PSYC620 Intervention and Behavior Support
CLINICAL HANDBOOK OF PSYCHOLOGICAL DISORDERS
Also from David H. Barlow
Anxiety and Its Disorders: The Nature and Treatment of Anxiety and Panic, Second Edition
David H. Barlow
Handbook of Assessment and Treatment Planning for Psychological Disorders, Third Edition
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Neuroticism: A New Framework for Emotional Disorders and Their Treatment
Shannon Sauer-Zavala and David H. Barlow
CLINICAL HANDBOOK OF PSYCHOLOGICAL DISORDERS A Step-by-Step Treatment Manual
S I X T H E D I T I O N
edited by
DAVID H. BARLOW
THE GUILFORD PRESS New York London
Copyright © 2021 The Guilford Press A Division of Guilford Publications, Inc. 370 Seventh Avenue, Suite 1200, New York, NY 10001 www.guilford.com
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The authors have checked with sources believed to be reliable in their efforts to provide information that is complete and generally in accord with the standards of practice that are accepted at the time of publication. However, in view of the possibility of human error or changes in behavioral, mental health, or medical sciences, neither the authors, nor the editors and publisher, nor any other party who has been involved in the preparation or publication of this work warrants that the information contained herein is in every respect accurate or complete, and they are not responsible for any errors or omissions or the results obtained from the use of such information. Readers are encouraged to confirm the information contained in this book with other sources.
Last digit is print number: 9 8 7 6 5 4 3 2 1
Library of Congress Cataloging-in-Publication Data
Names: Barlow, David H., editor. Title: Clinical handbook of psychological disorders : a step-by-step treatment manual / edited by David H. Barlow. Description: Sixth edition. | New York : The Guilford Press, [2021] | Includes bibliographical references and index. Identifiers: LCCN 2021014995 | ISBN 9781462547043 (hardcover) Subjects: LCSH: Behavior therapy—Handbooks, manuals, etc. | Medical protocols—Handbooks, manuals, etc. | BISAC: PSYCHOLOGY / Psychopathology / General | PSYCHOLOGY / Clinical Psychology Classification: LCC RC489.B4 C584 2021 | DDC 616.89/142—dc23 LC record available at https://lccn.loc.gov/2021014995
v
David H. Barlow, PhD, ABPP, is Professor Emeritus of Psychology and Psychiatry and Founder and Director Emeritus of the Center for Anxiety and Related Disorders at Boston University. Dr. Barlow has published over 650 articles and chapters and over 90 books and clinical manuals, primarily on the nature and treatment of emotional disorders and clini- cal research methodology. His books and manuals have been translated into more than 20 languages. Dr. Barlow’s numerous awards and citations include psychology’s three highest honors: the Distinguished Scientific Award for the Applications of Psychology from the American Psychological Association, the James McKeen Cattell Fellow Award from the Association for Psychological Science, and the Gold Medal Award for Life Achievement in the Practice of Psychology from the American Psychological Foundation.
About the Editor
vii
Idan M. Aderka, PhD, Department of Psychology, University of Haifa, Haifa, Israel
David H. Barlow, PhD, ABPP, Center for Anxiety and Related Disorders, Boston University, Boston, Massachusetts
Aaron T. Beck, MD, University of Pennsylvania Perelman School of Medicine and Beck Institute for Cognitive Behavior Therapy, Philadelphia, Pennsylvania
Kate H. Bentley, PhD, Department of Psychiatry, Massachusetts General Hospital/ Harvard Medical School, Boston, Massachusetts
Katherine Berry, PhD, Division of Psychology and Mental Health, University of Manchester, Manchester, United Kingdom
Kathryn L. Bleiberg, PhD, Department of Psychology, Weill Cornell Medicine, New York, New York
Kathleen M. Chard, PhD, Cincinnati VA Medical Center, Cincinnati, Ohio
Andrew Christensen, PhD, Department of Psychology, University of California, Los Angeles, Los Angeles, California
Zafra Cooper, DPhil, Department of Psychiatry, Yale School of Medicine, New Haven, Connecticut
Michelle G. Craske, PhD, Department of Psychology and Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, California
Sona Dimidjian, PhD, Renée Crown Wellness Institute and Department of Psychology and Neuroscience, University of Colorado Boulder, Boulder, Colorado
Brian D. Doss, PhD, Department of Psychology, University of Miami, Coral Gables, Florida
Kristen K. Ellard, PhD, Department of Psychiatry, Massachusetts General Hospital/ Harvard Medical School, Boston, Massachusetts
Contributors
viii Contributors
Elizabeth E. Epstein, PhD, Department of Psychiatry, University of Massachusetts Medical School, Worcester, Massachusetts
Elizabeth H. Eustis, PhD, Center for Anxiety and Related Disorders, Boston University, Boston, Massachusetts
Todd J. Farchione, PhD, Center for Anxiety and Related Disorders, Boston University, Boston, Massachusetts
Edna B. Foa, PhD, Center for the Treatment and Study of Anxiety, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania
Martin E. Franklin, PhD, Rogers Behavioral Health, Philadelphia, Pennsylvania
Allison G. Harvey, PhD, Department of Psychology, University of California, Berkeley, Berkeley, California
Sarah H. Heil, PhD, Vermont Center on Behavior and Health and Departments of Psychiatry and Psychological Science, University of Vermont, Burlington, Vermont
Ruth Herman‑Dunn, PhD, private practice and Department of Psychology, University of Washington, Seattle, Washington
Stephen T. Higgins, PhD, Vermont Center on Behavior and Health and Departments of Psychiatry and Psychological Science, University of Vermont, Burlington, Vermont
Stefan G. Hofmann, PhD, Center for Anxiety and Related Disorders, Boston University, Boston, Massachusetts
Samuel Hubley, PhD, Renée Crown Wellness Institute and Department of Psychology and Neuroscience, University of Colorado Boulder, Boulder, Colorado
Neil S. Jacobson, PhD (deceased), formerly of Department of Psychology, University of Washington, Seattle, Washington
Katherine A. Kaplan, PhD, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California
Marsha M. Linehan, PhD, ABPP, Department of Psychology, University of Washington, Seattle, Washington
Joseph S. Maimone, BA, Department of Psychology, Massachusetts General Hospital/ Harvard Medical School, Cambridge, Massachusetts
John C. Markowitz, MD, Department of Psychiatry, Columbia University Vagelos College of Physicians and Surgeons, New York State Psychiatric Institute, New York, New York
Christopher R. Martell, PhD, Department of Psychological and Brain Sciences, University of Massachusetts Amherst, Amherst, Massachusetts
Barbara S. McCrady, PhD, Center on Alcohol, Substance Use, and Addictions (CASAA) and Department of Psychology, The University of New Mexico, Albuquerque, Albuquerque, New Mexico
David J. Miklowitz, PhD, Max Gray Child and Adolescent Mood Disorders Program, Division of Child and Adolescent Psychiatry, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, Los Angeles, California
Contributors ix
Candice M. Monson, PhD, Department of Psychology, Ryerson University, Toronto, Ontario, Canada
Rebecca Murphy, DClinPsych, Department of Psychiatry, University of Oxford, Oxford, United Kingdom
Andrada D. Neacsiu, PhD, Cognitive Behavioral Research and Therapy Program, Department of Psychiatry and Behavioral Sciences, and Department of Family Medicine, Duke University Medical Center, Durham, North Carolina
Matthew K. Nock, PhD, Department of Psychology, Harvard University, Cambridge, Massachusetts
K. Maria Nylocks, PhD, Emory Healthcare Veterans Program, Emory University School of Medicine, Atlanta, Georgia
Susan M. Orsillo, PhD, Department of Psychology, Suffolk University, Boston, Massachusetts
John D. Otis, PhD, Center for Anxiety and Related Disorders, Boston University, Boston, Massachusetts
Laura A. Payne, PhD, Department of Psychiatry, McLean Hospital/Harvard Medical School, Belmont, Massachusetts
Kelly R. Peck, PhD, Vermont Center on Behavior and Health and Departments of Psychiatry and Psychological Science, University of Vermont, Burlington, Vermont
Lizabeth Roemer, PhD, Department of Psychology, University of Massachusetts Boston, Boston, Massachusetts
Jayne L. Rygh, PhD, private practice, New York, New York
Philippe Shnaider, PhD, Department of Psychiatry and Behavioral Neurosciences, McMaster University, Hamilton, Ontario, Canada
Nicholas Tarrier, PhD, FBPsS, FBA, Emeritus Professor, Department of Psychology, University of Manchester, Manchester, United Kingdom
Erin F. Ward-Ciesielski, PhD, Center for Anxiety and Related Disorders, Boston University, Boston, Massachusetts
Arthur D. Weinberger, PhD, formerly of Cognitive Therapy Center of New York, New York, New York
Jennifer G. Wheeler, PhD, Pacific Evaluation, Consultation, and Treatment Services, PLLC, Seattle, Washington
Kate Wolitzky-Taylor, PhD, Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, Los Angeles, California
Jeffrey E. Young, PhD, Schema Therapy Institute, New York, New York
Noga Zerubavel, PhD, Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina
xi
Evidence-based practice (EBP) is one of those ideas that comes along occasionally and takes the world by storm. Although some of the tenets of EBP have been around for
decades (as has this handbook), it is only in the past 20 years that EBP has been formally identified as a systematic method of delivering clinical care (Institute of Medicine, 2001; Sackett, Strauss, Richardson, Rosenberg, & Haynes, 2000).
Since that time, the “tipping point” (Gladwell, 2000) for EBP has clearly occurred, and health care policymakers and governments, as well as professional societies around the world, have collectively decided that the delivery of health care, including behavioral health care, should be based on evidence (e.g., Silverman et al., 2015; American Psycho- logical Association, 2015; Barlow, 2004; Institute of Medicine, 2015; McHugh & Barlow, 2010). Fulfilling this mandate is the goal of EBP, and has also been the goal of this book since the first edition was published in 1985, and almost all clinical practice guidelines from leading behavioral health care delivery systems worldwide recommend treatment pro- tocols described in this book. This includes the Veterans Health Administration (www. healthquality.va.gov) and the National Institute for Health and Care Excellence within the National Health Service in the United Kingdom (www.nice.org.uk/guidance).
The sixth edition of this handbook continues to represent a distinct departure from any number of similar books reviewing advances in the treatment of psychological disor- ders from the perspective of EBP. Over the past two decades, we have developed a technol- ogy of behavior change that necessarily differs from disorder to disorder (and increasingly for classes of disorders).
This technology comprises a variety of techniques or procedures with more or less proven effectiveness for specific presentations of psychopathology. Naturally, we have more evidence of the effectiveness of these treatments for some disorders than for others. It also has become more apparent since the earlier editions that considerable clinical skill is required to apply this technology most effectively. Therefore, this handbook, in its sixth edition, is not another review of therapeutic procedures for a given problem, with recom- mendations for further research. Rather, it is a detailed description of actual treatment protocols in which experienced clinicians implement the technology of behavior change in the context of the most frequently encountered disorders or classes of disorders.
Preface
xii Preface
In this edition, the originators of some of the best-known treatment protocols have revised and updated the descriptions of their interventions to reflect the latest develop- ments in an increasingly powerful array of psychological therapies. Among these revisions to existing chapters, several deserve comment. Monson, Shnaider, and Chard (Chapter 2) have updated their chapter on posttraumatic stress disorder, describing the tragic case of a soldier fresh from the battlefields of Iraq. Their successful treatment of this individual suffering from the unspeakable (and intolerable) trauma of war is one consequence of today’s headline news stories that seldom makes it into print. Drug abuse continues as a scourge that ruins individual lives, the functioning of families, and the very fabric of soci- ety. Higgins, Heil, and Peck (Chapter 15) present the latest iterations of their approach, with a focus in this edition on the scourge of opiate abuse. Chapters on schizophrenia and other psychotic disorders, borderline personality disorder, bipolar disorder, and a number of anxiety disorders, along with depression, written in almost all cases by the originators of these leading protocols, have been updated considerably to reflect the latest evidence for the most effective approaches to these common but debilitating problems.
In addition, three original treatment protocols make their appearance for the first time in this edition. Chronic pain is the most common and most costly single disorder pre- senting to health care systems, easily outranking cancer, cardiovascular disease, and every other psychological disorder in this book. Brief psychological treatments for chronic pain are the first-line treatment, and the protocol in this book by Otis (Chapter 17), one of the leading investigators and clinicians in this area, reflects decades of research and refinement and is one of the success stories in EBP.
Self-injurious thoughts and behaviors (SITBs) have attracted increasing attention from health care policymakers and delivery systems as a broad area of concern associated with many different disorders, and on occasion occurring independently of additional psy- chopathology. With suicide rates alone climbing since 2010, the application of a transdiag- nostic protocol targeting this class of behaviors originated by Bentley, Maimone, and Nock (Chapter 11), leading investigators from Harvard and Massachusetts General Hospital, is a welcome addition to this book.
Also making a first appearance in this edition are Aderka and Hofmann (Chapter 3), illustrating a newer cognitive-behavioral intervention called “process-based therapy.” This third-wave approach, originated by Hayes and Hofmann (2018), goes beyond the static DSM approach to diagnosis and more standardized treatment protocols by emphasizing a very idiographic or individual approach to assessment and treatment in the specific context of the patient, along with continual processing and feedback. This intervention is nicely illustrated in the assessment and treatment of the case of “Mark,” suffering from social anxiety disorder.
Finally, there is growing consensus that the future of EBP will be to distill principles of effective change that cut across diagnostic conditions, making them more generally applicable. Two of these “unified” or “transdiagnostic” protocols appear in this sixth edi- tion. In Chapter 6 (Payne, Ellard, Farchione, & Barlow), we present our own unified trans- diagnostic approach to emotional disorders. Cooper and Murphy (Chapter 18) describe a transdiagnostic approach to eating disorders that they originated in collaboration with their colleagues.
In all chapters, the nuts and bolts of clinical application are emphasized. As with the previous editions, this book was motivated by countless clinical psychology graduate stu-
Preface xiii
dents, psychiatric residents, and other mental health professionals, either in training or in practice, asking, “But how do I do it?” Realizing that there is no single source in which to find step-by-step treatment protocols for use as a guide to practice, this book attempts to fill the void. To accomplish this purpose, a number of specific topics are common to most chapters. Each chapter begins with a brief review of our knowledge of the specific disorder (or class of disorders), followed by a description of the particular model or mini-theory that guides the technology utilized with the disorder in question. This model, or mini-theory, typically answers the question What particular facets of the disorder should be assessed and treated? While clinical application always dilutes theoretical models, clinicians will recognize cognitive-behavioral and systems approaches, with some psychodynamic contri- butions, as the predominant theoretical context.
This model is followed by a description of the typical setting in which the treatment is carried out. The setting varies from disorder to disorder, ranging from the more usual office setting to the home environment of the patient. Authors provide similar detailed descriptions of the social context of treatment (e.g., the importance of the involvement of family or friends) as well as therapist and client variables that are important within the con- text of the particular problem. For example, therapist variables that may be important in implementing techniques for treatment of agoraphobia or couple distress are described. In addition, authors discuss the implications for treatment of client variables, such as depen- dency and unassertiveness in individuals with panic disorder with agoraphobia.
A detailed description of the actual step-by-step process of assessment and treatment follows, liberally sprinkled in many chapters with transcripts of therapy sessions. Important components of this process are the specifics of the rationale given to the patient before treat- ment, as well as typical problems that arise during the implementation of the technology. Where data exist, authors provide information on clinical predictors of success or failure.
In accomplishing the rather ambitious goals just described, I was very fortunate in this edition of the book, as in previous editions, to have leading clinicians and researchers document in some detail how they actually treat their patients. Once again, these authori- ties reported that the number of details they had to include in order to convey how they actually applied their treatment programs went far beyond their expectations. My hope is that practicing clinicians and clinical students everywhere will benefit from acquaintance with these details.
In closing, I would like to express my deep appreciation to Bethany Harris, my research and administrative assistant during the editing of this book. She worked with me and the authors every step of the way. I am sure this information will come in handy as she is now pursuing her own doctorate in clinical psychology.
REFERENCES
American Psychological Association. (2015). Professional practice guidelines: Guidance for developers and users. American Psychologist, 70(9), 823–831.
Barlow, D. H. (2004). Psychological treatments. American Psychologist, 59(9), 869–878. Gladwell, M. (2000). The tipping point: How little things can make a big difference. Boston: Little,
Brown. Hayes, S. C., & Hofmann, S. G. (Eds.). (2018). Process-based CBT: The science and core clinical compe-
tencies of cognitive behavioral therapy. Oakland, CA: New Harbinger.
xiv Preface
Institute of Medicine. (2001). Crossing the quality chasm: A new health system for the 21st century. Wash- ington, DC: National Academies Press.
Institute of Medicine. (2015). Psychosocial interventions for mental and substance use disorders: A frame- work for establishing evidence-based standards. Washington, DC: National Academies Press.
McHugh, R. K., & Barlow, D. H. (2010). Dissemination and implementation of evidence-based psy- chological interventions: A review of current efforts. American Psychologist, 65(2), 73–84.
Sackett, D. L., Strauss, S. E., Richardson, W. S., Rosenberg, W., & Haynes, R. B. (2000). Evidence- based medicine: How to practice and teach EBM (2nd ed.). London: Churchill Livingstone.
Silverman, J. J., Galanter, M., Jackson-Triche, M., Jacobs, D. G., Lomax, J. W., Riba, M. B., et al. (2015). The American Psychiatric Association Practice Guidelines for the Psychiatric Evaluation of Adults. American Journal of Psychiatry, 172(8), 798–802.
xv
1. Panic Disorder and Agoraphobia 1 Michelle G. Craske, Kate Wolitzky‑Taylor, and David H. Barlow
2. Posttraumatic Stress Disorder 64 Candice M. Monson, Philippe Shnaider, and Kathleen M. Chard
3. Social Anxiety: A Process‑Based Treatment Approach 108 Idan M. Aderka and Stefan G. Hofmann
4. Obsessive–Compulsive Disorder 133 Martin E. Franklin and Edna B. Foa
5. Generalized Anxiety Disorder: An Acceptance‑Based 184 Behavioral Therapy Lizabeth Roemer, Elizabeth H. Eustis, and Susan M. Orsillo
6. Emotional Disorders: A Unified Protocol 217 for Transdiagnostic Treatment Laura A. Payne, Kristen K. Ellard, Todd J. Farchione, and David H. Barlow
Contents
xvi Contents
7. Cognitive Therapy for Depression 257 Jeffrey E. Young, Erin F. Ward‑Ciesielski, Jayne L. Rygh, Arthur D. Weinberger, and Aaron T. Beck
8. Interpersonal Psychotherapy for Depression 317 Kathryn L. Bleiberg and John C. Markowitz
9. Behavioral Activation for Depression 339 Sona Dimidjian, Christopher R. Martell, Ruth Herman‑Dunn, and Samuel Hubley
10. Borderline Personality Disorder 381 Andrada D. Neacsiu, Noga Zerubavel, K. Maria Nylocks, and Marsha M. Linehan
11. Addressing Self‑Injurious Thoughts and Behaviors 443 within the Context of Transdiagnostic Treatment for Emotional Disorders Kate H. Bentley, Joseph S. Maimone, and Matthew K. Nock
12. Bipolar Disorder 480 David J. Miklowitz
13. Schizophrenia and Other Psychotic Disorders 522 Nicholas Tarrier and Katherine Berry
14. Alcohol Use Disorders 555 Barbara S. McCrady and Elizabeth E. Epstein
15. Substance Use Disorders 612 Stephen T. Higgins, Sarah H. Heil, and Kelly R. Peck
16. Treatment of Sleep Disturbance 638 Katherine A. Kaplan and Allison G. Harvey
17. Cognitive‑Behavioral Therapy for Chronic Pain 670 John D. Otis
Contents xvii
18. Eating Disorders: A Transdiagnostic Protocol 705 Zafra Cooper and Rebecca Murphy
19. Couple Distress 742 Andrew Christensen, Jennifer G. Wheeler, Brian D. Doss, and Neil S. Jacobson
Author Index 773
Subject Index 799
1
The treatment protocol described in this chapter represents one of the success stories in the devel- opment of evidence-based psychological treatments. Results from numerous studies indicate that this approach provides substantial advantages over placebo medication or alternative psychosocial approaches containing “common” factors, such as positive expectancies and helpful therapeutic alli- ances. In addition, this treatment forms an important part of every clinical practice guideline in either public health or other sources from countries around the world, describing effective treatments for panic disorder and agoraphobia. Results from numerous studies evaluating this treatment protocol, both individually and in combination with leading pharmacological approaches, suggest that this approach is equally effective as the best pharmacological approaches in the short term and more durable over the long term. But this treatment protocol has not stood still. For example, we have learned a great deal in recent years about neurobiological mechanisms of action in fear reduction, and the best psychological methods for effecting these changes, particularly strategies for optimizing inhibitory learning and retrieval. Newly developed acceptance-based procedures have also proven efficacious. In this chapter we present the latest version of this protocol, incorporating these changes and additions, all as illustrated in a comprehensive account of the treatment of “Julie.” —D. H. B.
Advances continue in the development of biopsycho- social models and cognitive-behavioral treatments
for panic disorder and agoraphobia. The conceptu- alization of panic disorder as an acquired fear of cer- tain bodily sensations, and agoraphobia as a behavioral response to the anticipation of related bodily sensa- tions or their crescendo into a full-blown panic attack, continues to be supported by experimental, clinical, and longitudinal research. Furthermore, the efficacy of cognitive-behavioral treatments that target fear of bodily sensations and associated agoraphobic situations is well established. In addition to presenting an up-to- date review of treatment outcome data, this chapter covers recent theoretical and empirical developments in reference to etiological factors, the role of comorbid diagnoses in treatment, ways to optimize learning dur-
ing exposure therapy, and the effect of medication on cognitive-behavioral treatments. The chapter concludes with a detailed, session-by-session outline of cognitive- behavioral treatment for panic disorder and agorapho- bia. This protocol has been developed in our clinics; the full protocol is detailed in available treatment manuals (Barlow & Craske, 2007; Craske & Barlow, 2007).
NATURE OF PANIC AND AGORAPHOBIA
Panic Attacks
Panic attacks are discrete episodes of intense fear or dis- comfort, accompanied by physical and cognitive symp- toms, as listed in the DSM-5 panic attack checklist (American Psychiatric Association, 2013). Panic attacks
C H A P T E R 1
Panic Disorder and Agoraphobia
Michelle G. Craske Kate Wolitzky‑Taylor David H. Barlow
2 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
are discrete by virtue of their sudden or abrupt onset and brief duration, as opposed to gradually building anxious arousal. Panic attacks in panic disorder often have an unexpected quality, which means that from the patient’s perspective, they appear to happen without an obvious trigger or at unexpected times. Indeed, the diagnosis of panic disorder is defined by recurrent “un- expected” panic attacks, followed by at least 1 month of persistent concern about their recurrence and their consequences, or by a significant change in behavior consequent to the attacks (American Psychiatric Asso- ciation, 2013).
As with all basic emotions (Izard, 1992), panic at- tacks are associated with strong action tendencies: Most often, these are urges to escape, and less often, urges to fight. These fight or flight tendencies usually involve elevated autonomic nervous system arousal needed to support such fight–flight reactivity. Furthermore, per- ceptions of imminent threat or danger, such as death, loss of control, or social ridicule, often accompany such fight–flight reactivity. However, the features of urgency to escape, autonomic arousal, and perception of threat are not present in every self-reported occurrence of panic. For example, despite evidence for elevated heart rate or other indices of sympathetic nervous system acti- vation during panic attacks on average (e.g., Wilkinson et al., 1998), Margraf, Taylor, Ehlers, Roth, and Agras (1987) found that 40% of self-reported panic attacks were not associated with accelerated heart rate. More- over, in general, patients with panic disorder are more likely than nonanxious controls to report arrhythmic heart rate in the absence of actual arrhythmias (Barsky, Cleary, Sarnie, & Ruskin, 1994). Heightened anxiety about signs of autonomic arousal may lead patients to perceive cardiac events when none exist (Barlow, Brown, & Craske, 1994; Craske & Tsao, 1999). We believe that self-reported panic in the absence of heart rate accel- eration or other indices of autonomic activation reflects anticipatory anxiety rather than true panic (Barlow et al., 1994), especially because more severe panic attacks are more consistently associated with accelerated heart rate (Margraf et al., 1987). Sometimes individuals re- port intense abrupt fear in the absence of perceptions of threat or danger. This has been termed noncognitive panic (Rachman, Lopatka, & Levitt, 1988; see Kircan- ski, Craske, Epstein, & Wittchen, 2009). Finally, the urgency to escape is sometimes weakened by situational demands for continued approach and endurance, such as performance expectations or job demands, thus cre-
ating discordance between behavioral responses on the one hand, and verbal or physiological fear responses on the other.
A subset of individuals with panic disorder experi- ence nocturnal panic attacks. Nocturnal panic refers to waking from sleep in a state of panic, with symptoms that are very similar to panic attacks during wakeful states (Craske & Barlow, 1989; Uhde, 1994). Noctur- nal panic does not refer to waking from sleep and pan- icking after a lapse of waking time, or nighttime arous- als induced by nightmares or environmental stimuli (e.g., unexpected noises). Instead, nocturnal panic is an abrupt waking from sleep in a state of panic, without an obvious trigger. Nocturnal panic attacks reportedly most often occur between 1 and 3 hours after sleep onset, and only occasionally more than once per night (Craske & Barlow, 1989). Surveys of select clinical groups suggest that nocturnal panic is relatively com- mon among individuals with panic disorder: 44–71% report having experienced nocturnal panic at least once, and 30–45% report repeated nocturnal pan- ics (Craske & Barlow, 1989; Krystal, Woods, Hill, & Charney, 1991; Mellman & Uhde, 1989; Roy-Byrne, Mellman, & Uhde, 1988; Uhde, 1994). Individuals who suffer frequent nocturnal panic often become fearful of sleep and attempt to delay sleep onset. Avoid- ance of sleep may result in chronic sleep deprivation, which in turn precipitates more nocturnal panic inci- dents (Uhde, 1994).
“Nonclinical” panic attacks occur occasionally in ap- proximately 3–5% of people in the general population who do not otherwise meet criteria for panic disorder (Norton, Cox, & Malan, 1992). Also, panic attacks occur across a variety of anxiety and mood disorders (Barlow et al., 1985), as well as substance use, personal- ity disorders and psychoses (Craske et al., 2010) and are not limited to panic disorder. Indeed, the ubiquity of panic attacks has been emphasized in DSM-5 (Ameri- can Psychiatric Association, 2013), in which panic attacks are designated as a potential specifier for any DSM disorder. As stated earlier, the defining feature of panic disorder is not the presence of panic attacks per se, but involves additional anxiety about the recurrence of panic or its consequences, or a significant behavioral change because of the panic attacks. It is the additional anxiety about panic combined with catastrophic cogni- tions in the face of panic that differentiate between the person with panic disorder and the occasional nonclini- cal panicker (e.g., Telch, Lucas, & Nelson, 1989) or the
Panic Disorder and Agoraphobia 3
person with other anxiety disorders who also happens to panic. The following scenario exemplifies the latter point.
PATIENT: Sometimes I lay awake at night thinking about a million different things. I think about what is going to happen to my daughter if I get sick. Who will look after her, or what would happen if my hus- band died and we didn’t have enough money to give my daughter a good education? Then I think about where we would live and how we would cope. Some- times I can work myself up so much that my heart starts to race, my hands get sweaty, and I feel dizzy and scared. So I have to stop myself from thinking about all those things. I usually get out of bed and turn on the TV—anything to get my mind off the worries.
THERAPIST: Do you worry about the feelings of a rac- ing heart, sweating, and dizziness happening again?
PATIENT: No. They’re unpleasant, but they are the least of my concerns. I am more worried about my daugh- ter and our future.
This scenario illustrates the experience of panic that is not the central focus of the person’s anxiety. More likely, this woman has generalized anxiety disorder, and her uncontrollable worry leads her to panic on occa- sion. The next example is someone with social anxiety disorder, who becomes very concerned about panicking in social situations, because the possibility of a panic attack increases her concerns about being judged nega- tively by others.
PATIENT: I am terrified of having a panic attack in meetings at work. I dread the thought of others no- ticing how anxious I am. They must be able to see my hands shaking, the sweat on my forehead, and worst of all, my face turning red.
THERAPIST: What worries you most about others notic- ing your physical symptoms?
PATIENT: That they will think that I am weird or strange.
THERAPIST: Would you be anxious in the meetings if the panic attacks were gone?
PATIENT: I would still be worried about doing or saying the wrong thing. It is not just the panic attacks that worry me.
THERAPIST: Are you worried about panic attacks in any other situations?
PATIENT: Formal social events and sometimes when I meet someone for the first time.
In this case, even though the patient experiences panic attacks, the real concern is about being judged negatively by others consequent to panic attacks, and the panic attacks do not occur in situations other than social ones. Hence, this presentation is most aptly de- scribed as social anxiety.
Agoraphobia
Agoraphobia refers to avoidance or endurance with dread of situations from which escape might be diffi- cult or when help is unavailable in the event of a panic- like symptoms (including but not limited to panic at- tacks) or other incapacitating symptoms, such as loss of bowel control or vomiting, disorientation (especially in children), or sense of falling (especially in older adults) (American Psychiatric Association, 2013). Typical ago- raphobic situations include shopping malls, waiting in line, movie theaters, traveling by car or bus, crowded restaurants, and being alone. “Mild” agoraphobia is exemplified by the person who hesitates about driving long distances alone but manages to drive to and from work, prefers to sit on the aisle at movie theaters but still goes to movies, and avoids crowded places. “Moderate” agoraphobia is exemplified by the person whose driving is limited to a 10-mile radius from home and only if accompanied, who shops at off-peak times and avoids large supermarkets, and who avoids flying or travel- ing by train. “Severe” agoraphobia refers to very lim- ited mobility, sometimes even to the point of becoming housebound.
Relationship between Panic and Agoraphobia
The relationship between panic and agoraphobia is complex. On the one hand, not all persons who panic develop agoraphobia, and the extent of agoraphobia that emerges is highly variable (Craske & Barlow, 1988). Various factors have been investigated as potential pre- dictors of agoraphobia. Although agoraphobia tends to increase as history of panic lengthens, a significant proportion of individuals panic for many years without developing agoraphobic limitations. Nor is agorapho-
4 CliniCal Handbook of PsyCHologiCal disorders
bia related to age of onset or frequency of panic (Cox, Endler, & Swinson, 1995; Craske & Barlow, 1988; Kikuchi et al., 2005; Rapee & Murrell, 1988). Some studies report more intense physical symptoms during panic attacks when there is more agoraphobia (e.g., de Jong & Bouman, 1995; Goisman et al., 1994; Noyes, Clancy, Garvey, & Anderson, 1987; Telch, Brouillard, Telch, Agras, & Taylor, 1989). Others fail to find such differences (e.g., Cox et al., 1995; Craske, Miller, Ro- tunda, & Barlow, 1990). On the one hand, fears of dying, going crazy, or losing control do not relate to level of agoraphobia (Cox et al., 1995; Craske, Rapee, & Barlow, 1988). On the other hand, concerns about social consequences of panicking may be stronger when there is more agoraphobia (Amering et al., 1997; de Jong & Bouman, 1995; Rapee & Murrell, 1988; Telch, Brouilard, et al., 1989). In addition, Kikuchi and col- leagues (2005) found that individuals who develop agoraphobia within 6 months of the onset of panic dis- order have a higher prevalence of generalized anxiety disorder but not major depression. However, whether social evaluation concerns or comorbidity are precur- sors or are secondary to agoraphobia remains to be de- termined. Occupational status also predicts agorapho- bia, accounting for 18% of the variance in one study (de Jong & Bouman, 1995). Perhaps the strongest predictor of agoraphobia is sex; the ratio of males to females shifts dramatically in the direction of female predominance as level of agoraphobia worsens (e.g., Thyer, Himle, Curtis, Cameron, & Nesse, 1985).
On the other hand, not everyone with agoraphobia has a history of panic attacks or even panic-like symp- toms, although a history of panic is much more com- mon in treatment-seeking samples of individuals with agoraphobia than in epidemiological samples (Witt- chen, Gloster, Beesdo-Baum, Fava, & Craske, 2010). Nonetheless, the prevalence of agoraphobia without a history of panic disorder, panic attacks, or panic-like symptoms was reported to be at least as high as the combined rates of panic disorder with and without agoraphobia across all epidemiological studies (Witt- chen et al., 2010). Approximately 50% of individuals from community samples who endorse agoraphobia do not endorse panic attacks. Furthermore, agoraphobia without panic-like features appears to be as impairing as panic disorder without agoraphobia, although the combination is usually associated with even more im- pairment. In addition, some differences exist between them in terms of incidence, comorbidity, and response to treatment (Wittchen et al., 2010). For these reasons,
panic disorder and agoraphobia are now recognized as two distinct, albeit highly comorbid, disorders in DSM-5 (American Psychiatric Association, 2013).
PRESENTING FEATURES
From the latest epidemiological study in the United States, the National Comorbidity Survey Replication (NCS-R; Kessler, Berglund, Demler, Jin, & Walters, 2005; Kessler, Chiu, Demler, & Walters, 2005), 12- month prevalence estimates for panic disorder are ap- proximately 2% in adults and adolescents. Lower esti- mates have been reported for some Asian, African, and Latin American countries, ranging from 0.1 to 0.8% (Lewis-Fernandez et al., 2010). However, a recent mul- tinational epidemiological study of individuals in 25 countries reported a similar lifetime prevalence esti- mate of 1.7% (de Jonge et al., 2016). The 12-month rates for agoraphobia are approximately 1.7%, and the lifetime morbid risk is 3.7% (Kessler, Petukhova, Sampson, Zaslavsky, & Wittchen, 2012).
The modal age of onset for panic disorder is late teen- age years and early adulthood (Kessler, Berglund, et al., 2005). In fact, although panic disorder is rare below the age of 14, a substantial proportion of adolescents report panic attacks (e.g., Hayward et al., 1992), and panic disorder in children and adolescents tends to be chronic and comorbid with other anxiety, mood, and disrup- tive disorders (Biederman, Faraone, Marrs, & Moore, 1997). Treatment is usually sought much later, around age 34 (e.g., Noyes et al., 1986). Similarly, agorapho- bia may occur in childhood, but the incidence peaks in late adolescence and early adulthood (Beesdo, Knappe, & Pine, 2007; Bittner et al., 2007); the mean age of onset is 17 years (Kessler et al., 2012), and older in the absence of history of panic disorder or panic attacks. Rates of panic disorder decline in older adults, possi- bly diminishing to subclinical levels (Wolitzky-Taylor, Castriotti, Lenze, Stanley, & Craske, 2010). Similarly, 12-month prevalence rates for agoraphobia reduce to 0.4% in individuals over the age of 65 years (Kessler et al., 2006). The overall ratio of females to males is ap- proximately 2:1 (Kessler et al., 2006) and, as mentioned already, the ratio shifts dramatically in the direction of female predominance as level of agoraphobia worsens (e.g., Thyer et al., 1985).
Rarely do the diagnoses of panic disorder or agoraphobia occur in isolation. Indeed, a multinational epidemiological study found that 80.2% of individu-
Panic Disorder and Agoraphobia 5
als who met lifetime diagnostic criteria for panic dis- order had another lifetime comorbid mental disorder (de Jonge et al., 2016). Commonly co-occurring Axis I conditions included specific phobias, social phobia, dysthymia, generalized anxiety disorder, major depres- sive disorder, and substance abuse (e.g., Brown, Camp- bell, Lehman, Grishman, & Mancill, 2001; Goisman, Goldenberg, Vasile, & Keller, 1995; Kessler, Chiu, et al., 2005). Also, 25–60% of persons with panic disor- der also meet criteria for a personality disorder, mostly avoidant and dependent personality disorders (e.g., Chambless & Renneberg, 1988). However, the nature of the relationship with personality disorders remains unclear. For example, comorbidity rates were highly dependent on the method used to establish Axis II di- agnosis, as well as the co-occurrence of depressed mood (Alneas & Torgersen, 1990; Chambless & Renneberg, 1988). Moreover, the fact that abnormal personal- ity traits improve and some “personality disorders” even remit after successful treatment of panic disorder (Black, Monahan, Wesner, Gabel, & Bowers, 1996; Mavissakalian & Hamman, 1987; Noyes, Reich, Suel- zer, & Christiansen, 1991) raises questions about the validity of Axis II diagnoses. The issue of comorbidity with personality disorders and its effect on treatment for panic disorder and agoraphobia is described in more detail in a later section.
Finally, panic disorder and agoraphobia tend to be chronic conditions, with severe financial and inter- personal costs (Wittchen et al., 2010). Only a minor- ity of untreated individuals remit without subsequent relapse within a few years if not treated (Emmelkamp & Wittchen, 2009; Katschnig & Amering, 1998; Roy- Byrne & Cowley, 1995). Also, individuals with panic disorder overutilize medical resources compared to the general public and individuals with other “psychiatric” disorders (e.g., Katon et al., 1990; Roy-Byrne et al., 1999).
HISTORY OF PSYCHOLOGICAL TREATMENT FOR PANIC DISORDER AND AGORAPHOBIA
It was not until the publication of DSM-III (Ameri- can Psychiatric Association, 1980) that panic disorder with or without agoraphobia was recognized as a dis- tinct anxiety problem. Until that time, panic attacks were viewed primarily as a form of free-floating anxi- ety. Consequently, psychological treatment approaches were relatively nonspecific. They included relaxation
and cognitive restructuring for stressful life events in general (e.g., Barlow, O’Brien, & Last, 1984). Many presumed that pharmacotherapy was necessary for the control of panic. In contrast, the treatment of agora- phobia was quite specific from the 1970s onward, with primarily exposure-based approaches to target fear and avoidance of specific situations. However, relatively little consideration was given to panic attacks in either the conceptualization or treatment of agoraphobia. The development of specific panic control treatments in the middle to late 1980s shifted interest away from agoraphobia. Interest in agoraphobia was subsequently renewed, specifically in terms of whether panic control treatments are sufficient for the management of agora- phobia, and whether their combination with treatments that directly target agoraphobia is superior overall. We address these questions in more detail after describing the conceptualization that underlies cognitive-behav- ioral approaches to the treatment of panic and agora- phobia.
CONCEPTUALIZATION OF ETIOLOGICAL AND MAINTAINING FACTORS FOR PANIC DISORDER AND AGORAPHOBIA
Several independent lines of research (Barlow, 1988; Clark, 1986; Ehlers & Margraf, 1989) converged in the 1980s on the same basic conceptualization of panic disorder as an acquired anxiety focused on bodily sensations, particularly sensations associated with au- tonomic arousal. Psychological and biological predis- positions are believed to enhance the vulnerability to acquire such anxiety. These interacting vulnerabilities have been organized into an etiological conception of anxiety disorders in general, referred to as “triple vul- nerability theory” (Barlow, 1988, 2002; Barlow, Ellard, Sauer-Zavala, Bullis, & Carl, 2014; Suárez, Bennett, Goldstein, & Barlow, 2008). First, genetic contribu- tions to the development of anxiety and negative affect constitute a generalized (heritable) biological vulnera- bility. Second, evidence supports a generalized psycho- logical vulnerability to experience anxiety and related negative affective states, characterized by a diminished sense of control arising from early developmental ex- periences. Although the unfortunate co-occurrence of generalized biological and psychological vulnerabilities may be sufficient to produce anxiety and related states, particularly generalized anxiety disorder and depres- sion, and perhaps, neuroticism itself, a third vulnerabil-
6 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
ity seems necessary to account for the development of at least some specific anxiety disorders, including panic disorder; that is, early learning experiences in some instances seem to focus anxiety on particular areas of concern. In panic disorder, the experience of certain so- matic sensations becomes associated with a heightened sense of threat and danger. This specific psychological vulnerability, when coordinated with the generalized biological and psychological vulnerabilities mentioned earlier, seems to contribute to the development of panic disorder. Fear conditioning, avoidant responding, and information-processing biases are believed to perpetu- ate such fear. It is the perpetuating factors that are tar- geted in the cognitive-behavioral treatment approach. What follows is a very brief review of some contributory factors with practical relevance for panic disorder.
Vulnerability Factors
Genetics and Temperament
The temperament most associated with anxiety disor- ders, including panic disorder, is neuroticism (Eysenck, 1967; Gray, 1982), or proneness to experience negative emotions in response to stressors. A closely linked con- struct, negative affectivity, is the tendency to experience a variety of negative emotions across a variety of situa- tions, even in the absence of objective stressors (Wat- son & Clark, 1984). Structural analyses confirm that negative affect/neuroticism is a higher-order factor that distinguishes individuals with each anxiety disorder (and depression) from controls with no mental disor- der: Lower-order factors discriminate among anxiety disorders, with “fear of fear” (more accurately, anxiety focused on somatic symptoms of the emotion of fear) being the factor that discriminates panic disorder from other anxiety disorders (Brown, Chorpita, & Barlow, 1998; Prenoveau et al., 2010; Zinbarg & Barlow, 1996). The anxiety disorders load differentially on negative af- fectivity, with more pervasive anxiety disorders, such as generalized anxiety disorder, loading more heavily, panic disorder loading at an intermediate level, and social anxiety disorder loading the least (Brown et al., 1998).1 However, these findings derive from cross- sectional datasets.
Longitudinal prospective evidence for the role of neuroticism in predicting the onset of panic disorder is relatively limited. Specifically, neuroticism predicted the onset of panic attacks in adolescents (Hayward, Killen, Kraemer, & Taylor, 2000; Schmidt, Lerew, &
Jackson, 1997, 1999), and “emotional reactivity” at age 3 was a significant variable in the classification of panic disorder in 18- to 21-year-old males (Craske, Poulton, Tsao, & Plotkin, 2001).
Numerous multivariate genetic analyses of human twin samples consistently attribute approximately 30–50% of variance in neuroticism to additive genetic factors (Barlow, Ellard, et al., 2014; Eley, 2001; Lake, Eaves, Maes, Heath, & Martin, 2000). In addition, anxiety and depression appear to be variable expressions of the heritable tendency toward neuroticism (Kendler, Heath, Martin, & Eaves, 1987). Symptoms of panic (i.e., breathlessness, heart pounding) may be addition- ally explained by a unique source of genetic variance that is differentiated from symptoms of depression and anxiety (Kendler et al., 1987) and neuroticism (Martin, Jardine, Andrews, & Heath, 1988).
Analyses of specific genetic markers remain prelimi- nary and inconsistent. For example, panic disorder has been linked to a locus on chromosome 13 (Hamilton et al., 2003; Schumacher et al., 2005) and chromo- some 9 (Thorgeirsson et al., 2003), but the exact genes remain unknown. Findings regarding markers for the cholecystokinin B receptor gene have been inconsistent (cf. Hamilton et al., 2001; van Megen, Westenberg, Den Boer, & Kahn, 1996). Also, association and link- age studies implicate the adenosine receptor gene in panic disorder (Deckert et al., 1998; Hamilton et al., 2004). An allele of the neuropeptide S receptor gene on chromosome 7 was linked in a male-specific manner to panic disorder and not to schizophrenia or atten- tion deficit disorder (Okamura et al., 2011), whereas the same gene was linked in a female-specific man- ner to panic disorder compared to healthy controls ( Domschke et al., 2011). Thus, at this stage, the re- sults are rather piecemeal and sometimes inconsistent, and there is no evidence at this point for a specific link between genetic markers and temperament on the one hand, and panic disorder on the other. Rather, neuro- biological factors seem to comprise a nonspecific bio- logical vulnerability.
Anxiety Sensitivity
As described earlier, neuroticism is viewed as a higher- order factor characteristic of all anxiety disorders, with “fear of fear” being more unique to panic disorder. The construct “fear of fear” overlaps with the construct “anxiety sensitivity,” or the belief that anxiety and its associated symptoms may cause deleterious physical,
Panic Disorder and Agoraphobia 7
social, and psychological consequences that extend beyond any immediate physical discomfort during an episode of anxiety or panic (Reiss, 1980). Anxiety sen- sitivity is elevated across most anxiety disorders, but it is particularly elevated in panic disorder (e.g., Taylor, Koch, & McNally, 1992; Zinbarg & Barlow, 1996; Olatunji & Wolitzky-Taylor, 2009), especially the Phys- ical Concerns subscale of the Anxiety Sensitivity Index (Barlow, Sauer-Zavala, Carl, Bullis, & Ellard, 2014; Zinbarg & Barlow, 1996; Zinbarg, Barlow, & Brown, 1997). Therefore, beliefs that physical symptoms of anxiety are harmful seem to be particularly relevant to panic disorder and may comprise a specific psychologi- cal vulnerability.
Anxiety sensitivity is presumed to confer a risk factor for panic disorder, because it primes fear reactivity to bodily sensations. In support, anxiety sensitivity pre- dicts subjective distress and reported symptomatology in response to procedures that induce strong physical sensations, such as CO2 inhalation (Forsyth, Palav, & Duff, 1999), balloon inflation (Messenger & Shean, 1998), and hyperventilation (Sturges, Goetsch, Ridley, & Whittal, 1998) in nonclinical samples, even after re- searchers control for the effects of trait anxiety (Rapee & Medoro, 1994). In addition, several longitudinal studies indicate that high scores on the Anxiety Sensi- tivity Index predict the onset of panic attacks over 1- to 4-year intervals in adolescents (Hayward et al., 2000), college students (Maller & Reiss, 1992), and commu- nity samples with specific phobias or no anxiety disor- ders (Ehlers, 1995). The predictive relationship remains after researchers control for prior depression (Hayward et al., 2000). In addition, Anxiety Sensitivity Index scores predicted spontaneous panic attacks and worry about panic (and anxiety more generally), during an acute military stressor (i.e., 5 weeks of basic training), even after researchers control for history of panic at- tacks and trait anxiety (Schmidt et al., 1997, 1999), and Anxiety Sensitivity Index scores predicted spontaneous panic attacks (and anxiety disorder diagnoses) in a non- clinical adult sample over a 2-year longitudinal period (Schmidt, Zvolensky, & Maner, 2006). Finally, panic attacks themselves elevated anxiety sensitivity over a 5-week period in adults (Schmidt et al., 1999), and over a 1-year period in adolescents, albeit to a lesser extent (Weems, Hayward, Killen, & Taylor, 2002).
However, Bouton, Mineka, and Barlow (2001) have noted that the relationship between anxiety sensitivity and panic attacks in these studies is relatively small, not exclusive to panic, and weaker than the relationship
between panic and neuroticism. Furthermore, these studies have evaluated panic attacks and worry about panic but not the prediction of diagnosed panic disor- der. Thus, the causal significance of anxiety sensitivity for panic disorder remains to be fully understood.
History of Medical Illness and Abuse
Other studies highlight the role of medical illnesses as contributing to a specific psychological vulnerability for panic disorder. For example, using the Dunedin Multidisciplinary Study database, we found that expe- rience with personal respiratory disturbance (and pa- rental poor health) as a youth predicted panic disorder at age 18 or 21 (Craske et al., 2001). This finding is con- sistent with reports of more respiratory disturbance in the history of patients with panic disorder compared to other patients with anxiety disorders (Verburg, Griez, Meijer, & Pols, 1995). Furthermore, first-degree rela- tives of patients with panic disorder had a significantly higher prevalence of chronic obstructive respiratory dis- ease, and asthma in particular, than first-degree rela- tives of patients with other anxiety disorders (van Beek, Schruers, & Friez, 2005). Beyond respiratory disease, other medical illnesses have been shown to contribute to panic disorder onset. A longitudinal study found that the number of physical diseases endorsed on a list of medical problems (e.g., heart problems, asthma, mi- graines) was positively associated with subsequent panic disorder diagnosis (Rudaz, Craske, Becker, Ledermann, & Margraf, 2010).
Childhood experiences of sexual and physical abuse may also prime panic disorder. Retrospective reports of such childhood abuse were associated with panic disor- der onset at ages 16–21 years in a longitudinal analysis of New Zealanders from birth to age 21 (Goodwin, Fer- gusson, & Horwood, 2005). This finding is consistent with multiple cross-sectional studies in both clinical and community samples (e.g., Asselmann, Wittchen, Lieb, & Beesdo-Baum, 2016; Bandelow et al., 2002; Kendler et al., 2000; Kessler, Davis, & Kendler, 1997; Moisan & Engels, 1995; Stein et al., 1996). The association with childhood abuse is stronger for panic disorder than for other anxiety disorders, such as social phobia (Safren, Gershuny, Marzol, Otto, & Pollack, 2002; Stein et al., 1996) and obsessive–compulsive disorder (Stein et al., 1996). In addition, some studies reported an associa- tion between panic disorder and exposure to violence between other family members, generally interparental violence (e.g., Bandelow et al., 2002; Moisan & Engels,
8 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
1995), whereas another study did not (Goodwin et al., 2005). Retrospective reporting of childhood abuse and familial violence in all of these studies, however, limits the findings, and it may be that these early experiences are more strongly related to neuroticism than any one disorder (Barlow, Ellard, et al., 2014)
Interoceptive Awareness
Patients with panic disorder, as well as nonclinical pan- ickers, appear to have heightened awareness of, or abil- ity to detect, bodily sensations of arousal (e.g., Ehlers & Breuer, 1992, 1996; Ehlers, Breuer, Dohn, & Fei- genbaum, 1995; Zoellner & Craske, 1999). Discrepant findings (e.g., Antony et al., 1995; Rapee, 1994) exist but have been attributed to methodological artifact (Ehlers & Breuer, 1996). Ability to perceive heartbeat, in particular, appears to be a relatively stable individu- al-difference variable given that it does not differ be- tween untreated and treated patients with panic dis- order (Ehlers & Breuer, 1992), or from before to after successful treatment (Antony, Meadows, Brown, & Barlow, 1994; Ehlers et al., 1995). Thus, interoceptive accuracy may be a predisposing trait for panic disorder that increases the probability of perceiving sensations that in turn may trigger a panic attack. Whether in- teroceptive awareness is learned, and represents another specific psychological vulnerability, or is more disposi- tional remains to be determined.
Separate from interoception is the issue of propensity for intense autonomic activation. As noted earlier, some evidence points to a unique genetic influence on the reported experience of breathlessness, heart pounding, and a sense of terror (Kendler et al., 1987). Conceiv- ably, cardiovascular reactivity presents a unique physi- ological predisposition for panic disorder. In support of this, cardiac symptoms and shortness of breath predict later development of panic attacks and panic disorder (Keyl & Eaton, 1990). Unfortunately, these data derive from report of symptoms, which is not a good index of actual autonomic state (Pennebaker & Roberts, 1992) and may instead reflect interoception.
Initial Panic Attacks
From an evolutionary standpoint, fear is a natural and adaptive response to threatening stimuli. However, the fear experienced during the first unexpected panic at- tack is often unjustified due to the lack of an identifi- able trigger or antecedent; hence, it represents a “false
alarm” (Barlow, 1988, 2002). The large majority of ini- tial panic attacks are recalled as occurring outside of the home while driving, walking, at work, or at school (Craske et al., 1990), generally in public (Lelliott, Marks, McNamee, & Tobena, 1989), and on a bus, plane, subway, or in social-evaluative situations (Shul- man, Cox, Swinson, Kuch, & Reichman, 1994). Barlow (1988) and Craske and Rowe (1997) believe situations that set the scene for initial panic attacks are ones in which bodily sensations are perceived as posing the most threat because of impairment of functioning (e.g., driving), entrapment (e.g., air travel, elevators), negative social evaluation (e.g., job, formal social events), or dis- tance from safety (e.g., unfamiliar locales). Entrapment concerns may be particularly salient for the subsequent development of agoraphobia (Faravelli, Pallanti, Bion- di, Paterniti, & Scarpato, 1992).
Maintenance Factors
Acute “fear of fear” (or, more accurately, anxiety fo- cused on somatic sensations) that develops after initial panic attacks in vulnerable individuals refers to anxiety about certain bodily sensations associated with panic attacks (e.g., racing heart, dizziness, paresthesias) (Bar- low, 1988; Goldstein & Chambless, 1978), and is attrib- uted to two factors. The first is interoceptive condition- ing, or conditional fear of internal cues, such as elevated heart rate, because of their association with intense fear, pain, or distress (Razran, 1961). Specifically, interocep- tive conditioning refers to low-level somatic sensations of arousal or anxiety becoming conditional stimuli, so that early somatic components of the anxiety response come to elicit significant bursts of anxiety or panic (Bouton et al., 2001). An extensive body of experimen- tal literature attests to the robustness of interoceptive conditioning (e.g., Dworkin & Dworkin, 1999), par- ticularly with regard to early interoceptive drug-onset cues becoming conditional stimuli for larger drug ef- fects (e.g., Sokolowska, Siegel, & Kim, 2002). In addi- tion, interoceptive conditional responses are not depen- dent on conscious awareness of triggering cues (Razran, 1961); thus, they have been observed in patients under anesthesia (e.g., Block, Ghoneim, Fowles, Kumar, & Pathak, 1987). Within this model, then, slight changes in relevant bodily functions that are not consciously recognized may elicit conditional anxiety or fear and panic due to previous pairings with panic (Barlow, 1988; Bouton et al., 2001); the result would be an unex- pected panic attack. Further support for a conditioning
Panic Disorder and Agoraphobia 9
model comes from evidence that individuals with panic disorder, as well as other anxiety disorders, show ele- vated fear conditioning and weakened fear extinction in laboratory paradigms (Lissek et al., 2005), suggest- ing that they are more prone to developing fear through negative associations, and once acquired, their fear is less likely to diminish with time. This pattern seems to be compounded for individuals with panic disorder who additionally show impaired safety learning (Lissek et al., 2009) and greater fear generalization (Lissek et al., 2010) in laboratory paradigms. In other words, once fear of specific bodily sensations is acquired, individu- als with panic disorder may have difficulty perceiving other sensations as being harmless and may be more likely to generalize their fear to various bodily states.
The second factor, offered by Clark (1986) to explain acute fear of panic-related body sensations, is cata- strophic misappraisals of bodily sensations (misinter- pretation of sensations as signs of imminent death, loss of control, etc.). We have taken issue with the purely cognitive model of panic disorder by stating that it cannot account for panic attacks devoid of conscious cognitive appraisal without turning to constructs such as “automatic appraisals,” which prove to be untestable (Bouton et al., 2001). Catastrophic misappraisals may accompany panic attacks because they are a natural part of the constellation of responses that go with panic, or because they have been encouraged and reinforced much like sick role behaviors during childhood. In ad- dition, such thoughts may become conditioned stimuli that trigger anxiety and panic, as demonstrated via panic induction through presentation of pairs of words involving sensations and catastrophic outcomes (Clark et al., 1988). In this case, catastrophic cognitions may well be sufficient to elicit conditioned panic attacks, but not necessary.
Whether cognitively or noncognitively based, ex- cessive anxiety over panic-related bodily sensations in panic disorder is well supported. Persons with panic disorder endorse strong beliefs that bodily sensations associated with panic attacks cause physical or men- tal harm (e.g., Chambless, Caputo, Bright, & Galla- gher, 1984; McNally & Lorenz, 1987). They are more likely to interpret bodily sensations in a catastrophic fashion (Clark et al., 1988) and to allocate more at- tentional resources to words that represent physical threat, such as disease and fatality (e.g., Ehlers, Mar- graf, Davies, & Roth, 1988; Hope, Rapee, Heimberg, & Dombeck, 1990); catastrophe words, such as death and insane (e.g., Maidenberg, Chen, Craske, Bohn, &
Bystritsky, 1996; McNally, Riemann, Louro, Lukach, & Kim, 1992); and heartbeat stimuli (Kroeze & van den Hout, 2000); however, attentional bias is not al- ways found (e.g., DeCort, Hermans, Spruyt, Griez, & Schruers, 2008). Also, individuals with panic disorder show enhanced brain potentials in response to panic- related words (Pauli, Amrhein, Muhlberger, Dengler, & Wiedemann, 2005). In addition, they are more likely to become anxious in procedures that elicit bodily sen- sations similar to the ones experienced during panic attacks, including benign cardiovascular, respiratory, and audiovestibular exercises (Antony, Ledley, Liss, & Swinson, 2006; Jacob, Furman, Clark, & Durrant, 1992), as well as more invasive procedures, such as CO2 inhalations, compared to patients with other anxiety disorders (e.g., Perna, Bertani, Arancio, Ronchi, & Bellodi, 1995; Rapee, 1986; Rapee, Brown, Antony, & Barlow, 1992) or healthy controls (e.g., Gorman et al., 1994). The findings are not fully consistent, however, because patients with panic disorder did not differ from patients with social phobia in response to an epineph- rine challenge (Veltman, van Zijderveld, Tilders, & van Dyck, 1996). Nonetheless, individuals with panic disorder also fear signals that ostensibly reflect height- ened arousal and false physiological feedback (Craske & Freed, 1995; Craske, Lang, et al., 2002; Ehlers, Mar- graf, Roth, Taylor, & Birnbaumer, 1988).
Distress over bodily sensations is likely to generate ongoing distress for a number of reasons. First, in the immediate sense, autonomic arousal generated by fear in turn intensifies the feared sensations, thus creating a reciprocating cycle of fear and sensations that is sus- tained until autonomic arousal abates or the individual perceives safety. Second, because bodily sensations that trigger panic attacks are not always immediately obvi- ous, they may generate the perception of unexpected or “out of the blue” panic attacks (Barlow, 1988) that causes even further distress (Craske, Glover, & De- Cola, 1995). Third, the perceived uncontrollability, or inability to escape or terminate bodily sensations, again, is likely to generate heightened anxiety (e.g., Maier, Laudenslager, & Ryan, 1985; Mineka, Cook, & Miller, 1984). Unpredictability and uncontrollability, then, are seen as enhancing general levels of anxiety about “When is it going to happen again?” and “What do I do when it happens?” which thereby contributes to high levels of chronic anxious apprehension (Bar- low, 1988, 2002). In turn, anxious apprehension in- creases the likelihood of panic by directly increasing the availability of sensations that have become condi-
10 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
tioned cues for panic and/or attentional vigilance for these bodily cues. Thus, a maintaining cycle of panic and anxious apprehension develops. Also, subtle avoid- ance behaviors are believed to maintain negative beliefs about feared bodily sensations (Clark & Ehlers, 1993). Examples include holding onto objects or persons for fear of fainting, sitting and remaining still for fear of a heart attack, and moving slowly or searching for an escape route because one fears acting foolish (Salkov- skis, Clark, & Gelder, 1996). Such avoidance includes experiential avoidance, or being unwilling to remain in contact with particular private experiences, in this case bodily sensations and catastrophic cognitions. Experi- ential avoidance is believed to contribute to overall dis- tress and dysfunction in general (Hayes, Wilson, Gif- ford, & Follette, 1996), and appears to correlate with panic-related worries and disability in individuals with panic disorder (Kampfe et al., 2012). Further support for the role of experiential avoidance comes from evi- dence for instructions to accept symptoms of panic to result in less fear and avoidance in patients with panic disorder (Campbell-Sills, Barlow, Brown, & Hofmann, 2006; Eifert & Heffner, 2003), including CO2 inha- lation challenges (Levitt, Brown, Orsillo, & Barlow, 2004). Finally, anxiety may develop over specific con- texts in which the occurrence of panic would be par- ticularly troubling (i.e., situations associated with im- pairment, entrapment, negative social evaluation, and distance from safety). These anxieties may contribute to agoraphobia, which in turn maintains distress by preventing disconfirmation of catastrophic misapprais- als and extinction of conditioned responding. Clearly, this model targets panic disorder and agoraphobia, and is not as relevant to agoraphobia in the absence of panic attacks or panic-like symptoms.
TREATMENT VARIABLES
Setting
There are several different settings for conducting cog- nitive-behavioral therapy for panic disorder and agora- phobia. The first, the outpatient clinic–office setting, is suited to psychoeducation, cognitive restructuring, assignment, and feedback regarding homework assign- ments and role-play rehearsals. In addition, certain exposures can be conducted in the office setting, such as interoceptive exposure to feared bodily sensations we describe later. Outpatient settings have extended from mental health settings to primary care suites (e.g.,
Craske, Roy-Byrne, et al., 2002; Craske et al., 2011; Roy-Byrne, Craske, et al., 2005; Roy-Byrne et al., 2010; Sharp, Power, Simpson, Swanson, & Anstee, 1997). This extension is particularly important because of the higher prevalence of panic disorder in primary care set- tings (e.g., Shear & Schulberg, 1995; Tiemens, Ormel, & Simon, 1996). However, whether a mental health or a primary care office is being used, the built-in safety signals of such an office may limit the generalizability of learning that takes place in that setting. For example, learning to be less afraid in the presence of the therapist, or in an office located near a medical center, may not necessarily generalize to conditions in which the thera- pist is not present, or when the perceived safety of a medical center is not close by. For this reason, home- work assignments to practice cognitive-behavioral skills in a variety of different settings are particularly impor- tant.
In the second setting, the natural environment, cog- nitive restructuring and other anxiety management skills are put into practice as the patient faces feared situations. The latter is called in vivo exposure and can be conducted with the aid of the therapist or alone. Therapist-directed exposure is particularly useful for patients who lack a social network to support in vivo ex- posure assignments, and more valuable than self-direct- ed exposure for patients with more severe agoraphobia (Holden, O’Brien, Barlow, Stetson, & Infantino, 1983). Therapist-directed exposure is essential to “guided mas- tery exposure,” in which the therapist gives corrective feedback about the way the patient faces feared situ- ations to minimize unnecessary defensive behaviors. For example, patients are taught to drive in a relaxed position and to walk across a bridge without holding the rail. On the one hand, guided mastery exposure has been shown to be more effective than “stimulus expo- sure” when patients attempt simply to endure the situ- ation alone until fear subsides, without the benefit of ongoing therapist feedback (Williams & Zane, 1989). On the other hand, self-directed exposure is very valu- able also, especially to the degree that it encourages in- dependence and generalization of the skills learned in treatment to conditions in which the therapist is not present. Thus, the most beneficial approach in the nat- ural environment is to proceed from therapist-directed to self-directed exposure.
In telephone-guided treatment, an interesting varia- tion that combines the office and the natural envi- ronment, therapists direct patients with agoraphobia by phone to conduct in vivo exposure to feared situa-
Panic Disorder and Agoraphobia 11
tions (NcNamee, O’Sullivan, Lelliott, & Marks, 1989; Swinson, Fergus, Cox, & Wickwire, 1995) or provide instruction in panic control skills (Côté, Gauthier, La- berge, Cormier, & Plamondon, 1994). In addition, one small study showed that cognitive-behavioral therapy was as effective when delivered by videoconference as in person (Bouchard et al., 2004).
Self-directed treatments, with minimal direct thera- pist contact, take place in the natural environment and are beneficial for highly motivated and educated pa- tients (e.g., Ghosh & Marks, 1987; Gould & Clum, 1995; Gould, Clum, & Shapiro, 1993; Lidren et al., 1994; Schneider, Mataix-Cols, Marks, & Bachofen, 2005; Mitsopoulou et al., 2020). On the other hand, self-directed treatments are less effective for more se- verely affected patients (Holden et al., 1983); for those with more comorbidity (Hecker, Losee, Roberson-Nay, & Maki, 2004), less motivation, and less education; or for patients who are referred as opposed to recruited through advertisement (Hecker, Losee, Fritzler, & Fink, 1996). Self-directed treatments have expanded beyond workbooks and manuals to computerized and Internet versions (e.g., Carlbring, Ekselius, & Anders- son, 2003; Richards, Klein, & Austin, 2006; Richards, Klein, & Carlbring, 2003). In general, these treat- ments yield very positive results with strong effect sizes (Andrews, Cuijpers, Craske, McEvoy, & Titov, 2010), and at least two studies indicate that they are as ef- fective as therapist-led cognitive-behavioral therapy for panic disorder (Carlbring et al., 2005; Kiropoulos et al., 2008). However, attrition rates may be higher with self-directed computer/Internet programs in the absence of any therapist contact (e.g., Carlbring et al., 2003; Nordgreen et al., 2016). Recent models of Internet-based cognitive-behavioral therapy for panic disorder that include online support by a clinician have demonstrated effectiveness in reducing panic disorder symptoms severity yet still experience high attrition (Hedman et al., 2013).
The third setting, the inpatient facility, is most ap- propriate when conducting very intensive cognitive- behavioral therapy (e.g., daily therapist contact) or treating severely disabled persons who can no longer function at home. In addition, certain medical or drug complications may warrant inpatient treatment. The greatest drawback to the inpatient setting is poor gener- alization to the home environment. Transition sessions and follow-up booster sessions in an outpatient clinic– office or in the patient’s own home facilitate generaliza- tion.
Format
Cognitive-behavioral therapy for panic disorder and agoraphobia may be conducted in individual or group formats. Several clinical outcome studies have used group treatments (e.g., Bohni, Spindler, Arendt, Hou- gaaard, & Rosenberg, 2009; Craske, DeCola, Sachs, & Pontillo, 2003; Craske et al., 2007; Evans, Holt, & Oei, 1991; Feigenbaum, 1988; Hoffart, 1995; Telch et al., 1993). The fact that their outcomes are generally consistent with the summary statistics obtained from individually formatted treatment suggests that group treatment is as effective as individual therapy. In direct comparisons, albeit few in number, a slight advantage is shown for individual formats. Specifically, Néron, La- croix, and Chaput (1995) compared 12–14 weekly ses- sions of individual or group cognitive-behavioral thera- py (N = 20), although the group condition received two additional 1-hour individual sessions. The two condi- tions were equally effective for measures of panic and agoraphobia at posttreatment and 6-month follow-up. However, the individual format was more successful in terms of generalized anxiety and depressive symptoms by the follow-up point. In addition, individual treat- ments resulted in more clinically significant outcomes than group formats in primary care (Sharp, Power, & Swanson, 2004). Furthermore, 95% of individuals assigned to the wait-list condition in the latter study stated a clear preference for individual treatment when given the choice at the end of the wait list.
Most studies of cognitive-behavioral therapy for panic and agoraphobia involve 10–20 weekly treatment sessions. Several studies show that briefer treatments may be effective as well. Evans and colleagues (1991) compared a 2-day group cognitive-behavioral treatment to a waiting-list condition, although without random assignment. The 2-day program comprised lectures (3 hours); teaching skills, such as breathing, relaxation, and cognitive challenge (3 hours); in vivo exposure (9 hours); and group discussion plus a 2-hour support group for significant others. Eighty-five percent of treated patients were reported to be either symptom- free or symptomatically improved, and these results were maintained 1 year later. In contrast, the waiting- list group did not demonstrate significant changes. A pilot study similarly indicated effectiveness with inten- sive cognitive-behavioral therapy over 2 days (Deacon & Abramowitz, 2006). Other studies have evaluated the effectiveness of cognitive-behavioral therapy when delivered over fewer sessions. A five-session cognitive
12 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
behavioral therapy protocol for panic disorder that fo- cuses largely on interoceptive exposure demonstrated large effect sizes in two studies (Otto et al., 2010; Na- tions et al., 2012). In a randomized study, patients with panic disorder with agoraphobia who awaited phar- macotherapy treatment were assigned to four weekly sessions of either cognitive-behavioral therapy or sup- portive nondirective therapy (Craske, Maidenberg, & Bystritsky, 1995). Cognitive-behavioral therapy was more effective than supportive therapy, particularly with less severely affected patients, although the results were not as positive as those typically seen with more sessions. Also, we found that up to six sessions (aver- age of three sessions) of cognitive-behavioral therapy combined with medication recommendations yielded significantly greater improvements on an array of mea- sures, including quality of life, compared to treatment as usual for individuals with panic disorder in primary care settings (Roy-Byrne, Craske, et al., 2005). Notably, however, the treatment effects substantially increased as the number of cognitive-behavioral therapy sessions (up to six) and follow-up booster phone call sessions (up to six) increased (Craske et al., 2006). In our subsequent primary care study, an average of seven sessions of cognitive-behavioral therapy and/or medication recom- mendations was superior to usual care, and in this case, usual care often involved several active treatment ele- ments (Craske et al., 2011). Finally, in a direct compari- son, results were equally effective whether cognitive- behavioral therapy was delivered across the standard 12 sessions or across approximately six sessions (Clark et al., 1999).
Interpersonal Context
Interpersonal context variables have been researched in terms of the development, maintenance, and treatment of agoraphobia. The reason for this research interest is apparent from the following vignette:
“My husband really doesn’t understand. He thinks it’s all in my head. He gets angry at me for not being able to cope. He says I’m weak and irresponsible. He resents having to drive me around, and doing things for the kids that I used to do. We argue a lot because he comes home tired and frustrated from work only to be frustrated more by the problems I’m having. But I can’t do anything without him. I’m so afraid that I’ll collapse into a helpless wreck without him, or that I’ll be alone for the rest of my life. As cruel as
he can be, I feel safe around him because he always has everything under control. He always knows what to do.”
This first vignette illustrates dependence on the significant other for a sense of safety despite a non- sympathetic response that may only serve to increase background stress for the patient. The second vignette illustrates inadvertent reinforcement of fear and avoid- ance through attention from the significant other:
“My boyfriend really tries hard to help me. He’s al- ways cautious of my feelings and doesn’t push me to do things that I can’t do. He phones me from work to check on me. He stays with me and holds my hand when I feel really scared. He never hesitates to leave work to help me if I’m having a bad time. Only last week we visited some of his friends, and we had to leave. I feel guilty because we don’t do the things we used to enjoy doing together. We don’t go to the mov- ies anymore. We used to love going to ball games, but now it’s too much for me. I am so thankful for him. I don’t know what I would do without him.”
Perhaps some forms of agoraphobia represent a con- flict between desire for autonomy and dependence in interpersonal relationships (Fry, 1962; Goldstein & Chambless, 1978). In other words, the “preagorapho- bic” individual is trapped in a domineering relationship without the skills needed to activate change. However, the concept of a distinct marital system that predispos- es toward agoraphobia lacks empirical evidence. This is not to say that marital or interpersonal systems are unimportant to agoraphobia. For example, interperson- al discord/dissatisfaction may represent one of several possible stressors that precipitate panic attacks. Also, interpersonal relations may be negatively impacted by the development of agoraphobia (Buglass, Clarke, Hen- derson, & Presley, 1977) and in turn contribute to its maintenance. Not unlike one of the earlier vignettes, consider the woman who has developed agoraphobia and now relies on her husband to do the shopping and other errands. These new demands on the husband lead to resentment and marital discord. The marital distress adds to background stress, making progress and recov- ery even more difficult for the patient.
Aside from whether interpersonal dysregulation con- tributes to the onset or maintenance of panic disorder or agoraphobia, some studies suggest that poor marital relations adversely impact exposure-based treatments
Panic Disorder and Agoraphobia 13
(Bland & Hallam, 1981; Dewey & Hunsley, 1990; Milton & Hafner, 1979). However, other studies show no relationship between marital distress and outcome from cognitive-behavioral therapy (Arrindell & Em- melkamp, 1987; Emmelkamp, 1980; Himadi, Cerny, Barlow, Cohen, & O’Brien, 1986). Another line of re- search suggests that involving significant others in every aspect of treatment may override potential negative im- pacts of poor marital relations on phobic improvement (Barlow et al., 1984; Cerny, Barlow, Craske, & Himadi, 1987). Furthermore, involvement of significant others resulted in better long-term outcomes from cognitive- behavioral therapy for agoraphobia (Cerny et al., 1987). Similarly, communications training with significant others, compared to relaxation training, after 4 weeks of in vivo exposure therapy, resulted in significantly greater reductions on measures of agoraphobia by post- treatment (Arnow, Taylor, Agras, & Telch, 1985), an effect that was maintained over an 8-month follow-up. Together, these studies suggest the value of including significant others in the treatment for agoraphobia. On the other hand, treatment focused specifically on interpersonal relationships, via interpersonal therapy, was not as effective as cognitive-behavioral therapy for panic disorder and agoraphobia (Vos, Huibers, Diels, & Arntz, 2012).
Yet another question is the degree to which treatment for panic disorder and agoraphobia influences marital/ interpersonal relations. Some have noted that successful treatment can have deleterious effects (Hafner, 1984; Hand & Lamontagne, 1976). Others note that it has no effect or a positive effect on marital functioning (Barlow et al., 1984; Himadi et al., 1986) and interper- sonal functioning in general (Hoffart, 1997). Barlow, O’Brien, Last, and Holden (1983) suggested that when negative effects do occur, it may be because exposure therapy is conducted intensively, without the significant other’s involvement, which causes major role changes that the significant other perceives as being beyond his/ her control. This again speaks to the value of involving significant others in the treatment process.
Therapist Variables
Only a few studies have evaluated therapist variables in relation to cognitive-behavioral treatments for anxiety disorders, let alone panic disorder or agoraphobia. Wil- liams and Chambless (1990) found that patients with agoraphobia who rated their therapists as caring/in- volved, and as modeling self-confidence, achieved bet-
ter outcomes on behavioral approach tests. However, an important confound in this study was that patient ratings of therapist qualities may have depended on patient responses to treatment. Keijsers, Schaap, Hoog- duin, and Lammers (1995) reviewed findings on thera- pist relationship factors and behavioral outcome. They concluded that empathy, warmth, positive regard, and genuineness assessed early in treatment predict positive outcome; patients who view their therapists as under- standing and respectful improve the most, and patient perceptions of therapist expertness, self-confidence, and directiveness relate positively to outcome, although not consistently. In their own study of junior thera- pists who provided cognitive-behavioral treatment for panic disorder with or without agoraphobia, Keijsers and colleagues found that more empathic statements and questioning occurred in Session 1 than in later ses- sions. In Session 3, therapists became more active and offered more instructions and explanations. In Session 10, therapists employed more interpretations and con- frontations than previously. Most importantly, direc- tive statements and explanations in Session 1 predicted poorer outcome. Empathic listening in Session 1 related to better behavioral outcome, whereas empathic listen- ing in Session 3 related to poorer behavioral outcome. Thus, they demonstrated the advantages of different in- teractional styles at different points in therapy. Interest- ingly, one study found that the therapist contribution to the therapy alliance predicted attrition (with greater al- liance factors as reported by the patient associated with less dropout), but did not predict treatment outcomes (Huppert et al., 2014). A study using independent raters of therapeutic alliance, which overcomes some of the methodological limitations described earlier, found that ratings of therapeutic alliance were positively associated with improvement in patients’ agoraphobic avoidance (Weck et al., 2016).
Most clinicians assume that therapist training and experience improve the chances of successful outcome. Some believe this to be the case particularly with respect to the cognitive aspects of cognitive-behavioral therapy (e.g., Michelson et al., 1990), and some indirect evi- dence for this supposition exists. Specifically, cognitive- behavioral therapy conducted by “novice” therapists in a medical setting (Welkowitz et al., 1991) was some- what less effective in comparison to the same therapy conducted by inexperienced but highly trained thera- pists in a psychological setting (Barlow, Craske, Czerny, & Klosko, 1989), or by experienced and highly trained therapists in a community mental health setting (Wade,
14 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
Treat, & Stuart, 1998). Huppert and colleagues (2001), who directly evaluated the role of therapist experience, found that, in general, therapist experience positively related to outcome, seemingly because these therapists were more flexible in administering the treatment and better able to adapt it to the individual being treated. In contrast, there is some evidence that adherence (i.e., fol- lowing the protocol) but not competence (i.e., degree to which the treatment is delivered skillfully) is predictive of treatment outcome in cognitive-behavioral therapy for panic disorder (Weck et al., 2016). Obviously, there is a need for more evaluation of the role of therapist ex- perience and training in cognitive-behavioral therapy.
In our primary care work, we developed a computer guide to assist novice clinicians in implementing a cog- nitive-behavioral program for panic disorder (plus other anxiety disorders and depression) (Craske et al., 2001), called Calm Tools for Living (CALM). The clinician and patient sit side by side as both view the program on- screen. Throughout, the program prompts clinicians to engage in specific tasks, such as helping patients to es- tablish a fear hierarchy, demonstrating breathing skills, practicing cognitive skills, conducting interoceptive ex- posure, or designing in vivo exposure assignments. The program also provides learning tools for patients, such as didactic information, interactive exercises, video vi- gnettes, and quizzes. The goal of the computerized pro- gram is to enhance the integrity of cognitive-behavioral therapy in the hands of novice and relatively untrained clinicians.
Patient Variables
There has been interest in the effect of comorbidity on the outcomes of cognitive-behavioral therapy for panic disorder and agoraphobia. Brown, Antony, and Barlow (1995) found that comorbidity with other anxiety dis- orders did not predict response to cognitive-behavioral therapy overall, although social phobia was unexpected- ly associated with superior outcome for panic disorder and agoraphobia. In contrast, Tsao, Lewin, and Craske (1998) found a trend for comorbidity that comprised mostly other anxiety disorders to be associated with slightly lower rates of overall success. In a subsequent study, however, we replicated the finding by Brown and colleagues (1995) of no relationship between baseline comorbidity comprising mostly other anxiety disorders, and either immediate or 6-month outcome for panic disorder and agoraphobia (Tsao, Mystkowski, Zucker, & Craske, 2002).
Research on how comorbid depression affects the course and outcome of panic disorder treatment has yielded mixed results. Studies focused on cognitive- behavioral therapy for all anxiety disorders and treat- ment participation have found that comorbidity with depression is associated with increased rates of refusal to enter treatment (Issakidis & Andrews, 2004); however, once patients have entered treatment, the comorbidity has no effect on rates of attrition (Allen et al., 2010; Brown et al., 1995). Preliminary research investigating the effects of comorbidity on engagement with treat- ment has revealed that comorbid depression has no ef- fect on compliance with cognitive-behavioral therapy homework (McLean, Woody, Taylor, & Koch, 1998) or compliance with cognitive-behavioral treatment as a whole (Murphy, Michelson, Marchione, Marchione, & Testa, 1998), though it does increase levels of dis- tress associated with treatment (Murphy et al., 1998). Interestingly, comorbid depression has no effect on the response to cognitive-behavioral therapy for panic disorder at posttreatment or follow-up and in both referred and primary care settings (Allen et al., 2010; McLean et al., 1998; Roy-Byrne, Craske, et al., 2005). It seems contradictory that comorbid depression would have significant impact on the severity and persistence of panic disorder (Baldwin, 1998) but would not affect the outcomes of panic disorder treatment. This may be a product of limitations to the current treatment litera- ture. For example, studies have recruited patients for the treatment of panic disorder and have often excluded patients who are very extremely depressed or suicidal. Thus, the majority of patients are mildly to moderately depressed. Many of these studies also exclude patients with bipolar disorder, and therefore exclude an entire group of individuals who experience major depressive episodes. However, it may also be that the effects of cognitive-behavioral therapy for panic disorder are suf- ficiently potent to impact depressive symptoms either directly or indirectly.
A relatively high co-occurrence exists between panic disorder and agoraphobia, and avoidant, dependent, and histrionic personality disorders (e.g., Reich et al., 1994). Questions of diagnostic reliability and validity aside, comorbid personality disorders are sometimes as- sociated with poorer response than usual to cognitive- behavioral therapy for panic disorder or agoraphobia (e.g., Hoffart & Hedley, 1997; Marchand, Goyer, Du- puis, & Mainguy, 1998). However, closer examina- tion reveals that although individuals with comorbid personality disorders have greater severity of panic
Panic Disorder and Agoraphobia 15
or agoraphobia pre- and post–cognitive-behavioral therapy, the rate of decrease in panic or agoraphobia symptoms usually is not affected by the comorbid per- sonality disorder. Thus, Dreessen, Arntz, Luttels, and Sallaerts (1994) and van den Hout, Brouwers, and Oomen (2006) found that comorbid personality dis- orders did not affect response to cognitive-behavioral therapy for panic or agoraphobia. Moreover, Hofmann and colleagues (1988) found that scores on question- naire subscales reflecting Axis II personality disorders did not predict panic disorder treatment response to either cognitive-behavioral therapy or to medication. In fact, some personality traits may associate positively with outcome, as was reported by Rathus, Sanderson, Miller, and Wetzler (1995) with respect to compulsive personality features.
Substance use disorders also commonly co-occur with panic disorder and agoraphobia, but very few treat- ment studies have addressed this important comorbid- ity. In a series of single cases (N = 3), Lehman, Brown, and Barlow (1998) demonstrated successful control of panic attacks in individuals who were abusing alcohol. Also, the addition of anxiety treatment to a relapse pre- vention program for abstinent individuals with a pri- mary diagnosis of alcohol dependence and a comorbid diagnosis of panic disorder or social phobia decreased anxiety symptoms relative to a relapse prevention pro- gram alone (Schade et al., 2005). However, adding the anxiety treatment did not affect rates of alcohol relapse in that study. More recent work has attempted to fully integrate the cognitive-behavioral therapy for panic disorder into substance use disorder treatment more seamlessly, with more promising effects on both panic disorder symptoms and substance use symptoms (Kushner et al., 2006, 2013). Our own work adapting Calm Tools for Living (Craske et al., 2009) for clients with comorbid substance use disorders and anxiety dis- orders (including panic disorder and agoraphobia) has shown that a computer-assisted but therapist-directed integrated cognitive-behavioral treatment for comorbid anxiety and substance use disorders showed greater im- provement in anxiety and substance use outcomes than a substance use disorder treatment alone (Wolitzky- Taylor et al., 2018). More work is needed in this area, though recent data suggest that panic disorder can improve when substance use disorders are present, and that treating both simultaneously can improve panic/ anxiety symptoms and substance use severity.
Another source of comorbidity is medical conditions, such as cardiac arrhythmias or asthma, that may slow
improvement rates given the additional complications involved in discriminating between anxiety and disease symptomatology, increases in actual medical risk, and the stress of physical diseases. We found that medically ill patients with panic disorder, although more severely affected than their nonmedically ill counterparts at baseline, responded just as favorably to cognitive- behavioral therapy with psychotropic medication rec- ommendations (Roy-Byrne, Stein, et al., 2005). Also, cognitive-behavioral therapy for panic disorder has been shown to alleviate self-reported physical health symptoms (Schmidt et al., 2003). Similarly, we found that cognitive-behavioral therapy and/or psychotropic medication recommendations for anxiety disorders (in- cluding panic disorder) significantly improve physical health functioning (Niles et al., 2013).
Other patient variables include socioeconomic status and general living conditions. We evaluated perceived barriers to receiving mental health treatment in our pri- mary care study of panic disorder (Craske, Golinelli, et al., 2005). Commonly reported barriers included in- ability to find out where to go for help (43%), worry about cost (40%), lack of coverage by one’s health plan (35%), and inability to get an appointment soon enough (35%). Also, in our multicenter trial, attrition from cognitive-behavioral and/or medication treatment for panic disorder with minimal agoraphobia was pre- dicted by lower education, which in turn was dependent on lower income (Grilo et al., 1998). Similarly, levels of education and motivation were associated with dropout rates in another sample, although the effects were small (Keijsers, Kampman, & Hoogduin, 2001). Low educa- tion–income may reflect less discretionary time to en- gage in activities such as weekly treatment. Consider a woman who is the mother of two, a full-time clerk, whose husband is on disability due to a back injury, or the full-time student who works an extra 25 hours a week to pay his way through school. Under these con- ditions, treatment assignments of daily in vivo exposure exercises are much less likely to be completed. Frustra- tion with lack of treatment progress is likely to result. Therapeutic success requires either a change in lifestyle that allows the cognitive-behavioral treatment to be- come a priority or termination of therapy until a later time, when life circumstances are less demanding. In fact, these kinds of life circumstance issues may explain the trend for African Americans to show less treatment benefit in terms of mobility, anxiety, and panic attacks than European Americans (Friedman & Paradis, 1991; Williams & Chambless, 1994). Although, in contrast
16 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
to these two studies, Friedman, Paradis, and Hatch (1994) found equivalent outcomes across the two ra- cial groups, and the results from another study yielded outcomes from a female African American sample that were judged to be comparable to those of European Americans (Carter, Sbrocco, Gore, Marin, & Lewis, 2003). The influence of ethnic and cultural differences on treatment outcome and delivery clearly needs more evaluation.
Finally, patients’ understanding of the nature of their problem may be important to the success of cognitive- behavioral treatments. Given the somatic nature of panic disorder, many patients seek medical help first. Beyond that, however, differences in the way the prob- lem is conceptualized could lead to the perception that pharmacological or analytical treatment approaches are more credible than cognitive-behavioral treatment ap- proaches. For example, individuals who strongly believe their condition is due to “a neurochemical imbalance” may be more likely to seek medication and to refute psychological treatments. Similarly, individuals who at- tribute their condition to “something about my past—it must be unconscious influences” may resist cognitive- behavioral interpretations. Also, Grilo and colleagues (1998) found that patients with panic disorder or agoraphobia who attributed their disorder to specific stressors in their lives were more likely to drop out of cognitive-behavioral or medication treatment, perhaps because they saw the offered treatment as irrelevant.
Concurrent Pharmacological Treatment
Many more patients receive medications than cogni- tive-behavioral therapy for panic disorder and agora- phobia, partly because primary care physicians are usu- ally the first line of treatment. Thus, one-half or more of patients with panic disorder who attend psychology research clinics already are taking anxiolytic medica- tions. The obvious questions, therefore, are the extent to which cognitive-behavioral therapy and medications have a synergistic effect, and how medications impact cognitive-behavioral therapy.
Results from large clinical trials, including our own multisite trial (Barlow, Gorman, Shear, & Woods, 2000), suggest no advantage during or immediately after treatment of combining cognitive-behavioral and pharmacological approaches. Specifically, both indi- vidual cognitive-behavioral and drug treatment, and a combination treatment were immediately effective fol- lowing treatment. Furthermore, following medication
discontinuation, the combination of medication and cognitive-behavioral therapy fared worse than cogni- tive-behavioral therapy alone, suggesting the possibility that state- (or context-) dependent learning in the pres- ence of medication may have attenuated the new learn- ing that occurs during cognitive-behavioral therapy. In contrast, in the primary care setting, we found that the addition of even just one component of cognitive- behavioral therapy to medications for panic disorder re- sulted in statistically and clinically significant improve- ments at posttreatment and 12 months later (Craske, Golinelli, et al., 2005).
More recently, our multisite collaborative team has been investigating long-term strategies in the treatment of panic disorder. We examined sequential combina- tion strategies to determine whether this approach is more advantageous than simultaneously combining treatments. In the initial phase, 256 patients with panic disorder and all levels of agoraphobia completed 3 months of initial treatment with cognitive-behavioral therapy (Aaronson et al., 2008; White et al., 2010). Patients were then triaged into two clinical trials. Re- sponders were randomized to 9 months of monthly booster sessions (N = 79) or no booster sessions (N = 78), then followed for an additional 12 months with- out treatment (White et al., 2013). Booster sessions produced significantly lower relapse rates (5.2%) and reduced work and social impairment compared to the assessment-only condition without booster sessions (18.4%) at 21-month follow-up. Multivariate Cox pro- portional hazards models showed that residual symp- toms of agoraphobia at the end of acute-phase treat- ment were independently predictive of time to relapse during 21-month follow-up (hazard rate = 1.15, p < .01). Thus, booster sessions aimed at reinforcing acute treatment gains to prevent relapse and offset disorder recurrence improved long-term outcome for panic dis- order with and without agoraphobia. Fifty-eight of the original patients did not reach an optimal level of functioning (high end-state functioning) and entered a trial in which they received either continued cogni- tive-behavioral therapy for 3 months or paroxetine for 3 months. Patients doing well with one treatment or the other continued with the respective treatment for an additional 9 months. Results indicated significantly lower panic disorder symptoms for individuals in the paroxetine condition compared to those in continued cognitive-behavioral therapy at 3 months. However, group differences had disappeared 9 months later. Re- sults were maintained when excluding individuals with
Panic Disorder and Agoraphobia 17
comorbid major depression. These data suggest a more rapid treatment response when switching to paroxetine after not responding optimally to cognitive-behavioral therapy; however, both treatments ultimately achieved similar outcomes.
In another study with similar results, patients who did not respond to cognitive-behavioral therapy also benefited more from the addition of a serotonergic drug (paroxetine) to continued cognitive-behavioral therapy than from the addition of a drug placebo, with substan- tially different effect sizes (Kampman, Keijsers, Hoog- duin, & Hendriks, 2002). Conversely, individuals who are resistant to pharmacotherapy may respond positive- ly to cognitive-behavioral therapy, although these find- ings were part of an open trial without randomization (Heldt et al., 2006).
Findings from the combination of fast-acting anx- iolytics, specifically, the high-potency benzodiazepines, and behavioral treatments for agoraphobia are contra- dictory (e.g., Marks et al., 1993; Wardle et al., 1994). Nevertheless, several studies have reliably demonstrated the detrimental effects of chronic use of high-potency benzodiazepines on short-term and long-term out- come in cognitive-behavioral treatments for panic or agoraphobia (e.g., Otto, Pollack, & Sabatino, 1996; van Balkom, de Beurs, Koele, Lange, & van Dyck, 1996; Wardle et al., 1994). Specifically, there is evidence for more attrition, poorer outcome, and more relapse with chronic use of high-potency benzodiazepines. In addi- tion, use of benzodiazepines as needed was associated with poorer outcome than regular use or no use in one small naturalistic study (Westra, Stewart, & Conrad, 2002).
Finally, the cost-effectiveness of cognitive-behavioral and medication treatments alone rather than in com- bination requires further evaluation; currently, cogni- tive-behavioral therapy is considered to be more cost- effective (e.g., disability costs, work days missed, health care use) than pharmacotherapy (Heuzenroeder et al., 2004).
Understanding the ways in which psychotropic medications influence cognitive-behavioral therapy may prove useful for developing methods that optimize the combination of these two approaches to treatment. First, medications, particularly fast-acting, potent medications that cause a noticeable shift in state and are used on an as-needed basis (e.g., benzodiazepines, beta-blockers), may contribute to relapse, because ther- apeutic success is attributed to them rather than to cog- nitive-behavioral therapy. Patients’ resultant lack of per-
ceived self-control may increase relapse potential when medication is withdrawn or contribute to maintenance of a medication regimen under the assumption that it is necessary to functioning. In support, attribution of therapeutic gains to alprazolam, and lack of confidence in coping without alprazolam, even when given in con- junction with behavioral therapy, predicted relapse (Ba- soglu, Marks, Kilic, Brewin, & Swinson, 1994). Sec- ond, medications may assume the role of safety signals, or objects to which persons erroneously attribute their safety from painful, aversive outcomes. Safety signals may contribute to maintenance of fear and avoidance in the long term (Hermans, Craske, Mineka, & Lovibond, 2006) and may interfere with corrections of misapprais- als of bodily symptoms (see below for further discussion of this issue). Third, medications may reduce the mo- tivation to engage in practices of cognitive-behavioral skills, yet completion of between-session assignments is a positive predictor of outcome from cognitive-behav- ioral therapy (e.g., Glenn et al., 2013). Finally, learning that takes place under the influence of medications may not necessarily generalize to the time when medications are removed, thus contributing to relapse (Bouton & Swartzentruber, 1991). Some of these points are illus- trated in the following vignettes:
“I had been through a program of cognitive-behav- ioral therapy, but it was really the Paxil that helped. Because I was feeling so much better, I considered tapering off the medication. At first, I was very con- cerned about the idea. I had heard horror stories about what people go through when withdrawing. However, I thought it would be OK as long as I ta- pered slowly. So, I gradually weaned myself off. It re- ally wasn’t that bad. Well, I had been completely off the medication for about a month when the problem started all over again. I remember sitting in a res- taurant, feeling really good because I was thinking about how much of a problem restaurants used to be for me before, and how easy it seemed now. Then, whammo. I became very dizzy and I immediately thought, ‘Oh no, here it comes.’ I had a really bad panic attack. All I could think of was why didn’t I stay on the medication?”
“I started to lower my dose of Xanax. I was OK for the first couple of days. . . . I felt really good. Then, when I woke up on Friday morning, I felt strange. My head felt really tight and I worried about having the same old feelings all over again. The last thing
18 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
I want to do is to go through that again. So I took my usual dose of Xanax and, within a few minutes, I felt pretty good again. I need the medication. I can’t manage without it right now.”
In what ways might such negative effects of medi- cations be offset? One possibility is that continuation of exposure after medication is withdrawn may offset relapse, because it enhances attributions of personal mastery and reduces the safety signal function of medi- cations. In addition, opportunities to practice exposure and cognitive and behavioral strategies without the aid of medication overcome state dependency and enhance generalization of therapeutic gains once treatment is over.
CASE STUDY
Julie, a 33-year-old mother of two, lives with Larry, her husband of 8 years. For the past 3 years, she has been chronically anxious and panic stricken. She de- scribes her panic attacks as unbearable and increasing in frequency. The first time she felt panicky was just over 3 years ago, when she was rushing to be by her grandmother’s side in the last moments before she died. Julie was driving alone on the freeway. She remembers feeling as if everything were moving in slow motion, as if the cars were standing still, and things around her seemed unreal. She recalled feeling short of breath and detached. However, it was so important to reach her destination that she did not dwell on how she felt until later. After the day was over, she reflected on how lucky she was not to have had an accident. A few weeks later, she experienced the same feeling again when driving on the freeway. This time it occurred without the pressure of getting to her dying grandmother. It scared Julie, be- cause she was unable to explain the feelings. She pulled to the side of the road and called her husband, who came to meet her. She followed him home, feeling anx- ious the entire way.
Now, Julie has these feelings in many situations. She describes her panic attacks as feelings of unreality, detachment, shortness of breath, a racing heart, and a general fear of the unknown. It is the unreality that scares her the most. Consequently, Julie is sensitive to anything that produces “unreal” types of feelings, such as the semiconsciousness that occurs just before fall- ing asleep, the period when daylight changes to night, bright lights, concentrating on the same thing for long
periods of time, alcohol or drugs, and being anxious in general. Even though she has a prescription for Klono- pin (a high-potency benzodiazepine), she rarely, if ever, uses it because of her general fear of being under the influence of a drug, or of feeling an altered state of consciousness. She wants to be as alert as possible at all times, but she keeps the Klonopin with her in the event that she has no other way of managing her panic. She does not leave home without the Klonopin. Julie is very sensitive to her body in general; she becomes scared of anything that feels a little different than usual. Even coffee, which she used to enjoy, is distressing to her now because of its agitating and racy effects. She was never a big exerciser, but to think of exerting herself now is also scary. Julie reports that she is constantly waiting for the next panic attack to occur. She avoids freeways, driving on familiar surface streets only. She limits her- self to a 10-mile radius from home. She avoids crowds and large groups as well, partly because of the feeling of too much stimulation and partly because she is afraid to panic in front of others. In general, she prefers to be with her husband or her mother. However, she can do most things as long as she is within her “safety” region.
Julie describes how she differs from the way she used to be: how weak and scared she is now. The only other incident that is similar to her current panic attacks oc- curred in her early 20s, when she had a negative reac- tion to smoking marijuana. Julie became very scared of the feeling of losing control and feared that she would never return to reality. She has not taken drugs since then. Otherwise, there is no history of serious medi- cal conditions or any previous psychological treatment. Julie had some separation anxiety and was shy as a young child and throughout her teens. However, her social anxiety improved throughout her 20s, to the point that until the onset of her panic attacks, she was mostly very comfortable around people. Since the onset of her panic attacks, Julie has become concerned that others will notice that she appears anxious. However, her social anxiety is limited to panic attacks and does not reflect a broader social phobia.
In general, Julie’s appetite is good, but her sleep is restless. At least once a week she wakes abruptly in the middle of the night, feeling short of breath and scared, and she has great difficulty going to sleep when her husband travels. In addition to worrying about her panic attacks, Julie worries about her husband and her children, although these latter worries are secondary to her worry about panicking and not excessive. She has some difficulty concentrating but is generally able to
Panic Disorder and Agoraphobia 19
function at home and at work because of the familiar- ity of her environment and the safety she feels in the presence of her husband. Julie works part-time as the manager of a business that she and her husband own. She sometimes becomes depressed about her panic and the limitations on how far she can travel. Occasionally she feels hopeless about the future, doubting whether she will ever be able to escape the anxiety. Although the feelings of hopelessness and the teariness never last than more than a few days, Julie has generally had a low- grade depressed mood since her life became restricted by the panic attacks.
Julie’s mother and her uncle both had panic attacks when they were younger. Julie is now worried that her oldest child is showing signs of being overly anxious, because he is hesitant about trying new things or spend- ing time away from home.
ASSESSMENT
A functional behavioral analysis depends on several dif- ferent modes of assessment, which we describe next.
Interviews
An in-depth interview is the first step in establishing diagnostic features and the profile of symptomatic and behavioral responses. Several semistructured and fully structured interviews exist. The Anxiety Disorders In- terview Schedule for DSM-IV (ADIS-IV; Di Nardo, Brown, & Barlow, 1994) and for DSM-5 (ADIS-5; Brown & Barlow, 2014) primarily assesses anxiety dis- orders, as well as mood and somatoform disorders. Psy- chotic and drug conditions are screened by this instru- ment also. The ADIS facilitates gathering the necessary information to make a differential diagnosis among anxiety disorders and offers a means to distinguish between clinical and subclinical presentations of a dis- order. Data on the frequency, intensity, and duration of panic attacks, as well as details on avoidance behav- ior, are embedded within the ADIS; this information is necessary for tailoring treatment to each individual’s presentation. The value of structured interviews is their contribution to a differential diagnosis and interrater reliability. Interrater agreement ranges from satisfactory to excellent for the various anxiety disorders using the ADIS-IV (Brown, Di Nardo, Lehman, & Campbell, 2001). Similar analyses for the ADIS-5 are underway (Brown & Tung, 2018).
Similarly, the Schizophrenia and Affective Disor- ders Schedule—Lifetime Version (modified for the study of anxiety) produces reliable diagnoses for most of the anxiety disorders (generalized anxiety disorder and simple phobia are the exceptions) (Manuzza, Fyer, Liebowitz, & Klein, 1990), as does the Structured Clin- ical Interview for DSM (SCID), now in its fifth edition (American Psychiatric Association, 2013).
Differential diagnosis is sometimes difficult because, as described earlier, panic is a ubiquitous phenomenon (Barlow, 1988) that occurs across a wide variety of emo- tional disorders. It is not uncommon for persons with specific phobias, social phobia, generalized anxiety dis- order, obsessive–compulsive disorder, and posttraumat- ic stress disorder to report panic attacks. For Julie, there was a diagnostic question regarding differentiation be- tween social anxiety disorder versus panic disorder and/ or agoraphobia. Shown in Figure 1.1 are the ADIS-5 questions that address this differentiation (Julie’s an- swers are in italics).
As demonstrated in Figure 1.1, Julie experiences panic attacks in social situations and is concerned about being negatively evaluated by others if her anxiety be- comes visibly apparent. However, despite her history of shyness, Julie’s current social discomfort is based primarily on the possibility of panicking. Because of this, and because she meets the other criteria for panic disorder (i.e., unexpected/nonsocial panic attacks and pervasive apprehension about future panic attacks), the social distress is best subsumed under the domain of panic disorder and agoraphobia. If Julie reported that she experiences panic attacks in social situations only, or that she worries about panic attacks in social situa- tions only, then a diagnosis of social anxiety disorder would be more probable. A report of unexpected panic attacks, as well as self-consciousness about things that she might do or say in social situations regardless of the occurrence of panic, would be consistent with a dual diagnosis of panic disorder–agoraphobia and social anxiety disorder. In general, an individual with panic disorder may continue to feel anxious even when play- ing a passive role in a social setting, whereas a patient with social phobia is more likely to feel relaxed when he/she is not the center of attention and does not an- ticipate being evaluated or judged (Dattilio & Salas- Auvert, 2000).
The same types of diagnostic questioning are useful for distinguishing between panic disorder–agoraphobia and claustrophobia. Other differential diagnostic is- sues can arise with respect to somatoform disorders, real
20 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
FIGURE 1.1. Julie’s responses (in italics) to ADIS-5 questions.
Parts of ADIS-5 Panic Disorder Section
Do you currently have times when you feel a sudden rush of intense fear or discomfort? Yes.
In what kinds of situations do you have those feelings? Driving, especially on freeways . . . alone at home . . . at parties or in crowds of people.
Do you ever have those feelings come “from out of the blue,” for no apparent reason, or in situations where you did not expect them to occur? Yes.
How long [does/did] it usually take for the rush of fear/discomfort to reach its peak level? It varies, sometimes a couple of seconds and at other times it seems to build more slowly.
How long [does/did] the fear or discomfort usually last at its peak level? Depends on where I am at the time. If it happens when I’m alone, sometimes it is over within a few minutes or even seconds. If I’m in a crowd, then it seems to last until I leave.
In the last month, how much have you been worried or concerned about having another panic attack or about the potential consequences of having another attack (circle rating)?
0 1 2 3 4 5 6 7 8
No worry/ no fear
Rarely worried/ mild fear
Occasionally worried/
moderate fear
Frequently worried/
severe fear
Constantly worried/
extreme fear
Parts of ADIS-5 Social Phobia Section
In social situations, where you might be observed or evaluated by others, or when meeting new people, do you feel fearful, anxious, or nervous? Yes.
Are you overly concerned that you might do and/or say something that might embarrass or humiliate yourself in front of others, or that others may think badly of you? Yes.
What are you concerned will happen in these situations? That others will notice that I am anxious. My face turns white and my eyes look strange when I panic. I am worried that I’ll flip out in front of them, and they won’t know what to do.
Are you anxious about these situations because you are afraid that you will have a panic attack? Yes (either a panic or that I’ll feel unreal).
Other than when you are exposed to (specify social situations), have you experienced an unexpected rush of fear/anxiety? Yes.
Panic Disorder and Agoraphobia 21
medical conditions, and avoidant or dependent person- ality disorders.
Following completion of a diagnostic assessment, a dimensional assessment specifically designed for panic disorder, such as the Panic Disorder Severity Scale (PDSS; Shear et al., 1997), may be helpful. This cli- nician-completed scale rates seven areas of responding using a 0- to 4-point severity rating scale: panic attack frequency; distress; anticipatory anxiety; agoraphobic and interoceptive-related fears; avoidant behavior; and work and social impairment. A cutoff score of 8 on the PDSS identifies patients with panic disorder with high sensitivity and acceptable specificity (Shear et al., 2001).
Medical Evaluation
A medical evaluation is generally recommended, be- cause several medical conditions should be ruled out before assigning the diagnosis of panic disorder. These include thyroid conditions, caffeine or amphetamine intoxication, drug withdrawal, or pheochromocytoma (a rare adrenal gland tumor). Furthermore, certain medical conditions can exacerbate panic disorder, al- though panic disorder is likely to continue even when the symptoms are under medical control. Mitral valve prolapse, asthma, allergies, and hypoglycemia fall into this latter category. According to the model described earlier, these medical conditions exacerbate panic disor- der to the extent that they elicit the feared physical sen- sations. For example, mitral valve prolapse sometimes produces the sensation of a heart flutter, asthma pro- duces shortness of breath, and hypoglycemia produces dizziness and weakness, all of which overlap with symp- toms of panic and may therefore become conditional cues for panic.
Self‑Monitoring
Self-monitoring is a very important part of assessment and treatment for panic disorder and agoraphobia. Retrospective recall of past episodes of panic and anxi- ety, especially when made under anxious conditions, may inflate estimates of panic frequency and intensity (Margraf et al., 1987; Rapee, Craske, & Barlow, 1990). Moreover, such inflation may contribute to apprehen- sion about future panic. In contrast, ongoing self-mon- itoring generally yields more accurate, less inflated es- timates (for a comprehensive review of self-monitoring for panic and anxiety, see Craske & Tsao, 1999). Also, ongoing self-monitoring is believed to contribute to an
objective self-awareness. Objective self-monitoring re- places negative, affect-laden self-statements such as “I feel horrible. This is the worst it has ever been—my whole body is out of control” with “My anxiety level is 6. My symptoms include tremulousness, dizziness, un- real feelings, and shortness of breath—and this episode lasted 10 minutes.” Objective self-awareness usually re- duces negative affect. Finally, self-monitoring provides feedback for judging progress and useful material for in-session discussions.
Panic attacks are recorded in the Panic Attack Re- cord, a version of which is shown in Figure 1.2. This re- cord, which is to be completed as soon as possible after a panic attack occurs, is therefore carried on-person (wal- let size). Daily levels of anxiety, depression, and worry about panic are monitored with the Daily Mood Re- cord shown in Figure 1.3. This record is completed at the end of each day. Finally, activities may be recorded by logging daily excursions in a diary, or by checking off activities completed from an agoraphobia checklist.
A common problem with self-monitoring is noncom- pliance. Sometimes noncompliance is due to misunder- standing or lack of perceived credibility in self-moni- toring. Most often, however, noncompliance is due to anticipation of more anxiety as a result of monitoring. This is particularly true for individuals whose pre- ferred style of coping is to distract themselves as much as possible because thoughts of panic might otherwise become overwhelming: “Why should I make myself worse by asking myself how bad I feel?” In Julie’s case, the self-monitoring task was particularly difficult, be- cause explicit reminders of her anxiety elicited strong concerns about losing touch with reality. Prompting, reassurance that anxiety would subside with persever- ance at self-monitoring, and emphasis on objective versus subjective self-monitoring were helpful for Julie. In addition, therapist attention to the self-monitored information and corrective feedback about the method of self-monitoring at the start of each treatment session reinforced Julie’s self-monitoring.
Standardized Inventories
Several standardized self-report inventories provide use- ful information for treatment planning and are sensitive markers of therapeutic change. The Anxiety Sensitiv- ity Index (Reiss, Peterson, Gursky, & McNally, 1986) and the multidimensional Anxiety Sensitivity Index–3 (Taylor et al., 2007) have received wide acceptance as a trait measure of threatening beliefs about bodily sensa-
22 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
0——1——2——3——4——5——6——7——8——9——10
None Mild Moderate Strong Extreme
Date Average anxiety
Average depression
Average worry about panic
7572/16
5452/17
5442/18
4342/19
1122/21
2222/22
5442/29
FIGURE 1.3. Julie’s Daily Mood Record.
Date Time began
Triggers
Expected Unexpected
Maximum Fear 0——1——2——3——4——5——6——7——8——9——10
None Mild Moderate Strong Extreme
Check all symptoms present to at least a mild degree:
Chest pain or discomfort Sweating
Heart racing/palpitations/pounding Nausea/upset stomach
Short of breath Dizzy/unsteady/lightheaded/faint
Shaking/trembling Chills/hot flushes
Numbness/tingling Feelings of unreality
Feelings of choking Fear of dying
Fear of losing control/going crazy
Thoughts:
Behaviors:
2/16/06 Home alone and shortness of breath x
x x x x
x
x
I am going crazy, I will lose control Called my mother
5:20 P.M.
FIGURE 1.2. Julie’s Panic Attack Record.
Panic Disorder and Agoraphobia 23
tions. Both display good psychometric properties and tend to discriminate panic disorder and agoraphobia from other anxiety disorders (e.g., Taylor et al., 1992; Telch, Sherman, & Lucas, 1989), especially the Physical Concerns subscale (Zinbarg et al., 1997). More specific information about which particular bodily sensations are feared most and what specific misappraisals occur most often may be obtained from the Body Sensations Questionnaire and the Agoraphobia Cognitions Ques- tionnaire, respectively (Chambless et al., 1984). Both scales have strong to excellent psychometric proper- ties and are sensitive to change following treatment (see Keller & Craske, 2008). The Mobility Inventory (Chambless, Caputo, Gracely, Jasin, & Williams, 1985) lists agoraphobic situations, which are rated in terms of degree of avoidance when alone and when accompa- nied. This instrument is very useful for establishing in vivo exposure hierarchies and, again, is well supported psychometrically. As described earlier, the PDSS (Shear et al., 2001) is a commonly used, brief dimensional measure of panic disorder symptom severity with good psychometric properties. Finally, the Panic Appraisal Inventory assesses cognitive maintaining factors of panic disorder and includes three 15-item subscales in- cluding anticipated panic, perceived consequences of panic, and perceived self-efficacy to cope with panic (Telch et al., 1989).
In addition, we have developed two standardized self- report inventories that are useful for panic disorder and agoraphobia. The first, the Albany Panic and Phobia Questionnaire (Rapee, Craske, & Barlow, 1995), as- sesses fear and avoidance of activities that produce feared bodily sensations (e.g., exercise, caffeine), as well as more typical agoraphobia and social situations. Factor analy- ses confirmed three distinct factors labeled Agoraphobia, Social Phobia, and Interoceptive Fears. The question- naire has adequate psychometric properties and is useful in profiling agoraphobic versus interoceptive avoidance. The second, the Anxiety Control Questionnaire, assess- es perceived lack of control over anxiety- related events and occurrences, such as internal emotional reactions or externally threatening cues (Rapee, Craske, Brown, & Barlow, 1996). This scale is designed to assess locus of control, but in a more specific and targeted manner rel- evant to anxiety and anxiety disorders compared to more general locus-of-control scales. A revised, 15-item version yields three factors—Emotion Control, Threat Control, and Stress Control—with a higher-order dimension of perceived control (Brown, White, Forsyth, & Barlow, 2004). Changes in this scale from pre- to posttreatment
predicted reductions in comorbidity at follow-up in one study (Craske et al., 2007). A more detailed review of each questionnaire listed herein and the complete assess- ment for panic disorder and agoraphobia is provided by Keller and Craske (2008).
Behavioral Tests
The behavioral test is a useful measure of degree of avoidance of specific interoceptive cues and external sit- uations. Behavioral approach tests can be standardized or individually tailored. The standardized behavioral test for agoraphobic avoidance usually involves walk- ing or driving a particular route, such as a 1-mile loop around the clinic setting. Standardized behavioral tests for anxiety about physical sensations involve exercises that induce panic-like symptoms, such as spinning in a circle, running in place, hyperventilating, and breath- ing through a straw (Barlow & Craske, 2006). Anxiety levels are rated at regular intervals throughout the be- havioral tests, and actual distance or length of time is measured. The disadvantage of standardized behavioral tests is that the specific task may not be relevant to all patients (e.g., a 1-mile walk or running in place may be only mildly anxiety provoking to some but highly dis- tressing to others); hence, the value of individually tai- lored tasks. In the case of agoraphobia, this usually en- tails attempts at three to five individualized situations that the patient has identified as ranging from Some- what difficult to Extremely difficult, such as driving two exits on freeway, waiting in a bank line, or shopping in a local supermarket for 15 minutes. For anxiety about physical sensations, individually tailored behavioral tests entail exercises designed specifically to induce the sensations feared most by a given patient (e.g., nose plugs to induce sensations of difficulty breathing). As with standardized tests, ongoing levels of anxiety and degree of approach behavior are measured in relation to individually tailored behavioral tests.
Individually tailored behavioral tests are more in- formative for clinical practice, although they confound between-subject comparisons for research purposes. Behavioral tests are an important supplement to self- report of agoraphobic avoidance, because patients tend to underestimate what they can actually achieve (Craske et al., 1988). In addition, behavioral tests often reveal important information for treatment planning of which the individual is not yet fully aware. For ex- ample, the tendency to remain close to supports, such as railings or walls, may not be apparent until one ob-
24 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
serves the patient walking through a shopping mall. In Julie’s case, the importance of change from daylight to night was not apparent until she was asked to drive on a section of road as a behavioral test. Her response was that it was too late in the day to drive, because dusk made her feel as if things were unreal. Similarly, it was not until Julie completed a behavioral test that we rec- ognized the importance of air-conditioning when she was driving. Julie believed that the cool air blowing on her face helped her to remain “in touch with reality.” Fi- nally, we noticed that her physical posture while driving was a factor that contributed to anxiety: Julie’s shoul- ders were hunched, and she leaned toward the steering wheel and held it very tightly. All of these were targeted in the treatment: Driving at dusk was included in her hierarchy; air-conditioning was regarded as a safety sig- nal from which she should be weaned; and driving in a more relaxed position was part of mastery exposure.
Psychophysiology
Ongoing physiological measures are not very practi- cal tools for clinicians, but they can provide important information. In particular, the discrepancy described earlier between reports of symptoms and actual physi- ological arousal (i.e., report of heart rate acceleration in absence of actual heart rate acceleration) may serve as a therapeutic demonstration of the role of attention and cognition in symptom production. Similarly, actual re- cordings provide data to disconfirm misappraisals such as “My heart feels like it’s going so fast that it will ex- plode” or “I’m sure my blood pressure is so high that I could have a stroke at any minute.” Finally, resting lev- els of physiological functioning, which are sometimes dysregulated in anxious individuals, may be sensitive measures of treatment outcome (e.g., Craske, Lang, Ai- kins, & Mystkowski, 2005).
Functional Analysis
The various methods of assessment provide the mate- rial for a full functional analysis for Julie. Specifically, the topography of her panic attack is as follows: The most common symptoms include a feeling of unreal- ity, shortness of breath, and racing heart; average fre- quency of panic attacks is three per week; each panic attack on average lasts from a few seconds to 5 minutes, if Julie is not in a crowd, where the panicky feelings last until she exits the crowd; in terms of apprehension, Julie worries about panic 75% of the day; and most of
her panic attacks are expected, but she has some unex- pected ones as well. Julie has both situational and in- ternal antecedents to her panic attacks. The situational antecedents include driving on freeways; crowds of peo- ple; being alone, especially at night; restaurants; dusk; reading and concentrating for long periods of time; and aerobic activity. The internal antecedents include heart rate fluctuations, lightheaded feelings, hunger feelings, weakness due to lack of food, thoughts of the “big one” happening, thoughts of not being able to cope with this for much longer, and anger. Her misappraisals about panic attack symptoms include beliefs that she will never return to normality, that she will go crazy or lose control, and that others will think she is weird. Her behavioral reactions to panic attacks include escape behaviors such as pulling off to the side of the road, leaving restaurants and other crowded places, calling her husband or mother, and checking for her Klonopin. Her behavioral reactions to the anticipation of panic at- tacks include avoidance of driving long distances alone, driving on unfamiliar roads and freeways or at dusk, crowded areas, exercise, quiet time with nothing to do, and doing one thing for a long period of time. In addition, she tries not to think about anxiety or feel- ings of unreality. Her safety signals and safety-seeking behaviors include having her Klonopin on hand at all times, always knowing the location of her husband, and having the air-conditioning on. The consequences of her panic disorder with agoraphobia affect her fam- ily: Julie’s husband is concerned and supportive, but her mother thinks she should pull herself together because “it’s all in her head.” In addition, Julie works but has cut back the number of hours, and she travels and socializes much less. Her general mood includes some difficulty concentrating and sleeping, restlessness, headaches, and muscular pains and aches. In addition, she is occasion- ally tearful, sad, and hopeless, and generally feels down.
COMPONENTS OF COGNITIVE‑BEHAVIORAL THERAPY
The components of the cognitive-behavioral treatment described in this section are integrated into a session- by-session treatment program in the next section.
Education
The treatment begins with education about the nature of panic disorder, the causes of panic and anxiety, and
Panic Disorder and Agoraphobia 25
the ways panic and anxiety are perpetuated by feed- back loops among physical, cognitive, and behavioral response systems. In addition, specific descriptions of the psychophysiology of the fight–flight response are provided, as well as an explanation of the adaptive value of the various physiological changes that occur during panic and anxiety. The purpose of this education is to correct the common myths and misconceptions about panic symptoms (i.e., beliefs about going crazy, dying, or losing control) that contribute to panic and anxiety. The survival value of alarm reactions (i.e., panic at- tacks) is emphasized throughout.
Education also distinguishes between the state of anxiety and the emotion of fear/panic, both conceptu- ally and in terms of its three response modes (subjective, physiological, and behavioral). This distinction is cen- tral to the model of panic disorder and to the remainder of the treatment. Anxiety is viewed as a state of prepara- tion for future threat, whereas panic is the fight–flight emotion elicited by imminent threat. Panic/fear is characterized by perceptions of imminent threat, sud- den autonomic discharge, and fight–flight behavior. In contrast, anxiety is characterized by perceptions of future threat and chronic tension, cautiousness, avoid- ance, and disruption of performance.
Self‑Monitoring
Self-monitoring is essential to the personal scientist model of cognitive-behavioral therapy. Self-monitoring is introduced as a way to enhance objective self-aware- ness and increase accuracy in self-observation. As noted earlier, patients are asked to keep at least two types of records. The first, the Panic Attack Record, is com- pleted as soon after each panic attack as possible; this record provides a description of cues, maximal distress, symptoms, thoughts, and behaviors. The second, the Daily Mood Record, is completed at the end of each day to record overall or average levels of anxiety, de- pression, and whatever else is considered important to record. Additionally, patients may keep a daily record of activities or situations completed or avoided.
Breathing Retraining and Capnometry‑Assisted Respiratory Training
Breathing retraining is a central component early on in the development of panic control treatments, because many patients with panic describe symptoms of hyper- ventilation as being very similar to their panic attack
symptoms. It is noteworthy, however, that a hyperven- tilation symptom report does not always accurately rep- resent hyperventilation physiology: Only 50% or fewer patients show actual reductions in end-tidal CO2 values during panic attacks (Hibbert & Pilsbury, 1989; Holt & Andrews, 1989; Hornsveld, Garssen, Fiedelij Dop, & van Spiegel, 1990).
In early conceptualizations, panic attacks were related to stress-induced respiratory changes that provoke fear either because they are perceived as threatening or they augment fear already elicited by other phobic stimuli (Clark, Salkovskis, & Chalkley, 1985). Several studies illustrated a positive effect of breathing retraining, in- volving slow abdominal breathing exercises (e.g., Kraft & Hoogduin, 1984). The value of breathing retrain- ing was subsequently questioned. For example, several studies suggested that the addition of breathing retrain- ing alone did not improve on in vivo exposure (e.g., de Beurs, van Balkom, Lange, Koele, & van Dyck, 1995). We found breathing retraining to be slightly less effec- tive than interoceptive exposure when each was added to cognitive restructuring and in vivo exposure (Craske, Rowe, Lewin, & Noriega-Dimitri, 1997), and in anoth- er study, the inclusion of breathing retraining resulted in poorer outcomes than cognitive-behavioral therapy without breathing retraining, although the findings were not robust (Schmidt et al., 2000). From their re- view of efficacy and mechanisms of action, Garssen, de Ruiter, and van Dyck (1992) concluded that breathing retraining probably effects change not through breath- ing per se but through distraction and/or a sense of con- trol. Thus, breathing retraining is no longer considered a central component of cognitive-behavioral therapy for panic disorder. Furthermore, to the extent that it might become misused as a means for avoiding physical symp- toms, it may even be countertherapeutic. That being said, there may be occasions when breathing retrain- ing is a useful tool, such as for the individual showing obvious signs of irregular breathing (e.g., rapid, shallow breathing, frequent deep breaths), as long as breathing retraining does not become a method of avoidance or safety seeking.
In contrast to traditional breathing retraining, cap- nometry-assisted respiratory training (CART) targets respiratory dysregulation, in particular hypocapnia (Meuret, Rosenfield, Seidel, Bhaskara, & Hofmann, 2010; Meuret, Wilhelm, Ritz, & Roth, 2008). CART is a brief, 4-week training that uses immediate feedback of end-tidal partial pressure CO2 (pCO2) to teach patients how to raise their subnormal levels of pCO2 (hyperven-
26 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
tilation) and thereby gain control over dysfunctional re- spiratory patterns and associated panic symptoms (e.g., shortness of breath, dizziness). The device, a portable capnometer, offers breath-by-breath feedback of expired CO2 and rate of breathing (both measured via a nasal canula). Due to the novelty of CART, randomized controlled trials are limited but promising. In a first randomized controlled study, Meuret and colleagues (2008) tested the efficacy of 4 weeks of CART (N = 20) compared to a delayed wait-list control group (WL, N = 17). CART, but not WL, led to sustained increases in pCO2 levels and reduced panic severity and frequency. Reductions in panic symptom severity (PDSS; Shear et al., 1997) were comparable to standard cognitive- behavioral therapy, and improvements were maintained at 12-month follow-up. In a second study, patients with panic disorder were randomly assigned to receive either 4 weeks of CART (N = 21) or cognitive therapy (N = 20). An initial 4 weeks of skills training was followed by three sessions of in vivo exposure and a fourth session at a 2-month follow-up. Respective skills acquisition trainings led to significant and comparable reductions in panic symptom severity and panic-related cogni- tions, irrespective of modality. However, only CART, not cognitive therapy, led to a correction of hypocapnic levels of pCO2 (Meuret et al., 2010; Seidel, Rosenfield, Bhaskara, Hofmann, & Meuret, 2009). However, an evaluation of the degree to which CART augments exposure therapy (relative to exposure therapy alone) awaits testing.
Applied Relaxation
A form of relaxation known as applied relaxation has shown good results as a treatment for panic at- tacks. Two studies by Öst (Öst & Westling, 1995; Öst, Westling, & Hellström, 1993) indicate that ap- plied relaxation is as effective as in vivo exposure and cognitive therapy. In contrast, Barlow and colleagues (1989) found that applied progressive muscle relaxation (PMR) is relatively ineffective for panic attacks, al- though we excluded all forms of interoceptive exposure from the hierarchy of tasks to which PMR was applied, which was not necessarily the case in the studies by Öst (Öst, 1988; Öst & Westling, 1995; Öst, Westling, & Hellström, 1993). Clark and colleagues (1994) found cognitive therapy to be superior to applied PMR when conducted with equal amounts of in vivo exposure, whereas Beck, Stanley, Baldwin, Deagle, and Averill (1994) found very few differences between cognitive
therapy and PMR when each was administered without exposure procedures.
Cognitive Restructuring
Cognitive restructuring is a skills set in which patients learn to recognize cognitive errors and generate alter- native, noncatastrophic explanations for the sensations that are feared during panic attacks. Cognitive therapy begins with a treatment rationale and discussion of the role of thoughts in generating emotions. Next, thoughts are recognized as hypotheses rather than as fact, and are therefore open to being questioned and challenged. De- tailed self-monitoring of emotions and associated cogni- tions is instituted to identify specific beliefs, appraisals, and assumptions. Once identified, relevant cognitions are categorized into types of typical errors that occur during heightened emotion, such as overestimations of risk of negative events or catastrophization of mean- ing of events. The process of categorization, or label- ing of thoughts, is consistent with a personal scientist model and facilitates an objective perspective by which the validity of the thoughts can be evaluated. Thus, in labeling the type of cognitive distortion, the patient is encouraged to use an empirical approach to examine the validity of his/her thoughts by considering all of the available evidence. Therapists use Socratic questioning to help patients make guided discoveries and question their anxious thoughts. Next, more evidence-based alternative hypotheses are generated. In addition to surface-level appraisals (e.g., “That person is frowning at me because I look foolish”), core-level beliefs or sche- mas (e.g., “I am not strong enough to withstand fur- ther distress” or “I am unlikable”) are questioned in the same way. Importantly, cognitive restructuring is not intended as a direct means of minimizing fear, anxiety, or unpleasant symptoms. Instead, cognitive restructur- ing is intended to correct distorted thinking; eventually fear and anxiety are expected to subside, but their dimi- nution is not the first goal of cognitive therapy.
Cognitive therapy is often intermingled with behav- ioral techniques (e.g., “behavioral experiments,” “hy- pothesis testing,” “instructions” involving exposure) that complicate direct testing of the efficacy of cogni- tive therapy in its “pure” form (e.g., Hoffart, Sexton, Hedley, & Martinsen, 2008; Hofmann et al., 2007; Öst et al., 1993; Teachman, Marker, & Smith-Janik, 2008). Nonetheless, there is some evidence that training in cognitive procedures in full isolation from exposure and behavioral procedures is efficacious in reducing aspects
Panic Disorder and Agoraphobia 27
of panic (Beck et al., 1994; Meuret et al., 2010; Salkov- skis, Clark, & Hackmann, 1991; van den Hout, Arntz, & Hoekstra, 1994). Similarly, in a study by Bouchard and colleagues (1996), cognitive restructuring was as effective as exposure therapy in reducing panic symp- toms. However, the effects of cognitive therapy alone on agoraphobia are unclear. One study found that cog- nitive therapy was less effective than exposure therapy for agoraphobia (Williams & Falbo, 1996). In another study, Hoffart (1995) found that cognitive therapy was as effective as guided mastery exposure delivered inten- sively over 6 weeks for individuals with moderate to se- vere agoraphobia, although some elements of exposure (e.g., hyperventilation tests to elicit sensations) were in- cluded in the cognitive therapy condition.
A few studies have evaluated the effects of cogni- tive therapy combined with exposure in comparison to exposure alone or in combination with other coping skills. Most often, cognitive therapy combined with ex- posure does not yield an additional benefit over in vivo exposure alone (Öst, Thulin, & Ramnero, 2004; van den Hout et al., 1994; see Murphy et al., 1998, for an exception).
Exposure
Exposure is a critical phase of treatment and, once begun, is a major focus of treatment sessions as well as between-treatment session homework, since limited exposure practice is of small benefit and may even be detrimental. The exposure is designed to disconfirm misappraisals and extinguish conditional emotional re- sponses to external situations and contexts, through in vivo exposure, as well as to bodily sensations, through interoceptive exposure. Growing evidence suggests that exposure represents the most powerful component of cognitive-behavioral therapy for panic disorder and agoraphobia, including meta-analyses that fail to show any additional benefit of either cognitive restructuring or somatic coping skills beyond exposure therapy alone (Norton & Price, 2007). A large trial reported a dose– response relationship between exposure and improve- ment in agoraphobia (Gloster et al., 2011).
In Vivo Exposure
In vivo exposure refers to repeated and systematic, real- life exposure, in this case, to agoraphobic situations. A long history of research has established the efficacy of in vivo exposure for agoraphobia.
Most often, in vivo exposure is conducted in a grad- uated manner, proceeding from the least to the most anxiety-provoking situations on an avoidance hierar- chy. However, there is some evidence to suggest that intensive or ungraduated exposure may be effective. In a study by Feigenbaum (1988), treatment sessions were conducted in a massed format over the course of 6–10 consecutive days. One group received ungraded expo- sure (N = 25), beginning with the most feared items from avoidance hierarchies. Another group received graded exposure (N = 23), beginning with the least feared hierarchy items. Approximately one-third of this severely agoraphobic sample was housebound at initial assessment. At posttreatment and 8 months later, the conditions proved to be equally effective (although, in- triguingly, the graded group reported the treatment to be more distressing). However, ungraded exposure was clearly superior at the 5-year follow-up assessment: 76% of the intensive group versus 35% of the graded group reported themselves to be completely free of symptoms. When 104 subjects were added to the intensive expo- sure format, the same results were obtained. Of 129 subjects, 78% were reportedly completely symptom-free 5 years later. This dramatic set of results suggests that an intensive approach, which is likely to produce higher levels of arousal than a graduated approach, can be very beneficial (at least when conducted in a massed format). Unfortunately, the validity of the outcome measures in this study is somewhat questionable, and replication by independent investigators has yet to be reported.
The amount of time devoted to in vivo exposure is very dependent on the patient’s agoraphobia profile. Obviously, more time is needed for patients with more severe agoraphobia.
Interoceptive Exposure
In interoceptive exposure, the goal is deliberately to in- duce feared physical sensations a sufficient number of times, and long enough each time, so that misappraisals about the sensations are disconfirmed and conditional anxiety responses are extinguished. A standard list of exercises, such as hyperventilating and spinning, is used to establish a hierarchy of interoceptive exposures. With a graduated approach, exposure begins with the less dis- tressing physical exercises and continues with the more distressing exercises. It is essential that the patient en- dure the sensations beyond the point at which they are first noticed, for at least 30 seconds to 1 minute, be- cause early termination of the task may eliminate the
28 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
opportunity to learn that the sensations are not harm- ful and that the anxiety can be tolerated. The exercise is followed by a discussion of what the patient learned about the physical sensations. These interoceptive exer- cises are practiced daily outside of the therapy session to consolidate the process of learning. Interoceptive ex- posure extends to naturalistic activities that induce so- matic sensations (e.g., caffeine consumption, exercise).
A series of studies reported on the effects of intero- ceptive exposure independent of other therapeutic strategies. Early on, Bonn, Harrison, and Rees (1971) and Haslam (1974) observed successful reduction in reactivity with repeated infusions of sodium lactate (a drug that produces panic-type bodily sensations). However, panic was not monitored in these investiga- tions. Griez and van den Hout (1986) compared six sessions of graduated CO2 inhalations to a treatment regimen of propranolol (a beta-blocker chosen because it suppresses symptoms induced by CO2 inhalations), both conducted over the course of 2 weeks. CO2 inha- lation treatment resulted in a mean reduction from 12 to four panic attacks, which was superior to the results from propranolol. In addition, inhalation treatment resulted in significantly greater reductions in reported fear of sensations. A 6-month follow-up assessment suggested maintenance of treatment gains, although panic frequency was not reported. Beck and Shipherd (1997) similarly found a positive effect from repeated CO2 inhalations, although it had little effect on agora- phobia (Beck, Shipherd, & Zebb, 1997). Broocks and colleagues (1998) tested the effects of exercise (with once-weekly supportive contact from a therapist) in comparison to clomipramine or drug placebo over 10 weeks. The exercise group was trained to run 4 miles, three times per week. Despite high attrition from ex- ercise (31%), exercise was more effective than the drug placebo condition. However, clomipramine was supe- rior to exercise.
In the first comparison to other cognitive and be- havioral treatments, Barlow and colleagues (1989) compared applied PMR, interoceptive exposure plus breathing retraining and cognitive restructuring, their combination with applied PMR, and a wait-list con- trol in a sample with panic disorder with limited ago- raphobia. The two conditions involving interoceptive exposure, breathing retraining and cognitive restruc- turing, were significantly superior to applied PMR and wait-list conditions. The results were maintained 24 months following treatment completion for the group receiving interoceptive exposure, breathing retraining,
and cognitive restructuring without PMR, whereas the combined group tended to deteriorate over follow-up (Craske, Brown, & Barlow, 1991). As already men- tioned, we compared interoceptive exposure, cognitive therapy, and in vivo exposure to breathing retraining, cognitive therapy, and in vivo exposure for individuals with varying levels of agoraphobia. The condition that included interoceptive exposure was slightly superior to breathing retraining at posttreatment and 6 months later (Craske et al., 1997). Similarly, Ito, Noshirvani, Basoglu, and Marks (1996) found a trend for those who added interoceptive exposure to their self-directed in vivo exposure and breathing retraining to be more like- ly to achieve at least a 50% improvement in phobic fear and avoidance. However, the combination of breathing education, breathing retraining, and repeated intero- ceptive exposure to hyperventilation did not increase the effectiveness of in vivo exposure for agoraphobia (de Beurs, Lange, van Dyck, & Koele, 1995).
Interoceptive exposure is now a standard compo- nent of cognitive-behavioral therapy for panic disorder (e.g., Barlow et al., 2000; Craske, Lange, et al., 2005), although different groups give different emphases to interoceptive exposure, with some emphasizing it as a means for extinguishing fear responses (Barlow & Craske, 2006) and others, as a vehicle for disconfirm- ing misappraisals (Clark, 1996). Indeed, dismantling studies indicate that interoceptive exposure may be a particularly active ingredient of cognitive-behavioral therapy for panic disorder. One analogue study with in- dividuals high in anxiety sensitivity compared one ses- sion of interoceptive exposure to interoceptive exposure plus cognitive restructuring to interoceptive exposure plus cognitive restructuring and breathing retraining (Deacon et al., 2012). All three groups showed greater improvement in anxiety symptoms compared to a con- trol condition, with no differences between the three active treatment groups, suggesting that there was no benefit to adding cognitive restructuring or breathing retraining. However, the benefits of cognitive restruc- turing and breathing retraining may not be observed in a single session.
Optimizing Learning during Exposure
Our understanding of the mechanisms of exposure therapy has evolved over time. One of the most influen- tial theories, emotional processing theory, emphasized habituation of fear responding within an exposure trial as a necessary precursor to habituation across treatment
Panic Disorder and Agoraphobia 29
sessions that in turn leads to long-term corrective learn- ing (Foa & Kozak, 1986; Foa & McNally, 1996). Most recently, we have emphasized optimizing inhibitory learning and its retrieval in ways that are not necessar- ily dependent on reductions in fear throughout trials of exposure (Craske et al., 2008); we discuss this approach below.
Emotional processing theory emphasizes mecha- nisms of habituation as precursors to cognitive correc- tion. Specifically, emotional processing theory purports that the effects of exposure therapy derive from activa- tion of a “fear structure” and integration of information that is incompatible with it, resulting in the develop- ment of a non-fear structure that replaces or competes with the original one. Incompatible information derives first from within-session habituation, or reduction in fear responding with prolonged exposure to the fear stimulus. Within-session habituation is seen as a pre- requisite for the second piece of incompatible informa- tion, which derives from between-session habituation over repeated occasions of exposure. Between-session habituation is purported to form the basis for long-term learning and to be mediated by changes in “meaning,” or lowered probability of harm (i.e., risk) and lessened negativity (i.e., valence) of the stimulus. Emotional processing theory guides clinicians to focus on the ini- tial elevation of fear followed by within- and between- session reductions in fear as signs of treatment success. Although enticing in its face validity, support for the theory has been inconsistent at best (Craske et al., 2008; Craske, Liao, Brown, & Vervliet, 2012). Rather, the evidence suggests that the amount by which fear ha- bituates from the beginning to the end of an exposure practice is not a good predictor of overall outcomes, and that evidence for between-session habituation is mixed (Craske et al., 2008, 2012).
A return to the science of fear learning and extinction may help to explain the effects of exposure therapy and thereby optimize its implementation. It is now thought that inhibitory learning is central to extinction (Bou- ton, 1993). Inhibitory pathways are also recognized in the neurobiology of fear extinction (see Sotres-Bayon, Cain, & LeDoux, 2006). Within a Pavlovian condi- tioning approach, inhibitory learning means that the original conditioned stimulus–unconditioned stimulus (CS-US) association learned during fear conditioning is not erased during extinction, but rather is left intact as a new, secondary learning about the CS-US devel- ops (Bouton, 1993). The degree to which inhibitory as- sociations shape fear responding at retest (the index of
strength and stability of new “learning”) is independent of fear levels expressed throughout extinction and in- stead is dependent on factors such as context and time.
Based on the inhibitory retrieval model of extinction, outcomes may be enhanced by strategies that do not rely on fear reduction within a trial of exposure (Craske et al., 2008, 2012). Indeed, fear reduction may become a safety behavior for persons with panic disorder (since fear reduction eradicates the very thing that is feared), such that a more appropriate goal may be to maintain high levels of fear and anxiety in order to disconfirm the expectancy of negative consequences. One trans- lational possibility is “deepened extinction” (Rescorla, 2006), in which multiple fear conditional stimuli are first extinguished separately before being combined during extinction, and in animal studies, decrease spon- taneous recovery and reinstatement of fear. Indeed, this is what is essentially done when interoceptive exposure is conducted in feared agoraphobic situations (Barlow & Craske, 1994), and recent experimental data support the beneficial effects of deepened extinction in human conditioning studies (Culver, Vervliet, & Craske, 2015).
In addition, the effects of exposure therapy may be enhanced by the prevention or removal of “safety sig- nals” or “safety behaviors.” Common safety signals and behaviors for clients with panic disorder are the pres- ence of another person, therapists, medications, or food or drink. In the experimental literature, safety signals alleviate distress in the short term, but when they are no longer present, the fear returns (Lovibond, Davis, & O’Flaherty, 2000), an effect that may derive in part from interference with the development of inhibitory associations. In phobic samples, the availability and use of safety signals and behaviors has been shown to be detrimental to exposure therapy (Sloan & Telch, 2002), whereas instructions to refrain from using safe- ty behaviors improved outcomes (Salkovskis, 1991). Similarly, the use of safety signals was associated with poorer outcomes for panic (Helbig-Lang & Petermann, 2010). However, recent data have presented contradic- tory findings (Rachman, Shafran, Radomsky, & Zysk, 2011).
Further options include stimulus variability throughout exposure, since variability has been shown to enhance the storage capacity of newly learned in- formation. Two studies with clinical analogues have demonstrated positive benefits in terms of spontane- ous recovery (Lang & Craske, 2000; Rowe & Craske, 1998), while a third showed trends only (Kircanski et al., 2011). In the treatment for panic disorder with ago-
30 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
raphobia, this implies conducting exposure for varying durations, at varying levels of intensity, rather than continuing exposure in one situation until fear declines before moving to the next situation. Notably, such vari- ability typically elicits higher levels of anxiety during exposure but without detrimental effects and some- times with beneficial effects in the long term.
Based on evidence of the weakening of fear extinc- tion by antagonists of the glutamate receptors in the amygdala, Walker and Davis (2002) tested and dem- onstrated that drug agonists of the same receptors, and in particular, D-cycloserine, enhance extinction in animal studies. In a meta-analysis of the efficacy of D-cycloserine for anxiety disorders, Norberg, Krystal, and Tolin (2008) reported effect sizes of d = 0.60 at posttreatment and 0.47 at follow-up in clinical anxiety samples. D-Cycloserine in combination with interocep- tive exposure for panic clients has resulted in a greater reduction in symptom severity, and a greater likelihood of achieving a change in clinical status at posttreatment and 1-month follow-up compared to exposure plus pla- cebo (Otto et al., 2010). Notably, D-cycloserine has been shown to have positive effects without influencing the level of fear during exposure per se.
A number of options for enhancing retrieval of the extinction memory have been tested. One option dur- ing extinction training is to include retrieval cues to be used in other contexts once extinction is over. This has been shown to be effective in animal studies and human conditioning studies (see Craske et al., 2012, for a review). In clinical analogue samples, the effects of a retrieval cue upon context renewal were very weak in one study (Culver, Stoyanova, & Craske, 2012), although instructions to reinstate what was learned mentally during exposure had more robust effects in re- ducing context renewal in another study (Mystkowski, Craske, Echiverri, & Labus, 2006). In the treatment of panic disorder, this approach simply suggests that cli- ents carry with them cues (e.g., a wristband) to remind them what they learned during exposure therapy (as long as the cues do not become safety signals), or are prompted to remind themselves of what they learned in exposure therapy each time they experience previously feared sensations or situations.
Another option is to provide multiple contexts in which extinction takes place. This approach has been shown to offset context renewal in rodent samples, and in a clinical analogue study of exposure therapy (Vansteenwegen et al., 2007), although the results are not always consistent (Neumann, Lipp, & Cory, 2007).
In the treatment of panic disorder and agoraphobia, this would mean asking clients to conduct their interocep- tive and in vivo exposures in multiple different contexts, such as when alone, in unfamiliar places, or at varying times of day or varying days of the week.
A recent (re)discovery is that retrieving already stored memories induces a process of reconsolidation (Nader, Schafe, & LeDoux, 2000), since the memory is writ- ten into long-term memory again, requiring de novo neurochemical processes. Thus, it may be possible to change memories during the reconsolidation time frame upon retrieval. Propranolol, a beta-blocker, has been shown to block the reconsolidation of memories, and Debiec and LeDoux (2004) found that infusions of propranolol blocked the reconsolidation of a previously formed CS-US memory, and led to erasure of the fear response and resistance to reinstatement effects. This suggests that propranolol upon retrieval may be a useful clinical tool, and indeed, two fear conditioning studies in healthy humans (Kindt, Soeter, & Vervliet, 2009; Soeter & Kindt, 2010) have replicated the effects. How- ever, the effects have not been tested in the context of exposure therapy for panic disorder.
Role of Acceptance during Exposure
Cognitive and somatic coping skills are central to cognitive-behavioral therapy and are taught to facili- tate and improve exposure therapy. Newer approaches that explore acceptance and cognitive defusion (e.g., acceptance and commitment therapy; Hayes, Strosahl, & Wilson, 1999) have been gaining interest, especially given evidence that experiential avoidance is a correlate of anxious psychopathology and acceptance increases willingness to experience and lessens emotional distress over induced anxiety symptoms in individuals with panic disorder (e.g., Campbell-Sills et al., 2006; Eifert & Heffner, 2003), including CO2 inhalation challeng- es (Levitt et al., 2004). Interestingly, the acceptance approach is entirely consistent with our formulation of interoceptive exposure, in which patients are encour- aged to experience the feared physical sensations with- out any attempt to lessen them or to think differently about them in the moment of exposure. We recently extended this model of acceptance during interoceptive exposure to acceptance during in vivo exposure in an open trial of 11 patients with panic disorder (Meuret, Twohig, Rosenfield, Hayes, & Craske, 2012). In gen- eral, the exposures were an opportunity for patients to behave with their panic-related thoughts, feelings, and
Panic Disorder and Agoraphobia 31
bodily sensations; in other words, patients were encour- aged to realize that they can drive for and reach life goals, even in the presence of unpleasant inner experi- ences. To that end, it was explicitly stated that the level of anxiety or fear was not the determining factor. Rath- er, it was explained that “willingness can do surprising things to one’s inner experiences. If one is willing to experience anxiety it may or may not show up. Thus, we are not going to judge the success of these exposures on how high the anxiety gets, but instead in how open you are to what might show up.” To plan effectively for interoceptive (i.e., eliciting panic sensations such as a racing heart or shortness of breath) and in vivo expo- sures (i.e., seeking places and situations that one previ- ously avoided because of the fear of panic sensations), a hierarchy of least to most anxiety-provoking items was created. Movement up the hierarchy was not based on reductions in anxiety at the preceding step but on high willingness to experience panic-related inner experienc- es. During the exposures, patients were encouraged to maintain an open, nonjudgmental stance toward what- ever thoughts, feelings, and bodily sensations arose in a given moment, experiencing them for what they were, and moving toward them while anxious. Treatment was associated with clinically significant improvements in panic symptom severity, willingness to allow inner experiences to occur, and reductions in avoidant be- havior. In another study of a mixed anxiety disorder sample, we found very few differences in outcome be- tween acceptance and commitment therapy (Hayes et al., 1999) and cognitive-behavioral therapy, although the treatments were matched on amount of time spent on exposure therapy, albeit framed differently within for each condition (Arch et al., 2012). Thus, the data to date suggest that both a cognitive therapy coping approach and an acceptance-based exposure approach are effective.
OVERALL EFFICACY OF COGNITIVE‑BEHAVIORAL THERAPY
An extensive body of research has evaluated the efficacy of cognitive-behavioral therapy for panic disorder and agoraphobia. Cognitive-behavioral therapy, involving most or all of the components just listed, yields panic- free rates in the range of 70–80% and high end-state rates (i.e., within normative ranges of functioning) in the range of 50–70% for panic disorder with mini- mal agoraphobia (e.g., Barlow et al., 1989; Clark et al.,
1994). Although agoraphobic avoidance is sometimes associated with less positive response (e.g., Dow et al., 2007), the overall within-group effect size for change in panic disorder and agoraphobia from pre- to post- treatment is very large (e.g., effect size = 1.53; Norton & Price, 2007). Moreover, the between-group effect size is substantial in comparison to wait-list conditions (e.g., effect size = 0.64; Haby, Donnelly, Corry, & Vos, 2006). However, more research is needed comparing cognitive-behavioral therapy to alternative active treat- ment conditions.
The effectiveness extends to clients who experience nocturnal panic attacks (Craske, Lang, et al., 2005). Furthermore, cognitive-behavioral therapy results in improvements in rates of comorbid anxiety and mood disorders (e.g., Craske et al., 2007; Tsao, Mystkowksi, Zucker, & Craske, 2005), although one study sug- gested that the benefits for comorbid conditions may lessen over time, when assessed 2 years later (Brown et al., 1995). Finally, applications of cognitive-behav- ioral therapy lower relapse rates upon discontinuation of high-potency benzodiazepines (e.g., Spiegel, Bruce, Gregg, & Nuzzarello, 1994). The effects of cognitive- behavioral therapy are sustained over time, as meta- analyses show little change (i.e., maintenance of treat- ment effects) from posttreatment to follow-up (effect size = 0.12; Norton & Price, 2007).
With regard to long-term maintenance of gains after cognitive-behavioral therapy, in a review of meta-analy- ses for cognitive-behavioral therapy across all disorders, Butler, Chapman, Forman, and Beck (2006) concluded that evidence for maintenance of treatment gains was particularly strong for panic disorder, where the rate of relapse was almost half the rate of relapse following pharmacotherapy. Continuing improvement after acute treatment is facilitated by involvement of significant others in every aspect of treatment for agoraphobia (e.g., Cerny et al., 1987). Also, booster sessions enhance long-term outcomes and prevent return of symptoms and relapse (Craske et al., 2006; White et al., 2013). There is some evidence to suggest that although long- term maintenance is observed over a 24-month period for individuals who received cognitive-behavioral ther- apy for panic disorder and agoraphobia, improvement in agoraphobic avoidance is maintained to a greater ex- tent for those who receive in-person therapy compared to those who receive self-help therapy (Gloster et al., 2013), indicating that treatment effects may be more stable over the long term when treatment is provided by a therapist.
32 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
Efficacy data from research settings are now being complemented by effectiveness data from real-world, primary care settings. In a randomized controlled trial in primary care settings with novice therapists, cognitive-behavioral therapy combined with expert recommendations for medication regimens was more effective than treatment as usual (Roy-Byrne, Craske, et al., 2005). The effects appeared primarily to be due to cognitive-behavioral therapy rather than medication (Craske, Golinelli, et al., 2005). In the more recent CALM study (Craske et al., 2011), the effectiveness of cognitive-behavioral therapy for panic disorder in pri- mary care settings was demonstrated in the hands of nonexperienced therapists with the aid of a computer- ized guide, combined with expert recommendations for medication, relative to treatment as usual.
Even though cognitive-behavioral therapy for panic disorder and agoraphobia is efficacious and effective, there is room for improvement. In one study, Brown and Barlow (1995) estimated that 30% of clients con- tinue to function poorly at follow-up, and only 48% reached high end-state status. In a landmark study (Barlow et al., 2000), only 32% of clients with panic disorder assigned to cognitive-behavioral therapy alone demonstrated strong treatment response 12 months after acute treatment. Finally, of those who do start treatment, the mean dropout rate is 19%, with a range of 0–54% (Haby et al., 2006).
TREATMENT DESCRIPTION: PROTOCOL
What follows is a description of a 12-session cognitive- behavioral therapy for panic disorder and agoraphobia tailored to Julie’s presentation. Of course, the degree to which the various components of treatment are empha- sized vary by the functional assessment conducted for each patient.
Overview
The basic aim of the treatment protocol is to influence directly the catastrophic misappraisals and avoidance of bodily sensations and agoraphobic situations. This is done first through the provision of accurate informa- tion as to the nature of the fight–flight response. By provision of such information, patients are taught that they experience sensations that are normal and harm- less. Second, treatment aims to teach a set of skills for
developing evidence-based appraisals regarding bodily sensations and agoraphobic situations. At the same time, specific information concerning the effects of hyperventilation and its role in panic attacks is pro- vided, with practice of breathing retraining, if deemed appropriate. Then, the crux of the treatment involves repeated exposure to feared internal cues and agorapho- bic situations.
Session 1
The goals of Session 1 are to describe fear and anxi- ety; to help patients understand the cyclical influ- ences among behavioral, physiological, and cognitive responses; to understand that panic attack symptoms are not harmful; and to begin self-monitoring, if it was not already begun with the initial assessment. Therapy begins with identifying anxiety patterns and the situ- ations in which anxiety and panic attacks are likely to occur. Many patients have difficulty identifying specif- ic antecedents, reporting that panic can occur at almost any time. Therapists help patients to identify internal triggers, specifically, negative verbal cognitions, cata- strophic imagery, and physical sensations. The follow- ing interchange took place for Julie:
THERAPIST: In what situations are you most likely to panic?
JULIE: Crowded restaurants and when I’m driving on the freeway. But sometimes I am driving along, feel- ing OK, when all of a sudden it hits. And other times I can be sitting at home feeling quite relaxed and it just hits. That’s when I really get scared because I can’t explain it.
THERAPIST: So, when you are driving on the freeway, what is the very first thing you notice that tells you you’re about to panic?
JULIE: Well, the other cars on the road look as if they are moving really slowly . . . it’s as if I am in a dream.
THERAPIST: And what is the first thing you notice when you’re at home?
JULIE: An unreal feeling, like I’m floating. THERAPIST: So, what does that tell you? What is the
common factor that started these two panic attacks? JULIE: The feeling as if things are unreal? Wow, I al-
ways thought the physical feelings were the panic at- tack, but maybe they start the panic attack.
Panic Disorder and Agoraphobia 33
Next, the three-response system model for describ- ing and understanding anxiety and panic is introduced. This model contributes to an objective self-awareness— to becoming a personal scientist—and provides the groundwork for an alternative conceptual framework for explaining panic and anxiety that replaces the pa- tient’s own misassumptions. Patients are asked to de- scribe cognitive, physiological, and behavioral aspects to their responding: to identify the things that they feel, think, and do when they are anxious and panicky. As described earlier, differences between the response profiles of anxiety and panic are highlighted. After grasping the notion of three responses that are partially independent, interactions among the response systems are described. The patient is asked to describe the three- response system components in a recent panic attack and to identify ways in which they interacted to pro- duce heightened distress, as in the following example:
THERAPIST: How would you describe the three parts to the panic attack you had at home last week?
JULIE: Well, physically, my head felt really light, and my hands were clammy. I thought that I would ei- ther pass out or that I would somehow dissolve into nothingness. My behavior was to lie down and phone my husband.
THERAPIST: Ok that’s a great description of your thoughts, physical feelings, and behaviors. Now let’s look at the sequence of events. What was the very first thing you noticed?
JULIE: When I stood up, my head started to feel really weird, as if it was spinning inside.
THERAPIST: What was your very next reaction to that feeling?
JULIE: I held onto the chair. I thought something was wrong. I thought it could get worse and that I’d col- lapse.
THERAPIST: So it began with a physical sensation, and then you had some very specific thoughts about those sensations. What happened next?
JULIE: I felt very anxious. THERAPIST: And what happened next? JULIE: Well, the dizziness seemed to be getting worse
and worse. I became really concerned that it was dif- ferent from any other experience I had ever had. I was convinced that this was “it.”
THERAPIST: So, as you became more anxious, the physi- cal feelings and the thoughts that something bad was going to happen intensified. What did you do next?
JULIE: I called my husband and lay on the bed until he came home. It was horrible.
THERAPIST: Can you see how one thing fed off another, creating a cycle? That it began with a sensation, then some anxious thoughts, then feeling anxious, then more sensations and more thoughts, and more fear, and so on?
Next, the reasons why panic attacks first began are addressed briefly. Patients are informed that it is not necessary to understand the reasons why they began to panic to benefit from the treatment, because factors involved in onset are not necessarily the same as the factors involved in the maintenance of a problem. Nev- ertheless, the initial panic attack is described as a mani- festation of anxiety/stress. The stressors surrounding the time of the first panic attack are explored with the patient, particularly in terms of how stressors may have increased levels of physical arousal and primed certain danger-laden cognitive schemas.
Also, the therapist briefly describes the physiology un- derlying anxiety and panic, and the myths about what the physical sensations might mean. The main concepts covered in this educational phase are (1) the survival value or protective function of anxiety and panic; (2) the physiological basis to the various sensations experienced during panic and anxiety, and the survival function of the underlying physiology; and (3) the role of specific learned and cognitively mediated fears of certain bodily sensations. The model of panic we described earlier in this chapter is explained. In particular, the concepts of misappraisals and interoceptive conditioning are ex- plained as accounting for panic attacks that seem to occur from out of the blue—that are triggered by very subtle internal cues or physical sensations that may occur at any time. Not only does this information reduce anxi- ety by decreasing uncertainty about panic attacks but it also enhances the credibility of the subsequent treatment procedures. This information is detailed in a handout given to the patient to read over the next week (for the handout, see Barlow & Craske, 2006).
This information was very important for Julie, be- cause the inability to explain her panic attacks was a major source of distress. Here are some of the questions she asked in her attempt to understand more fully:
34 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
JULIE: So, if I understand you correctly, you’re saying that my panic attacks are the same as the fear I expe- rienced the time we found a burglar in our house. It doesn’t feel the same at all.
THERAPIST: Yes, those two emotional states—an unex- pected panic attack and fear when confronted with a burglar—are essentially the same. However, in the case of the burglar, where were you focusing your attention—on the burglar or on the way you were feeling?
JULIE: The burglar, of course, although I did notice my heart was going a mile a minute.
THERAPIST: And when you have a panic attack, where are you focusing your attention—on the people around you or on the way you are feeling?
JULIE: Well, mostly on the way I’m feeling, although it depends on where I am at the time.
THERAPIST: Being most concerned about what’s going on inside can lead to a very different type of experi- ence than being concerned about the burglar, even though basically the same physiological response is occurring. For example, remember our description of the way fear of sensations can intensify the sensa- tions.
JULIE: I get that. But what about the feelings of unreal- ity? How can they be protective or how can feeling unreal help me deal with a dangerous situation?
THERAPIST: OK, remember that it’s the physiological events that are protective—not the sensations. The sensations are just the end result of those events. Now, feelings of unreality can be caused by changes in your blood flow to your brain (although not dan- gerously so), or from overbreathing, or from concen- trating too intensely on what’s going on inside you. So the unreality sensation may not be protective, but the changes in blood flow and overbreathing are.
JULIE: I understand how I can create a panic attack by being afraid of my physical feelings, like my heart racing or feeling unreal. But sometimes it happens so quickly that I don’t have time to think.
THERAPIST: Yes, these reactions can occur very quickly, at times automatically. But remember, we are tuned to react instantaneously to things that we believe to be dangerous. Imagine yourself walking through a dark alley, and you have reason to believe that some- where in the darkness lurks a killer. Under those con- ditions, you would be extremely attentive to any sign,
any sound, or any sight of another person. If you were walking through the same alley and were sure there were no killers, you might not hear or detect the same signals you picked up on in the first case. Now let’s translate this to panic; the killer in the dark alley is the panic attack, and the signs, sounds, and smells are the physical sensations you think signal the possibility of a panic attack. Given the acute de- gree of sensitivity to physical symptoms that signal a panic attack, it is likely that you are noticing normal “noises” in your body that you would otherwise not notice, and on occasion, immediately become fearful because of those “noises.” In other words, the sen- sations are often noticeable because you attend to them.
Next, the method of self-monitoring was described and demonstrated with in-session practice of complet- ing a Panic Attack Record. Julie was concerned that self-monitoring would only elevate her distress, by re- minding her of the very thing she was afraid of (panic and unreality). The therapist clarified the difference between objective and subjective self-monitoring, and explained that distress would subside as Julie persevered with self-monitoring.
The homework for this session was to self-monitor panic attacks, daily anxiety, and mood, and to read the handout. In fact, we encourage patients to reread the handout several times and to actively engage in the material by circling or marking the most personally relevant sections or areas in need of clarification, be- cause effort enhances long-term retention of the mate- rial learned. Of course, for some patients, reading the material draws their attention to things they fear (just as with self-monitoring). In this case, therapists can dis- cuss the role of avoidance, and how, with repeated read- ings, distress levels will most likely subside.
At the end of the session, Julie suddenly became highly anxious. She felt unable to tolerate either the treatment procedures or her anticipation of them. She became very agitated in the office and reported feel- ings of unreality. She opened the office door to find her husband, who was waiting outside. The therapist helped Julie understand how the cycle of panic had emerged just at that moment: (1) The trigger was the treatment description—having to face eventually feared sensations and situations; (2) this was anxiety produc- ing, because Julie believed that she could not cope with the treatment demands, that the treatment would cause her so much anxiety that she would “flip out” and lose
Panic Disorder and Agoraphobia 35
touch with reality permanently, or that she would never improve because she could not tolerate the treatment; (3) the current anxiety in the office elicited sensations of unreality and a racing heart; (4) Julie began to worry that she might panic and lose touch with reality per- manently within the next few minutes; (5) the more anxious Julie felt, and the stronger her attempts to es- cape and find safety, the stronger the physical sensa- tions became; and (6) she felt some relief upon finding her husband, because his presence reassured her that she would be safe. Julie was reassured that treatment would progress at a pace with which she was comfortable, but at the same time she was helped to understand that her acute distress about the feeling of unreality would be the precise target of this type of treatment, therefore attesting to the relevance of this treatment for her. She was also calmed by preliminary cognitive restructur- ing of the probability of permanently losing touch with reality. After a lengthy discussion, Julie became more receptive to treatment. A team approach to treatment planning and progress was agreed upon, so that Julie did not feel that she would be forced to do things she did not think she could do.
Session 2
The goals of this session are to begin the development of a hierarchy of agoraphobic situations and coping skills of breathing retraining and cognitive restructur- ing. The individualized hierarchy comprises situations that range from mild to moderate anxiety, all the way up to extreme anxiety. These situations become the basis of graduated in vivo exposure. Although in vivo exposure exercises are not scheduled to take place until Session 4, the hierarchy is introduced now, so that cog- nitive restructuring skills can be practiced in relation to each situation on the hierarchy before in vivo exposure begins. Moreover, the hierarchy will be refined as a re- sult of the cognitive restructuring practice, because the latter highlights specific features of agoraphobic situa- tions that are most anxiety provoking.
Julie was asked to develop a hierarchy over the fol- lowing week. She expressed some doubt that she would ever be able to accomplish any, let alone all, of the items on her hierarchy. The therapist helped Julie by asking her to think of any situation in her lifetime that used to be difficult but became easier with practice. Julie remembered how anxious she used to be when she first started working with customers at her husband’s office—and how that discomfort subsided over time.
This was used to help Julie realize that the same might happen with the situations listed on her hierarchy. Ju- lie’s final hierarchy comprised the following situations: driving home from work alone; sitting in a crowded movie theater; spending 2 hours alone at home during the day; being alone at home as day turned to night; driving on surface streets to her brother’s house (10 miles) alone; driving two exits on Freeway 444, with her husband following in the car behind; driving two exits on Freeway 444, alone; driving four exits on Free- way 444; and driving on the freeway to her brother’s house alone. Then, Julie was to repeat all of these tasks without taking Klonopin, and without knowing the lo- cation of her husband.
Breathing retraining also is begun in this session. Pa- tients are asked to hyperventilate voluntarily by stand- ing and breathing fast and deep, as if blowing up a balloon, for 1½ minutes. With prompting and encour- agement from the therapist, patients can often complete the full 1½ minutes, after which time they are asked to sit, close their eyes, and breathe very slowly, paus- ing at the end of each breath, until the symptoms have abated. The experience is then discussed in terms of the degree to which it produced symptoms similar to those that occur naturally during anxiety or panic. Approxi- mately 50–60% of patients report that the symptoms of hyperventilation are very similar to their panic attack symptoms. Often, however, similarity of the symptoms is confused with similarity of the anxiety. Because the exercise is conducted in a safe environment and the symptoms have an obvious cause, most patients rate the experience as less anxiety provoking than if the same symptoms had occurred naturally. This distinction is important to make, because it demonstrates the signifi- cance of perceived safety for the degree of anxiety expe- rienced. Julie rated the hyperventilation exercise as very anxiety provoking (8 on a 0- to 10-point scale), and rated the symptoms as being quite similar to her panic symptoms (6 on a 0- to 10-point scale). She terminated the task after approximately 40 seconds in anticipation of experiencing a full-blown panic attack. The therapist and Julie discussed this experience in terms of the three response systems, and the role of misappraisals and in- teroceptive conditioning described during the previous session.
Then, Julie was briefly educated about the physio- logical basis to hyperventilation (see Barlow & Craske, 2006). As before, the goal of the didactic presentation was to allay misinterpretations of the dangers of over- breathing, and to provide a factual information base
36 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
on which to draw when actively challenging misinter- pretations. The educational content is tailored to the patient’s own educational level and covered only to the degree that it is relevant to the patient.
In the next step, the therapist teaches breathing re- training, which begins by teaching patients to rely more on the diaphragm (abdomen) than on chest muscles. In addition, patients are instructed to concentrate on their breathing by counting on their inhalations and think- ing the word “relax” on exhalations. (Slow breathing is introduced in Session 3.) Therapists model the sug- gested breathing patterns, then provide corrective feed- back to patients while they practice in the office setting. (Note that CART uses a different method of breathing retraining that is based on raising levels of CO2 in the blood through biofeedback.)
Initial reactions to the breathing exercise may be negative for patients who are afraid of respiratory sen- sations, because the exercise directs their attention to breathing. It also can be difficult for patients who are chronic overbreathers, and patients for whom any inter- ruption of habitual breathing patterns initially increases respiratory symptomatology. In both cases, continued practice is advisable, with reassurance that sensations such as shortness of breath are not harmful. The goal is to use breathing skills training to encourage continued approach toward anxiety and anxiety-producing situa- tions. On occasion, patients mistakenly view breathing retraining as a way of relieving themselves of terrifying symptoms, thus falling into the trap of fearing dire con- sequences should they not succeed in correcting their breathing. This is what happened for Julie:
JULIE: So, all I have to do is to slow down my breathing, then everything will be OK?
THERAPIST: Certainly, slowing down your breathing will help to decrease the physical symptoms that you feel, but I am not sure what you mean when you ask whether everything will be OK.
JULIE: That proper breathing will prevent me from los- ing touch with reality—that I won’t disappear.
THERAPIST: Breathing retraining will help you to regu- late your breathing, which may lessen your physical symptoms, including the sense of unreality. Your question, though, is the reason for our next treat- ment skill of changing your thinking, so you can learn that the sense of unreality is not a sign of actual loss of touch with reality and disappearance.
The homework is to practice diaphragmatic breath- ing for at least 10 minutes, two times a day in relaxing environments.
Therapists introduce cognitive restructuring in this session, by explaining that everyone has errors in think- ing when anxious, thus helping the patient to expect his/her thinking to be distorted. Patients are informed that these distortions have an adaptive function: Chances of survival are greater if we perceive danger as probable and worthy of attention rather than mini- mize it. Therefore, anxiety leads us to judge threatening events as being more likely and more threatening than they really are. However, the cognitive distortions are unnecessary, because there is no real threat in the case of panic disorder.
Then, patients are taught to treat their thoughts as hypotheses or guesses rather than as facts. The notions of automatic thinking and discrete predictions are also explained, to emphasize the need to become an astute observer of one’s own habitual self-statements in each situation. This leads to a “downward arrow technique” to identify specific predictions made at any given mo- ment, as shown with Julie.
THERAPIST: What is it that scared you about feeling detached in the movie theater last night?
JULIE: It is just such a horrible feeling. THERAPIST: What makes it so horrible? JULIE: I can’t tolerate it. THERAPIST: What makes you think you cannot tolerate
it? What is the feeling of detachment going to do to you that makes you think it is horrible and intoler- able?
JULIE: It might become so intense that it overwhelms me.
THERAPIST: And if it overwhelms you, what would happen?
JULIE: I could become so distressed that I lose touch with reality.
THERAPIST: What would it mean if you lost touch with reality?
JULIE: That I would be in a different mind state forev- er—I would never come back to reality. That I would be so crazy that I would have to be carted out of the movie theater to a mental hospital and locked away forever.
Panic Disorder and Agoraphobia 37
Overly general self-statements, such as “I feel ter- rible—something bad could happen,” are insufficient, nontherapeutic, and may serve to intensify anxiety by virtue of their global and nondirective nature. Instead, detail in thought content, such as “I am afraid that if I get too anxious while driving, then I’ll lose control of the wheel and drive off the side of the road and die,” permits subsequent cognitive restructuring.
Analysis of anxious thought content yields two broad factors that are labeled as risk and valence. These two main types of cognitive errors are described to patients. Risk translates to overestimation, or jumping to con- clusions by viewing negative events as being probable events, when in fact they are unlikely to occur. The pa- tient is asked to identify overestimations from the anxi- ety and panic incidents over the past couple of weeks: “Can you think of events that you felt sure were going to happen when you panicked, only to find out in the end that they did not happen at all?” Usually, patients can identify such events easily, but with protestations, as in the following example:
JULIE: Well, several times I thought that I really was going to lose it this time . . . that I would flip out and never return to reality. It never actually happened, but it could still happen.
THERAPIST: Why do you think “it” could still happen? JULIE: Part of me feels like I’ve always managed to es-
cape it just in time, by either removing myself from the situation or by having my husband help me, or by holding on long enough for the feeling to pass. But what if I can’t hold on the next time?
THERAPIST: Knowing what we know about our thoughts when we are anxious, can you classify any of the ideas you just expressed, of “just holding on” or “just escaping in time,” as overestimations?
JULIE: I suppose you’re saying that I can hold on or I can always escape in time.
THERAPIST: More that you feel the need to hold on and the need to escape because you are overestimating the likelihood of flipping out and never returning to reality.
JULIE: But it really feels like I will. THERAPIST: The confusion between what you think
will happen and what actually happens is the very problem that we are addressing in this session.
The reasons why overestimations persist despite re- peated disconfirmation are explored. Typically, patients misattribute the absence of danger to external safety signals or safety behaviors (e.g., “I only made it because I managed to find help in time,” “If I had not taken Xanax last week when I panicked in the store, I’m sure I would have passed out,” or “I wouldn’t have made it if I hadn’t pulled off the road in time”), or to “luck,” instead of realizing the inaccuracy of the original pre- diction. Similarly, patients may assume that the only reason they are still alive, sane, and safe is because the “big one” has not happened. In this case, patients err by assuming that intensity of panic attacks increases the risk of catastrophic outcomes.
The method for countering overestimation errors is to question the evidence for probability judgments. The general format is to treat thoughts as hypotheses or guesses rather than as facts, and to examine the evi- dence and generate alternative, more realistic predic- tions. This is best done by the therapist using a Socratic style, so that patients learn the skill of examining the content of their statements and arrive at alternative statements or predictions after they have considered all of the evidence. Questioning of the logic (e.g., “How does a racing heart lead to heart attack?”), or the bases from which judgments are made (e.g., misinformation from others, unusual sensations) is useful in this regard. Continuing with the previous example from Julie, the questioning took the following course:
THERAPIST: One of the specific thoughts you have identified is that you will flip out and never return to reality. What specifically leads you to think that that is likely to happen?
JULIE: Well, I guess it really feels like that. THERAPIST: Describe the feelings? JULIE: Well, I feel spacey and unreal, like things around
me are different and that I’m not connected. THERAPIST: And why do you think those feelings mean
that you have actually lost touch with reality? JULIE: I don’t know—it feels as if I have. THERAPIST: So, let’s examine that assumption. What is
your behavior like when you feel unreal? For exam- ple, do you respond if someone asks you a question during those episodes?
JULIE: Well, I respond to you even though I feel that way sometimes in here.
38 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
THERAPIST: OK, and can you walk or write or drive when you feel that way?
JULIE: Yes, but it feels different. THERAPIST: But you do perform those functions de-
spite feeling detached. So, what does that tell you? JULIE: Well, maybe I haven’t lost complete touch with
reality. But what if I do? THERAPIST: How many times have you felt detached? JULIE: Hundreds and hundreds of times. THERAPIST: And how many times have you lost touch
with reality permanently? JULIE: Never. But what if the feelings don’t go away?
Maybe I’ll lose it then? THERAPIST: So what else tells you that this is a pos-
sibility? JULIE: Well, what about my second cousin? He lost it
when he was about 25, and now he’s just a mess. He can hardly function at all, and he is constantly in and out of psychiatric hospitals. They have him on a bunch of heavy-duty drugs. I’ll never forget the time I saw him totally out of it. He was talking to himself in jibberish.
THERAPIST: So, do you make a connection between him and yourself?
JULIE: Yes. THERAPIST: What are the similarities between the two
of you? JULIE: There are none really. It’s just that he is what I
think I will become. THERAPIST: Did he ever feel the way you feel now? JULIE: I don’t know. THERAPIST: And if another one of your cousins had
severe back problems, would you be concerned that you would end up with severe back problems?
JULIE: No. THERAPIST: Why not? JULIE: Because it never crosses my mind. It is not some-
thing that I worry about. THERAPIST: So, it sounds like you think you will end
up like your cousin because you are afraid of ending up like him.
JULIE: I suppose so. THERAPIST: So, let’s look at all of the evidence and
consider some alternatives. You have felt unreal hun-
dreds of times, and you’ve never lost touch with real- ity because you’ve continued to function in the midst of those feelings, and they have never lasted. You are afraid of becoming like your cousin, but there are no data to show that you and he have the same problem. In fact, the data suggest otherwise, because you func- tion and he does not. So what is the realistic prob- ability that you will lose touch with reality perma- nently? Use a scale of 0 to 100, where 0 = No chance at all and 100 = Definitely will happen.
JULIE: Well, maybe it is lower than I thought. Maybe 20%.
THERAPIST: So that would mean that you have actually lost touch with reality in a permanent way once every five times you have felt unreal.
JULIE: When it’s put like that, I guess not. Maybe it’s a very small possibility.
THERAPIST: Yes, so what is an alternative explanation? JULIE: Perhaps the feelings of unreality are caused by
feeling anxious or overbreathing, and having those feelings does not mean that I am actually losing touch with reality, and that I am not like my cousin at all.
For homework, in addition to continuation of self- monitoring and practice of diaphragmatic breathing, Julie was asked to identify her anxious thoughts in rela- tion to every item on her agoraphobia hierarchy, and to use the in-session steps of examining the evidence and generating alternative evidence-based interpretations for errors of overestimating the risk. She was to do the same for every panic attack that occurred over the next week.
Session 3
The goals of this session are to develop breathing re- training and to continue active cognitive restructuring. The therapist reviews the patient’s week of diaphrag- matic breathing practice. Julie was disappointed with her attempts to practice.
JULIE: I just didn’t seem to be able to do it the right way. Sometimes I would start off OK and then the more I tried, the more it felt like I was running out of air, and I’d have to take a big gulp between breaths. At other times, I felt dizzy and the unreal feelings would start, at which point I would stop and do “busy work” to keep my mind occupied.
Panic Disorder and Agoraphobia 39
THERAPIST: It sounds like quite a few things were going on. First of all, remember that this is a skill, just like learning to ride a bike, and you cannot expect it to be easy from the get-go. Second, it sounds like you experienced some uncomfortable physical symptoms that worried you. You said it felt like you were run- ning out of air. Based on what we talked about last week, what do you think might have caused that feel- ing?
JULIE: Well, maybe I wasn’t getting enough air into my lungs because it’s really hard for me to use my dia- phragm muscle. I felt like I was suffocating myself.
THERAPIST: Possibly it’s just a matter of learning to use the diaphragm muscle, but were you really suffocat- ing or was it an interpretation that you might be suf- focating?
JULIE: I don’t know. I’ve had the feeling of suffocat- ing before, especially when I’m trapped in a crowded room.
THERAPIST: So, how do you know you were suffocat- ing?
JULIE: I don’t know. It just felt that way. THERAPIST: So, let’s put the evidence together. You’ve
had the feelings before and never suffocated. As we discussed last time, anxiety can sometimes create a sensation of shortness of breath even though you are getting plenty of air. Can you think of an alternative explanation?
JULIE: Well, maybe I wasn’t suffocating. Maybe it just felt like that.
Julie’s complaints represent typical concerns that should be addressed. The next step is to slow the rate of breathing until the patient can comfortably span a full inhalation and exhalation cycle of 6 seconds. Again, the therapist models slowed breathing, then provides cor- rective feedback on practice in the session. The patient is instructed to continue to practice slow breathing in “safe” or relaxing environments, and is discouraged from applying slow breathing when anxious or panick- ing, until fully skilled in its application.
Also, cognitive restructuring is continued by ad- dressing the second cognitive error, which involves viewing an event as “dangerous,” “insufferable,” or “catastrophic.” Typical examples of catastrophic errors are “If I faint, people will think that I’m weak, and that would be unbearable” or “Panic attacks are the worst thing I can imagine,” and “The whole evening is ruined
if I start to feel anxious.” Decatastrophizing means to face the worst, to realize that the occurrences are not as “catastrophic” as stated, and to think about actual ways to cope with negative events rather than how “bad” they are. A key principle underlying decatastrophiz- ing is that events can be endured even though they are uncomfortable. Recognition of the time-limited na- ture of discomfort contributes to the development of a sense of being able to cope. The critical distinction here is that although patients might prefer that these events not occur, they can tolerate the discomfort, if necessary. Thus, for the person who states that negative judgments from others are unbearable, it is important to discuss what he/she would do to cope should some- one else make a direct negative judgment. Similarly, for the person who states that the physical symptoms of panic are intolerably embarrassing, the following type of questioning is helpful:
JULIE: I am really worried that I might lose control and do something crazy, like yell and scream.
THERAPIST: Let’s face the worst and find out what is so bad about it. What would be so horrible about yell- ing and screaming?
JULIE: I could never live it down. THERAPIST: Well, let’s think it through. What are the
various things you could do in the situation? You have just yelled and screamed—now what?
JULIE: Well, I guess the yelling and screaming would eventually stop.
THERAPIST: That’s right—at the very least you would eventually exhaust yourself. What else?
JULIE: Well, maybe I would explain to the people around me that I was having a really bad day but that I would be OK. In other words, reassure them.
THERAPIST: Good. What else? JULIE: Maybe I would just get away—find someplace to
calm down and reassure myself that the worst is over. THERAPIST: Good. JULIE: But what if the police came and took me away,
locked me up in a mental ward? THERAPIST: Again, let’s face the worst. What if the po-
lice did come when you were yelling and screaming, and what if the police did take you away? As scary as that may sound to you, let’s consider what actually would happen.
40 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
JULIE: I have this image of myself not being able to tell them what is really going on—that I am so out of it I don’t have the ability to let them know I am just anxious.
THERAPIST: If you were so distraught that you could not clearly communicate, how long would that last?
JULIE: You’re right. I would eventually exhaust myself and then I could speak more clearly. But what if they didn’t believe me?
THERAPIST: What if they did not believe you at first? How long would it take before they would realize that you were not crazy?
JULIE: I guess that after a while they would see that I was OK, and maybe I could call a friend or my doc- tor to explain what was going on.
The homework for this session, in addition to contin- ued self-monitoring, is to practice slow and diaphrag- matic breathing in relaxing environments, and to iden- tify errors of catastrophizing in relation to each item on the agoraphobia hierarchy, followed by practice of decatastrophizing and generation of ways to cope. In addition, Julie was to use the skill of decatastrophizing for panic attacks that occurred over the following week.
Session 4
The main goal of this session is to use breathing retrain- ing skills as a coping tool, to review cognitive restruc- turing skills, and to begin in vivo exposure to the first item on the agoraphobia hierarchy.
Now that patients have practiced slow and diaphrag- matic breathing sufficiently in relaxing environments, they are ready to use these methods in distracting en- vironments and in anxious situations. Patients are en- couraged to use breathing skills as a coping technique as they face fear, anxiety, and anxiety-provoking situ- ations. Some patients use breathing skills as a safety signal or a safety behavior; in other words, they believe that they will be at risk for some mental, physical, or social calamity if they do not breathe correctly. This issue came up with Julie:
JULIE: When I panicked during the week, I tried to use the breathing. It didn’t work. It made me feel worse.
THERAPIST: It sounds as if you might have attempted to use the breathing exercise as a desperate attempt to control the feelings you were experiencing.
JULIE: Yes, that’s right. THERAPIST: What did you think would have happened
if you had not been able to control the feelings? JULIE: I was really worried that I might not be able to
handle the feelings. THERAPIST: And if you weren’t able to handle the feel-
ings, what would happen? JULIE: It just feels like I will lose it, permanently. THERAPIST: So this is one of those thoughts that we
were talking about last time. What does your evi- dence tell you about the likelihood of losing touch with reality permanently?
JULIE: So you mean even if I don’t control my breath- ing, then I will be OK?
THERAPIST: Well, you had not lost touch with reality permanently before you learned the breathing exer- cise. So what does that tell you?
JULIE: OK, I get it. THERAPIST: The breathing exercise is best thought of as
a tool to help you face whatever is provoking anxiety. So, as you face situations and your anxiety increases, use the breathing exercise to help you to face rather than run away from anxiety. The breathing exercise can be helpful for helping you approach or stay in these situations, but you don’t actually need it to face these situations and tolerate your anxiety.
Patients who consistently use the breathing skills as a safety behavior might be discouraged from using the breathing skills, because they learn that what they are most worried about either does not happen or it can be managed without using the breathing skills.
In terms of the cognitive restructuring, therapists give corrective feedback to patients on the methods of questioning the evidence to generate realistic prob- abilities, facing the worst, and generating ways to cope with each item on the agoraphobia hierarchy and any panic attacks that occurred over the past week. Partic- ular “corrective” feedback is given when patients lack specificity in their cognitive restructuring (e.g., patients who record that they are most worried about panicking should be encouraged to detail what it is about pan- icking that worries them) or rely on blanket reassur- ance (e.g., patients who record that “Everything will be OK” as their evidence and/or ways of coping should be encouraged to list the evidence and/or generate actual coping steps).
Panic Disorder and Agoraphobia 41
Next, attention is given to how to practice the first item on the agoraphobia hierarchy. If appropriate, rea- sons why previous attempts at in vivo exposure may have failed are reviewed. Typical reasons for patients’ past failures at in vivo exposure include attempts that are too haphazard and/or brief or spaced too far apart, and attempts conducted without a sense of mastery, or while maintaining beliefs that catastrophe is very pos- sible. Julie had tried to face agoraphobic situations in the past, but each time she had escaped, feeling over- whelmed by panic and terrified of losing touch with reality permanently. The therapist helped Julie realize how to approach the agoraphobic situations differently to benefit from the exposure. Julie’s typical safety sig- nals were the presence of her husband, or at least know- ing his whereabouts, and Klonopin (which she carried but rarely used). The therapist discussed the impor- tance of eventual weaning from those safety signals.
As mentioned earlier, the goal of exposure therapy is not immediate reduction in fear and anxiety; rather, the goal is for the patient to learn something new as a result of exposure. Clarification of what patients are most worried about as they face their feared situations and the conditions that best help them to learn that what worries them most never or rarely happens, and/ or that they can cope with the situation and tolerate anxiety, is essential for effective exposure. If a patient is most worried that fear and anxiety will remain elevated for the duration of the practice, then corrective learn- ing involves toleration of sustained anxiety. For Julie, the first situation on her hierarchy was to drive home from work, alone. She stated that what most worried her in that situation was that she would panic and lose touch with reality, and as a result, lose control of the car and die in an accident. She also stated that to drive at dusk was the condition under which she was most convinced of these eventualities. Thus, the task that the therapist considered most effective in teaching Julie that she would not lose touch with reality, or that she could cope with the sensations of unreality and panic, was to drive home from work at dusk.
Delineate the exposure task as concretely as possible, so that patients clearly understand exactly what the practice entails (e.g., “Walk around inside of mall for 10 minutes by myself”). Importantly, the practice should not be ended because of anxiety (e.g., “Continue driving on the freeway until I feel anxious”), because the expo- sure practice would then reinforce avoidance of anxiety.
Julie was reminded that she could use her coping skills should she panic as she practiced the task; that is,
in moments of fear, patients are encouraged to use their breathing and thinking skills to complete the assigned task, if needed to stay in engaged in the task; the coping skills are not intended as means to reduce fear and anxi- ety, but to tolerate it. Acceptance and nonjudgmental observation of physical sensations and thoughts can be another strategy to use in the midst of exposure therapy.
Patients are encouraged to maintain a regular sched- ule of repeated in vivo exposure practices at least three times per week and to conduct these practices regard- less of internal (e.g., having a “bad day,” feeling ill) or external (e.g., inclement weather, busy schedules) fac- tors that may prompt postponement of practices. Julie expressed some concerns about being able to practice at least three times over the following week:
JULIE: I don’t know if I can practice three times, be- cause more days than not I feel pretty worn down; maybe I can practice on just Monday and Tuesday, because they are the days I typically feel better.
THERAPIST: What is it you are worried about happen- ing if you practice on a day when you already feel worn down?
JULIE: I feel more fragile on those days. THERAPIST: And if you feel more fragile, what might
happen? JULIE: I just don’t think I could do it. It would be too
hard. I might really freak out and lose touch with reality for ever.
THERAPIST: OK, so let’s think about that thought. What does your experience tell you? How many times have you permanently lost touch with reality, including days when you were worn down?
JULIE: Well, never. THERAPIST: So, what does that tell you? JULIE: OK, but it still feels difficult to drive on those
days. THERAPIST: How about you start with Monday or
Tuesday, but quickly move to the other days of the week when you are feeling worn down, so that you get a really good opportunity to learn whether you permanently lose touch with reality or not?
Julie’s homework for this session involves continued self-monitoring, continued use of cognitive restructur- ing and breathing retraining in the event of elevated anxiety or panic, and practicing the first item on the
42 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
agoraphobia hierarchy at least three times, with at least one of those times being without her husband Larry.
Session 5
The goals of this session are to review the practice of in vivo exposure, to design another exposure task to be practiced over the next week, and to begin interoceptive exposure. Note that in vivo and interoceptive exposure can be done simultaneously or sequentially. For Julie, in vivo exposure was begun in Session 4, whereas in- teroceptive exposure was begun in this session, but they could easily have been done in the opposite order.
It is essential to review the week’s practice of in vivo exposure. An objective evaluation of performance is considered necessary to offset subjective and damag- ing self-evaluations. As demonstrated in experimental literature on learning and conditioning, appraisals of aversive events after they have occurred can influence anxiety about future encounters with the same types of aversive events. Any practice that is terminated prema- turely is to be reviewed carefully for contributing fac- tors that can then be incorporated into subsequent trials of in vivo exposure. Recognition of the precipitant to escape is very important, because the urge to escape is usually based on the prediction that continued endur- ance would result in some kind of danger. For example, patients may predict that the sensations will become intense and lead to an out-of-control reaction. This pre- diction can be discussed in terms of jumping to con- clusions and blowing things out of proportion. At the same time, escape itself need not be viewed catastrophi- cally (i.e., as embarrassing, or as a sign of failure). In addition, therapists reinforce the use of breathing and cognitive skills (or acceptance skills), if needed, to help patients remain in the situation until the specified dura- tion or task has been completed, despite uncomfortable sensations. However, if patients are able to remain in the situation without explicit use of coping skills, that is perfectly fine. In fact, this approach may aid patients in learning that they can tolerate anxiety without at- tempting to manage it, or even that it may go away on its own as corrective learning takes place, without the use of coping skills.
Again, it is important for patients to recognize that the goal is repeatedly to face situations despite anxiety, not to achieve a total absence of anxiety. Toleration of fear rather than immediate fear reduction is the goal for each exposure practice; this approach leads to an eventual fear reduction over time. Anxiety that does
not decline over repeated days of in vivo exposure may result from too much emphasis on immediate fear and anxiety reduction; that is, trying too hard or wishing too much for anxiety to decline typically maintains anxiety.
Julie had success with her first in vivo exposure prac- tice; she managed to drive home from work at dusk, alone, four different times. She noted that the first time was easier than she had expected; the second was harder, and one time she pulled off to the side of the road. The therapist helped Julie identify the thoughts and sensa- tions that led her to “escape” from the situation: the sensations of unreality and fears of losing touch with re- ality. Julie had waited for a few minutes, then continued driving home—an action that was highly reinforced by the therapist. The third and fourth times were easier.
Julie’s husband, Larry, attended Session 5, so that he could learn how to help Julie overcome her panic and agoraphobia. He was supportive and eager to help in any way possible, expressing frustration at having had no idea how to help in the past.
There are general principles for involvement of sig- nificant others in treatment. First, a treatment concep- tualization is provided to the significant other to reduce his/her frustration and/or negative attributions about the patient’s emotional functioning (e.g., “Oh, she’s just making it up. There’s nothing really wrong with her” or “He has been like this since before we were mar- ried, and he’ll never change”). The way in which the agoraphobic problem has disrupted daily routines and distribution of home responsibilities is also explored and discussed. Examples might include social activities, leisure activities, and household chores. The therapist explains that family activities may be structured around the agoraphobic fear and avoidance to help the patient function without intense anxiety. At the same time, reassignment of the patient’s tasks to the significant other may actually reinforce the agoraphobic pattern of behavior. Consequently, the importance of comply- ing with in vivo exposure homework instructions, even though the patient may experience some distress ini- tially, is emphasized.
The significant other is encouraged to become an active participant by providing his/her perception of the patient’s behavior and fearfulness, and the impact on the home environment. Sometimes the significant other provides information of which the patient is not fully aware, or did not report, particularly in relation to how the patient’s behavior affects his/her own daily functioning. Larry, for example, described how he felt
Panic Disorder and Agoraphobia 43
restricted at home in the evenings; whereas, before, he occasionally played basketball with his friends at the local gym, he now stays at home, because he feels guilty if he leaves Julie alone.
The next step is to describe the role of the significant other regarding in vivo exposure tasks. The significant other is viewed as a coach, and the couple is encouraged to approach the tasks as a problem-solving team. This includes deciding exactly where and when to practice in vivo exposure. In preparation for practices, the patient identifies his/her misappraisals about the task and gen- erates cognitive alternatives. The significant other is en- couraged to help the patient question his/her own “anx- ious” thoughts. Role plays of this type of questioning of the patient by the significant other may be conducted in the session, so that the therapist can provide corrective feedback to each partner. Throughout in vivo exposure, the significant other reminds the patient to apply cop- ing skills, whether it be cognitive challenges, breath- ing skills, or acceptance skills. Because the significant other is usually a safety signal, tasks are less anxiety provoking. However, the patient must be weaned from the safety signal eventually. Therefore, initial attempts at facing agoraphobic situations are conducted with the significant other, and later trials are conducted alone. Weaning from the significant other may be graduated, as in the case of Julie (1) driving first with Larry in the car, (2) with him in a car behind, (3) meeting him at a destination point, and (4) driving alone.
Very important to the success of this collaboration is style of communication. On the one hand, the signifi- cant other is discouraged from magnifying the experi- ence of panic and encouraged to help the patient apply coping statements when anxious. On the other hand, the significant other is encouraged to be patient given the fact that progress for the patient may be erratic. The patient and the significant other are instructed to use a 0- to 10-point rating scale to communicate with each other about the patient’s current level of anxiety or distress, as a way of diminishing the awkwardness associated with discussion of anxiety, especially in public situations. The patient is warned about the po- tential motivation to avoid discussing his/her feelings with the significant other, due to embarrassment or an attempt to avoid the anxiety for fear that such discus- sion and concentration on anxiety may intensify his/ her distress level. Avoidance of feelings is discouraged, because distraction is viewed as less beneficial in the long term than objectively facing whatever is distressing and learning that predicted catastrophes do not occur.
The patient is reassured that the initial discomfort and embarrassment will most likely diminish as the part- ners become more familiar with discussing anxiety lev- els and their management. Furthermore, the patient’s concerns about the significant other being insensitive or too pushy are addressed. For example, a significant other may presume to know the patient’s level of anxi- ety and anxious thoughts without confirmation from the patient, or the significant other may become angry at the patient for avoiding or escaping from situations, or being fearful. All of these issues are described as rela- tively common and understandable patterns of commu- nication that are nevertheless in need of correction. In- session role playing of more adaptive communication styles during episodes of heightened anxiety is a useful learning technique. On occasion, more specific com- munications training may be beneficial, especially if the partners frequently argue in their attempts to generate items or methods for conducting in vivo exposure.
The next in vivo exposure task for Julie was to sit in a crowded movie theater, gradually moving away from the aisle, toward the middle of the row, because that was the condition in which she was most concerned that she would lose control and draw attention to herself. Julie and Larry rehearsed their approach to the in vivo expo- sure task in session, while the therapist provided cor- rective feedback using the principles of communication and coping described earlier. They were instructed to practice this task at least three times over the next week. On at least one occasion, Julie was to practice the task alone.
Next, interoceptive exposure was introduced. As with in vivo exposure, through repeated exposures to feared sensations, patients learn that they are not harmed by the sensations, and they achieve increased confidence in their ability to tolerate symptoms of anxiety. The procedure begins with assessment of the patient’s response to a series of standardized exercises. The therapist models each exercise first. Then, after the patient has completed the exercise, the therapist records the sensations, anxiety level (0–10), sensation intensity (0–10), and similarity to naturally occurring panic sensations (0–10). The exercises include shaking the head from side to side for 30 seconds; placing the head between the legs for 30 seconds and lifting the head to an upright position quickly; running in place or using steps for l minute; holding one’s breath for as long as possible; complete body muscle tension for 1 minute or holding a push-up position for as long as pos- sible; spinning in a swivel chair for 1 minute; hyper-
44 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
ventilating for 1 minute; breathing through a narrow straw (with closed nasal passages) or breathing as slowly as possible for 2 minutes; and staring at a spot on the wall or at one’s mirror image for 90 seconds. If none of these exercises produce sensations at least moderately similar to those that occur naturally, other, individually tailored exercises are generated. For example, tightness around the chest may be induced by a deep breath be- fore hyperventilating; heat may be induced by wearing heavy clothing in a heated room; choking sensations may be induced by a tongue depressor, a high-collared sweater, or a necktie; and startle may be induced by an abrupt, loud noise in the midst of relaxation. For Julie, the sensations produced by hyperventilating, spinning, and staring at a spot on the wall were most anxiety pro- voking.
Patients who report little or no fear because they feel safe in the presence of the therapist are asked to attempt each exercise alone, either at home or with the thera- pist out of the office. At the same time, discussing the influence of perceived safety as a moderating factor in the amount of fear experienced reinforces the value of cognitive restructuring. For a minority of patients, the known cause and course of the sensations override the fear response; that is, because the sensations are predict- ably related to a clear cause (the interoceptive exercise), and because the sensations can be relatively easily con- trolled by simply terminating the interoceptive exercise, fear is minimal. Under these conditions, discussion can productively center on the misassumptions that render naturally occurring sensations more frightening than the ones produced by the interoceptive exercises. Typi- cally, these misassumptions are that naturally occurring sensations are unpredictable; that unpredictable sensa- tions are more harmful; and that if naturally occurring sensations are not controlled, then they pose a potential threat. The majority of patients fear at least several of the interoceptive exercises despite knowing the cause of the sensations and their controllability.
Interoceptive exercises rated as producing at least somewhat similar sensations to naturally occurring panic (at least 3 on the 0- to 10-point scale) are selected for repeated exposure. A graduated approach is used for interoceptive exposure, beginning with the lowest item on the hierarchy established in Session 4. For each trial of exposure, the patient is asked to begin the induction, to indicate when the sensations are first experienced (e.g., by raising a hand), and to continue the induction for at least 30 seconds longer to permit corrective learn- ing. After terminating the induction, anxiety is rated,
and the patient is given time to apply cognitive and breathing coping skills, if needed, to keep the patient engaged. Although some cognitive restructuring may naturally occur as patients see that their predictions are not coming true during interoceptive exposure, ex- plicit use of cognitive restructuring or diaphragmatic breathing skills in between interoceptive exposure tri- als is not necessary. Allowing patients to experience and tolerate anxiety during the exercise, take a short break, and begin a new trial without efforts to manage anxiety is appropriate. Finally, the therapist reviews the induction experience. During this review, the therapist emphasizes the importance of experiencing the sensa- tions fully during the induction, of concentrating ob- jectively on the sensations versus distracting from them, and of identifying specific cognitions and challenging them by considering all of the evidence. In addition, the therapist asks key questions to help the patient real- ize his/her safety (e.g., “What would have happened if you had continued spinning for another 60 seconds?”), and to generalize to naturally occurring experiences (e.g., “How is this different from when you feel dizzy at work?”). In other words, cognitive restructuring ex- tends the cognitive reprocessing already taking place implicitly as a result of repeated interoceptive exposure.
Specific, previously unrecognized cognitions some- times become apparent during repeated exposure. For example, when Julie began to conduct repeated expo- sures to hyperventilation and spinning, she became more aware of her implicit assumption that sensations of spaciness or lightheadedness would lead her to lose control of her limbs. This related to her concern about causing an accident when driving. During repeated hy- perventilation exercises, and with prompting of “what ifs” from the therapist, Julie discovered her fear of not being able to move her arms or legs. The therapist then behaviorally challenged this assumption by having Julie overbreathe for longer periods of time, followed imme- diately by walking, picking up objects, and so on.
Homework practice is very important, because safety signals present in the clinic setting or that derive from the therapist per se may, again, prevent generalizability to the natural setting. Patients are instructed to practice the interoceptive items conducted in session on a daily basis, three times each day. Julie was to practice hyper- ventilation over the following week. She expressed some concern at doing the exercises alone, so the therapist helped Julie to use her cognitive restructuring skills in relation to being alone. In addition, more graduation of homework was suggested, so that Julie would practice
Panic Disorder and Agoraphobia 45
hyperventilating when her husband was at home the first couple of days, then when he was not at home the rest of the time.
Sessions 6 and 7
The primary goal of these sessions is to review the past week of in vivo exposure practices, design new expo- sures, review between-session practices of interocep- tive exposure, conduct repeated interoceptive exposure in session, and assign those as homework for the next week.
The in vivo exposure is reviewed, as in the previous session. In this case, Julie and Larry had done well with the movie theater practice. Julie even practiced going to the movies on her own. On that occasion, she reported higher anxiety than when she was with Larry for fear of having to get up and leave the theater and worries about bothering others in the audience. The therapist helped Julie to identify what worry led her to think about leav- ing in the first place; in other words, what did she think might happen if she could not leave? When Julie indi- cated that she had thoughts of losing control and caus- ing a scene, she was then prompted to apply her cogni- tive restructuring skills of evidence-based analyses and decatastrophizing. She was ready to move to the next items on her hierarchy: to spend 2 hours alone at home during the day and to stay alone at home as day turned to night. As with every in vivo exposure task, Julie iden- tified what she most feared happening in those situa- tions, and the best practice conditions under which to learn that either those eventualities would not happen and/or she could cope with the worst.
The past week of interoceptive exposure practice is reviewed in session with a mind toward avoidance: either overt failure to practice or covert avoidance by minimizing the intensity or duration of the sensations induced, or by limiting practice to the presence of a safety signal (e.g., a significant other) or times when background anxiety is minimal. Reasons for avoidance may include continued misinterpretation of the dangers of bodily sensations (i.e., “I don’t want to hyperven- tilate, because I’m afraid that I won’t be able to stop overbreathing and no one will be there to help me”) or the belief that anxiety will not reduce with repetition of the task.
For the first week, Julie practiced interoceptive expo- sure exercises about half of the days between sessions. The therapist used a “downward arrow” method to ex- plore Julie’s reasons for not practicing every day.
JULIE: I tried hyperventilating on my own. However, I wasn’t very successful because I felt too scared and I stopped it as soon as I noticed the strange feelings.
THERAPIST: What did you think would happen if the sensations became more intense?
JULIE: I thought the feelings would get worse and worse and worse, and just overwhelm me. I didn’t want to have that feeling of panic again.
THERAPIST: If you did become overwhelmed, then what would happen to you?
JULIE: Then I’d feel really terrible. THERAPIST: And if you felt really terrible? JULIE: Well, nothing. I’d just feel terrible. THERAPIST: The word terrible carries a lot of meaning.
Let’s see if we can pin down your anxious thoughts that make the feelings so terrible.
JULIE: I just can’t tolerate the feeling. THERAPIST: What tells you that you cannot tolerate it?
How do you know you can’t tolerate it?
And the discussion continued, so that Julie realized what was most important for her to learn by the repeated hyperventilation: She could tolerate the sensations and anxiety. However, after the subsequent week of repeated practice, Julie remained cautious for fear that the ex- ercises would cause her to revert to her state of several weeks earlier; that is, she was concerned that the induc- tions would leave her in a persistent symptomatic state. Furthermore, she was particularly reluctant to practice interoceptive exposure at the end of the day, when she was more likely to feel unreal, or on a day when an im- portant social event was scheduled. Again, these avoid- ance patterns were related to fears that the symptoms would become too intense or result in some type of men- tal or social catastrophe. These types of avoidance pat- terns are addressed in the following vignette:
THERAPIST: When did you practice deliberately spin- ning and hyperventilating?
JULIE: Usually in the mornings. One day I left it until the end of the day, and that turned out to be a bad idea. I felt terrible.
THERAPIST: Let’s think about that a bit more. What made it terrible when you practiced at the end of the day?
JULIE: Well, I was already feeling pretty unreal—I usu-
46 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
ally do around that time of the day. So I was much more anxious about the symptoms.
THERAPIST: Being more anxious implies that you thought the symptoms were more harmful. Is that what happened on the day that you practiced in- teroceptive exposure when you were already feeling unreal?
JULIE: Yes, I felt that because I was already feeling un- real, I was on the edge, and that I might push my- self over the edge if I tried to increase the feelings of unreality.
THERAPIST: What do you mean by “push myself over the edge”?
JULIE: That I would make the feelings so intense that I really would lose it—go crazy.
THERAPIST: So there is one of those hypotheses: to feel more intense unreality means to be closer to going crazy. Let’s examine the evidence. Is it necessarily the case that more intense unreality means you are closer to craziness?
In sessions, the therapist continued practice of in- teroceptive exposure with the next item on Julie’s hi- erarchy, which was to stare at a spot on the wall and to spin around.
The homework from this session is to continue self- monitoring, in vivo exposure to an item from the agora- phobia hierarchy at least three times, and daily practice of interoceptive exposure.
Sessions 8 and 9
The primary goals of these sessions are to continue in vivo exposure, as described in the prior sessions, and to extend interoceptive exposure to natural activities. Julie had practiced staying at home for 2 hours alone dur- ing the day and as daylight turned to dusk, with good results. In particular, despite experiencing a couple of panic attacks during these in vivo exposure practices, she continued with the assigned practice. This was criti- cal for Julie, because it allowed her to learn that she could survive the feeling of panic; it was the first time she had remained in a situation despite panicking.
In reviewing the week’s practice of interoceptive ex- posure, it became apparent that Julie was separating the practices from real-life experiences of bodily sensations in a way that would limit generalization. This was ad- dressed as follows:
JULIE: After spinning and hyperventilating several times, I really do feel much less anxious. I was terri- fied at the start, but now I am only mildly anxious, if at all. But this is different than what happens to me when I’m on the freeway or at home.
THERAPIST: How is it different? JULIE: I don’t know when the feelings of dizziness and
unreality are going to hit. THERAPIST: From our previous discussions, let’s think
of potential reasons why you might feel dizzy or un- real at a particular time?
JULIE: I know. I have to keep remembering that it could be my breathing, or just feeling anxious, or tired, or a bunch of different things.
THERAPIST: OK. And why is it so important to know when those feelings will occur?
JULIE: Because I don’t want them to be there at all. THERAPIST: And why not . . . what are you afraid of? JULIE: I guess it’s the same old thing . . . that I’ll lose it
somehow? THERAPIST: So let’s go back to the cognitive restructur-
ing that you have been doing. What specifically are you afraid of? How likely is it to happen? What are the alternatives?
JULIE: I understand. THERAPIST: So, now you see that whether the sensa-
tions of dizziness or unreality are produced by anxi- ety, overbreathing, diet, or the exercises we do here, they’re all the same—they are just uncomfortable physical sensations. The only reason they perturb you more when you are driving or at home is because of the meaning you still give to them in those situ- ations.
Naturalistic interoceptive exposure refers to exposure to daily tasks or activities that have been avoided or en- dured with dread because of the associated sensations. Typical examples include aerobic exercise or vigorous physical activity, running up flights of stairs, eating foods that create a sensation of fullness or are associated with sensations of choking, saunas or steamy showers, driving with the windows rolled up and the heater on, caffeine consumption, and so on. (Of course, these ex- ercises may be modified in the event of actual medical complications, such as asthma or high blood pressure.) From a list of typically feared activities and generation of items specific to the individual’s own experience, a
Panic Disorder and Agoraphobia 47
hierarchy is established. Each item is ranked in terms of anxiety ratings (0–10). Julie’s hierarchy was as fol- lows: looking out through venetian blinds (anxiety = 3); watching One Flew over the Cuckoo’s Nest (anxiety = 4); playing tennis (anxiety = 4); scanning labels on a supermarket shelf (anxiety = 5); concentrating on needlework for an hour (anxiety = 6); driving with win- dows closed and heater on (anxiety = 7); a nightclub with strobe lights (anxiety = 8); and rides at Disneyland (anxiety = 10).
Like the symptom exercises, the activity exercises are designed to be systematically graduated and repetitive. Patients may apply the breathing and cognitive skills while the activity is ongoing, if needed, to stay engaged in the activity. This is in contrast to the symptom in- duction exercises, in which coping skills are used only after completion of the symptom exercise (if at all), because the activities often are considerably longer than the symptom induction exercises. Nevertheless, patients are encouraged to focus on the sensations and experience them fully throughout the activity, and not use the coping skills to prevent or remove the sensa- tions.
Patients are instructed to identify maladaptive cogni- tions and rehearse cognitive restructuring before begin- ning each activity. In-session rehearsal of the cognitive preparation allows therapists to provide corrective feed- back. Julie did this with her therapist for her first two naturalistic activities, which were to look at venetian blinds and to watch One Flew over the Cuckoo’s Nest. Julie realized that she was most worried about sensa- tions of unreality and fears of going crazy, although, as a result of her various exposure exercises up to this point, she quickly was able to recognize that such sensa- tions were harmless and that she could tolerate them, and that such fears were unrealistic based on the evi- dence.
As with all exposures, it is important to identify and remove (gradually, if necessary) safety signals or protec- tive behaviors, such as portable phones, lucky charms, walking slowly, standing slowly, and staying in close proximity to medical facilities. These safety signals and behaviors reinforce catastrophic misappraisals about bodily sensations. Julie’s safety behaviors were identi- fied as checking the time on the clock (as a reassurance that she was in touch with reality) and pinching her- self (again, to feel reality). She was asked to practice the two naturalistic interoceptive exposures at least three times each before the next treatment session, without the safety behaviors.
Sessions 10 and 11
The primary goals of these sessions are to review the in vivo and naturalistic exposure exercises over the past week, and to combine exposure to feared and avoided agoraphobic situations with deliberate induction of feared sensations into those situations. As with ear- lier interoceptive exposure homework assignments, it is important to evaluate and correct tendencies to avoid naturalistic interoceptive exposure tasks, mainly by considering the underlying misassumptions that lead to avoidance. Remember also that a form of avoidance is to rely on safety signals or safety behaviors, so careful questioning of the way in which the naturalistic expo- sure was conducted, and under what conditions, may help to identify inadvertent reliance on these unneces- sary precautions. Julie reported that she was successful in looking at the venetian blinds, even though she expe- rienced sensations of unreality. She had more difficulty watching One Flew over the Cuckoo’s Nest because it tapped directly into her worst fears of losing touch with reality permanently; she tried but terminated the film early. The second time, she watched it with Larry, who prompted Julie to remember her cognitive and breath- ing skills, and she was able to watch the entire film. She watched the film one more time on her own. Two new naturalistic exposure items were selected for the com- ing week, with special attention to weaning or remov- ing safety signals and safety behaviors, and rehearsal of cognitive restructuring in session. For Julie, these were playing tennis (something she had avoided for years) and scanning items on supermarket shelves.
The notion of deliberately inducing feared bodily symptoms within the context of feared agoraphobic sit- uations derives from the evidence that compound rela- tionships between external and internal cues can be the most potent anxiogenic agent (i.e., deepened extinction, as reviewed in earlier sections); that is, neither just the situation nor just the bodily sensation triggers distress. It is the combination of the bodily sensation and the situation that is most distressing. Thus, effective expo- sure targets both types of cues. Otherwise, patients run the risk of later return of fear. For example, repeated practice walking through a shopping mall without feel- ing dizzy does not adequately prepare patients for occa- sions on which they feel dizzy walking through a shop- ping mall, and without such preparation, patients may be likely to panic and escape should they feel dizzy in this or similar situations in the future. Wearing heavy clothing in a restaurant helps patients to learn to be less
48 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
afraid of not only the restaurant but also of feeling hot in a restaurant. Other examples include drinking cof- fee before any of the agoraphobic tasks, turning off the air-conditioning or turning on the heater while driving, breathing very slowly in a crowded area, and so on.
Patients choose an item from their hierarchy of ago- raphobia situations, either one already completed or a new item, and also choose which symptom to induce and ways of inducing that symptom in that situation. Julie’s task was to drink coffee as she went to a movie. She expressed the following concerns:
JULIE: Do you really think I am ready to drink coffee and go to the movie?
THERAPIST: What worries you about the combination of coffee and the movie theater?
JULIE: Well, I’ve practiced in the movie theaters a lot, so that feels pretty good, but the coffee is going to make me feel very anxious.
THERAPIST: And if you feel very anxious in the movie theater, then what?
JULIE: Then, I don’t know what. Maybe I will get those old feelings again, like I have to get out.
THERAPIST: Based on everything you have learned, how can you manage those feelings?
JULIE: Well, I guess my number one rule is never to leave a situation because I am feeling anxious. I will stick it out, no matter what.
THERAPIST: That sounds great. It means you are ac- cepting the anxiety and taking the opportunity to learn that you can tolerate it. What else?
JULIE: I can ask myself what is the worst that can hap- pen. I know I am not going to die or go crazy. I will probably feel my heart rate going pretty fast because of the coffee.
THERAPIST: And if your heart rate goes fast, what does that mean?
JULIE: I guess it just means that my heart rate will go fast.
THERAPIST: This will be a really good way for you to learn that you can tolerate the anxiety and the symp- toms of a racing heart.
The homework for this session is to continue self- monitoring, to practice in vivo exposure combined with interoceptive exposure, and to continue naturalistic in- teroceptive exposure.
Session 12
The last treatment session reviews the principles and skills learned and provides the patient with a template of coping techniques for potentially high-risk situations in the future. Julie finished the program after 12 ses- sions, by which time she had not panicked in 8 weeks, rarely experienced dizziness or feelings of unreality, and was driving further distances. There were some situa- tions still in need of exposure practices (e.g., driving very long distances away from home and on the freeway at dusk). However, Julie and Larry agreed to continue in vivo exposure practices over the next few months to consolidate her learning and to continue her improve- ment.
CONCLUSION
As we noted earlier in this chapter, cognitive-behavior- al treatments for panic disorder and agoraphobia are highly effective and represent one of the success stories of psychotherapy. Between 80 and 100% of patients undergoing these treatments will be panic-free at the end of treatment and maintain these gains for up to 2 years. These results reflect substantially more durability than medication treatments. Furthermore, between 50 and 80% of these patients reach a point of “high end state,” which means their symptoms and functioning are within normative realms, and many of the remain- der have only residual symptomatology. Nevertheless, major difficulties remain.
First, these treatments are not foolproof. As many as 50% of patients retain substantial symptomatology despite improvement from baseline, and this is par- ticularly likely for those with more severe agoraphobia. Further research must determine how treatments can be improved or better individualized to alleviate con- tinued suffering. For example, one of us (D. H. B.) saw a patient several years ago who had completed an initial course of treatment but required continued periodic visits for over 4 years. This patient was essentially im- proved for approximately 9 months but found himself relapsing during a particularly stressful time at work. A few booster sessions restored his functioning, but he was back in the office 6 months later with reemerging symptomatology. This pattern essentially continued for 4 years and was characterized by symptom-free periods followed by (seemingly) stress-related relapses. Further- more, the reemerging panic disorder would sometimes
Panic Disorder and Agoraphobia 49
last from 3 to 6 months before disappearing again, per- haps with the help of a booster session.
Although this case was somewhat unusual in our ex- perience, there was no easy explanation for this pattern of relapses and remissions. The patient, who has a grad- uate degree, understood and accepted the treatment model and fully implemented the treatment program. There was also no question that he fully comprehended the nature of anxiety and panic, and the intricacies of the therapeutic strategies. While in the office, he could recite chapter and verse the nature of these emotional states, as well as the detailed process of his own reac- tion while in these states. Nevertheless, away from the office, the patient found himself repeatedly hoping that he would not “go over the brink” during a panic attack, despite verbalizing very clearly the irrationality of this concept while in the office. In addition, he continued to attempt to reduce minor physiological symptoms as- sociated with anxiety and panic, despite a full rational understanding of the nature of these symptoms (includ- ing the fact that they are the same symptoms he experi- enced during a state of excitement, which he enjoyed). His limited tolerance of these physical sensations was also puzzling in view of his tremendous capacity to en- dure pain.
Any number of factors might account for what seemed to be “overvalued ideation” or very strongly held irrational ideas during periods of anxiety, including the fact that the patient has several relatives who have repeatedly been hospitalized for emotional disorders (seemingly mood disorders or schizoaffective disorder). Nevertheless, the fact remains that we do not know why this patient did not respond as quickly as most people. Eventually, he made a full recovery, received several promotions at work, and considered treatment to be the turning point in his life. But it took 5 years.
Other patients, as noted earlier, seem uninterested in engaging in treatment, preferring to conceptualize their problems as chemical imbalances. Still others have difficulty grasping some of the cognitive strategies, and further attempts are necessary to make these treatments more “user-friendly.”
It also may seem that this structured, protocol-driv- en treatment is applied in a very standard fashion across individuals. Nothing could be further from the truth. The clinical art involved in this, and in all treatments described in this book, requires a careful adaptation of these treatment strategies to the individual case. Many of Julie’s symptoms revolved around feelings of unreal- ity (derealization and depersonalization). Emphasizing
rational explanations for the production of such feel- ings, as well as adapting cognitive and exposure exercis- es to maximize these sensations, is an important part of this treatment program. Although standard interocep- tive provocation exercises seemed sufficient to produce relevant symptomatology in Julie’s case, we have had to develop new procedures to deal with people with more idiosyncratic symptoms and fears, particularly those in- volving feelings of unreality or dissociation. Other in- novations in both cognitive and behavioral procedures will be required by individual therapists as they apply these procedures.
Although these new treatments seem highly success- ful when applied by trained therapists, treatment is not readily available to individuals with these disorders. In fact, these treatments, although brief and structured, are far more difficult to deliver than, for example, phar- macological treatments (which are also often misap- plied). Furthermore, few people are currently skilled in the application of these treatments. What seems to be needed for these and other successful psychosocial treatments is a new method of disseminating them, so that they reach the maximum number of patients. Modification of these treatment protocols into more user-friendly formats, as well as brief periods of training for qualified therapists to a point of certification, would be important steps in successfully delivering these treat- ments. This may be difficult to accomplish.
NOTE
1. Specific phobias were not assessed, but by being most cir- cumscribed, they would be hypothesized to load the least on negative affectivity.
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Severe, unexpected trauma may occur in less than a minute but have lifelong consequences. The tragedy that is posttraumatic stress disorder (PTSD) is brought into stark relief when the origins of the trauma occur in the context of people’s inhumanity to others. In this chapter, the case of “Tom” illustrates the psychopathology associated with PTSD in all its nuances and provides a very personal account of its impact. In one of any number of events summarized dryly every day in the middle pages of the newspaper, Tom, in the fog of war in Iraq, shoots and kills a pregnant woman and her young child in the presence of her husband and father. The impact of this event devastates him. The sensi- tive and skilled therapeutic intervention described in this chapter is a model for new therapists and belies the notion that, in these severe cases, manualized therapy can be rote and automated. In addi- tion, “cognitive processing therapy,” the evidence-based treatment for PTSD utilized with this case, is sufficiently detailed to allow knowledgeable practitioners to incorporate this treatment program into their practice. This comprehensive treatment program takes advantage of the latest developments in our knowledge of the psychopathology of trauma impact by incorporating treatment strategies specifically tailored to overcome trauma-related psychopathology and does so in the context of the significant changes to diagnostic criteria in DSM-5. —D. H. B.
PREVALENCE
Epidemiological studies document significant rates of trauma exposure and posttraumatic stress disorder (PTSD) across the world (e.g., Atwoli, Stein, Koenen, & McLaughlin, 2015; Kessler, Sonnega, Bromet, Hughes, & Nelson, 1995; Kessler, Berglund, et al., 2005; Kes- sler, Chiu, Demler, Merikangas, & Walters, 2005; Kil- patrick, Saunders, Veronen, Best, & Von, 1987; Kulka et al., 1990). In a national (U.S.) random probability sample of 4,008 women, Resnick, Kilpatrick, Dansky, Saunders, and Best (1993) found a high rate of trauma experiences (69%). When they extrapolated their re- sults to the U.S. population based on census statistics for 1989, they estimated that 66 million women in the United States had experienced at least one major trau-
matic event. Of those who had experienced a criterion A stressor, Resnick and colleagues found the following lifetime PTSD rates: completed rape, 32%; other sexual assault, 31%; physical assault, 39%; homicide of fam- ily or friend, 22%; any crime victimization, 26%; and noncrime trauma (e.g., natural and manmade disasters, accidents, injuries), 9%.
In the first large national civilian prevalence study of the psychological effects of trauma, Kessler and col- leagues (1995) surveyed a representative U.S. national sample of 5,877 persons (2,812 men and 3,065 women). They assessed 12 categories of traumatic stressors and revealed that a majority of people had experienced at least one major traumatic event. They found that, whereas 20.4% of women and 8.2% of men were likely to have PTSD following exposure to trauma, the rates
C H A P T E R 2
Posttraumatic stress Disorder
Candice M. Monson Philippe Shnaider Kathleen M. Chard
Posttraumatic Stress Disorder 65
for specific traumas were often much higher. For ex- ample, rape was identified as the trauma most likely to lead to PTSD among men, as well as women. Moreover, 65% of men and 46% of women who identified rape as their most distressing trauma were diagnosed with PTSD. Among men who identified other traumas as most distressing, the probability of having PTSD was 39% for those with combat exposure, 24% for those who suffered childhood neglect, and 22% of those who experienced childhood physical abuse. Among women, aside from rape, PTSD was associated with physical abuse in childhood (49%), threat with a weapon (33%), sexual molestation (27%), and physical attack (21%). As with Resnick and colleagues’ (1993) study, accidents and natural disasters were much less likely to precipitate PTSD among men and women. On the other hand, Norris (1992) pointed out that although motor vehicle accidents (MVAs) occur less frequently than some trau- mas (e.g., tragic death or robbery) and are less traumatic than some events (sexual and physical assault), when both frequency and impact are considered together, MVAs may be the single most significant event. The lifetime frequency of MVAs is 23%, and the PTSD rate is 12%, which results in a rate of 28 seriously distressed people for every 1,000 adults in the United States, just from one type of event. Kessler, Berg lund, and colleagues (2005) reported on another large National Comorbidity Survey with over 9,200 respondents. The overall prevalence of PTSD was 6.8% in this study; this compares to the 7.8% population prevalence reported in the 1995 study.
Atwoli and colleagues (2015) reviewed PTSD preva- lence from a more global perspective. They noted that the rates of experiencing trauma, and even the type of trauma experienced, can vary significantly by country or region, often due to social or political reasons (e.g., civil war or state-sanctioned discrimination). They found that trauma exposure rates were higher in lower- income countries, and PTSD rates were highest in post- conflict settings. Of the countries surveyed, most re- ported global lifetime rates between 1.3% (Japan) and 2.4% (Italy), with Northern Ireland reporting the high- est rate of 8.8%. Using 26 population surveys from the World Health Organization, Koenen and colleagues (2017) found an overall lifetime PTSD prevalence of 5.6% in those who had been exposed to a traumatic event.
The largest study of combat veterans to date, the National Vietnam Veterans Readjustment Study (NVVRS; Kulka et al., 1990), was mandated by the
U.S. Congress in 1983 to assess PTSD and other psy- chological problems following the Vietnam War. Dur- ing the years of the war, over 8 million people served in the U.S. military. Of those, 3.1 million served in Vietnam (theater veterans) and the remainder served in other areas abroad or in the U.S. (era veterans). Women comprised 7,200 of those serving in Vietnam, and over 255,000 of those serving elsewhere during the Vietnam era. The NVVRS conducted in-depth interviews and assessments with three groups: 1,632 Vietnam theater veterans, 716 Vietnam era veterans, and 668 nonvet- erans/civilian counterparts, for a total of 3,016 partici- pants.
The results of the NVVRS indicated that the major- ity of Vietnam theater veterans made a successful read- justment to civilian life and did not suffer from PTSD or other problems. However, the researchers also found that 31% of men and 27% of women veterans had a diagnosis of PTSD at some time during their lives. Fur- thermore, 15% of men and 9% of women veterans had PTSD at the time of the study, over a decade after the end of the war. These rates translated to 479,000 Viet- nam veterans with current PTSD at the time that the study was conducted.
Data from the NVVRS were reevaluated using very strict criteria that only included those incidents that could be verified through historical records. Dohren- wend and colleagues (2006) found very little falsifica- tion of events and a strong relationship between the amount of trauma exposure and rates of PTSD (i.e., dose–response relationship). They did, however, find lower rates of PTSD after controlling for people who developed PTSD before or after their deployment to Vietnam and eliminating those people with unverifi- able events. Using these stricter criteria, they found that 18.7% of the veterans met criteria for war-related PTSD at some point, and 9.1% still had PTSD when assessed 11 to 12 years later. These rates should be con- sidered minimum likelihood rates given that people can be traumatized by events that may not be verifiable in historical accounts of war (e.g., rape, accidents). A follow-up study, the National Vietnam Veterans Lon- gitudinal Study (NVVLS; Marmar et al., 2015), evalu- ated the long-term effects of trauma exposure in the same sample. The researchers were able to obtain data from 78.8% of the original sample (N= 1,450), and they found a current PTSD rate of 4.5% and a lifetime rate of 17%, 40 years after the war had ended.
The wars in Iraq and Afghanistan saw the first at- tempts to assess PTSD during a war (Hoge et al., 2004;
66 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
Hoge, Auchterlonie, & Milliken, 2006). Hoge and his colleagues (2004) studied 2,530 Army soldiers and Marines before and 3,671 after deployment to Iraq or Afghanistan. They found that mental health problems were significantly greater among those who returned from deployment than among those not yet deployed, and that mental health problems were greater in those who deployed to Iraq compared with Afghanistan. Prior to deployment, 9% of the service personnel ex- ceeded the self-reported PTSD symptom cutoff score used for likely PTSD, whereas 11.5% of those deployed to Afghanistan and 18–20% of those deployed to Iraq exceeded the cutoff. There was a linear relationship be- tween the number of firefights reported and the sever- ity of PTSD. Being wounded or otherwise physically injured was also associated with greater PTSD symp- tomatology.
Because the U.S. military began screening all mili- tary personnel for PTSD following deployment, a population-based study of 303,905 Army soldiers and Marines who deployed to Afghanistan, Iraq, or other locations could be conducted for a 1-year period (May 2003 to April 2004; Hoge et al., 2006). As with the pre- vious report, servicemen and women were more likely to report mental health problems after serving in Iraq (19.1%) than after serving in Afghanistan (11.3%) or other locations (8.5%). In this study, they also assessed 32,500 women, comprising 10.7% of the total sample. There was an overall gender difference in mental health concerns, with 23.6% of women compared with 18.6% of men reporting a mental health concern. However, this gender comparison did not take into account pre- existing traumas or PTSD, exposure to combat traumas or sexual assault, or other variables that might explain these differences (Street, Gradus, Vogt, Giasson, & Resick, 2013).
The National Health Study for a New Generation of U.S. Veterans (NewGen; Dursa, Reinhard, Barth, & Schneiderman, 2014) was launched by the U.S. De- partment of Veterans Affairs to determine the rates of PTSD in Iraq and Afghanistan veterans (15.8%) com- pared with nondeployed veterans (10.9%). They found higher rates of PTSD among African Americans (odds ratio [OR] = 1.61), those who served in the Army (OR = 2.67) and those on active duty (OR = 1.69). A meta- analysis (Fulton et al., 2015) of 33 studies published between 2007 and 2013 revealed a PTSD prevalence rate among veterans who served in Iraq and/or Afghan- istan of around 23% (range 1.4–60%). The authors found that disparities in prevalence were often related
to methods of obtaining diagnosis, anonymity of re- porting, degree of combat exposure, and military sta- tus (e.g., active duty vs. reserve). In keeping with prior research, non-White veterans were more likely to have a diagnosis of PTSD; however, in this study, men were more likely than women to have PTSD.
THEORETICAL MODELS
As researchers and clinicians began to study and treat survivors of rape trauma and Vietnam veterans in the 1970s, they began to draw on learning theory as an ex- planation for the symptoms they were observing. Mow- rer’s two-factor theory (1947) of classical and operant conditioning was first proposed to account for post- trauma symptoms (Becker, Skinner, Abel, Axelrod, & Cichon, 1984; Holmes & St. Lawrence, 1983; Keane, Zimering, & Caddell, 1985; Kilpatrick, Veronen, & Best, 1985; Kilpatrick, Veronen, & Resick, 1982). Clas- sical conditioning was used to explain the high levels of distress and fear observed in trauma victims in reaction to trauma-related stimuli. Operant conditioning ex- plained the onset of PTSD avoidance symptoms, as well as the maintenance of fear over time, despite the fact that the unconditioned stimulus, the traumatic stressor, does not recur. Because the trauma memory and other cues (conditioned stimuli) elicit fear and anxiety (con- ditioned emotional responses), people avoid (or escape from) these cues, and the result is a reduction in fear and anxiety. In this manner, avoidance of the condi- tioned stimuli is negatively reinforced, which prevents deterioration of the link between the trauma cues and anxiety that would normally be expected without rep- etition of the trauma itself.
Although learning theory accounts for much of the onset and maintenance of the fear and avoidance in PTSD, it does not fully explain intrusion symptoms. Based on Lang’s (1977) information processing theory of anxiety development, Foa, Steketee, and Rothbaum (1989) suggested that PTSD emerges due to the devel- opment of a fear network in memory that elicits escape and avoidance behavior. Mental fear structures include stimuli, response, and meaning elements. Anything as- sociated with the trauma may elicit the fear structure or schema and subsequent avoidance behavior. The fear network in people with PTSD is thought to be stable and to generalize broadly, so that it is easily accessed. Chemtob, Roitblat, Hamada, Carlson, and Twentyman (1988) proposed that these structures are always at least
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weakly activated in individuals with PTSD and guide their interpretation of events as potentially dangerous. When the fear network is activated by reminders of the trauma, the information in the network enters con- sciousness (intrusive symptoms). Attempts to avoid this activation result in the avoidance symptoms of PTSD. According to information processing theory, repetitive exposure to the traumatic memory in a safe environ- ment results in habituation of fear and subsequent changes in the fear structure. As emotion decreases, clients with PTSD begin to modify their meaning el- ements spontaneously, and consequently change their self-statements and reduce their generalization.
Social-cognitive theories are also concerned with in- formation processing, but they focus on the semantic content of the survivor’s belief system and the adjust- ments that are necessary to reconcile a traumatic event with prior beliefs and expectations. The first and most influential cognitive theorist, Horowitz (1986), moved from a more psychodynamic view to a cognitive pro- cessing theory. Horowitz proposed that processing is driven by a “completion tendency,” the psychological need for new, incompatible information to be inte- grated with existing beliefs. The completion tendency keeps the trauma information in active memory until the processing is complete and the event is resolved. Horowitz also theorized that there is a basic conflict between the person’s need to resolve and reconcile the event into his/her history, and the desire to avoid emo- tional pain. When images of the event (flashbacks, nightmares, intrusive recollections), thoughts about the meanings of the trauma, and emotions associated with the trauma become overwhelming, psychological defense mechanisms take over, and the person exhibits numbing or avoidance. Horowitz suggested that a per- son with PTSD oscillates between phases of intrusion and avoidance, and that if successfully processed, the oscillations become less frequent and less intense. Ac- cording to this theory, chronic PTSD occurs because the trauma remains in active memory without becom- ing fully integrated; therefore, it is still able to stimulate intrusive and avoidant reactions.
Several other social-cognitive researchers and theo- rists propose that basic assumptions about the world and oneself are “shattered” following exposure to a trau- matic event. Constructivist theories are based on the idea that people actively create their own internal rep- resentations of the world (and themselves). New experi- ences are assigned meaning based on a person’s model of the world (Janoff-Bulman, 1985, 1992; Mahoney &
Lyddon, 1988; McCann & Pearlman, 1990). The task for recovery is to reconstruct fundamental beliefs and establish equilibrium. Janoff-Bulman (1985) suggested that this process is accomplished by reinterpreting the event to reduce the distance between the prior beliefs and the new beliefs. Other theorists have proposed that if one’s preexisting beliefs are particularly positive or particularly negative, then more severe PTSD symp- toms result (McCann & Pearlman, 1990; Resick, Mon- son, & Chard, 2017; Resick & Schnicke, 1992). Foa et al. (1989) focused particularly on beliefs regarding the predictability and controllability of the trauma, where- as McCann and Pearlman (1990) proposed that several areas of cognition might be either disrupted or seem- ingly confirmed, that is, beliefs regarding safety, trust, power/control, esteem, and intimacy. Resick, Monson, and Chard (2017) model focuses particularly on the “just world” myth and the human desire (and illusion) that we can predict and control our lives.
In a social-cognitive model, affective expression is needed, not for habituation but for the trauma memory to be processed fully. It is assumed that the natural af- fect, once accessed, dissipates rather quickly, and that the work of accommodating the memory with beliefs can begin. Once faulty beliefs regarding the event (e.g., inappropriate self- or other-blame) and overgeneralized beliefs about oneself and the world (e.g., safety, trust, power/control, esteem, intimacy) are challenged, then the secondary or manufactured emotions also decrease, along with the intrusive reminders. The fact that both stress inoculation training without trauma exposure ex- ercises (Foa, Rothbaum, Riggs, & Murdock, 1991; Foa et al., 1999) and cognitive therapy without written or oral accounts of the traumatic experience (e.g., Ehlers et al., 2003; Resick et al., 2008; Resick, Wachen, et al., 2017; Tarrier et al., 1999) are effective treatments for PTSD undermines the assumption that habituation is the sole mechanism of change. In fact, recent work has suggested that cognitive change may be a central mech- anism by which exposure-based therapies treat PTSD (e.g., Zalta et al., 2014).
Ehlers and Clark (2000) proposed a cognitive model of PTSD that focuses on perceived threat and memory. Although the event occurred in the past, Ehlers and Clark propose that people with PTSD are unable to see the event as time-limited and assume that it has larger implications for the future. Individuals with PTSD ap- praise the event such that they believe themselves to be currently at risk. There are several ways in which this misappraisal happens. One is to overgeneralize based
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on the event and assume that normal activities are more dangerous than they objectively are. Individuals may overestimate the probability that the event will recur. After the trauma happens, they may misconstrue the meaning of their PTSD symptoms such that they per- ceive themselves to be in greater danger (false alarms are assumed to be true alarms) or interpret their symp- toms to mean that they cannot cope with events in the future.
Ehlers and Clark’s (2000) cognitive theory also considers the apparent memory disturbance that oc- curs, such that persons with PTSD may have trouble intentionally accessing their memory of the event but have involuntary intrusions of parts of the event. They propose that because memory encoded at the time of the trauma is poorly elaborated and integrated with other memories with regard to details, context of time, sequence, and so forth, this might explain why people with PTSD have poor autobiographical memory, yet may be triggered to have memory fragments that have a here-and-now quality (no time context) or lack appro- priate posttrauma appraisals (e.g., “I did not die”). Like the emotional processing models, Ehlers and Clark also propose that strong associative learning is paired with fear responses and may generalize. In response to perceptions of threat, people with PTSD adopt vari- ous maladaptive coping strategies, depending on their appraisals. For example, people who believe they will go crazy if they think about the traumatic event try to avoid thoughts about the trauma and keep their minds occupied as much as possible. Someone who believes he/she must figure out why the traumatic event oc- curred to keep it from happening again will ruminate about how it could have been prevented. Those who think they were being punished for their actions may become immobilized and be unable to make decisions. These maladaptive strategies, most often avoidance be- haviors, may (1) increase symptoms, (2) prevent change in negative appraisals, or (3) prevent change in the trau- ma memory.
In an attempt to reconcile the theories of PTSD, Brewin, Delgleish, and Joseph (1996; Brewin, Gregory, Lipton, & Burgess, 2010) proposed a dual-representa- tion theory that incorporates both information pro- cessing and social-cognitive theories, and incorporates research and theory from neuroscience with regard to memory. They suggest that the concept of a single emo- tional memory is too narrow to describe the full range of memory that has been evident in research and clini- cal observations. Based on prior research, they proposed
that sensory input is subject to both low-level and high- level memory and representation. High-level memory and representations comprise information that is con- textually bound and represented (contextual memory [C-memory]). Contextual representations (C-reps) of these memories can be deliberately retrieved and ma- nipulated. C-reps contain some sensory information, information about emotional and physical reactions, and the personal meaning of the event. Although C- reps might be reasonably detailed, they may also be very selective, because attention is narrowed under con- ditions of stress, and short-term memory capacity may be decreased.
In contrast, low-level memory and representation consists of sensory and affective elements (sensation- based memory [S-memory]). Representations of these memories (S-reps) cannot be accessed deliberately and are not as easily altered or edited as the more explic- itly accessed C-reps. Accordingly, S-reps are typically experienced as intrusive sensory images or flashbacks accompanied by physiological arousal.
Dual-representation theory posits two types of emo- tional reactions: One type is conditioned during the event (e.g., fear, anger), recorded in the S-memory, and activated along with reexperienced sensory and physi- ological information. The other type, secondary emo- tions, result from the consequences and implications (meaning) of the trauma.
Brewin and colleagues (1996) proposed that emo- tional processing of trauma has two elements. One element of the processing is the activation of S-reps (as suggested by information processing theories), the purpose of which is to aid in cognitive readjustment by supplying detailed sensory and physiological informa- tion concerning the trauma. The activation of S-reps may eventually diminish in frequency when they are blocked by the creation of new S-reps, or when they are altered by the incorporation of new information. Even- tually, if the S-reps are replaced or altered sufficiently, there is a reduction in negative emotions and a subse- quent reduction in attentional bias and accessibility of the memory.
The second element (as proposed by the social- cognitive theorists) is the conscious attempt to search for meaning, to ascribe cause or blame, and to resolve conflicts between the event and prior expectations and beliefs. The goal of this process is to reduce the nega- tive emotions and to restore a sense of relative safety and control in one’s environment. To obtain this second goal, the traumatized person may have to edit his/her
Posttraumatic Stress Disorder 69
autobiographical memory (C-reps) to reconcile con- flicts between the event and his/her belief system.
Brewin and colleagues (1996) suggest that for cases in which the emotions are primary and driven by S- reps, exposure therapy may be all that is needed. How- ever, when secondary emotions such as guilt or shame are present, cognitive therapy may be needed. Although both exposure and cognitive therapies have been found to be effective in treating PTSD, no research thus far has matched types of therapy to client profiles.
Another multirepresentational cognitive model called the schematic, propositional, analogue, and as- sociative representational system (SPAARS; Dalgleish, 2004) was originally proposed to explain everyday emotional experience and was then applied to PTSD. This model also endeavors to encompass previous theo- ries. The model proposes four types or levels of mental representation systems: schematic, propositional, ana- logue, and associative. The schematic level represents abstract generic information, or schemas. Proposition- al-level information has verbally accessible meanings, similar to C-reps, whereas information at the analogue level is stored as “images” across all types of sensory sys- tems, similar to S-reps. Associative representations are similar to the fear structures hypothesized in emotional processing theory as representing the connections be- tween other types of representations. In the SPAARS model, emotions are generated through two routes. One, similar to Ehlers and Clark’s (2000) cognitive model, is through appraisals at the schematic level, in which events are compared against important goals. A person appraises an event to be threatening if it blocks an important goal, then experiences fear. Because trau- matic events are threats to survival, they are appraised as threatening and elicit fear. The second route to emo- tion is through associative learning, which is automatic and similar to the fear activation described by Foa and colleagues (1989).
Within the SPAARS model, a traumatic event trig- gers intense appraisal-driven fear, helplessness, or hor- ror, as well as a range of other emotions. Information about the traumatic event is encoded in the schematic, propositional, and analogue levels simultaneously. Be- cause the memory of the traumatic event represents an ongoing threat to goals, the person is left with low-level fear activation, cognitive bias to attend to threat ap- praisals, and intrusive sensory images and appraisals. The trauma memory exists across different levels of mental representation but is unincorporated into the person’s larger mental representations; the memory may
be elicited as flashbacks or nightmares. Such strong memory and emotional intrusions result in efforts to cope through avoidance.
Research on intimate relationship problems associ- ated with PTSD (Taft, Watkins, Stafford, Street, & Monson, 2011) has highlighted the importance of the interpersonal context in which PTSD exists and has led to the development of treatment innovations to address these concerns (e.g., Monson & Fredman, 2012). In this vein, interpersonal models of PTSD have been pro- posed to account for the occurrence of, maintenance of, and reciprocal associations between PTSD and inter- personal relationship problems. These models include cognitive-behavioral interpersonal theory (C-BIT) of PTSD (Monson, Fredman, & Dekel, 2010), as well as the couple adaptation to stress (CATS) model (Nelson Goff & Smith, 2005), which frame PTSD within a dy- adic relationship. C-BIT proposes that individual-level cognitive, behavioral, and emotional factors within each partner, as well as shared relationship-level factors that exist within the dyadic relationship, serve to in- fluence recovery, the psychological well-being of one’s partner, and relationship functioning following expo- sure to a traumatic event. Each factor is considered to uniquely contribute to, as well as interact with, other factors in the model to impact each partner and their relationship adjustment (Monson et al., 2010). Similar- ly, the CATS model proposes three factors that influ- ence adaptation posttrauma: each partner’s individual functioning, predisposing factors and resources, and couple-level functioning. These factors are considered to interact with one another to influence each partner’s posttraumatic reactions (Nelson Goff & Smith, 2005). Both C-BIT and the CATS model highlight the inter- personal nature of PTSD, proposing bidirectional re- lationships between both individual psychopathology and relationship functioning.
ASSESSMENT
Any comprehensive assessment of PTSD must capture whether or not a life event meets the requirements of a traumatic stressor (criterion A), as well as the presence and severity of the 20 associated symptoms (criteria B–E) listed in the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5; Ameri- can Psychiatric Association, 2013). Although interview- based measures are considered the “gold standard” for assessing PTSD, a number of self-report measures have
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been developed in recent years to provide a quicker, less resource-heavy method for assessing PTSD.
Assessment of Traumatic Events
The first essential step in the assessment of PTSD is to identify traumas in the patient’s history. Often this is difficult to achieve, because many trauma survivors, especially rape and child sexual abuse trauma survivors, do not spontaneously disclose their trauma history. This is consistent with general patterns of avoidance of trauma-related reminders and may reflect shame, embarrassment, and self-blame regarding the inci- dents. Even when seeking treatment for mental health problems, trauma survivors often fail to recognize that their psychological difficulties may be associated with their trauma histories. There are other reasons survi- vors might not be forthcoming with this information, including fear of a negative reaction to disclosure, es- pecially if previous disclosure has resulted in disbelief or blame. Additionally, many trauma survivors do not recognize or label their experience as “trauma,” “rape,” or “abuse,” especially if the assailant was an acquain- tance or a relative, or if the trauma was experienced by many people, as in combat. Finally, in the absence of a strong alliance with the therapist, many people choose not to disclose such deeply personal information. It is therefore important for the clinician to forge a positive alliance as early as possible and be forthcoming about the purpose of the questioning, any limits of confiden- tiality, and how obtained information may be used (i.e., diagnosis, treatment planning, research purposes).
In terms of questions regarding the presence of trau- matic experiences, a behavioral, descriptive prompt such as “Has anyone ever touched you when you did not want them to or made you have unwanted sexual contact?” is more detailed and is preferable to asking, “Have you ever been raped?” In the latter case, someone who is married (or dating) and has been sexually assaulted may say “no,” because “rape” might not be a term that they associate with forced sex by one’s partner. The same problem may exist with child abuse. A client may indicate that he was not abused as a child but readily admit, when asked, that a parent whipped him with a belt until he had welts. In general, it is recommended that clinicians always begin with broad questions about experiences, then move to more specific, behaviorally anchored questions.
Some structured interviews have been developed with the primary purpose of assessing traumas in more
detail. The Potential Stressful Events Interview (Kil- patrick, Resnick, & Freedy, 1991) has behaviorally an- chored questions that are particularly good for assessing interpersonal victimization, as well as a range of other traumatic stressors. The Clinician-Administered PTSD Scale for DSM-5 (CAPS-5; Weathers et al., 2018), reviewed in more detail later, includes a self-report screening scale (Life Events Checklist), followed by in- terviewer prompts to establish whether a trauma meets criterion A.
In addition to the Life Events Checklist, the Brief Trauma Questionnaire (BTQ; Schnurr, Spiro, Viel- hauer, Findler, & Hamblen, 2002) the Trauma History Questionnaire (THQ; Hooper, Stockton, Krupnick, & Green, 2011), the Traumatic Life Events Questionnaire (TLEQ; Kubany et al., 2000), and the Trauma History Screen (Carlson et al., 2011) all assess a number of dif- ferent types of trauma, including accidents, natural di- sasters, sexual assault, and threats of, or actual, physical harm. The Posttraumatic Stress Diagnostic Scale (PDS; Foa et al., 2016) has two sections prior to assessment of symptoms. The first section assesses 13 potentially traumatic events, whereas the second section has ques- tions to determine whether an event meets criterion A.
Structured Diagnostic Interviews
The CAPS-5 (Weathers et al., 2018), a “gold-standard” assessment measure, is one of the most widely used di- agnostic interviews for PTSD. In addition to a detailed assessment of individual trauma experiences with the Life Events Checklist, it assesses both severity and fre- quency of symptoms using specific criteria related to behavior change following the traumatic event. The CAPS-5 also includes questions on associated features of PTSD, including dissociation, survivor guilt, and so- cial and occupational impairment. The CAPS-5 has a large body of research demonstrating its reliability and validity across a wide variety of trauma populations. One disadvantage is its length of administration, an av- erage of about 45 minutes, and the need for administra- tion by a mental health clinician.
The Structured Clinical Interview for DSM-5 (SCID-5; First, Williams, Karg, & Spitzer, 2016), one of the most widely used diagnostic interview scales, in- cludes a Trauma- and Stressor-Related Disorders mod- ule, and was developed for use by experienced clini- cians. Although it assesses all of the symptoms of PTSD and can provide information about whether an individ-
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ual meets criteria for the diagnosis, it is important to note that this interview does not assess for frequency or severity of individual symptoms. Thus, one can only determine a count of the number of positive symptoms, thereby limiting its utility in research or clinical set- tings in which a continuous measure of severity may be desirable.
The PTSD Symptom Scale—Interview for DSM-5 (PSS-I-5; Foa et al., 2016) has a particular advantage in its ease of administration and brevity. The PSS-I-5 consists of 24 items that match the 20-symptom PTSD criteria in DSM-5, as well as questions related to the distress level, onset, and duration of symptoms. The PSS-I-5 can result in continuous scores to reflect fre- quency of symptoms or to determine PTSD diagnosis.
Self‑Report Instruments
There are a number of self-report scales of PTSD that have good psychometric properties and are consistent with the DSM-5 nomenclature. The two most widely known are the PDS-5 (Foa et al., 2016) and the PTSD Checklist–5 (PCL-5; Weathers et al., 2013). The 20- item PCL-5 also has a longer version that includes an exploration of criterion A experiences. With any self- report measure, there are limitations to relying exclu- sively on questionnaires for diagnosis or symptom se- verity. Used in conjunction with structured interviews, however, they can be useful for screening purposes and for demonstrating changes over time as a result of a particular intervention. There is also evidence that self- report and clinician interview of PTSD symptoms are correlated over the course of treatment (Monson et al., 2008).
In response to a need to screen large numbers of people for PTSD after combat or disasters, or in medi- cal settings when time is limited, a brief PTSD screen has been developed for use in primary care settings or for large-group administrations, such as those with military personnel following deployment. The Primary Care PTSD Screen for DSM-5 (PC-PTSD-5; Prins et al., 2016) was developed for such a purpose and is now being used routinely in the United States with anyone returning from military deployment or receiving any kind of treatment in the VA medical system (Hoge et al., 2006). This scale includes an initial item to deter- mine trauma exposure, followed by five yes–no items that represent the five major symptom clusters found in most PTSD factor-analytic studies that separate effort-
ful avoidance from numbing. A cutoff of 3 is recom- mended as an optimally efficient score for both men and women, and a cutoff of 2 is recommended for max- imum sensitivity.
Other Assessment Considerations
The ideal assessment for PTSD includes measure- ment in multiple response channels, including bio- logical changes or responses. This is especially true in PTSD assessment, because physiological reactivity to trauma cues is one of the criteria of the disorder. Re- search attempting to identify biological underpinnings for PTSD, including organic, cellular, and molecular levels, has exploded over the past 20 years, with a po- tential goal of establishing a biological test for PTSD. This work has focused on the areas of structural and functional neuroimaging, endocrinological, genetic and molecular biological studies. Although the state of the research, costs, required technology, and neces- sary expertise may prevent psychophysiological testing in clinical settings, it is important to be aware of the research in this area and to be alert to obvious physi- ological symptoms in patients when talking about their trauma experiences (e.g., signs of agitation, sweat- ing, flushing). Research has demonstrated consistent group differences in physiological reactivity between individuals with and without PTSD when exposed to trauma-related stimuli, such as through the use of in- dividualized trauma scripts (for a systematic review of this body of research, see Pitman et al., 2012). Vietnam veterans with PTSD have consistently been found to be more reactive to combat imagery than combat veterans without PTSD, even when the comparison samples had other anxiety disorders or other psychological prob- lems (Keane et al., 1998; Pitman, Orr, Forgue, & Alt- man, 1990). Similar results have been found in people with PTSD as a result of MVAs and child sexual abuse (Blanchard, Hickling, Buckley, & Taylor, 1996; Orr et al., 1998).
In general, there are two major aims in assessment in clinical practice: diagnosis and treatment plan- ning. Whether the primary purpose of assessment is diagnosis or treatment planning, a multidimensional, multimethod approach is desirable. Certainly, for the purposes of treatment, ongoing assessment of symp- tom patterns and treatment effectiveness is essential. In addition, given the likelihood of comorbid conditions and problems, objective assessment of these potential
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symptoms and problems is recommended. Given the significant comorbidity between PTSD and depressive disorders, and the role of depression in increasing sui- cide risk in clients with PTSD, depression should also be assessed in patients with a probable PTSD diagnosis (Panagioti, Gooding, & Tarrier, 2012; Stanley, Rogers, Hanson, Gutierrez, & Joiner, 2019). Second, a growing body of research suggests that individuals with PTSD are at increased risk of perpetrating physical aggression against others. McFall, Fontana, Raskind, and Rosen- heck (1999) found that male Vietnam veteran inpatients with PTSD were more likely than inpatients without PTSD or a community sample of Vietnam veterans to perpetrate acts of violence toward objects or others. This finding was replicated in a survey of 1,388 veter- ans from the wars in Iraq and Afghanistan, showing that veterans with PTSD and alcohol misuse (35.9%) and those with PTSD alone (10%) were more likely to commit violence than those without a PTSD diagnosis (5.3%; Elbogen et al., 2014). Given also that one of the DSM-5 symptoms of PTSD is outbursts of anger, it is important that history of aggressive acts (under crite- rion E), as well as current impulses toward aggression (e.g., angry mood in criterion D), be carefully assessed and addressed.
TREATMENT
Types of Therapy for PTSD
Treatment guidelines and reviews have identified four general types of evidence-based therapies for PTSD: exposure-based treatments, cognitive therapy, eye movement desensitization and reprocessing (EMDR) and skills-focused treatments (e.g., Ostacher & Cifu, 2019; Schnyder & Clotire, 2015). In addition, there are several promising treatments that have done well in ini- tial studies but need additional independent research to determine their efficacy, including cognitive-behavioral conjoint therapy (CBCT; Monson & Fredman, 2012), dialectical behavior therapy/prolonged exposure (DBT/ PE; Harned, Korslund, & Linehan, 2014), interperson- al psychotherapy (IPT; Bleiberg & Markowitz, 2019), narrative exposure therapy (NET; Schauer, Neuner, & Elbert, 2011), skills training in affective and inter- personal regulation (STAIR; Cloitre, Koenen, Cohen, & Han, 2002), and written exposure therapy (WET; Sloan & Marx, 2019). Before reviewing the research on treatment outcomes for PTSD, we describe the most empirically supported treatment protocols.
Exposure Techniques
Beginning in the early 1980s, forms of exposure thera- py were investigated as a treatment for PTSD. Although systematic desensitization (SD) has been demonstrated to be effective for treating PTSD in a number of case study reports and controlled studies, it was not widely adopted as a preferred treatment (Bowen & Lambert, 1986; Brom, Kleber, & Defares, 1989; Shalev, Orr, & Pitman, 1992). Because people with PTSD may fear and avoid a wide range of trauma-related stimuli, SD may require a number of hierarchies that can be quite inefficient.
Extended exposure to feared cues or to the trauma memory itself is a more efficient treatment and has been employed more widely. Known variously as direct therapeutic exposure (DTE), flooding, or prolonged ex- posure (PE), these exposure techniques require clients to confront feared situations in vivo, to imagine them- selves in a fear-producing situation, or to recall their particular trauma for extended periods of time. In ad- dition, several researchers have demonstrated that ima- ginal exposure can be facilitated using virtual reality techniques (virtual reality exposure therapy [VRET]; Kothgassner et al., 2019; Rothbaum, Hodges, Ready, Graap, & Alarcon, 2001). VRET is often utilized with veterans with PTSD and allows them to take a virtu- al helicopter trip in Vietnam, complete with gunfire, or drive a vehicle in Middle Eastern streets, as well as experience other stimuli that may evoke memories of traumatic events.
Foa and colleagues (1991) were the first to focus ex- tensively on the specific trauma memory rather than fear-producing stimuli. PE is conducted individually in eight to 15 weekly or biweekly 90-minute sessions. The first two sessions are for information gathering, treatment planning, and explanation of the treatment rationale. A hierarchical list of major stimuli that are feared and avoided is created. Clients are instructed to confront feared cues for at least 30–45 minutes a day, starting with a moderately anxiety-provoking stimulus on the hierarchy. Beginning with Session 3, the trauma scene is relived in imagination, and the client is asked to describe it aloud in the present tense. The level of detail is left to the client for the first two exposures, but thereafter he/she is encouraged to include more and more detail about external cues and internal cues, such as thoughts, physiological responses, and feared consequences. Descriptions are repeated several times each session (for 30–45 minutes) and audio-recorded.
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Clients are assigned as homework listening to the re- cording and engaging in in vivo tasks. Care is taken in sessions to ensure that the client’s anxiety decreases be- fore the session is terminated, aided by the therapist, if necessary (Foa, Hembree, Rothbaum, & Rauch, 2019).
Cognitive Interventions
Cognitive therapy for PTSD has generally taken two forms. One form is more present-focused and typically uses daily diaries or monitoring forms to elicit current thoughts that the client has recorded during the week. These homework sheets form the basis of the cogni- tive interventions that occur during treatment through the use of teaching and Socratic questioning. Clients are taught to identify and to dispute their unrealistic or exaggerated thoughts about themselves, the world, and their futures with more probabilistic reasoning and evidence-based argument. Examples of research- ers who have used this model of cognitive restructuring are Blanchard and colleagues (2003) and Foa and col- leagues (2005).
The other form of cognitive therapy, trauma-focused and constructivist (e.g., Ehlers & Clark, 2000; Resick et al., 2017), focuses on the particular meanings that the traumatic event(s) has for the client and how those interpretations of the event contradict or seemingly confirm previously held beliefs about self and others. These distorted assumptions about the event (e.g., “I should have been able to stop the event, so it is my fault that it happened”) may maintain a belief in a just world or a sense of controllability, but at the cost of reduced self-esteem, shame, or guilt. The focus of treatment is on how clients may have distorted the event itself to maintain prior beliefs about justice or the role of oth- ers (assimilation), or conversely, how they may have changed their beliefs about themselves and the world too much (overaccommodation) in an attempt to regain a sense of control or safety in the present or the future (“I cannot trust other people at all any more”). Treat- ment includes Socratic dialogue and use of cognitive worksheets to teach clients to challenge their thinking about their traumatic events and the implications they have constructed.
Cognitive processing therapy (CPT) initially was de- veloped specifically to treat the PTSD in sexual assault survivors (Resick & Schnicke, 1992, 1993), but it has since been updated and applied to a range of trauma survivors (Resick et al., 2017). CPT, which can be de- livered in individual, group, or combined formats, is a
12-session (with option to end earlier or later depending on symptom response) structured therapy program that is predominantly a cognitive therapy. After an intro- duction to PTSD symptoms and the therapy, clients are asked to write an Impact Statement, which is a descrip- tion of how their most distressing traumatic event has affected them. Clients are asked to focus on any guilt or self-blame they experience regarding the trauma and the effects of the event on their beliefs about self and others. This statement is used to understand how they may have distorted the cause of the event or overgener- alized its meaning, such that their functioning has been compromised. For example, if someone thinks that he/ she should have been able to stop the event, then the individual might feel guilt afterward. If a client has de- cided that the event means no one is to be trusted, then he/she will behave as though this is true. These dis- torted assumptions are labeled as Stuck Points that have prevented the client from recovering and then placed on a log for future examination.
Before challenging Stuck Points in depth, the client is taught to label emotions and recognize the connec- tion among events, thoughts, and feelings. The thera- pist helps the client begin to examine his/her problem- atic thinking about the traumatic event with Socratic dialogue, then teaches the client the skill of challeng- ing thoughts and assumptions with Socratic questions through a series of worksheets. The client is first taught to question a single Stuck Point, then to look for patterns of problematic thinking, and, finally, to generate alter- native, more balanced thoughts about the event itself, then overgeneralized assumptions about self and world. In the last five sessions, clients are provided modules to assist them in thinking about specific themes that are commonly disrupted following traumatic events: safety, trust, power and control, esteem, and intimacy. An al- ternative form of CPT, CPT+A, asks the client to write an account of their most traumatic event after Sessions 3 and 4 and to read it to themselves every day and to the therapist in the following sessions. While reading the account, the client is encouraged to feel his/her natural emotions resonating from the event, and to identify any Stuck Points associated with the event(s).
Eye Movement Desensitization and Reprocessing
Eye movement desensitization and reprocessing (EMDR) is a controversial therapy that evolved not from theory or application of effective techniques for other disorders but from a personal observation. As
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originally developed by Shapiro (2018), EMDR was based on a chance observation that troubling thoughts were resolved when her eyes followed the waving of leaves during a walk in the park. Shapiro developed EMDR on the basis of this observation and argues that lateral eye movements facilitate cognitive processing of the trauma. Subsequently, EMDR has been alterna- tively conceptualized as a cognitive-behavioral treat- ment aimed at facilitating information processing of traumatic events and cognitive interventions for nega- tive, trauma-related cognitions and/or as an exposure therapy focused on replaying the traumatic memories in the mind.
EMDR for PTSD typically follows a course similar to the other trauma therapies, including weekly 60- to 90-minute sessions for up to 3 months. EMDR is an eight-phase treatment that includes history taking, client preparation, target assessment, desensitization, installation, body scan, closure, and reevaluation of treatment effects. Most EMDR sessions include expo- sure and cognitive components, as well as the lateral eye movements. In the basic EMDR protocol, clients are asked to identify and focus on a traumatic image or memory (target assessment phase). Next, the therapist elicits negative cognitions or belief statements about the memory. Clients are asked to assign a rating to the memory and negative cognitions on an 11-point scale of distress and to identify the physical location of the anxiety. The therapist helps clients generate positive cognitions that would be preferable to associate with the memory. These are rated on a 7-point scale of how much the client believes the statement. Once the thera- pist has instructed a client in the basic EMDR proce- dure, he/she is are asked to do four things simultane- ously (desensitization phase): (1) visualize the memory; (2) rehearse the negative cognitions; (3) concentrate on the physical sensations of the anxiety; and (4) visually track the therapist’s index finger. While the client does this, the therapist rapidly moves his/her index finger back and forth from right to left, 30–35 centimeters from the client’s face, with two back-and-forth move- ments per second (there are light bars available to do this). These are repeated up to 24 times. Then, the cli- ent is asked to blank out the memory and take a deep breath. Subsequently, the client brings back the memo- ry and cognitions and rates the level of distress. Sets of eye movements (saccades) are repeated until the distress rating equals 0 or 1. At this point, the client is asked how he/she feels about the positive cognition and gives a rating for it (installation phase).
Skills‑Focused Treatments
Two therapies have focused less on the traumatic memories or thoughts resonating from the memories, and place more emphasis on learning skills to manage clients’ current unhealthy relationships or behavioral interactions. Both therapies have been used as com- parison treatments in outcome studies and have been utilized with varied populations.
STRESS INOCULATION TRAINING
Based on Meichenbaum’s (1985) approach to anxiety, the aim of SIT is to give clients a sense of mastery over their fears by teaching a variety of coping skills. Origi- nally described as an approach specifically for use with rape survivors (Kilpatrick & Amick, 1985; Kilpatrick et al., 1982), SIT has been used with individuals with other traumas, including veterans (Jackson, Baity, Bobb, Swick, & Giorgio, 2019). The approach is tai- lored to the individual problems and needs of each cli- ent, so it is flexible and can be used in individual or group settings. SIT typically lasts around 3 months and includes 60- to 90-minute weekly sessions that are approached in phases. The first phase, preparation for treatment, includes an educational element to provide an explanatory or conceptual framework from which the client can understand the nature and origin of his/ her fear and anxiety, and make sense of the trauma and its aftermath. In SIT, a social learning theory expla- nation is used. Along with this, fear and anxiety reac- tions are explained as occurring along three channels (Lang, 1968): (1) the physical or autonomic channel; (2) the behavioral or motoric channel; and (3) the cogni- tive channel. Specific examples are given for each, and the patient identifies his/her own reactions within each channel. Interrelationships among the three channels are explained and discussed. The second phase of SIT is the training of coping skills directed at each of these channels of response. It includes, in sequence, a defini- tion of the coping skill, a rationale, an explanation of the mechanism by which the skill works, a demonstration of the skill, application by the client of the skill to a prob- lem area unrelated to the target behaviors, a review of how well the skill worked, and, finally, application and practice of the skill with one of the target fears. Skills taught most often for coping with fear in the physical channel are muscle relaxation and breathing control.
For the behavioral channel, covert modeling and role playing are the coping skills usually taught. The
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client is taught to visualize a fear- or anxiety-provoking situation and to imagine confronting it successfully. For the cognitive channel, the client is taught guided self-dialogue. The client is taught to focus on his/her internal dialogue and trained to label negative, irratio- nal, and maladaptive self-statements. The client is then taught to substitute more adaptive self-verbalizations. Self-dialogue is taught in four categories: preparation, confrontation and management, coping with feelings of being overwhelmed, and reinforcement. For each of these categories, a series of questions and/or statements is generated that encourages the client to assess the ac- tual probability that the negative event will occur, to manage the overwhelming fear and avoidance behavior, to control self-criticism and self-devaluation, to engage in the feared behavior, and finally to reinforce him/ herself for making the attempt and following the steps.
PRESENT-CENTERED THERAPY
Present-centered therapy (PCT; Frost, Laska, & Wampold, 2014; Schnurr et al., 2003) was originally designed as a control condition for treatment outcome studies that accounted for the nonspecific elements of psychotherapy. The main elements of change include psychoeducation regarding the impact of trauma, ex- amination of the present maladaptive relationship or behavioral patterns and problem-solving techniques. The treatment does not involve a direct examination of the traumatic events, and homework is minimal, with a focus only on problem-solving choices identified by the client. The therapy typically entails nine to 15 weekly sessions and can be conducted in an individual or group format.
Evidence for Treatment Efficacy
Meta-analyses and systematic reviews underpinning treatment guidelines have summarized the vast number of clinical trials that have been conducted to investigate the efficacy of various interventions for PTSD. Across meta-analyses, trauma-focused cognitive-behavioral therapies such as exposure therapy, including PE, and cognitive therapy, including CPT, as well as EMDR, have demonstrated significant large effect size increases for the treatment of PTSD (Cusak et al., 2016; Forbes, Bisson, Monson, & Berliner, 2021; Watts et al., 2013). When examining and factoring in the strength of the evidence supporting these treatments, multiple treat- ment guidelines for PTSD have recommended trauma-
focused exposure and trauma-focused cognitive therapy, as well as EMDR, as first line treatments (Department of Veterans Affairs & Department of Defense, 2017; Forbes et al., 2021; National Institute for Health and Care Excellence, 2018; Phoenix Australia Centre for Posttraumatic Mental Health, 2013). In contrast, oth- ers have indicated stronger support for trauma-focused cognitive-behavioral therapies over EMDR (American Psychological Association, 2017).
Meta-analyses have also revealed that trauma-focused cognitive-behavioral therapies and EMDR are sig- nificantly more effective than wait-list and treatment- as-usual conditions, and generally better than therapies designed to control for the essential and nonspecific elements of efficacious psychotherapy (Forbes et al., 2021). Moreover, comparisons of trauma-focused ex- posure and trauma-focused cognitive therapies, as well as trauma-focused cognitive-behavioral therapies and EMDR, have demonstrated equivocal findings (Forbes et al., 2021) or have indicated insufficient evidence to suggest a difference (Cusack et al., 2016).
Evidence for skills-focused interventions, often re- ferred to as non-trauma-focused therapies, which in- clude SIT and PCT, has been more modest in com- parison to that of trauma-focused cognitive-behavioral interventions and EMDR reviewed earlier. Although these interventions have been shown to lead to sig- nificant improvements compared to wait-list and treat- ment-as-usual conditions, the relatively limited number of studies hampers their support (Cusak et al., 2016; Forbes et al., 2021; Watts et al., 2013). Where com- parisons have been possible, evidence supports the use of trauma-focused cognitive-behavioral therapies over PCT (Forbes et al., 2021). Existing treatment guide- lines have been more tentative in their endorsement of these interventions, typically indicating that they may be considered in cases where trauma-focused therapies are unavailable or have not sufficiently addressed symp- toms, as well as in cases in which an individual is un- willing to participate in a trauma-focused therapy for PTSD (Department of Veterans Affairs & Department of Defense, 2017; Forbes et al., 2021; National Institute for Health and Care Excellence, 2018; Phoenix Austra- lia Centre for Posttraumatic Mental Health, 2013).
Numerous interventions have also recently garnered attention and emerged as promising practices in the treatment of PTSD. These interventions have built on research on factors associated with PTSD and its treat- ment to develop novel ways to provide care for those with this condition. Building on research on comorbid
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borderline personality disorder and PTSD, as well as increased suicidality across these conditions, Harned and colleagues (2014) have investigated an approach that combines DBT with PE. Similarly, appreciating the interpersonal context of trauma recovery, Mon- son and Fredman (2012) developed CBCT for PTSD, which has now been tested in a number of studies (see Liebman, Whitfield, Sijercic, Ennis, & Monson, 2020). Finally, examining whether there is a need for exposure to be included in the treatment of PTSD, Markowitz and colleagues (2015), investigated the efficacy of IPT. Results of these studies have demonstrated preliminary efficacy for these interventions. Although the evidence for these approaches is still emerging, they represent unique and novel ways to provide care for individuals with PTSD.
Moderators of and Process Factors Associated with Treatment
As the evidence for treatments for PTSD grows, there has been increasing attention on factors that may mod- erate treatment outcomes. This has included an ex- amination of how specific client- and treatment-level variables impact outcomes. Notably, given that trauma- focused therapies for PTSD have received the most research, examination of these moderating variables is largely limited to these interventions.
Among the available research, there is some evidence to suggest that client factors such as gender and civil- ian versus veteran status may be associated with treat- ment outcome. Extant work suggests that women may be more likely to benefit from psychotherapy for PTSD, and that men may be more likely to drop out of treat- ment (Wade et al., 2016). In contrast, others have in- dicated that these differences may be better explained by confounding variables, underrepresentation of gen- ders in treatment studies of samples of specific types of trauma exposure (e.g., underrepresentation of men in studies of sexual assault and of women in studies of combat trauma), as well as studies not being designed or being underpowered to evaluate gender differences (see Blain, Galovski, & Robinson, 2010 for review). With regard to civilian versus veteran status, studies have documented differences in treatment response, such that veteran samples exhibit smaller effect size improve- ments with treatment in comparison to those of civilian samples (Dillon, LoSavio, Henry, Murphy, & Resick, 2019; Gobin et al., 2018; Goodson et al., 2011; Mor- land et al., 2015).
Treatment-level factors associated with clinical deci- sions on how to move forward with treatment based on symptom presentation and comorbid issues have also been the focus of recent investigation. This has includ- ed research on how best to proceed when individuals present with comorbid PTSD and substance use dis- orders. The high rate of comorbidity between PTSD and substance use disorders has been well documented (Pietrzak, Goldstein, Southwick, & Grant, 2011), lead- ing clinicians to wonder whether substance use needs to be treated effectively before endeavoring to treat PTSD. The extant research, however, suggests that de- spite poorer outcomes among individuals with comor- bid PTSD and substance use disorders, trauma-focused therapies confer some benefit (Roberts, Roberts, Jones, & Bisson, 2016), resulting in treatment guidelines sug- gesting that treatment for PTSD should be offered to individuals with this comorbidity (Department of Vet- erans Affairs & Department of Defense, 2017).
Within CPT, preliminary research suggests differen- tial effects based on the presence of dissociative symp- toms. In a dismantling trial of CPT for women who were victims of interpersonal violence, Resick, Suvak, Johnides, Mitchell, and Iverson (2012) documented a differential effect of the treatments based on dissocia- tion symptoms. Women with higher levels of pretreat- ment dissociation demonstrated a better treatment response when they received the version of CPT that in- cluded written trauma accounts (CPT+A). In contrast, women with low levels of pretreatment dissociation had a better treatment response when they received the ver- sion without written trauma accounts (CPT; Resick et al., 2012). The study authors suggested that this differ- ential response may be explained by the written trauma accounts serving to help reconstruct a fragmented trau- ma memory among those who are highly dissociative, prior to assisting them in processing the trauma mem- ory and challenging maladaptive cognitions associated with it through Socratic dialogue.
Recent work has also raised the question of whether existing treatments for PTSD adequately address the distinct but related construct of moral injury. Moral in- jury involves the violation of one’s deeply held beliefs or expectations, and can occur via the perpetration of acts, as well as witnessing or learning about them (see Litz et al., 2009, for summary). Traumatic events, particularly those of an interpersonal nature, may often include an element of moral injury. With growing research in this area, some have purported that existing treatments for PTSD may not adequately address moral injury, high-
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lighting issues associated with PTSD initially being conceptualized as a fear-based disorder, as well as its treatment being developed in response to this fear- based conceptualization. Moreover, some have argued that cognitions underlying moral injury may be fun- damentally different than those underlying PTSD re- sulting from other traumatic events (see Held, Klassen, Brennan, & Zalta, 2018, for summary). In response to these critiques, preliminary work has examined the ap- plication of existing first-line treatments for PTSD to those considered to have moral injury. Although lim- ited to case studies, preliminary findings support that existing interventions for PTSD, such as CPT and PE, can adequately address this issue without modifications (Held et al., 2018).
Factors associated with the mode and format of treat- ment delivery have also been examined in an effort to more efficiently deliver services to those in need. De- livery of treatment in a group format is often a con- sideration in settings in which the availability of ser- vices is scarce, in an effort to more efficiently treat a larger number of individuals. Although limited, there is some evidence that group interventions for PTSD can be beneficial (Resick et al., 2015, 2017; Schnurr et al., 2003), with studies favoring trauma-focused cognitive- behavioral therapy groups over PCT groups (Forbes et al., 2021). However, it is important to note that the bulk of the evidence favors individual over group therapy for PTSD (Cusak et al., 2016; Forbes et al., 2021; Resick et al., 2017; Watts et al., 2013).
Advances in technology have also allowed for delivery of treatments via telehealth (i.e., services delivered via videoconferencing or telephone). Studies of treatment for PTSD delivered via telehealth have been found to be efficacious in the treatment of PTSD and not inferior to treatment delivered in person. Additionally, dropout rates do not appear to be negatively impacted when treatment is delivered via telehealth, and may even be better than in face-to-face therapy (see Moring et al., 2020, for review). Although factors related to ensuring privacy and confidentiality, setting clients’ expectations related to their participation via telehealth, and file/ document sharing require adjustments when transition- ing to telehealth delivery, the existing research suggests that these are surmountable barriers and that telehealth presents a unique opportunity to effectively deliver treatment for PTSD.
Finally, studies have also examined the importance of treatment fidelity when delivering protocol therapies for PTSD (Farmer, Mitchell, Parker-Guilbert, & Ga-
lovski, 2017; Holder, Holliday, Williams, Mullen, & Surís, 2018; Marques et al., 2019). These studies have tested whether adherence to the “essential elements” of protocoled therapies for PTSD, as well as competence in delivering them, is associated with treatment outcomes. Although the pattern of findings has differed among studies, as a whole, they suggest that both adherence and competence are associated with improvements in PTSD and comorbid symptoms (Farmer et al., 2017; Holder et al., 2018; Marques et al., 2019). Moreover, when considering therapists’ modifications during the delivery of a protocol therapy, modifications that are classified as fidelity-consistent appear to be associated with greater reductions in PTSD and comorbid symp- toms compared to those classified as fidelity-inconsis- tent (Marques et al., 2019). These findings highlight the importance of therapist adherence and competence in delivering the essential ingredients of evidence-based treatments for PTSD, while demonstrating that it is possible to make treatment adaptations to better serve one’s clients in a way that preserves fidelity to these pro- tocoled therapies.
CASE STUDY
“Tom” is a 25-year-old, married, male who presented for treatment approximately 1 year after a traumatic event that occurred during his military deployment to Iraq. Tom received CPT while on active duty.
Background
Tom was the third of four children born to his parents. He described his father as an alcoholic who was fre- quently absent from the home due to work travel prior to his parents’ divorce. Tom indicated that his father was always emotionally distant from the family, espe- cially after the divorce. Tom had close relationships with his mother and siblings. He denied having any significant mental health or physical health problems in his childhood. However, he described two signifi- cant traumatic events in his adolescence. Specifically, he described witnessing his best friend commit suicide by gunshot to the head. Tom indicated that this event severely affected him, as well as his entire community. He went on to report that he still felt responsible for not preventing his friend’s suicide. The second traumatic event was the death of Tom’s brother in an automobile accident when Tom was 17 years old. Tom did not re-
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ceive any mental health treatment during his childhood or after these events, though he indicated that he began using alcohol and illicit substances after these traumatic events in his youth. He admitted using cannabis nearly daily during high school, as well as daily use of alcohol, drinking as much as a 24-pack of beer per day until he passed out. Tom reported that he decreased his alcohol consumption and ceased using cannabis after his enlist- ment.
Tom served in the Infantry. He went to Basic Train- ing, then attended an advanced training school prior to being deployed directly to Iraq. While in Iraq, Tom witnessed and experienced a number of traumatic incidents. He spoke about fellow soldiers who were killed and injured in service, as well as convoys that he witnessed being hit by improvised explosive devices (IEDs). However, the traumatic event that he identified as most distressing and anxiety-provoking was shooting a pregnant woman and child.
Tom described this event as follows: Suicide bomb- ers had detonated several bombs in the area where Tom served, and a control point had been set up to contain the area. During the last few days of his deployment, Tom was on patrol at this control point. It was dark outside. A car began approaching the checkpoint, and officers on the ground signaled for the car to stop. The car did not stop in spite of these warnings. It continued to approach the control point, entering the area where the next level of Infantrymen were guarding the en- trance. Per protocol, Tom fired a warning shot to stop the approaching car, but the car continued toward the control point. About 25 yards from the control point gate, Tom and at least one other soldier fired upon the car several times.
After a brief period of disorientation, a crying man with clothes soaked with blood emerged from the car with his hands in the air. The man quickly fell to his knees, with his hands and head resting on the road. Tom could hear the man sobbing. According to Tom, the sobs were guttural and full of despair. Tom looked over to find in the pedestrian seat a dead woman who was apparently pregnant. A small child in the backseat was also dead. Tom never confirmed this, but he and his fellow soldiers believed that the man crying on the road was the husband of the woman and the father of the child and fetus.
Tom was immediately distressed by the event, and a Combat Stress Control unit in the field eventually had him sent back to a Forward Operating Base because of his increasing intrusive and arousal symptoms. Tom
was eventually brought to a major Army hospital, where he received individual CPT.
Tom was administered the CAPS at pretreatment; his score was in the severe range, and he met diagnos- tic criteria for PTSD. He also completed the Patient Health Questionnaire–9 (PHQ-9) and the General- ized Anxiety Disorder–7 (GAD-7). His depression and anxiety symptoms at pretreatment were in the severe range. Tom was provided feedback about his assess- ment results in a session focused on an overview of his psychological assessment results and on obtaining his informed consent for a course of CPT. After providing feedback about his assessment, the therapist gave Tom an overview of CPT, with an emphasis on its trauma- focused nature, expectation of out-of-session practice adherence, and the client’s active role in getting well. Tom signed a “CPT Treatment Contract” detailing this information and was provided a copy of the contract for his records. The CPT protocol began in the next session.
Session 1
Tom arrived 15 minutes early to his first scheduled ap- pointment of CPT. He sat down in the chair the ther- apist gestured that he sit in, but he was immediately restless and repositioned frequently. Tom quickly asked to move to a different chair in the room, so that his back was not facing the exterior door and his gaze could monitor both the door and the window. He asked the therapist how long his session would take and whether he would have to “feel anything.” The therapist re- sponded that this session would last 50–60 minutes, and that, compared with other, future sessions, she would be doing most of the talking. She added that, as discussed during the treatment contracting session, the focus would be on Tom’s feelings in reaction to the traumatic event but that the current session would focus less on this. The therapist also explained that she would have the treatment manual in her lap, and would refer to it throughout to make sure that she delivered the psychotherapy as it was prescribed. She encouraged Tom to ask any questions he might have as the session unfolded.
The therapist explained that at the beginning of each session they would develop an agenda for the session. The purposes of the first therapy session were to (1) de- scribe the symptoms of PTSD; (2) give Tom a frame- work for understanding why these symptoms had not remitted; (3) present an overview of treatment to help
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Tom understand why practice outside of session and therapy attendance were important to elicit cooperation and to explain the progressive nature of the therapy; (4) build rapport between Tom and the therapist; and (5) give Tom an opportunity to talk briefly about his most distressing traumatic event or other issues.
The therapist then proceeded to give didactic infor- mation about the symptoms of PTSD. She asked Tom to provide examples of the various clusters of PTSD symptoms he was experiencing, emphasizing how in- trusive symptoms are related thoughts and emotions about the trauma, which are tied to arousal symptoms. She emphasized how hyperarousal symptoms elicit a desire to avoid or become numb. The paradoxical ef- fect of avoidance and numbing in maintaining, or even increasing, PTSD symptoms was also discussed. Tom indicated that this was the first time someone had ex- plained the symptoms of PTSD in this way, putting them “in motion” by describing how they interact with one another.
The therapist transitioned to a description of trauma aftereffects within an information processing frame- work. She described in lay terms how traumas may be schema-discrepant events; traumatic events often do not fit with one’s prior beliefs about oneself, others, or the world. To incorporate this event into one’s memory, the person may alter his/her perception of the event (assimi- late the event into an existing belief system). Examples of assimilation include looking back on the event and believing that some other course of action should have been taken (“undoing” the event) or blaming oneself because it occurred. The therapist went on to explain that Tom could have also attempted to change his prior belief system radically to overaccommodate the event to his prior beliefs. Overaccommodationwas described as changing beliefs too much as a result of the traumatic event (e.g., “I can’t trust myself about anything”). She explained that several areas of beliefs are often affected by trauma, including safety, trust, power/control, es- teem, and intimacy. She further explained that these beliefs could be about the self and/or others. The thera- pist also pointed out that if Tom had negative beliefs prior to the traumatic event relative to any of these top- ics, the event could serve to strengthen, and seemingly confirm, these preexisting negative beliefs.
At this point, Tom described his childhood and ado- lescent experiences, and how they had contributed to his premilitary trauma beliefs. The therapist noted that Tom tended to blame himself and to internalize the bad things that had happened in his family and the suicide
of his friend. She also noted his comment, “I wonder if my father drank to cope with me and my siblings.” In Tom’s case, it seemed likely that the traumatic experi- ence served more to confirm his preexisting beliefs that he had caused or contributed to bad things happening around and to him.
Tom then spent some time describing how drastical- ly things had changed after his military traumas. Prior to his military experiences and, specifically, the shoot- ing of the woman and child, Tom described himself as “proud of being a soldier” and “pulling his life together.” He indicated that the military structure had been very good for him in developing self-discipline and improv- ing his self-esteem. He indicated that he felt good about serving his country. He felt camaraderie with his fellow soldiers and was planning a career in the military. He denied any authority problems and in fact believed that his commanding officers had been role models of the type of leader he wished to be. After his return from Iraq, Tom indicated that he did not trust anyone, es- pecially anyone associated with the U.S. government. Tom expressed his disillusionment with the war effort and distrust of the individuals who commanded his unit. He also articulated distrust of himself: “I always make bad decisions when the chips are down.” He stat- ed that he felt completely unsafe in his environment. In his immediate postdeployment period, Tom had occa- sionally believed snipers on the base grounds had placed him in their crosshairs to kill him. He indicated that he minimally tolerated being close to his wife, including sexual contact between the two of them.
The therapist introduced the notion of Stuck Points, or ways of making sense of the trauma or of think- ing about himself, others, and the world, as getting in the way of Tom’s recovery from the traumatic events. The therapist noted that a large number of individuals are exposed to trauma. In fact, military personnel are among the most trauma-exposed individuals. However, most people recover from their trauma exposure. Thus, a primary goal of the therapy was to figure out what had prevented Tom from recovering (i.e., how his thinking had got him “stuck,” leading to the maintenance of his PTSD symptoms).
The therapist then asked Tom to provide a 5-minute account of his index traumatic event. Tom immediately responded, “There were so many bad things over there. How could I pick one?” The therapist asked, “Which of those events do you have the most thoughts or images about? Which of those events do you dislike thinking about the most?” The therapist indicated that Tom did
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not need to provide a fine-grained description of the event, but rather a brief overview of what happened. Tom provided a quick account of the shooting of the woman and child. The therapist praised Tom for shar- ing about the event with her and asked about his feel- ings as a result of sharing the information. Tom said that he felt anxious and wanted the session to be over. The therapist used this as an opportunity to describe the differences between natural and manufactured emotions.
The therapist first described naturalemotions as those automatic feelings that are commensurate reactions to experiences that have occurred. These feelings require minimal conscious processing. For example, if some- one has violated us, it is natural to feel anger. If we en- counter a threatening situation, it is natural to feel fear. Natural emotions have a self-limited and diminishing course. If we allow ourselves to feel these natural emo- tions, they will naturally dissipate. The therapist used the analogy of the energy contained in a bottle of car- bonated soda to illustrate this concept. If the top of the bottle is removed, the pressure initially comes out with some force, but that force subsides and eventually has no energy forthcoming. On the other hand, there are manufacturedemotions, or emotions that a person has a role in making. Our conscious thoughts contribute to the nature and course of these emotions. The more that we “fuel” these emotions with our self-statements, the more we can increase the “pressure” of these emotions. For example, if a person tells himself over and over that he is a stupid person and reminds himself of more and more situations in which he perceived that he made mistakes, then he is likely to have more and more anger toward himself. The therapist summarized for Tom the three major goals of the therapy: (1) to remember and accept what happened to him by not avoiding those memories and associated emotions; (2) to allow him- self to feel his natural emotions and let them run their course, so the memory could be put away without such strong feelings still attached; and (3) to balance beliefs that had been disrupted or reinforced, so that Tom did not manufacture unhelpful emotions.
The therapist made a strong pitch for the importance of out-of-session practice adherence before assigning Tom the first practice assignment. The therapist told Tom that there appeared to be no better predictor of response to the treatment than how much effort a pa- tient puts into it. She pointed out that of the 168 hours in a week, Tom would be spending 1–2 hours of that week in psychotherapy sessions (Note: We have found it
helpful to do twice-weekly sessions, at least in the initial portion of the therapy, to facilitate rapport building, to overcome avoidance, and to capitalize on early gains in the therapy.) If Tom only spent the time during psycho- therapy sessions focused on these issues, he would be spending less than 1% of his week focused on his recov- ery. To get better, he would be using daily worksheets and other writing assignments to promote needed skills in his daily life and to decrease his avoidance. The therapist also pointed out that at the beginning of each session they would review the practice assignments that Tom had completed. The therapist asked Tom if this made sense, and he responded, “Sure. It makes sense that you get out of it what you put into it.”
Tom’s first assignment was to write an “Impact State- ment” about the meaning of the event to determine how he had made sense of the traumatic event, and to help him begin to determine what assimilation, accom- modation, and overaccommodation had occurred since the event. Stuck Points that get in the way of recovery are identified with this first assignment. Tom was in- structed to start writing the assignment later that day to address directly any avoidance about completing the assignment. He was specifically reminded that this was not a trauma account and that this assignment was spe- cifically designed to get at the meaning of the event in his life, and how it had impacted his belief systems.
The specific assignment was as follows:
“Please write at least a one-page statement on why you think your most distressing traumatic event occurred. You are not being asked to write specific details about this event. Write about what you have been thinking about the cause of this event. Also, consider the effects this traumatic event has had on your beliefs about yourself, others, and the world in the following areas: safety, trust, power/control, es- teem, and intimacy. Bring this statement with you to the next session.”
Session 2
The purposes of the second session are to (1) discuss the meaning of the event and (2) to help Tom begin to recognize thoughts, label emotions, and see the connec- tion between what he says to himself and how he feels. Tom arrived with obvious anger and appeared defen- sive throughout most of the session. He stated that he had been feeling quite angry all week, and that he was “disgusted” with society and particularly politicians,
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who were “all self-interested or pandering to those with money.” He expressed a great deal of anger over the re- ports of alleged torture at Abu Ghraib prison, which was a major news item during his therapy. The therapist was interested in the thinking behind Tom’s anger about the events at Abu Ghraib. However, she first reviewed Tom’s practice assignment, writing the first Impact Statement, to reinforce the completion of this work and to maintain the session structure she had outlined in the first session.
The therapist asked Tom to read his Impact State- ment aloud. Clients in individual CPT are always asked to read their practice assignments aloud. Should the therapist read them, the client could dissociate or oth- erwise avoid his/her own reactions to the material. Tom had written:
“The reason that this traumatic event happened is be- cause I was friggin’ stupid and made a bad decision. I killed an innocent family, without thinking. I mur- dered a man’s wife and child. I can’t believe that I did it. I took that man’s wife and child, and oh, yeah, his unborn child, too. I feel like I don’t deserve to live, let alone have a wife and child on the way. Why should I be happy when that man was riddled with despair, and that innocent woman, child, and unborn child died? Now, I feel like I’m totally unsafe. I don’t feel safe even here on the hospital grounds, let alone in the city or back home with my family. I feel like someone is watching me and is going to snipe at me and my family because the terrorists had information about the situation and passed it on. I also don’t feel that people are safe around me. I might go off and hurt someone, and God forbid it be my own family. With my wife pregnant, I am really concerned that I might hurt her. I don’t trust anyone around me, and especially the government. I don’t even trust the mil- itary treating me. I also don’t trust myself. If I made a bad decision at that time, who is to say that I won’t make a bad decision again? About power and control, I feel completely out of control of myself, and like the military and my commanding officer have complete control over me. My self-esteem is in the toilet. Why wouldn’t it be given the crappy things that I have done? I don’t think there are many positive things that I’ve done with my life, and when the chips are down, I always fail and let others down. I’m not sure what other-esteem is, but I do like my wife. In fact, I don’t think she deserves to have to deal with me, and I think they would be better without me around. I don’t want to be close to my wife, or anyone for that
matter. It makes me want to crawl out of my skin when my wife touches me. I feel like I’ll never get over this. It wasn’t supposed to be like this.”
The therapist first reinforced Tom for completing the assignment. She then asked Tom what it was like to write and then read the Impact Statement aloud. Tom responded that it had been very difficult, and that he had avoided the assignment until the evening before his session. She used the opportunity to gently address the role of avoidance in maintaining PTSD symptoms. She asked specific Socratic questions aimed at elucidating the distress associated with anticipatory anxiety, and wondered aloud with Tom about what it would have been like to have completed the assignment earlier in the week. She also asked Socratic questions aimed at highlighting the fact that Tom felt better, not worse, after completing the assignment.
Tom’s first Impact Statement and the information he shared in the first session made evident the Stuck Points that would have to be challenged. In CPT, areas of as- similation are prioritized as the first targets of treat- ment. Assimilation is targeted first, because changes in the interpretation of the event itself are integrally related to the other, more generalized beliefs involved in overaccommodation. In Tom’s case, he was assimi- lating the event by blaming himself. He used the term murdererto describe his role in the event, disregarding important contextual factors that surrounded the event. These beliefs would be the first priority for challeng- ing. Tom’s overaccommodation is evident in his general distrust of society and authority figures, and his belief that he will make bad decisions in difficult situations. His overaccommodation is also evident in his sense of threat in his environment (e.g., snipers) and low esteem for others and himself.
The therapist returned to Tom’s anger about Abu Ghraib to get a better sense of possible Stuck Points and also to experiment with Tom’s level of cognitive rigid- ity or openness to cognitive challenging. The following exchange ensued between Tom and the therapist:
THERAPIST: Earlier you mentioned that you were feel- ing angry about the reports from Abu Ghraib. Can you tell me what makes you angry?
TOM: I can’t believe that they would do that to those prisoners.
THERAPIST: What specifically upsets you about Abu Ghraib?
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TOM: Haven’t you heard the reports? I can’t believe that they would humiliate and hurt them like that. Once again, the U.S. military’s use of force is unacceptable.
THERAPIST: Do you think your use of force as a mem- ber of the U.S. military was unacceptable?
TOM: Yes. I murdered innocent civilians. I am no dif- ferent than those military people at Abu Ghraib. In fact, I’m worse because I murdered them.
THERAPIST: Murder. That’s a strong word. TOM: Yeah? THERAPIST: From what you’ve told me, it seems like you
killed some people who may or may not have been “innocent.” Your shooting occurred in a very specific place and time, and under certain circumstances.
TOM: Yes, they died at my hands. THERAPIST: Yes, they died, and it seems, at least in
part, because of your shooting. Does that make you a murderer?
TOM: Innocent people died and I pulled the trigger. I murdered them. That’s worse than what happened at Abu Ghraib.
THERAPIST: (quietly) Really, you think it is worse? TOM: Yes. In one case, people died, and in another they
didn’t. Both are bad, and both were caused by sol- diers, but I killed people and they didn’t.
THERAPIST: The outcomes are different—that is true. I’m curious if you think how it happened matters?
TOM: Huh? THERAPIST: Does it matter what the soldiers’ intentions
were in those situations, regardless of the outcome? TOM: No. The bottom line is killing versus no killing. THERAPIST: (realizing that there was minimal flexibility
at this point) I agree that there is no changing the fact that the woman and child died, and that your shooting had something to do with that. However, I think we might slightly disagree on the use of the term murder. It is clear that their deaths have been a very difficult thing for you to accept, and that you are trying to make sense of that. The sense that you appear to have made of their deaths is that you are a “murderer.” I think this is a good example of one of those Stuck Points that seem to have prevented you from recovering from this traumatic event. We’ll definitely be spending more time together on under- standing your role in their deaths.
In addition to testing Tom’s cognitive flexibility, the therapist also wanted to plant the seeds of a different interpretation of the event. She was careful not to push too far and retreated when it was clear that Tom was not amenable to an alternative interpretation at this point in the therapy. He was already defensive and somewhat angry, and she did not want to exacerbate his defensive- ness or possibly contribute to dropout from the therapy.
From there, the therapist described how important it was to be able to label emotions and to begin to iden- tify what Tom was saying to himself. The therapist and Tom discussed how different interpretations of events can lead to very different emotional reactions. They generated several examples of how changes in thoughts result in different feelings. The therapist also reminded Tom that some interpretations and reactions follow naturally from situations and do not need to be altered. For example, Tom indicated that he was saddened by the death of the family; the therapist did not challenge that statement. She encouraged Tom to feel his sadness and to let it run its course. He recognized that he had lost something, and it was perfectly natural to feel sad as a result. At this point Tom responded, “I don’t like to feel sad. In fact, I don’t like to feel at all. I’m afraid I’ll go crazy.” The therapist gently challenged this be- lief. “Have you ever allowed yourself to feel sad?” Tom responded that he worked very hard to avoid any and all feelings. The therapist encouraged Tom, “Well, given that you don’t have much experience with feeling your feelings, we don’t know that you’re going to go crazy if you feel your feelings, right?” She also asked him whether he had noticed anyone in his life who had felt sad and had not gone crazy. He laughed. The therapist added, “Not feeling your feelings hasn’t been working for you so far. This is your opportunity to experiment with feeling these very natural feelings about the trau- matic event to see whether it can help you recover now from what has happened.”
Tom was given a number of A-B-C Worksheets (Ac- tivating Event, Belief, Consequence) as practice assign- ments to begin to identify what he was telling himself and his resulting emotions, including at least one sheet related to his most traumatic event. In the first column, under A, “Something happens,” Tom was instructed to write down an event. Under the middle column, B, “I tell myself something,” he was asked to record his thoughts about the event. Under column C, “I feel and/ or do something,” Tom was asked to write down his behavioral and emotional responses to the event. The
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therapist pointed out that if Tom says something to himself a lot, it becomes automatic. After a while, he can go straight to the feeling. It is important to stop and recognize automatic thoughts to decide whether they either make sense or should be challenged and changed.
Session 3
Tom handed the therapist his practice assignments as soon as he arrived. The therapist went over the indi- vidual A-B-C Worksheets Tom had completed and emphasized that he had done a good job in identifying his feelings and recognizing his thoughts. Some of this work is shown in Figure 2.1.
The purpose of reviewing this work at this point in the therapy is to identify thoughts and feelings, not to heavily challenge the content of those thoughts. The therapist did a minor correction of Tom’s identification of the thought “I feel like I’m a bad person” (bolded in Figure 2.1) as a feeling. She commented that feel- ings are almost always one word and what you feel in your “gut,” and that adding the stem “I feel . . .” does not necessarily make it a feeling. The therapist noticed
the pattern of thoughts that Tom tended to record (i.e., internalizing and self-blaming), as well as the character- istic emotions he reported.
The therapist noted the themes of assimilation that again emerged (i.e., self-blame) and chose to focus on mildly challenging these related thoughts. She specifi- cally chose to focus on Tom’s thoughts and feelings re- lated to his wife’s pregnancy, which ultimately seemed to be related to his assimilation of the traumatic event.
THERAPIST: You don’t think you deserve to have a fam- ily? Can you say more about that?
TOM: Why should I get to have a family when I took someone else’s away?
THERAPIST: OK, so it sounds like this relates to the first thought that you wrote down on the A-B-C Worksheet about being a murderer. When you say to yourself, “I took someone else’s family away,” how do you feel?
TOM: I feel bad. THERAPIST: Let’s see if we can be a bit more precise.
FIGURE 2.1. A-B-C Worksheet for Tom. Adapted from Resick, Monson, and Chard (2017). Copyright © 2017 The Guil- ford Press. Adapted by permission.
Activating Event Belief/Stuck Point Consequence A B C
“Something happens” “I tell myself something” “I feel something”
I killed an innocent family.
My wife is pregnant.
Abu Ghraib
Going to therapy
“I am a murderer.”
“I don’t deserve to have a family.”
“The government sucks.”
“I’m weak. I shouldn’t have PTSD. PTSD is only for the weak.”
I feel like I’m a bad person. Avoid talking about it. Guilty
Angry
Angry
Are my thoughts above in column B realistic or helpful? Yes.
What can I tell myself on such occasions in the future? ?
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What brand of bad do you feel? Remember how we talked about the primary colors of emotion? Which of those might you feel?
TOM: I feel so angry at myself for doing what I did. THERAPIST: OK. Let’s write that down—anger at self.
So, I’m curious, Tom, do the other people you’ve told about this situation, or who were there at the time, think what you did was wrong?
TOM: No, but they weren’t the ones who did it, and they don’t care about the Iraqi people like I do.
THERAPIST: Hmm . . . that makes me think about something, Tom. In the combat zone in which you were involved in Iraq, how easy was it to determine who you were fighting?
TOM: Not always particularly easy. There were lots of insurgents who looked like everyday people.
THERAPIST: Like civilians? Innocent civilians? (pause) TOM: I see where you are going. I feel like it is still
wrong because they died. THERAPIST: I believe you when you say that it feels that
way. However, feeling a certain way doesn’t neces- sarily mean that it is based on the facts or the truth. We’re going to work together on seeing whether that feeling of guilt or wrongdoing makes sense when we look at the situation very carefully in our work to- gether.
Because the goal is for Tom to challenge and dis- mantle his own beliefs, the therapist probed and plant- ed seeds for alternative interpretations of the traumatic event but did not pursue the matter too far. Although Tom did move some from his extreme stance within the session, the therapist was not expecting any dramatic changes. She focused mostly on helping Tom get the connections among thoughts, feelings, and behaviors, and developing a collaborative relationship in which cognitive interventions could be successfully delivered.
The therapist praised Tom for his ability to recognize and label thoughts and feelings, and gave him the as- signment to complete an A-B-C Worksheet each day fo- cused on his thoughts about the index trauma of shoot- ing the pregnant woman and child at the checkpoint.
Session 4
Tom came to the session having done an A-B-C Work- sheet each day prior to the session. The therapist praised
Tom for his hard work, then asked him to share the sheets that he thought were most helpful and/or dif- ficult for him. One of the trauma-related sheets that Tom shared was related to the thought, “I murdered an innocent child” and the associated feelings of guilt and shame. The therapist took the opportunity to jump off this worksheet to engage in Socratic dialogue with Tom about his self-blame, and to also encourage him to feel his natural feelings that he had been avoiding.
THERAPIST: Tom, are you OK if I ask you some follow- up questions about these thoughts?
TOM: Sure. Would it really matter if I said no? (Tom and therapist chuckle.)
THERAPIST: Of course I can’t make you talk about this Tom. . . . That said, I do believe you can get better by talking about it. Can you explain to me a bit more about the scene that leads to your conclusion that you murdered her?
TOM: I’m starting to feel sick to my stomach—like I felt at the time when I saw her in the back seat with all that blood and her doll. She was lifeless just like that doll. I really think I might throw up. I am also disgusted and sad. I killed an innocent child. There are so many things I could have done differently not to have taken her life.
[The therapist is aware of the assimilation process in Tom’s use of hindsight bias about the “many things he could have done not to have taken her life.” She stores that informa- tion away for future reference for challenging because she wants to make sure that Tom is feeling as many of his natu- ral emotions as possible about the traumatic event.] THERAPIST: Continue to feel those feelings. Don’t run
away from them. Anything else that you’re feeling? TOM: I feel mad at myself and guilty. THERAPIST: Were you feeling mad at yourself and
guilty at the time? TOM: No. I was horrified. THERAPIST: OK, let’s stay with that feeling. TOM: (Pauses.) I don’t want to feel this anymore. THERAPIST: I know you don’t want to feel this any-
more. You’re doing a great job of not avoiding your feelings here. In order to not feel like this for a long time, you need to feel these absolutely natural feel- ings. Let them run their course. They’ll decrease if you stay with them.
Posttraumatic Stress Disorder 85
After a period in which Tom experienced his feelings related to the situation and allowed them to dissipate, a discussion ensued regarding how hurtful it was to Tom to hear other people’s reaction to the war. He expressed specific frustration with administration and its policy on the war. The therapist gently redirected Tom’s more philosophical discussion of international policy to the effects of the trauma on him. Tom then told a story of how he had shared his traumatic experience with a high school friend. He felt that this person had a negative reaction to him as a result of sharing the story. Tom felt judged and unsupported by this friend. Since this experience with his friend, Tom had refrained from tell- ing others about his combat experience. Using Socratic questioning, the therapist asked Tom if there might be any reason, outside of his actions, that someone might have a negative reaction to hearing about the shooting. Through this exchange, Tom was able to recognize that when others hear about traumatic events, they also are trying to make sense of these experiences in light of their existing belief systems. In other words, others around him might fall prey to the “just world” belief that bad things only happen to bad people. They also might not take into account the entire context in which Tom shot the passengers in the car. This recognition resulted in Tom feeling less angry at his friend for this perceived judgment. He was also somewhat willing to admit that his interpretation of his friend’s reaction might have been skewed by his own judgment of him- self. In fact, later in the therapy, when Tom was able to ask his friend directly about the perceived reaction, the friend indicated that it had been hard for him to hear, but that he had not been judging Tom at all. In actu- ality, he was thinking about the terrible predicament Tom had endured at the time.
The therapist returned to Stuck Points she had heard in the course of reviewing the sheets and Socratic dia- logue. The following dialogue then occurred:
TOM: I’m not sure what the Stuck Points are, but from what you’ve been asking me, I guess you question whether or not I murdered this family.
THERAPIST: That’s true. I think it is worthwhile for us to discuss the differences between blame and respon- sibility. Let’s start with responsibility. From your ac- count, it sounds like you were responsible for shooting the family. It sounds like other people may have been responsible, too, given that you were not the only person who shot at them.
[The therapist stores this fact in her mind to challenge Tom later about the appropriateness of his actions. This also provides a good opportunity to reinforce Tom for perform- ing well in a stressful situation.] THERAPIST: The bottom line is that responsibility is
about your behavior causing a certain outcome. Blame has to do with your intentionality to cause harm. It has to do with your motivations at the time. In this case, did you go into the situation with the motivation and intention to kill a family?
TOM: No, but the outcome was that they were mur- dered.
THERAPIST: Some died. That is true. From what you’ve shared, if we put ourselves back into the situation at the time, it doesn’t seem like it was your intention for them to die. They were coming down the road too fast, not responding to the very clear efforts to warn them to stop. Your own and others’ intentions were to get them to stop at the checkpoint. Your intention at the time did not seem to be to kill them. In fact, wasn’t your intention quite the opposite?
TOM: Yes. (Begins to cry.) THERAPIST: (Pauses until Tom’s crying subsides some-
what.) It doesn’t seem that your intention was to kill them at all. Thus, the word blame is not appropriate. Murder or considering yourself a murderer does not seem accurate in this situation. The reason I’ve ques- tioned the term murder or murderer all along was be- cause it doesn’t seem like your intention was to have to shoot them.
TOM: But why do I feel like I am to blame? THERAPIST: That’s a good question. What’s your best
guess about why that is? TOM: (still crying) If someone dies, someone should
take responsibility. THERAPIST: Do you think it is possible to take respon-
sibility without being to blame? What would be a better word for a situation that is your responsibility, but that you didn’t intend to happen? If a person shot someone but didn’t intend to do that, what would we call that?
TOM: An accident, I guess. THERAPIST: That’s right. In fact, what would you call
shooting a person when you are trying to protect something or someone?
TOM: Self-defense.
86 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
THERAPIST: Yes, very good. Weren’t you responsible for guarding the checkpoint?
TOM: Yeah. THERAPIST: So, if you were responsible for guard-
ing that checkpoint, and they continued through, wouldn’t that have put the area at risk?
TOM: Yes, but it was a family—not insurgents. THERAPIST: How did you know that at the time? TOM: There was a woman and child in the car. THERAPIST: Yes—we know how the story ended now.
Did you know that at the time? TOM: No. THERAPIST: So only in hindsight do you know that it
was a family that might have had no bad intention. We actually don’t know the family’s intention, do we? They didn’t heed the several warnings, right?
TOM: Yes. (Pauses.) I hadn’t thought that they would be looking to do something bad with a woman and child in the car.
THERAPIST: We don’t know, and won’t ever know, un- fortunately. However, what we do know is what you knew at the time. What you knew at the time is that they did not heed the warnings, that you were respon- sible for securing the checkpoint, and that you took action when you needed to take action to protect the post. Thinking about those facts of what happened and what you knew at the time, how do you feel?
TOM: Hmm . . . I guess I’d feel less guilty. THERAPIST: You’d feel less guilty. Or, you feel less
guilty? TOM: When I think through it, I do feel less guilty. THERAPIST: There may be points when you start feel-
ing guiltier again. It will be important for you to hold onto the facts of what happened versus going to your automatic interpretation that you’ve had for a while now. Is there any part of it that makes you proud?
TOM: Proud? THERAPIST: Yes. It seems like you did exactly what you
were supposed to do in a stressful situation. Didn’t you show courage under fire?
TOM: It’s hard for me to consider my killing them as courageous.
THERAPIST: Sure. You haven’t been thinking about it in this way for a long time, but it is something to consider.
The therapist’s Socratic dialogue was designed to help Tom consider the entire context in which he was operating. She also began to plant the seed that Tom not only did nothing wrong but he also did what he was supposed to do to protect the checkpoint. Whenever possible, pointing out acts of heroism or courage can be powerful interventions with trauma survivors.
The therapist noted that another of Tom’s sheets contained overaccommodated beliefs about the U.S. military. He had entered the service with a very positive view of the military. Tom had a family history of mili- tary service and believed in service to country and the “rightfulness” of the military. Subsequent to his trau- matic event and military service in Iraq, he developed a negative view of the military that had extended to the Federal government in general. The therapist used this content to introduce the first series of tools to help chal- lenge Tom’s Stuck Points. She also emphasized how he would gradually be taking over as his own therapist, ca- pable of challenging his own patterns of thinking that kept him “stuck.”
THERAPIST: It seems that you have some very strong beliefs about the military and the U.S. government since your service. I’d like to use those beliefs to in- troduce some new material that will be helpful to you in starting to challenge Stuck Points on your own. You’ve done an outstanding job of considering the way that you think and feel about things. You’ve been very open to considering alternative interpreta- tions of things. Starting in this session, I’m going to help you to become your own therapist and to attack your own Stuck Points directly.
TOM: OK. THERAPIST: We’re going to be building your skills over
the next few sessions. The first tool is a sheet called the Challenging Questions Worksheet. Our first step is to identify a single belief you have that may be a Stuck Point. As I mentioned before, I’d like us to use your beliefs about the Federal government now. So, if you were to boil down what you believe about the Federal government or the military, what is it?
TOM: I don’t know. I’m not sure. I guess I’d say that the U.S. military is extremely corrupt.
THERAPIST: Good. That is very clear and to the point. So, let’s go over these questions and answer them as they relate to this belief. The first question you ask yourself is “What’s the evidence for and against this idea?”
Posttraumatic Stress Disorder 87
TOM: The evidence for this is Abu Ghraib. Can you believe that they would do that? I would have also put my own shooting under the “for” list, but I’m beginning to question that.
THERAPIST: What other evidence is there of corrup- tion?
TOM: Oh, and these defense contractors . . . what a scam! That leads me to the current administration and its vested interests in going to war to make money on defense contracting. And, oh, of course, to make money on the oil coming out of these coun- tries!
THERAPIST: OK. Sounds like you have some “for” evi- dence. What about the “against” evidence?
TOM: Well, some of my fellow soldiers were very good. They were very committed in their service and to the mission. I also had mostly good leaders, although some of them were real pigs. Some were really power- hungry a—holes, frankly.
THERAPIST: So, it sounds like you have some pros and cons that support your belief that the U.S. military is completely corrupt. In the process of changing, it is common to have thoughts on both sides. That means that you are considering different alternatives, and are not “stuck” on one way of seeing things. Let’s look at the next one. . . .
The therapist spent the balance of the session going over the list of questions to make sure that Tom un- derstood them. Although most of the questions focused on the issue of corruption in the military, other issues were also brought in to illustrate the meaning of the questions. For example, the therapist introduced the probability questions with the example from Tom’s life in which he believed that he was going to be shot by an insurgent sniper while back home. These questions are best illustrated with regard to issues of safety. The therapist pointed out that perhaps not all of the ques- tions applied to the belief on which Tom was working. The question “Are you thinking in all-or-none terms?” seemed to resonate with Tom the most, because it ap- plied to his belief about the military. He commented that he was applying a few examples of what seemed to be corruption to the entire military. Tom also indicated that his description of the military as “extremely” cor- rupt was consistent with the question “Are you using words or phrases that are extreme or exaggerated?” In- dicative of his grasp of the worksheet, Tom also noticed
that the question “In what ways is your Stuck Point not including all of the information?” applied to his prior view of his behavior as a murder in the traumatic event.
For his practice assignment prior to Session 5, Tom agreed to complete one Challenging Questions Work- sheet each day. He and the therapist brainstormed about potential Stuck Points prior to the end of the session to facilitate practice assignment completion. These Stuck Points included “I don’t deserve to have a family,” “I murdered an innocent family,” and “I am weak because I have PTSD.” Prior to ending the session, the therapist inquired about his reaction to the therapy session. Tom commented that it had been very difficult, but that he felt better than he expected in going into the “nitty- gritty” of what happened. He also noted that there were things he had not considered about the event that were “food for thought.”
Session 5
Tom arrived at Session 5 looking brighter and making more eye contact with the therapist. His self-reported PTSD symptoms were decreased, and he spontaneously noted that he was experiencing less guilt.
THERAPIST: You mentioned that you’re feeling less guilt now. Why is that?
TOM: I’m beginning to realize that I was not the only one there that was trying to stop them. Several of us were trying to get them to stop. There is still some guilt that I was the one who shot them.
THERAPIST: If one of the other guards had shot them, would you blame him or her for the shooting? Would you expect him or her to feel guilty for their behav- ior?
TOM: (Laughs.) I started thinking about that this week. It made me wonder if it was really me who even shot them. As I was writing and thinking about it more, I realized that there is a possibility that another of the guards may have been shooting at the same time.
THERAPIST: What would it mean if they were shooting at the same time?
TOM: If he was shooting at the same time, it means that he thought that shooting at them might be the right thing to do in that situation.
THERAPIST: Might have been the right thing to do? TOM: (smiling) Yeah, I still have questions that we
might have been able to do something else.
88 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
THERAPIST: It seems like you’re still trying to “undo” what happened. I’m curious, what else could you have done?
TOM: Not have shot at them. THERAPIST: Then what would have happened? TOM: They might have stopped. (Pauses.) Or I guess
they could have gone through the checkpoint and hurt other people past the checkpoint. I guess they could have also been equipped with a car bomb that could have hurt many other people. That seems hard to believe, though, because of the woman and child in the car.
THERAPIST: It is impossible for us to know their inten- tions, as we discussed before. The bottom line is that you’ve tended to assume that doing something dif- ferent, or doing nothing, would have led to a better outcome.
TOM: That is true. I still feel sad. THERAPIST: Sure you do—that’s natural. I take it as
a good sign that you feel sad. Sadness seems like a very natural and appropriate reaction to what hap- pened—much more consistent with what happened than the guilt and self-blame that you’ve been expe- riencing.
Tom and the therapist discussed how the goal of the therapy was not to forget what had happened, but to have the memory without all of the anxiety, guilt, and other negative emotions attached to it. Tom indicated that he was becoming less afraid and more able to tol- erate his feelings, even when they were intense. Tom acknowledged that talking about his trauma, doing the worksheets, and coming to psychotherapy sessions were becoming easier and that his negative feelings were be- ginning to diminish.
Tom completed Challenging Questions Worksheets about all of the Stuck Points he and the therapist had generated. The therapist reviewed these worksheets to determine whether Tom had used the questions as de- signed. She asked Tom which of the worksheets he had found least helpful. He responded that he had had the most difficulty completing the sheet about deserving to have a family. The therapist then reviewed this sheet in detail with Tom (see Figure 2.2).
THERAPIST: So, I notice that in your answer about the evidence for and against this idea about deserving a family, you included as evidence that you took some
other man’s family. I’m glad to see that you didn’t include the word murder—that’s progress. But, how is that evidence for you not deserving a family?
TOM: It is evidence because I feel like I took someone else’s; therefore, I don’t deserve one for myself. It seems fair.
THERAPIST: Remind me to make sure and look at what you put for the question about confusing feelings and facts. For now, though, help me understand the math of why you don’t deserve your family, and your hap- piness about your family, because of what happened?
TOM: I don’t know—it just seems fair. THERAPIST: Fair? That implies that you did something
bad that requires you to be punished. TOM: As I’ve been thinking about it more, I don’t think
I did something wrong when I really look at it, but it still feels like I did something wrong and that I shouldn’t have something good like a wife and child in my life.
THERAPIST: Maybe we should look at your response to that feelings versus facts question. What did you put in response to the question “In what ways is your Stuck Point based on feelings rather than facts?”
TOM: I wrote, “I’m feeling guilty, like I did something wrong when the truth is that I did what I was sup- posed to do.” I try to remember what we talked about—that part about them not responding to the warnings and my shooting them, which may have prevented something else that was bad. I still feel bad—not as bad as I did—but I still feel like I did something wrong.
[The therapist uses this as an opportunity to talk about the need for practicing new alternative thoughts in order to elicit emotional change.] THERAPIST: You are well on your way, Tom, to recover-
ing. Your head is starting to get it, and your feelings need to catch up. You’ve been thinking about what happened and what you did in a certain way for a while now. You blamed yourself over and over and over again, telling yourself that you did something wrong. You gave yourself a steady diet of that type of thinking, which resulted in you feeling guilty about what happened. It is like a well-worn rut of thinking in your brain that automatically leads you down the path of feeling guilty. What you need to do now is start a new road of more realistic and truthful think- ing about the situation that will eventually be a well-
Posttraumatic Stress Disorder 89
Below is a list of questions to be used in helping you challenge your Stuck Points or problematic beliefs. Not all questions will be appropriate for the belief you choose to challenge. Answer as many questions as you can for the belief you have chosen to challenge below.
Belief: I don’t deserve to have a family.
1. What is the evidence for and against this Stuck Point?
For: I took some other man’s family.
Against: I didn’t want to have to shoot anyone. An “eye for an eye” does not apply here.
2. Is your Stuck Point a habit or based on facts?
It is a habit for me to think this way. The facts are that I didn’t do something wrong to deserve to be punished in this way.
3. In what ways is your Stuck Point not including all of the information?
My interpretation of the original situation has been fairly unrealistic, which is where I get this belief.
4. Does your Stuck Point include all-or-none terms?
N/A
5. Does the Stuck Point include words or phrases that are extreme or exaggerated (e.g., “always,” “forever,” “never,” “need,” “should,” “must,” “can’t,” and “every time”)?
I guess maybe “deserve” could be an extreme word.
6. In what way is your Stuck Point focused on just one piece of the story?
Yes, like #3, I tend to forget what all was going on at the time of my shooting.
7. Where did this Stuck Point come from? Is this a dependable source of information on this Stuck Point?
No, I’m not very reliable these days.
8. How is your Stuck Point confusing something that is possible with something that is likely?
N/A
9. In what ways is your Stuck Point based on feelings rather than facts?
I’m feeling guilty like I did something wrong when the truth is that I did what I was supposed to do.
10. In what ways is this Stuck Point focused on unrelated parts of the story?
Maybe my deserving a family has nothing to do with someone else losing theirs?
FIGURE 2.2. Challenging Questions Worksheet for Tom. Adapted from Resick, Monson, and Chard (2017). Copyright © 2017 The Guilford Press. Adapted by permission.
90 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
worn path. What is the more realistic view of your role in this event?
TOM: (tearfully) I had to shoot at the car, and people died.
THERAPIST: That’s right. And, let’s pretend for a second that you really do believe that thought. If so, what would you feel?
TOM: I’d feel so much lighter. I wouldn’t feel guilty. I’d continue to feel sad about this horrible situation, but I wouldn’t blame myself.
THERAPIST: Let’s take it to the next step. If you didn’t blame yourself and feel guilty, then would you be- lieve that you deserve to be happy with your wife and the baby that will soon be here?
TOM: Sure. THERAPIST: So, Tom, your work is to practice, prac-
tice, practice this new and more accurate way of looking at what happened and your role in it. With practice, your feelings will start matching the truth about what happened and the fact that you are not to blame.
TOM: It is kind of like training to use a weapon. They made us do certain things with our guns over and over and over again, until it was automatic. It was very automatic after a while.
THERAPIST: That’s right. There are other questions on this sheet that might be helpful in convincing you of the truth about this in your practice.
This dialogue illustrates a common occurrence at this stage in the therapy. Tom was starting to experi- ence cognitive change, but his emotional change was lagging. The therapist reinforced the need to practice the new ways of thinking to feel different. It is also important to highlight clients’ gains in changing their thinking, even if their feelings have not changed or are ambivalent. A change in thinking is framed as more than halfway to a change in feeling. In effect, changed thinking involves competing thoughts or learning, and with more repetitions of the new thought, the associ- ated feelings follow and eventually win out.
In the latter portion of this session the therapist in- troduced the Patterns of Problematic Thinking Work- sheet and provided an explanation of how this list was different from the Challenging Questions Worksheet (see Figure 2.3). More specifically, she indicated that the Patterns of Problematic Thinking Worksheet per-
tains to more general patterns of thinking versus chal- lenging individual thoughts that Tom might have. The Patterns of Problematic Thinking Worksheet lists seven types of faulty thinking patterns (e.g., oversimplifying, overgeneralizing, emotional reasoning).
Tom and the therapist went through the list and gen- erated examples for each of the patterns. For example, for “Ignoring important parts of a situation,” the thera- pist pointed out something that Tom had brought up several times during therapy. Initially, Tom had not in- cluded the important information that he and the other guards had attempted to stop the car before shooting at it. She also pointed out that emotional reasoning was similar to confusing a feeling with a fact, which had been a primary focus of the session.
When they got to the item “Overgeneralizing from a single incident,” Tom said he noticed that he was begin- ning to change his thoughts about the government and its leaders. He commented that it had been very power- ful for him to consider that, in a number of instances, his fellow soldiers had operated with integrity and were committed to the mission, and to the safety and protec- tion of others. Tom said spontaneously, “I guess that is also kind of like drawing conclusions when evidence is lacking or even contradictory.” He said that he had started stereotyping after the traumatic event—apply- ing negative attributes and opinions to everyone in the military and the government too broadly. Tom and the therapist discussed how the goal of the therapy was to have a balanced and realistic view of things versus the overly ideal version he had pretrauma or the overly pes- simistic version he had posttrauma. In other words, the goal was to find shades of gray and balance in his think- ing about the government, the military, and their lead- ership. Tom added an example of this thinking: “There are at least some people in government who want to do good for others.”
Tom was given the practice assignment to read over the list in the Patterns of Problematic Thinking Work- sheet and to note examples of times he used each of the problematic thinking patterns.
Session 6
Tom began the session by stating that he was feeling better, and that his wife had also noted a difference in him and was feeling less concerned about the therapy making him worse rather than better. The therapist asked whether Tom had completed his practice assign- ment, the Patterns of Problematic Thinking Work-
Posttraumatic Stress Disorder 91
sheet. He indicated that he had not, but that he had thought about it over the week. He also laughed and said that he had noticed the thinking patterns in his wife and others. The therapist asked Tom to complete some of the sheet in session. At this point in therapy, the therapist was sitting back more as Tom took on the role of challenging his own cognitions. The therapist provided both minimal clarification and additional ex- amples that she had noticed in working with Tom.
In this session, the therapist introduced the Chal- lenging Beliefs Worksheet. She was careful to point out that the worksheet integrated all of the previous work
Tom had done and added a few new elements. The following dialogue illustrates the introduction of this sheet (see Figure 2.4).
THERAPIST: I want to show you the final worksheet that we’re going to be using for the rest of the therapy.
TOM: OK. Wow—that looks complicated! THERAPIST: Actually, you’ve done pretty much ev-
erything on this worksheet already. This worksheet brings together into one place everything that we’ve been working on.
FIGURE 2.3. Patterns of Problematic Thinking Worksheet for Tom. Adapted from Resick, Monson, and Chard (2017). Copyright © 2017 The Guilford Press. Adapted by permission.
Listed below are several different patterns of problematic thinking that people use in different life situations. These patterns often become automatic, habitual thoughts that cause people to engage in self- defeating behavior. Considering your own Stuck Points, or samples from your everyday thinking, find examples for each of these patterns. Write in the Stuck Point or typical thought under the appropriate pattern, and describe how it fits that pattern. Think about how that pattern affects you.
1. Jumping to conclusions or predicting the future.
I tend to jump to the conclusion that I have done something wrong when bad things happen. I assume things are my fault.
2. Exaggerating or minimizing a situation (blowing things way out of proportion or shrinking their importance inappropriately).
I minimize the things that I have done well in the military.
3. Ignoring important parts of a situation.
In the past I have tended to neglect the important aspect that several of us tried to stop the car from going through the checkpoint.
4. Oversimplifying things as “good–bad” or “right–wrong.”
I can sometimes think of all the Iraqis as all bad.
5. Overgeneralizing from a single incident (e.g., a negative event is seen as a never- ending pattern).
I have assumed that because of my traumatic event, I could not be safe with my baby to be born.
6. Mind reading (assuming that people are thinking negatively of you when there is no definite evidence for this).
I assume that everyone thinks I am a terrible person, a murderer, because of what I did.
7. Emotional reasoning (using your emotions as proof—e.g., “I feel fear, so I must be in danger”).
This one is easy—I feel guilty, and there I must be.
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st ea
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:
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)
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)
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a st
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ifo rm
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t he
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.” (1
0 0 % )
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er (
8 0 % )
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( 3 0 % )
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ab it t
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on ’t k
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.” (6
0 % )
“I f he
d oe
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hi
s sh
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er , I do
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kn ow
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ha t
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ab ou
t— m
ay be
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al
on e
ha vi ng
s er
ve d
in Ir
aq .”
(8 0 % )
3 5 %
A ng
er ( 2 0 % )
Fe ar
( 1 5 % )
Posttraumatic Stress Disorder 93
TOM: I’ll take your word for it, Doc. THERAPIST: Remember the A-B-C Worksheets from
way back when? TOM: Yes. THERAPIST: (pointing to first two columns on the Chal-
lenging Beliefs Worksheet) This is A, B, and C. You have in column A the situation, or “Activating Event” that you had on the A-B-C Worksheet. In column B you have “Automatic Thoughts,” which is the “Be- lief/Stuck Point” portion of the A-B-C Worksheet. Last, section C, “Emotions,” is the “Consequence” portion of the A-B-C Worksheet.
TOM: OK. So far, so good. THERAPIST: Section D is where you identify the “Chal-
lenging Questions” from that sheet that apply to the thought or Stuck Point that you’re working on. In section E, you identify the type of “Patterns of Prob- lematic Thinking” that apply to the thought or Stuck Point that you’re working on. Make sense?
TOM: Yes. THERAPIST: So, only section F, “Alternative Thought,”
is new. Here you identify alternative thoughts that you could have about the situation. In other words, we’re looking for alternative statements that you can tell yourself or different interpretations of the event. In sections G and H, you get to see how your belief in your original thoughts may change and how the new thoughts affect your feelings.
TOM: OK. THERAPIST: So, let’s pick a Stuck Point and start using
this Challenging Beliefs Worksheet. What Stuck Point would you like to learn with?
TOM: Well, I still wonder if there are people out in the world who want to hurt me, even if I now realize that no sniper is going to take me out.
THERAPIST: So, let’s pick a specific event—the more specific, the better.
TOM: I was in the grocery store, and I had my uniform on. There was this guy who seemed to have a chip on his shoulder about it—like he hated me or some- thing.
THERAPIST: So, write down the event in Section A. (Pauses.) What was your thought? You’ve already mentioned one of them.
TOM: This guy has a chip on his shoulder about me because I’m in the military.
THERAPIST: Good. How strongly do you believe that thought?
TOM: 100%. THERAPIST: OK, let’s write that next to the thought.
We are now rating how much you believe in your thoughts because you’re going to see at the end how much your thought has changed. What feeling or feelings are associated with that thought?
TOM: Definitely anger. THERAPIST: Makes sense, given your thought. How
much anger from 0 to 100%, with 100% being as much anger as you could possibly imagine having?
TOM: Hmm . . . I’d say 80%. THERAPIST: Any other feelings? You can have more
than one. TOM: I guess when I stop and think about it, there is
some fear there, too. THERAPIST: That makes sense, too. How much fear
from 0 to 100%? TOM: Oh, maybe 30%. It’s not the strongest feeling,
but it’s there, because I’m wondering if he is going to say something or do something.
THERAPIST: Nice job. Let’s move onto the next column that relates to the Challenging Questions Worksheet you’ve already done. Take a look at this list. What questions might apply here?
TOM: I guess I might be confusing a habit with a fact. It seems like it is a habit for me to assume that every- one dislikes me because I was in Iraq. I really don’t know if that is why he seemed to have a chip on his shoulder. I guess I also don’t know for sure if he had a chip on his shoulder. He didn’t say anything to me. (Pauses.) I guess that is also an example of the source of information being unreliable, and that source is me! (Laughs.)
THERAPIST: While you were talking, I was thinking that the same questions applied. You can also pick out other challenging questions that might apply, but usually two or three will do the trick. In the next column, we’re going to refer to the Patterns of Prob- lematic Thinking Worksheet. What might fit here?
TOM: I guess one jumps out—mind reading. THERAPIST: How so? TOM: I’m assuming that he is thinking the worst about
me and about my having served my country. I’m good at that.
94 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
THERAPIST: Write that down. You can add others later if something seems to apply. The next column is very important. This is where you start coaching yourself to come up with alternative thoughts or perceptions about the situation. Based on having asked yourself these questions and noticing the problematic think- ing patterns, what other ways might you think about this situation?
TOM: I guess one thing I could say to myself is, “I don’t know if he has a chip on his shoulder.” I could also say, “If he does have a chip on his shoulder, I don’t know what it is about—maybe it isn’t even about me, let alone about my having served in Iraq.”
THERAPIST: Wow! You’re doing great at this. Let’s get those written down. Let’s also add how much you believe those two new thoughts. Below those alterna- tive thoughts is the section that asks you to recon- sider how much you believe your original thoughts over here in section B. How much do you believe them after walking through this process? Before you said 100%.
TOM: Oh, I’d say now it is only about 35%. THERAPIST: That is a big change. You went from 100%
certainty to 35% certainty that he had a chip on his shoulder because you fought in the war.
TOM: I’m a little surprised by that myself. THERAPIST: Let’s take it the final step. How about your
feelings now? Let’s rerate those here. TOM: My anger is way down—I’d say only about 20%.
The anxiety is still there because I really wouldn’t want to have to protect myself, and he might have had a chip on his shoulder at me. It is down a little, though, because I realize I’m not 100% certain he was out to get me. I’d say maybe 15% on fear.
THERAPIST: Do you have questions about what we just did here?
TOM: Not at the moment. I’ll get back to you. THERAPIST: I’m going to ask that you do one of these
sheets on a Stuck Point per day until I see you again. I’m also going to give you some example sheets other patients have done that might be helpful to you.
TOM: OK. Should be interesting. . . .
The therapist cautioned Tom that he should not ex- pect his beliefs and feelings always to change complete- ly in the process of doing the sheet. The old thought would need to be completely dismantled, and the new
thought would need to become more habitual for him to see a more permanent change. The therapist sug- gested that Tom read the sheets he completed over to himself a number of times to facilitate the process. Tom was instructed to complete a Challenging Beliefs Work- sheet each day prior to the next session, taking thoughts off his Stuck Points Log to challenge. The therapist also reminded Tom that he needed to finish the Patterns of Problematic Thinking Worksheet assignment from last session.
Session 7
Tom arrived at the session having completed the Pat- terns of Problematic Thinking Worksheet, as well as two Challenging Beliefs Worksheets. The therapist spent a little time looking at his answers to the Patterns of Problematic Thinking Worksheet, because she did not want to send the message inadvertently that com- pleting the assignments was unimportant. She asked Tom to read the patterns that he had completed at home, as opposed to those in their previous session.
Tom completed only two Challenging Beliefs Work- sheets. Thus, the therapist emphasized how Tom might use this process more generally in his day-to-day life, and highlighted how more practice would lead to more results. She noted that using the process on less emo- tionally distressing topics could actually be very help- ful in getting the process down. It is always easier to learn something when one is not dealing with the most challenging circumstances. She used a military analogy with Tom about learning to load and shoot a gun—best learned in a nonconflict situation, so that it is a more rote behavior when under fire.
The therapist skimmed the two sheets Tom had com- pleted and noticed that he had struggled most coming up with alternative statements related to his wife’s im- pending delivery of their child. The following dialogue ensued (see Figure 2.5):
THERAPIST: I notice that you might have had the most trouble coming up with alternative thoughts about how safe you can be with your wife and your child who is about to be born.
TOM: Yeah, I don’t really like to talk about it. It freaks my wife out. I’m uncomfortable being around my wife, which makes her feel bad, but I’m just afraid I’m going to hurt her or the child.
THERAPIST: Let’s take your first thought because it is
95
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b e
vi ol
en t
96 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
kind of general. How is it that you think you’re going to hurt them? Are we talking physically or mentally?
TOM: Oh, physically is what I mean. I don’t know how exactly, but somehow, some way, I guess.
THERAPIST: That makes it a bit more concrete. How do you physically think you’re going to hurt them? Do you think you’ll shoot them, given your trauma history?
TOM: No. Absolutely not. THERAPIST: So, what have you considered in your
mind? TOM: I guess I’m worried that, out of nowhere, I’ll get
physically violent. THERAPIST: OK, now we’re cooking. Let’s write that
down. “Out of nowhere I’ll get physically violent.” I noticed that in section C you didn’t mention any- thing about confusing possibilities with certainties. Safety issues are almost always about gauging prob- abilities. The world is not a completely safe place, and every day we all make calculated risks about our safety based on the probability of bad things happen- ing to us or to someone else. How do you think that question might apply?
TOM: Are you getting at the idea that I’m confusing how likely it is to be?
THERAPIST: Precisely. How do you think that applies here?
TOM: I’m convinced that “somehow, some way” I’m going to hurt my family, so I believe that it is a high potential that it will happen and not a low possibility. I think you think that the possibility I will do that is low. But, I’m still concerned about it.
THERAPIST: Let’s talk about the actual likelihood. How often have you hurt your family physically?
TOM: Never. Are you kidding? THERAPIST: I thought as much, but you made it sound
like it was very likely to happen. I guess that’s part of the problem, right?
TOM: You’re right. THERAPIST: How often have you been physically vio-
lent against anyone? TOM: I haven’t, besides the shooting. And it surely
hasn’t been unexpected. Now that we’re talking through it, it feels a little silly.
THERAPIST: So, it sounds like figuring out the actual probability of this is right where we needed to go.
Given what we’ve talked about, what is an alternative statement you can tell yourself and how much do you believe it?
TOM: It is unlikely that I’ll hurt my family, and even more unlikely that it will be sudden and unexpected given that it has never happened.
THERAPIST: Let’s keep going to see how that might change how you feel. You wrote that you had 85% fear. What is that rating now?
TOM: Less than 10%. There is some fear now that I know I am capable of hurting a family, but like we’ve talked about before—and what I have to remem- ber—is that it occurred in a certain situation and not in my everyday life now as a civilian in my family.
This exchange between Tom and the therapist il- lustrates the hallmark role of probability in assessments and beliefs about safety, the first of the themes that is introduced in this session. It is important to realize that there are some objectively unsafe situations or behav- iors, and these should not be minimized or challenged. If there are unreasonable safety precautions or beliefs, the actual probability of harm should be carefully eval- uated, keeping in mind that 100% safety is rarely, if ever, guaranteed.
The Safety module was then introduced. Safety is the first of five modules (two- to three-page handouts) that also include Trust, Power/Control, Esteem, and Intimacy. The therapist oriented Tom to the format of the module, which included discussion about how beliefs about the self and others in this area can be dis- rupted or seemingly confirmed after a traumatic event, depending on one’s history prior to the traumatic event. The modules describe how these problematic beliefs are manifested emotionally and behaviorally (e.g., not leav- ing one’s home because of the belief that the world is unsafe). It also provides alternative self-statements that are more balanced and realistic in each area.
Tom had felt safe with others before the traumatic event occurred, and this sense of safety about others had been disrupted, as evidenced by his sense that oth- ers around him were out to get him. Pretrauma, Tom had also felt as though he was not a danger to others. Posttrauma, he believed that he could not be safe with others, which specifically manifested in his concerns about being around his pregnant wife. The therapist suggested that Tom complete at least one worksheet on his Stuck Points about others being safe, as well as his being a possible danger to others.
Posttraumatic Stress Disorder 97
Session 8
Tom did an excellent job of completing Challenging Beliefs Worksheets on a daily basis, including ones on the theme of safety. About half of the session was spent on Tom sharing with the therapist about these work- sheets and the two of them collaboratively improving completion of them for Tom’s benefit.
The therapist transitioned the session to introduce the Trust module. Tom noted that he had pretty good trust of himself and others prior to his best friend com- mitting suicide when they were in high school. Tom said that after the experience, he sometimes did not trust his judgments about other people, and that he felt respon- sible for not anticipating his friend’s suicide. The mili- tary traumatic event served to confirm his belief that he could not trust his judgments about others’ intentions. Tom’s concerns about his ability to be safe with his wife and unborn child also dovetailed with the issue of trust. The therapist and Tom went over the information in the Trust module handout, and Tom seemed to reso- nate with all of the potential effects. He reported that he had really been trying to open up with his wife and not avoid her. He noted that they were communicating more, which made both of them more relaxed and com- fortable in the final days of her pregnancy.
The therapist closed the session by assigning daily Challenging Beliefs Worksheets, asking Tom to do at least one on the topic of trust. She reminded him that, like other areas, the goal is to develop balanced alternative thoughts. In the case of trust, she noted that Stuck Points about trust often revolve around making all-or-none judgments, either trusting or not. The goal is to consider trust as multidimensional, with different types of issues resulting in different levels of trust in different situations. Tom also agreed to complete the Trust Star Worksheet, which is designed to help the client identify these different types of trust and levels of each type.
Session 9
Tom arrived at this session having completed a num- ber of Challenging Beliefs Worksheets. Several of them were about trust, including his level of trust of the gov- ernment and trust of himself in being a father. He had also used the worksheets on non-trust-related topics related to his daily life. He commented that the work- sheets had been helpful in working out his thinking be- fore he behaved impulsively or felt miserable.
The therapist praised Tom for completing the work- sheets so well, and asked him whether he felt he could use assistance with any of the worksheets. Tom quickly responded that he wanted to focus on the sheet about fatherhood because he was experiencing so much anxi- ety about his child’s impending birth. In turning their attention to this worksheet, the therapist immediately noticed that Tom had probably struggled with this worksheet, because he had listed so many different types of thoughts that were fueling his anxiety about becoming a father. She used this as an opportunity to fine-tune Tom’s use of the worksheets. The therapist’s choice in thoughts to challenge first also illustrates the prioritization of treatment targets in the therapy. She chose to go after the more directly trauma-relat- ed thoughts that contained remnants of assimilation. Tom’s thoughts about deserving to be happy about starting a family given the death of the woman, fetus, and child suggested that he had not fully accepted the traumatic event and the circumstances surrounding it. Thus, she addressed this thought first (see Figure 2.6).
THERAPIST: Wow, you’ve got lots of thoughts going on in your head about becoming a father, don’t you? I’m going to suggest that we use a different worksheet for each of the clusters of thoughts you’re having on this topic. I think that will make your use of the Chal- lenging Beliefs Worksheet better. It seems that some thoughts are directly related to your traumatic expe- rience, others are specifically related to your wife’s labor and delivery, and still others are related more generally to being a parent. Let’s focus on those that are directly related to your trauma. You wrote that one of your feelings was guilt (85%), and I’m assum- ing that it is related to your thought that it isn’t right that you’re happy with a soon-to-be-born baby given what happened.
TOM: That’s right. If I’m really honest, I still feel guilty that the Iraqi woman was pregnant and getting ready to have a child, and the shooting deprived her of the ability to have that child and be happy, and I’m get- ting ready to have that happiness.
THERAPIST: We’ve talked about this before, but we’ve been more focused on the man and the child in- volved in the situation.
TOM: Yeah, I think the closer my wife gets to delivery, the more I think about the Iraqi woman. I’ve been imagining that she wasn’t part of a potential plot for terrorist activity and was more an innocent partici-
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Posttraumatic Stress Disorder 99
pant. Then, I go back and forth, thinking that she might have actually been involved and didn’t care that she was pregnant. Or maybe it was just an ac- cident, and they truly didn’t understand that they needed to stop. Uggghhhh, it is exhausting.
THERAPIST: And we’ll never know. If your friend were saying all of this to you, what would be your response to him?
TOM: I’d be telling him to quit beating himself up and feeling guilty.
THERAPIST: Easier said than done. Anything else? Maybe it would help to look at the Challenging Questions and Patterns of Problematic Thinking Worksheets. I’m wondering if you are focusing on unrelated parts of the story—item 10 on the Chal- lenging Questions Worksheet.
TOM: Hmm . . . what is unrelated in this case? THERAPIST: How relevant are her intentions to deserv-
ing to be happy yourself about having a child? TOM: (Pauses.) I’m going to have to think about that
for a second. THERAPIST: Aren’t your intentions in that situation
what is relevant? Were your intentions at that time to deprive her of the right to bear her child and live happily ever after?
TOM: No, not at all. THERAPIST: So, why guilt? What did you do wrong
that you should be punished about? TOM: Oh, wow. I hadn’t thought of that. Her inten-
tions are irrelevant. It only makes me crazy to try to get in her head. I guess that would be mind reading, now wouldn’t it?
THERAPIST: Very good—a different spin on mind reading. So, what is the alternative, more balanced and realistic thought?
TOM: My intentions are what matter. I didn’t intend for her to lose her own or her baby’s life.
THERAPIST: Go on . . . do you have a right to experi- ence happiness?
TOM: I guess I do. It just feels weird. THERAPIST: Sure—it feels different. It is different than
what you’ve been thinking about it for a while. I’m curious—what would you feel if you said to yourself, “I did not intentionally do anything to deprive some- one else of family happiness. I deserve to be happy in becoming a father.”
TOM: I’d feel less guilty for sure, and even happy. THERAPIST: Let’s get this all written down. Now you
have the job of holding on to these new insights and practicing them. Read over this worksheet every day until you see me again. I’d also like you to take these other thoughts on your original Challenging Beliefs Worksheet about this topic and put them on separate worksheets and work through them. Can you com- mit to doing that?
TOM: Yes, I already feel better. THERAPIST: This is an exciting time—you’ve got to
continue to work on this, so that you can have the enjoyment you deserve!
At this point, the therapist introduced the Power/ Control module. Tom admitted that prior to the trau- matic event, he was someone who liked to be in control. He did not like unpredictability, and he noticed that this tendency had gotten especially bad after his friend’s suicide. The military lifestyle seemed to be congruent with this tendency. Tom indicated that he had not had authority issues prior to the traumatic event, but he had noticed himself questioning authority much more since his military trauma. As with previous sessions, Tom was given the practice assignment to complete Challenging Beliefs Worksheets every day prior to the next session, and at least one was assigned on power/control.
Session 10
Tom began the session by saying that his wife had gone to her obstetrician the previous day, and that her labor would be induced in 1 week if she did not naturally go into labor before then. Tom indicated that the last session had been very good in helping him to become happier about his child’s impending birth, and that he had read the Challenging Questions Worksheet about deserving to be happy several times since the last ses- sion. He believed it more and more. He stated that he was still having some anxiety about becoming a father, and about everything going OK with his wife’s labor and delivery. The therapist normalized some of Tom’s anxiety, stressing how it was very natural for a first-time father, and Tom was able to recognize the typicality of this anxiety in others he had witnessed becoming par- ents.
Tom stated that since reading the Power/Control module after the last session, he had started to realize that not everyone in authority over him had wielded
100 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
their authority malevolently. This was very important in light of Tom’s preexisting history of desiring to exert control; he had directly confronted his illusion of con- trol. The therapist and Tom went over this worksheet.
Tom went on to describe how his belief that he could and should have control over everything had resulted in low self-esteem. In general, when things did not go as he desired, Tom felt as though he was a failure for not controlling the outcome. This belief structure led him to think that he should have been able to control his friend and stop him from committing suicide. It also led him to believe that he should have been able to create a positive outcome in the military traumatic event. This discussion served as a natural segue to the next topic—esteem. Tom admitted that he had become someone who thrived too much on accomplishment. This had affected his self-esteem and was especially rel- evant to his belief that he had not accomplished his goal in the military because he had to be taken from the field after the traumatic event at the checkpoint.
After reviewing the Esteem module, the therapist asked Tom to complete Challenging Beliefs Worksheets on his remaining Stuck Points, as well as any Stuck Points relating to esteem. He was also given two other assignments: to practice giving and receiving compli- ments every day, and to do one nice thing for himself every day that was not contingent on “achieving” some- thing. These assignments were to help him with his self- and other-esteem.
Session 11
Tom completed a worksheet on self-esteem related to his belief that he had not achieved his goal within the military. The therapist and Tom went over this work- sheet, and both noted that he had made significant progress by using the worksheet to change the way he thought and felt about himself. He asserted that he was beginning to see that people are much more than their professional accomplishments. They also have other activities and relationships with their families, friends, and themselves.
The therapist inquired about the assignment of giv- ing and receiving compliments. Tom replied that it had gone well, even though it felt a bit awkward and forced. He was even able to notice that when he gave compli- ments and was more positive toward other people, he seemed to get more positive responses back from them. The therapist noticed that several of the compliments were to his wife, and she pointed out that Tom seemed
more connected to his wife. He said that he was ac- tually beginning to feel glimmers of excitement about the birth of their child. He reported that he was still feeling some anxiety about becoming a father, and about how the labor and delivery would go, but that the anxiety was less and more manageable. When the therapist asked about Tom receiving compliments, he reported more difficulties. She asked what Tom typi- cally did when he received compliments, and it became clear that he often deflected or minimized them. Cor- respondingly, Tom also said that he had only done one nice thing for himself since the last session, and that it had felt uncomfortable. This pattern seemed to fit with Tom’s overall schema of being unworthy and un- deserving. The following dialogue ensued between the therapist and Tom:
THERAPIST: It seems like you have a hard time letting someone be nice to you and being nice to yourself.
TOM: Yes. THERAPIST: Why do you think that is? TOM: I don’t know. (Pauses.) I don’t like it. It feels like
they shouldn’t be nice to me, and I shouldn’t be nice to me.
THERAPIST: Hmm . . . I wonder if there is anything “off” about that thinking? What do you think?
TOM: As I hear myself say it, it sounds a little weird. It sounds like I don’t deserve to have nice things for me. Kind of like not deserving to have a family . . .
THERAPIST: This seems like a larger tendency in your life—one of those problematic thinking patterns. What pattern do you hear in your thinking? Look at the worksheet if you want to.
TOM: Maybe emotional reasoning. I feel like I don’t de- serve it; therefore, I must not deserve it. That seems like the best one. Maybe I’m also drawing a conclu- sion when the evidence is lacking.
THERAPIST: I agree. Given how much you seem to fol- low this pattern of thinking, I’m betting it has been around for a while—maybe even before the shooting occurred in Iraq.
TOM: It has. I think it had to do with my dad, his alco- holism, and not being close to me. As a kid, I always thought I had done something wrong, or that I was so bad that he didn’t want to be around me.
THERAPIST: Now, with adult eyes, what do you think about your dad not being close to you?
Posttraumatic Stress Disorder 101
TOM: I figure that he drank for a reason, and that it might have been me and my other brothers and sis- ters.
THERAPIST: Why do you assume that he drank because of you kids?
TOM: I don’t know. I figure it was stressful having four kids.
THERAPIST: It probably was at times, but as you hear yourself talk about this, what is amiss in how you’ve made sense of his drinking and being close to you?
TOM: I’ve known other people who had four kids and didn’t have drinking problems. There were a lot of big families where I grew up. Plus, I know that he and my mom had money problems when we were young, and that they fought a lot.
THERAPIST: So, again, why then do you assume it was you who caused his drinking and alienation?
TOM: When we talk about it, I guess I see that it might not have been me alone.
THERAPIST: Or not even you at all. Everybody has a choice about how they handle their stress, and it seems that he was distant from everyone, not just you.
TOM: True. It still feels that way. THERAPIST: There seems to be a well-worn path in your
brain that when something goes wrong, you blame yourself. The next step is that you deserve to be pun- ished, or at least you don’t deserve anything good. I don’t think this tendency is going to change over- night. You’re going to need to work hard at talking to yourself more rationally to change how you feel. For that new path to get worn, you’re going to have to walk down it a number of times. Pretty soon, the path will be more worn and automatic. It will take some effort, but you can change the way you auto- matically feel. I’d like you to do a Challenging Be- liefs Worksheet about what we’ve just talked about. Once we get a good one about it, you can read and refer to it as part of forging that new path. Can you do that?
TOM: Yes. I think it would be good.
This exchange regarding Tom’s dad dovetailed nicely with the final module, Intimacy. The therapist noted that people tend to think of intimacy as it relates to romantic relationships, and especially in terms of sexual intimacy. She stressed that there are all kinds of intima-
cy with different people. In essence, intimacy relates to how close and open we feel with other people. She went on to discuss the notion of self-intimacy, or how well we take care of, support, and soothe ourselves. In other words, it reflects how good a relationship we have with ourselves. Tom admitted that he struggled with being close to other people, which had most obviously mani- fested in the work he had done relative to his wife and unborn child. As noted earlier, Tom also struggled with doing nice things and taking good care of himself. Both of these areas seemed to be affected by Tom’s underly- ing schema that he was undeserving and unworthy.
The therapist assigned daily Challenging Beliefs Worksheets, continuation of the behavioral assign- ments, and requested that Tom do worksheets on being nice to himself and being close to his wife. In addition, she asked Tom to write a final Impact Statement, spe- cifically about his understanding of the trauma now, after all the work he had done. The therapist asked him to write about his current thoughts/beliefs in the areas of safety, trust, power/control, esteem, and intimacy.
Session 12
The day after Session 11, Tom left a message indicat- ing that his wife had delivered a healthy baby girl. He indicated in his voice-mail message that he felt happy and relieved. He went on about how beautiful the baby was, how well his wife had done in labor and delivery, and how he had enjoyed holding his daughter in his arms the first time. The 12th session was delayed a bit because of the baby’s arrival.
Tom’s wife and new daughter accompanied him to the final session. The therapist spent some time admir- ing Tom’s new baby and congratulating his wife be- fore starting the final session. Tom seemed genuinely proud and happy about his daughter, and noted that becoming a father had been more natural than he had anticipated. He commented that he had been worried that he would not want to hold the infant for fear of hurting her or because he would do something wrong. Instead, he found it almost “instinctual” to hold her, and that soothing her had come more naturally than he expected. Tom seemed surprised about how natural his role as a father had come.
The therapist inquired about how the assignments had gone. Tom said that he had not done as much as he had hoped given the baby’s arrival, but that he had done worksheets about his father and about being close to his wife. The therapist looked over these worksheets,
102 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
which Tom had done very well. She asked Tom about how helpful they had been, and he reported that they had been very helpful. He added that he was still strug- gling about his father, but that he was beginning to think that it was not all about him, which had made him feel better about himself and less guilty in general. He mentioned that he was considering writing a let- ter to his father about his daughter’s arrival, and that he was thinking about asking his father about why he drank and distanced himself from his family. The therapist reinforced Tom for considering this and for not blindly making assumptions about his role in his father’s drinking. However, she also attempted to inoc- ulate Tom to the possibility that his father could blame him or his siblings for his alcoholism (given that she did not know his father or his history), and that this did not necessarily mean that it was true. She reminded him that he needed to consider the source of information, and that any good detective would get multiple reports. Tom seemed to like the idea of getting more informa- tion from others, mentioning that he and his siblings had never really talked about his belief that they were to blame for their father’s alcoholism.
Tom also shared that he better understood the idea of having intimacy, without sex, in his relationship with his wife. He said that since the birth of their child, he felt closer to his wife and had generally been more open and present to her. The therapist asked him about doing nice things for himself, and Tom laughed and said that he was more open to that but was finding less time to do it with a new baby.
The therapist then asked Tom to read the final Im- pact Statement about the meaning of the event for him after the work that he had done. He read:
“There is no doubt that this traumatic event has deep- ly impacted me. My thoughts about myself, others, and the world were changed. When I started thera- py, I believed that I was a murderer. I blamed myself completely. Now, I believe that I shot a family, but I did not murder them. I realize that I and others around me had to do what we did at the time, and that we chose to shoot because we had to. I will never know what that man, or maybe even the family, was trying to do by going through that checkpoint, but I know now that I had no choice but to shoot to stop them. Regarding safety, I used to think that there were people out to get me, but now I realize that the probability of that is slim. I still feel a little anxious about me, my wife, and now my daughter, getting
hurt, but not by a sniper. That seems unlikely. Now I worry about the stuff that everyone worries about— like crazy drivers, illness, or some accident. About safety, I used to worry that I was going to go ‘off ’ and hurt my family. I don’t believe that I will do that, because I’ve never done that before and basically this trauma messed with my head about how likely I would be to hurt someone unless I had to. I’m trust- ing myself more in terms of the decisions I make, and I have some more faith and trust in my government now that I realize I really needed to shoot in that situation. I think I may always struggle with wanting to have power and control over things, but I’m work- ing on not having control over everything. The fact is, I don’t have control, even though I like to think that I do. My self-esteem is improving. I have to re- member that not every bad thing that happens is my fault, and that I deserve to be happy even if I don’t fully believe it yet. One of the biggest things that seems to be changing is that I’m enjoying being close to my wife and my new daughter. I used to avoid my wife, because I thought I didn’t deserve to be happy and that I might hurt her. Slowly I’m realizing that it is not very likely that I’ll hurt my wife or my new daughter, or at least hurt them intentionally. My wife seems much happier now. I want to hold on to this time in my life and provide a good life for my daugh- ter and wife. I’m happy to know that my daughter is not going to know someone who thought that snipers were out to get him, and who was anxious, avoiding everything and everyone. It sounds silly, but I’m kind of glad that I went through this because I think I’m going to be a better dad and person because of it.”
Tom was a bit teary as he finished reading. The ther- apist asked Tom whether he remembered what he wrote the first time. Tom said no, so the therapist read to him his first Impact Statement. She pointed out that Tom had come a long way, and he agreed. The therapist and Tom reviewed the whole therapy process, what they had covered, and the Stuck Points that Tom had challenged. Tom said that he was going to continue using the work- sheets, because they had been so helpful in making him slow down to think about things instead of just react- ing. They did some relapse planning, and the therapist asked Tom what he could do if he sensed that he was struggling with PTSD or depressive symptoms, or sec- ond-guessing his new ways of thinking. He mentioned that he was going to share the materials with his wife, because she was very good at helping him to “get his
Posttraumatic Stress Disorder 103
head on straight.” He also included on his list a review of the materials he had completed during the course of therapy. The therapy session ended with a discussion of Tom’s goal to write his father a letter and to increase his contact with his siblings. He was planning to use these contacts to discover more about the reasons his father was alcoholic and had seemed to abandon the family. Tom also shared his goals about the type of father and husband he hoped to be, and what his professional fu- ture held as he left the military. The therapist congratu- lated Tom on his willingness to do the hard work to recover from what happened to him and wished him the best with his family and future. Tom expressed his appreciation for the therapy.
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Many people are very shy and somewhat inhibited. For this reason, the suffering associated with social anxiety disorder is often minimized as a common trait in the population that does not require a heavy artillery of formalized treatment interventions (either drugs or psychological treatments). Noth- ing could be further from the truth. For members of a very large segment of the population with de- bilitating social anxiety (over 12% and increasing), at some point in their lives, the seemingly simple process of interacting with people or forming relationships provokes overwhelming terror and is often avoided. The effects on career and quality of life can be devastating. As is increasingly true of our new generation of psychological interventions, cognitive-behavioral approaches have proven to be significantly better than equally credible but less focused psychological interventions, and its effects are increasingly powerful over time. This chapter by Aderka and Hofmann is new to this edition and illustrates a newer cognitive-behavioral approach called “process-based therapy” (PBT) as applied to social anxiety disorder. PBT goes beyond the static DSM approach to diagnosis and more stan- dardized treatment by emphasizing a very idiographic or individual approach to assessment and treatment in the specific context of the patient, along with continual processing and feedback. Thus, treatment may end up looking relatively different from one patient to the next in both content and se- quence. This approach is illustrated in the assessment and treatment of “Mark,” which demonstrates nicely the maturity and clinical sophistication of this remarkable approach to social anxiety. —D. H. B.
We have all felt social anxiety at some point in our lives. Whether it is presenting in front of others,
being on a date, talking in a group, going to a party, or being observed while we are completing a task, so- cial anxiety is ubiquitous and is a natural response in many social situations. However, for some people, so- cial anxiety is so severe that it can lead to substantial impairment in many aspects of daily life. Individuals with social anxiety disorder (SAD) typically fear and avoid situations in which others can evaluate them. In these situations, they fear that they will act in a way (or show anxiety symptoms) that will be embarrassing
or humiliating. Thus, individuals with SAD typically avoid anxiety-provoking social situations or endure them with substantial distress. However, it is important to note that social anxiety is a culture-related experi- ence (Hofmann, Asnaani, & Hinton, 2010) ranging from normative social anxiety that causes little distress or impairment to severe social anxiety and avoidance that can significantly impair one’s ability to function in important areas of life.
SAD is one of the most common psychological dis- orders, and a large epidemiological study conducted in the United States (National Comorbidity Survey Repli-
C H A P T E R 3
social Anxiety A Process‑Based Treatment Approach
Idan M. Aderka Stefan G. Hofmann
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cation Study) found a lifetime prevalence rate of 12.1% for the disorder (Kessler, Chiu, Demler, & Walters, 2005). In a review of community studies from around the world, Furmark (2002) concluded that the preva- lence of SAD is 7–13% in Western countries.
Impairment in SAD can affect all facets of daily life, including relationships, work, and studies (Aderka et al., 2012). Compared to individuals without SAD, those with the disorder are more likely to drop out of school prematurely (Stein & Kean, 2000), to have lower educational attainment (Katzelnick & Greist, 2001; Wittchen, Stein, & Kessler, 1999), to hold jobs below their level of qualification (Katzelnick & Greist, 2001), to have lower income and to be unemployed (Lecru- bier et al., 2000), and even when employed, tend to miss eight times more work days (Wittchen, Fuetsch, Sonntag, Müller, & Liebowitz, 2000). Individuals with SAD report poor quality of life (Alonso et al., 2004), are more likely to attempt suicide (Wunderlich, Bronisch, & Wittchen, 1998), and are more likely to have alcohol and nicotine dependence (Wittchen et al., 1999).
A number of important gender differences exist in SAD. First, women are more likely to have SAD, and this has been replicated in studies across the world (for reviews, see Asher, Asnaani, & Aderka, 2017; Fehm, Pelissolo, Furmark, & Wittchen, 2005; Furmark, 2002). This gender difference in prevalence is greatest among adolescents and seems to diminish along the course of life. In addition to having greater prevalence, women also report greater clinical severity, as indicat- ed by more severe symptoms (Asher & Aderka, 2018), higher levels of social fears (Crome, Baillie, & Taylor, 2012), and a greater number of social fears (Xu et al., 2012). As is true for all anxiety disorders, SAD is more disabling in women than in men, particularly among White women and to some extent also among Hispanic women (McLean, Asnaani, Litz, & Hofmann, 2011). Interestingly, whereas women are more likely to suffer from SAD and demonstrate greater clinical severity, men with the disorder may seek treatment to a greater extent (Asher, Hermesh, Gur, Marom, & Aderka, 2019).
PSYCHOLOGICAL THERAPIES FOR SAD
Researchers have examined the efficacy of many psy- chological treatments for SAD including (but not lim- ited to) cognitive and behavioral treatments, acceptance and commitment therapy (ACT), interpersonal psy- chotherapy (IPT), mindfulness training, attention bias
modification, interpretation training, psychodynamic therapy, and social skills training. A large number of treatment formats have also been examined, includ- ing individual therapy, group therapy, virtual reality exposure treatment, Internet-delivered treatment, and computerized administration (i.e., for attention-bias modification). While a comprehensive and exhaustive review of each of these therapies and treatment formats is beyond the scope of this chapter, we present a general overview of the treatment outcome literature for SAD, with a focus on cognitive-behavioral therapy (CBT), ACT, and other evidence-supported and process-based interventions (e.g., Hofmann & Hayes, 2018).
CBT is the most widely researched treatment for SAD. In a meta-analysis of randomized controlled tri- als for SAD (Carpenter et al., 2018), the authors found a mean controlled effect size of 0.41 of CBT as compared to a placebo condition. Importantly, CBT for SAD has also been found to be effective under less-controlled, real-world conditions (Stewart & Chambless, 2009). Finally, the efficacy of CBT has been demonstrated meta-analytically in individual therapy (Aderka, 2009; Carpenter et al., 2018; Mayo-Wilson et al., 2014), in group therapy (e.g., Wersebe, Sijbrandij, & Cuijpers, 2013), in virtual reality exposure treatment (e.g., Carl et al., 2019; Chesham, Malouff, & Schutte, 2018) and in Internet-delivered treatments (e.g., Kampmann, Em- melkamp, & Morina, 2016).
ACT has also been found to be effective in treating SAD. In a review of studies examining ACT for SAD, moderate to large effect sizes were found across 10 stud- ies (Swain, Hancock, Hainsworth, & Bowman, 2013). Moreover, in a relatively recent trial, ACT was found to be comparable to CBT on most outcome measures of SAD (Craske et al., 2014). ACT was also found to be efficacious in group formats (Kocovski, Fleming, Haw- ley, Huta, & Antony, 2013) and as an Internet-delivered treatment (Ivanova et al., 2016), and was found to be effective in naturalistic settings (Dalrymple & Herbert, 2007).
A number of studies have examined IPT for the treatment of SAD. Lipsitz et al. (2008) examined 70 individuals with SAD who were treated with either IPT or supportive therapy. They found that IPT resulted in significant improvement during treatment. However, IPT was not significantly superior to supportive ther- apy in that study. In another study, Borge et al. (2008) examined 80 individuals with chronic and severe SAD in a residential setting who received either CBT or IPT. They found that both treatments were effective
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and found no differences between the two treatments. Finally, Stangier, Schramm, Heidenreich, Berger, and Clark (2011) randomized 117 individuals with SAD to wait list, cognitive therapy, and IPT. They found that both cognitive therapy and IPT outperformed wait-list. However, CBT was found to be significantly more ef- ficacious than IPT. More recently, Dagöö et al. (2014) examined Internet-delivered versions of CBT and IPT. They found that CBT significantly outperformed IPT in this medium of administration. Thus, most studies find IPT to be an effective treatment for SAD, but in most studies CBT results in superior outcomes.
Mindfulness-based stress reduction (MBSR) was also examined as a treatment for SAD. In a random- ized controlled trial, Goldin et al. (2016) examined the effect of MBSR, CBT, and wait-list on 108 individuals with SAD. They found that CBT and MBSR resulted in similar improvements in social anxiety symptoms and in most additional outcome measures. In contrast, Koszycki, Benger, Shlik, and Bradwejn (2007), who examined CBT and MBSR, found that whereas both treatments improved social anxiety, CBT resulted in better outcomes. Thus, mindfulness may be an effec- tive treatment for SAD, but more studies are required in order to draw firm conclusions on the effect of mind- fulness on social anxiety symptoms.
A PSYCHOLOGICAL MODEL OF SOCIAL ANXIETY
Hofmann (2007) developed an integrated CBT model describing the process by which social anxiety is main- tained and exacerbated. Before we describe the model, it is important to consider that the experience of social anxiety and SAD is heterogeneous (Hofmann, Hein- richs, & Moscovitch, 2004) and not all of the main- tenance factors in the model play an important role for each individual. Rather, it is more likely that some of the maintenance factors are more salient for some individuals than for others. Therefore, an idiographic approach assessing which maintaining processes are relevant for each individual and in different contexts is needed in order to tailor interventions to particular clients (Hayes et al., 2019; Hofmann & Hayes, 2018).
Core Social Anxiety‑Provoking Process
The model describes a circular process that maintains or exacerbates social anxiety (see Figure 3.1). Accord- ing to the model, socially anxious individuals have a
strong desire to make a favorable impression on others but have doubt and uncertainty about their ability to do so (Clark & Wells, 1995; Leary, 2010; Trower & Gil- bert, 1989). This can also be understood as a discrep- ancy between perceived social standards and perceived social abilities (Alden, Bieling, & Wallace, 1994). More specifically, socially anxious individuals perceive social standards to be high while perceiving their own social abilities to be low (Moscovitch, Orr, Rowa, Reimer, & Antony, 2009). This discrepancy results in social ap- prehension regarding one’s performance in social situa- tions and regarding the ability to make a favorable im- pression on others.
Importantly, social standards do not necessarily need to be high to create social apprehension. Research has shown that social apprehension might also arise when standards are ambiguous or poorly defined. For in- stance, Moscovitch and Hofmann (2007) examined individuals with SAD and nonanxious controls who were exposed to cues indicating that standards for per- formance were high, low, or ambiguous prior to being asked to perform a socially threatening task. The results showed that individuals with SAD rated their perfor- mance as being worse in the high and even more so in the ambiguous standards conditions. No group dif- ference in appraisal was observed in the low standards condition. Thus, when standards are poorly defined or ambiguous, individuals with SAD perceive their social abilities as lower and experience enhanced social appre- hension.
Self‑Focused Attention
Social apprehension can lead to heightened self-focused attention, in which individuals shift their attention in- ward and engage in a process of detailed monitoring and observation of themselves (Hirsch, Clark, Mathews, & Williams, 2003). This shift in attention has a number of negative consequences that can enhance anxiety. First, physiological symptoms are perceived as more salient when attention is directed to them. Thus, so- cially anxious individuals become more aware of their anxiety-related physiological symptoms (e.g., blushing, trembling, sweating) and the symptoms are perceived as more salient, thus increasing anxiety (“What if some- one would notice my blushing/trembling/sweating?”). Second, under conditions of high self-focused attention, socially anxious individuals experience spontaneous, re- current, and excessively negative self-images that they believe to be accurate at the time they occur (Hack-
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mann, Surawy, & Clark, 1998; Hackmann, Clark, & McManus, 2000; Hofmann & Heinrichs, 2003). These negative images can also exacerbate anxiety. Third, self-focused attention can lead to reduced externally fo- cused attention and can lead socially anxious individu- als to miss important positive cues from others during social interactions (e.g., someone smiling).
Cognitive and Emotional Processes Enhanced by Self‑Focused Attention
Self-focused attention experienced in socially threaten- ing situations can also spark or enhance a number of additional cognitive and emotional processes. One such process is negative self-perception, in which cognitions about the inferiority, inadequacy, or flaws of the self are experienced more saliently (Beck & Emery, 1985;
Clark & Wells, 1995; Rapee & Heimberg, 1997). An- other such cognitive process is perceived poor social skills, in which socially anxious individuals underestimate their skills, abilities, and actual performance in social situations (e.g., Rapee & Lim, 1992). A third cognitive process is high estimated social cost, in which the conse- quences of one’s inability to meet social standards are perceived as catastrophic or disastrous. Consistently, socially anxious individuals believe that negative so- cial events are more likely to occur than positive social events (Lucock & Salkovskis, 1988), and assume that most people are inherently critical of others and are likely to evaluate them negatively (Leary & Kowalski, 1995). The fourth process enhanced by self-focused at- tention is low perceived emotional control. Specifically, socially anxious individuals believe that they have little control over their emotional response in threatening so-
Social Apprehension
Heightened Self- Focused Attention
High Estimated Social Cost
Low Perceived Emotional Control
Perceived Poor Social Skills
Postevent Rumination
Negative Self- Perception
Anticipation of Social Mishap
Avoidance and Safety Behaviors
High Perceived Social Standards and Poorly Defined Social Goals
FIGURE 3.1. A psychological model of social anxiety. Copyright © 2007 Stefan G. Hofmann. Used by permission.
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cial situations and that this lack of control can be easily noticed by other people.
Emotional Processes
Whereas the model developed by Hofmann (2007) focused specifically on emotional control, more recent theoretical thinking (e.g., Hofmann, 2014), as well as empirical studies (e.g., Kashdan & Steger, 2006; Kash- dan et al., 2013), have identified a number of emotional processes related to social anxiety and SAD. Thus, in this chapter, we present an update and expansion of the Hofmann (2007) model based on theoretical models and empirical studies of emotion in social anxiety and SAD. Specifically, we focus on three emotional pro- cesses: emotion differentiation, experiential avoidance, and emotion regulation. All three emotional processes can be viewed as contributing to the lack of control over emotions associated with social anxiety and SAD.
Emotion differentiation is defined as the degree to which a person is able to classify felt experiences into discrete emotion categories (Kashdan & Farmer, 2014). It also refers to the level of specificity with which peo- ple distinguish between their emotional states (Erbas, Ceulemans, Koval, & Kuppens, 2015). A number of re- searchers (e.g., Boden, Thompson, Dizén, Berenbaum, & Baker, 2013; Kashdan, Barrett, & McKnight, 2015) have proposed that effective emotion regulation is large- ly dependent on knowledge of experienced emotions that are targeted for regulation. Put differently, it is harder to regulate or control emotions one cannot name or differentiate as a distinct state. Individuals with SAD have been found to have difficulties differentiating be- tween negative (but not positive) emotions (Kashdan & Farmer, 2014) and this can contribute to low perceived emotional control about anxiety and other negative emotions experienced in social situations.
Experiential avoidance reflects efforts to control or avoid unpleasant internal events, such as distressing emotions, negative thoughts, and unwanted physical sensations (Hayes, Wilson, Gifford, Follette, & Stro- sahl, 1996). Experiential avoidance can lead to low perceived emotional control, because when emotions are avoided, they become more difficult to regulate or influence. In addition, experiential avoidance may re- sult in paradoxical effects and increase the experience of the emotion one is trying to avoid (e.g., Campbell-Sills, Barlow, Brown, & Hofmann, 2006; Gross & Levenson, 1997). This can result in a flood of negative emotions that are then more difficult to control. In two examina-
tions of individuals with and without SAD using expe- rience sampling, Kashdan et al. (2013, 2014; Study 1) found that compared to healthy controls, individuals with SAD reported greater use of experiential avoidance in their daily, face-to-face interactions, and this associa- tion could not be attributed to comorbid anxiety and depressive disorders. Moreover, the experiential avoid- ance–social anxiety association was greater for individ- uals with SAD compared to healthy controls (Kashdan et al., 2014, Study 1). Finally, Dalrymple and Herbert (2007), examined individuals with SAD who under- went ACT. Results showed that treatment resulted in reductions in both experiential avoidance and SAD symptoms. Moreover, changes in experiential avoid- ance predicted subsequent changes in SAD symptoms along the course of therapy.
Emotion regulation can also contribute to low per- ceived emotional control. Specifically, individuals with SAD have been found to rely excessively on expressive suppression, which is associated with negative social and emotional consequences, and to use cognitive reappraisal ineffectively, thus inhibiting the potential positive emo- tional benefits of this strategy (see Dryman & Heim- berg, 2018, for a review). These difficulties in regulating emotions may lead to low perceived emotional control.
Avoidance and Safety Behaviors
Avoidance and safety behaviors constitute a central part in the model, as they create a feedback loop that maintains anxiety. Whereas the term avoidance reflects avoidance of certain anxiety-provoking situations be- fore they occur (this is similar to the concept of situ- ation selection in emotion regulation models; Gross, 1998), safety behaviors reflect any attempt to reduce anxiety or avoid it within social situations (this mirrors the concept of situation modification in emotion regu- lation models). Both forms of avoidance are the result of anxiety and serve as potentially maladaptive strategies to regulate anxiety, and both forms of avoidance inad- vertently increase anxiety in the long term, thus cre- ating the maintaining feedback loop. Adopting safety behaviors in social situations has been found to lead to diverse negative effects for socially anxious individuals, such as impaired performance (Rowa et al., 2015), in- creased momentary anxiety (for a review, see Piccirillo, Taylor Dryman, & Heimberg, 2016), and even feelings of inauthenticity and interpersonal rejection, which further fuel future anxiety (Plasencia, Taylor, & Alden, 2016; Taylor & Alden, 2010).
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Postevent Processing
Postevent processing refers to a process that follows stress- ful social situations. During postevent processing, so- cially anxious individuals mentally review the social interaction in detail, with a focus on anxious feelings and negative self-perceptions. This process of focusing on negative aspects typically leads socially anxious in- dividuals to recall the interaction as being more nega- tive than it actually was and results in elevated anxiety regarding future situations. For example, Abbott and Rapee (2004) found that compared to individuals with- out social anxiety, individuals with SAD had a more negative appraisal of an impromptu speech task imme- diately following the task. In addition, whereas indi- viduals with SAD maintained their negative appraisal through the week following the task and engaged in more rumination and postevent processing, individuals without social anxiety developed a more positive atti- tude about their performance along the week.
PROCESS‑BASED THERAPY OF SOCIAL ANXIETY
The treatment described in this chapter is based on a process-based approach (Hayes & Hofmann, 2018; Hofmann & Hayes, 2018). Rather than have a predeter- mined structure to treatment, with certain sessions in- cluding specific interventions in a particular order, the process-based approach strives to provide therapists and clients with more flexibility. The approach describes a wide range of possible interventions that can be applied flexibly based on an idiographic analysis that is tailored to the client and to a particular context. For instance, some individuals with SAD have very salient negative self-perceptions and perceptions of poor social skills, and these may be treated by cognitive reappraisal and modifying core beliefs, whereas others’ social anxiety may have a strong emotional component, with difficul- ty differentiating between negative emotions and a fear of anxiety and related emotions, and these are better treated by psychoeducation on emotions, working on emotion differentiation, and cultivating psychological acceptance. Even for the same individual, salient fac- tors may vary between contexts. For instance, socially anxious individuals may be extremely concerned with physiological symptoms and the possibility that oth- ers will notice and judge them negatively when giving a presentation in front of a class, but be much more
concerned with their appearance and poor social skills (“I’ll say something stupid, or boring”) when on a date. Thus, a careful idiographic analysis that considers the individual and context represents an important first step in the selection and implementation of any inter- vention in this treatment.
Based on the large interpersonal diversity and diver- sity in contexts, interventions to consider can include contingency management, stimulus control, shaping, self-management, arousal reduction, coping and emo- tion regulation, problem solving, exposure strategies, behavioral activation, interpersonal skills, cognitive reappraisal, modifying core beliefs, cognitive defusion, cultivating psychological acceptance, values choice and clarification, mindfulness practice, enhancing motiva- tion, and crisis management (for a detailed description of these interventions, see Hayes & Hofmann, 2018). In this chapter we focus on three of these interventions that we consider especially relevant to most individuals with SAD and high social anxiety: cognitive restructur- ing, exposures and behavioral experiments, and emo- tion differentiation and regulation.
Stages of PBT of Social Anxiety
PBT of social anxiety includes a three-stage process that is repeated throughout treatment: contextual id- iographic assessment, intervention, and processing and feedback. It begins with a contextual idiographic as- sessment that identifies a target for intervention. This assessment is intended to be collaborative process in which both client and therapist examine a particular context or situation and use the client’s unique knowl- edge of him/herself and the therapist’s unique knowl- edge of psychology (e.g., the model described earlier) to formulate a shared understanding of the process occur- ring in that particular context and to identify targets for intervention. For instance, sometimes clients share that they have stressful situations in their immediate future, such as a party, a presentation, or a date, and these situ- ations become the focus of inquiry. Other times, the therapist can suggest a possible context based on his/ her familiarity with the client. However, this process of generating a shared understanding of the situation and choosing a target for intervention is always collabora- tive. Many times, the process also includes drawing a schematic of the relevant processes (i.e., drawing a sim- plified version of the model that is person- and context- specific). This contextual model or schematic captures the joint understanding of client and therapist, and it
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is important that clients feel that the model is a good representation of their experience.
Once a collaborative understanding has emerged, and a target for intervention is identified, we enter the intervention stage, which includes choosing, planning, and implementing an intervention. For instance, if the model identified an important safety behavior in a certain context (e.g., rehearsing topics for conversation before a date), then planning an exposure while drop- ping the safety behavior represents a valid option (e.g., asking questions based on what the partner said rath- er than preplanned topics). However, for every target identified, there are usually multiple potential interven- tions. For instance, cognitive reappraisal focusing on rehearsing topics may also be an option, as well as strat- egies cultivating acceptance of the anxiety experienced due to the uncertainty of not knowing the topics of conversation before an actual conversation takes place. Choosing an intervention is also a collaborative process that takes into account context, client preferences and values, and therapist experience and knowledge.
After an intervention is chosen and implemented, processing the intervention and eliciting feedback can take place. Processing the intervention includes discuss- ing the client’s experiences during the intervention. It may also include discussing what was learned as a result of the intervention, or what went wrong and prevented meaningful learning. Finally, receiving feedback on the intervention is essential in order to decide whether to adapt or change the intervention and conduct it again (e.g., if something went wrong, was misunderstood, was not properly planned), whether to choose a different in- tervention for the same target, or whether to move on to a different context or therapeutic target. Thus, elicit- ing feedback provides essential information that can in- form the next cycle, beginning with idiographic assess- ment (i.e., the second cycle of idiographic assessment will include information about the client’s experiences and processing of the first intervention).
To summarize, the PBT manual for social anxiety operates differently than some manuals. Whereas man- uals typically arrange content and interventions along sessions (e.g., first, three sessions of cognitive restruc- turing, followed by six sessions of exposure exercises), PBT flexibly includes any content or intervention based on a contextual idiographic assessment. One way to fa- cilitate and guide contextual idiographic assessment is by using a functional-analytic network based on the ex- tended evolutionary meta-model (EEMM; Hayes et al., 2019). This is by no means the only way to conduct or
organize a contextual idiographic assessment; rather, it represents a specific comprehensive assessment scheme that considers the potential contribution of various di- mensions and levels to the particular problem space of a given individual.
The EEMM (Figure 3.2) utilizes a number of dimen- sions to describe target problems. Specifically, problems can be described as having one or more of the following facets or existing on one or more of the following di- mensions: affective, cognitive, attentional, self-related, motivational, and overt behavioral. For each of these dimensions, problems can involve variation, selection, retention, and context issues. For instance, if a client has a negative automatic thought every time he/she talks to a particular person at the office, this problem can be conceptualized as belonging to the cognitive dimension and involving low variation (i.e., the client has access to this thought but not to other, alternative thoughts) and a strong context component (a particu- lar person at the office). Potential interventions could target variation (e.g., developing alternative thoughts) and facilitate selection of appropriate and helpful ways of thinking. Applying such interventions in a way that takes context into account (e.g., applying them at the office) and maximizes retention (e.g., applying them with other people in the office first and with the target person later) is also important. Specific treatment strat- egies for target problems are discussed below.
Cognitive Reappraisal
Cognitive reappraisal refers to the process of changing the meaning of a stimulus or situation, in order to alter emotional responses (Gross, 1998). This process can in- clude helping clients to adopt new perspectives; to think about themselves, others, their lives, and everyday situ- ations in different ways; and to consider multiple view- points on important issues. Cognitive reappraisal can be divided into three stages: identifying maladaptive thinking, evaluating maladaptive thinking, and modi- fying maladaptive thinking (Wenzel, 2018).
Identifying maladaptive thinking, the first stage of cognitive reappraisal, typically involves identifying a context or situation in which clients recently expe- rienced high levels of negative affect and asking them questions to elicit their thoughts. Clinicians can ask questions such as “What was going through your mind during the situation?” or “What were you thinking about when X happened?” Whereas these may seem like easy questions to answer, not all clients find it
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easy to verbally describe their thoughts. When eliciting thoughts is difficult for clients, therapists can ask them to guess their own thoughts, or to guess what some- one else may have been thinking in a similar situation. Therapists can also suggest several possible thoughts and see whether clients identify with one or more of these thoughts.
Identifying maladaptive thinking can be seen as the basis for later stages of cognitive reappraisal, but it can also have therapeutic value in and of itself. Specifi- cally, the process of identifying maladaptive thoughts increases awareness of internal psychological processes and facilitates a connection with one’s experiences. This can serve to reduce experiential avoidance and increase one’s ability to fully experience the present moment.
Once thoughts are identified, and clients and therapists become familiar with clients’ maladaptive thoughts, a process of evaluation can begin. In evaluat- ing maladaptive thoughts, it is important for therapists to refrain from adopting an overly challenging, criti- cal, or superior stance. Rather, joining clients from a position of curiosity, while attempting to facilitate discovery of additional information and examination of additional possible points of view, usually leads to
better results. The idea is to evaluate thoughts together and learn more about them. Questions that facilitate this evaluation may include “What is the evidence for and against this thought?”; “What additional explana- tions exist?”; “What is the best, the worst, and the most realistic things that can happen?”; “What would you tell a friend or family member if they were in a similar situation?”; “What are the consequences of focusing on this thought versus thinking differently or focusing on something else?” This list of questions is by no means exhaustive, but it can serve as an example of possible questions that may spark a process of jointly discover- ing more about clients’ thoughts and becoming familiar with additional perspectives.
Modifying maladaptive thinking, the third and final stage of cognitive reappraisal, refers to a collaborative process in which clients (with therapist guidance) de- velop alternative, more balanced thoughts using the discoveries made in the evaluation stage. The goal of this stage is not to remove maladaptive thoughts, re- place maladaptive thoughts, or discard thoughts that are “wrong.” Rather, the goal is to incorporate new in- formation into existing thoughts to create a more bal- anced or a multifaceted way of thinking.
FIGURE 3.2. The extended evolutionary meta-model (EEMM) for organizing target problems and identifying appropriate interventions. Copyright © 2019 Steven C. Hayes and Stefan G. Hofmann. Used by permission.
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For instance, a male client of one of the authors (I. M. A.) was anxious about an upcoming date. He identified a number of maladaptive thoughts related to his anticipatory anxiety, but a central and representa- tive thoughts was “I’ll mess it up. She’ll hate me and won’t want to see me anymore.” During the evaluation stage, the therapist asked the client whether this chain of events is bound to happen and represents 100% of all possible scenarios. When the client replied negatively, it sparked a discussion of alternative scenarios for the date. Incorporating these scenarios with the original thought, the client was able to develop the following perspective: “It is absolutely possible that I will mess it up, that she’ll hate me and never want to see me again. In fact, it is an integral part of any date. However, it is also possible that things won’t be that bad. We could get along, she may like me, and we could see each other again. It’s also possible I won’t like her and won’t want to keep seeing her. Actually, I won’t really know until we go on the date.” This type of flexible and multi- faceted thinking retains the original thought but views it as a single outcome among many possible outcomes, while accepting the inherent uncertainty when meeting someone new.
To summarize, cognitive reappraisal is a process of collaboratively identifying, evaluating, and modifying maladaptive thoughts. As mentioned earlier, a number of maladaptive thoughts can play an important role in maintaining social anxiety (e.g., negative self-percep- tions and perceived poor social skills). The process of cognitive reappraisal can be used to target these ele- ments (or additional thoughts pertaining to anticipa- tory anxiety, postevent processing, and other sections of the model).
Exposure and Behavioral Experiments
Exposure is a collaborative process in which the client (with the therapist’s guidance) chooses to systematically enter situations or approach stimuli that provoke fear, anxiety, or other negative emotions. This definition highlights three important characteristics of exposure. First, it is a collaborative process. Thus, effective ex- posures are not “prescriptions” administered to clients by therapists. Rather, choosing exposures and planning them is part of a collaborative discussion in which goals, rules, and definitions of success are discussed and mu- tually agreed upon. Second, the client makes an explicit choice to enter situations or approach stimuli. Thus, client agency and volition are extremely important in
exposure and represent the approach behavior required to facilitate new learning. Third, exposure is systematic and includes planning, gradual progression, and appro- priate repetition. Exposure can be divided into three stages: establishing the rationale for exposure, choos- ing and planning exposures, and processing exposures (after their completion).
Establishing the rationale for exposure is extremely important, as clients are unlikely to engage in expo- sures without a clear and compelling rationale. As PBT aims to enhance flexibility and use individually tailored interventions based on idiographic assessment, we pro- vide three possible rationales for exposure that can be presented to different clients with different character- istics. The first is the behavioral rationale for exposure that is centered on habituation. According to this ratio- nale, repeated exposure to anxiety-provoking situations results in habituation, and emotional experiences and reactions to these situations gradually decline with re- peated exposures. The second rationale is the cognitive rationale for exposure, centered on creating cognitive change or achieving new learning as a result of expo- sure. Exposures with this rationale are typically referred to as behavioral experiments. This rationale is based on the idea that without exposure, clients do not test their thoughts and beliefs about themselves, others, or anxi- ety (or only do so only in a philosophical or theoretical way). However, during exposure, clients can test beliefs and use their real-world experience to guide new learn- ing and facilitate cognitive change. This rationale is also similar to the concept of collaborative empiricism, in which therapist and client design experiments (i.e., ex- posures) to test beliefs. The third rationale for exposure, the emotional rationale, focuses on fully experiencing emotions and cultivating acceptance of these emotions (i.e., reducing experiential avoidance). According to this rationale, exposure is used to approach emotions that are typically avoided, and to experience these emo- tions without fighting them or avoiding them. Such an experience reduces fear of emotions, and enhances acceptance and tolerance of emotions. These rationales can be used separately or in combination to facilitate discussions with clients on exposure.
Choosing and planning exposures is the second stage of this intervention. To facilitate appropriate selection of exposures, a hierarchy can be jointly established to guide decision making. In a hierarchy, situations or po- tential exposures are organized by level of anxiety or difficulty. When selecting exposures, we typically rec- ommend starting with situations that elicit 30–40% of
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the maximum anxiety and gradually increase levels of anxiety in subsequent exposures based on client prog- ress. An alternative strategy for selecting exposures is to choose situations that not only provoke anxiety that is clearly experienced (or situations that the client per- ceives as significantly difficult), but also exposures that the client feels he/she can complete. Exposures that are perceived as both difficult and possible are typically chosen.
Once an exposure has been chosen, planning can begin. As we described in the model, individuals with SAD typically have ambiguous standards or poorly de- fined goals in social situations. Thus, when planning exposures, goals must be clearly defined to prevent pathological maintaining processes from undermining the intervention. Goals need to be objectively defined and must include behaviors that are under the cli- ent’s control. Having a 15-minute conversation with a stranger is an example of a poorly defined goal, because it not specific and involves other people who are not under the client’s control. However, initiating a conver- sation with an employee at the supermarket and asking two questions is a much better goal, because it is more clearly defined and under the client’s control. Goals must be individually tailored to specific clients, con- texts, and the particular thoughts or beliefs that need to be examined. When planning exposures, eliciting predictions from clients can be very helpful (e.g., “The anxiety will last for hours”, “Everyone will be mean to me the entire time”). Eliciting predictions that are clear and objectively defined can facilitate cognitive change by being juxtaposed with actual outcomes when pro- cessing completed exposures.
The final stage of exposure includes the processing of completed exposures. If the goals for the exposure are met, therapists should praise clients and highlight cli- ents’ achievement, accomplishment, and success (e.g., “You’ve just done something that you’ve avoided for so long! I’m sure it was tempting to skip this exposure and find an excuse not to do it, but you chose to take the hard way, and this is quite an accomplishment”). While devoting time to bolster clients’ sense of achievement may be easily overlooked in therapy, recent research clearly demonstrates its centrality in treatment. For in- stance, in one of the largest treatment studies, which in- cluded over 90,000 sessions, therapist praise was found to be the best predictor of therapeutic outcomes in CBT (Ewbank et al., 2019). Along these lines, increases in self-efficacy as a result of completing exposures were found to predict improvement from exposure therapy
(Jones & Menzies, 2000). If exposure goals are not met, therapist and client should discuss the exposure to un- derstand what might have gone wrong and decide on alterations to be made for future exposures (e.g., reduc- ing the difficulty level of the next exposure, changing goals, or selecting a different context).
Another important part in the processing of expo- sures is discussing the meaning of the exposure, and what was learned in the exposure. Important questions to ask clients include “What have you learned from completing this exposure?” and “What do you know now that you didn’t know before?” Discussing the out- comes of exposure and the new learning that occurred are important to facilitate consolidation of cognitive change.
To summarize, the exposure is one of the most ef- fective interventions for social anxiety. The rationale for exposures should be discussed, and clients need to “buy-in” before exposures can be implemented. Expo- sures are then systematically planned and executed; fi- nally, exposures are processed after they are completed in order to enhance client self-efficacy, to elicit feed- back and gather information to be used in future inter- ventions, and to consolidate new learning.
Enhancing Emotional Processes
Individuals with SAD and socially anxious individu- als display a reduced capacity to differentiate between negative emotions. This is important, as it is almost im- possible to regulate emotions or accept emotions one cannot differentiate. Thus, for some socially anxious individuals, work on emotion differentiation may be a prerequisite for work on emotion regulation and emo- tional acceptance.
Work on emotion differentiation can utilize a num- ber of tools or techniques. First, psychoeducation on emotions is extremely important, not only psychoedu- cation on emotions in general, their function, and their patterns of experience (as is done in many treatments), but also psychoeducation on discrete emotions, their definitions, and the differences between them. For in- stance, discussing the differences between shame and guilt, anger and frustration, and despair and loneliness, and delineating the contexts in which these emotions are experienced and the cognitions associated with them provides a good foundation for emotion differ- entiation. Another important tool in facilitating emo- tion differentiation is an Emotion Log, in which clients monitor and record emotions during the week. This log
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(which also includes context/situation and thoughts) can help clients recognize different emotions and is also discussed and processed in therapy to further enhance learning. A third tool for enhancing emotion differen- tiation is reading vignettes and guessing others’ emo- tions. For clients who find it difficult to identify their own emotions, practicing emotion identification and differentiation using vignettes of others may be a help- ful alternative.
Once clients become better at identifying and nam- ing their emotions, and better at differentiating be- tween them, work on emotional regulation or emo- tional acceptance can begin. One way to help clients improve their emotion regulation capabilities is to prac- tice cognitive reappraisal (see the previous section) in multiple contexts, and for multiple emotions (Aldao & Plate, 2018). This is important, as regulating certain emotions may be more difficult than others for a par- ticular client and context. For example, even if socially anxious clients experience heightened levels of anxiety, practicing reappraisal when experiencing anger, guilt, loneliness, or shame may prove very valuable. Practicing reappraisal in different contexts (e.g., within the ses- sion, at home alone, with close others, with strangers, and at work) is also very helpful for enhancing clients’ capacity to regulate their emotions.
Another emotional skill that can be viewed as com- plementary to emotion regulation is emotional accep- tance (Forsyth & Ritzert, 2018). Emotional acceptance reflects a focus on accepting emotions as they are and adopting an intentionally open, receptive, flexible, and nonjudgmental posture with respect to moment-to- moment experience (Hayes, Strosahl, & Wilson, 2012). Practicing mindfulness of one’s emotions is an excel- lent way to facilitate emotional acceptance. In mindful- ness exercises, clients practice observing their emotions, along with the physical sensations that accompany them, in a nonjudgmental and curious way. Mindful- ness helps clients experience their emotions as they are, without trying to change or alter them, and without struggling with them or avoiding them. Another set of exercises that facilitate emotional acceptance is defu- sion exercises. In these exercises, the focus is on creat- ing distance between internal stimuli, such as thoughts and emotions, and the self. When we are “fused” with our emotions, these emotions determine our behavior without additional input. Thus, defusion strives to cre- ate distance between emotions and the self, so that val- ues and other considerations can also guide behavior. When experiencing emotions in this way, there is no
need to fight them, avoid them, or alter them in any way. Rather, one can experience these emotions as they are, and still make decisions and behave according to one’s values. Thus, defusion can help facilitate emo- tional acceptance.
While in no way an exhaustive list, cognitive reap- praisal, exposure, and behavioral experiments and emo- tion-focused interventions represent important inter- ventions to consider when treating social anxiety. PBT includes the flexible implementation of these interven- tions based on repeated contextual idiographic assess- ment conducted throughout treatment. The following case study exemplifies the use of these strategies.
CASE STUDY
Presenting Problem
“Mark,” a 25-year-old man, sought treatment due to intense anxiety he experienced in interpersonal interac- tions. Mark reported that he was constantly concerned about saying something strange, odd, silly, or irrelevant and fearing that other people would judge him, think negatively of him, and ultimately decide to keep their distance. Mark described one-on-one conversations as particularly distressing and mentioned that he rarely shared personal information about himself, as well as thoughts and feelings, with others in an attempt to keep conversations as brief as possible. He described himself as insecure and his voice as too soft. Interacting with women was intimidating and anxiety provoking to Mark, and he shared that he had never been in a romantic relationship, and in fact had never been on a date. Mark said that there was a girl in college who had shown romantic interest in him, but he felt he could not handle the anxiety of meeting her, being on a date, and disclosing personal information about himself, and he ultimately decided to avoid her. When reflecting on this, Mark said he both wanted the relationship but was even more terrified of it, which led to his decision to withdraw.
History
Mark, the youngest of three siblings, described his re- lationship with his parents as close and caring. Mark was raised in a Jewish household and felt that religion was an important part of his life. At school, Mark ex- celled academically and never had any behavior prob- lems. However, some interpersonal difficulties emerged
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as early as elementary school. Mark did not like talk- ing in front of the class and refrained from answering questions even when he knew the correct answers. He had a few close friends (two or three) but always found it difficult to form new relationships, and he typically avoided parties and other social events in his teens. After graduating from high school, Mark studied soft- ware engineering in college. He reported experiencing substantial test anxiety that was compounded by the competitive atmosphere in college. Specifically, he had trouble sleeping before tests and found it difficult to concentrate while studying or while taking some of the tests. Despite this anxiety, Mark did well academically and graduated with good grades. Socially, Mark avoid- ed parties and many social activities. He said that such parties (with alcohol or drugs) were inconsistent with his religious values, but, in fact, he also avoided other social activities he was interested in (e.g., writing class). Mark made some friends during college, but he viewed these connections as superficial and did not keep in touch after graduating. Instead, he remained in touch with his childhood friends, with whom he felt more comfortable. After graduation, Mark began to work at a software company and rented a small apartment. Mark’s childhood friends were all in romantic relation- ships, and some were engaged to be married. To Mark, this, as well as his difficulties forming new relationships at work, indicated that something was clearly “wrong” with him. As time went by, he felt increasingly isolated and began to think that his social anxiety would never go away, and would prevent him from living a full, sat- isfying life. He decided to seek psychological treatment.
Pretreatment Assessment
Mark underwent a structured diagnostic interview: the Anxiety Disorders Interview Schedule for DSM-5 (ADIS-5; Brown & Barlow, 2014). Mark met criteria for primary SAD, with a clinician severity rating of 5 (on a scale of 0–8, with 4 being the clinical cutoff), and also met criteria for comorbid major depressive dis- order, with a clinical severity rating of 4. Mark com- pleted a number of self-report measures, including the Liebowitz Social Anxiety Scale—Self-Report version (LSAS-SR; Liebowitz, 1987), the Social Phobia Inven- tory (SPIN; Connor et al., 2000), the Social Anxiety Questionnaire (SAQ; Caballo, Arias, Salazar, Irurtia, & Hofmann, 2015), the Social Thoughts and Beliefs Scale (STABS; Turner, Johnson, Beidel, Heiser, & Lyd- iard, 2003), the Beck Depression Inventory–II (BDI-II;
Beck, Steer, & Brown, 1996), and the Sheehan Disabil- ity Scale (SDS; Sheehan, 1983).
Mark’s total score on the LSAS-SR was 72. This score is above the cutoff of 60, which indicates clini- cal levels of severity (Rytwinski et al., 2009). Similarly, Mark’s score on the SPIN was 39, which is above the clinical cutoff of 20 (Connor et al., 2000) and repre- sents moderate to high levels of clinically significant social anxiety. Finally, Mark’s score on the SAQ was 110, which is above the clinical cutoff of 89 for men (Caballo et al., 2015). Importantly, the LSAS-SR focus- es on 24 commonly encountered social situations (e.g., going to a party) and assesses anxiety and avoidance for each of these situations. In contrast, the SPIN ex- amines symptoms of social anxiety in general, without necessarily referring to a particular situation (e.g., fear of criticism or blushing in general). Thus, these mea- sures can be seen as complementary, with the LSAS-SR being highly contextualized but focused only on symp- toms of anxiety and avoidance, whereas the SPIN is less contextualized but includes many additional symptoms (e.g., physiological and cognitive symptoms). Finally, a unique aspect or advantage of the SAQ over both the LSAS-SR and SPIN is having separate empirically de- rived cutoffs for men and women. This is extremely im- portant, as gender differences play an important role in social anxiety (Asher et al., 2017). Thus, the SAQ can be viewed as more gender-sensitive.
Mark’s score on the STABS (a measure of social anx- iety-related cognitions) was 50, which is above the clini- cal cutoff of 40 (Turner et al., 2003). Mark’s score on the BDI-II was 21, which indicated a moderate level of depression. He did not endorse any suicidal thoughts. His scores on the SDS were 6 for work, 9 for social life, and 4 for home. This indicates a moderate impairment at work, a marked impairment in social life, and a mild impairment in family life or home responsibilities.
Establishing the Therapeutic Alliance and Identifying Treatment Goals
Establishing a strong therapeutic alliance is important in every treatment, and creating a strong science of the therapeutic relationship is an important aspect of pro- cess-based therapies (Hofmann & Hayes, 2018). The therapeutic alliance has been shown to predict treat- ment outcome above and beyond therapeutic orienta- tions (for a meta-analysis, see Flückiger, Del, Wampold, & Horvath, 2018), and this predictive utility may hold even when symptom improvement is taken into ac-
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count (e.g., Zilcha-Mano, Dinger, McCarthy, & Bar- ber, 2014). The therapeutic alliance has three impor- tant facets: bond, goals and tasks (Bordin, 1979). Bond refers to the emotional connection between therapist and patient (e.g., the extent to which both members of the therapeutic dyad like, respect, and trust one an- other). Goals refers to agreement on the goals in therapy (or the therapeutic focus at any given point in therapy), and tasks refers to agreement on the actions needed to achieve these goals (e.g., the interventions used, the roles of the therapist and patient in these interventions). A strong therapeutic alliance can facilitate many of the interventions in treatment (e.g., exposure is likely to be facilitated when trust exists in the therapeutic dyad) and may also be beneficial in and of itself (having a strong alliance with the therapist may serve as a positive implicit model for other relationships in the patient’s life). For a detailed discussion of these two potential contributions of the therapeutic alliance to cognitive and behavioral interventions see Persons (2008).
During the first session, the therapist asked Mark a number of open-ended questions about the reasons that led him to seek treatment, and about his main areas of difficulty. This is typically a good way to help cli- ents to talk and share their thoughts and feelings, and can generally lead to good rapport. However, Mark’s replies were very brief, and it seemed that he had a hard time elaborating and disclosing personal information. He would typically respond with two or three brief sen- tences, then become anxious over the ensuing silence. The therapist quickly adjusted and began to take a more active role in the session. Specifically, the thera- pist began asking questions that were more specific and helped guide Mark through the story (“And what hap- pened then?”; “How did you feel when this happened?”; “What was going through your mind?”; Did anything else happen before this occurred?”). In addition, the therapist decided not to focus solely on Mark’s expe- rience during the session but also to begin discussing certain aspects of the model described earlier and to examine whether Mark felt those aspects were relevant to him or resonated with him. This type of back-and- forth helped the conversation flow more smoothly, and helped to foster an atmosphere of curiosity about what the therapist and treatment had to offer.
Over the next few sessions, the therapist focused on facilitating a strong therapeutic alliance by discuss- ing and agreeing on goals and priorities, and broadly discussing what would be required to meet these goals (i.e., addressing the tasks facet). Specifically, Mark and
the therapist discussed Mark’s depression and social anxiety and how to prioritize these issues. The therapist asked Mark what he wanted to focus on in treatment, and whether he viewed depression or social anxiety as his bigger concern. The therapist also used the “magic wand” metaphor and asked Mark whether he believed his social anxiety would remain if the therapist were able to use a wand to magically remove the depression, and whether he believed his depression would remain if the therapist were able to magically remove the so- cial anxiety. Mark replied that his social anxiety would probably remain if the depression were removed, but that he would not be depressed if his social anxiety ceased to be an issue. As a result of this collaborative decision-making process, Mark and the therapist col- laboratively decided that addressing social anxiety would be their priority in treatment. Once this decision was made, the therapist and Mark began to discuss vari- ous contexts in which Mark felt impaired by his social anxiety and began to prioritize these contexts. Mark and the therapist decided that despite the fact that ro- mantic relations represented the context in which Mark felt most impaired, they would initially focus on other, less impaired contexts (i.e., work) to begin practicing skills. Then, they would target the more difficult con- texts using the skills acquired and the lessons learned from work-related contexts.
Once goals and overarching strategy were set, the therapist shared his thoughts on the interventions that would likely be helpful. He told Mark that they would probably spend some of their time in therapy examin- ing Mark’s thoughts, and getting to know them. He also added that they might devote time to discussing and developing new ways of thinking about social situa- tions and about Mark’s experience and behavior in such situations. Finally, the therapist noted that the idea that thoughts are merely thoughts, and do not always ad- equately represent the world or ourselves, might also be explored. This would mean developing a different way of thinking about thoughts or of relating to them. The therapist also discussed the importance of exposure to social situations. He initiated a discussion of avoidance and anxiety, and the relationship between them, and also guided Mark in examining his previous behavior problems (which included a fair amount of avoidance) and their long-term consequences. The therapist then suggested that the approach in treatment could be one that strives to engage in previously avoided situations to reduce anxiety in the long term by experiencing it in the short term. Finally, the therapist said that they might
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adopt a focus on feelings in some sessions. Emotion- focused interventions could help Mark get to know his own emotions (and emotions in general) to a greater extent. In this approach, feeling emotions and describ- ing the experience would be goals even if the feelings were unpleasant. These discussions served a number of goals: (1) to prepare Mark for future interventions; (2) to involve Mark in decisions regarding potential in- terventions as part of a collaborative process; and (3) to receive Mark’s input and thoughts regarding these interventions (such input can facilitate clinical decision making further along the course of treatment).
In addition to working on the therapeutic alliance and reaching agreement on goals and tasks (as well as cultivating an atmosphere of collaboration), Mark and the therapist began to conduct contextual idiographic assessment. Specifically, they reviewed three possible work-related situations and drew a model for each situ- ation or context (based on the general model of SAD presented earlier; i.e., Hofmann, 2007). These situa- tions included asking a coworker for help, asking Mark’s boss for a day off in person (rather than via e-mail), and initiating a conversation with someone at work he does not know (or has not spoken to before). These were all situations Mark had indicated were difficult and anxi- ety provoking for him, and through the contextual id- iographic assessment, Mark and the therapist were able to learn much about the processes occurring in these contexts, the similarities between them, and the unique aspects of each one. For instance, while negative self- perception played a role in all three contexts, perceived poor social skills and anticipation of mishap were es- pecially pertinent when initiating a conversation with someone at work he did not know. Mark’s thoughts for that situation were “I wouldn’t know what to say”; “I’m not good at making small-talk”; “I’ll say something awkward or irrelevant”; “He/she will not want to talk to me.” Safety behaviors were also different for each context. Mark and the therapist were able to identify specific safety behaviors Mark might use when asking for help (e.g., beginning the request with an apology or a lengthy explanation of the reasons for asking help), when requesting a day off in person (e.g., not making eye contact with his boss), and when initiating small- talk with someone for the first time (e.g., rehearsing topics for conversation in advance). Using contextual idiographic assessment, Mark and the therapist were able to enhance their understanding of Mark’s social anxiety and the processes maintaining it in each of these contexts. Figure 3.3 is a schematic of the model
drawn during one of these sessions (based on a dynamic network approach; Hofmann, Curtiss, & Hayes, 2020).
Cognitive Restructuring
During contextual idiographic assessment, Mark and the therapist were able to identify a large number of negative automatic thoughts Mark experienced dur- ing social situations at work. Mark seemed to learn this skill quickly and was able to formulate his thoughts and put them into words with relative ease. He also made several statements that suggested he was able to view these thoughts as irrational—at least in the context of therapy. For instance, in the discussion about asking his boss for a day off, Mark said he was worried that his boss would be upset with him for the request, or angry because it might cause delays in Mark’s work. After identifying that thought, Mark immediately went on to say that he knows days off are part of his job, that his coworkers take days off regularly, and that this does not seem to have any negative effect on their productivity or on their relationships with the boss. Mark’s ability to easily identify negative automatic thoughts, as well as his ability to view them as inaccurate or exaggerated, suggested to the therapist that using cognitive restruc- turing in this context was likely to be helpful.
To facilitate cognitive restructuring, the therapist used a technique that differentiates between Mark and his social anxiety, and creates some distance or defu- sion between the two (e.g., Barrera, Szafranski, Rat- cliff, Garnaat, & Norton, 2016; Kocovski, Fleming, & Rector, 2009; Kross, Gard, Deldin, Clifton, & Ayduk, 2012). In this way, negative automatic thoughts are at- tributed to social anxiety, whereas the more rational view is attributed to the self (i.e., Mark). This implicitly helps Mark identify with more rational alternatives and creates an alliance between Mark and the therapist in their joint effort to deal with (the distanced or defused) social anxiety. In addition, thinking of social anxiety as an entity that is (in part) distinct from Mark has the advantage of facilitating discourse between Mark and his social anxiety.
THERAPIST: What do you think would go through your mind if you were to ask your boss for a day off in person?
MARK: I think I would be worried that he would be disappointed or mad that I was taking time off. That maybe it would delay some of the things I am cur- rently working on.
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THERAPIST: I can completely understand. By taking some time off, you are concerned that your boss would think you are abandoning some of your work or your responsibilities. Do you think you could write those thoughts down and formulate them the same way we did with those previous thoughts?
MARK: Sure. (writing and reading aloud) “My boss will be disappointed or mad at me for taking time off.” (looking at the text) I mean, I know it doesn’t make any sense. Everyone can take time off, and my co- workers do it all the time, and everything is just fine. It’s just when I need to do it, I get anxious.
THERAPIST: I think you are saying something impor- tant here. You know that, realistically, there is noth- ing wrong with asking for time off. Yet when you do, it’s as if the social anxiety is telling you that it is wrong. That your boss will be mad at you or disap- pointed in you. And that makes you start to waver. You get anxious.
MARK: I’ve never thought of it in that way before. THERAPIST: That sounds like a good sign to me. We’re
here to see if we can think about things differently. What do you think you could say back to the social
anxiety after it says that your boss would be disap- pointed or mad?
MARK: Well, exactly what I said before—that other people do it all the time and it’s fine.
THERAPIST: Those are great replies! Is there anything else you can say back?
MARK: I’m not sure. THERAPIST: What about thinking about previous times
you asked for time off? Did your boss ever express disappointment or anger?
MARK: No. He was always perfectly fine with things. THERAPIST: So you could probably reply to the social
anxiety that in all previous instances, things went smoothly.
MARK: That’s right. (taking some time to think) I could also say that my boss takes time off, too. In fact, he was gone for quite a while recently.
THERAPIST: Great job! I like where you’re going with this. What do you think you would tell a friend who came to you with such an issue? How would you sug- gest the friend think about it, or what should he/she say to his/her social anxiety?
FIGURE 3.3. Dynamic network model for Mark. Thicker arrows represent stronger connections between model compo- nents.
Asking for a Day Off Feeling
Anxious
Negative Automatic Thoughts
“He’ll refuse my request”
Safety Behaviors
Apologize in Advance
Self-Efficacy Diminished
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MARK: That the friend shouldn’t care too much about what the boss thinks. He/she can take a day off if he/ she wants to, that he/she is entitled to days off, even if the boss doesn’t like it.
THERAPIST: That sounds great. So we have a number of possible replies to the social anxiety in this situation if it tries to stress you out again. How does that feel?
MARK: It feels pretty good. I think I was so busy being anxious, I never thought I could answer back and change things.
THERAPIST: You’re absolutely right. When we think differently, we often feel differently as well. I think you just experienced that.
Mark responded very well to cognitive restructuring in work contexts. With the therapist’s guidance, he was able to develop alternative thoughts (i.e., replies to his social anxiety) and use them. Mark felt empowered by this skill, and his ability to distance himself from his so- cial anxiety and “talk back” to it helped him feel more confident and increased his self-efficacy.
Exposure and Behavioral Experiments
Encouraged by Mark’s success with cognitive restruc- turing, Mark and the therapist turned their attention to exposures/behavioral experiments at work. They began planning such exposures, with an emphasis on defin- ing goals in a precise, objective, and clearly defined way (because ambiguous goals have been shown to increase and maintain social anxiety; e.g., Moscovitch & Hof- mann, 2007), as well as ensuring that goals always re- main within Mark’s control and do not include others’ responses or Mark’s own anxiety. For instance, the goal of having a conversation when everyone else responds positively or displays interest is clearly out of our control and therefore not a helpful goal in exposure. Similarly, having a conversation while experiencing no anxiety or minimal anxiety is also not particularly helpful as a goal, as it involves emotions that are not under our di- rect or explicit control. In addition, it might convey the (inaccurate) message that anxiety is “bad” and should be reduced as much as possible (as opposed to anxiety being a natural human emotion that needs to be expe- rienced in full, yet does not always have to dictate our actions).
While planning exposures, Mark and the therapist recorded their decisions and other important informa- tion by creating an exposure form (in Mark’s handwrit-
ing). An example of this form for the exposure of initi- ating a conversation with a coworker appears in Figure 3.4. This form includes both a planning section that is completed with the therapist in the session before the exposure takes place, and a processing section that is completed with the therapist in the following session.
THERAPIST: As we did for the previous exposures, we are only setting goals that are under your control. This way, success or failure depends solely (or as much as possible) on you.
MARK: I remember. But how can we do that when it is a conversation with someone else? Don’t things always depend on the other person?
THERAPIST: That is an excellent question. Just like you said, when we have a conversation with someone else, the conversation always depends on the other per- son. However, in an exposure we can set goals that only depend on your behavior. For example, we can decide that the first goal is to initiate the conversa- tion. So the goal would be to make sure you are the one that approaches and begins talking, rather than being the one who responds to something someone else says. Another goal could be asking two ques- tions. Meeting the goal doesn’t depend on whether the other person answers or the way he/she responds. It just has to do with you asking the questions. Even if someone is in a hurry, you can usually get to ask a couple of questions. For example, asking how the person’s weekend was, and if he/she is in a rush and can’t talk right now, you can still ask when would be a good time to chat. So even in this worst-case sce- nario, it is possible to ask two questions.
MARK: I understand. But it would be pretty terrible if someone responded that way. I am sure it wouldn’t feel like success. That’s probably the worst thing that could happen. It means that just like I thought, peo- ple don’t want to talk to me because I’m weird and I don’t know how to have a conversation.
THERAPIST: I completely understand. If your goal is to have a conversation with someone, then not being able to do so would feel like a failure. But in our case, we are interested in something else. You can’t control other people, and you’re right that you could poten- tially experience rejection. However, I am suggesting that success in our case is being able to risk being re- jected. Rejection can happen. We’ve all been rejected, and I know it feels terrible and none of us like it, but
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FIGURE 3.4. Exposure form (planning and processing sections).
Exposure 3: Initiating conversation with a coworker with whom I have never spoken before Exposure Planning Time and place Monday morning (before lunch time) at work
Goals 1. Initiate conversation with Jack, a coworker of mine.
2. Ask Jack at least two open-ended questions.
3. Do not do anything to end the conversation.
Things that may appear to be goals but are not 1. Jack’s responses (Even if Jack answers briefly, shows little interest, can’t talk when I initiate the
conversation, ignores me, or says something mean—my success depends only on my three goals.)
2. My experience of anxiety and other emotions (My anxiety and emotions are not under my direct control, so they can’t define my success. Even if I get very anxious, I can succeed if I meet my three goals. In fact, if I meet goals while being extremely anxious, it can even be considered a bigger success.)
Safety behaviors 1. Not making eye contact (I am dropping this safety behavior.)
2. Rehearsing topics or questions for conversation (Is OK for now, but I will drop this next time.)
Negative automatic thoughts (or predictions) 1. I will say something stupid or weird.
2. Jack will not want to talk to me.
Alternative thoughts 1. It’s possible I’ll say something stupid, but most of the time I say things that are fine.
2. Even if I say something stupid and Jack will not want to talk to me, I will feel bad for a couple of days, but the feeling will go away and it’s not the end of the world.
Exposure Processing What actually happened? Jack was really nice. We talked for a few minutes and things were fine. We also started saying hello in the mornings after our talk.
What have I learned from this exposure? Things aren’t always as bad as they are in my thoughts. I can do things even if I’m anxious.
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it’s out of our control. But being able to risk rejection is extremely important, and that’s what we are prac- ticing here. Taking a risk instead of avoiding things in the first place, that is success.
MARK: Risking rejection . . . (mulling it over) That’s very different from what I’ve always done, isn’t it? It’s not easy.
THERAPIST: Absolutely. It’s very hard, and may require mustering all our strength, but it can also be very helpful.
MARK: So I just walk up to someone and start asking questions?
THERAPIST: In a way. We will plan it, get all the details right, and make sure that you are able to benefit the most from doing this. Let’s start with who the per- son will be. Do you have someone in mind? Someone from work that you haven’t really spoken to?
MARK: Well, there is this one person. His office is down the hall from mine. He seems nice, but I’ve never really talked to him.
THERAPIST: So definitely a possibility. What’s his name?
MARK: Jack. THERAPIST: Anyone else you think we should consider?
Maybe a woman from the office? MARK: (looking terrified) No, no. That’s much harder.
I’ll probably freeze and won’t be able to talk at all. THERAPIST: OK, so it sounds like we’ll be starting with
a man, and then see how things go and what the next steps can be. When would be a good time to approach someone and start talking?
Mark and the therapist then went on to discuss and record all the details of the exposure (see Figure 3.4). In our experience, the more time devoted to agreeing on all the relevant details, to discussing possible scenarios, to addressing others’ possible responses and Mark’s anxiety (and how they are unrelated to success in the exposure), and the more individually tailored the ex- posure is, the better the results. Thus, especially in the first exposures, spending a substantial amount of time preparing for exposures can be very helpful.
Over a number of sessions, Mark and the therapist planned and executed a series of exposures at work. After every exposure, the therapist devoted time to pro- cess Mark’s experience during the exposure, to praise him for conducting the exposure and meeting his goals,
and to discuss what Mark learned from the exposure and how that changes his perceptions of himself, his anxiety, and others (see Figure 3.4 for an example). Mark reported substantial improvements at work: His anxiety dropped, alternative thoughts began emerging, and Mark’s belief in them grew, and he was able to ex- pand his behavioral repertoire by initiating conversa- tions with coworkers, asking for help, and joining oth- ers for lunch. Mark reported that he felt much better at work, that he was more comfortable, and less anxious.
Strategies Focusing on Emotional Processes
Despite Mark’s improvement at work, his difficulties in romantic relationships remained unchanged for the most part. Thus, there was little generalization of new learning from work contexts to social life/romantic re- lations contexts. Mark and the therapist conducted an- other contextualized idiographic assessment to increase their understanding of this context and the potential challenges and barriers to change that may be present. This analysis provided a wealth of important informa- tion.
First, Mark shared an experience of being completely overwhelmed by his emotions, “freezing up,” not being able to talk or move, and just feeling terrified of what was happening to him. The feeling was so aversive that even thinking about it or imagining it made Mark want to escape it and talk about something else. This strong, overwhelming, and paralyzing emotional response was not present in work contexts and represented a unique aspect of the context of romantic relations. When the therapist discussed this feeling with Mark and referred to it as anxiety, Mark replied that it felt like “much more” than anxiety. The therapist inquired about this feeling, but Mark only said that the feeling was some sort of wave of emotion that came crashing down on him. Mark would frequently talk about the intensity of the emotions and their overwhelming nature, but his descriptions were always broad and general, and lacked emotional granularity or specificity. For Mark, the con- text of romantic relations included a strong component of lack of control over emotions that was related to dif- ficulty differentiating between emotions, regulating emotions, and experiential avoidance. The therapist believed that the emotional barrage that Mark was feel- ing represented a core component maintaining Mark’s social anxiety in romantic relations.
A second factor that arose during this contextual idiographic assessment involved Mark’s values and,
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in particular, his religion and spirituality. Both values (Hayes et al., 2012), and religion and spirituality in particular (Rosmarin, Pargament, & Mahoney, 2009; Rosmarin, Auerbach, Bigda-Peyton, Björgvinsson, & Levendusky, 2011), can play an important role in psy- chotherapy. Specifically, during the contextual idio- graphic assessment, the therapist suggested that as part of the strategy in treatment, Mark could create a profile on a dating site, write women he was interested in meet- ing, and work toward dating. Mark’s reply made it clear that this suggestion was not aligned with his values. He replied that in his community, dating was typically ar- ranged by family members or acquaintances who would introduce single individuals for this purpose. Mark said that he preferred meeting women this way and that he viewed dating sites as being “only for sex.”
Following the contextual idiographic assessment, it was clear to the therapist that an exposure-based strat- egy would be a poor fit for Mark in this context, despite being successful in other contexts. Mark’s emotional response was too substantial and was likely to interfere with developing the sense of self-efficacy needed in ex- posures. Moreover, relying on others to arrange dates meant that this was not under Mark’s direct control, and that the number of potential dates may be limit- ed. PBT is ideal for these situations, because it allows flexibility in the use of therapeutic interventions rather than adherence to a strict session-based protocol. Using the information gathered from contextual idiographic assessment, Mark and the therapist decided to dedicate the next sessions to emotion-focused interventions.
As a first step, Mark and the therapist engaged in psychoeducation on emotions. This psychoeducation included a discussion of emotions in general, their function, and their patterns of experience, as is done in many treatments for anxiety. Importantly, the therapist emphasized that emotions represent a natural part of human experience, that emotions change quite rapidly, and that they provide important information for us about ourselves and others. While this information can and should be used to inform daily decisions, it should not be relied upon solely, and other factors (e.g., think- ing rationally, values) should also contribute to our decision-making process. This balance, or reliance on multiple sources of information (including emotions) was discussed as a healthy way to make decisions in our lives. Thus, Mark and the therapist began discussing two goals for the emotion-focused interventions: (1) to experience emotions as fully and completely as possible
(without fighting them or avoiding them) and (2) to base decisions on multiple considerations including not only emotions but also values, future goals, and rational thinking.
In addition to this common form of psychoeduca- tion, Mark and the therapist began to focus on discrete emotions to increase familiarity with them, and facili- tate differentiation and granularity. A greater focus was given to negative emotions, as individuals with SAD have been shown to have impaired differentiation of negative but not positive emotions (Kashdan & Farmer, 2014). Specifically, Mark and the therapist discussed anxiety, frustration, envy, guilt, embarrassment, shame, anger, loneliness, sadness, and despair. They described these emotions, defined them, and discussed the con- texts that commonly lead to these emotions, as well as associated thoughts, bodily sensations, and metaphors for these emotions.
For instance, when discussing envy, they described and defined it as an emotion arising when someone else possesses something (either material or immaterial) that we desire yet do not perceive ourselves to have. We can envy others for having more money than we do, for their appearance, for certain traits that they possess (whereas we do not), and so forth. They also discussed a number of facts about this emotion (derived from research in psychology). For instance, that the more similarity ex- ists between the envied individual and the self (in ev- erything but the desired feature) the greater the envy (Smith & Kim, 2007). Similarly, the more central the desired trait or feature is to one’s self-esteem, the greater the envy (Smith & Kim, 2007). Finally, they talked about how, sometimes, envy can be associated with a desire “to become” the other person and sometimes it can be associated with thoughts of harming the other person to reduce the perceived discrepancy between the self and the envied individual (van de Ven, Zeelenberg, & Pieters, 2009). When discussing envy, Mark noted that the Bible included a number of stories about this emotion, such as Joseph’s story (his brothers envied him, wronged him, and were ultimately punished for it). This was an important moment in therapy, because Mark was able to connect the content discussed in the sessions with his values, religious beliefs, and spiritual- ity. The therapist and Mark discussed how the broth- ers were punished not for experiencing the emotion in the first place, but for acting on it and harming some- one else. This contributed to the distinction between experiencing emotions (which is viewed as a natural
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part of human experience) and acting solely based on these emotions, without considering the consequences (which may lead to adverse outcomes).
After Mark and the therapist concluded their discus- sion of discrete emotions, they began to practice identi- fying these emotions and differentiating between them. The therapist described hypothetical daily scenarios that were likely to evoke certain emotions, and Mark was tasked with identifying the emotions. Mark and the therapist then discussed these scenarios and how Mark was able to determine the likely emotion experienced by the protagonist. Then, the therapist asked Mark to describe a situation in which he felt that particular emo- tion. This enhanced Mark’s ability to identify emotions and differentiate between them, with regard to others’ behavior and to himself. Mark was encouraged to iden- tify three situations during the week in which he saw other people behave or speak in way that suggested they were experiencing a certain emotion, as well as three situations in which he experienced an emotion (three different emotions). Mark logged these situations, de- scribed them, and brought the log in to the following session for processing.
In the final step of the work on identifying and dif- ferentiating between emotions, Mark began to differen- tiate and disentangle the lump of emotions he felt when interacting with women, and especially in romantic contexts. Mark imagined previous interactions he had with women at the office and at school, and identified his emotional response. Mark was able to see that he did experience not only anxiety in these situations (“She’ll think I’m weird and won’t want to talk to me”) but also frustration (“Why do I always feel like this when I talk to women?”), shame (“I hope she won’t see how anx- ious I am”), envy (“How come everyone else can do this so easily but I can’t?”), and despair (“I’m a lost cause. I’ll never be able to have a normal relationship with a woman”). This represented a significant improvement in Mark’s ability to identify and differentiate between his emotions, and he began seeing his emotional re- sponse as a number of different emotions rather than as a nameless lump of overwhelming emotional experi- ence.
The therapist and Mark also conducted two in-ses- sion exposures. Specifically, the therapist invited two fe- male therapists (one in each session) to conduct “getting acquainted” conversations with Mark. Mark’s goals in these interactions were (1) to feel his emotions as fully as possible, without fighting them or avoiding them;
(2) to continue to interaction regardless of emotional reactions; and (3) following the interaction, to identify, discuss, and process his emotional experience with the therapist. While these can be considered exposures, it is important to note that the rationale for using these interventions was not to facilitate habituation of emo- tional responses, nor was it to examine beliefs or pre- dictions Mark had about himself and/or others in such situations. The sole focus was on experiencing emotions and processing them in a way that enhanced Mark’s emotional vocabulary and reduces fear and avoidance of these emotions (i.e., reduces experiential avoidance).
Mark was extremely anxious about these conversa- tions, and the therapist reminded him that these were opportunities to practice date-like situations, to experi- ence the associated emotions, to get to know them bet- ter, and to make sure they did not solely control Mark’s behavior. The therapist told Mark that, in a way, he was gradually owning more and more of his emotional space rather than avoiding it and leaving the emotions to run rampant. Mark benefited greatly from these exposures and was able to complete the interactions despite being highly distressed. Mark learned that he could talk to women while being distressed and did not necessarily need to avoid his emotions or run from them. More- over, feedback from interaction partners that his inner turmoil was less visible to others than he perceived was also valuable to Mark, as it helped him realize that the presence of his emotions did not mean that conversa- tions needed to be avoided.
In the last portion of Mark’s therapy, he began to go on dates (for the first time in his life). Mark quickly found that dates were not necessarily the terrifying en- counters he had feared and were more akin to everyday conversations. In one of these sessions, Mark compared dating to a job interview that, while being stressful, did not need to be overwhelming. Mark was surprised at first that women showed interest in him, but he gradu- ally became more confident as this process continued. At this point in therapy, the therapist focused on pro- cessing these dates with Mark, on Mark learning new things about himself and others in a dating context, and on helping Mark both disclose information so that his dates could get to know him and do his best to get to know his dating partners.
Whereas therapy did not conclude with Mark in a ro- mantic relationship, he was able to date several women (one for a period of 4 weeks) and felt that his anxiety and impairment were greatly reduced. Mark suggested
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that he could continue on his own, and that he had overcome the barriers that made dating a herculean task for him. He felt his next challenge was to find a partner with whom he felt he had a good fit.
At termination, Mark’s scores on self-report measures were 35 on the LSAS, 12 on the SPIN, 80 on the SAQ, 20 on the STABS, and 6 on the BDI-II. He reported that his impairment was 3 for work, 4 for social life, and 2 for home. These scores reflect substantial improve- ment, and symptom levels were below clinical levels.
PREDICTORS OF TREATMENT SUCCESS
A number of predictors of success (and failure) have been addressed throughout this chapter (e.g., the thera- peutic alliance). In addition to such predictors, we would like to emphasize the importance of client mo- tivation and client preferences, and their relationship with the process-based model we described.
Clients who are not motivated to change, or who experience high levels of ambivalence toward change, are at higher risk for treatment failure in any treat- ment (Miller & Rollnick, 2012). Thus, using contex- tual idiographic assessment to assess client motivation is important and can inform therapeutic interventions. For some clients, evoking motivation and reducing bar- riers for change is extremely important and may be a prerequisite for the success of other empirically based processes. Motivation-focused strategies (e.g., motiva- tional interviewing; Miller & Rollnick, 2012) should be utilized and prioritized in such cases.
Client preferences regarding interventions should also be taken into consideration. This was true for Mark in the case presented in this chapter, and it has also been empirically supported across contexts and treat- ments (see Lindhiem, Bennett, Trentacosta, & McLear, 2014, for a meta-analysis). Client preferences should be assessed during contextual idiographic assessment and used to inform treatment decisions. Interventions that are perceived by clients as inappropriate, insufficient, irrelevant, or inferior to other options are unlikely to be successful. In such cases, conducting an in-depth discussion with clients regarding the intervention and its rationale is important, but if clients do not “buy-in,” alternative interventions should be used by therapists. Typically, multiple interventions can be used to achieve any particular goal or therapeutic target. This allows therapists the flexibility needed to tailor treatment to particular clients and their preferences.
SUMMARY
In this chapter, we have described PBT and how it can be applied to the treatment of social anxiety. We believe that this treatment offers flexibility to clients and thera- pists and can be used to provide individually tailored, empirically supported interventions that can reduce so- cial anxiety and its associated impairment and improve quality of life among individuals with social anxiety and SAD.
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It will not take the reader long to see that successful therapy for obsessive–compulsive disorder (OCD) is markedly different in both structure and content from the usual therapeutic approaches. For this reason, regrettably, few therapists feel self-efficacious enough to undertake this therapy, yet this approach is clearly the treatment of choice for the most beneficial short- and long-term effects in OCD according to clinical trials. The information provided in this detailed chapter should be sufficient for any reasonably well-trained mental health professional to undertake this treatment, particularly if few other options are available. The suffering involved with OCD can be extraordinary, and even imperfect attempts at therapy can relieve much of this suffering. This chapter describes the detailed conduct of intensive daily sessions involving both imaginal and direct in vivo practice. Also noticeable is the ingenuity required of therapists (e.g., “Where do you find dead animals?”). The importance of involving significant others continues a theme first described by Craske, Wolitzky-Taylor, and Barlow in Chapter 1 of this volume, in which spouses/partners or other people close to the individual with the problem become an important and integral part of treatment. Finally, this chapter contains an up-to- date review of the current status of psychological and pharmacological approaches to OCD. —D. H. B.
Advances in cognitive-behavioral and pharmaco- logical treatments in the last four decades have
improved the prognosis for patients with obsessive– compulsive disorder (OCD). In this chapter we first discuss diagnostic and theoretical issues of OCD and review the available treatments, then describe assess- ment procedures and illustrate in detail how to imple- ment intensive cognitive-behavioral treatment (CBT) involving exposure and ritual prevention (EX/RP) for OCD. Throughout the chapter, we use case material to illustrate interactions that occur between therapist and patient to demonstrate the process that occurs during treatment.
DEFINITION
According to the 11th edition of the International Clas- sification of Diseases (ICD-11; World Health Organiza- tion, 2021), OCD is characterized by recurrent obses- sions and/or compulsions that interfere substantially with daily functioning (Stein et al., 2016). Common obsessions are repeated thoughts about causing harm to others, contamination, and doubting whether one locked the front door. Common compulsions include handwashing, checking, and counting. OCD is cat- egorized among obsessive–compulsive and related dis- orders (e.g., Stein et al., 2010, 2016), which highlight
C H A P T E R 4
Obsessive–Compulsive Disorder
Martin E. Franklin Edna B. Foa
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the formal and functional similarity between OCD and several other disorders that involve intense anxi- ety and associated compulsions (e.g., body dysmorphic disorder [BDD]), as well as those involving repetitive behaviors that appear to be driven by appetitive urges (e.g., trichotillomania [hair pulling], excoriation [skin picking] disorder; Stein et al., 2016).
The functional link between obsessions and compul- sions is emphasized: Obsessions are defined as thoughts, images, or impulses that cause marked anxiety or dis- tress, and compulsions are defined as overt (behavioral) or covert (mental) actions that are performed in an at- tempt to reduce the distress brought on by obsessions or according to rigid rules. This modification was sup- ported by findings from a large field trial on OCD, in which over 90% of participants reported that the aim of their compulsions was either to prevent harm associated with their obsessions or to reduce obsessional distress (Foa et al., 1995).
Data from that same large field study also indicated that the vast majority (over 90%) of individuals with OCD manifest both obsessions and behavioral rituals. When mental rituals are also included, only 2% of the sample report “pure” obsessions (Foa et al., 1995). Be- havioral rituals (e.g., handwashing) are equivalent to mental rituals (e.g., silently repeating special prayers) in their functional relationship to obsessions: Both serve to reduce obsessional distress, to prevent feared harm, or to restore safety. Thus, whereas all obsessions are in- deed mental events, compulsions can be either mental or behavioral. Identification of mental rituals is an espe- cially important aspect of treatment planning, because obsessions and compulsions are addressed via different techniques. For example, we once treated a patient who described himself as a “pure obsessional,” who would ex- perience intrusive and unwanted images of harm com- ing to his girlfriend by an animal attack. The patient would quickly and intentionally insert his own image into the scene to become the victim of the animal maul- ing, thereby reducing his distress and, in his estimation, reducing the likelihood that some future harm would come to his girlfriend. The substitution of his own image into the scene constituted a mental ritual, and the success of imaginal exposure exercises required that the patient refrain from this form of compulsion.
Increased consensus about a continuum of insight in individuals with OCD (e.g., Foa et al., 1995; Insel & Akiskal, 1986) led to designation of a subtype of OCD “with poor insight” to include individuals who
indeed have obsessions and compulsions but fail to rec- ognize their senselessness (Stein et al., 2016), although clinicians had difficulty applying a three-level insight qualifier ( fair-to-good insight, poor insight, no insight) to OCD case vignettes (Kogan et al., 2020). Individuals are classified as having good or fair insight, poor in- sight, or absent insight/delusional beliefs, reflecting an even greater recognition of a continuum of insight in OCD (Leckman et al., 2010). Clinically, it is impor- tant to evaluate the degree of insight prior to initiating CBT, because fixed belief about the consequences of re- fraining from compulsions and avoidance behaviors has been found to be associated with attenuated treatment outcome (e.g., Foa, Abramowitz, Franklin, & Kozak, 1999; Neziroglu, Stevens, Yaryura-Tobias, & McKay, 2000; Visser et al., 2017).
To be diagnosed with OCD, obsessions and/or com- pulsions must be found to be of sufficient severity to cause marked distress, be time-consuming, and inter- fere with daily functioning. If another Axis I disorder is present, the obsessions and compulsions cannot be restricted to the content of that disorder (e.g., preoc- cupation with food in the presence of eating disorders).
PREVALENCE AND COURSE
Once thought to be an extremely rare disorder, the 12-month prevalence of OCD was estimated at 1.0% in the National Comorbidity Survey Replication in- volving over 9,000 adult participants in the United States (Kessler et al., 2005). Epidemiological studies with children and adolescents suggest similar lifetime prevalence rates in these samples (e.g., Dalsgaard et al., 2020; Flament et al., 1988; Valleni-Basille et al., 1994). Slightly more than half of adults suffering from OCD are female (Rasmussen & Tsuang, 1986), whereas a 2:1 male to female ratio has been observed in several pedi- atric clinical samples (e.g., Hanna, 1995; Swedo, Rapo- port, Leonard, Lenane, & Cheslow, 1989). Age of onset typically ranges from early adolescence to young adult- hood, with earlier onset in males; modal onset is ages 13–15 in males, and ages 20–24 in females (Rasmus- sen & Eisen, 1990). However, cases of OCD have been documented in children as young as age 2 (Rapoport, Swedo, & Leonard, 1992).
Development of the disorder is usually gradual, but acute onset has been reported in some cases. Although chronic waxing and waning of symptoms are typical,
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episodic and deteriorating courses have been observed in about 10% of patients (Rasmussen & Eisen, 1989). In some cases of pediatric OCD and tic disorders, onset is very sudden and associated with streptococcal infection; treatment of the infection is associated with substantial reduction of symptoms, but recurrence of infection is again associated with symptom exacerbation (Swedo et al., 1998). Presentation of OCD in these cases, which is much more typical in males than in females, came to be known as “pediatric autoimmune neuropsychiatric dis- orders associated with streptococcal infection” (PAN- DAS) and has more recently been revised and broad- ened under the umbrella term “pediatric autoimmune neuropsychiatric syndrome” (PANS; Swedo, Leckman, & Rose, 2012); the prevalence of PANDAS or PANS has yet to be determined. OCD is frequently associ- ated with impairments in general functioning, such as disruption of gainful employment (Koran, 2000; Leon, Portera, & Weissman, 1995; Torres et al., 2006) and interpersonal relationship difficulties (Emmelkamp, de Haan, & Hoogduin, 1990; Riggs, Hiss, & Foa, 1992; Torres et al., 2006). Adolescents identified as having OCD (Flament et al., 1988) reported in a subsequent follow-up study that they had withdrawn socially to prevent contamination and to conserve energy for ob- sessive–compulsive behaviors (Flament et al., 1990). Many individuals with OCD suffer for years before seeking treatment (e.g., García-Soriano, Rufer, Del- signore, & Weidt, 2014). In one study, individuals first presented for psychiatric treatment over 7 years after the onset of significant symptoms (Rasmussen & Tsu- ang, 1986). The disorder may cause severe impairment in functioning that results in job loss and disruption of marital and other interpersonal relationships. Marital distress is reported by approximately 50% of married individuals seeking treatment for OCD (Emmelkamp et al., 1990; Riggs et al., 1992).
COMORBIDITY
Convergent epidemiological and clinical data indicate that OCD rarely occurs in isolation: Although the rates of comorbidity differ across studies due to selec- tion of population and methodology, comorbidity is generally high. For example, Weissman and colleagues (1994) found that 49% of individuals diagnosed with OCD suffered from a comorbid anxiety disorder and 27% from comorbid major depressive disorder (MDD).
Among studies conducted specifically within anxiety clinics, there is great variability, but comorbid condi- tions are generally common (for a review, see Ledley, Pai, & Franklin, 2007). In the largest of the studies conducted in the context of an anxiety clinic, Brown, Campbell, Lehman, Grisham, and Mancill (2001) found that 57% of 77 adults with a principal diagnosis of OCD had a current comorbid Axis I condition; the rate rose to 86% for lifetime comorbid Axis I condi- tions. Notably, when OCD co-occurs with other anxi- ety disorders, it is typically the principal diagnosis (e.g., the diagnosis of greatest severity; see Antony, Downie, & Swinson, 1998). It also appears to be the case that MDD onset tends to follow that of OCD, suggesting that depression might be a response to OCD symptoms (Bellodi, Sciuto, Diaferia, Ronchi, & Smeraldi, 1992; Diniz et al., 2004).
The data are equivocal with respect to the influence of comorbidity on OCD presentation. In one study, Denys, Tenney, van Megen, de Geus, and Westenberg (2004) found that comorbidity did not influence OCD symptom severity, whereas others (Angst, 1993; Tukel, Polat, Ozdemir, Aksut, & Turksov, 2002) found a rela- tionship between comorbidity and OCD symptom se- verity. A more consistent finding is that comorbidity is associated with poorer quality of life, particularly in the case of comorbid depression (Lochner & Stein, 2003; Masellis, Rector, & Richter, 2003).
With respect to the effect of comorbid anxiety and depression on treatment outcome, the influence of de- pression has received more empirical attention to date. Some studies have found that higher levels of depres- sion at pretreatment are related to poorer outcome (e.g., Keijsers, Hoogduin, & Schaap, 1994; Steketee, Chamb- less, & Tran, 2001), whereas others have found little or no effect (Mataix-Cols, Marks, Greist, Kobak, & Baer, 2002; O’Sullivan, Noshirvani, Marks, Monteiro, & Lelliott, 1991; Steketee, Eisen, Dyck, Warshaw, & Rasmussen, 1999). Some have suggested that, more specifically, the severity of the comorbid depression might influence its effects on OCD treatment outcome: Abramowitz, Franklin, Street, Kozak, and Foa (2000) found that only severely depressed patients were less likely to respond to EX/RP therapy for OCD. Simi- larly, highly depressed patients with OCD seem to be at greater risk for relapse following treatment discon- tinuation (Abramowitz & Foa, 2000; Basoglu, Lax, Kasvikis, & Marks, 1988). The influence of comorbid anxiety disorders on outcome has received less attention
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thus far: One study reported that patients with OCD and comorbid generalized anxiety disorder (GAD) ter- minate OCD treatment at higher rates than other pa- tients (Steketee et al., 2001), and another found that the presence of posttraumatic stress disorder (PTSD) in patients with OCD attenuated response to EX/RP (Gershuny, Baer, Jenike, Minichiello, & Wilhelm, 2002). Within pediatric OCD specifically, comorbidity other than a second anxiety disorder (e.g., externaliz- ing disorder, mood disorder) was associated with poorer acute response to CBT (Storch et al., 2008), and an- other report indicated that comorbid attention-deficit/ hyperactivity disorder (ADHD) specifically attenuated CBT outcomes at follow-up among children and ado- lescents (Farrell, Waters, Milliner, & Ollendick, 2012). Notably, the mechanisms by which these comorbid conditions influence outcome have yet to be explored.
Tourette syndrome and other tic disorders also ap- pear to be related to OCD, although not sufficiently to be grouped within obsessive–compulsive and related disorders (Stein et al., 2016). Estimates of the comor- bidity of Tourette syndrome and OCD range from 28 to 63% (Comings, 1990; Kurlan et al., 2002; Leckman & Chittenden, 1990; Pauls, Towbin, Leckman, Zahn- er, & Cohen, 1986). Conversely, up to 17% of patients with OCD are thought to have Tourette syndrome (Comings, 1990; Kurlan et al., 2002; Rasmussen & Eisen, 1989). The relationship between tic comorbidity and treatment outcome are complex: in one study the presence of tics was associated with poorer treatment outcome (Matsunaga et al., 2005) while in another trial, tic comorbidity decreased pharmacotherapy treat- ment outcome but not outcome of CBT (March et al., 2007). In a more recent trial of CBT augmentation in youth on an SRI, tic status did not predict outcome to any treatment (Conelea et al., 2014); tics also did not predict outcome to CBT alone in a large trial of youth with OCD who were not receiving any SRIs (Højgaard et al., 2017).
DIFFERENTIAL DIAGNOSIS
The high comorbidity of OCD with other disorders noted earlier, as well as the similarity between the crite- ria for OCD and other psychiatric disorders, can pose diagnostic quandaries. Below we review some of the more common diagnostic difficulties likely to confront clinicians and provide recommendations for making these difficult diagnostic judgments.
Obsessions versus Depressive Rumination
It is sometimes difficult to differentiate between de- pressive ruminations and obsessions. The distinction rests primarily on thought content and the patient’s re- ported resistance to such thoughts. Unlike obsessions, ruminations are typically pessimistic ideas about the self or the world, and ruminative content frequently shifts. Additionally, depressive ruminators tend to not make repeated attempts to suppress their ruminations the way individuals with OCD try to suppress obses- sions. When depression and OCD co-occur, both phe- nomena may be present, but only obsessions should be targeted with exposure exercises. We have also found clinically that the generally pessimistic presentation of depressed patients can undermine hopefulness about improvement during EX/RP; thus, these beliefs may require therapeutic intervention even though they are not obsessional.
Anxiety Disorders
OCD has been classified previously as an anxiety dis- order, and it often co-occurs with anxiety disorders. Diagnostic criteria are sometimes similar among these related (anxiety) disorders, but the symptoms associ- ated with each diagnosis can usually be distinguished. For example, the excessive worries characteristic of GAD may appear similar to those in OCD but, un- like obsessions, worries are excessive concerns about real-life circumstances and are experienced by the in- dividual as appropriate (ego-syntonic). In contrast, obsessive thinking is more likely to be unrealistic or magical, and obsessions are usually experienced by the individual as inappropriate (ego-dystonic). There are, however, exceptions to this general rule: Individuals with either GAD or OCD may worry about everyday matters, such as their children getting sick. However, when worried about their children catching cold, par- ents with GAD might focus their concern on the long- term consequences (e.g., falling behind in school, de- velopment of a lifelong pattern of debilitation), whereas parents with OCD might focus more on the contami- nation aspect of illness (e.g., their child being infested with “cold germs”). The problem of distinguishing between obsessions and worries in a particular patient is most relevant when the patient exhibits no compul- sions, but, as we mentioned earlier, pure obsessionals comprise only about 2% of individuals with OCD (Foa et al., 1995).
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In the absence of rituals, the avoidance associated with specific phobias may also appear similar to OCD. For example, excessive fear of germs and specific phobia both may result in persistent fear of dogs. However, un- like an individual with OCD, a person with a specific phobia can successfully avoid dogs for the most part, or reduce distress quickly by escaping dogs when avoid- ance is impractical. In contrast, the individual with OCD who is obsessed with “dog germs” continues to feel contaminated even after the dog is gone, and some- times knowing that a dog was in the vicinity several hours earlier can also produce obsessional distress even if there is no possibility that the dog will return. This distress often prompts subsequent avoidance behaviors (e.g., taking off clothing that might have been near the contaminating dog) not typically observed in specific phobias.
Body Dysmorphic Disorder
The preoccupation with imagined physical defects of BDD is formally similar to the obsessions of OCD, and BDD is grouped with obsessive–compulsive and related disorders. The best way to differentiate between this disorder and OCD is to examine for content specificity of the fear-provoking thoughts. Most individuals with BDD are singly obsessed, whereas most individuals with OCD have multiple obsessions.
Tourette Syndrome and Tic Disorders
To differentiate the stereotyped motor behaviors that characterize Tourette syndrome and tic disorders from compulsions, the functional relationship between these behaviors and any obsessive thoughts must be examined. Motor tics are generally experienced as involuntary and are not aimed at neutralizing distress brought about by obsessions. There is no conventional way to differentiate them from “pure” compulsions, but OCD with “pure” compulsions is extremely rare (Foa et al., 1995). As we noted earlier, there appears to be a high rate of comor- bidity between OCD and tic disorders (e.g., Pauls et al., 1986); thus, both disorders may be present simultane- ously in a given patient. Interestingly, tics were similarly responsive to an EX/RP protocol when compared in a randomized study to habit-reversal training in which a competing response is substituted for the tic; this find- ing suggests that the conceptual model underlying the treatment of tics might require modification (Verdellen, Keijsers, Cath, & Hoogduin, 2004).
Delusional Disorder and Schizophrenia
Individuals with OCD may present with obsessions of delusional intensity (for a review, see Kozak & Foa, 1994). Approximately 5% of patients with OCD report complete conviction that their obsessions and compul- sions are realistic, with an additional 20% reporting strong but not fixed conviction. Therefore, it is impor- tant to consider the diagnosis of OCD “with poor in- sight” even if these beliefs are very strongly held. The differentiation between delusional disorder and OCD can depend on the presence of compulsions in OCD (Eisen et al., 1998). In OCD, obsessions of delusional intensity are usually accompanied by compulsions.
It is also important to recognize that the content of obsessions in OCD may be quite bizarre, as in the delu- sions of schizophrenia, but bizarreness in and of itself does not preclude a diagnosis of OCD. For example, one patient seen at our center was fearful that small bits of her “essence” would be forever lost if she passed too close to public trash cans. This patient did not report any other symptoms of formal thought disorder, such as loose associations, hallucinations, flat or grossly in- appropriate affect, and thought insertion or projection. Following a course of EX/RP that focused on exercises designed to expose the patient to the loss of her “es- sence” (e.g., driving by the city dump), her OCD symp- toms were substantially reduced. On occasion patients do meet diagnostic criteria for both OCD and schizo- phrenia, and a dual diagnosis is appropriate under these circumstances. Importantly, EX/RP with such patients should proceed only if the associated treatment exer- cises do not exacerbate the comorbid thought disorder symptoms.
COGNITIVE AND BEHAVIORAL MODELS
Mowrer’s (1939) two-stage theory for the acquisition and maintenance of fear and avoidance behavior has been commonly adopted to explain phobias and OCD. As elaborated by Mowrer (1960), this theory proposes that in the first stage, a neutral event becomes associ- ated with fear by being paired with a stimulus that by its nature provokes discomfort or anxiety. Through conditioning processes, objects, as well as thoughts and images, acquire the ability to produce discomfort. In the second stage of this process, escape or avoidance responses are developed to reduce the anxiety or dis- comfort evoked by the various conditioned stimuli and
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are maintained by their success in doing so. Dollard and Miller (1950) adopted Mowrer’s two-stage theory to explain the development of phobias and obsessive– compulsive neurosis. As noted earlier, because of the intrusive nature of obsessions, many situations that provoke obsessions cannot readily be avoided. Passive avoidance behaviors, such as those utilized by phobics, are also less effective in controlling obsessional distress. Active avoidance patterns in the form of ritualistic be- haviors are then developed and maintained by their suc- cess in alleviating this distress.
In light of equivocal empirical support for the two- stage theory and its limitations, Rescorla (1982) pro- posed a model of learning theory that emphasizes change in expectations as the mechanism of change in conditioning and extinction. Influenced by their theo- ry, Foa, Yadin, and Lichner (2012) adopted emotional processing theory (Foa & Kozak, 1986) to explain the mechanism of exposure and response prevention, sug- gested that disconfirmation of beliefs underlies the ef- fects of this treatment (i.e., patients learn that the nega- tive outcome they expected from being exposed to their fear situation did not materialize).
Another explanation was offered by Salkovskis’s (1985) cognitive analysis of OCD. He posited that intrusive obsessional thoughts are stimuli that may provoke certain types of negative automatic thoughts. Accordingly, an intrusive thought leads to mood dis- turbances only if it triggers negative automatic thoughts through interaction between the unacceptable intru- sion and the individual’s belief system (e.g., only bad people have sexual thoughts). According to Salkovskis, exaggerated senses of responsibility and self-blame are the central themes in the belief system of a person with OCD. Neutralization, in the form of behavioral or cog- nitive compulsions, may be understood as an attempt to reduce this sense of responsibility and to prevent blame. In addition, frequently occurring thoughts regarding unacceptable actions may be perceived by the individ- ual with OCD as equivalent to the actions themselves, so, for example, even if the person has not sinned, the thought of sinning is as bad as sinning itself.
Salkovskis (1985) further proposed that five dysfunc- tional assumptions characterize individuals with OCD and differentiate them from persons without OCD:
(1) Having a thought about an action is like perform- ing the action; (2) failing to prevent (or failing to try to prevent) harm to self or others is the same as having caused the harm in the first place; (3) responsibility is not
attenuated by other factors (e.g., low probability of oc- currence); (4) not neutralizing when an intrusion has oc- curred is similar or equivalent to seeking or wanting the harm involved in that intrusion to actually happen; (5) one should (and can) exercise control over one’s thoughts. (p. 579)
Thus, while the obsession may be ego-dystonic, the automatic thought it elicits will be ego-syntonic. By extension, this model suggests that treatment of OCD should largely focus on identifying the erroneous as- sumptions and modifying the automatic thoughts. This theory paved the way for various elaborations on the cognitive models, experimental studies of the model, and the development of cognitive therapies that derive from the central role of these key cognitive factors.
Salkovskis’s (1985) theory sparked examination of the role of responsibility in the psychopathology of OCD (Ladoucer et al., 1995; Rachman, Thordarson, Shafran, & Woody, 1995; Rhéaume, Freeston, Dugas, Letarte, & Ladoucer, 1995). Further attention has been paid to what Rachman (1998) referred to as thought– action fu- sion (TAF), wherein individuals believe that simply hav- ing an unacceptable thought increases the likelihood of the occurrence of a feared outcome, and that thoughts of engaging in repugnant activities are equivalent to actu- ally having done so. Contemporary cognitive theorists would then suggest that obsessive– compulsive beliefs such as TAF, exaggerated responsibility, and intolerance of uncertainty likely result in increased and ultimately futile efforts at thought suppression and other ill- advised mental control strategies, which would then yield in- creased frequency of such thoughts and associated dis- tress (Purdon & Clark, 2002). Hence, a vicious cycle of avoidance maintains and strengthens the OCD, and the cognitive therapies that derive from these contemporary models would directly target these obsessive–compulsive beliefs in an effort to break the cycle.
In an integrated cognitive-behavioral account, Foa and Kozak (1985, 1986) conceptualized anxiety dis- orders in general as specific impairments in emotional memory networks. Following Lang (1979), they view fear as an information network existing in memory that includes representation about fear stimuli, fear respons- es, and their meaning. With regard to the fear content, Foa and Kozak (1986) suggested that fear networks of individuals with anxiety disorders are characterized by the presence of erroneous estimates of threat, un- usually high negative valence for the feared event, and excessive response elements (e.g., physiological reactiv-
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ity), and are resistant to modification. This persistence may reflect failure to access the fear network because of either active avoidance or the content of the fear network precludes spontaneous encounters with situa‑ tions that evoke anxiety in everyday life. Additionally, anxiety may persist because of some impairment in the mechanism of extinction. Cognitive defenses, excessive arousal with failure to habituate, faulty premises, and erroneous rules of inference are all impairments that would hinder the processing of information necessary for modifying the fear structure to reduce fear behavior.
Foa and Kozak (1985) suggested that several forms of fear occur in individuals with OCD. The patient who fears contracting venereal disease from public bathrooms and washes to prevent such harm has a fear structure that includes excessive associations between the stimuli (e.g., bathrooms) and the anxiety/distress responses, as well as mistaken beliefs about the harm re‑ lated to the stimulus. For other individuals with OCD, fear responses are associated with mistaken meaning rather than with a particular stimulus. For example, some patients who are disturbed by perceived asymme‑ try, and who reduce their distress by rearranging ob‑ jects, do not fear the objects themselves, nor do they an‑ ticipate disaster from the asymmetry. Rather, they are upset by their view that certain arrangements of stimuli are “improper.”
Like Reed (1985), Foa and Kozak (1985) proposed that in addition to the pathological content of the ob‑ sessions, OCD is distinguished from other disorders by pathology in the mechanisms underlying information processing. Specifically, they suggested that patients with OCD experience impairments in taking into ac‑ count the rules for making inferences about harm, often concluding that a situation is dangerous based on the absence of evidence for safety, and that they often fail to make inductive leaps about safety from informa‑ tion about the absence of danger. Consequently, rituals performed to reduce the likelihood of harm can never provide safety and must be repeated. In an elaboration on emotional processing theory and the mechanism by which exposure works, Foa, Huppert, and Cahill (2006) suggested that in vivo exposure to the feared stimulus in the absence of the anticipated harm cor‑ rects the exaggerated probability estimates; imaginal exposure not only corrects the exaggerated cost but also strengthens the discrimination between “thoughts about harm” and “real harm,” thus altering the asso‑ ciations between threat meaning of stimulus and/or re‑ sponse elements in the fear structure.
Animal models of fear conditioning and extinction (see Bouton, 1993) have suggested that the original con‑ ditioned stimulus–unconditioned stimulus (CS‑US) as‑ sociation learned during fear conditioning is not erased during an extinction procedure, but rather rendered am‑ biguous as new information is learned when the CS no longer predicts the US. This process means that the CS now has two meanings: the original excitatory mean‑ ing, plus an additional inhibitory one (Craske, Treanor, Conway, Zbozinek, & Vervliet, 2014). With respect to application in humans, Craske and colleagues have pos‑ ited that anxious individuals show deficits in the mech‑ anisms thought to be central to extinction learning; accordingly, there is great clinical value in optimizing inhibitory learning during exposure therapy to maxi‑ mize treatment outcomes. One such strategy involves overtly setting up exposures as tests of patient expectan‑ cies so as to provide maximal opportunity for violation of said expectancies. In order to do so, it is important to shift language away from whether a patient is ha‑ bituating, focusing instead on whether he/she is learn‑ ing that his/her expectations of negative outcome do not occur. In addition, the application of an inhibitory learning model in treatment would include emphasiz‑ ing the importance of decontextualizing inhibitory as‑ sociations, as well as helping the patient develop distress tolerance (Blakey & Abramowitz, 2016). Experimental tests of the relative efficacy of this approach to con‑ ducting exposure versus other approaches (e.g., models that emphasize within‑session habituation) have yet to be undertaken specifically with patients with clinical OCD. It will also be important to determine whether patients with OCD with explicit feared consequences (e.g., “I will kill my baby if I do not ritualize in response to thoughts of harming her”) fare better using the in‑ hibitory learning model when compared to those whose urges to ritualize are driven more by disgust or by “not just right” experiences without fear related to specific external consequences.
TREATMENTS
Exposure and Ritual Prevention
The prognostic picture for OCD has improved dra‑ matically since Victor Meyer (1966) first reported on two patients who responded well to a treatment that included prolonged exposure to obsessional cues and strict prevention of rituals. This procedure, known at the time as “exposure and ritual prevention” (EX/RP),
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was later found to be extremely successful in 10 of 15 cases and partly effective in the remainder. Patients treated with this regimen also appeared to maintain their treatment gains: At a 5-year follow-up, only two of these patients had relapsed (Meyer & Levy, 1973; Meyer, Levy, & Schnurer, 1974).
As was the case with Meyer’s program, current EX/RP treatments typically include both prolonged exposure to obsessional cues and procedures aimed at blocking rituals. Exposure exercises are often done in real-life settings (in vivo), for example, by asking the patient who fears accidentally causing a house fire by leaving the stove on, to leave the house without checking the burners. When patients report specific feared conse- quences of refraining from rituals, these fears may also be addressed via imaginal exposure. In fact, in vivo and imaginal exposure exercises are designed specifically to prompt obsessional distress. It is believed that repeated, prolonged exposure to feared thoughts and situations provides information that disconfirms mistaken associ- ations and evaluations held by the patients and thereby promotes habituation (Foa & Kozak, 1986). Exposure is usually done gradually by confronting situations that provoke moderate distress before confronting more up- setting ones. Exposure homework is routinely assigned between sessions, and patients are also asked to refrain from rituals.
Since Meyer’s (1966) initial positive report of the ef- ficacy of EX/RP, many subsequent studies of EX/RP have indicated that most EX/RP treatment completers make and maintain clinically significant gains. Ran- domized controlled trials (RCTs) have indicated that EX/RP is superior to a variety of control treatments, including placebo medication (Marks, Stern, Mawson, Cobb, & McDonald, 1980; Foa et al., 2005), relaxation (Fals-Stewart, Marks, & Schafer, 1993; Simpson et al., 2008), and anxiety management training (Lindsay, Crino, & Andrews, 1997). Recent meta-analytic find- ings examining randomized trials clearly support the efficacy of CBT for both adult (Öst, Havnen, Hansen, & Kvale, 2015) and pediatric OCD (Öst, Riise, Werge- land, Hansen, & Kvale, 2016). Moreover, several studies have now indicated that these encouraging findings for EX/RP are not limited to highly selected RCT samples (Franklin, Abramowitz, Kozak, Levitt, & Foa, 2000; Kay, Eken, Jacobi, Riemann, & Storch, 2016, Roth- baum & Shahar, 2000; Valderhaug, Larsson, Gote- stam, & Piacentini, 2007; Warren & Thomas, 2001).
In general, EX/RP has been found quite effective in ameliorating OCD symptoms and has produced great
durability of gains following treatment discontinua- tion. In our review of the literature, it also was appar- ent that among the many variants of EX/RP treatment, some are relevant for outcome and others are not. We review the literature on the relative efficacy of the ele- ments that comprise EX/RP to help clinicians decide which EX/RP components are most essential.
EX/RP Treatment Variables
EXPOSURE VERSUS RITUAL PREVENTION VERSUS EX/RP
To separate the effects of EX/RP on OCD symptoms, Foa, Steketee, Grayson, Turner, and Latimer (1984) randomly assigned patients with washing rituals to treatment by exposure only (EX), ritual prevention only (RP), or their combination (EX/RP). Each treatment was conducted intensively (15 daily 2-hour sessions conducted over 3 weeks) and followed by a home visit. Patients in each condition were found to be improved at both posttreatment and follow-up, but EX/RP was superior to the single-component treatments on almost every symptom measure at both assessment points. In comparing EX and RP, patients who received EX re- ported lower anxiety when confronting feared contami- nants than did patients who had received RP, whereas the RP group reported greater decreases in urge to ritu- alize than did the EX patients. Thus, it appears that EX and RP affected different OCD symptoms. The findings from this study clearly suggest that EX and RP should be implemented concurrently; treatments that do not include both components yield inferior out- come. It is important to convey this information to pa- tients, especially when they are experiencing difficulty either refraining from rituals or engaging effectively in exposure exercises during and between sessions.
IMPLEMENTATION OF RITUAL PREVENTION
Promoting abstinence from rituals during treatment is thought to be essential for successful treatment out- come, but the preferred method of RP has changed over the years. In Meyer’s (1966) EX/RP treatment program, hospital staff members physically prevented patients from performing rituals (e.g., turning off the water supply in a patient’s room). However, physical intervention by staff or family members to prevent pa- tients from ritualizing is no longer typical or recom- mended. It is believed that such prevention techniques
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are too coercive to be an accepted practice today. More- over, physical prevention by others may actually limit generalizability to nontherapy situations in which oth- ers are not present to intercede. Instead, instructions and encouragement to refrain from ritualizing and avoidance are now recommended. As noted earlier, al- though exposure itself can reduce obsessional distress, it is not so effective in reducing compulsions. To maxi- mize treatment effects, the patient needs to refrain vol- untarily from ritualizing, while engaging in systematic exposure exercises. The therapist should strongly em- phasize the importance of refraining from rituals and help the patient with this difficult task by providing support, encouragement, and suggestions about alter- natives to ritualizing.
USE OF IMAGINAL EXPOSURE
Treatment involving imaginal plus in vivo EX/RP at follow-up was superior to an in vivo EX/RP program that did not include imaginal exposure (Foa, Steketee, Turner, & Fischer, 1980; Steketee, Foa, & Grayson, 1982). However, a second study did not find that the addition of imaginal exposure enhanced long-term ef- ficacy compared to in vivo exposure only (De Araujo, Ito, Marks, & Deale, 1995). The treatment program in the former study (Foa et al., 1980) differed from that of De Araujo and colleagues on several parameters (e.g., 90-minute vs. 30-minute imaginal exposures, respec- tively); thus, the source of these studies’ inconsistencies cannot be identified.
In our clinical work, we have found imaginal ex- posure to be helpful for patients who report that di- sastrous consequences will result if they refrain from rituals. Because many of these consequences cannot be readily translated into in vivo exposure exercises (e.g., burning in hell), imaginal exposure allows the patient an opportunity to confront these feared thoughts. Also, the addition of imagery to in vivo exposure may circumvent the cognitive avoidance strategies used by patients who intentionally try not to consider the con- sequences of exposure while confronting feared situa- tions in vivo. In summary, although imaginal exposure does not appear essential for immediate outcome, it may enhance long-term maintenance and be used as an adjunct to in vivo exercises for patients who fear disastrous consequences. For patients who only report extreme distress as a consequence of refraining from rituals and avoidance behaviors, imaginal exposure may not be needed.
GRADUAL VERSUS ABRUPT EXPOSURES
No differences in OCD symptom reduction were de- tected in a study comparing patients who confronted the most distressing situations from the start of thera- py to those who confronted less distressing situations first, yet patients preferred the more gradual approach (Hodgson, Rachman, & Marks, 1972). However, be- cause patient motivation and agreement with treatment goals are core elements of successful EX/RP, situations of moderate difficulty are usually confronted first, fol- lowed by several intermediate steps, before the most dis- tressing exposures are attempted. Thus, we emphasize that exposure will proceed at a pace that is acceptable to the patient, and that no exposure will ever be attempted without the patient’s approval. At the same time, it is preferable to confront the highest item on the treatment hierarchy relatively early in treatment (e.g., within the first week of intensive treatment) to allow sufficient time to repeat these difficult exposures over the later sessions.
DURATION OF EXPOSURE
Duration of exposure was once believed to be impor- tant for outcome in that prolonged, continuous expo- sure was found to be more effective than short, inter- rupted exposure (Rabavilas, Boulougouris, & Perissaki, 1979). Indeed, reduction in anxiety (habitation) across sessions has been associated with improvement fol- lowing exposure-based treatments for OCD and for PTSD (e.g., Jaycox, Foa, & Morral, 1998; Kozak, Foa, & Steketee, 1988; van Minnen & Hagenaars, 2002). However, several studies have not found a strong rela- tionship between within-session habituation and fear and symptom reduction (Jaycox et al., 1998; Kozak et al., 1988; Mathews, Johnston, Shaw, & Gelder, 1974; Rowe & Craske, 1998). In an elaboration on emotional processing theory, Foa and colleagues (2006) found that the recent deemphasis of the relationship between within-session habituation and outcome is not critical to emotional processing theory, because the proposed mechanism underlying symptom reduction is the mod- ification of the relevant erroneous associations through disconfirming information, not through habituation per se. In practical terms, this means patients should be instructed that although, optimally, they should persist with exposure until the anxiety is substantially reduced, the more important factor is repeating the same expo- sures, to promote reduction of associated anxiety over time. Patients with OCD might be particularly vul-
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nerable to fears of ending exposures “too soon,” hence, doing the treatment incorrectly, so this new instruc- tion might help encourage patients to go about their business without ritualizing or avoiding, regardless of whether anxiety still lingers on from an exposure task. The deemphasis of the critical importance of habitu- ation in the moment is more pronounced procedur- ally when using acceptance and commitment therapy (e.g., Twohig et al., 2010), but, generally speaking, this viewpoint appears to be gaining acceptance among cog- nitive-behavioral therapists as well. For example, clini- cally we often remind patients that whether they are anxious is less relevant than what they do (or do not do) when they are anxious, since ritualizing and avoidance will maintain fear down the line.
FREQUENCY OF EXPOSURE SESSIONS
Optimal frequency of exposure sessions has yet to be established. Intensive exposure therapy programs that have achieved excellent results (e.g., Foa, Kozak, Steke- tee, & McCarthy, 1992) typically involve daily ses- sions over the course of approximately 1 month, but quite favorable outcomes have also been achieved with more widely spaced sessions (e.g., Abramowitz, Foa, & Franklin, 2003; De Araujo et al., 1995; Franklin et al., 1998). A recent RCT in pediatric OCD found no dif- ference between intensive and weekly treatment (Storch et al., 2007). Clinically, we have found that less frequent sessions may be sufficient for highly motivated patients with mild to moderate OCD symptoms, who readily understand the importance of daily exposure home- work. Patients with very severe symptoms, or those who for various reasons cannot readily comply with EX/RP tasks between sessions, are typically offered intensive treatment.
THERAPIST-ASSISTED VERSUS SELF-EXPOSURE
Evaluations of the presence of a therapist during ex- posure have yielded inconsistent results. In one study, patients with OCD receiving therapist-assisted expo- sure were more improved immediately posttreatment than those receiving clomipramine and self-exposure, but this difference was not evident at follow-up (Marks et al., 1988). However, these results are difficult to in- terpret in light of the study’s complex design. A sec- ond study using patients with OCD also indicated that therapist-assisted treatment was not superior to self-exposure at posttreatment or at follow-up (Em-
melkamp & van Kraanen, 1977), but the number of patients in each condition was too small to render these findings conclusive. In contrast to the negative find- ings of Marks and colleagues (1988) and Emmelkamp and van Kraanen (1977), therapist presence yielded superior outcome of a single, 3-hour exposure session compared to self-exposure for persons with specific phobia (Öst, 1989). Because specific phobias are, on the whole, less disabling and easier to treat than OCD, one may surmise that therapist presence should also influ- ence treatment outcome with OCD. Moreover, using meta-analytic procedures, Abramowitz (1996) found that therapist-controlled exposure was associated with greater improvement in OCD and GAD symptoms compared to self-controlled procedures. Comparable outcomes were found for patients receiving EX/RP with therapist assistance and those who received teletherapy (Lovell et al., 2006), which further raises the question of whether therapist assistance is required for good out- come. In light of these inconsistent findings, no clear answer is available on the role of therapist assistance with exposure tasks in OCD treatment. However, we have found clinically that the presence of a therapist can be useful in helping patients to remain engaged in ex- posures while anxiety is high, to avoid subtle rituals or avoidance behaviors during exposure (e.g., distraction, mental rituals), and to remain sufficiently motivated despite distress. Researchers have begun to examine the question of whether telephone therapy or Skype would also be effective, including adapted CBT protocols for Tourette syndrome (Himle, Olufs, Himle, Tucker, & Woods, 2010) and OCD specifically (e.g., Bachofen et al., 1999; Comer et al., 2017); such research may pro- vide greater confidence that these methods can be used efficaciously, which will help to address the ongoing problem of the paucity of OCD treatment expertise that plagues most communities.
EX/RP versus Other Treatment Approaches
In this section we review the literature on the efficacy of standard individual EX/RP treatment versus other therapeutic approaches, including group treatment, family-based EX/RP treatment, cognitive therapy, and pharmacotherapy.
INDIVIDUAL VERSUS GROUP EX/RP
Intensive individual EX/RP, although effective, can pose practical obstacles, such as high cost for treatment,
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and scheduling problems for patient and therapist alike. Additionally, because experts in EX/RP treat- ment are few and far between, patients may need to wait for long periods or travel substantial distances to be treated. Thus, some researchers have begun to exam- ine the efficacy of more affordable and efficient treat- ment modalities. One such alternative is group treat- ment. Fals-Stewart and colleagues (1993) conducted a controlled study in which patients with OCD were randomly assigned to individual EX/RP, group EX/RP, or a psychosocial control condition (relaxation). Each of the active treatments was 12 weeks long, with sessions held twice weekly, and included daily exposure home- work. Significant improvement in OCD symptoms was evident in both active treatments, with no differences detected between individual and group EX/RP imme- diately posttreatment or at 6-month follow-up. Profile analysis of OCD symptom ratings collected through- out treatment did indicate a faster reduction in symp- toms for patients receiving individual treatment. These results offer evidence for the efficacy of group treat- ment. However, because patients were excluded from this study if they were diagnosed with any personality disorder or with comorbid depression, it may be that the sample was somewhat atypical. In addition, none of the participants had received previous OCD treatment, which is also unusual for this population and suggestive of a less symptomatic sample. Thus, inferences about the broader OCD population merit caution until these results are replicated.
Barrett, Healy-Farrell, and March (2004) found that individual and group CBT were highly and simi- larly efficacious for children and adolescents with OCD relative to a wait-list control; this raises the possibility that group interventions might hold particular promise in the treatment of youth with OCD. Also in youth, Asbahr and colleagues (2005) found group CBT and sertraline comparable at posttreatment, but there was less relapse in the former condition. Another Australian research group found comparable outcomes for group treatment compared to individual treatment, both of which were superior to a wait-list control (Anderson & Rees, 2007); not surprisingly, though, individual treat- ment was associated with more rapid response.
FAMILY INVOLVEMENT VERSUS STANDARD EX/RP TREATMENT
Emmelkamp and colleagues (1990) examined whether family involvement in treatment would enhance the
efficacy of EX/RP for OCD. Patients who were mar- ried or living with a romantic partner were randomly assigned to receive EX/RP either with or without part- ner involvement in treatment. Results indicated that OCD symptoms were significantly lowered following treatment for both groups. No differences between the treatments emerged, and initial marital distress did not predict outcome. However, the reduction in anxiety/ distress reported for the sample as a whole was mod- est (33%), which may have resulted from the relatively short treatment sessions and absence of in vivo exposure exercises in treatment sessions.
Mehta (1990) also examined the effect of family involvement on EX/RP treatment outcome. To adapt the treatment to serve the large numbers of young un- married people seeking OCD treatment and the “joint family system” prevalent in India, Mehta used a family- based rather than spouse-based treatment approach. Patients who did not respond to previous pharmaco- therapy were randomly assigned to receive treatment by systematic desensitization and EX/RP, either with or without family assistance. Sessions in both conditions were held twice weekly for 12 weeks; response preven- tion was described as “gradual.” In the family condition, a designated family member (parent, spouse, or adult child) assisted with homework assignments, supervised relaxation therapy, participated in response prevention, and was instructed to be supportive. On self-reported OCD symptoms, a greater improvement was found for the family-based intervention at posttreatment and at 6-month follow-up. Although this study had meth- odological problems that complicate interpretation of findings (e.g., use of self-report OCD measures only, unclear description of treatment procedures), it offers some preliminary evidence that family involvement may be helpful in OCD treatment. Clinically, we rou- tinely enlist the support of family members in EX/RP, providing psychoeducation about the illness and its consequences during the early stages of treatment plan- ning, and advice and encouragement in managing the patient’s request for assurances, his/her avoidant behav- iors, and violation of EX/RP rules between sessions. We also try to reduce family members’ criticism of the patient and unconstructive arguing about OCD and related matters when these issues arise in the therapy.
Published randomized studies of CBT for OCD with youth have each included parents at least to some extent in treatment (Barrett et al., 2004; de Haan, Hoogduin, Buitelaar, & Keijsers, 1998; Pediatric OCD Treatment Study Team, 2004), and a direct comparison
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of CBT, with and without a family component, using an otherwise identical protocol has yet to be conducted in pediatric OCD. Research on whether family involve- ment enhances individual CBT outcomes in other anxiety disorders has generally yielded mixed findings, however, and a large RCT indicated that both forms of treatment are efficacious and essentially equivalent to one another (Bogels & Bodden, 2005). Higher family dysfunction in general was associated with poorer long- term outcome in one study (Barrett, Farrell, Dadds, & Boulter, 2005), as was family accommodation of OCD rituals specifically (Peris et al., 2012), and at this point it might be clinically prudent to include a more com- prehensive family component when family members are very directly involved in the patient’s rituals (e.g., reassurance seeking) or when family psychopathology threatens generalizability of treatment gains to a chaot- ic home environment. It also may be that greater family involvement in treatment is needed when the patient is very young (Freeman et al., 2003, 2007, 2014).
EX/RP VERSUS COGNITIVE THERAPIES
Increased interest in cognitive therapy (e.g., Beck, 1976; Ellis, 1962), coupled with dissatisfaction with formula- tions of treatment mediated by processes such as extinc- tion (Stampfl & Levis, 1967) or habituation (Watts, 1973), prompted examination of the efficacy of cogni- tive procedures for anxiety disorders in general and for OCD in particular. A number of early studies found few differences between standard behavioral treat- ments and behavioral treatments enhanced with vari- ous cognitive approaches (e.g., Emmelkamp & Beens, 1991; Emmelkamp, Visser, & Hoekstra, 1988). Re- cent advances in cognitive conceptualizations of OCD have apparently yielded more efficacious and durable cognitive treatments. Freeston and colleagues (1997) found a cognitive-behavioral intervention efficacious compared to a wait-list control group for patients with “pure” obsessions. Several other studies (Cottraux et al., 2001; McLean et al., 2001; Vogel, Stiles, & Götestam, 2004; Whittal, Thordarson, & McLean, 2005) have suggested equivalent results for CBT and EX/RP, re- spectively, although some procedural overlap between the two conditions in these studies makes their find- ings difficult to interpret. In concert with studies at- testing to the utility of cognitively oriented approaches for conditions that are quite similar to OCD, such as hypochondriasis (Barsky & Ahern, 2004; Warwick, Clark, Cobb, & Salkovskis, 1996), it does appear that
cognitive therapies hold promise for the treatment of OCD and might be an efficacious potential alternative to EX/RP (Öst et al., 2015). However, Whittal, Woody, McLean, Rachman, and Robichaud (2010) failed to find a difference between cognitive therapy and stress management training (SMT) for a sample with primary obsessions and mental rituals, although this appeared to be due to the fact that SMT yielded substantial and lasting benefit compared to pretreatment rather than because cognitive therapy did not.
The question of whether cognitive therapy improves the efficacy of EX/RP is generally difficult to discern, because both exposure therapy and cognitive therapy are intended to modify mistaken cognitions. An RCT that compared “pure” forms of CT or EX/RP, with or without medication, found similar, yet somewhat at- tenuated, outcomes relative to what might typically be expected from either treatment (van Balkom et al., 1998). Foa and Kozak (1986) argued that the discon- firmation of erroneous associations and beliefs is a crucial mechanism underlying the efficacy of exposure treatments, hence disputing discussions that mistaken cognitions from EX/RP might be expected to hamper outcome. For example, a patient and therapist sitting on the bathroom floor in a public restroom conduct- ing an exposure to contaminated surfaces routinely discuss risk assessment, probability overestimation, and so forth, as the therapist helps the patient achieve the cognitive modification necessary for improvement. The practical issue of interest is how to maximize efficacy: Is informal discussion of cognitive distortions during the exposure exercises sufficient, or should the therapist engage in formal Socratic questioning of hypothesized distortions, such as inflated responsibility? Notably, in a meta-analytic review, cognitive therapies for OCD that included some form of exposure to feared stimuli were superior to those that did not, suggesting that exposure may be necessary to maximize outcomes (Abramowitz, Franklin, & Foa, 2002).
To expand on this point further, Hiss, Foa, and Kozak (1994) investigated whether formal relapse prevention techniques following intensive EX/RP en- hanced maintenance of gains. Notably, all discussions about cognitive factors typically included during the core treatment (e.g., discussion of lapse vs. relapse, posttreatment exposure instructions, themes of guilt and personal responsibility, and feared consequences) were removed. Patients received this modified EX/RP, followed by either a relapse prevention treatment or a psychosocial control treatment (associative therapy). All
Obsessive–Compulsive Disorder 145
patients in both conditions were classified as respond- ers at posttreatment (defined as 50% or greater reduc- tion in OCD symptoms), with treatment gains better maintained in the relapse prevention group than in the associative therapy condition at 6-month follow- up. The percentages of responders at follow-up were 75% in the relapse prevention condition and 33% in associative therapy. The higher than usual observed relapse rate in the associative therapy condition may have resulted from the removal of cognitive techniques typically utilized during the core treatment, such as discussion of feared consequences. These findings, and those discussed earlier, further underscore our belief that blended treatment designed to provide patients the opportunity to disconfirm their erroneous cognitions makes the most sense clinically. Accordingly, our ap- proach clearly incorporates informal cognitive proce- dures, and discussions of the outcome of exposures are geared toward challenging mistaken beliefs; this is ac- complished in the context of a treatment approach that still emphasizes the importance of EX/RP in bringing about such changes.
Serotonergic Medications
Effectiveness of Medications
The use of serotonergic medications in the treatment of OCD has received a great deal of attention. Of the tricyclic antidepressants, clomipramine (CMI) has been studied most extensively. In controlled trials, CMI has consistently been found to be superior to placebo (e.g., DeVeaugh-Geiss, Landau, & Katz, 1989). Similar re- sults have been obtained with the selective serotonin reuptake inhibitors (SSRIs) fluoxetine, fluvoxamine, and sertraline (see Öst et al., 2015). Accordingly, each of these medications has been approved by the U.S. Food and Drug Administration (FDA) as treatments for adult OCD. On the whole, these studies suggest that up to 60% of patients show some response to treatment with SSRIs. However, even the average treatment gain achieved by treatment responders is moderate at best (Greist, 1990). In addition, amelioration of obsessive– compulsive symptoms is maintained only as long as the drug is continued: For example, in an early controlled, double-blind discontinuation study, 90% of patients re- lapsed within a few weeks after being withdrawn from CMI (Pato, Zohar-Kadouch, Zohar, & Murphy, 1988). More recent discontinuation studies with slower taper periods have not yielded such dramatic results, but
they nevertheless converge to suggest that maintenance treatment is necessary to sustain achievements attained with pharmacotherapy alone for OCD (Dougherty, Rauch, & Jenike, 2002).
EX/RP versus Pharmacotherapy
Many controlled studies have indicated that serotoner- gic antidepressants are superior to placebo in ameliorat- ing OCD symptoms (for a review, see Greist, Jefferson, Kobak, Katzelnick, & Serlin, 1995). However, only a few controlled studies have directly compared the rela- tive or combined efficacy of antidepressant medications and EX/RP, and several studies that have made such a comparison included complex designs that make it difficult to draw confident conclusions about relative and combined efficacy (e.g., Marks et al., 1980, 1988). Cottraux and colleagues (1990) compared fluvoxamine (FLV) with antiexposure instructions, FLV plus weekly EX/RP, and pill placebo (PBO) plus EX/RP, and found FLV + EX/RP and FLV + antiexposure instructions su- perior to PBO + EX/RP; there was a trend toward an advantage for combined treatment, but it failed to reach significance. Hohagen and colleagues (1998) compared EX/RP + FLV to EX/RP + PBO and found that both groups improved significantly and comparably on com- pulsions, but the patients who received EX/RP + FLV were significantly better at posttreatment on obsessions than those who received EX/RP + PBO. Subanalyses indicated that patients with secondary depression also fared better if they were receiving EX/RP + FLV.
The relative and combined efficacy of CMI and in- tensive EX/RP was examined in a multicenter, RCT conducted at our center (Penn) and at Columbia Uni- versity. Findings with both treatment completer and in- tention-to-treat (ITT) data indicated at posttreatment that the active treatments were superior to placebo, EX/ RP was superior to CMI, and the combination of the two treatments was not superior to EX/RP alone (Foa et al., 2005); relapse was more evident following treat- ment discontinuation in the CMI group than in either treatment that included intensive EX/RP (EX/RP, EX/ RP + CMI; Simpson et al., 2004). However, the design used in the Penn–Columbia study may not have op- timally promoted an additive effect for CMI, because the intensive portion of the EX/RP program was largely completed before patients reached their maximum dose of CMI. In addition, combined treatment effects may be more evident when intensive EX/RP is not used (Foa, Franklin, & Moser, 2002). Notably, an additive effect
146 CliniCal Handbook of PsyCHologiCal disorders
for combined treatment was found in a study in pedi- atric OCD at Penn, Duke, and Brown (Pediatric OCD Treatment Study Team, 2004), although examination of effect sizes by site indicated that the CBT monother- apy effect at Penn was very large, and no additive effect for combined treatment was found at this site.
In summary, although there is clear evidence that both pharmaceutical treatment with serotonergic medi- cations and EX/RP treatments are effective for OCD, information about their relative and combined efficacy remains scarce, because most of the studies that exam- ined these issues have been methodologically limited. Nevertheless, no study has found clear, long-term supe- riority for combined pharmacotherapy plus EX/RP over EX/RP alone. The absence of conclusive findings not- withstanding, many experts continue to advocate com- bined procedures as the treatment of choice for OCD (e.g., Greist, 1992). In clinical practice, it is common to see patients in EX/RP treatment who are taking SSRIs concurrently. In uncontrolled examinations of EX/RP treatment outcome for adults (Franklin, Abramowitz, Bux, Zoellner, & Feeny, 2002) and youth (Franklin et al., 1998; Piacentini, Bergman, Jacobs, McCracken, & Kretchman, 2002) treated in OCD outpatient clinics, no posttreatment differences in OCD symptom sever- ity were detected between patients who received EX/RP alone and those who received SSRI medication when receiving EX/RP. From these data we can surmise that concomitant pharmacotherapy is not required for every patient to benefit substantially from EX/RP, and that concomitant pharmacotherapy does not appear to in- hibit EX/RP treatment response. With respect to EX/ RP augmentation in SSRI partial responders, there is now evidence from randomized trials that EX/RP aug- mented treatment outcome compared to medication alone in youth (Franklin et al., 2011) and compared to stress management training in adults (Simpson et al., 2010). More definitive conclusions about the effects of augmenting pharmacotherapy with EX/RP await a more carefully controlled examination, however.
ASSESSMENT
Following a diagnostic interview to ascertain the pres- ence of OCD, it is advisable to quantify the severity of the OCD symptoms with one or more of the instru- ments described below. Quantification of symptom se- verity assists the therapist in evaluating how successful treatment was for a given patient. In our clinic, we use
several assessment instruments. As in most OCD clini- cal research studies, however, the primary measure of OCD symptom severity used in our center is the Yale– Brown Obsessive–Compulsive Scale (Y-BOCS; Good- man et al., 1989a, 1989b).
Yale–Brown Obsessive–Compulsive Scale
The Y-BOCS (Goodman et al., 1989a, 1989b), a stan- dardized, semistructured interview, takes approximately 30 minutes to complete. The Y-BOCS Severity scale in- cludes 10 items (five assess obsessions and five, compul- sions), each of which is rated on a 5-point scale ranging from 0 (No symptoms) to 4 (Severe symptoms). Assessors rate the time occupied by the obsessions and compul- sions, the degree of interference with functioning, the level of distress, attempts to resist the symptoms, and level of control over the symptoms. The Y-BOCS has shown adequate interrater agreement, internal consis- tency, and validity (Goodman et al., 1989a, 1989b). The Y-BOCS served as the primary measure of outcome in most of the published OCD pharmacotherapy and CBT treatment studies conducted during the 1990s.
Self‑Report Measures
Obsessive–Compulsive Inventory—Revised
The Obsessive–Compulsive Inventory—Revised (OCI-R; Foa, Huppert, et al., 2002) is an 18-item, self- report measure that assesses the distress associated with obsessions and compulsions. In addition to the total score, six separate subscale scores are calculated by add- ing the three items that comprise each subscale: Wash- ing, Checking, Ordering, Obsessing, Hoarding, and Neutralizing. Foa, Huppert, and colleagues reported good internal consistency, test–retest reliability, and discriminant validity in clinical patients with OCD, PTSD, generalized social phobia, and nonanxious con- trols. The total score ranges from 0 to 72, and each sub- scale ranges from 0 to 12.
Other Self‑Report Measures
A few self-report instruments for assessing OCD symp- toms, such as the Leyton Obsessional Inventory (Ka- zarian, Evans, & Lefave, 1977) and the Lynfield Ob- sessional/Compulsive Questionnaire (Allen & Tune, 1975), are also available. These instruments are limited in that they assess only certain forms of obsessive–
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compulsive behavior and/or they include items that are unrelated to OCD symptoms. More recently, Storch and colleagues (2009) have developed the Children’s Florida Obsessive–Compulsive Inventory, which is in- tended primarily for screening purposes.
INITIAL INTERVIEW
After a diagnosis of OCD has been established, and be- fore actually beginning treatment, the therapist should schedule 4–6 hours of appointments with the patient. In these sessions, the therapist needs to accomplish three important tasks. First, the sessions are used to collect the information necessary to develop a treat- ment plan. Specifically, the therapist must first identify specific cues that cause the patient distress (threat cues), avoidance, rituals, and feared consequences. Second, the therapist should develop a good rapport with the patient, who will engage in exposure exercises designed to elicit anxiety and distress during intensive EX/RP; the lack of a good relationship between therapist and the patient may compromise outcome. Third, the thera- pist needs to explore the patient’s beliefs about OCD and the perceived consequences of refraining from ritu- als and avoidance, because this information guides the informal discussions of cognitive processes that take place throughout EX/RP.
Threat cues may be either (1) tangible objects in the environment or (2) thoughts, images, or impulses that the person experiences (for lack of better terms, we have labeled them “external cues” and “internal cues,” re- spectively). Passive avoidance and ritualistic behavior (sometimes called “active avoidance”) both serve to re- duce the distress associated with the threat cues. Ritu- als may be further divided into overt or covert (mental) forms. It is essential that patients understand the dif- ference between obsessions and mental compulsions, because obsessions are treated with systematic exposure and mental compulsions, with ritual preventions. Dur- ing treatment, patients should be instructed to report any mental compulsions to the therapist, because per- forming such compulsions during exposure exercises attenuates the effects of these exercises in the same way that behavioral compulsions do.
External Fear Cues
Most individuals with OCD experience fear in reaction to specific environmental cues (objects, persons, or situ-
ations), but each patient has his/her own idiosyncratic threat cues. For example, individuals who fear con- tamination from toilets may differ as to whether they fear all toilets or only those open to the public. One patient may fear only the toilet itself, whereas another may also fear bathroom floors, doorknobs, and faucets. Similarly, two individuals may experience distress at the prospect of a fire burning down their home, but whereas one experiences the distress only when she is the last person to leave the house, the other experiences distress before going to bed at night when his children are present.
The therapist needs to gather specific information about cues that elicit the patient’s distress to identify the basic sources of the fear. Identification of the basic source is important for planning the treatment pro- gram. Confronting the source of the fear is essential for successful behavioral treatment of OCD. Often, when such exposure does not take place during treat- ment, relapse occurs. For example, a patient who feared contamination by her hometown was treated with EX/ RP 3,000 miles away from the town. Because of the distances involved, direct exposure to the town was impossible, so treatment comprised exposure to objects contaminated directly or indirectly by contact with the town. Although the patient habituated to the objects used in the exposure sessions, she continued to fear her hometown. Within 1 year after treatment, she had de- veloped fears to new objects related to her hometown. Not until she engaged in repeated exposures to the town itself did she experience lasting improvement.
It is important that the therapist conduct a thorough investigation of objects, situations, and places that evoke obsessional distress for the patient at the time of presentation and at onset. Such information helps to identify the source of the distress. To facilitate com- munication with the patient about situations that evoke distress, a Subjective Units of Discomfort Scale (SUDS) ranging from 0 to 100 points is introduced. Patients are asked to rate each situation with respect to the level of distress they expect to experience upon exposure. The source of the distress is expected to be 100. The follow- ing dialogue between therapist and patient illustrates the process of gathering information about distressing situations.
THERAPIST: When do you get the urge to wash your hands?
PATIENT: In a lot of places. There are so many places.
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THERAPIST: Are there any places where the urges are particularly strong?
PATIENT: Well when I am sitting in my living room, particularly near the fireplace. Also in the laundry room, which I never go to. Also, when I walk in the park.
THERAPIST: Let’s talk about your living room. How upset are you when you are sitting next to your fire- place?
PATIENT: That’s bad. I guess about a 90. THERAPIST: Can you tell me what makes you so upset
in your living room? PATIENT: Well that is a long story . . . and I know it
doesn’t make sense. THERAPIST: Go on. It’s important that we understand
what makes you uncomfortable and fearful in your living room.
PATIENT: About 2 years ago, I got up in the morn- ing and went into the living room, and I saw a dead squirrel in the fireplace. I guess he got in through the chimney. So, I figured that if the squirrel was dead, he must have been sick. I know that a lot of squirrels have rabies, so I thought that if the squirrel died of rabies, then there are germs all over the chimney.
THERAPIST: Have you tried to have the chimney and the fireplace cleaned?
PATIENT: Yes, we did have a company come in and clean the whole area, but I’m not sure that they can clean away the germs.
THERAPIST: I understand. How about the laundry room? How upsetting is it to be in the laundry room?
PATIENT: That would be a 100; that’s why I don’t go in there.
THERAPIST: How did the laundry room become dan- gerous?
PATIENT: Oh, that’s another story. Until a year ago, my children used to keep their guinea pigs in the laun- dry room. One day we found the female guinea pig dead. So I thought that it probably died of rabies, too.
THERAPIST: Oh, I understand. So you are generally afraid you will contract rabies if you come in contact with things that you think are contaminated with rabies germs. Is this true?
PATIENT: Exactly. That’s why I don’t like to walk in
the woods or the park. You know, those places have all kind of animals, and you can never tell where the germs might be.
It is clear from this conversation that it was not liv- ing rooms, laundry rooms, or parks per se that the patient feared. Rather, any situation or object that, in her mind, had some probability of being infested with rabies germs became a source of contamination. Some contamination-fearful patients, however, cannot spec- ify feared consequences of coming into contact with stimuli they perceive to be contaminated. For these patients, the primary fear is that they will not be able to tolerate the extreme emotional distress generated by being contaminated. With such patients, it is also im- portant to probe further to discern whether they have fears about the long-term health consequences of expe- riencing high and unremitting anxiety in response to stimuli that prompt obsessions.
Internal Fear Cues
Anxiety and distress may also be generated by images, impulses, or abstract thoughts that the individual finds disturbing, shameful, or disgusting. Examples of such cues include impulses to stab one’s child, thoughts of one’s spouse injured in an accident, or images of reli- gious figures engaged in sexual activity. Clearly, inter- nal threat cues may be produced by external situations, such as the sight of a knife triggering the impulse to stab one’s child. Some patients may become distressed when they experience certain bodily sensations, such as minor pains triggering the fear of having cancer.
In many cases, patients may be reluctant to ex- press their obsessive thoughts, because they are either ashamed of them or fear that expressing them will make the consequence more likely to occur. In these cases, the therapist needs to encourage the expression of these thoughts through direct questioning and a matter-of- fact attitude. Sometimes it helps to tell the patient that many people with and without OCD have unwanted thoughts (as many as 85% of normal individuals; Rach- man & DeSilva, 1978). It may also be helpful to remind the patient that talking about the obsessions will be a part of therapy; the evaluation session provides an op- portunity to begin this process.
THERAPIST: So tell me, when is it that you feel the urge to count?
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PATIENT: It seems like I’m always counting something, but it’s mostly when I think about certain things.
THERAPIST: What kind of things? PATIENT: I don’t know. Bad things. THERAPIST: Can you give me some examples of bad
thoughts that will make you want to count? PATIENT: (brief silence) I really prefer not to talk about
them. It makes things worse. THERAPIST: You mean it makes the counting worse? PATIENT: Yes. THERAPIST: All right, I know now that when you think
or talk about certain bad things, you have an urge to count, but I still don’t know what those bad things are. How about you tell me so that I can help you with them?
PATIENT: I’d really rather not. Can’t we talk about something else?
THERAPIST: It is important that I know what the thoughts are to plan your treatment. I’ll try to help you. Do the thoughts involve someone being hurt?
PATIENT: Yes. THERAPIST: Do the thoughts involve only certain peo-
ple getting hurt or could it be anyone? PATIENT: Mostly my family. THERAPIST: OK, what else can you tell me about the
thoughts? PATIENT: I really don’t want to say any more. THERAPIST: I know this is scary, but remember that
facing your fears is what this treatment is all about. PATIENT: OK. It’s not always thoughts. Sometimes I
see pictures in my mind, where my brother or my mom and dad are killed. I’m afraid when I talk about these thoughts and pictures that they really will die.
THERAPIST: A lot of people have thoughts that they don’t like to have. Even people without OCD. Just because you have these thoughts, or talk about them, doesn’t mean that bad things will actually happen or that you want them to come true.
It is important to reassure the patient that unpleas- ant thoughts occur often and to emphasize the dis- tinction between thoughts and reality. Many patients with OCD have magical ideas in which the distinction between “thinking about” and “making things hap- pen” is blurred, a process labeled by Salkovskis (1985)
as “thought–action fusion” (TAF). It is important to point out to the patient that thoughts are different from actions. Also, many patients think that if negative thoughts enter their mind, then it means they wish the bad thing will happen. The therapist should assure the patient that thinking about bad things does not mean that one wants them to happen. These sorts of infor- mal discussions of mistaken beliefs are an integral part of correct implementation of EX/RP. Such discussions should accompany the treatment planning process and be reiterated as needed during exposure exercises. It is, however, important that such discussions accompany EX/RP exercises rather than replace them.
Feared Consequences
Many individuals with OCD are afraid that something terrible will happen if they fail to perform their rituals. Such patients with washing rituals, for example, typi- cally fear that they and/or someone else will become ill or disabled, or die, as a result of being contaminated. Many patients with checking rituals fear that because of their negligence, certain catastrophes will occur, such as their homes burning down, or that they might kill someone while driving. Some patients have only a vague notion of what these negative consequences might be (e.g., “I don’t know exactly what will happen, but I feel that if I don’t count to 7, something bad will happen to my family”). Others do not fear catastrophes at all, but they cannot tolerate the emotional distress they ex- perience if they do not perform rituals. Some fear that unless they ritualize, anxiety will increase continually, until they have a nervous breakdown. Approximately two-thirds of patients with OCD could clearly identify consequences other than emotional distress that would result when they refrained from performing rituals, whereas the remainder could report no such conse- quences (Foa et al., 1995).
It is important to identify the specific details of the patient’s feared consequences to plan an effective expo- sure program. For example, the content of the imaginal exposure of a patient who checks while driving for fear of having hit a pedestrian and being sent to jail differs from that of a patient who fears that hitting a pedestri- an will result in punishment by God. Similarly, patients who ritualistically place objects in a specific order may differ with respect to their feared catastrophes. Some perform the ritual to prevent catastrophic consequences (e.g., death of parents), whereas others do so only to re- duce distress elicited by disordered objects. The former
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would benefit from treatment that includes both imagi- nal and in vivo exposure, whereas the latter is likely to profit from in vivo exposure alone.
Strength of Belief
Clinical observations have led to suggestions that in- dividuals with OCD who have poor insight do not respond well to exposure and response prevention, al- though two later studies failed to find a linear relation- ship between strength of belief in feared catastrophes and improvement following exposure and response pre- vention (Foa et al., 1999; Lelliott, Noshirvani, Basoglu, Marks, & Monteiro, 1988). Two issues need to be con- sidered in evaluating these collective findings. First, the reliability and validity of the strength of belief measures used in previous studies are unknown. Second, the re- lationship between overvalued ideation and treatment outcome may not be linear. Clinical observation sug- gests that only patients who express extreme belief in their obsessional ideation show poor outcome. Indeed, Foa and colleagues (1999) found that only extremely strong belief (fixed belief) was associated with attenuat- ed outcome. Such patients may appear delusional when discussing their feared catastrophes. We hypothesize that the effect of fixed belief on outcome may be me- diated by treatment compliance: Patients who are con- vinced that feared disasters will ensue if they engaged in prescribed exercises probably will not complete the tasks as assigned.
When assessing the strength of belief, it is important to remember that a patient’s insight into the senseless- ness of his/her belief often fluctuates. Some patients readily acknowledge that their obsessional beliefs are irrational, but the beliefs still cause marked distress. A few individuals firmly believe that their obsessions and compulsions are rational. In most patients, though, the strength of belief fluctuates across situations, making it difficult to ascertain the degree to which they believe the obsessions are irrational. The following example is an inquiry into the strength of a patient’s belief in her obsessional fear of contracting acquired immune defi- ciency syndrome (AIDS).
THERAPIST: How likely is it that you will contract AIDS from using a public restroom?
PATIENT: I’m really terrified that I will get AIDS if I use a bathroom in a restaurant.
THERAPIST: I know that you are afraid of getting AIDS,
but if you think logically, how likely do you think you are to get AIDS by sitting on a public toilet?
PATIENT: I think I will get AIDS if I use a public toilet. THERAPIST: So do you mean to say that there is a 100%
chance of you getting AIDS if you sit on a public toilet once?
PATIENT: Well, I don’t know about once, but if I did it again and again I would.
THERAPIST: What about other people? Will they get AIDS if they use a public toilet?
PATIENT: I guess so. I’m not sure. THERAPIST: Since most people use public bathrooms,
almost everyone should have AIDS by now. How do you explain the fact that a relatively small number of people have AIDS?
PATIENT: Maybe not everybody is as susceptible to AIDS as I am.
THERAPIST: Do you think that you are more suscep- tible than other people?
PATIENT: I don’t know for sure. Maybe the likelihood of my getting AIDS is only 50%.
Based on the interaction just described, the thera- pist concluded that the patient was not an “overvalued ideator”; thus, the prognosis for this patient is brighter than it would be if she continued strongly to hold her original belief. Accordingly, the implementation of EX/ RP for this patient would follow the standard guide- lines.
Avoidance and Rituals
To maximize treatment efficacy, all avoidance and ritu- alistic behaviors, even seemingly minor ones, should be prevented. Therefore, the therapist should gather complete information about all passive avoidance and rituals. When the therapist is in doubt as to whether a particular avoidance behavior is related to OCD, he/she might suggest an “experiment” in which the patient is exposed to the avoided situation. If the patient experi- ences anxiety or distress, the avoidance behavior should be prevented as part of treatment. Similarly, if it is un- clear whether a given action constitutes a ritual, a re- sponse prevention “experiment” may be implemented. If refraining from performing the action evokes dis- tress, the action is identified as a ritual and should be addressed in therapy.
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Individuals with OCD, like those with specific pho- bias, often attempt to avoid anxiety-evoking situations. Most passive avoidance strategies are fairly obvious (e.g., not entering public restrooms, not preparing meals, and not taking out the trash). However, the therapist also needs to be attentive to subtle forms of avoidance, such as carrying money in one’s pockets to avoid opening a wallet, wearing slip-on shoes to avoid touching laces, and using drinking straws to avoid contact with a glass or a can. Patients with obsessive–compulsive checking rituals also engage in subtle avoidance behaviors that are important to explore, such as arranging their work schedules to ensure that they are rarely, if ever, the last person to leave the business, thus ensuring that the re- sponsibility for checking the safe falls on a coworker.
Active rituals, such as passive avoidance, may be ex- plicit (e.g., prolonged washing, repeated checks of the door, and ordering of objects) and/or subtle (e.g., wip- ing hands on pant legs, blinking, and thinking “good” thoughts). It is important that the therapist identify both explicit and subtle rituals, so that both may be ad- dressed during treatment.
Although compulsive rituals are intended to reduce the distress associated with obsessions, patients some- times report that the performance of these rituals is aversive in itself. For example, Ms. S, who was obsessed with the orderliness of objects on her shelves, found re- ordering the shelves aversive, because she was unable to find the “perfect” place for everything. Similarly, Mr. J, who felt contaminated by chemicals, found the act of decontaminating himself by repeated handwash- ing aversive, because he was unable to decide when his hands were sufficiently clean; therefore, he washed until his hands became raw. Rituals may also become aversive because of their intrusion into other aspects of the person’s life. For example, Mr. J, who would take 2-hour-long showers to feel adequately clean, was rep- rimanded repeatedly by his supervisor for arriving late to work.
When certain compulsions become aversive, some patients decrease the time they spend performing the ritual by increasing avoidance behaviors, or by substi- tuting other, less time-consuming rituals. For example, Ms. E, who was obsessed with fears of contamination by funeral-related objects (e.g., cemeteries and people returning from a funeral), responded with hours of showering and handwashing. She eventually retreated into her bedroom and avoided all contact with the outside world. Mr. J, described earlier, avoided taking a shower for days at a time, but between showers he
wiped his hands compulsively and avoided touching his wife. In some cases, seemingly “new” rituals may de- velop during the course of treatment to function in the place of those previously identified and eliminated. For example, Mr. F, who was concerned about his hands becoming contaminated, successfully resisted the urge to wash his hands, but soon after response prevention was implemented, he started to rub his hands together vigorously to “decontaminate” them. When such a sub- stitute ritual is identified, it also needs to be addressed in treatment with ritual prevention. Therapists must re- main alert to not only such shifts in ritualistic behaviors but also alert patients to the possibility of such shifts.
History of Main Complaint and Treatment History
Many individuals with OCD are unable to give a de- tailed account of the onset of their symptoms because the symptoms began subtly, many years ago. Neverthe- less, therapists should attempt to collect as much infor- mation as possible about the onset and course of the disorder. Such information may provide clues about as- pects of the fear network and variables associated with the maintenance of symptoms, and may help to antici- pate difficulties that may arise during treatment (e.g., old obsessions or rituals that may resurface as more prominent ones diminish).
Many such individuals also have an extensive his- tory of psychological and pharmacological treatments, and it is important to make a detailed inquiry about the outcome of previous treatments. If the patient has been treated with EX/RP, the therapist should assess whether the treatment was implemented appropri- ately and the patient was compliant with treatment demands. Knowledge that a patient experienced diffi- culty complying with response prevention instructions, or that previous therapy failed to provide adequate ex- posure experiences or response prevention instructions, is important for designing the behavioral program. Other factors that may have prevented successful out- come or caused relapse, such as job stress, death in the family, or pregnancy, should be discussed. At the same time, a prior failed course of EX/RP should not neces- sarily be viewed as prognostic, especially if the patient recognizes why the therapy was less successful in the past. One of our patients, who had failed multiple trials of less intensive EX/RP, came to our center with the knowledge that his noncompliance with exposure exer- cises between weekly sessions greatly reduced the effects of treatment. He also noted that the slow progress he
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observed in these previous therapies demoralized him and caused further disengagement from the treatment. When offered a choice of daily versus twice-weekly ses- sions, he opted for the daily treatment, noting that the more intensive approach might decrease the chance of similar lapses. He has now successfully completed the intensive regimen.
In our clinic we have observed that a substantial majority of our outpatients have been treated, or are currently being treated, with serotonergic medications. Some seek EX/RP to augment the partial gains they have achieved with the medication. Others wish to dis- continue the medication because it was ineffective, it had side effects, or they do not want to continue taking medicine indefinitely. Assessment of the patient’s treat- ment goals is necessary for planning his/her treatment program.
Social Functioning
Obsessive–compulsive symptoms may severely disrupt the daily functioning of patients. Therapists should as- sess the impact of OCD symptoms on the various areas of functioning. When appropriate, this information should be used to design suitable exposure exercises. For example, Ms. D experienced difficulties completing as- signments at work, because she repeatedly checked each task. Treatment included exposures to performing tasks at work without checking. Even if the client is not cur- rently working, exposures simulating work situations may be necessary if symptoms created difficulties in previous jobs.
OCD clearly has a deleterious effect on the intimate relationships of many patients. About half of married individuals seeking treatment for OCD experience marital distress (Emmelkamp et al., 1990; Riggs et al., 1992). Other family and social relationships may also suffer as a result of OCD symptoms. The impairment in social functioning may arise because social contact is either perceived as threatening (e.g., “I may spread germs to other people”) or so much of the patient’s time and energy is invested in performing rituals and plan- ning ways to avoid distressing situations. Again, infor- mation about the relation of social dysfunction to OCD symptoms may lead the therapist to include specific ex- posures aimed at ameliorating these social difficulties.
The assessment of social functioning should also in- clude an evaluation of what role, if any, other people play in the patient’s compulsive rituals. If the patient re- lies on others for reassurance or compliance with rituals
(e.g., family members must remove their shoes before entering the house), the therapist should instruct fam- ily members how to respond appropriately when asked to participate in the patient’s rituals. A careful analysis of the relationship is called for before specific instruc- tions are given to significant others. Moreover, if family members tend to criticize the patient when obsessional distress arises, it is important to address these negative exchanges in treatment. We have often addressed this issue with a combination of empathic discussion of the frustration experienced by the family member and role playing of more effective responses.
Mood State
Although some patients with serious depression and OCD may benefit from behavioral therapy for OCD (Foa, Franklin, et al., 1992), research suggests that severe depression may limit the extent of reduction of OCD symptoms and the maintenance of those gains (e.g., Abramowitz et al., 2000). Therefore, it is impor- tant to assess the mood state of the patient prior to be- ginning behavioral therapy. Patients with severe depres- sion should be treated with antidepressant medication or cognitive therapy to reduce the depressive symptoms prior to implementing behavioral therapy for the OCD. Treatment with serotonergic antidepressants may re- duce OCD symptoms, as well as depression. Because the effects of such medication on OCD symptoms may not be evident until 3 months after treatment begins, the therapist needs to use his/her clinical judgment to decide whether to begin EX/RP when the depression decreases or wait until the effects of the medication on OCD symptoms can be assessed.
Choice of Treatment
How should a therapist determine the most suitable treatment for a given patient? As discussed earlier, EX/RP, as well as serotonergic medications, have dem- onstrated efficacy for OCD. Therapist and patient are faced with the choice of EX/RP, pharmacotherapy, or a combination of the two. Neither treatment is effective with all patients, and no consistent predictors of who will benefit most from which treatment modality have been identified. Therefore, unless the patient has been particularly successful or unsuccessful with some previ- ous course of treatment, the decision should be based on factors such as availability of treatment, amount of time the patient is able or willing to invest in treatment,
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and his/her motivation and willingness to tolerate side effects.
The intensive treatment requires a considerable in- vestment of time over a period of several weeks. Many patients are unable, or unwilling, to devote 4–5 hours a day to treatment. These patients should be advised to try pharmacological treatment, which does not require the same extensive time commitment. Recent investiga- tions of the effects of a twice-weekly EX/RP regimen compared to intensive treatment suggested comparable outcomes at follow-up (Abramowitz et al., 2003; Storch et al., 2007); thus, in our center, we routinely offer either program to patients considering EX/RP. Some patients may be unwilling (sometimes expressed as “I can’t do that”) to experience the temporary discomfort caused by EX/RP. These patients, too, may be advised to try medications. The need to develop “readiness programs” designed to prepare such patients to accept EX/RP treatment is often cited in light of the relatively high refusal rate among patients offered EX/RP. Such programs may include testimonials from previously treated patients, cognitive strategies designed to help the patient calculate objective risks more accurately, psychoeducation about OCD and EX/RP, and a review of the outcome literature for various treatments (Tolin, Maltby, Diefenbach, Hannan, & Worhunsky, 2004). An initial RCT of EX/RP plus motivational interview- ing (MI) did not yield outcomes that were superior to EX/RP alone (Simpson et al., 2010), but the study did not specifically recruit patients who were experiencing low motivation. Manualizing programs specifically for those patients and examining the acceptance rate and efficacy of EX/RP infused with MI constitutes the next step in this line of research.
Patients who are concerned about the potential (or have already experienced) side effects of medications or their unknown long-term effects often prefer EX/RP. Other patients are concerned with the prospect of en- tering an “endless” treatment because, according to present knowledge, relapse occurs when medication is withdrawn (Pato et al., 1988; Thorén, Asberg, Chron- holm, Jörnestedt, & Träskman, 1980). This concern is particularly relevant for women who plan to bear chil- dren and need to withdraw from the medication during pregnancy. EX/RP should be recommended to these patients because its effects are more enduring.
As discussed earlier, the long-term effects of combin- ing EX/RP and medication are unclear; therefore, it is premature to recommend treatment programs that combine the two therapies. However, some patients
who present for treatment are already on antidepressant medication. Because these medications were found not to interfere with the effectiveness of EX/RP (Franklin et al., 2000), it is recommended that patients continue to take the medication if they have experienced some improvement in either obsessive–compulsive symp- toms or depression. However, if the patient has not ex- perienced improvement with medication, withdrawal of the medication before or during EX/RP should be considered. Special consideration should be given to patients with severe depression concurrent with their OCD. It is recommended that these patients be treat- ed with antidepressants or cognitive therapy for the depression prior to entering intensive EX/RP for the OCD given recent findings of somewhat attenuated outcome for severely depressed patients (Abramowitz et al., 2000).
INTENSIVE EX/RP PROGRAM
The intensive treatment program comprises four phas- es: (1) information gathering, (2) intensive EX/RP, (3) a home visit, and (4) maintenance and relapse prevention.
Information Gathering and Treatment Planning
The first stage of information gathering consists of a thorough diagnostic evaluation to determine that the patient’s main psychopathology is OCD. The second step is to assess whether the patient is appropriate for EX/RP. We recommend that individuals who are abus- ing drugs or alcohol should be treated for the substance abuse prior to intensive treatment for OCD. Patients who have clear delusions and hallucinations are also poor candidates for intensive treatment. Individuals with severe MDD should be treated for depression be- fore beginning treatment for OCD. The patient’s mo- tivation to comply with the demands of intensive treat- ment should be carefully evaluated. It is important to describe the treatment program in enough detail that the patient is not surprised when treatment begins. If the patient does not express strong motivation and commitment to treatment, it might be preferable to delay implementation of intensive treatment or to offer alternative treatments, such as medication. As noted earlier, a study of less intensive EX/RP for patients who appear otherwise motivated, yet cannot accommodate the daily regimen into their schedules, suggested an outcome comparable to intensive treatment; future re-
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search with much larger samples is needed to determine whether patient factors predict differential outcome to either treatment schedule.
Once a patient is judged to be appropriate for in- tensive treatment, information gathering for treatment planning begins. This phase typically comprises 4–6 hours of contact with the patient over a period of 2–3 days. During this phase, the therapist collects informa- tion about the patient’s obsessive–compulsive symp- toms, general history, and the history of treatment for OCD, as described earlier. During these sessions, the therapist discusses the rationale for treatment, describes the program in detail, teaches patients to monitor their rituals, and develops a treatment plan.
First Information‑Gathering Session
It is very important to discuss the rationale for treat- ment and to describe the treatment program in detail. The program requires that the patient abandon his/ her obsessive–compulsive habits, therefore temporarily experiencing substantial discomfort. If patients do not understand why they are asked to suffer this short-term distress or are not convinced that treatment will work, they are unlikely to comply with treatment instruc- tions. The treatment rationale is explained as follows:
“You have a set of habits that, as you know, are called obsessive–compulsive symptoms. These are habits of thinking, feeling, and acting that are extremely unpleasant, wasteful, and difficult to get rid of on your own. Usually, these habits involve thoughts, im- ages, or impulses that habitually come to your mind, even though you don’t want them. Along with these thoughts you have unwanted feelings of extreme dis- tress or anxiety and strong urges to do something to reduce the distress. To try to get rid of the anxiety, people get into the habit of engaging in various spe- cial thoughts or actions, which we call ‘rituals.’
“Unfortunately, as you know, the rituals do not work all that well, and the distress decreases for a short time only, then comes back again. Eventually, you may find yourself doing more and more ritual- izing to try to reduce anxiety, but even then the re- lief is temporary and you have to do the ritual all over again. Gradually, you find yourself spending so much time and energy ritualizing—which does not work that well anyway—that other areas of your life are seriously disrupted.
“The treatment we are about to begin is called exposure and response prevention. It is designed to break two types of associations. The first association is between sensations of anxiety and the objects, situ- ations, or thoughts that produce this distress. [The therapist uses information collected as examples; e.g., ‘Every time you touch anything associated with urine you feel anxious, distressed, or contaminated.’] The second association we want to break is that between carrying out ritualistic behavior and the feeling of less anxiety or less distress. In other words, after you carry out [specifies the identified rituals], you tem- porarily feel less distress. Therefore, you continue to engage in this behavior frequently. The treatment we offer breaks the automatic bond between the feelings of discomfort/anxiety/contamination of [specifies the obsession] and your rituals. It will also train you not to ritualize when you are anxious.”
After presenting the treatment rationale, the thera- pist should begin to collect information about the pa- tient’s OCD symptoms. The rationale for information gathering and a description of the treatment is present- ed as follows:
“In the next two sessions, I will ask you specific questions about the various situations and thoughts that generate discomfort or anxiety in you. We will order them according to the degree of distress they generate in you on a scale from 0 to 100, where 0 means No anxiety and 100 means Maximum anxiety or panic. The exposure treatment program involves confronting you with situations and thoughts that you avoid because they generate anxiety and urges to carry out ritualistic behavior. Why do we want to expose you to places and objects that will make you uncomfortable, situations that you have attempted to avoid even at much cost? We know that when people are exposed to situations that they fear, anxiety grad- ually declines. Through exposure, then, the associa- tion between anxiety and [specifies the obsession] weaken because you are repeatedly exposed to these situations, so that the previously evoked anxiety de- creases with time.
“For many people with OCD the obsessions occur within their imagination and rarely take place in real- ity. This makes it impossible to practice exposure by actually confronting those situations for prolonged periods. For example, if a person fears that her home
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will burn down, we certainly do not wish to have her house catch on fire in order to practice exposure. Similarly, someone who fears that he has run over a person who is now lying in the road cannot in reality be exposed to such a situation.
“If confrontation with the feared situation is nec- essary to reduce obsessions, how can you improve without directly confronting the situation? You can confront these fears through imagery, in which you visualize the circumstances that you fear will hap- pen. In imagery practice, you create in your mind detailed pictures of the terrible consequences that you are afraid will occur if you do not engage in the ritualistic behavior. During prolonged exposure to these images, the distress level associated with them gradually decreases.
“When people with OCD encounter their feared situations or their obsessional thoughts, they become anxious or distressed and feel compelled to perform the ritualistic behavior as a way to reduce their distress. Exposure practices can cause this same distress and urge to ritualize. Usually, performing rituals strength- ens the pattern of distress and rituals. Therefore in treatment, ritual prevention is practiced to break the habit of ritualizing. This requires that you stop ritual- izing, even though you are still having urges to do so. By facing your fears without resorting to compulsions, you gradually become less anxious. Behavior thera- pists call this process habituation. Therefore, during the 3 weeks of intensive exposure, the association be- tween relief from anxiety and carrying out [specifies the patient’s rituals] will become weaker because you will not be allowed to engage in such behaviors; there- fore, you will find out that your anxiety decreases even if you do not resort to these activities.”
The initial information-gathering session is also used to begin training the patient to monitor his/her rituals accurately. Accurate reports of the frequency and dura- tion of ritualistic behavior are important to evaluate the progress of treatment and to demonstrate the reality of changes to the patient. In some cases, the monitoring also serves an active role in treatment. Patients begin to recognize that rituals do not truly occur “all day long” and the act of monitoring the rituals may decrease their frequency and duration.
“It is very important for the treatment program that we have an accurate picture of the extent to which
you engage in obsessive thinking and compulsive be- havior. Having a clear picture of how much of your time is taken up by your problem will help us to monitor your progress and adjust the treatment pro- gram accordingly. Therefore, during this week, while I am still collecting information to form a treatment program, I would like you to record your symptoms every day. It is not easy to report accurately on how much you engage in your obsessive–compulsive be- havior; therefore, we will spend some time now and in the next session going over some rules for how to record your symptoms. Here are some monitoring forms on which you will record your thoughts and rituals.”
The therapist should specify which ritual(s) the pa- tient is to record, go over the instructions carefully with the patient, and practice filling out the form with the patient using an “imaginary day” of his/her life. The following rules are helpful in monitoring rituals:
1. Use your watch to monitor the time you spend on your rituals.
2. Do not guess the time of ritualizing; be exact. 3. Write the time immediately on your monitoring
form. 4. Do not save the recording to the end of the day or
the beginning of the next day. 5. Write a short sentence to describe the trigger for
ritualizing.
Prior to beginning treatment, the patient identifies an individual (e.g., parent, spouse, or close friend) who can serve as a support person during the intensive treatment program. The patient is instructed to rely on this person for support during exposures, and the support person is asked to help monitor compliance with response preven- tion instructions. If the patient experiences difficulty resisting the urge to ritualize, then the support person is contacted for support. Because the support person is involved in the therapy, the therapist allocates time during the information-gathering phase to describe the treatment and discuss its rationale with him or her.
The therapist makes an effort to ensure that the sup- port person and the patient mutually agree that the support person will offer constructive criticism and observations. In making these suggestions, the sup- port person should be sensitive to any difficulties that have arisen in the past. For example, Mr. B, who served
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as his wife’s primary source of reassurance, also criti- cized her severely when he “caught” her performing her handwashing ritual. To prevent these responses from hampering treatment, to help the husband supervise his wife’s response prevention, the therapist spent time with the couple negotiating appropriate, uncritical re- sponses to the wife’s requests for reassurance.
The support person is in regular (at least twice week- ly) contact with the therapist and is not only informed about the specific homework exposures that the patient has to accomplish but also relays his/her observations about the patient’s behavior outside the therapy session. In addition, with the consent of the patient, the support person should contact the therapist if major treatment violations occur (e.g., refusing to do homework or en- gaging in ritualistic behavior).
Second Information‑Gathering Session
At the beginning of the second information-gathering session, the therapist devotes time to the patient’s self- monitoring form, which includes examining the de- scriptions of situations that trigger ritualistic behavior and offering constructive comments when necessary. The therapist reminds the patient to use short phrases or sentences to describe the trigger situations, assesses the accuracy of the patient’s time estimates, and empha- sizes the need for accurate measurements.
Generating a Treatment Plan
The bulk of the second information-gathering session is allotted to gathering detailed information about the patient’s symptoms and, based on what is learned about the symptoms, developing a treatment with the patient. It is important to explain to the patient how the ex- posure exercises that comprise his/her treatment will reduce the OCD symptoms. For, example, the patient with religious obsessions is told that the imaginal expo- sure to burning in hell in excruciating detail is designed to reduce his obsessional distress when a less elaborate image of burning in hell comes into his mind. It is im- portant that patients understand the rationale under- lying the central concept in EX/RP, that confronting obsession-evoking stimuli during treatment increases their suffering in the short run but will reduce it in the long run. We often tell patients that the difficulties they experience during the first week of exposure sessions are likely to diminish with proper implementation of EX/RP.
Describing Homework
At the end of the second information-gathering ses- sion, the therapist describes the homework assignments included in the treatment program. The homework, which usually requires 2–3 hours, in addition to the 2-hour treatment session, comprises additional expo- sure exercises to be done between treatment sessions at the patient’s home or elsewhere (e.g., a shopping mall or a relative’s home). We suggest that the patient monitor his/her SUDS level every 10 minutes during the home- work exposures. In some cases, when it is impossible for the patient to maintain an exposure for 45–60 minutes, the therapist works with the patient to develop a plan that allows the exposure to be prolonged. For example, instead of asking the patient to spend 45 minutes sit- ting in the restroom of a local restaurant, the therapist might suggest that he/she contaminate a handkerchief on the toilet seat and carry this “contamination rag” in a pocket.
Treatment Period
The treatment program at our center typically com- prises fifteen 2-hour treatment sessions conducted daily for 3 weeks. Clinical observation suggests that massed sessions produce better results than do sessions spread out over time; therefore, we recommend a minimum of three sessions per week. Each session begins with a 10- to 15-minute discussion of homework assignments and the previous day’s ritual monitoring. The next 90 minutes are divided into 45 minutes each of imaginal and in vivo exposure. The final 15 minutes are spent discussing the homework assignment for the following day. This format may be adjusted when necessary. For example, if an in vivo exposure requires that therapist and patient travel to a local shopping mall to contami- nate children’s clothing, the entire session is devoted to this activity. Some patients have difficulty engaging emotionally in imaginal exposures (i.e., the images fail to elicit distress). In these cases, treatment should focus exclusively on in vivo exercises.
We recommend that the therapist discuss the plan for that session with the patient in the beginning of the ses- sion. Barring any unusual circumstances (e.g., patient’s stated objection to proceeding with the planned expo- sure), it is important to limit these discussions to no more than 15 minutes. Patients with OCD are usually very fearful of engaging in exposure tasks, and elabo- rate discussion of the task at hand may serve as a form
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of avoidance of going ahead with the exposure. These preexposure discussions are also fertile ground for as- surance seeking (i.e., the patient asking the therapist if he/she is certain that the proposed exercise is safe). The therapist should answer such questions carefully, avoid- ing either extreme (i.e., neither providing compulsive reassurance nor conveying to the patient that the pro- posed exposure is objectively dangerous).
Imaginal exposure exercises are typically conducted prior to in vivo exercises in each session, often as a pre- lude to the scheduled in vivo exercise. During imaginal exposure the patient is seated in a comfortable chair and is given the following instructions:
“Today you will be imagining [describes scene]. I’ll ask you to close your eyes so that you won’t be dis- tracted. Please try to picture this scene as fully and vividly as possible, not like you are being told a story, but as if you were experiencing it now, right here. Every few minutes I will ask you to rate your anxiety level on a scale from 0 to 100. Please answer quickly and try not to leave the image.”
The imaginal exposure sessions are audiotaped, and the patient is asked to repeat the exposure by listening to the tape as part of that day’s homework. The situ- ations included in in vivo exposure vary greatly from patient to patient (particularly with patients with prom- inent checking rituals). Below are some examples of in- structions that might be offered to patients during in vivo exposure exercises.
For patients with prominent washing rituals:
“Today, you will be touching [specifies item(s)]. This means that I will ask you to touch it with your whole hand, not just the fingers, and then to touch it to your face, hair, and clothing, all over yourself, so you feel that no part of you has avoided contamination. Then I’ll ask you to sit and hold it and repeatedly touch it to your face, hair, and clothes during the rest of the session. I know that this is likely to make you upset, but remember the anxiety will eventually decrease. I also want you to go ahead and let yourself worry about the harm you are afraid will occur— for example, disease—since you won’t he washing or cleaning after this exposure. I am sorry that this treatment has to be difficult and cause so much dis- comfort, but I’m sure you can do it. You’ll find it gets easier as time goes on. OK, here it is, go ahead and touch it.”
The therapist should give the patient the object to hold, ask him/her to touch it, then ask the patient to touch the object or the “contaminated” hands directly to his/her face, hair, and clothing. Every 10 minutes the patient should be asked, “What is your level of anxiety or discomfort from 0 to 100 right now as you focus on what you’re touching?” This can be shortened to “What is your SUDS level?” once the patient understands the question.
For patients with prominent checking rituals:
“Now, I’d like you to [e.g., write out your checks to pay your monthly bills without looking at them after you’ve finished; just put them in the envelope and then we will mail them right away, without checking even once after you’ve done it]. Then we will go on and do [e.g., drive on a bumpy road without look- ing in the rearview mirror] in the same way. While doing this, I would like you to worry about what harm might occur because you aren’t checking your actions, but don’t let the thoughts interfere with ac- tually doing those activities.”
Patients should be reminded of the specific instruc- tions for response prevention on the first day of treat- ment and periodically during treatment. We have found that giving patients a printed copy of the rules for response prevention can help them to understand and remember the rules. If the rules as outlined for the patient do not adequately cover the type of ritual(s) the patient exhibits, the therapist should provide a written set of instructions modeled after these forms.
During the last few sessions of treatment, the patient should be introduced to rules of “normal” washing, cleaning, or checking. Response prevention require- ments should be relaxed to enable the patient to return to what is considered a normal routine.
Home Visit
It is important to ensure that the patient’s gains from the treatment program generalize to the home envi- ronment. Usually, homework assignments function to produce this generalization, but we have found that vis- its by the therapist to the patient’s home can be quite helpful, especially when the patient is not able to return home daily during the intensive treatment phase (e.g., patients who are from out of town or are hospitalized). The home visit also offers therapist and patient an op- portunity to discuss guidelines for “normal” behavior.
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The therapist should discuss the plans for these visits with the patient and his/her family before the treatment ends. It is also important to note that, in some cases, the majority of the treatment sessions need to be conduct- ed at the patient’s home, for example, when treating a hoarder. Determining the frequency of home visits dur- ing the core treatment should be based on whether the patient’s OCD symptoms are readily “transportable” to situations outside the home, or whether they are spe- cific to the home. For patients with prominent wash- ing rituals, with “safe” rooms and areas in their houses, contamination of these areas is imperative and also quite difficult; it is often advisable that the therapist as- sist directly with these home-based exposures when it is questionable whether the patient can contaminate these “sanctuaries” successfully on his/her own.
Typically, the home visit comprises 4-hour sessions held on each of 2 days at the end of the treatment pro- gram. The bulk of the time in these sessions is used to conduct additional exposures to obsessive stimuli in and around the patient’s home or workplace. For example, the therapist might accompany the patient as he/she con- taminates objects around the house or at the local gro- cery store. Similarly, the patient might be asked to turn the stove on and off without checking and leave the house with the therapist. Most patients, particularly those who were able to return home during treatment, report little or no discomfort when doing these exposures, because they represent repetition of homework assignments. In some cases, though, the therapist will discover areas that the patient has not contaminated, or some areas at home that continue to generate distress despite previous expo- sures. The home visit should focus on exposure to situa- tions or objects that remain problematic.
With more recent development of platforms such as Skype, Zoom, and so forth, home visits become expen- sive in therapist’s time and travel. The goals of the home visits can be achieved through the computer platforms.
Maintenance Period
In addition to prescribing continued self-exposure tasks to help the patient maintain therapy gains, the therapist may wish to schedule regular maintenance sessions. These sessions may be used to plan additional exposures, to refine guidelines for normal behavior, and to address issues that arise as the patient adjusts to life without OCD.
There is some evidence that patients benefit from continued contact with the therapist following the in-
tensive therapy sessions. In one study, 12 weekly sup- portive therapy sessions (no exposure exercises) ap- peared to reduce the number of relapses in a sample of individuals with OCD treated with 3 weeks of intensive EX/RP (Foa et al., 1992). In another study, following the intensive treatment with 1 week of daily cognitive- behavioral sessions, followed by eight brief (10-minute) weekly telephone contacts, resulted in better long-term outcome than following intensive treatment with 1 week of treatment with free association (Hiss et al., 1994).
Therapeutic Setting
It is advisable for patients to remain in their normal en- vironments during intensive treatment. This is particu- larly important for patients whose fears are cued mainly by stimuli in their home environment. The hospital may be an artificially protected setting, particularly for patients with prominent checking rituals, who may not feel responsible for their surroundings and as a result do not experience their usual urges to check. If patients live too far away to commute for daily sessions, we recom- mend that they rent an apartment or hotel room near the clinic. When this is not possible, hospitalization should be considered. Hospitalization is recommended for patients deemed to be at risk for suicide or psychotic breakdown, and for those who need close supervision but lack a support system sufficient to aid them during treatment.
If a patient is employed and his/her OCD symptoms are work related, he/she should be encouraged to con- tinue working, so that relevant exposures can he includ- ed in treatment. However, since treatment requires 5–6 hours per day, the patient may opt to work half-days during the intensive treatment.
When the patient’s symptoms are unrelated to work, he/she may decide not to continue working during in- tensive treatment. Because of the time-consuming na- ture of the treatment, we often suggest that patients take some time off from work. If it is not possible for the patient to take 3 full weeks off from work, the therapist might suggest that the patient work half-days or take time off from work during the first and second weeks of the treatment program.
Therapist Variables
Intensive treatment with exposure to feared situations and response prevention of ritualistic behavior provoke
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considerable stress for patients. Their willingness to un- dergo such “torture” attests to their strong motivation to rid themselves of the OCD symptoms. The intensive treatment regimen requires that the therapist main- tain a delicate balance between pressuring the patient to engage in the treatment and empathizing with his/ her distress. Clinical observations and findings from a study by Rabavilas and colleagues (1979) suggest that a respectful, understanding, encouraging, explicit, and challenging therapist is more likely to achieve a suc- cessful outcome than a permissive, tolerant therapist. Notably, patients of well-supervised, nonexpert EX/RP therapists appear to fare well with EX/RP (Franklin, Abramowitz, Furr, Kalsy, & Riggs, 2003; Valderhaug et al., 2007).
During treatment, patients’ behavior may range from extreme cooperation and willingness to partici- pate in exposures to blatant manipulation and refusal to follow the therapist’s instructions. An individual patient may fluctuate depending on what exposure is conducted during a particular session. To a great ex- tent, the “art” of conducting behavioral therapy for OCD involves knowing when to push, when to con- front, and when to be more flexible. Such decisions re- quire that the therapist carefully observe the patient’s reactions and make a judgment based on his/her expe- rience. As much as possible, the therapist should dis- play an attitude that counteracts the harshness of the treatment program, while maintaining the rules for therapy established at the beginning of the program. The therapist should assure the patient that he/she will not use force to implement exposure, and that no ex- posure will be planned without the patient’s consent. If the patient cannot trust that the therapist will adhere to these essential guidelines, the treatment is likely to be compromised. We also assure patients that family members will be asked not to present unplanned expo- sures to the patient (e.g., taking out the garbage) with- out discussing it.
Patient Variables
A primary factor that influences a patient’s potential for benefiting from intensive behavioral treatment is the level of his/her motivation. Because EX/RP causes high distress, patients need to be highly motivated to un- dertake the treatment. Often the level of motivation is related to the severity of the patient’s symptoms. When symptoms are sufficiently intolerable, patients are more likely to tolerate considerable discomfort for a short pe-
riod to gain relief from their symptoms in the long run. Tolin and colleagues (2004) have also discussed the im- portance of motivational readiness in EX/RP and have suggested specifically how best to prepare patients for the often grueling treatment regimen.
Sometimes individuals are pressured into entering therapy by their families, and they agree to participate in treatment only to appease a spouse or a parent. These patients are unlikely to follow the therapist’s instruc- tions strictly; therefore, they are less likely to make last- ing gains in therapy. In light of these observations, we do not recommend that patients enter into EX/RP if they are not committed to follow such instructions; al- ternative treatment strategies are typically recommend- ed in such circumstances.
It is important that the therapist clearly explain to the patient that 1 month of therapy, albeit intensive, is unlikely to eliminate all OCD symptoms. Rather, pa- tients should expect that their anxiety and the urges to ritualize will diminish and become more manageable. An expectation of becoming symptom free at the end of treatment may lead to disappointment and can poten- tiate relapse, because maintenance of treatment gains usually requires continued effort over time following the intensive treatment. Thus, in the initial interview, we tell patients that we do not have a “cure” for OCD; rather, we have a treatment that is likely to help them substantially reduce their symptoms in both the short and the long run.
It is also important to explain to patients that EX/RP treatment is not a panacea for all of their psychological and interpersonal problems. This treatment is aimed specifically at reducing patients’ obsessions and urges to ritualize. Problems that existed prior to treatment (e.g., marital discord or depression) are likely to remain, although they may be somewhat alleviated after treat- ment.
As mentioned earlier, patients with severe depression and/or an extremely strong belief in the reality of the ob- sessive fear may not benefit from EX/RP. An additional factor that has been identified as a potential hindrance to the cognitive-behavioral and pharmacological treat- ment of OCD is concurrent schizotypal personality disorder (Jenike, Baer, Minichiello, Schwartz, & Carey, 1986). Although some questions have been raised about the method used to diagnose schizotypy (see Stanley, Turner, & Borden, 1990), therapists should be alerted to the probability that patients with schizotypal per- sonality disorder may respond poorly to treatment for OCD.
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CASE STUDY
In this section we demonstrate through verbatim ma- terial the process of gathering information relevant to treatment, planning the treatment program, and con- ducting exposure sessions.
Case Description
“June,” a 26-year-old married woman who had just completed her bachelor’s degree in nursing, sought treatment for a severe washing and cleaning problem. She was extremely agitated in the first interview and de- scribed herself as “crying a whole lot” during the previ- ous 6 weeks. She arrived in the company of her husband of 6 months and her sister-in-law, whom she considered a good friend. Previous treatment by systematic desen- sitization, antidepressants, tranquilizers, and cognitive restructuring had proven ineffective. June had been un- able to seek employment as a nurse due to her symptoms.
This information was collected at June’s initial evalu- ation for participation in EX/RP treatment. After as- certaining the absence of psychosis, drug and alcohol abuse, and organic disorders, June was assigned a thera- pist.
Information Gathering
Current Symptoms
First, the therapist sought information from June about the obsessional content, including external and internal fear cues, beliefs about consequences, and information about passive avoidance patterns and types of rituals. Because rituals are the most concrete symptom, it is often convenient to begin the inquiry by asking for a description of this behavior.
THERAPIST: I understand from Dr. F that you are hav- ing a lot of difficulty with washing and cleaning. Can you tell me more about the problem?
JUNE: I can’t seem to control it at all recently. I wash too much. My showers are taking a long time, and my husband is very upset with me. He and my sister- in-law are trying to help, but I can’t stop it. I’m upset all the time and I’ve been crying a whole lot lately (on the verge of tears). Nothing seems to help.
THERAPIST: I see. You look upset right now. Please try to explain what your washing has been like in the
past few days, so I can understand. How much wash- ing have you been doing?
JUNE: Much too much. My showers use up all the hot water. And I have to wash my hands, it seems like, all the time. I never feel clean enough.
THERAPIST: About how long does a shower take? How many minutes or hours would you say?
JUNE: About 45 minutes, I guess. I try to get out sooner. Sometimes I ask Kenny to make me stop.
THERAPIST: And how often do you take one? JUNE: Usually only twice, once in the morning and
once at night before bed, but sometimes, if I’m really upset about something, I could take an extra one.
THERAPIST: And what about washing your hands? How much time does that take?
JUNE: You mean how many times do I wash? THERAPIST: How long does it take each time you wash
your hands, and how often do you wash your hands in a day?
JUNE: Umm, maybe 20 times a day. It probably takes me 5 minutes each time, maybe more sometimes. I always have the feeling they’re not really clean, like maybe I touched them to the side of the sink after I rinsed and then I think they’re dirty again.
The therapist now had some basic information about the most prominent rituals. Some further questioning clarified whether other compulsions were also in evi- dence.
THERAPIST: Do you do anything else to make yourself feel clean?
JUNE: Yes, I alcohol things. I wipe with alcohol, like the car seat before I sit down.
THERAPIST: Do you wipe yourself with alcohol? JUNE: No, only things that I think are dirty. THERAPIST: Can you tell me how much you do that? JUNE: I use about a bottle of alcohol a week.
Here the therapist had to choose whether to inquire about what objects June cleans or to ask about possible additional rituals. The therapist chose to continue the inquiry about ritualistic actions, and to turn to the subject of “contaminants” as soon as the inquiry was completed.
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THERAPIST: OK, can you think of any other things that you do to clean yourself, or other things around you that you feel are dirty?
JUNE: That’s all I can think of right now. THERAPIST: What about other kinds of what we call
“compulsive” type of activities? Do you have to check or repeat things over and over?
JUNE: No, except when I wash, if I don’t feel it’s enough. Then I wash again.
THERAPIST: No other repetitive actions besides wash- ing?
Since this patient did not appear to have multiple types of ritualistic behaviors, the therapist turned to the obsessional content. External cues are usually solicited first.
THERAPIST: What are the things that make you feel you want to wash? For instance, why do you wipe the car seat with alcohol?
JUNE: I think that maybe I got dog dirt on it when I got in from before, or Kenny might have.
THERAPIST: From your shoes? JUNE: Yes, I also worry about the hem of my dress
touching the seat. I’ve been worrying that my shoe could kick my skirt hem or when I step up a step, like to go in a building, the dress could touch the step.
THERAPIST: A dress like this? June was wearing a dress that came to just below her knee. [The likelihood that it could have touched a curb or sole of her shoe was very slim.]
JUNE: Yes. THERAPIST: Has your skirt ever had dog dirt on it? JUNE: I don’t think so, but in my mind I think that
maybe it could have gotten some on it. I suppose it would be hard for that to happen, wouldn’t it?
Thoughts that highly improbable events might have occurred are common in OCD. Such distortions may be the result of intense anxiety. Doubts about “safety” often lead to requests for reassurance or to rituals. Reas- suring June that her dress is unlikely to be soiled would have been countertherapeutic, because it perpetuates the neurotic fears. Rather, the therapist inquired fur- ther about the obsessional content.
THERAPIST: Is dog “dirt” the most upsetting thing that you worry about?
JUNE: Probably. Yes, I think so, but bathroom germs are pretty bad, too.
THERAPIST: What sort of germs? JUNE: From toilets. You know, when you go to the
bathroom. THERAPIST: Urine and feces? JUNE: Yes, urine doesn’t bother me as much as the other. THERAPIST: Why? JUNE: Because I learned in nursing school that it’s al-
most sterile. I had a hard time in the course about microbiology, because it upset me to try to learn about bacteria and microorganisms. They make it sound like there are all kinds of germs everywhere that are real dangerous. I didn’t learn it very well; I tried to avoid thinking about it.
June’s concerns with both dog dirt and bathroom germs suggested that her fear structure includes ap- prehension about potential illness. The therapist ques- tioned her to better understand the nature of the feared consequences of contamination.
THERAPIST: Are you afraid of diseases that could come from feces?
JUNE: Yes, I guess so. The thing of it is, though, I know other people don’t worry about it like I do. To them, you know, they just go to the bathroom and wash their hands and don’t even think about it. But I can’t get it out of my head that maybe I didn’t get clean enough.
THERAPIST: If you didn’t wash enough, would you get sick or would you cause someone else to get sick?
JUNE: Mostly I worry that I’ll get sick, but sometimes I worry about Kenny, too.
THERAPIST: Do you worry about a particular kind of disease?
JUNE: I’m not sure. Some kind of illness.
It is not uncommon for patients who fear harm that may ensue from not ritualizing to be unable to identify a specific feared consequence. Patients with prominent checking rituals often fear they will forget or throw out something important, but they do not always know ex-
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actly what this will be. Repeaters may fear that some- thing bad will happen to loved ones but often cannot specify what particular disaster will befall them. How- ever, many individuals with OCD do fear specific con- sequences (e.g., blindness or leukemia). At this point, the therapist may choose either to complete the inquiry about external threat cues or pursue the investigation about the feared consequences and the belief that such harm is indeed likely to occur. The latter course was selected here.
THERAPIST: Let’s say that you did actually touch dog feces or human feces, and you weren’t aware of it, so you didn’t wash to remove it. What is the likelihood that you or Kenny would really get seriously ill?
JUNE: Well, I feel like it really could happen. THERAPIST: I understand that when it happens and you
become very distressed, it feels like you will actually become sick, but if I ask you to judge objectively, right now, how likely is it that you will get sick from touching feces and not washing? For example, if you were to touch feces 10 times, how many times would you get sick?
JUNE: Oh, I know it’s pretty unlikely, but sometimes it seems so real.
THERAPIST: Can you put a number on it? What’s the percent chance that if you touched a small amount of feces and didn’t wash that you’d get sick?
JUNE: I’d say low, less than 25%. THERAPIST: That means that one time in every four
you’d get sick. JUNE: No, that’s not right. I guess it’s really less than
1%.
From this dialogue, it is clear that June did not strongly believe that her feared disasters would actu- ally occur, although her initial estimate of the likeli- hood was high. A person with poor insight regarding the senselessness of his/her OCD symptoms would have assigned higher probabilities (usually over 80%) and would insist on the accuracy of his/her estimate even in the face of persistent questioning. Note also that this exchange is an example of the informal cognitive re- structuring accompanying EX/RP that we discussed earlier. The therapist may need to repeat this discussion during subsequent exposure sessions when June, highly anxious about confronting contaminants, readjusts her
likelihood estimates when anxious. Strength of belief can change in a given patient but is stronger when the patient perceives threat.
THERAPIST: OK. Now, besides disease, what else could happen if you got feces on you?
JUNE: I suppose I’m also afraid of what other people might think if I got dog feces on my shoe or on my dress. Somebody would see it or smell it and think it was really disgusting, and I was a dirty person. I think I’m afraid they would think I’m not a good person.
The therapist then questioned June further about this feared consequence, inquiring about the possibil- ity of others evaluating her character negatively because she had feces on her dress. The material regarding feared consequences was collected for later inclusion in the imaginal exposure scenes. To conclude the inquiry about the nature of the obsessions, the therapist further elucidated the external feared stimuli.
THERAPIST: Besides dog and human feces and toilets, what else can “contaminate” you? Is it OK if I use the word contaminated to describe how you feel if you handle these things?
JUNE: Yes, it’s like I can feel it on my skin, even if I can’t see it. Umm, I also get upset if I see “bird doo” on my car.
THERAPIST: Bird droppings? The whitish spots? JUNE: Yeah, I have to hold my skirt close to me so that I
don’t touch any of these spots with my clothes. THERAPIST: OK, bird doo, what else? JUNE: Dead animals, like on the roadside. I feel like
the germs, or whatever it is, get on the tires from the pavement and get on the car. Even if I don’t run over it. Like it’s spread around the street near it.
THERAPIST: What do you do if you see a dead animal? JUNE: I swerve wide around it. Once I parked the car
and as I got out, I saw this dead cat right behind the car. I had to wash all my clothes and take a shower right away. It was really a mess that day.
THERAPIST: It sounds like that was very difficult for you. Is there anything else besides dead animals that contaminates you?
JUNE: I can’t think of any. There are lots of places I
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avoid now, but that’s because of what we just talked about.
The therapist questions June further about other items that are likely to be contaminated because of their potential relationship to the ones she has already noted.
THERAPIST: What about trash or garbage? JUNE: Yeah, that bothers me. And I also avoid gutters
on the street. THERAPIST: What’s in the gutter that upsets you? JUNE: Dead animals, I guess. And then the rain spreads
the germs down the street. Also rotten garbage. It’s really dirty. Sometimes the gutters are really disgust- ing.
THERAPIST: Um hmm. Are you afraid you could get sick from dead animals and garbage?
JUNE: Yes, it’s like the toilets or dog dirt.
To prepare for an exposure program in which ob- jects are presented hierarchically with respect to their ability to provoke discomfort, June was asked to rank her major contaminants. Here she also provided infor- mation about avoidance behaviors associated with her contaminants.
THERAPIST: Now, let’s make a list of the main things that upset you. I’m going to ask you how distressed you would be on a 0- to 100-point scale if you touched the thing I’ll name. Zero indicates no dis- tress at all and 100 means you’d be extremely upset, the most you’ve ever felt.
JUNE: OK. THERAPIST: What if you touched dog dirt? JUNE: And I could wash as much as I wanted? THERAPIST: No, let’s say you couldn’t wash for a while. JUNE: 100. THERAPIST: A dead animal. JUNE: Also 100. THERAPIST: Bird doo on your car. JUNE: That depends on whether it is wet or dry. THERAPIST: Tell me for both. JUNE: 100 wet and 95 dry. THERAPIST: Street gutter.
JUNE: 95. THERAPIST: Garbage in your sink at home. JUNE: Not too bad. Only 50. But, the trash can out-
doors would be 90. THERAPIST: Why the difference? JUNE: Because the inside of the trash can is dirty from
lots of old garbage. THERAPIST: I see. What about a public toilet seat? JUNE: That’s bad. 95. THERAPIST: Car tires? JUNE: Usually 90. But if I just passed a dead animal,
they’d be 99. THERAPIST: What about a doorknob to a public bath-
room? JUNE: The outside knob is low, like 40. But the inside
knob is 80, because people touch it right after they’ve used the bathroom, and I’ve seen that some don’t wash their hands.
THERAPIST: I understand. How about grass in a park where dogs are around?
JUNE: If I did walk in the grass, it would be about 80 or 85, but I don’t usually do it. I also have a lot of trouble on sidewalks. You know, the brown spots on the concrete. I guess most of it is just rust or other dirt, but I think maybe it could be dog dirt.
THERAPIST: How much does that bother you? JUNE: To step on a brown spot? About 90. I always walk
around them.
The therapist should continue in this manner until a list of 10–20 items is formed. More items may be neces- sary for patients with multiple obsessional fears or ritu- als. The items are ordered from low- to high-level fear in preparation for treatment by exposure. Items equivalent with regard to their level of disturbance are grouped to- gether. Moreover, it is important to probe the rationale for one stimulus differing from another, because it pro- vides further information about the patient’s particular “OCD logic.” This information is highly relevant for the construction of the exposure hierarchy and for the informal cognitive discussions about risk assessment, responsibility, and so forth.
Considerable information about avoidance patterns and rituals emerged from the previous interview about external threat cues. More details may be obtained by
164 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
asking the patient to provide a step-by-step descrip- tion of a typical day’s activities from the time he/she awakens until he/she goes to sleep. Usually, patients are not entirely accurate when describing their compulsive behaviors during the interview because, as one patient told us, they have not “thought of their OCD in that way before.” Thus, the self-monitoring tasks assist pa- tients in raising their awareness about the OCD pat- terns and provide the therapist with more accurate data about rituals and avoidant behaviors.
We were particularly concerned by June’s bathroom routines, her shower, use of the toilet, handling of tow- els and dirty clothes, and dressing and putting on shoes. Additional information about avoidance patterns may be ascertained by inquiring about other routine activi- ties, such as shopping, eating out, housecleaning, pre- paring meals, working, and so on. The following dia- logue exemplifies the degree of detail desired.
THERAPIST: June, for us to plan your treatment care- fully, I need to know what you avoid in your daily routine. Why don’t you start by describing what you do first when you wake up?
JUNE: I go to use the bathroom first. THERAPIST: Nightgown on or off? JUNE: I take off my nightgown, because I don’t want it
to touch the toilet. That way it’s clean at night after I shower.
THERAPIST: Go on. JUNE: I go to the toilet. I suppose I use a lot of toilet
paper because I don’t want to get anything on my hand. Then I have to shower after a bowel movement.
THERAPIST: How do you get ready to shower? JUNE: I have to put a new towel on the rod near the
shower. I don’t like it to touch anything before I use it. Oh, and I put my slippers facing the door, near the shower, so I can put them on without stepping on the bathroom floor when I get out of the shower. Then I get into the shower.
THERAPIST: You said you shower for 45 minutes. Why does it take so long?
JUNE: I have to wash myself in a special order and I count how many times I wash each part. Like I wash my arm four times. That’s why it takes so long.
THERAPIST: What is the order you use? JUNE: First I wash my hands, then my face and hair,
and then I go from the top down.
THERAPIST: What about the genital and anal area? [This area should disturb this patient most, because she fears contamination from fecal “germs.”]
JUNE: Oh yes, those are last, after my feet.
Such a detailed description helps the therapist to anticipate possible avoidance by the patient during treatment and to plan specific exposure instructions. Supervision of normal washing behavior at the end of treatment will address June’s tendency to count and to order her washing. During the initial session of infor- mation gathering, June was instructed to self-monitor the frequency and duration of her compulsions.
THERAPIST: Between now and our next session, I’d like you to record all the washing and cleaning that you do, including wiping things with alcohol. You can use this form (Hands her a self-monitoring of rituals form.) Please write down every time you wash, how long you washed, what made you wash, and how anxious you were before you washed. This kind of record will help us identify any sources of contamination you’ve forgotten to mention, and we can also use it to measure your progress during treatment.
JUNE: Do you want me to write in each space for each half-hour?
THERAPIST: No, only when you wash or use alcohol. JUNE: OK.
History of Symptoms and Treatment History
After assessing the patient’s current symptoms, the therapist sought information about the onset of the problem, with particular reference to the presence of specific stressors at the time and whether these stressors are still present.
THERAPIST: How long have you been washing like this? JUNE: It started about 2 years ago in my first year of
nursing school. It wasn’t real bad right away. It start- ed with the city. I had to go into the city to classes, and the city seemed real dirty.
THERAPIST: Did nursing have something to do with it? JUNE: Maybe. I was under a lot of tension. I had to quit
working as a secretary, and it was pretty hard without an income and a lot of school bills. My mother and dad weren’t much help. And then we started to learn
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all the sterilizing techniques, and I already told you about the course in microbiology.
THERAPIST: Did it gradually get worse? JUNE: Mostly, but I did notice that it was a lot worse
after a rotation on surgery, where I was really worried about germs contaminating the instruments. That’s when I started to wash more than usual.
THERAPIST: Did you seek help at that time? JUNE: I was already seeing Dr. W at the university, and
he tried to help. THERAPIST: You were already in treatment with him?
For what reason? JUNE: He was helping me with an eating problem. I had
anorexia. I’d been seeing him for about a year when the washing started.
THERAPIST: Anorexia? Did treatment help? JUNE: Yes. I was down to 85 pounds, and I’m up around
105 now. He mostly asked me to increase my weight every week and he did “cognitive therapy,” I think it’s called.
THERAPIST: I see. What about the washing problem? JUNE: He tried the same type of therapy, but it didn’t
work for that. That’s why I’m here. My sister-in-law heard about it, and Dr. W said I should come.
THERAPIST: What about drugs? Were you ever given medication for this problem?
JUNE: Yes, I tried Anafranil [clomipramine] for a while and it helped a little, but it made me dizzy and sleepy, so I decided to stop taking it. Also, I heard that you can’t take the medication when you are pregnant, and Kenny and I want to have a baby soon. Before that, I took Xanax [alprazolam]; it calmed me down but didn’t stop the washing.
THERAPIST: Have you tried any other treatments? JUNE: Only for the anorexia. I went to another counsel-
ing center at the university for about a year, but that didn’t really help at all.
June’s history was unusual only in the relatively re- cent onset of her symptoms. Typically, patients in our clinic present a much longer duration of symptoms, with the mean around 8 years. Other centers in Eng- land and Holland report similar figures. June’s treat- ment history of trying various psychotherapeutic and pharmacological treatments prior to seeking EX/RP was quite typical. Since previous failure with nonbe-
havioral treatments has not been found to influence outcome with EX/RP, the clinician should not be dis- couraged by such a history. However, because of a pos- sible skeptical attitude about the value of treatment, the therapist should provide the patient with a clear ratio- nale for EX/RP treatment along the lines discussed ear- lier and demonstrated below.
THERAPIST: Before I continue to collect more informa- tion about your problem, let me tell you about our treatment.
JUNE: Well, Dr. F told me something about it, but I’m still not sure what this treatment is going to be like.
THERAPIST: The treatment is called exposure and ritual prevention. I’ll be asking you to confront situations and things that frighten you or make you feel con- taminated. We will do this gradually, working up to the hardest things. For example, we may begin with the outside door handles of bathrooms and work our way up to toilet seats and bird doo. We’ll do this to- gether, and I’ll be there to help you. The sessions will last 1½ or 2 hours, and we’ll meet every weekday. In addition, I’ll assign you homework to do similar things between the therapy sessions.
JUNE: You mean I have to touch them, even dog dirt? THERAPIST: Yes, to get over these kinds of fears, people
must learn to confront what they’re afraid of and stay with it until the discomfort decreases.
JUNE: Even if I did, it would probably take me a year to get used to it.
THERAPIST: Remember, you didn’t always feel like this about dog dirt. When you were younger, did you ever step in dog dirt and just wipe it off on the grass and go on playing?
JUNE: Yeah, I forget that. It seems such a long time ago. I used to not think twice about this stuff.
THERAPIST: To get you back to how you used to feel, we need to expose you directly to what you’re afraid of. Now, there’s a second part to treatment. I’m also going to ask you not to wash for 3 days at a stretch. No handwashing or showering for 3 days. Then you can take a shower, but you will have to limit it to 10 minutes. After the shower, you will have to contami- nate yourself again, then wait another 3 days for your next shower.
JUNE: I can’t believe it! I’ll never be able to do that. If I could, I wouldn’t be here. How can I not wash? Every
166 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
day I resolve to stop, but I always give in. You mean I wouldn’t be able to wash after I use the bathroom or before I eat? Other people wash after they use the toi- let. Why can’t I just wash less, like normal people do?
THERAPIST: Other people don’t have OCD. Remem- ber, for you, washing makes you feel less “contami- nated” and less anxious. Right?
JUNE: Yes. THERAPIST: If you wash, even briefly, whenever you
feel “contaminated,” you never get a chance to learn that the feeling of contamination would go away by itself without washing. If you are really very anx- ious, it might take a while, even several hours, be- fore you feel better, but it will eventually happen. On the other hand, if you wash, even briefly, every few hours, it will reinforce your idea that you have to wash to feel better.
JUNE: But why 3 days? Couldn’t I shower once a day like other people?
THERAPIST: For the same reason. You’d still feel relief, even if you waited 24 hours between washings. And that would strengthen your belief that you need to “decontaminate” by washing yourself. You must learn to use soap and water to feel clean and fresh but not to “decontaminate” yourself.
JUNE: I think I understand. I know I shower now to get the things I’m afraid of off my body. I used to shower just to get sweat and dirt off, and feel nice. I’m still not sure I could stand it though, not washing for that long.
THERAPIST: The treatment is very demanding. Be- fore we start the treatment program you will need to make a commitment to yourself that even though you will feel very uncomfortable and even quite upset at times, you won’t wash. I’ll try to help you as much as I can by planning the treatment so you know what to expect each day and by supporting you whenever you need it. Someone will have to be available to help supervise and support you any time you need it. Between sessions, you can always call me here or at home if a problem comes up. I know the treatment won’t be easy for you, but I’m sure you can do it if you make up your mind.
At this point, the therapist should not request a firm commitment. Rather, the patient should be made aware of what will be required so that he/she can adjust to these expectations and plan activities during the treat-
ment period accordingly. The patient should make the arrangements necessary to attend daily treatment ses- sions for 3–4 weeks. As we discussed earlier, two to three sessions per week may be sufficient for patients with less severe symptoms. It is important that the therapist not minimize the difficulty of the treatment regimen, so that the patient is prepared to struggle and enters treatment with a readiness to mobilize inner re- sources and emotional support from family and friends.
The history of the patient is usually taken in the first session. Because collecting histories of individuals with OCD does not differ from collecting histories of other psychiatric patients, details are not provided here.
Treatment Planning
The therapist began the second session by briefly re- viewing the patient’s self-monitoring of rituals form. The remainder of the session was devoted to developing a treatment plan.
THERAPIST: OK, now I want to discuss our plan for each day during the first week of therapy. We need to expose you both in imagination and in reality to the things that bother you, which we talked about in our first sessions. As I said already, we’ll also limit your washing. The scenes you imagine will focus on the harm that you fear will occur if you do not wash. The actual exposures will focus on confronting the things that contaminate you. Restricting your wash- ing will teach you how to live without rituals. In imaginal exposure, you will picture yourself touch- ing something you’re afraid of, like toilet seats, and not washing, and then becoming ill. We can have you imagine going to a doctor who can’t figure out what’s wrong and can’t fix it. That’s the sort of fear you have, right?
JUNE: Yes, that and Kenny getting sick, and it being my fault.
THERAPIST: OK, so in some scenes you’ll be sick, and in others Kenny will get sick. Should I add that other people blame you for not being careful? Is this what you’re afraid of?
JUNE: Yes, especially my mother. THERAPIST: OK. We’ll have her criticize you for not
being careful enough. Can you think of anything else we should add to the image?
JUNE: No, that’s about it.
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THERAPIST: We can compose the scenes in detail after we plan the actual exposures. Let’s review the list of things you avoid or are afraid to touch and make sure that we have listed them in the right order. Then we’ll decide what to work on each day. OK?
JUNE: OK.
June reviewed the list, which included items such as trash cans, kitchen floor, bathroom floor, public hall- way carpet, plant dirt, puddles, car tires, dried dog “dirt,” and bird “doo.” Changes were made as needed.
THERAPIST: Good. Now let’s plan the treatment. On the first day we should start with things that you rated below a 60. That would include touching this carpet, doorknobs that are not inside bathrooms, books on my shelves, light switches, and stair rail- ings. On the second day, we’ll do the 60- to 70-level items, like faucets, bare floors, dirty laundry, and the things on Kenny’s desk. [The therapist continued to detail Sessions 3–5, increasing the level of difficulty each day.] In the second week, we will repeat the worse situations like gutters, tires, public toilets, bird doo, and dog dirt, and we’ll also find a dead animal to walk near and touch the street next to it.
On rare occasions, direct confrontation with a feared object (e.g., pesticides or other chemicals) may have some likelihood of producing actual harm. In such cases, the therapist’s judgment should be exercised to find a middle ground between total avoidance and endangerment. With chemicals, for example, patients are exposed to small quantities that are objectively nonharmful. In June’s case, the therapist decided that direct contact with a dead animal was not called for, and that stepping on the animal’s fur with her shoe and then touching the shoe sole constituted sufficient exposure. In general, the therapist must weigh the level of obsessional distress that will be evoked by a given exposure with the objective risks entailed in complet- ing that exposure. Patients with OCD have difficulty assessing such risks realistically; thus, it is the respon- sibility of the therapist to evaluate whether exposure is warranted. For example, patients with fears of con- tracting HIV would certainly be highly distressed if asked to handle a dirty hypodermic needle found in a city gutter, but because exposure to such stimuli is objectively risky, they should not be included on the treatment hierarchy.
THERAPIST: How does this plan sound? JUNE: The first week is OK, but I’m really scared about
the second week. I’m not sure I’ll be ready to do the bathrooms and dog dirt by then.
THERAPIST: Many people feel this way at the begin- ning, but by the end of the first week, you won’t be as frightened as you are now about touching tires or public toilets. Remember, I will be here to help you, because it will probably be difficult in the beginning.
JUNE: Yes, I know it. I feel like I don’t really have a choice anyhow. This washing is crazy and I’m disgusted with myself. I suppose I’m as ready as I’ll ever be.
THERAPIST: Good. Now remember, I’ll ask you to keep working on these things for 2–3 hours at home after each session, but you will already have done them with me, so I don’t think it will be too hard. I take it that you talked to Kenny about assisting us with supervising, since I saw him out in the waiting room.
JUNE: Yes, he said that’s fine. He wanted to know what he should do.
THERAPIST: Let’s call him in. Did you talk to your sister-in-law about being available when Kenny is at work during the day?
JUNE: Yes, she was really good about it, but she couldn’t come today because of the kids.
THERAPIST: If it’s difficult for her to come, I could talk to her on the phone. Why don’t you go get Kenny now?
Treatment
June was seen for 15 treatment sessions, held every weekday for 3 weeks. During the fourth week, the therapist visited her twice at her home for 4 hours each time. During these visits, under the therapist’s supervi- sion, June contaminated her entire house and exposed herself to objects at home and in her neighborhood that provoked distress. Thereafter, once-weekly follow-up sessions were instituted to ensure maintenance of gains and to address any other issues of concern to her.
As discussed earlier, treatment begins with exposure to moderately difficult items on the hierarchy and pro- gresses to the most disturbing ones by the beginning of the second week. The most distressing items are re- peated during the remainder of the second and third weeks. The following sequence, which occurred on the sixth day of treatment, exemplifies this process.
168 CliniCal Handbook of PsyCHologiCal disorders
THERAPIST: How was your weekend? JUNE: Not that great. I suppose it was as good as I could
expect. I took my shower Sunday night and I was so nervous about finishing in time I don’t even know if I washed right.
THERAPIST: Most people feel the same way. Remember though, you aren’t supposed to wash “right,” just to wash. Did Kenny time it?
JUNE: Yes, he called out the minutes like you said, “5, 7, 9,” and then “stop.”
THERAPIST: You stopped when he said to? JUNE: Yes, but it still wasn’t easy. THERAPIST: I know. I’m really pleased that you were
careful to follow the rules. JUNE: I have pretty much decided that this is my chance
to get better, so I’m trying my best. THERAPIST: Good. I am glad you feel so positive. How
was the homework? JUNE: I touched the floor and the soles of my shoes and
the cement. It is all written on the daily sheet there. On Saturday, I went to my sister’s, so I could play with the kids like we said. They stepped on me when I lay on the floor and I tried to touch their bottoms when I held them. On Sunday, Kenny and I went to the park. I didn’t sit in the grass, but I did walk around and touched my shoes afterward.
THERAPIST: The soles? JUNE: Yeah. We also went downtown and I threw some
things in the trash cans and pushed them down, and tried to touch the sides. It’s sort of hard because I felt conspicuous, but I did it anyway.
THERAPIST: That sounds really good. I’m glad to hear it. How about your doormat and going into the garden?
JUNE: I did the doormat and I stood in the garden, but I couldn’t touch the dirt. The neighbor’s dog always runs all over. I know I should have touched it, but I just couldn’t get up the courage.
THERAPIST: Well, you did do many other things. Let’s plan to go outside today and do it together, so it will be easier for you to walk in the garden when you go home.
JUNE: OK.
June was very compliant with the treatment regimen. Some patients occasionally lapse on response preven-
tion, particularly during the first week of the treatment program. The therapist should reinforce the patient for partial compliance but emphasize the need to comply fully with treatment instructions. With regard to expo- sure homework, it is not uncommon for patients to ne- glect completing some assignments. Again, they should be reinforced for what they have achieved and encour- aged to complete all of the assignments.
THERAPIST: How are you and Kenny doing? JUNE: He got mad on Sunday night after the shower,
because I started to ask him how he showered and if I was clean enough. I think I nagged him too much, so he lost his temper. We just watched TV, and after a while we talked a bit and he sort of apologized for getting mad. But I understand; I ask too many ques- tions. Otherwise, the rest of the weekend was OK.
THERAPIST: Well, it’s unfortunate that Kenny got mad, but it’s good that he didn’t answer your questions. He’s not supposed to reassure you about cleanliness.
JUNE: I think he has a hard time knowing when to an- swer me and when not to. I am not real sure either. Could you talk to him before Wednesday, when I shower again?
THERAPIST: That’s a good idea. I’ll call him after we’re done with today’s session. Now, today we’ll start with the scene about you driving your car to an ap- pointment with me, and you get a flat tire and have to change it. The cars splash water in the puddle near you, and it lands on the car and on you. Then you notice a dead animal when you walk behind the car, and it’s right behind you. You really feel contaminat- ed. You walk to the gas station nearby to see if they can fix the tire and you have to urinate so badly that you have to use their restroom. They agree to fix the tire if you remove it and bring it to them, because, otherwise, they are too busy. Of course, that means you will have to handle the tire that is contaminated by the dead animal. We’ll add some bird doo on the street and on the sidewalk, too. Then, later you start to feel sick, and you feel like it’s from the dead ani- mal. Sound awful enough?
JUNE: Yeah. Ugh. That one is really bad. Do I have to? Never mind, I know the answer.
THERAPIST: OK. I want you to close your eyes now and imagine that you are driving your car on West Avenue.
Obsessive–Compulsive Disorder 169
Note that the therapist checked the patient’s assign- ment from the previous day to verify that she completed it and did not engage in avoidance and rituals. This provided an opportunity to reinforce efforts at self- exposure. It is important to keep track of completion of homework, because patients do not always volunteer in- formation about omissions. They will, however, admit failure to comply if directly asked and are likely to carry out the next assignment if reinforced adequately.
With regard to the conflict between June and Kenny, it is our experience that, like Kenny, most family mem- bers are quite willing to help. Difficulty may, however, arise when they are unable to help without becoming upset, thereby increasing the patient’s tension. Provid- ing them with an opportunity to ventilate their frustra- tion by contacting the therapist, who also may coach them in alternative reactions, may reduce familial ten- sion.
That same session also included imaginal exposure to do a scenario planned in advance. Since that scenario had already been discussed in detail with the patient, it posed no surprises for her. It is presented for up to 1 hour, or until a substantial decrease in anxiety is evi- dent. Next, the patient is confronted in vivo with situa- tions like those included in the fantasized scene.
THERAPIST: It’s time to do the real thing now. I looked for a dead animal by the side of the road yesterday and I found one about a mile away. I think we should go there.
JUNE: Yuck, that’s terrific. Just for me you had to find it.
THERAPIST: Today’s our lucky day. You knew we were going to have to find one today anyhow. At least it’s close.
JUNE: Great.
Humor is encouraged and can be quite helpful if the patient is capable of responding to it. At the same time, it is important that the therapist laugh with rather than at the patient. Patients and therapists often develop a shorthand lexicon for discussing OCD and its treat- ment that is specific to them and aimed at promoting compliance with treatment. For example, one patient– therapist pair began to discuss exposure homework as “swallowing the frog,” based on a proverb that the pa- tient introduced. When the therapist asked the patient if she had “swallowed the frog” that morning, it con-
veyed the difficulty of the exposure tasks she needed to do between sessions. It is important for the therapist to observe the patient’s interpersonal style to determine whether such banter is likely to promote the therapeutic goals.
THERAPIST: (outside the office) There it is, behind the car. Let’s go and touch the curb and street next to it. I don’t think that you need to touch it directly, because it’s a bit smelly, but I want you to step next to it, then touch the sole of your shoe.
JUNE: Yuck! It’s really dead. It’s gross! THERAPIST: Yeah, it is a bit gross, but it’s also just a
dead cat if you think about it plainly. What harm can it cause?
JUNE: I don’t know. Suppose I get germs on my hand? THERAPIST: What sort of germs? JUNE: Dead cat germs. THERAPIST: What kind are they? JUNE: I don’t know. Just germs. THERAPIST: Like the bathroom germs that we’ve al-
ready handled? JUNE: Sort of. People don’t go around touching dead
cats. THERAPIST: They also don’t go running home to show-
er or alcohol the inside of their car. It’s time to get over this. Now, come on over and I’ll do it first. (June follows.) OK. Touch the curb and the street. Here’s a stone you can carry with you and a piece of paper from under its tail. Go ahead, take it.
JUNE: (looking quite uncomfortable) Ugh! THERAPIST: We’ll both hold them. Now, touch it to
your front and your skirt, and your face and hair. Like this. That’s good. What’s your anxiety level?
JUNE: Ugh! 99. I’d say 100, but it’s just short of panic. If you weren’t here, it’d be 100.
THERAPIST: You know from past experience that this will be much easier in a while. Just stay with it and we’ll wait here. You’re doing fine.
JUNE: (A few minutes pass in which she looks very upset.) Would you do this if it weren’t for me?
THERAPIST: Yes, if this were my car and I dropped my keys here, I’d just pick them up and go on.
JUNE: You wouldn’t have to wash them?
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THERAPIST: No. Dead animals aren’t delightful, but they’re part of the world we live in. What are the odds that we’ll get ill from this?
JUNE: Very small, I guess. I feel a little bit better than at first. It’s about 90 now.
THERAPIST: Good! Just stay with it now.
The session continued for another 45 minutes, or until anxiety decreased substantially. During this pe- riod, conversation focused generally on the feared situ- ations and the patient’s reaction to them. The thera- pist inquired about June’s anxiety level approximately every 10 minutes. It is important to note that June and the therapist have engaged in conversation throughout the exposure task, discussing issues such as habitua- tion, risk, responsibility, and long-term outcomes. At the same time, it is imperative to refocus the patient on the exposure task at hand to ensure that he/she remains engaged with it. Thus, asking for SUDS ratings serves two purposes: It provides data about fear reduction, and it refocuses the patient on the exposure. However, if the informal discussion serves as a distractor, helping the patient “not think about” what he/she is doing, the therapist should limit such conversations.
THERAPIST: How do you feel now? JUNE: Well, it is easier, but I sure don’t feel great. THERAPIST: Can you put a number on it? JUNE: About 55 or 60, I’d say. THERAPIST: You worked hard today. You must be
tired. Let’s stop now. I want you to take this stick and pebble with you so that you continue to be con- taminated. You can keep them in your pocket and touch them frequently during the day. I want you to contaminate your office at work and your apartment with them. Touch them to everything around, in- cluding everything in the kitchen, chairs, your bed, and the clothes in your dresser. Oh, also, I’d like you to drive your car past this spot on your way to and from work. Can you do that?
JUNE: I suppose so. The trouble is going home with all of this dirt.
THERAPIST: Why don’t you call Kenny and plan to get home after he does, so he can be around to help you. Remember, you can always call me if you have trouble.
JUNE: Yeah. That’s a good idea. I’ll just leave work after he does. See you tomorrow.
This scenario illustrates the process of in vivo ex- posure. The therapist answered clearly the questions raised without detouring from the essential purpose of the session, exposure to the feared contaminant. After the initial increase, the anxiety may begin to drop rela- tively quickly for some patients and may require longer for others. As noted previously, it is advisable to contin- ue the exposure until the patient appears visibly more at ease and reports a substantial decrease in anxiety (40 or 50%).
After 10–15 sessions, the patient’s reported anxiety level is expected to decrease considerably. At the 15th session, June reported a maximum discomfort of 70 SUDs (still somewhat high, although reduced from 99 SUDs) that lasted for a few minutes. Her minimal anxiety was 35 SUDs. Her average anxiety level during this session was 45 SUDs. Ideally, by the end of treat- ment, the highest level should not exceed 50 SUDs and should drop below 20 SUDs at the end of the session. In June’s case, more follow-up sessions were required, because her anxiety was still quite high.
To facilitate a transition to normal washing and cleaning behavior, the therapist instituted a normal washing regimen during the third week of treatment. The patient was allowed one 10-minute shower daily and no more than five 30-second handwashes when there was visible dirt on her hands or when they were sticky.
When the therapist arrived for a home treatment ses- sion the next week, the following conversation ensued:
THERAPIST: How did it go over the weekend? JUNE: Not too bad. But I got sort of upset Saturday.
We went to a picnic and there were several piles of dog dirt around. I had on my flip-flops and I wanted to play volleyball. You can’t in flip-flops, so I went barefoot.
THERAPIST: That’s great! I’m glad to hear it. JUNE: Yeah, but then I got really upset about going
home and carrying it into the apartment. I did it. I walked all over barefoot and with the flip-flops, but I worried about it for another whole day, until I talk- ed to Kenny about my thoughts on Sunday around noon. I felt better when he said he wouldn’t worry about it. It seems like I feel guilty or something, like
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the house isn’t clean enough. But lately if he says it is clean, I’ve been able to take his word for it.
THERAPIST: Well, in time you’ll be able to make this kind of judgment yourself. How about your washing and cleaning?
JUNE: It was all right. I washed for half a minute before I ate, because I was dusty from playing volleyball. I deliberately didn’t wash when I got home, because I felt bad and I knew that if I did, it would be to “de- contaminate” myself. I showered Saturday night and I did feel relieved, but I knew I should go and walk around barefoot and touch the floors I’d walked on. So I did that.
THERAPIST: That’s great! It sounds like you handled it fine. I’m really pleased. You avoided washing when it would mean reducing feelings of contamination, and you exposed yourself when you felt concerned about germs. That’s excellent. Now, let’s go over the problem situations that still need work here at home. What things still disturb you?
JUNE: The basement. I haven’t done much with the kitty litter box and old shoes that I threw down there a year ago, because they got contaminated. The closet still has some contaminated clothes. And I still worry about the backyard some. Also, the porch. Pi- geons have been perching on the roof, and there are droppings on the railing now, so I thought I’d wait until you came to do that.
THERAPIST: OK. Let’s start low and work up. Which is easiest?
JUNE: The basement and closets. THERAPIST: Fine, down we go.
Exposure to contaminants during the home visit is conducted in the same manner as that during treat- ment sessions. Typically, home sessions last longer, from 2 to 4 hours, until all “dirty” items are touched and “clean” places are contaminated. These visits should be repeated if the patient expresses considerable concern about his/her ability to adopt a permanent regimen of nonavoidance.
Follow‑Up Sessions
June was seen weekly for 3 months, until she experienced a setback following the development of a new obsession. She became concerned about hitting a pedestrian while
driving. Thoughts that she “might have hit someone” intruded, particularly after turning a corner or glancing in the mirror to change lanes. Once evoked, they per- sisted for several hours. To overcome this new problem, the therapist directed June to increase her driving and refrain from retracing her path or looking in the mirror to check for casualties. June was told that she could stop her car only if she knew for certain that she hit someone. Thoughts that it “might” have occurred were to be ig- nored. To reduce June’s anxiety about having obsessions (e.g., “Oh, my God, here it is again. This is terrible”), she was advised to expect occasional recurrences of obses- sive thoughts. The frequency of obsessions about hitting someone decreased from several each day to once weekly after 3 weeks of self-exposure; the associated anxiety di- minished from 95 to 50 SUDs or less.
Of June’s germ-related obsessions, only that of dog feces partially recurred. Fears of public bathrooms and dead animals remained low. The therapist felt that June’s fear of dog feces had received insufficient atten- tion during treatment. To address this return of fear, June was seen three times a week for 1-hour exposure sessions, in which she touched brown spots on the side- walk and walked near, and eventually stepped on, dog feces. Homework included going to parks, walking on sidewalks without looking, stepping on dog feces, and stepping on the grass where she thought dogs had been. This treatment continued for 4 weeks and was reduced to twice a week for an additional 3 weeks. Thereafter, June came once weekly for another 6 weeks, during which the therapist assigned self-exposure and dealt with June’s everyday concerns. News media coverage of herpes led to a brief concern about public toilets, but this dissipated within a few days.
In the dialogue below, the therapist reviewed with June her progress at a 9-month follow-up.
THERAPIST: I’d like to know how you feel compared to when you first came here 9 months ago.
JUNE: I’m definitely a lot better. But I still have some bad days when I worry a lot about something, and I get down on myself. But when I remember how upset I was last summer and all that washing I did, it’s re- ally a whole lot better. Maybe about 80% better. I’m not ready to be a floor nurse yet, but the job I got after treatment is pretty good for now. Kenny and I are doing fine, except he’s real sensitive if I bring up one of my fears. I wish he’d just listen and say, “OK”
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or something, instead of looking worried about me. It’s like he’s afraid I’m going to get upset again. It makes it hard for me to talk freely, but sometimes he does handle it fine. I really can’t complain. He’s been through a lot, too, when I was really a mess last year and before that.
THERAPIST: I’m glad to hear you feel so much better. You look a lot more at ease. You laugh more now. I don’t know if you recall, but you never did in the beginning.
JUNE: I remember. THERAPIST: What’s left now, the other 20%? JUNE: Obsessions, I guess. I can still work on my fear
of driving over someone. Mostly it lasts less than 15 minutes, but now and then it hangs on through an evening.
THERAPIST: How often? JUNE: Once every week or two, I think. And I still have
an urge to avoid walking on the grass in parks. Like I’m hyperalert. I do it pretty often, but I’m self-con- scious.
THERAPIST: You mean you have to remind yourself not to avoid dog feces?
JUNE: Yeah. And I tend to see things in black and white, all good or all bad. I catch myself feeling guilty for dumb things like eating dessert after a full meal. I can stop, but it’s like I’m out to punish myself or think badly about what I did. I have to watch out for it. Still, the thoughts are nothing like they used to be. I can have fun now. And work is pretty absorbing, so I can go whole days without getting down on myself for something. Will I always do that?
THERAPIST: Maybe to some extent. We know that you have a tendency to obsess. Most people who have had an obsessive–compulsive problem say that the rituals and urges to do them decrease more quickly than the obsessive ideas. You might have disturbing thoughts for a while, but you can expect them to become less frequent if you’re careful not to attempt to control them through rituals or by avoiding things. Can you handle that?
JUNE: I suppose so. They’re not a lot of fun, but I feel like I’m living a normal life again. I suppose everyone has some problems to deal with.
Rarely do patients report complete remission of all obsessions. It is unrealistic to lead a patient to expect
that 4 weeks of treatment will result in a total absence of obsessions and rituals. Patients should expect some con- tinued struggle with obsessions and urges to ritualize. Strategies for coping with such occasional difficulties should be rehearsed.
COMPLICATIONS DURING BEHAVIORAL TREATMENT
Obviously, difficulties may arise during implementa- tion of EX/RP treatment for OCD. Several of these are described below and possible solutions are discussed.
Noncompliance with Response Prevention
Individuals with OCD often report engaging in rituals despite the response prevention instructions. In most cases, these represent brief “slips” that the therapist ad- dresses by reiterating the rationale for the treatment regimen and the need to follow the response prevention instructions strictly. The therapist also may offer ways the ritual might be “undone” (e.g., recontaminating or turning the stove on and off again).
Sometimes the patient’s support person reports vio- lations of response prevention to the therapist. The therapist should discuss the violations with the patient, emphasizing the fact that continued failure to comply with the response prevention instructions may result in treatment failure. The following is an example of how violations of response prevention may be presented to the patient.
“I understand from your father that on three occa- sions this weekend he saw you checking the front door lock five or six times before you left the house. As we agreed in the first session, he called to inform me about your checking. I am sure you remember that we agreed that you would check the doors only once, and that if you had a problem, you would dis- cuss it with your father or me right away, so we could help you overcome your urge to ritualize. Will you explain to me what happened?”
If the patient acknowledges the slip and responds with a renewed agreement to follow instructions, the therapist need not pursue the issue further. However, if a second significant infraction of the response pre- vention instructions occurs, the therapist should again remind the patient of the therapy rules and the rationale
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for these rules, and “troubleshoot” with the patient how to implement ritual prevention successfully. During the course of this discussion, if it becomes evident that the patient is unwilling to consider these recommendations and remains committed to rituals and avoidance as a means to reduce obsessional distress, then the therapist may broach the subject of discontinuing treatment, un- less the patient is ready to comply.
“It seems that right now you aren’t able to stop ritu- alizing. For treatment to be successful, it is essential that you completely stop your rituals. Every time that you relieve your discomfort by ritualizing, you prevent yourself from learning that anxiety would have de- clined eventually without rituals, and you don’t permit your obsessional fears to be disconnected from distress and anxiety. Exposing you to feared situations without stopping your rituals won’t be helpful. If you cannot follow the no-rituals rule quite strictly, then we ought to stop treatment now and wait until you are really pre- pared to follow through with all the requirements. It is very hard for people to resist the urge to ritualize, and it may be that you are just not ready yet and will feel more able to do so in the future. It is much better for us to stop treatment now than to continue under condi- tions where you are unlikely to benefit from treatment. That would only leave you feeling more hopeless about future prospects for improvement.”
As discussed earlier, patients sometimes replace iden- tified rituals with less obvious avoidance patterns. For example, a patient may use hand lotion to “decontami- nate” the hands instead of the excessive washing that was done originally. If this occurs, the therapist should immediately instruct the patient to stop the new ritual. Other examples of replacement washing rituals include brushing off one’s hands or blowing off “germs”; exten- sive checks are often replaced with quick glances. Di- rect questioning of the patient to solicit such informa- tion should proceed as follows:
“Now that you’ve stopped your washing rituals, do you find yourself doing other things to relieve your anxiety? For example, some people start to wipe their hands with paper towels or tissues as a substitute for washing with soap and water. Are you doing any- thing like this?”
If the answer is “yes,” the therapist should identify these new behaviors as rituals and instruct the patient
to resist engaging in them in the same manner as he/she resists other compulsions.
Continued Passive Avoidance
Patients who continue to avoid situations likely to evoke obsessional distress are also likely to experience attentu- ated outcome in EX/RP. For example, a patient may put “contaminated” clothing back in the closet as in- structed, but in doing so he/she may ensure that the contaminated clothes do not touch clean garments. Such avoidance reflects an ambivalent attitude toward treatment and hinders habituation of anxiety to feared situations. Because such processes may hinder outcome, the presence of continued and frequent avoidance be- havior calls for the therapist and patient to reevaluate whether the patient should continue treatment.
THERAPIST: Jim, let’s make sure that you are doing your homework the right way. I know that you had a problem putting your dirty underwear in with your other dirty clothes. How are you doing with it now?
PATIENT: Well, I was afraid you might ask that. I still haven’t mixed them up. I was too scared to do it.
THERAPIST: We discussed this several days ago and you were instructed to do it that night. It would have been better had you told me the next day that you weren’t able to. What I’d like you to do for tomorrow is to bring in some dirty clothes. Bring in the under- wear and the other clothes in separate bags, and we will mix them here in the office. Are there any other things you have been avoiding that you haven’t told me about?
PATIENT: I don’t think so. THERAPIST: I want you to pay careful attention to
things you are doing, or not doing, and make a list of anything you are avoiding, particularly things that you are supposed to do for therapy. It is very impor- tant that you don’t protect yourself by avoiding dis- tressing situations, since if you don’t face these situ- ations, your obsessive–compulsive symptoms won’t get better. Let’s give it another try, but if you can’t bring yourself to confront these problematic situ- ations without these little avoidances, perhaps you would be better off delaying your treatment to a later time when you will be more ready to comply with the treatment program.
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Arguments
Some individuals who carry out the required exposure without ritualizing may attempt to engage the thera- pist in arguments about the assignments. It is quite tempting to get involved in arguments with patients over what they will or will not do during treatment. To avoid this, it is important for the therapist and the patient to agree on some ground rules before the inten- sive program begins. Patients must agree to follow the treatment plan that they developed in conjunction with the therapist, and to expose themselves to the distress- ing situations without argument. New, feared situations that are discovered should be discussed, and a new ex- posure program should be developed and agreed to, be- fore exposures to the new situations are carried out. If a patient balks at or attempts to alter a planned exposure, the therapist should acknowledge and empathize with the patient’s discomfort, inquire about the reasons for the hesitation, and encourage the patient to proceed in the following manner:
“I’m sorry to see that you are having so much trouble sitting on the floor. I know it’s difficult and that you’re frightened, but it won’t do you any good if we delay the exposure for another day or let you skip it all together. You really need to touch the floor, so let’s go ahead and do it now. We have agreed that today is the ‘floor’ day, and I wouldn’t be doing you a favor if I allowed you to avoid it. Remember, though, I am here to support you as much as I can when you become upset.”
In some instances, difficulties may be overcome by first exposing the patient to similar items that generate a lower level of distress. For example, if a patient refuses to touch a toilet seat, then the therapist may ask him/ her first to touch the bathroom floor or the door to the bathroom stall. Thereafter, the patient might touch the walls of the stall and the toilet handle before proceeding to the toilet seat itself.
Emotional Overload
Occasionally, during treatment, a patient will become overwhelmed by fear or another emotion that is not di- rectly related to his/her OCD symptoms. For example, a patient may be upset by a recent event (e.g., the death of a relative) or by fears of facing future plans (e.g., liv- ing on one’s own or getting a job). Implementing ex-
posure exercises is inadvisable when the patient is ex- tremely upset, because it is unlikely that the patient will adequately attend to the exposure stimulus; therefore, anxiety is unlikely to habituate. Instead, the therapist should discuss the distressing situation with the patient and proceed with exposure only when the patient is calmer. On rare occasions, exposure may be postponed altogether until the next day’s session. If this becomes a repetitive pattern, it may be advisable to interrupt treat- ment until the crisis is over.
Nonanxious Reactions to Exposures
Occasionally, patients respond to exposures with emo- tions other than anxiety or distress, such as anger or de- pression. Clinical observations suggest that anger often serves as a means for the patient to avoid the distress or anxiety that is the target of exposure. If this happens, the anger should be viewed as an avoidance. The thera- pist should refocus the patient on the anxiety-evoking aspects of the situation and point out to the patient that the anger only stands in the way of progress.
Sometimes, during imaginal exposure, when a pa- tient is exposed to the feared consequences of his/her behaviors, the patient becomes depressed. Such depres- sion and other emotional reactions may reduce the ef- ficacy of treatment, and the therapist needs to help the patient to focus on the anxiety-evoking cues. This may be done by directing the content of the imaginal ex- posure away from the feared consequences and toward the external threat cues. In some cases, such redirection does not resolve the problem, and the patient continues to display a depressive reaction to the exposure. When this happens, alternative scenarios that do not elicit de- pression should be developed.
Emergent Fears and Rituals
As mentioned earlier, sometimes patients develop “new” fears or rituals during treatment. Often, the content of these new symptoms is closely related to the original fears and may be treated by extending to these fears the EX/RP instructions given earlier in treatment. For example, following the successful implementation of response prevention for his compulsive handwash- ing, Mr. F began to rub his hands together to decon- taminate them. The therapist identified this as another ritual and instructed Mr. F to resist the urge to rub his hands together. Next, Mr. F began subtly to rub his fin- gers against the palms of his hands to cleanse his hands
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and to reduce anxiety. The therapist asked Mr. F to stop this ritual as he had the others and was again successful.
Some emergent fears may not be as clearly connect- ed to the patient’s original fears. For example, the fear that June developed of hitting someone while driving was not obviously related to her fears of contamina- tion. Further assessment often results in the discovery of a conceptual link between the two reported fears. In June’s case, her fear of being blamed for causing someone to become ill or die, and her concern about being thought of as a “bad person” because she killed someone, or because she smelled of dog feces, may have been the connection between her two identified fears. In such cases, it is important for the therapist to develop exposures that include cues for this more general fear. June’s therapist might conduct imaginal exposures that include images of people criticizing June or blaming her for causing someone to die.
Negative Family Reactions
Because family members have typically experienced years of frustration with the patient’s symptoms, it is not surprising that some are impatient, expecting treat- ment to progress smoothly and to result in total symp- tom remission. It is not uncommon for family members to become disappointed or angry when they perceive that the symptoms are not subsiding quickly enough. In such cases, the therapist should assure family members that occasional strong anxiety reactions are to be ex- pected and do not reflect failure. The family should be encouraged to respond calmly and be supportive should the patient experience a burst of anxiety.
Often, families have developed patterns of behavior designed to reduce the patient’s distress. Some family members may continue these patterns either in an at- tempt to protect the patient from upsetting situations or because it is difficult to break habits established over years of accommodating the patient’s requests. For example, Mr. P, who was accustomed to entering his home through the basement, immediately remov- ing his clothes, and showering for his wife’s sake, was instructed to enter through the front door and toss his overcoat on the couch. Similarly, family members may find themselves continuing to perform a variety of household activities that they have come to regard as their responsibility because of the patient’s wishes to avoid the distress that the activity caused. For instance, Mr. P was responsible for preparing all the family meals, because his wife was distressed by the possibil-
ity that she might inadvertently contaminate the food. Because such familiar patterns may hinder progress in treatment, the therapist should ask both the patient and family members about such habits and prescribe appro- priate alternative behaviors that maximize the patient’s exposure and minimize avoidance.
Functioning without Symptoms
At the end of treatment, many individuals with OCD find themselves left with a considerable void in their daily routines. The fact that they no longer need to al- locate a large portion of their day to performing rituals leaves them wondering what to do. The therapist should be sensitive to these issues and aid in planning new so- cial or occupational goals to be achieved following ther- apy. If needed, the therapist should conduct additional sessions or refer the patient to another therapist, who will focus on adjustment-related issues. It may also be the case that behavioral treatments such as acceptance and commitment therapy (ACT) are directly applicable to this problem given the explicit focus on functioning; patients with OCD might be especially vulnerable to the belief that they cannot move forward successfully in their lives unless their obsessions are gone, and ACT is particularly well suited to address these kinds of prob- lems. Preliminary evidence from a case series suggested the applicability of ACT to OCD (Twohig, Hayes, & Masuda, 2006), and an RCT provided stronger evi- dence for the efficacy of ACT (Twhohig et al., 2010).
Because they have spent years performing their ritu- als, patients may be unsure about what constitutes nor- mal behavior. The therapist should offer guidelines for appropriate washing, checking, repeating, or ordering. If rituals are still present, the therapist needs to instruct patients to continue the response prevention of some behaviors to ensure maintenance of treatment gains. A patient may also develop a fear that the OCD symp- toms will return. The therapist should reassure the pa- tient that a single washing of his/her hands does not signal the beginning of a relapse.
CONCLUSION
In this chapter, we have reviewed the literature on OCD and its treatment, and provided verbatim dialogue from patient–therapist interactions to demonstrate how EX/RP is implemented. Our review illustrates clearly that much is already known about CBT and pharmaco-
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therapy for OCD. In our clinical practice with adults, we are guided by the empirical research summarized in this chapter, although not all of our clinical deci- sions are unequivocally supported by empirical studies. For example, no controlled, direct comparison study has indicated that intensive EX/RP yields superior outcome to less intensive treatment, yet we typically provide intensive treatment to our adult patients with at least moderately severe OCD. Although our clinical experience suggests that weekly sessions are probably insufficient to produce meaningful gains in most adult patients with OCD, it has yet to be established whether two or three weekly sessions would yield results compa- rable to daily sessions both immediately after treatment and at follow-up. Future research should examine this important issue to establish a “dose–response” curve for EX/RP; in our view clinically, the patient’s initial severity, comorbidity, and motivational readiness to en- gage in the treatment influence our recommendations regarding the EX/RP visit schedule. Another important issue is how to best combine EX/RP with medication. Future research will allow us to identify the optimal treatment course for a particular patient.
Empirical results and clinical observations converge to indicate that psychosocial treatment for OCD must involve both EX and RP instructions, and that failure to conduct exposures to the most anxiety-evoking situ- ations is likely to compromise outcome. With respect to the therapist-assisted versus self-exposure issue, we routinely choose therapist-assisted exposure in our clinical practice. At present, eliminating therapist assis- tance with exposure exercises seems premature, because existing studies have methodological problems such as insufficient sample sizes, and an RCT in pediatric OCD indicated that EX/RP with in-session exposure was superior to a brief form of EX/RP that did not in- clude this procedural element (Franklin et al., 2011). With respect to the role of cognitive interventions in the treatment of OCD, the EX/RP program described in this chapter is a “cognitive-behavioral” treatment in that it targets both cognitions and behaviors; however, we do not typically include formal cognitive restruc- turing. Future research needs to delineate which cog- nitive and behavioral procedures are most effective for correcting particular pathological emotions. Cognitive procedures may also be utilized in “readiness programs” designed to help patients who are highly ambivalent about EX/RP realize that the treatment is both toler- able and effective. Empirical research to date suggests that although antidepressant medications for OCD do not interfere with the efficacy of CBT, combination
treatment is not necessarily more effective than EX/RP alone. However, the partial symptom reduction typi- cally found in pharmacotherapy studies for OCD may render some patients more willing to tolerate the dis- tress associated with EX/RP; thus, premedication may be helpful in promoting readiness in such cases.
What factors seem to enhance long-term efficacy of EX/RP for OCD? Studies suggest that patients with OCD who show great improvement immediately after CBT are more likely to retain their gains at follow-up than those who make only moderate posttreatment gains (e.g., Simpson et al., 2004). Thus, emphasis on procedures that are likely to lead to maximal short- term efficacy also serves to yield superior maintenance of gains. In our clinical experience, understanding of the treatment rationale, active engagement in exposure exercises, strict adherence to ritual prevention instruc- tions, willingness to design and implement exposure exercises between sessions, and willingness to confront even the most difficult tasks on the fear hierarchy are all factors associated with positive treatment outcome. Thus, verbal reinforcement of patients when they ac- complish these goals, and reinstruction when they do not, are important in promoting lasting improvement. In addition, relapse prevention techniques designed specifically for OCD have been found effective in pro- moting maintenance of gains at follow-up (Hiss et al., 1994). In clinical practice, we begin discussing relapse prevention procedures long before treatment is com- pleted, and we focus on maintaining gains in the last few active treatment sessions. Some continuing contact with the treating clinician is also thought to be of bene- fit; thus, brief follow-up sessions are held in the first few months after the active treatment is completed, with contact as needed following the formal follow-up phase. As part of relapse prevention, we often ask our patients to plan EX/RP exercises for hypothetical obsessions they might encounter in the future (e.g., “If you became obsessed in 6 months that touching tree bark would re- sult in your contracting a terrible illness, what exercises should you do?”) to encourage them to problem-solve around OCD issues for themselves rather than relying on the therapist’s instruction. We also emphasize that the occasional occurrence of obsessions should not be a cause of great alarm, provided that patients implement EX/RP to combat these recurring obsessions and urges to ritualize. The patients who are accepting of this real- ity are often the ones most able to apply what they have learned in treatment, and this process enables them to keep their OCD symptoms under control long after treatment has terminated.
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Generalized anxiety disorder (GAD) has been called the “basic” anxiety disorder, in the sense that generalized anxiety is, by definition, a component of other anxiety and related disorders. Indeed, GAD, although characterized by marked fluctuations, is chronic. Some have even considered that GAD might be better conceptualized as a personality disorder, or the clinical manifestation of the temperament of neuroticism itself, since many individuals with this problem cannot report a defini- tive age of onset; rather, they note that it has been with them all their lives. Psychological and drug treatments, although often evaluated, have not produced the robust results evident with some other anxiety disorders. For this reason, further study of new treatment protocols is all the more pressing.
The protocol presented in this chapter, developed by Drs. Roemer and Orsillo at our Center for Anxiety and Related Disorders, illustrates a cutting-edge, acceptance-based approach to GAD that has achieved a high rate of success. This protocol also illustrates, along with Chapter 3 describing process-based cognitive-behavioral therapy for social anxiety disorder, principles associated with the so-called “third-wave” cognitive-behavioral approach to psychological disorders. Clinicians and students interested in how this approach is actually implemented will find the case study of “Héctor” particularly fascinating. —D. H. B.
generalized anxiety disorder (GAD) is a chronic anx- iety disorder, centrally defined by excessive anxiety
and worry (see American Psychiatric Association, 2013, for diagnostic criteria). Epidemiological studies in the United States have revealed a lifetime prevalence of 5.7–9.0% for GAD using DSM-IV criteria (Kessler et al., 2005; Kessler, Petukhova, Sampson, Zaslavsky, & Wittchen, 2012), and 7.8% using DSM-5 criteria (Rus- cio et al., 2017). Lower lifetime prevalences have been reported in lower- and middle-income countries (Rus- cio et al., 2017).
GAD is associated with high levels of comorbidity with other psychological disorders. Over 90% of indi- viduals who meet criteria for GAD during their lifetimes
also meet criteria for at least one additional disorder (Bruce, Machan, Dyck, & Keller, 2001), and prospec- tive studies indicate that GAD is a specific risk factor for the development of other mental health disorders, par- ticularly major depression (Bruce et al., 2001). GAD is also associated with significantly reduced quality of life (Hoffman, Dukes, & Wittchen, 2008). Furthermore, individuals with GAD have more annual medical vis- its than other patients (Belanger, Ladouceur, & Morin, 2005) and are more likely to seek medical, rather than mental health, care for their symptoms (Wang et al., 2005). In fact, GAD is the most common anxiety dis- order found among primary care patients (Ballenger et al., 2001), and the mean annual medical cost of GAD
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generalized Anxiety Disorder An Acceptance‑Based Behavioral Therapy
Lizabeth Roemer Elizabeth H. Eustis Susan M. Orsillo
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is $2,138 higher than that for other anxiety disorders (mean = $6,475; Revicki et al., 2012). Given that GAD is associated with a host of physical complaints and con- ditions, including painful physical symptoms (Romera et al., 2010), gastrointestinal symptoms (Mussell et al., 2008), and cardiological complaints (Logue, Thomas, Barbee, & Hoehn-Saric, 1993), it is not surprising that patients with GAD have a tendency to overutilize medi- cal (Ballenger et al., 2001) and underutilize psychiatric (Kennedy & Schwab, 1997) services.
Although earlier diagnostic criteria for GAD incor- porated symptoms of autonomic arousal (e.g., acceler- ated heart rate), several lines of research converged to support removal of these criteria for DSM-IV. A large- scale study of reported associated symptoms indicated that autonomic symptoms were more rarely endorsed than symptoms of muscle tension, vigilance, and scan- ning, such as those described earlier (Marten et al., 1993). Furthermore, physiological studies revealed that GAD was more accurately characterized by reduced heart rate variability, most notably, vagal withdrawal during periods of worry and negative imagery (Levine, Fleming, Piedmont, Cain, & Chen, 2016), than by in- creased autonomic arousal (e.g., Thayer, Friedman, & Borkovec, 1996). Finally, experimental studies of worry revealed that worrying prior to exposure to a feared stimulus leads to less autonomic arousal than relaxation prior to exposure to a feared stimulus (e.g., Borkovec & Hu, 1990). Taken together, these studies suggest that autonomic arousal is not a necessary feature of GAD.
Instead, the central defining feature of GAD is ex- cessive worry, or repeatedly thinking about worst-case scenarios involving potential future events. Studies re- veal that worry content does not differ between indi- viduals who meet criteria for GAD and those who do not, except that those with GAD report worrying about miscellaneous topics, particularly minor matters, more than those who do not meet criteria (e.g., Roemer, Mo- lina, & Borkovec, 1997). As noted earlier, individuals with GAD report difficulty stopping their worry once it starts, and clients often note that worrying about one topic can lead to worry about another. These findings and observations suggest that worry is a cognitive habit, with clients who meet criteria for GAD getting “stuck” in cycles of worry about a wide range of topics that are difficult to stop once started. All cognitive-behavioral treatments for GAD emphasize interrupting this cycle, although methods for doing so vary.
Descriptive studies of GAD and worry have revealed affective, cognitive, and interpersonal correlates that
may have important treatment implications. Borkovec’s seminal research revealed that worry serves an avoidant function by its perceived association with decreasing the likelihood of already low base rate negative events, and by the reduction in physiological arousal noted earlier (Borkovec, Alcaine, & Behar, 2004), as well as distraction from more emotional topics by self-report (Borkovec & Roemer, 1995). Mennin, Holaway, Fresco, Moore, and Heimberg (2007) have demonstrated that GAD is associated with both self-reported deficits in emotion regulation and limits in implicit regulation of emotional processing (Etkin & Schatzberg, 2011). Studies in this area have also revealed that GAD is as- sociated with the fear of or distress about anxiety (and other emotions; Lee, Orsillo, Roemer, & Allen, 2010; Mennin et al., 2007), worry about worry (or meta- worry; Wells, 2005), and habitual avoidance of inter- nal experiences (i.e., experiential avoidance; Lee et al., 2010). Furthermore, in a clinical sample, both worry and GAD were uniquely associated with perceived un- controllability of emotional reactions, beyond shared variance with other known cognitive predictors of GAD (Stapinski, Abbott, & Rapee, 2010). Extensive research also documents an association between GAD and intolerance of uncertainty (the tendency to respond negatively to uncertain events and situations; Gentes & Ruscio, 2011), including an experimental study show- ing that manipulated uncertainty leads to increased worry (Ladouceur, Gosselin, & Dugas, 2000). In ad- dition, some researchers posit that worry in GAD may function to continue or maintain negative emotional states to avoid a shift or contrast in emotions that may be aversive (Newman & Llera, 2011; Crouch, Lewis, Erickson, & Newman, 2017). GAD is also associated with interpersonal problems (Przeworski et al., 2011), including increased marital distress (Whisman, 2007).
OVERVIEW OF EVIDENCE FOR PSYCHOLOGICAL TREATMENTS
Meta-analyses reveal that cognitive-behavioral thera- pies (CBTs) are efficacious for GAD, with large ef- fect sizes that are maintained over follow-up periods (Borkovec & Ruscio, 2001; Covin, Ouimet, Seeds, & Dozois, 2008; Cuijpers et al., 2014; Hanrahan, Field, Jones, & Davey, 2013), and evidence of comparative ef- ficacy over nondirective therapy (Borkovec & Costello, 1993). Within CBTs, a meta-analysis revealed compa- rable effects of cognitive therapy and relaxation therapy
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in treating GAD (Siev & Chambless, 2007), while another found some indication that CBT was more effective at 12-month follow-up, but not 24-month follow-up ( Cuijpers et al., 2014), with too few direct comparison studies to draw strong conclusions. How- ever, GAD remains one of the least successfully treated anxiety disorders (Waters & Craske, 2005), with most studies indicating that fewer than 65% of clients meet criteria for high end-state functioning at posttreatment (Ladouceur et al., 2000; Newman et al., 2011), and one meta-analysis finding that only 46% of clients at posttreatment, and 57% of clients at 12-month follow- up, were classified as recovered (based on a measure of worry; Hanrahan et al., 2013).
As briefly reviewed earlier, recent research has re- fined and expanded our understanding of GAD in an effort to identify causal and maintaining factors to target in therapy and improve its efficacy (see Behar, DiMarco, Hekler, Mohlman, & Staples, 2009, for an extensive review). Randomized controlled trials (RCTs) informed by these models indicate that targeting the interpersonal and emotion-focused aspects of GAD (Newman et al., 2011), and intolerance of uncertainty (Dugas et al., 2010), yield effects comparable to existing CBTs for GAD. An RCT comparing a treatment that targeted metacognition (e.g., metaworry) to CBT and wait-list control found that both metacognitive therapy (MCT) and CBT yielded better outcomes than wait list, and that MCT yielded significantly larger reduc- tions in worry at posttreatment and higher recovery rates (based on a measure of worry) at posttreatment and follow-up compared to CBT (Nordahl et al., 2018). Finally, an RCT comparing emotion regulation therapy (ERT; Mennin & Fresco, 2014; Renna, Quintero, Fres- co, & Mennin, 2017) for GAD to an attention control condition found that participants randomized to ERT reported significantly greater and clinically meaningful improvements in anxiety, depression, and quality of life via both assessor-rated and self-report measures (Men- nin, Fresco, O’Toole, & Heimberg, 2018).
We developed the acceptance-based behavioral ther- apy described in this chapter (which explicitly targets reactivity to [distress about] internal experiences, and experiential and behavioral avoidance, as described below) in an effort to better target GAD and comorbid disorders. We use the term acceptance-based behavioral therapy (ABBT; Roemer & Orsillo, 2020) to refer to the broad class of therapies that are based in cognitive- behavioral theory but explicitly incorporate methods to promote acceptance of internal experiences (e.g., accep-
tance and commitment therapy [ACT]; S. C. Hayes, Strosahl, & Wilson, 2012; dialectical behavior therapy [DBT]; Linehan, 1993; mindfulness-based cognitive therapy [MBCT]; Segal, Williams, & Teasdale, 2002). This ABBT for GAD, which draws from these treat- ments, as well as Borkovec’s CBT for GAD (Bork- ovec & Sharpless, 2004), has been examined through an open trial and two RCTs. The first RCT revealed significant, large effects on clinician and self-reported GAD symptoms, as well as depressive symptoms, along with marginally significant, medium effects on clini- cian-rated additional diagnoses and self-reported qual- ity of life (Roemer, Orsillo, & Salters-Pedneault, 2008). Significant large effects also emerged on self-reported experiential avoidance and mindfulness, two proposed mechanisms of change in the treatment. All effects were maintained at 9-month follow-up. Of those treated, 77% met criteria for high end-state functioning (fall- ing within normative range on the majority of anxiety measures) at posttreatment; this proportion increased slightly (nonsignificantly) over time. ABBT produced a significant increase in engagement in valued, or per- sonally meaningful, activities (Michelson, Lee, Orsillo, & Roemer, 2011). Moreover, ABBT significantly im- pacted outcome variables proposed in other models to be central to GAD (emotion regulation deficits, intoler- ance of uncertainty, and perceived control over anxiety- related events; Treanor, Erisman, Salters-Pedneault, Roemer, & Orsillo, 2011). Next, we conducted an RCT comparing ABBT with applied relaxation, an empiri- cally supported treatment for GAD, which revealed comparable effects on clinician-rated and self-reported GAD symptoms, clinician-rated comorbid diagnoses, and self-reported depressive symptoms and quality of life (Hayes-Skelton, Roemer, & Orsillo, 2013). A large proportion of clients in both conditions met criteria for high end-state functioning (some of the highest rates reported in the literature in each condition), and gains were maintained at 6-month follow up.
Finally, there is evidence that ABBT works through its proposed mechanisms. Session-by-session changes in acceptance of internal experiences and engagement in meaningful activities predicted outcome above and be- yond change in worry (S. A. Hayes, Orsillo, & Roemer, 2010). In addition, change in decentering has been found to precede and predict subsequent change in symptoms of anxiety, while change in anxiety did not precede and predict change in decentering (Hayes-Skel- ton, Calloway, Roemer, & Orsillo, 2015). Reductions in experiential avoidance were found to predict symptom
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and quality-of-life outcomes at posttreatment, above and beyond decentering (Eustis, Hayes-Skelton, Or- sillo, & Roemer, 2016). Furthermore, participants re- ported significant reductions in interpersonal problems across treatment, with increases in mindfulness predict- ing these reductions beyond shared variance with GAD severity (Millstein, Orsillo, Hayes-Skelton, & Roemer, 2015). Interestingly, in most of these secondary analy- ses, these mechanisms also emerged as predictive of out- come for participants in applied relaxation (see Hayes- Skelton, Usmani, Lee, Roemer, & Orsillo, 2012, for further discussion).
Arch and colleagues (2012) examined the relative ef- ficacy of ACT compared to CBT for a mixed-anxiety sample and found comparable effects across the full sample. Although the small size of the GAD subsample precluded within-subgroup analyses, examination of means suggests that ACT was effective in reducing cli- nician-rated and self-reported GAD symptoms in this study. A small RCT also found a significant reduction in self-reported GAD symptoms among individuals re- ceiving ABBT compared to those in a control condition (Zargar et al., 2012). Another RCT revealed significant effects of an Internet-delivered ABBT for GAD on GAD and depressive symptoms when compared to a wait-list control (Dahlin et al., 2016). Finally, a recent RCT revealed more rapid change in GAD and anxiety symptoms for a group-based ABBT treatment com- pared to a nondirective supportive group therapy (de Almeida Sampaio et al., 2020).
Taken together, these findings suggest that psycho- social treatments for GAD are efficacious, and adapta- tions of CBT that specifically target empirically deter- mined features of GAD are promising, with growing evidence supporting the efficacy of the ABBT presented in this chapter. As with all treatments based in behav- ioral theory, a well-developed case conceptualization is a necessary starting point to use evidence-based treat- ments effectively with a specific client.
AN ACCEPTANCE‑BASED BEHAVIORAL MODEL OF GAD
An acceptance-based behavioral model of GAD is grounded in behavioral learning theory. Consistent with other theories, we propose that individuals with GAD develop the habit of worry, repeatedly antici- pating potential dangers and threats. These habits are strengthened through repetition and reinforcing con-
sequences. This worry process is negatively reinforced by both the nonoccurrence of feared outcomes and the reduced physiological activation that is a positive con- sequence of engaging in worry (Borkovec et al., 2004).
Moreover, individuals with GAD come to associate universal, functional human states such as fear, anxi- ety, other emotional responses, and even worry with negative personal characteristics. As a result, individu- als with GAD respond to anxiety-related thoughts and emotional states with self-criticism and judgment. In an attempt to avoid or escape the uncomfortable, un- wanted experience of worry, and the associated nega- tive self-evaluation, individuals with GAD engage in a variety of potentially problematic behaviors. Although these behaviors interfere with quality of life, they pro- vide short-term relief from arousal and negative affect.
Drawing from decades of research on GAD, other anxiety disorders, and broader models of psychopathol- ogy (e.g., S. C. Hayes et al., 2012), we hypothesize that the following three learned behaviors contribute to the development and maintenance of GAD.
Reacting to Internal Experiences with Distress, Criticism, and Judgment (Leading to Entanglement/Fusion)
One of the most formative, consistent findings to emerge in the field of anxiety disorders has been that the experience of anxiety or fear, in and of itself (e.g., sensations of panic, worrisome thoughts, catastrophic images, recurrent painful memories), is not evidence of a disorder. Instead, reactions to these symptoms, or “re- actions to our reactions” (Borkovec & Sharpless, 2004) exacerbate their intensity and duration, cause distress, and interfere with quality of life, leading to the anxiety disorder diagnosis. The centrality of “reactions to re- actions” to the concept of psychological disorders has been documented in treatment research. Changes in reactivity to emotions predicted unique variance in all outcome variables, over and above changes in frequency of emotional responses in a study of the unified proto- col for transdiagnostic treatment of emotional disorders (Sauer-Zavala et al., 2012; see Payne, Ellard, Farchione, & Barlow, Chapter 6, this volume).
Individuals with GAD report increased anxiety sen- sitivity (i.e., fear of anxiety-related bodily sensations; Olatunji & Wolitzky-Taylor, 2009), negative reactiv- ity to their emotional responses (e.g., Lee et al., 2010; Mennin et al., 2007), and worry about their own worry (Wells, 2005). Furthermore, anxiety leads to a nar-
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rowed focus of attention (both external and internal) toward potential threat (Cisler & Koster, 2010), which likely both exacerbates these reactions and is strength- ened by reactivity, further perpetuating cycles of anx- ious responding. These reactions can lead individuals to become entangled with (Germer, 2005) or “hooked” on (Chodron, 2007) their experiences of anxiety and worry, so that the anxiety comes to seem self-defining and all-encompassing. Instead of viewing anxiety as a response that is elicited in a particular context, indi- viduals can come to define themselves as “anxious,” fusing their identity with these experiences (e.g., S. C. Hayes et al., 2012). Thus, negative reactivity to emo- tions can evolve into negative personal judgments (“I’m so weak!”; “Other people don’t worry the way I do”), which in turn can increase anxiety and worry.
Becoming entangled or fused with internal expe- riences makes it much harder to see the ways that thoughts, feelings, and sensations naturally rise, fall, and change over time. It can also interfere with one’s ability to understand and respond effectively to emo- tional states, leading to diffuse experiences of distress that do not provide clear motivational information. When fear, anxiety, and worry are perceived as distress- ing, defining, and unrelenting, they naturally elicit at- tempts to escape and avoid.
Rigid Attempts to Avoid Internal Distress (Experiential Avoidance)
Trying not to think about or feel or remember some- thing distressing is a natural response. All people use strategies to turn their attention away from internal dis- tress at times, in order to bring attention to the task at hand. Yet experimental studies show that rigid, repeated efforts to put thoughts, feelings, sensations or memo- ries out of our minds (e.g., experiential avoidance; S. C. Hayes, Wilson, Gifford, Follette, & Strosahl, 1996) are often unsuccessful and can actually increase distressing thoughts, feelings, or sensations (e.g., Gross, 2002; Lev- itt, Brown, Orsillo, & Barlow, 2004; Najmi & Wegner, 2008). Furthermore, instructed effort not to think of situations can increase reported anxiety associated with the target situation (Roemer & Borkovec, 1994), sug- gesting that experiential avoidance increases distress about thoughts and emotions. These studies suggest that rigid efforts to avoid distressing thoughts, feelings, sensations, and memories can increase the frequency of these experiences, as well as the distress associated with them, further strengthening the cycle of reactivity and avoidance. Efforts at experiential avoidance are likely
to reduce distress in the short term at least sometimes, leading to immediate negative reinforcement, further strengthening this habitual response.
Reports of experiential avoidance are associated with GAD diagnoses, even beyond shared variance with de- pressive symptoms (Lee et al., 2010). Furthermore, as described earlier, experimental studies demonstrate that worry itself serves an experientially avoidant function by reducing physiological arousal in response to feared stimuli and distracting individuals from more distress- ing topics (Borkovec et al., 2004).
Limited Engagement in Personally Meaningful Actions (Behavioral Avoidance)
Reactions to internal experiences and rigid experiential avoidance not only feed on each other in a continually escalating cycle but also naturally lead to avoidance of contexts that elicit anxiety or other experiences of distress. Behavioral avoidance is a core feature of other anxiety disorders, but it has historically been over- looked in GAD. However, individuals with GAD often avoid certain situations, spend extensive time preparing for situations, procrastinate or put off decision making, or seek reassurance, all in an effort to avoid distress, anxiety, and/or uncertainty (Andrews et al., 2010). Cli- ents with GAD reported significantly less consistent engagement in valued actions (i.e., doing what they find personally meaningful) than did individuals without this diagnosis (Michelson et al., 2011).
Clients with GAD limit their engagement in per- sonally meaningful actions in many different ways. We encounter clients who engage in overt behavioral avoidance, such as declining a date or turning down an opportunity to pursue a promotion at work. Clients vary in their awareness of the specific emotional trig- gers for these choices: Sometimes they are aware of their anxiety, fears of being rejected, or worry, while often they have a more generalized sense of trying to reduce “stress.” Other times, clients who seem to be engaging in a wide range of behaviors that are important (e.g., taking on challenges at work, being involved in activi- ties with their children) describe feeling disconnected from those activities, because they are constantly wor- rying about what is ahead rather than attending to what they are doing in the moment. Borkovec notes this focus on the future instead of the present as a core characteristic of GAD (e.g., Borkovec & Sharpless, 2004), and research indicates that GAD and worry are associated with reports of reduced mindfulness (aware- ness in the present moment; Roemer et al., 2009). This
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continual focus on what might go wrong in the future can lead clients to feel like spectators in their own lives: behaviorally, but not emotionally, engaged in actions that matter to them. We also see some clients whose lives are so busy with activities they feel compelled to complete in order to reduce stress (e.g., household chores, work-related tasks) or to control the uncontrol- lable (e.g., searching the Internet for ways to keep loved ones safe or for assurance that their child will grow up to be a happy adult), that they have little time left to engaged in values-based actions.
This conceptual model highlights three targets for intervention when treating clients with GAD and other comorbid disorders: (1) problematic ways of relating to internal experiences, (2) rigid strategies aimed at experi- ential avoidance, and (3) limited engagement in person- ally meaningful actions. Based on this model, the goals of an ABBT for GAD are (1) to cultivate an expanded (as opposed to narrowed) awareness and a compassionate (as opposed to critical and judgmental), decentered (as opposed to entangled and fused) stance toward internal experiences; (2) to increase acceptance of/willingness to have internal experiences; and (3) to engage mindfully in personally meaningful behaviors.
APPLYING ABBT
Context for Therapy
Our first case study of ABBT took place in group for- mat (Orsillo, Roemer, & Barlow, 2003). Although cli- ents benefited from the group context in some ways, they reported wanting a more individualized focus to help them clarify their values (i.e., what matters to them) and apply the treatment to their specific con- texts. As a result, all of our subsequent trials have used individual therapy. However, we think that the modal- ity of treatment can be adjusted to better fit specific settings. In fact, a group version of our protocol led to significant reductions in self-reported anxiety, worry, and GAD symptoms in a community setting (Heather- ington et al., 2014) and led to more rapid symptomatic change than a nondirective group therapy (de Almeida Sampaio et al., 2020). Furthermore, several elements of ABBT (e.g., psychoeducation, mindfulness practice, commitment to values-based actions) have been ef- fectively conducted in group settings in other, related treatment approaches (e.g., Evans et al., 2008; Kocov- ski, Fleming, Hawley, Huta, & Antony, 2013).
Given the prevalence of GAD in primary care con- texts, we are interested in adapting treatment so it can be
used as part of integrative primary care. Fuchs, Harad- hvala, and colleagues (2016) conducted a preliminary study that supported the feasibility of a group therapy using this approach. We wrote a self-help book (Orsillo & Roemer, 2011) and a workbook (Orsillo & Roemer, 2016) that may also be beneficial in this context. A pre- liminary RCT revealed that the workbook led to sig- nificantly greater decreases in anxiety and worry than a wait-list comparison (Serowik, Roemer, Suvak, Liver- ant, & Orsillo, 2020). We are also interested in the use of technology as one way to increase access to evidence- based care; as noted earlier, an Internet-delivered ABBT can be effective for GAD (Dahlin et al., 2016).
Briefer workshops (e.g., Blevins, Roca, & Spencer, 2011; Brown et al., 2011) may also be a useful modality for delivery of the conceptual model and suggestions for mindfulness and values-based action practices in contexts in which individual therapy is less feasible due to economic or time constraints. Our research groups have developed several brief, one-session prevention/in- tervention workshops based on our ABBT’s conceptual model for college students (Danitz & Orsillo, 2014; Danitz, Suvak, & Orsillo, 2016; Eustis et al., 2017; Eu- stis, Hayes-Skelton, Orsillo, & Roemer, 2018; Sagon, Danitz, Suvak, & Orsillo, 2018) that have yielded symptomatic improvement from both in-person and online delivery. These workshops include psychoeduca- tion on anxiety, stress, and the consequences of avoid- ance, and offer mindfulness, acceptance, and values clarification and values-based action as skills to use in response to anxiety and stress. Given the high preva- lence of racism and discrimination in the United States and the deleterious impacts these unjust experiences can have on mental health, another focus has been on developing and examining brief ABBT-informed in- terventions tailored specifically for coping with racism and discrimination. Examples of these interventions include a 1-hour computer-delivered program focused on racism-related stress for people of color that has been found to significantly reduce internalized racism (Martinez & Roemer, 2019), and an in-person cultur- ally adapted workshop for Latinx students that reduced symptoms of distress (Arbid, 2020).
Therapist Characteristics
A central aspect of ABBT involves modeling a way of responding to intense, challenging internal experiences with curiosity, awareness, compassion, and acceptance. Therefore, successful ABBT therapists are able to dis- cern emotions, validate and normalize their arising, and
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make room for clients’ distress in session. By continu- ally acknowledging emotions, turning toward them in an attempt to expand awareness and increase under- standing, validating their presence with compassion, and allowing them to be present while considering a range of behavioral options, ABBT therapists provide clients with an example of how they might respond dif- ferently to their own experiences and reduce the cycle of reactivity and avoidance that contributes to mainte- nance of their symptoms. Therapists also model a de- centered awareness of internal experiences in the way they talk about thoughts, emotions, internal sensations, and behavior. For example, rather than saying, “I can see you were very anxious in that situation,” the thera- pist might note, “It sounds like a lot of worry thoughts were present and you noticed sensations of tension and restlessness in your body.” These characteristics, com- bined with a clear understanding of the model and how to apply it to specific cases, help therapists to develop a strong, positive working alliance, which was signifi- cantly associated with outcome in our most recent trial (Calloway, Hayes-Skelton, Roemer, & Orsillo, 2017).
As we describe more fully below, ABBT is meant to be applied flexibly, with therapists adapting their ap- proach, strategies used, and between-session assign- ments to meet the presentation and context of clients. As such, flexibility may be an important therapist characteristic. In a small qualitative study, as part of an RCT, we interviewed clients who identified with marginalized backgrounds in terms of race, ethnicity, sexual orientation, socioeconomic status, or religion. Clients identified the flexibility of their therapist as an important factor in how helpful they found treatment and how well it fit with their particular context (Fuchs, West, et al., 2016).
Client Characteristics
In the studies we have conducted on ABBT for GAD, we have had very few exclusion criteria, in order to maximize the generalizability of our findings. Clients frequently present with comorbid diagnoses, most commonly major depressive disorder, social anxiety disorder, and other anxiety disorders. Because ABBT targets mechanisms that are likely to underlie these other disorders as well, treatment may positively impact these comorbid conditions (e.g., Roemer et al., 2008). However, outside the constraints of protocol therapy, we would recommend integrating elements of evidence- based methods (e.g., behavioral activation, exposure) when indicated. The disorders we have ruled out in our
RCTs, primarily because they warrant specific treat- ments, include substance dependence, bipolar disorder, schizophrenia, and autism spectrum disorders. Thus, we cannot determine the impact of ABBT on these co- morbid presentations.
To date, we have only preliminarily explored poten- tial predictors of response to ABBT. To date, our data suggest that gender, age, GAD severity, frequency and intensity of worry, depressive symptoms, and comorbid diagnoses do not significantly predict outcome (Orsillo, Roemer, & Salters-Pedneault, 2008).
As with most evidence-based treatments, consider- ably more research is needed to determine the ways an ABBT for GAD might be beneficial for people from marginalized or nondominant cultural backgrounds, as well as how to use ABBT strategies to address con- textual stressors such as discrimination and lack of re- sources. A meta-analysis indicated promising results for ABBTs more broadly (Fuchs, Lee, Roemer, & Orsillo, 2013). Our small, qualitative study revealed that clients from marginalized backgrounds generally found ABBT helpful (Fuchs, West, et al., 2016). Clients particularly noted that therapist flexibility and the focus on valued living helped them engage in treatment and find it rel- evant. However, some clients reported that therapist inflexibility or not connecting to specific mindfulness exercises was a barrier. As with all treatments, cultural considerations and adaptations are a necessary part of culturally responsive ABBT (for more in-depth dis- cussions of these considerations for mindfulness and acceptance-based therapies, see Hall, Hong, Zane, & Meyer, 2011; Harrell, 2018; Proulx et al., 2018; Roemer & Orsillo, 2020; Sobczak & West, 2013).
Concurrent Pharmacological Treatment
Pharmacotherapy, including selective serotonin reup- take inhibitors (SSRIs), serotonin and norepinephrine reuptake inhibitors (SNRIs), and pregabalin, is the most common mode of treatment for GAD (He et al., 2019) and is often considered a first-line treatment op- tion (Katzman et al., 2014). Benzodiazepines (BZs) continue to be commonly prescribed for GAD (Bald- win, Allgulander, Bandelow, Ferre, & Pallanti, 2012), despite the risks of tolerance and dependence (Baldwin, Hou, Gordon, Huneke, & Garner, 2017). A recent meta-analysis of pharmacotherapy for GAD demon- strated a small-to-medium effect of SSRIs, SNRIs, and BZs over placebo (Gomez, Barthel, & Hofmann, 2018). However, pharmacological interventions may produce adverse side effects, including sexual dysfunction,
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drowsiness, and weight gain, which lead many patients to stop treatment early (Baldwin et al., 2017); they are less cost-effective than psychotherapeutic approaches such as CBT (Heuzenroeder et al., 2004), and can be associated with increased health care utilization (Berger et al., 2011).
Clients who were stable on medications were en- rolled in our clinical trials. Within ABBT, medications are conceptualized as one of several ways to reduce the intensity of internal reactions, so that it is easier to ac- cept them, have compassion for oneself, and engage in meaningful actions. In this way, a nonexperientially avoidant function for medication can be highlighted (medication helps one to engage more fully in life and accept whatever comes), so that it is consistent with the rest of treatment.
Overview of Treatment Elements
In our clinical trials, we have followed a 16-session, weekly, individual protocol for ABBT, with the last two sessions tapered (every other week) and focused on re- lapse prevention. The first seven sessions focus on psy- choeducation and skills building, while the remaining sessions focus on application of skills, while the client engages in personally meaningful, values-based ac- tions. Here we provide a brief overview of each element of treatment, followed by a composite case example to illustrate the way each element is addressed across the course of therapy. Those interested in more details on our approach should consult our book for therapists (Roemer & Orsillo, 2020), our self-help book (Orsillo & Roemer, 2011), and our client workbook (Orsillo & Roemer, 2016).
Clinical Assessment to Develop an Acceptance‑Based Behavioral Conceptualization
To develop a case conceptualization that guides flexible application of treatment elements, we assess symptoms, context, and the three components of the model.
SYMPTOMS
Assessing the client’s anxiety and related symptoms provides useful information about targets for change, while also supporting the therapeutic goal of chang- ing a client’s relationship with anxiety. Assessment of anxiety-related thoughts, feelings, physical sensations, and behaviors, the contexts in which anxiety typically occurs, and the frequency and severity of symptoms,
helps clients begin to observe more accurately specific elements of their anxiety responses. Ongoing self-mon- itoring of daily anxiety symptoms, as well as guided imaginal recall, can provide a more accurate assessment of specific symptoms than general report given that cli- ents who engage in habitual avoidance or suppression of their anxiety often do not have an accurate perception of its frequency, duration, or variability over time. Brief but specific self-report measures (e.g., the Depression Anxiety Stress Scales [Lovibond & Lovibond, 1995] or the trait and weekly Penn State Worry Questionnaire [Meyer, Miller, Metzger, & Borkovec, 1990; Stöber & Bittencourt, 1998]), can also be used, both to obtain baseline measures of symptoms and to track weekly fluctuations in symptoms.
Semistructured clinical interviews such as the Anxi- ety Disorders Interview Schedule (Brown & Barlow, 2014) can be used to determine both principal and co- morbid disorders to guide the selection and emphasis of specific treatment strategies. Depression is an impor- tant target of assessment, as are other clinical presenta- tions, such as eating disorders and substance-use disor- ders, which may indicate specific avoidance strategies that need to be targeted in treatment.
REACTIONS TO INTERNAL EXPERIENCES
Assessing how clients respond to their anxiety symp- toms, as well as to internal experiences (e.g., thoughts, emotions, sensations, memories) more generally, con- tributes to case conceptualization. Therapists may ask questions (e.g., “When you notice you are worrying, what thoughts, feelings and sensations do you experience next?”; “Do you find yourself having critical thoughts about your experiences of anxiety?”; and “What kinds of thoughts do you have?”) or use self-report measures that capture these constructs. Self-criticism, judgment, and reactivity that arise for clients in response to their own thoughts and feelings are important targets for intervention. Measures such as the Affective Control Scale (Williams, Chambless, & Ahrens, 1997), a mea- sure of distress in response to anxiety, depression, anger, and positive emotions, and the Self-Compassion Scale (Neff, 2003) can help to identify reactivity to emotions and self-criticism.
EXPERIENTIAL AVOIDANCE
Therapists also assess the strategies that clients use in an attempt to suppress, avoid, or change internal experi- ences (S. C. Hayes et al., 1996). Experiential avoidance
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strategies may be internal, such as thought or emotion suppression (Gross & Levenson, 1997; Najmi & Weg- ner, 2008), or external, such as using substances, engag- ing in self-harm, or restricting eating. Therapists can ask clients what they do to try to manage their distress or anxiety, then listen for avoidant strategies. Efforts in which clients engage automatically or rigidly are most likely to lead to paradoxical increases in distress and symptoms. Therapists need to distinguish between ef- forts to modulate or regulate emotional distress and rigid efforts to avoid it; often, the difference is evident in what happens after the strategy is engaged. The former efforts are likely to be beneficial and may be strengths on which to build in therapy, if used flexibly, whereas the latter are more likely to lead to increased distress and interference. For instance, one client with whom we worked reported going for walks to try to clear her head of worry. When her therapist asked what she did when she returned, she reported that she was more able to focus on being with her children and enjoy their time together. On the other hand, another client who described regularly watching TV in order to dis- tract herself from her worries, said that as soon as she turned off the TV, her worried thoughts flooded back, so that she found herself watching TV for hours at a time rather than doing activities she had planned dur- ing the day. Whereas the first client’s walks might be incorporated into treatment as a way to care for herself and help her engage more effectively with her children, the second client’s therapist might help her develop al- ternative ways of responding to her anxiety. The Accep- tance and Action Questionnaire (Bond et al., 2011) and the Multidimensional Experiential Avoidance Ques- tionnaire (Gámez, Chmielewski, Kotov, Ruggero, & Watson, 2011) can help to identify experientially avoid- ant strategies; the Difficulties in Emotion Regulation Scale (Gratz & Roemer, 2004) assesses emotion regula- tion more broadly.
ENGAGEMENT IN VALUES-BASED ACTIONS
Therapists should also assess how clients are function- ing in their daily lives and the ways that anxiety and worry are interfering. Drawing from ACT (Wilson & Murrell, 2004), we focus particularly on the degree to which clients are doing what is important to them (i.e., what they value). We assess this with the Valued Liv- ing Questionnaire (Wilson, Sandoz, Kitchens, & Rob- erts, 2010), while also inviting clients to write about the ways anxiety interferes with their relationships, work–
school–household management, self-nourishment, and community involvement. This provides not only important information about current functioning but also a target and motivation for treatment to help cli- ents live fuller, more meaningful lives. This assessment often provides an important first step toward shifting the goal of therapy from anxiety reduction to enhance- ment of life.
CONTEXT AND HISTORY
As with all treatment approaches, assessing clients’ con- text is essential. Therapists need to learn how clients (as well as family and friends) understands their anxiety, their perspective on psychological challenges, and their views on psychotherapy. Therapists should also explore clients’ multifaceted cultural identity, with attention to culturally specific sources of coping and strength, culturally influenced views on emotions and emotional expression, comfort level with engaging in mindfulness practice, and the ways in which individualism or inter- dependence may influence personal values. Assessing for the presence of the contextual stressors in clients’ lives, including physical challenges, poverty, and dis- crimination, acknowledges the key role these stressors can play in maintaining psychological distress and in- creases the therapist’s awareness of potential obstacles that could arise over the course of treatment. In sum- mary, assessing culture and context helps to validate clients’ experiences, build therapeutic alliance, deepen case conceptualization, and help ensure that therapy proceeds in a culturally sensitive and responsive way (Hays, 2016; Sue & Sue, 2016).
This comprehensive assessment sets the stage for treatment elements aimed at (1) cultivating an expand- ed (as opposed to narrowed) awareness and a compas- sionate (as opposed to critical and judgmental), decen- tered (as opposed to entangled and fused) stance toward internal experiences; (2) increasing acceptance/willing- ness to have internal experiences; and (3) mindfully en- gaging in personally meaningful behaviors.
Therapeutic Relationship
The therapeutic relationship provides an important context for therapeutic change. In ABBT, the therapist provides acceptance and compassion that allows clients to begin to react differently toward their own internal experiences. Therapists explicitly validate the human- ness and naturalness of all responses that clients share,
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emphasizing the way biological makeup and learning history can easily lead to anxious responses and other emotional reactions, and the way that even apparently “irrational” thoughts can be learned from social and family influences. For instance, when a client noted in session that he knew he should not be anxious about a job interview, his therapist responded that anxiety be- fore an interview is a very natural response given that he really wants the position, and that we are hardwired to fear social rejection. This response modeled a differ- ent reaction to his anxiety and was the first step toward cultivating a new, less self-critical response.
It can be challenging to empathize with and vali- date some clients, particularly when they are hostile or unresponsive. Understanding the learning history and context that produces and maintains these difficult, but also in some ways functional, behaviors helps thera- pists cultivate compassion. When a therapist expresses genuine compassion toward a client, often the client’s reactions change, at least slightly, providing more op- portunities for connection, validation, empathy, and further change.
Another challenge to the therapeutic alliance can stem from differences between client and therapist in aspects of identity (e.g., age, gender, race, religion, eth- nicity, sexual orientation, immigration status, or social class; Hays, 2016; Sue & Sue, 2016). Initiating a discus- sion of potential differences early in therapy provides an opportunity for open communication about poten- tial sources of misunderstanding and may make a cli- ent feel more comfortable bringing up any issues that emerge throughout the course of therapy. Therapists take responsibility for learning about a client’s cultural context on their own, while remaining sensitive to each client’s individual experiences and life contexts, so that they can consider how cultural and systemic factors may play a role in clients’ responses and can be used to promote growth and positive adaptation. Commu- nicating awareness of, and sensitivity to, the therapist’s own areas of relative privilege can also contribute to a stronger therapeutic alliance.
Psychoeducation
Similar to other CBTs, psychoeducation is an impor- tant component of this ABBT. Therapists present con- cepts, using handouts, particularly during the first half of therapy (then revisit these concepts as needed in the second, application phase of treatment). For each con- cept, therapists draw examples from clients’ lives (using
monitoring forms, assessment material, or asking cli- ents specifically for examples) to ensure that the mate- rial is relevant.
Psychoeducation begins with a discussion about the nature of fear, anxiety, and worry (including a discus- sion of the function of worry), followed by exploration of the function of emotions more broadly, emphasizing the habitual nature of our emotional responding and how repetition strengthens these habits, while interrup- tion can weaken them. Therapists teach clients about the natural inclination to avoid painful or threatening cues, as well as the challenges and costs associated with trying to rigidly control internal experiences and avoid anxiety-eliciting situations. Therapists draw a distinc- tion between clear emotions (that provide information about a response to a current context) and muddy emo- tions (that may be diffuse, confusing, left over, or lon- ger lasting). They also differentiate worry from problem solving, highlighting the differences between events and outcomes over which we do and do not have influ- ence or control. Therapists also describe mindfulness skills, specifically noting the ways these skills can be used to clarify emotional responses and enhance par- ticipation in valued life activities.
Psychoeducation provides a rationale for the rest of treatment, encouraging engagement in behaviors that take significant time (e.g., mindfulness practice) or effort (e.g., engaging in values-based actions). Psycho- education on its own can also help to promote a new relationship to internal experiences. Realizing how one’s emotions become muddy and overwhelming as a result of a series of understandable processes (e.g., not getting enough sleep, still feeling upset about an earlier fight with a partner) can reduce self-criticism and judg- ment, which in turn can reduce muddiness and reac- tivity. For some clients, psychoeducation alone leads to engagement in new behaviors and to new learning that promotes accepting responses to internal experiences and increased engagement in life. However, experien- tial learning is often needed to supplement this clinical strategy.
Many challenges can arise when presenting psycho- educational material. First, it can be difficult to attend to specific client concerns while also presenting exten- sive new information. Using client examples as you teach and frequently asking clients to share their reac- tions can help to balance these competing demands. Also, sometimes clients disagree with material being presented. For instance, clients may insist that avoid- ance is an effective strategy. Arguing with clients is
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rarely productive, and it can weaken the therapeutic relationship. Furthermore, case conceptualizations are only hypotheses based on the literature and clinical ob- servation, so it is important not to cling rigidly to them. We find it useful, in this situation, to ask whether cli- ents are willing simply to observe the concept over the next few weeks to see whether they can learn anything new about their experience. This promotes a collabora- tive approach to treatment and helps to engage clients, while also encouraging valuable feedback on our con- ceptualization.
Mindfulness Skills Development
Mindfulness (Kabat-Zinn, 2003), or attending to the present moment with openness, curiosity, and compas- sion, is a central skill clients can use to change the na- ture of their relationship with their internal experiences (e.g., beginning to see thoughts as thoughts, or decen- tering), increase their willingness to have any reactions that arise, and promote engagement in fulfilling, mean- ingful lives. We use a wide range of methods to help cli- ents bring their awareness to the present moment, and we greet their experiences with curiosity, kindness, and compassion.
SELF-MONITORING
Self-monitoring is a common method used in all CBTs. Similar to these approaches, therapy begins with cli- ents monitoring situations in which worry arises. Each week, based on what is covered in session, new aspects of experience are added (e.g., emotions, efforts to avoid experience, engagement in values-based actions). The process of monitoring worry, other internal experiences, and behaviors helps to promote awareness and decenter- ing; clients turn toward their internal experiences rather than habitually turning away, and they see each aspect of their experience rather than blending the compo- nents together (e.g., noticing thoughts, emotions, and behaviors separately). As clients begin to notice the dis- tinction between emotion and behavior, they are more able to consider the variety of behavioral options avail- able to them even when strong emotions arise.
Self-monitoring can be challenging for some clients. They may forget to complete monitoring forms, see them as a “homework” requirement done only at the therapist’s request, or finish them in the waiting room as opposed to completing them in the moment. Thera- pists can help clients to see the usefulness of the practice
by clearly communicating the rationale for monitoring; describing how it helps build skills that can be used to clarify emotions, reduce distress, and increase engage- ment in valued activities; and reviewing the monitoring each session and connecting observations to treatment goals. Therapists can also flexibly adapt monitoring as- signments to fit with the client’s life (e.g., reduce moni- toring to one situation a day) while emphasizing the importance of doing some monitoring in the moment that a reaction occurs to facilitate the development of awareness as anxious habitual patterns unfold.
FORMAL MINDFULNESS PRACTICE
Mindfulness is a skill; therefore, practicing it regularly can be extremely helpful. Therapists help clients to de- termine when they can set aside some time in which to draw their awareness, again and again, to some aspect of their experience, such as the breath, physical sensa- tions, or thoughts. In mindfulness-based treatments such as MBCT, clients practice for 45 minutes a day; we generally use shorter mindfulness practices and allow clients to choose the length of their practice. We do have all clients practice an adapted progressive muscle relaxation in which clients tense and release a series of muscle groups, noticing the sensations they experience.1 This gives anxious clients an extended exposure to mindfulness, while providing a focus for attention that may facilitate more prolonged practice. Clients vary in how much they keep up this particular practice versus other, shorter practices.
In our approach, therapists teach clients a progression of practices across the course of treatment, beginning with focus on the breath and body, moving to aware- ness of taste and sounds, then on to more challenging practices of awareness of emotions and thoughts. Cli- ents and therapists practice together first in session, then discuss the client’s experience with the exercise. Initially, clients often label the practice as “good” or “bad,” “relaxing” or “stressful.” Therapists help clients move toward simply observing and describing their ex- perience during the practice, recognizing that all prac- tice is useful and so-called “bad” practice can teach a lot about how active one’s mind is and how to repeatedly bring awareness back to the moment despite a wander- ing mind.
When discussing in-session practice, therapists draw connections between the practice and clients’ present- ing problems. For instance, one client reported that when she practiced mindfulness of her breath, her mind
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kept wandering to her frustration with her roommate, and it was clear that she was “bad” at mindfulness and was not ever going to get better. Her therapist related these self-critical thoughts and negative predictions to those that often arose when the client took on a new task at work. The therapist suggested that if she prac- ticed observing critical thoughts with compassion and curiosity during formal mindfulness, she might be able to carry these same skills into challenging work situa- tions.
Clients often have trouble setting aside time to prac- tice mindfulness regularly. Use of traditional problem- solving strategies to help the client find moments (dur- ing a subway commute, just after putting the kids to bed) to practice and emphasis on the potential benefits of practice, including increased efficiency and alertness throughout the day, can be helpful. Clients can also use mindfulness as an avoidance strategy, particularly if they initially find the practice relaxing. Therapists need to attend to the function of practice behavior to be sure that clients are not using it to avoid unwanted internal experiences.
INFORMAL MINDFULNESS PRACTICE
Although setting aside time to practice can be an excel- lent way to develop any skill, the goal is always to use the skill while engaging in life. Clients practice mind- fulness informally by engaging mindfully in daily tasks such as washing the dishes (Nhat Hanh, 1992), eating, showering, or folding laundry. They gradually begin to practice in more challenging contexts, such as during conversations, dates, meetings at work, or community events. Therapists initially help clients to remember to practice mindfulness during sessions; over time, clients begin to remind themselves to come back to the present moment while engaging in therapy, strengthening this skill so they can use it more effectively in their lives.
Engaging in Actions
Finally, therapists help clients turn their attention and effort away from trying to control their internal experi- ences and instead focus on engaging more fully in their lives. Clients begin exploring what is important to them through a series of writing assignments. First, they de- scribe how anxiety has gotten in the way of their lives in several domains (relationships, work–school–house- hold management, and self-nourishment and commu- nity involvement). Next, they write about how they
would like to be in these areas, if they did not have any anxiety. Although these writing practices are one method of identifying the values that will become the focus of therapy moving forward, in-session exploration and clarification is often needed to supplement these as- signments. Clients may struggle to differentiate values from goals, articulate values that reflect perfectionistic standards, or focus too narrowly on particular values- based actions. Helping clients to clarify personal val- ues that can guide behavior and enhance their sense of purpose and meaning is a critical step toward effective behavior change. From here, therapy involves making behavioral plans each week to incorporate values-based actions into the client’s everyday life. This may include generating new activities a client can try (e.g., making a social connection, asserting oneself at work, or joining a community organization) or helping the client to iden- tify moments in life when he/she can choose responses that reflect values-based actions (e.g., considering per- sonal values when engaged in conflict and allowing values to guide responses). Clients are encouraged to use their mindfulness skills to recognize opportunities to engage in values-based actions, use intention rather than habit to guide behavior, and increase acceptance and willingness when challenging internal experiences such as anxiety arise.
Shifting from habitual avoidance to engagement is a long, ongoing process. Some clients have difficulty ar- ticulating their values, because all of their attentional and behavioral resources have been directed toward anxiety management for so long. Once clients have clarified what they find important, approaching these actions can be extremely anxiety provoking and hard to do. However, encouragement from the therapist, culti- vation of mindfulness skills, and breaking tasks down into specific manageable pieces (e.g., asking a coworker to lunch, or having one open conversation with a par- ent) can help a client become willing to make these first important behavioral changes even though anxiety will inevitably be present. Over time, the experience of engaging in valued activities can be naturally reinforc- ing. Nonetheless, continued awareness and practice are needed so as not to fall back into old, natural patterns of avoidance due to anxiety.
Many challenges arise in pursuing values-based ac- tions. First, as Hayes and colleagues (2012) note, clients often think in terms of goals (e.g., finding a partner, losing 15 pounds) as opposed to values (e.g., sharing intimate thoughts and feelings with others, engaging in health-promoting habits). Focusing on wanting to
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lose 15 pounds can lead to self-criticism in the moment, which might interfere with that goal. On the other hand, a person can take actions in the moment that are consistent with wanting to engage in health-promoting habits (e.g., going to the gym or eating a healthy lunch) that in turn also help with a goal. Therapists work to help clients identify the values and meaning that under- lie any stated goals, so that they can engage in actions in the moment that will be fulfilling and meaningful.
Therapists need to take care not to impose their own values onto clients. Cultural sensitivity is particularly important in this aspect of treatment. For instance, one client we treated with ABBT described a value of being able to provide financially for his parents, leading him to choose a profession that to him was less intrinsically interesting but would allow him to support his family. His therapist came from a more individualistic back- ground and had an initial reaction that choosing a more intrinsically rewarding profession was important. How- ever, the therapist recognized that this would impose his own values on the client rather than help the client to make choices consistent with his own values.
Therapists also need to be sensitive to the real-world constraints that can keep clients from engaging in ac- tions that matter to them. External constraints such as limited resources, inequities, racism, other forms of dis- crimination, and family contexts need to be validated and accounted for in developing treatment assignments. Relatedly, clients may want others in their lives to act differently. Although this is a very reasonable desire, changing other people is not always possible. Clients can request changes in others or take steps to address injustices in different contexts, but therapists cannot guarantee that these things will lead to clients’ hoped- for changes. Instead, the therapist can help the client make the best choices possible in the face of these con- straints, which can certainly include asking for changes and also leaving situations when possible, if necessary.
Relapse Prevention
Anxiety is a natural, habitual response, as is reactiv- ity to internal experiences and experiential avoidance. Therapists help clients develop a plan for maintaining the practices they have found most helpful in treat- ment, and to prepare for potential “lapses” in the fu- ture. Clients are encouraged to refer to their handouts and monitoring sheets when difficulties arise, and to revisit concepts and practices they found helpful in treatment.
CASE STUDY
This composite case is largely based on a single client but with details from other clients added to illustrate certain points. Identifying information is altered to protect confidentiality.
Background Information
“Héctor,” a 24-year-old Latino man, presented for treatment after being placed on academic probation. Although Héctor had an extremely strong academic re- cord as an undergraduate, he was struggling to keep up with the course demands in his first semester of medi- cal school. Héctor initially sought treatment from his primary care provider for a wide variety of stress-related symptoms, including frequent headaches, muscle ten- sion, and gastrointestinal distress. However, she urged him to seek therapy for what she believed to be an anxi- ety disorder.
In the initial assessment, Héctor endorsed symptoms consistent with GAD. He described a long history of worry that started in elementary school. His worry fo- cused centrally on his academic demands. He reported worrying constantly about the quality of his work, the sufficiency of his knowledge, and his ability to meet his own and others’ academic-related expectations. Héc- tor was the first person in his family to graduate from college, and his entire extended family was extremely proud of him and significantly invested in Héctor earn- ing a medical degree. Héctor’s mother had secured a second job to help meet his rising tuition costs, one of his uncles offered to cosign on a loan, and his cousin offered him a place to live rent-free. While he was ex- tremely grateful for their support, Héctor constantly worried about disappointing them.
Héctor was also troubled by worries about his moth- er’s health and well-being. He was concerned that she was overextending herself with two jobs, and he worried that she might have a heart attack or fall asleep when driving home and die in a car accident. Héctor also worried a fair amount about his two nephews. In his view, they spent far too much time watching television and playing video games, and needed more structure and guidance than his brother was providing.
Héctor described a number of aches and pains that he attributed to his constant, high level of physical tension. He noted that he had considerable difficulty falling asleep each night, as his mind constantly cycled through a variety of potentially negative outcomes the
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next day might bring. Not surprisingly, he described having a very difficult time concentrating, especially while he was in class and when he attempted to do his assigned reading. When his anxiety and worry became too severe, he would skip class and head to the gym. In the past, when he exercised long enough, he would become so physically fatigued that he would fall asleep immediately when his “head hit the pillow.” Unfortu- nately, that coping strategy had recently become less and less effective. First, he found that he was skipping class for the gym more and more frequently, to the point that he was unable to keep up his grades. More- over, although he was still falling asleep fairly quickly postexercise, recently, he would awaken after only 1 or 2 hours of sleep.
When he was in secondary school and college, Héc- tor also found that spending time with friends and family kept his GAD symptoms in check. However, 6 months earlier, he had left his support network behind in Miami and relocated to Boston for medical school. Although he initially went out to eat with some of his classmates and occasionally attended study sessions with them, he never felt entirely comfortable at these events. He worried that his classmates did not think he belonged at such a prestigious medical school, and Héc- tor was acutely aware that he was one of very few ethnic minority students.
Engagement Session
In this session, Héctor disclosed that his family did not know he was in therapy, and that he was too ashamed to tell them about his academic issues. Héctor acknowl- edged that keeping these secrets was painful and dis- tressing, particularly because it required him to dis- tance himself even further from his main source of social support.
Although Héctor had attended a few counseling ses- sions in his first semester of college, he had no other history of psychotherapy. Héctor described his brief course of previous therapy as primarily supportive. He noted that meeting a few times with his Latino thera- pist, mostly to talk about academic stressors, had been extremely helpful in his transition to college. This ex- perience made him cautiously optimistic about the cur- rent course of therapy, although he acknowledged a fear that his problems might now be too severe to overcome completely.
Given the considerable outside-of-therapy demands associated with ABBT, the therapist asked Héctor about
potential barriers to treatment. Although Héctor had a slightly reduced schedule because of his academic pro- bation, he was still taking three courses and working 20–30 hours a week. The therapist validated Héctor’s existing commitments, but she also wanted to be realis- tic in describing the additional time commitment that would be required, particularly in the first six to eight sessions of therapy. The therapist used the training for a marathon analogy to convey the importance of setting aside sufficient time for out-of-therapy assignments. She noted that Héctor’s worry habit was deeply ingrained, and that learning new methods of responding would require some commitment to practice. Athletes training for a marathon cannot keep the same work/life schedule while adding in training sessions. Instead, they need to make some temporary accommodations to make time to run. Similarly, a client with GAD cannot develop new habits while maintaining the same busy schedule. Some time and attention must be allocated temporarily to reflecting on the treatment and practicing new ways of responding.
Finally, the (White) therapist explored how her gen- der, race, and ethnicity might affect treatment.
THERAPIST: It sounds like one of the best things about your previous course of therapy was that you really felt understood by your therapist.
HÉCTOR: Yes, I was surprised that I felt so comfortable with him. I expected that my counselor would be a woman, and I was a little hesitant about talking with a man at first. . . . I thought he might think of me as weak for seeking therapy.
THERAPIST: I think most of us go to therapy with ex- pectations about our therapist. We might expect a therapist to be older or younger, male or female, or of a particular race or ethnicity. Depending on whether the therapist meets our expectations, we may be more or less comfortable, feel more or less understood. Did you have any expectations coming in today?
HÉCTOR: Honestly? I knew I was seeing a woman be- cause of your name. And I wasn’t sure of your eth- nicity. But frankly, I didn’t really expect to have a Latina therapist based on the providers I have seen at this center.
THERAPIST: Do you have any thoughts or concerns about working with me that you would like to talk about?
HÉCTOR: Not really . . .
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THERAPIST: My hope is that we can work really well together, but it would be understandable if you didn’t necessarily trust me or feel comfortable with me right off the bat. You don’t know me at all, and it can be really difficult to open up to a stranger. Also, I know that for some people it might matter that I’m not Latina, I’m White. Sometimes that can make some- one feel like I can’t understand some kinds of expe- riences, like those related to being a minority or a person of color. But my goal is to do whatever I can to be sensitive to, and understanding of, your unique experiences. I bring some general expertise about anxiety to our work, including ways that experiences with discrimination can relate to anxiety, sometimes in subtle ways, but you are the expert on your own experience. So I will always try to check in with you about the ways in which the things we discuss and the suggestions I make fit with your experience. Please feel free to let me know if I say or do some- thing insensitive, or if you feel like I am not fully understanding what you are telling me. I definitely make mistakes, but my intention is to try to help you as best I can achieve your goals for therapy.
The therapist ended the engagement session by pro- viding some activities for Héctor to complete before the next session. First, she explained a monitoring form used throughout treatment (although the domains to monitor are changed over time as new session material is introduced, this version includes only date, situation, and worry topic as columns) and asked Héctor to begin to notice when he engaged in worry. She also gave him a copy of the Valued Living Questionnaire to complete with the following instructions:
“Sometimes anxiety and worry can prevent us from taking some actions that are consistent with our val- ues. For example, you mentioned that you skip class when you feel too anxious, even though you also noted that you care deeply about being a good stu- dent. Anxiety and worry can also make people feel as if they are on automatic pilot, or that their lives are consumed by things they must do rather than things they choose to do. This questionnaire is a first step toward identifying some of the ways in which anxi- ety and worry might be interfering with your life. Sometimes it is painful to think about the ways our lives are not as we would wish them to be. But this awareness is a first step toward making a change. So,
notice any feelings that arise as you fill out the forms, and we will be sure to talk about them next week.”
Session 1
The goal of Session 1 is to provide an overview of the treatment structure (client and therapist roles, between- session assignments, etc.), and to plan and discuss the rationale for treatment that is informed by a person- alized ABBT conceptualization of the client’s present- ing problems. The therapist asked Héctor to engage in an experiential exercise that involved imagining him- self back in one of the anxiety-provoking situations he noted on his monitoring form. Using guided imagery, the therapist helped Héctor to notice that his experi- ence of anxiety was characterized by a cycle of interre- lated thoughts (worries), physiological sensations (tight- ness in his shoulders and chest), and behaviors (leaving class early, heading to the gym).
HÉCTOR: I didn’t realize so much was happening when I am anxious. Usually, as soon as I notice I’m anx- ious, I just do whatever I can to prevent it from es- calating.
THERAPIST: That doesn’t surprise me. You have de- veloped a strong habit. When you get anxious, you immediately try to distract your attention from your experience and seek out ways to control or dampen your emotions. How difficult was it to imagine your- self back in class on Monday?
HÉCTOR: It was surprisingly easy. I definitely felt just as anxious remembering how I felt as I did sitting in the classroom.
THERAPIST: That is a great thing to notice. Something that is uniquely human is our ability to remember and imagine events vividly. Like other animals, we are hardwired to experience fear in the face of a threat—as if a predator were charging at us. But humans can also simply imagine a threat in their minds and experience the same hardwired response to threat. Do you have any idea what you were imag- ining in class that day?
HÉCTOR: On Monday, my mind just went from 0 to 100—I was barely aware of what I was thinking. But when we went through the exercise today, I noticed a series of pictures in my mind. First, I thought, I am not prepared for class. Then I imagined the professor yelling at me, my classmates laughing at me, my fam- ily’s disappointment . . .
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THERAPIST: Hmm . . . if you imagined all those people rejecting you at the same time, it is not surprising that you would feel afraid. We are hardwired to seek social approval. If the entire academic community, your friends, and family all rejected you, you would have a pretty good reason for feeling afraid. Unfor- tunately, our minds don’t distinguish present threats from imagined ones.
The therapist and Héctor discussed the model of fear, anxiety, and worry guiding ABBT for GAD. The thera- pist explained that fear and anxiety serve adaptive func- tions. Anxiety allows us to imagine future threats and prepare for them. Fear energizes us to avoid and escape danger. In both of these states, our attention narrowly focuses on the threat and our escape plan, blocking out other information. Unfortunately, our ability to think, imagine (the future), and remember (the past) allows us to imagine endless threats and to respond with fear, even when no threat is present (i.e., our mental repre- sentations develop the same emotional properties as the events themselves, leading us to respond to threats that do not exist in the environment). Moreover, although we are hardwired to escape or avoid threat, sometimes, in order to do the things that matter to us, we have to approach situations that will likely elicit anxiety (e.g., allow ourselves to be vulnerable in order to gain intima- cy, take a risk at work in order to successfully negotiate a challenge). Many of us respond to this conundrum by harshly judging our natural responses and doing every- thing in our power to avoid experiencing them.
The therapist and Héctor also discussed the function of worry. Although worry is associated with clear nega- tive consequences (interferes with concentration, results in tension and fatigue), it too serves a function.
HÉCTOR: As much as my worry bothers me, in some ways, I am afraid to give it up. Sometimes it feels like the only thing I can do to control the uncontrollable.
THERAPIST: Great observation. Tell me more about that.
HÉCTOR: Well, sometimes it feels like if I stop worry- ing about my mother’s health, she will have a heart attack. Or I believe that if I don’t worry about a test, I won’t actually study.
THERAPIST: Some people notice that worrying about minor, everyday matters takes their mind off more painful thoughts and emotions. Have you ever no- ticed anything like that?
HÉCTOR: (beginning to tear up) Sometimes I think worrying about tests, or being late to class, or what I should wear to a school event is the only thing that keeps me from noticing how lonely I am. Sometimes I feel like if I stopped worrying, I would become so sad and depressed I might never get out of bed.
THERAPIST: That sounds really painful. When your mind is busy with worries, its challenging to concen- trate on anything else, and you experience tension and restlessness in your body. On the other hand, there is a real sadness here that you are away from your family and missing them, and worry can some- times distract from that sadness.
Near the end of the session, the therapist summed up her conceptualization and plan for treatment.
“Anxiety and worry narrow our focus and pull our attention toward the future. This cycle happens out- side of our awareness and can be difficult to change. In this treatment, we will use mindfulness skills to address this habit. Mindfulness increases and ex- pands our present-moment foc‘us and allows us to notice and break this cycle. We also have a tendency to judge and control our emotions because we think they are preventing us from having a satisfying life. In this treatment we will explore whether that reac- tion to our emotional responses is helpful or harm- ful, and we will consider alternative ways of respond- ing. Finally, worry is anticipatory; thus, it prevents us from engaging in activities that could be threaten- ing. But sometimes we want to approach these situa- tions—especially if they will help us to live the kind of life we value. In this treatment, we will learn to become more flexible—to consider different behav- ioral responses—rather than automatically avoiding potentially anxiety-provoking situations.”
At the end of Session 1, the therapist led Héctor in a mindfulness of breath exercise. She began by guiding him to notice the way he was sitting in the chair, then drew his attention to where he could feel his breath in his body. The therapist then guided Héctor to gently redirect his awareness back to the sensations of his in- halations and exhalations over the next several minutes, while deepening his breath, no matter how many times his mind wandered to other things. After the therapist and Héctor discussed his experience of this exercise, she asked him to practice it daily between sessions.
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Session 2
Session 2 primarily focuses on an introduction to mindfulness. The therapist led Héctor in a mindfulness of breath exercise, then engaged him in a debriefing.
THERAPIST: What did you notice? HÉCTOR: Well, I am pretty stressed out today. So the
exercise didn’t work as well as it did when I practiced this week.
THERAPIST: Tell me more about that. HÉCTOR: I used the breathing almost every night this
week to fall asleep. And it actually seemed to help. At least it calmed me down, so I could get to sleep quicker. But today, I just felt more stressed out.
THERAPIST: I can see why you might feel like your practice “worked” some days and not “others.” In the media, we often hear about breathing or mindful- ness practice as something we can do in a moment to feel less anxious. And as you’ve seen in your experi- ence, it can lead to a sense of calmness. Unfortunate- ly, as we’ve discussed, there really isn’t any strategy we can use in a particular moment that will make our anxiety go away. On the other hand, mindful- ness practice can help us become more aware of our experience. And this awareness can help to increase our self-compassion as we notice just how busy and critical our minds can be. Increased awareness can also help us notice habits that add to our distress and provide us with opportunities to try new ways of re- sponding. We will get to those later in therapy, but the focus now is on noticing and accepting whatever state we are in. What else did you notice?
HÉCTOR: I couldn’t keep my attention on my breath. It was all over the place. I am not sure I have the personality needed to be mindful.
THERAPIST: What a great observation. First, you no- ticed your attention was pulled in different direc- tions. I’ll bet that happens at other times in the day as well. It is useful to get to know just how busy our minds are.
HÉCTOR: I never thought of it like that. I guess it makes sense that I struggle to concentrate in class if I am having so many different thoughts all the time.
THERAPIST: I also want to gently remind you that I didn’t actually suggest that you should keep your at- tention on your breath. Just that you should notice
where your attention is and continually guide it back to the breath. Isn’t it interesting to see how quickly our minds judge whether we are doing something “right” or “wrong”?
HÉCTOR: (laughing) I sort of know what you are going to say here, but I also felt like I was breathing the wrong way. I kept breathing out of my mouth and it sounded so loud compared to your breath.
THERAPIST: (smiling) Great observation. If our minds are so judgmental about something as simple and natural as breathing, just imagine what judgmental thoughts are present when we are in class, at work, with friends. It sounds like you really used this ex- ercise as an opportunity to get to know the habits of your mind.
The therapist also led Héctor in the Raisin Exer- cise, which simply involves the practice of eating one raisin mindfully. Following this exercise, she focused on the mindfulness skill of “beginner’s mind,” essen- tially highlighting the ways in which “knowing” what to expect sometimes prevent us from accurately observ- ing different experiences. The session ended with the therapist leading Héctor through a slightly modified progressive muscle relaxation that was aimed at helping him to practice observing sensations and letting go of tension (rather than reduce anxiety).
Session 3
The therapist began Session 3 with the “mindfulness of sounds” mindfulness exercise. Héctor was able to see the similarity between this practice and the Raisin Ex- ercise in Session 2. Specifically, he noticed that it was difficult for his mind to observe the pitch, tone, and volume of the sounds around him without trying to label (a truck backing up) and judge (“That is loud and annoying”) his experience. The therapist was careful to normalize this response and to highlight the utility of becoming aware of what we are all naturally inclined to do.
After reviewing Héctor’s monitoring and mindful- ness homework, the therapist introduced a new psycho- educational topic—the function of emotions. Héctor quickly provided an example of the ways in which emo- tions such as fear can serve a communicative function. He described an incident when he was walking home from the library late at night. Although he did not hear or see anything out of the ordinary, Héctor had a sense
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that he was in danger, so he took a number of precau- tionary steps: He took his headphones off, crossed the street to be in an environment with more lighting, and called his roommate on his cell phone. The next morn- ing, Héctor read that there was a mugging the previous night on campus, and he was convinced that the fear signals he received protected him from being a victim. The therapist provided an example of the consequences of ignoring the messages our emotions provide.
THERAPIST: Imagine you are experiencing sadness and disappointment because your current job is not ful- filling. That sadness is uncomfortable, so you natu- rally want to get rid of it. You might spend your eve- nings zoning out watching television alone, trying to “relax,” or you might start staying out late at night with friends, drinking and trying to have a good time, so you don’t notice that you’re feeling sad in that area of your life. You might start finding reasons to miss work or start daydreaming when you’re at work. These strategies are all aimed at reducing your sadness. And they might work in the short term, but none of them resolves the problem. What is worse is that those strategies might even create new problems as you start sleeping less, doing less well at work, and running into more conflicts at work. Even though you are doing everything you can to avoid feeling sad, the sadness is there for a reason. The first step to moving forward in that situation is noticing that you are feeling sad and recognizing that your work situ- ation is eliciting these emotions. Only then can you decide what actions to take.
HÉCTOR: That makes sense. But what about the fear I feel when I think about asking a classmate to study with me?
THERAPIST: What do you think your fear is telling you in that situation?
HÉCTOR: That he might think up some excuse to reject me and say no.
THERAPIST: Absolutely. As humans we are hardwired to seek social support and approval. It can absolutely be risky to put ourselves out there to be accepted or rejected. But here is the thing. While it is impor- tant to acknowledge the message our emotions are sending, we don’t always have to follow their advice. Emotions are associated with action tendencies— when we feel fear, we are prepared to flee, when we feel anger, we are prepared to fight. But our emotions
don’t actually control our behavior. And often when we consider taking an action that could be really meaningful—opening up and appearing vulnerable to someone or taking on an academic challenge— our emotions will warn us that such a step is risky. In these cases, we need to acknowledge the message we are receiving, yet we can still choose to take the values-based action.
HÉCTOR: I guess that makes sense. I certainly knew that moving away from my family and starting medi- cal school was risky. I felt a lot of fear, but I did it anyway, because it is important to my family that I succeed. My abuela [grandmother] always says courage is acting with heart. Being afraid, but doing something anyway, because of love or passion.
However, Héctor also struggled a bit as he tried to determine the function of his emotions in some other contexts.
HÉCTOR: I can see how emotions sometimes can serve a function. But other times the function seems much less clear to me. For example, I know a little test anxiety can be helpful and motivating, but why do I feel terrified some nights when I am studying. I get so scared and anxious that I become paralyzed. My problem is that most of the time I am confused by my emotions and their intensity.
THERAPIST: We make the distinction between what we call “clear” and “muddy” emotions. Clear emotions refer to when we have a very strong emotional re- sponse to a particular situation; for instance, we feel strong fear when a car approaches us on the street, which is what we might call a “clear” emotional re- sponse. Emotions that are complex, confusing, or too intense and long-lasting for the situation are what we call “muddy.”
Together, Héctor and his therapist reviewed how fail- ures in self-care (e.g., not getting enough sleep or eating well, not exercising regularly) increase the likelihood of muddy emotions. They also considered ways that worry (which involves the ability to imagine things that have not yet happened) and rumination (which involves re- peatedly remembering past events) both can elicit emo- tions that are not at all related to whatever is unfolding in the present moment. Finally, they discussed the way our “reactions to our reactions” can muddy our emo- tional responses.
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“Another thing that can make our emotions confusing and muddied is that often when we have an emotion- al response, we don’t just have that one response—we have a series of responses that are triggered by that first emotion. For instance, we may feel scared, then angry that we got scared, then afraid the feeling will grow stronger, then ashamed that we are afraid, and so on. We may also have thoughts that come up as responses to a clear emotion, such as ‘I shouldn’t feel this way,’ ‘This is a sign that I am a weak person.’ One reaction that we often have is to try to control emotional responses. We will talk more about that in the next session. Finally, emotional responses can also seem much more intense when we start to feel defined by our emotions—when we see them as stable traits that represent our personality rather than natural human responses to events that come and go.”
Normally, Session 3 would end with a review of the first completed writing assignment (i.e., writing about how anxiety and worry interferes with relationships, work–school–household management, and self-nour- ishment and community involvement). However, Héc- tor admitted that he had not finished it. He noted that it had been a busy week with exams and that he found it hard to set aside time for himself. Together, Héctor and his therapist brainstormed ways he could schedule in the values writing. However, she also noted that sitting down and considering the ways that anxiety is interfer- ing with the things that matter most could be a very painful exercise. The therapist suggested that Héctor recognize that the pain served a function (letting Héc- tor know that changes were needed for him to live a more personally fulfilling life), and she pointed out that seeking therapy was a sign that he acknowledged that pain and was willing to make some changes. The thera- pist also gave Héctor new monitoring forms that added a column for emotions, so he could begin to monitor his emotional responses in addition to his worry.
Session 4
Héctor presented to Session 4 visibly upset. He had just returned from a visit back home to Miami, and he was extremely upset over his interactions with his brother. As he began to describe the situation, the therapist gen- tly interrupted.
“Excuse me for interrupting you, Héctor, but I have an important question. I can tell this visit was very
upsetting for you, and we will be sure to devote a good part of today’s session to talking about it. But if you are willing, I would like us to start out our ses- sion as we always do, with a brief mindfulness prac- tice. It can really be challenging to practice when you are experiencing a lot of emotions and thoughts, yet it can also be extremely helpful. If you are willing, I would like us to start by becoming aware of the physical sensations we are currently experiencing. I would like to hear about your visit, and then there is another mindfulness exercise that might help us fur- ther explore what you are feeling right now. Would that be all right with you?”
Héctor agreed, and the therapist introduced a mind- fulness exercise that involved increasing awareness of physical sensations. During the debriefing of the prac- tice, Héctor admitted that he found it particularly chal- lenging to keep redirecting his attention from images of his visit to his physical sensations in the moment. However, he noted that it became easier over time. The therapist remarked that Héctor seemed more centered than he had when he first walked in. Héctor replied that he did feel more present and ready to discuss his concerns.
THERAPIST: Did you use your monitoring sheet this weekend to help you work through some of the chal- lenges that arose during your visit home?
HÉCTOR: Absolutely, I was so upset that I needed to get my thoughts down on paper. As I wrote here, on Saturday, when I was at my parent’s house but only my brother and his sons were home, I was flooded with worries. My nephews used to be such sweet little boys, but now they will barely make eye contact with me when I greet them. They spend all their time glued to their electronic devices playing violent video games. And my brother completely ignores them— all he wants to do is talk to me about his latest dating adventures.
THERAPIST: Did you notice the specific worries you were experiencing?
HÉCTOR: Yes, I wrote I am worried that my brother and nephews are too much for my mother to handle. I am worried that they are draining her health and finances. I am worried that my nephews will not get a good education, and that they will get involved in the wrong crowd. And I am worried my brother is drinking too much and that he is too selfish.
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THERAPIST: Good job observing your responses. How about your emotions? Were you able to identify what emotion or emotions were present?
HÉCTOR: I was very upset. Mostly angry, I think. I don’t know—this is one of those situations where I felt confused about my feelings.
The therapist suggested that Héctor try a mindful- ness practice aimed at observing his emotional respons- es. She asked him to close his eyes and vividly imagine his interaction with his brother, and she instructed him to notice visual and auditory stimuli, to focus on the physical sensations in his body, to bring his attention to the thoughts running through his mind and finally to his emotions. She reminded him simply to notice his experience, bringing curiousness and compassion to what he was experiencing, observing what happened when he was feeling strong emotions, without altering or judging them. She reminded him to notice whether more than one emotion was present, and to observe any rise and fall in his emotions. After several moments, she asked him to open his eyes.
THERAPIST: What did you notice? HÉCTOR: At first, all I felt was angry. Then I noticed
I was feeling afraid. But what really surprised me is that I felt extremely sad. It’s interesting because at the time I thought I was just straight up angry, but thinking back on it I noticed that my emotions seemed to ebb and flow. I guess another thing that was interesting is that I started out just feeling the emotions. But throughout the exercise I started to notice I was observing them. It was really helpful to get some distance—before that I think I just felt con- sumed with emotion.
THERAPIST: Great observations. Tell me a bit more about your responses to those emotions. And any thoughts you have about their function.
HÉCTOR: I think I felt angry, because I disagree with how my brother is raising his sons. But then I got mad at myself for feeling angry. My brother hasn’t had the opportunities that I have. Thinking about that made me feel guilty.
THERAPIST: Did you notice any responses to your feel- ings of guilt?
HÉCTOR: I hate feeling guilty. It feels like a tremendous weight on my chest. I think I tried to distract myself from that feeling and then I just started imagining
all the problems that could result from my brother’s screwups and I got consumed with fear and worry. But then, when you prompted me, I returned back to observing my emotions. And then the more I focused on my emotions, I started to realize I felt really, re- ally sad. But what was interesting was I think I just accepted it was a sad situation. Usually I can’t stand feeling sad. I am afraid it means I am going to get depressed and retreat into my own world. But I think I recognized that this is just a sad situation. I miss my family. I wish I could fix my brother’s problems, but I can’t.
The therapist tied Héctor’s experience to the topic of clear and muddy emotions. She pointed out that anger is a natural response that arises when someone acts against your wishes. And sadness is a normal re- sponse to a painful situation. She also helped Héctor identify why his anger was initially so intense. In addi- tion to being angry about the situation on Saturday, he was also having anger about the many times in the past when his brother upset him. Héctor was also imagining that his brother would continue to “screw up,” which further fueled his anger. The “reactions to reactions” Héctor experienced also increased the intensity of his response. For example, when Héctor judged the feeling of anger as unacceptable, he started to feel guilty. And when the feeling of guilt was too painful, he distracted himself with multiple worries about the future.
Next, the therapist spent some time on the main concept of the session—the limits and consequence of internal control efforts. She asked Héctor to engage in a number of experiential exercises aimed at demonstrat- ing the often paradoxical effects of efforts to control internal experiences such as thoughts, emotions, and images. For example, the therapist asked Héctor to imagine that he “had to get a good night’s sleep” before a big test. She asked him what might happen if, alarmed by the late hour, he purposefully tried to induce a state of sleepiness. Héctor noted that this frequently hap- pened, and the more he tried, the more distressed and awake he became.
Finally, the therapist spent some time going over Héctor’s values assignment. Héctor easily identified many ways in which his anxiety was interfering with school and work. He noted that it was harder and hard- er to concentrate both during class and while doing his homework, because his mind was consumed with wor- ries—worries about failing class, about letting down his family, and about his family’s health and well-being.
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Héctor also noted that when his anxiety about his fam- ily became too intense, he would call or plan a visit with them. But he found that when he did make the time to talk with or be with his family, he was consumed with worry about the time he was taking away from his schoolwork. Héctor wrote about his fear that he would never find a life partner. He was far too busy with school and his family to date, and he believed it was his destiny to end up alone. He was terrified about this possibility because he described himself as extremely family-oriented.
As the session ended, the therapist gave Héctor a monitoring form that added a column for “efforts to control,” so that he could begin to notice these as they occurred throughout the week. She also provided for Héctor a second values assignment to complete for the next session. The therapist noted that often our at- tempts to avoid anxiety, worry, and stress cause us to make subtle shifts in our behavior, so that we begin doing whatever we are “supposed” to be doing and lose track of what we want to be doing, or what personally matters to us as individuals. She reviewed the distinc- tion between values and goals, emphasizing the impor- tance of identifying the direction that Héctor wants to move in rather than solely the goals to achieve. The therapist noted that this next assignment was aimed at further exploring three areas of living to see what changes might be necessary to improve Héctor’s quality of life.
“Choose two or three relationships that are important to you. You can either pick actual relationships (your relationship with your brother) or relationships you would like to have (“I would like to be part of a cou- ple,” “I would like to make more friends”). Briefly write about how you would like to be in those rela- tionships. Think about how you would like to com- municate with others (e.g., how open vs. private you would like to be, how direct vs. passive you would like to be in asking for what you need and in giving feedback to others). Think about what sort of sup- port you would like from other people and what sort of support you can give without sacrificing your own self-care. I also would like you to write briefly about the sort of work you would like and why that appeals to you. Next write about the student you would like to be with respect to your work habits and your re- lationships with your professors and peers. What is important to you about the product of your work/ studies? How would you like to communicate to others
about your work? How would you like to respond to feedback? What additional challenges would you like to take on? Finally, I would like you to briefly write about the ways in which you would like to spend your free time. What would you like to do to better nourish yourself (e.g., nutrition, exercise, spirituality) or contribute to your community?”
Sessions 5–7
In Sessions 5–7 of treatment, the focus is on encourag- ing the client to consider moving from a stance of re- sistance and avoidance to one of willingness. A number of mindfulness and other experiential exercises are used to help clients practice observing their thoughts, emo- tions, and physical sensations as transient events. For example, Héctor practiced imagining that his thoughts and feelings were going by on a movie screen in front of him. Once clients are able to defuse or decenter from their internal experiences, and they no longer feel de- fined or threatened by them, they are often more will- ing to approach and engage in a variety of activities.
Like many clients, Héctor initially struggled a bit with the concept of willingness. At first Héctor thought the therapist was suggesting that he should come to view his anxiety in a more positive light. Or that he should learn to accept his anxiety because it was what a “strong man” needed to do. Using a metaphor adapted from ACT, his therapist tried to clarify the concept of willingness, likening it to one’s willingness to wade through a swamp on a journey to a beautiful mountain.
“Taking a stance of willingness suggests that you will accept and move forward with the thoughts and feel- ings (rational or irrational) that appear as you make your way through life, taking the actions that will help you obtain the things in life that you value. For instance, let’s say that you want to ask your class- mates if you can join their study group. To do so will likely elicit feelings of fear, thoughts about possible rejection. However, you can be willing to experience those thoughts and feelings, if they are what arise when you take actions consistent with your value to engage in your schoolwork. You may not like the feelings, you may wish it could be another way, but you can be willing to experience whatever comes up in order to take a values-based action.
“It is as if you are on a journey to a beautiful mountain. But along the way you come to a disgust- ing, murky swamp. You don’t want to walk through
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the swamp, and it may not seem fair that you need to do so. But you can choose to walk through if you decide that the journey to the mountain is worth it to you.
“Now if the swamp is to the side of your path, you do not necessarily need to go through it. And, you don’t have to dive into the swamp and roll around in it. And you can put on boots, or walk across a plank, in an effort to avoid getting dirty. Yet you might still trip and fall in the swamp, and willingness means you accept that possibility as you move forward on the journey of your choosing.”
Several values assignments are used to help clients set their course or mountain “journey.” As noted earlier, Héctor was asked to write about his values in three spe- cific domains. This can be a challenging assignment, and often clients confuse values with goals, describe values that suggest the need for control or perfection, or focus on what they perceive to be insurmountable obstacles to living consistently with their values. Thus, often, several sessions are devoted to discussing the values assignment, and it is not uncommon for clients to revise their values multiple times in session and for homework. For example, Héctor’s initial writing assign- ment produced some values that could have been prob- lematic for him to pursue.
HÉCTOR: My value in the schoolwork domain is to achieve the highest grades in all of my coursework. I want to be the top student in my graduating class, so that I can make my family proud.
THERAPIST: Would aiming to receive a perfect score on an exam be an example of a value or a goal?
HÉCTOR: Right, grades are outcomes, so I guess those are goals.
THERAPIST: Imagine that you are working as a physi- cian. You are surfing the Internet and you stumble upon a webpage where patients rate, and leave com- ments about, their doctor. What would you want the page to say? My doctor scores well on standardized tests?
HÉCTOR: (chuckling) Well, no. I guess I would want them to say that I was caring and compassionate. And that I was willing to stick with a health problem until I came up with the right diagnosis and the best treatment I could provide.
THERAPIST: Great, those sound a bit more like values.
So, would it be fair to say you want to be engaged with the material you are learning? And that you want to be bring kindness and compassion to your interactions with patients and commit to learning what you can to help improve their health?
HÉCTOR: Yes, that is what I value. I keep thinking my grades matter most, but I know in my heart that is not why I am in medical school. I am not here to impress my instructors and classmates. I want to be a doctor who brings care and commitment to improv- ing the health of my patients.
Héctor also struggled a bit with articulating his rela- tionship values:
HÉCTOR: I wrote that I always wanted to be available to my mother, whenever she needed me. I want to be her rock. I get so angry at myself when I am too tired to return her phone calls at night. Or when she needs something to be fixed, like the leaky faucet in the kitchen, and I can’t take care of it because I am here in Boston and she is in Miami. Also, I feel bad when she is lonely. I want to prevent her from having to experience any more pain than she already has.
THERAPIST: I know you care deeply for your mother. And I can completely understand your desire to do all you can for her. And yet, much like it is humanly impossible to prevent yourself from feeling emo- tions, I think it is humanly impossible to ensure that our loved ones are never in pain or in need. Even if you dropped out of medical school and moved back home, there are limits to what you can do for her. And that can be a very difficult and painful thing to accept. It sounds to me like the value is that you want to maintain a strong, caring relationship with your mother. Would you agree?
HÉCTOR: Absolutely. THERAPIST: And fixing a faucet and returning a call
are actions that are consistent with those values. Are there other actions you can take that reflect your val- ues? In other words, if you are in Boston and she is in Miami, can you care for her without fixing her faucet?
HÉCTOR: Well, I could talk to her about it. She appre- ciates when I listen to her vent about her problems.
THERAPIST: Great, what else? HÉCTOR: I guess I could call a repair person for her. Or
ask my brother to help.
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THERAPIST: Wonderful. The point is, there are many actions one can take that are consistent with a value. If we define values-based action as just one or two responses, and for whatever reason, we can’t respond in those ways, we can end up feeling stuck and mis- erable. Living consistently with one’s values means flexibly considering multiple options to act in ways that are meaningful to us.
Héctor also struggled with articulating his values in relation to his brother and nephews:
HÉCTOR: I want to be close to my brother and his sons, but I can’t. It doesn’t matter how I treat them, they are selfish, and they never want to spend time with me.
THERAPIST: One of the most complicated things about relationship values is that we only have control over half of the relationship. You cannot control how your brother acts; you can only choose how you want to approach him.
HÉCTOR: Are you saying I should just let my brother live his life the way he currently does? Allow him to raise his sons to be disrespectful and rude?
THERAPIST: It is so painful for you to watch your brother make choices that are inconsistent with your values. And I know if you could control his behavior, you would. It seems like you keep trying and try- ing to figure out how to control a situation that just might be out of your control. Sometimes mindful- ness skills can help us to clearly accept the reality of a situation. And by “accept” I mean recognize the real- ity of the situation—I don’t mean that you should like or support his approach. But you may need to accept the reality that you only have control over some parts of this very painful situation. It seems to me that you can control how you choose to define your values regarding how you relate to your brother. But you can’t control his behavior. If you act lovingly toward him and try to establish a close relationship, your brother may respond in kind. And that bond might allow you to talk with him about your par- enting concerns. Or you might end up with a closer relationship and he could continue with his current habits. Or he may completely reject your efforts to become closer. Choosing our actions is like aiming an arrow. We can make choices about how we aim and when we release the arrow. We don’t have control over where the arrow lands. However, we may notice
where it lands and use that information to inform the way we aim or when we shoot the next time. In a similar way, we can choose the actions we want to take repeatedly, although we don’t have control over the consequences of our actions.
Héctor continued to work on defining his values, until he felt that he could clearly articulate what mat- tered to him in the domains of relationship, school- work, self-nourishment, and community involvement. Although it is necessary for clients to achieve this mile- stone, so that they can move into the next phase of treatment, it is important to recognize that values artic- ulation is a dynamic process. Having defined values is helpful in guiding the final nine sessions of treatment, but what is most important is for clients to adopt the general perspective that valuing can provide a compass for directing behavior and improving quality of life.
During these sessions, Héctor was given a final ver- sion of the monitoring form that represented an ap- plication of the full model. This included columns for date/time, situation, first reactions (thoughts, feelings, sensations), second reactions (efforts to control, mud- diness, willingness, acceptance), and actions/responses (e.g., avoidance, values-based actions, application of mindfulness skills).
Sessions 8–12
The goal of Sessions 8–12 was to personalize the con- cepts introduced in the first phase of treatment and help Héctor to apply mindfulness and engagement in valued activities to his daily life. At the beginning of each ses- sion, Héctor and the therapist worked together to pick a mindfulness practice. Each week they purposely chose exercises, including ones that Héctor found particularly challenging, those he found most useful, and those that seemed to best fit his needs given the particular struggle he was facing (see Table 5.1).
The bulk of these sessions used the mindfulness and acceptance strategies introduced during Phase I to in- crease Héctor’s willingness to engage in his personally articulated values-based actions. Héctor continued to monitor values-based actions taken, missed opportuni- ties, mindfulness, and obstacles to willingness (see Fig- ure 5.1).
For example, in Session 10, Héctor shared that he had missed an opportunity to engage in a valued ac- tion. Specifically, one of his favorite instructors had offered to meet with Héctor to discuss the process of
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TABLE 5.1. Choosing a Mindfulness Practice
Title Focus of attention How it can be helpful Where to find it
Mindfulness of Breath Breath • Portable • Can be centering • Great introduction to the habits of the mind
(busy, judgmental)
MP3 available onlinea; Kabat-Zinn (1990); Roemer & Orsillo (2020); Orsillo & Roemer (2011)
Mindfulness of Sounds Sounds • Helps us to notice our tendency to categorize/ judge
• Allows us to practice “beginner’s mind”— seeing things fully as they are, not as we imagine they will be
MP3 available online; Segal et al. (2002); Orsillo & Roemer (2011)
3-Minute Breathing Space
Physical sensations (including breath), thoughts, emotions
• Helps us get centered and present when moving from one activity to another
• Useful when we want to “check in” with ourselves
Segal et al. (2002); Roemer & Orsillo (2020); Orsillo & Roemer (2011)
Mindfulness of Physical Sensations
Physical sensations • Good practice for bringing curiosity and compassion to physical sensations that are typically feared and avoided
• Brings awareness to sensations in the body, without judgment or avoidance
MP3 available online; Orsillo & Roemer (2011)
Mindful Progressive Relaxation
Muscle tension/ relaxation
• Increases awareness of the sensations of tension and relaxation
• Concrete way to practice “letting go” • May elicit a relaxed state
MP3 available online; Orsillo & Roemer (2011)
Mindfulness of Emotions and Physical Sensations
Emotions and/ or accompanying physical sensations
• Increases awareness of the full range of emotions present
• Helpful when generally distressed or confused • Useful for evaluating clear and muddy
emotions
MP3 available online; Orsillo & Roemer (2011)
Mindfulness of Clouds and Sky
Thoughts and feelings, imagery
• Allows practice of viewing thoughts and feelings as transient and separate from self
• Helps with decentering/defusion
MP3 available online; Roemer & Orsillo (2020); Orsillo & Roemer (2011)
Inviting a Difficulty In and Working It through the Body
Physical sensations related to painful experience
• Helps to cultivate willingness to experience painful emotions
• Useful first step when a client is struggling against accepting a painful reality
MP3 available online; Williams et al. (2007); Roemer & Orsillo (2020); Orsillo & Roemer (2011)
Your Personal Experience with Self-Compassion/ Mindful Observation of Self-Critical Thoughts
Self-critical thoughts • Brings awareness to experiences of criticism in the past and the present
• Helps to identify barriers to self-compassion
MP3 available online; Orsillo & Roemer (2011)
Mountain Meditation Mountain imagery—transience of events external to the mountain
• Uses the image of a mountain to promote the experience of thoughts, feelings, and emotions as changing and impermanent
• Particularly helpful for cultivating a sense of inner strength or stability, even in the face of distress and reactivity
MP3 available online; Kabat-Zinn (1995); Orsillo & Roemer (2011)
aAt www.mindfulwaythroughanxiety.com.
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selecting rotations, but Héctor had cancelled the ap- pointment.
THERAPIST: What did you notice about your response to his offer?
HÉCTOR: At first, I was excited, but as time went on, I became more and more anxious.
THERAPIST: Can you identify the clear emotions that arose?
HÉCTOR: I actually used the mindfulness of emotion exercise to sort this out a bit. I felt excited about tak- ing the next step in my education, happy that my instructor singled me out, and nervous about the challenges that lie ahead for me in my career.
THERAPIST: Excellent. Were you also able to observe your reaction to your reactions?
HÉCTOR: Honestly, not until today. I think at the time I just got caught up in my reactions rather than observ- ing them. But during the mindfulness practice today,
I noticed some of the same old responses I always have. I was afraid to feel good about myself, and my pros- pects for the future. I had that same sense that worry- ing about what could go wrong was what I needed to do to ensure that I don’t mess up. I also became pretty critical and judgmental about my anxiety.
THERAPIST: What do you think you could have done differently?
HÉCTOR: I have become kind of lax when it comes to filling out the monitoring forms. But I was think- ing about what you said last week. I do think that the process of physically completing the form in the midst of my distress can help me to take a pause . . . and remember some of my skills.
Session 11 brought a more challenging issue into therapy. Héctor was extremely distressed over an inter- action he had with a university security officer. Héctor was on his way back home from a long night studying when he was approached by a security officer and asked
VALUED ACTIVITY LOG
Please complete this form at the end of each day.
This week, at the end of each day we would like you to think about an action that you took that was consistent with one of your values or an opportunity that you missed to take an action consistent with your value. Briefly describe the action and mark T for taken or M for missed.
On a scale of 0–100 rate how mindful you were during the action or the missed opportunity.
Note any obstacles that you noticed that stopped you from taking action (or could have).
There are no right or wrong answers to this assignment—we all choose not to engage in valued actions for a variety of reasons. This is just a way for us to start to get a better sense of what may be getting in the way for you so that you can make choices as to how you would like to proceed.
Date Action Taken (T) or missed (M)
Mindfulness (0–100) Obstacles
FIGURE 5.1. Values Monitoring Form.
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to produce his university identification card. Although it was close to midnight, Héctor observed at least five other students crossing the campus, yet he was the only one who was questioned. Héctor was already sensitive to the fact that he had been the only person of color in the library that night. He was stressed out over exams, missing his family and friends, and frankly tired of dealing with the subtle and obvious discrimination he encountered on a daily basis. Thus, he refused to pro- duce his identification card and reported that he “lost” it, and he shouted at the officer. Although the situation was eventually sorted out, Héctor was angry, embar- rassed over his behavior in the situation, and confused.
HÉCTOR: I am really struggling with this incident. My mind is racing, I feel tense all over, and I can’t sort out what is clear and what is muddy and, more im- portantly, what valued action I could have chosen.
THERAPIST: It is natural to experience a rush of con- flicting thoughts and emotions in such a painful en- counter. I am so sorry that given the racism inherent in our society, you are subjected to differential treat- ment because of how you look. This structural prob- lem exists outside of you and isn’t your fault. And I really understand how the pain and the anger can build up when you have to deal with things like this all the time. I certainly don’t want to suggest that you have to change who you are, when the system needs changing. However, if you think it would be helpful, I would like to try to work with you to find the least painful, most effective, values consistent way for you to respond when you are confronted with racism, be- cause, unfortunately, it is something you encounter in your daily life. If you are willing, a mindfulness practice might help us gain some clarity.
HÉCTOR: I don’t feel very open right now, but I do think it’s important for me to work on this. “Invit- ing a Difficulty In and Working with It through the Body” [see Figure 5.2] could be a first step.
Following the exercise, Héctor appeared more set- tled, although he also had tears in his eyes.
THERAPIST: What did you notice? HÉCTOR: It was pretty easy to locate the tension—it
was in the pit of my stomach. But I really struggled with opening up to it. My first response was “I don’t want to let go off the struggle against racism. Why
should I accept it?” But then I remembered the last time we did this exercise. And I reminded myself that I only had to be open to the present moment. I remembered that acceptance didn’t mean resigning myself to a situation. Instead, I focused on accepting that the incident had occurred and that I was rigidly holding tension in my body.
THERAPIST: I am really impressed that you were able to do that. What happened next?
HÉCTOR: I continued to breathe into my stomach and I worked on letting go of my tension. Once my body became more relaxed, I turned my attention to my thoughts about the incident.
THERAPIST: And what did you observe? HÉCTOR: I had thoughts about racism and how unjust
it is for people to be treated differently based on their appearance. I felt angry, which I think was a clear emotion, but then I started to feel ashamed of my behavior.
THERAPIST: Was that reaction clear or muddy? HÉCTOR: Well, I think a bit of both. I definitely was
able to bring some compassion to myself. No one wants to be treated differently based on their appear- ance.
THERAPIST: That is great. I know it is not easy for you to take a compassionate stance toward your thoughts and actions. What do you think was clear about the response?
HÉCTOR: I am ashamed of my behavior. It is inconsis- tent with my values to treat anyone the way I treated that officer, even if they deserve it. Frankly, I don’t care what he thinks of me, but I care what I think about myself.
THERAPIST: It sounds like you said and did some things that were inconsistent with your values and you were able to bring some compassion to yourself for that. This was a highly charged situation, and you were vulnerable going into it. In this moment, are there any values-based actions that come to mind?
HÉCTOR: This incident made me realize that my values have been a bit too off balance lately. I have been pay- ing a lot of attention to the schoolwork domain and a pretty good amount of attention to the relationship domain, but I think I need to take some actions con- sistent with my values regarding self-nourishment and community. At the beginning of the semester I
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grabbed a flyer for the Latinx Medical Student As- sociation, and I think I am going to contact them to see if there are some activities I can get involved with.
THERAPIST: That sounds great. HÉCTOR: I also think I might try and meet with some-
one from campus security. I think I want to apolo- gize for my behavior, but I also want to talk to them about cultural sensitivity training. And don’t worry, I didn’t forget about the arrow thing we talked about a few weeks ago. I can only aim the arrow; I can’t control where it lands. I know I might not change their practices, but these actions are consistent with my values.
Sessions 13–16
Héctor completed a treatment reflection writing assign- ment that set the stage for the final four sessions of thera- py. He identified a few specific values-based actions that he wanted to take before the end of therapy. He also rec- ognized that although he was maintaining a pretty steady formal mindfulness practice, he had paid less attention to informal mindfulness. Héctor also had made great gains in increasing his self-compassion, but he felt that he need- ed more practice while he still had the support of therapy.
Thus, Sessions 13–15 continued to follow the struc- ture of Sessions 8–12, but with added attention to is- sues of maintenance. The therapist became less and less
Before you begin this exercise, think of a difficulty you’re experiencing right now. It doesn’t have to be a significant difficulty, but choose something that you find unpleasant, something that is unresolved. It may be something you are worried about, an argument or misunderstanding you’ve had, something you feel angry, resentful, guilty, or frustrated about. If nothing is going on right now, think of some time in the recent past when you felt scared, worried, frustrated, resentful, angry, or guilty, and use that. Noticing the way you are sitting in the chair or on the floor. Noticing where your body is touching the chair or floor. Bringing you attention to your breath for a moment. Noticing the in-breath . . . and the out- breath. . . . Now gently widening your awareness, take in the body as a whole. Noticing any sensations that arise, breathing with your whole body. When you are ready, bringing to mind whatever situation has been bringing up difficult emotions for you. Bringing your attention to the specific emotions that arise and any reactions you have to those emotions. And as you are focusing on this troubling situation and your emotional reaction, allowing yourself to tune in to any physical sensations in the body that you notice are arising . . . becoming aware of those physical sensations . . . and then deliberately, but gently, directing your focus of attention to the region of the body where the sensations are the strongest in the gesture of an embrace, a welcoming . . . noticing that this is how it is right now . . . and breathing into that part of the body on the in-breath and breathing out from that region on the out-breath, exploring the sensations, watching their intensity shift up and down from one moment to the next. Now, seeing if you can bring to this attention an even deeper attitude of compassion and openness to whatever sensations, thoughts, or emotions you are experiencing, however unpleasant, by saying to yourself from time to time, “It’s OK. Whatever it is, it’s already here. Let me open to it.” Staying with the awareness of these internal sensations, breathing with them, accepting them, letting them be, and allowing them to be just as they are. Saying to yourself again, if you find it helpful, “It’s here right now. Whatever it is, it’s already here. Let me be open to it.” Softening and opening to the sensation you become aware of, letting go of any tensing and bracing. If you like, you can also experiment with holding in awareness both the sensations of the body and the feeling of the breath moving in and out as you breathe with the sensations moment by moment. And when you notice that the bodily sensations are no longer pulling your attention to the same degree, simply return 100% to the breath and continue with that as the primary object of attention. And then gently bringing your awareness to the way you are sitting in the chair, your breath, and, when you are ready, opening your eyes.
FIGURE 5.2. Inviting a difficulty in and working with it through the body. Adapted from Williams, Teasdale, Segal, and Kabat-Zinn (2007, pp. 151–152). Copyright © 2007 The Guilford Press. Adapted by permission.
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directive throughout this time, allowing Héctor to ad- dress obstacles and experience success himself. During this time, Hector began to date and expand his social network, feel more satisfied with his relationships with his family members, and find more success and satisfac- tion in his schoolwork.
During the final session, the therapist predicted that there would be times when Héctor would feel over- whelmed by emotion, drift away from his mindfulness practice, and lose sight of his values, despite all the no- table gains he reported. She described these “lapses” as a natural part of the process of life and helped Héctor to make plans for how to cope. Specifically, she sug- gested that he review the handouts in his binder, begin self-monitoring again, increase or reengage in mindful- ness practice, and consider doing some values writing. The therapist and Héctor collaboratively developed a personalized list of elements that were particularly help- ful for him and added that list to his binder. Héctor expressed sadness at saying good-bye to his therapist, and also excitement at feeling able to continue his prog- ress on his own and use the time allocated to therapy to engage in other values-based actions moving forward.
CONCLUSION
Evidence suggests that this ABBT for GAD can target symptoms of GAD, comorbid presenting problems, and proposed mechanisms that underlie these clinical pre- sentations, while helping clients to engage in their lives in satisfying ways. We have presented in this chapter a conceptual basis for this treatment, as well as guidelines for its flexible application, while remaining responsive to the specific context of a given client. More research is needed to better understand mechanisms and processes of change, as well as how to disseminate this treatment in community and primary care settings.
ACKNOWLEDGMENTS
We thank the therapists, students, and clients we have worked with over the years for all they have taught us, as well as Na- tional Institutes of Health for funding our work (Grant No. MH074589). We also thank Dave Barlow, Tim Brown, Bon- nie Brown, and the staff at the Center for Anxiety and Re- lated Disorders for supporting our treatment research. We dedicate this chapter to Tom Borkovec, whose seminal work in the treatment of GAD is the sturdy foundation on which our work stands.
NOTE
1. Audio recordings of this exercise, as well as other mind- fulness exercises we use, are available at www.mindfulway- throughanxiety.com. Scripts for many of these mindfulness exercises are available in Orsillo and Roemer (2011, 2016) and Roemer and Orsillo (2020).
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In this chapter we describe the Unified Protocol for Transdiagnostic Treatment of Emotional Dis- orders, one of the first treatment protocols of its kind, which has now been adopted worldwide and is translated into over 10 different languages. Developed through the Center for Anxiety and Related Disorders at Boston University, this “unified” transdiagnostic protocol distills therapeutic principles common to psychological treatment of the various emotional disorders and integrates these princi- ples into a single protocol that is, in theory, applicable to the full range of emotional disorders. What is unique about this approach is the systematic manner in which the treatment components are applied across disorders, as well as theoretical developments leading to reconceptualization of the principal target of treatment as a common, higher-order temperament undergirding disorders of emotion rather than specific DSM-defining system clusters. The protocol is deeply rooted in emotion science and, in particular, the evolutionarily adaptive function of emotions. The major advantage of a transdiagnostic approach, of course, in addition to greatly simplifying dissemination by eliminating numerous over- lapping single-disorder protocols, is that this approach also takes into consideration the extensive comorbidity often found among emotional disorders. In this chapter, we illustrate the unified protocol through a case study of the treatment of “Marianne.” —D. H. B.
The first edition of this book was published in 1985, in the dawn of evidence-based psychological treat-
ments. Descriptions of only those treatments with suf- ficient empirical support that were broadly applicable to large numbers of individuals with various forms of psychopathology at that time were included. Over suc- ceeding editions of this book some new treatment ap- proaches with wide appeal and strong empirical support have been added, whereas others have been deleted. In addition, the field has matured to the point that pub- lic health services around the world have directed that evidence-based psychological treatments become an
integral part of health care delivery systems due to their effectiveness, efficiency, and durability (Clark, 2012; Nathan & Gorman, 2007; Ruzek, Karlin, & Zeiss, 2012). It is also a sign of the maturity of a field to examine closely the limitations of existing evidence. Obviously, a considerable number of patients still do not respond as well as would be desirable to our current arsenal of psychological (or drug) treatments, and there is plenty of room for improvement.
Another problem that has become apparent, particu- larly in the context of emotional disorders, is that there now exists a plethora of treatment protocols for each
C H A P T E R 6
emotional Disorders A Unified Protocol for Transdiagnostic Treatment
Laura A. Payne Kristen K. Ellard Todd J. Farchione David H. Barlow
218 CliniCal Handbook of PsyCHologiCal disorders
of the discrete anxiety and mood disorders. Although these protocols, by and large, have proven useful and been well received, it takes a significant amount of training to become sufficiently familiar with the dis- tinct protocols to integrate them into clinical practice (Barlow, Bullis, Comer, & Ametaj, 2013). Unless these treatments become more “user-friendly” as recom- mended, clinicians are less likely to have a sufficient understanding of, or access to, these evidence-based treatments for the emotional disorders (McHugh & Barlow, 2012). In this chapter, we present a Unified Protocol (UP) for the transdiagnostic treatment of emotional disorders. “Emotional disorders” in our con- ception include not only the anxiety, depressive, obses- sive–compulsive, and trauma-related disorders but also other classes of disorders in which the experience and regulation of emotion plays a prominent role, such as the somatic disorders, dissociative disorders, and, to some extent, the eating disorders. Borderline personal- ity disorder can also be conceptualized as a disorder of extreme emotional dysregulation (Sauer-Zavala & Bar- low, 2014; Neacsiu, Zerubavel, Nylocks, & Linehan, Chapter 10, this volume) and may fit within our UP conceptualization (e.g., Lopez et al., 2015). Our science and practice have advanced sufficiently that there are now several strong arguments for this approach, in ad- dition to the very practical advantage of substantially reducing the number of existing protocols. We touch on these arguments here before describing the treatment components of the UP in some detail, in keeping with the long-standing format of this book.
RATIONALE FOR A UNIFIED APPROACH
Perhaps the strongest argument for a unified transdiag- nostic treatment approach to emotional disorders is an emerging body of evidence supporting commonalities in the etiology of these disorders that we have summa- rized in the form of an etiological model referred to as “triple vulnerability” (Barlow, 1991, 2000, 2002; Bar- low, Ellard, Sauer-Zavala, Bullis, & Carl, 2014; Suárez, Bennett, Goldstein, & Barlow, 2009). Since the time the UP first appeared in this volume, interest and re- search into transdiagnostic processes has grown expo- nentially, from 43 studies published between 2004 and 2009, to over 2,000 studies published between 2010 and 2020. Most notably, in 2010, the National Insti- tute of Mental Health launched the Research Domain Criteria (RDoC) initiative to promote research into
transdiagnostic dimensions of functioning across mul- tiple levels of analysis, from genes to molecules, neuro- circuits, behavior, and self-report, in an effort to more clearly elucidate and define etiology and markers of psychopathology beyond the bounds of DSM-defined diagnostic categories (Insel et al., 2010). Although re- search in this area is still in its early stages and shared etiological pathways or pathophysiological processes are not yet firmly established, emerging evidence on shared pathological processes is sufficiently strong at present to justify a transdiagnostic treatment approach, a point to which we return below.
A second argument focuses on conceptions of the major emotional disorders that emphasize their com- monalities rather than their differences. The “spec- trum” approach is one manifestation of this concep- tion. For example, high rates of comorbidity suggest considerable overlap among disorders. The observed effects of current psychological treatments on comorbid conditions also point to at least a partial nonspecificity of treatment response. From a phenomenological per- spective, emerging research on the latent structure of dimensional features of emotional disorders reveals a hierarchical structure that can accommodate these dis- orders. The sections to follow briefly review evidence relevant to these arguments.
Etiology
We have described in some detail a set of interacting vulnerabilities or diatheses relevant to the development of anxiety, anxiety disorders, and related emotional dis- orders. This “triple-vulnerability” theory encompasses a generalized biological vulnerability, a generalized psychological vulnerability, and a specific psychologi- cal vulnerability emerging from early learning (Barlow, 2000, 2002; Barlow, Ellard, et al., 2014; Sauer-Zavala & Barlow, 2021). Much of the research on generalized biological and psychological vulnerabilities has focused on a temperament labeled, variously, “neuroticism,” “negative affect,” “behavioral inhibition,” or “trait anxi- ety.” Although the relationships among these closely related traits and temperaments have yet to be worked out fully, it seems that they substantially overlap and represent a common theme associated with a biological vulnerability to develop emotional disorders (Barlow, 2000, 2002; Campbell-Sills, Liverant, & Brown, 2004; Suárez et al., 2009). We have come to refer to this tem- perament by its most traditional label, “neuroticism” (Barlow, Sauer-Zavala, Carl, Bullis, & Ellard, 2014;
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Eysenck, 1947; Sauer-Zavala & Barlow, 2021). A gener- alized biological vulnerability involves nonspecific ge- netic contributions to the development of neuroticism. Additionally, early life experiences fostering a sense that events, particularly negative events, are unpredictable or uncontrollable, contribute to a generalized psycho- logical vulnerability, or diathesis, to develop neuroti- cism later on. If a generalized biological and a general- ized psychological vulnerability happen to line up and are potentiated by the influence of life stress, the likely result is a development of the two closely related clinical syndromes of generalized anxiety disorder (GAD) and/ or depressive disorders. Notice that false alarms (panic attacks) may also occur as a function of stressful life events, facilitated by high levels of baseline anxiety. But these false alarms seem to have a different heritability than anxiety and are not necessarily implicated in a clinical disorder. For that to occur, an additional layer of a more specific psychological vulnerability must be considered.
We know from emotion science that learned asso- ciations between strong emotions and certain contexts, cues, or “meanings” become encoded into memory and serve to drive our behaviors in an automatic, reflexive way. Over time, we learn that “when I feel this, it means this about me and the world, and I respond in this way.” From an evolutionary standpoint, encoding these as- sociations in memory allows us to develop a unique “blueprint” of the world to guide our behaviors, so that we can respond to cues quickly and are not tasked with constantly reinterpreting meaning and reinventing re- sponses. However, this evolutionarily adaptive process can become maladaptive when associations among emotions, meanings, and responses are no longer help- ful or accurate. Thus, a psychological vulnerability to develop specific anxiety disorders can occur when the biological propensity to experience strong emotions is coupled with maladaptive learned associations. Certain learning experiences seem to focus anxiety on specific life circumstances, and these circumstances or events are associated with a heightened sense of threat or dan- ger. For example, specific early learning experiences seem to determine whether individuals may view so- matic sensations, intrusive thoughts, or social evalua- tion as specifically dangerous (Barlow, 2002; Bouton, Mineka, & Barlow, 2001); that is, to take one example, individuals with social anxiety often have in their back- ground admonitions from parents or family to always to be on their best behavior and to look their best, to avoid the dreaded consequence of being negatively eval-
uated or “disapproved of” by others. Children raised in environments in which the behavior of caregivers is unpredictable may learn to associate ambiguous social cues with threat, leading to the development of social anxiety, or with danger, leading to the development of GAD. It is this specific psychological vulnerability that, when coordinated with the generalized biological and psychological vulnerabilities mentioned earlier, seems to contribute to the development of discrete anxiety disorders such as social anxiety disorder, panic disor- der, and specific phobias. In other words, the specific symptom presentations that align with DSM diagnos- tic categories may in fact reflect circumstantial surface manifestations of underlying biological and psychologi- cal vulnerabilities. This model is also applicable to ob- sessive–compulsive, trauma-, and stressor-related dis- orders. For instance, in obsessive–compulsive disorder (OCD), individuals often report learning from author- ity figures that having a thought is as bad as engaging in the action (i.e., having the thought about shaking a newborn infant to quiet it is as bad as actually shaking the infant). Existing evidence for this triple-vulnerabili- ty model has been reviewed in detail elsewhere (Bouton et al., 2001; Chorpita & Barlow, 1998; Sauer-Zavala & Barlow, 2021) and is consistent with the overriding im- portance of common factors in the genesis and presen- tation of emotional disorders.
Latent Structure of the Emotional Disorders
Whereas the fourth and fifth editions of the Diagnos- tic and Statistical Manual of Mental Disorders (DSM- IV-TR and DSM-5; American Psychiatric Association, 2000, 2013) highlight a “splitting approach” to nosolo- gy in an attempt to achieve high rates of diagnostic reli- ability, this achievement may have come at the expense of diagnostic validity; that is, the current system may be highlighting categories that are minor variations of more fundamental underlying syndromes. Quantitative approaches such as structural equation modeling, prin- cipal component analyses, and machine learning are now capable of examining the full range of anxiety and mood disorders, and their interrelationships, without the constraints of existing (possibly) artificial categories (Brown, Chorpita, & Barlow, 1998; Chorpita, Albano, & Barlow, 1998; Clark, 2005; Clark & Watson, 1991; Grisanzio et al., 2018; Watson, 2005). We have been studying this question for a number of years. For exam- ple, Brown and colleagues (1998), using a sample of 350 patients with DSM-IV anxiety and mood disorders,
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confirmed a hierarchical structure to the emotional dis- orders. In this structure, trait negative affect and trait positive affect were identified as crucial higher-order factors to the DSM-IV disorder factors, with significant paths from negative affect to each of the five DSM-IV disorder factors (GAD, social phobia, panic disorder, OCD, and major depression). Interestingly, low positive affect emerged with significant paths to major depres- sion and social phobia only. In this model, autonomic arousal represents the phenomenon of panic, and this arousal emerges as a lower-order factor with significant paths from panic disorder and GAD (where the rela- tionship was negative).
In a separate study that followed 606 patients with DSM-IV anxiety and mood disorders over the course of 2 years, Brown (2007) found further support for this hierarchical model. Replicating earlier cross-sectional findings, the two higher-order temperament dimen- sions of neuroticism/behavioral inhibition/negative affectivity and behavioral activation/positive affectiv- ity accounted for virtually all of the covariance among DSM-IV disorder constructs (GAD, social phobia, and major depression). Furthermore, the rate of change in neuroticism/behavioral inhibition over the study period accounted for virtually all of the covariance among the rate of change in DSM-IV disorder constructs.
Computational approaches, such as machine learn- ing and graph-theoretical network-based analyses, have further confirmed underlying dimensions that cut across traditional DSM diagnostic categories. For ex- ample, a recent study used principal component analy- sis on the 21-item Depression Anxiety and Stress Scale (DASS-21; Lovibond & Lovibond, 1995) to identify dimensional clusters in a sample of 248 patients diag- nosed with a range of anxiety and mood disorders and 249 healthy controls. Three stable clusters emerged, identified by the authors as tension, anxious arousal, and anhedonia, which are constructs that overlap with high negative affect, low positive affect, and autonom- ic arousal (Grisanzio et al., 2018). Unsupervised ma- chine learning was then used to classify patients and controls within these three dimensions, resulting in six subtypes, defined as normative mood, tension, anxious arousal, general anxiety, anhedonia, and melancholia. Importantly, similar to our findings, the identified sub- types did not align with DSM diagnoses but instead cut across DSM diagnostic boundaries.
Findings such as these suggest that commonalities among emotional disorders outweigh the differences. We have concluded from this research that DSM emo-
tional disorder categories are best considered as use- ful concepts or constructs that emerge as “blips” on a general background of neuroticism/behavioral inhibi- tion but may not be the best way to organize nosology (Brown & Barlow, 2009).
Overlap among Disorders
At the diagnostic level, the overlap among the emo- tional disorders is most evident in the high rates of cur- rent and lifetime comorbidity (e.g., Brown, Campbell, Lehman, Grisham, & Mancill, 2001; Kessler et al., 1996; Roy-Byrne, Craske, & Stein, 2006; Tsao, Myst- kowski, Zucker, & Craske, 2002, 2005). Results from Brown, Campbell, and colleagues (2001) indicate that 55% of patients with a principal anxiety disorder had at least one additional anxiety or depressive disorder at the time of assessment. But if one examines for the presence of a disorder over the lifetime of the patient, whether it is present or not at the time of interview, this rate increases to 76%. To take one example, 60% of 324 patients diagnosed with panic disorder with or without agoraphobia (PD/A) were determined to meet criteria for either an additional anxiety or mood disorder, or both. Specifically, 47% presented with an additional anxiety disorder and 33%, with an additional mood disorder. When lifetime diagnoses are considered, the percentages rise to 77% experiencing any anxiety or mood disorder, breaking down to 56% for any anxiety disorder and 60% for any mood disorder. If posttrau- matic stress disorder (PTSD) or GAD was the principal (most severe) diagnosis, comorbidity rates were high- est. Merikangas, Zhang, and Aveneoli (2003) followed almost 500 individuals for 15 years and found that relatively few people suffer from anxiety or depression alone. When a single disorder did occur at one point in time, the additional mood state would almost certainly emerge later.
Several possible explanations for these high rates of comorbidity have been reviewed extensively elsewhere (Brown & Barlow, 2002). Among these are relatively trivial issues with overlapping definitional criteria; arti- factual reasons, such as differential base rates of occur- rence in our setting; and the possibility that disorders are sequentially related, and that the features of one dis- order act as risk factors for another disorder. For exam- ple, depression seems to follow PD/A, and PD/A seems to follow PTSD. But the more intriguing explanation, for our purposes, first offered by individuals such as Gavin Andrews and Peter Tyrer (Andrews, 1990, 1996;
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Tyrer, 1989; Tyrer et al., 1998), is that this pattern of comorbidity argues for the existence of what has been called a “general neurotic syndrome” (Barlow, Ellard, et al., 2014; Sauer-Zavala & Barlow, 2021). Andrews and Tyrer have suggested that the difference in the ex- pression of emotional disorder symptoms (individual variation in the prominence of social anxiety, panic at- tacks, anhedonia, etc.) is simply a trivial variation in the manifestation of a broader syndrome. This, in turn, is consistent with “triple vulnerability” models mentioned earlier, that anxiety (and mood) disorders emerge from shared psychosocial and biological/genetic diatheses. If this is the case, then a unified treatment protocol cut- ting across current diagnostic categories to address core features of the anxiety and mood disorders could be a more parsimonious and, perhaps, powerful option.
We have reviewed the genetic and neurobiological evidence on the commonalities among anxiety and de- pressive states in some detail elsewhere (Barlow, 2002, Chaps. 3, 6–8; Bouton, 2005; Brown, 2007; Suárez et al., 2009). For example, most work on genetic contri- butions to anxiety and depression supports the early dictum of Ken Kendler (1996; Kendler et al., 1995), “same genes, different environment” (Hettema, Neale, & Kendler, 2001; Rutter, Moffit, & Caspi, 2006). Consistent with a theory of an underlying genetic vul- nerability, genetic variations have been linked to both trait anxiety and negative emotionality (or neuroti- cism) (Montag, Fiebach, Kirsch, & Reuter, 2011; Stein, Campbell-Sills, & Gelernter, 2009; Tabak et al., 2020), and have been found to influence the later development of psychopathology following life stressors (Caspi et al., 2003). Recently, a growing body of literature in genet- ics has observed links between genetic polymorphisms and both the function and structure of neural pathways implicated in emotional processing, suggesting an asso- ciation between a genetic predisposition, inefficient or maladaptive emotion processing, and the development of emotional disorders. For example, genetic variations have been associated with hyperactivation in neural structures implicated in emotion generation (Drabant et al., 2012; Lonsdorf et al., 2011; Munafò, Brown, & Hariri, 2008; Tabak et al., 2020), reduced gray mat- ter volume in limbic regions, and reduced functional connectivity between emotion-generating regions and structures implicated in their inhibitory control (Mc- Teague et al 2020; Pezawas et al., 2005; Sharp, Miller, & Heller, 2015).
Increased perceptions of emotions as uncontrollable and intolerable, increased avoidant processing, and in-
creased attempts at emotional control have also been demonstrated across disorders (Campbell-Sills, Barlow, Brown, & Hofmann, 2006a, 2006b; Sloan et al., 2017; Weinberg & Hajcak, 2010; Weiser, Pauli, Weyers, Alp- ers, & Mühlberger, 2009). Intolerance of uncertainty and distress has been demonstrated across a full range of disorders, including depression, GAD, social anxi- ety, and OCD (Boelen, Vrinssen, & van Tulder, 2010; Boswell, Thompson-Holland, Farchione, & Barlow, 2013; Lee, Orsillo, Roemer, & Allen, 2010). In ad- dition, a growing number of studies have shown that individuals with anxiety and mood disorders tend to use maladaptive emotion regulation strategies, includ- ing attempts to avoid or dampen the intensity of un- comfortable emotions that ultimately backfire and contribute to the maintenance of their symptoms (e.g., Campbell-Sills et al., 2006a, 2006b; Liverant, Brown, Barlow, & Roemer, 2008; Mennin, Heimberg, Turk, & Fresco, 2005; Sloan et al., 2017; Tull & Roemer, 2007). Taken together, the evidence from genetics, neurosci- ence, behavioral studies, and psychopathology research suggests that a common, overlapping feature across disorders is the propensity toward increased emotional reactivity and inefficient or deficient regulatory con- trol that is coupled with a heightened tendency to view these experiences as aversive and is manifest in attempts to alter, avoid, or control emotional responding.
In summary, the existing literature supports several arguments for stepping back from individual DSM diagnostic categories and associated disorder-specific psychological protocols and considering a more unified transdiagnostic approach based on new findings on the nature of psychopathology and from the emerging field of emotion science. In addition, current evidence- based cognitive-behavioral therapy (CBT) protocols for emotional disorders have much in common and reduce to three broad principles of change: altering emotion- based misappraisals of salient events; preventing avoid- ance of negative, emotionally charged internal or exter- nal triggers, as well as modifying emotional behaviors (action tendencies) and facilitating extinction of fear; and reducing anxiety and distress over the experience of intense emotion (Mennin, Ellard, Fresco, & Gross, 2013).
EVIDENCE FOR THE EFFICACY OF THE UP
Since its inception in the early 2000s, the UP has amassed considerable empirical support as a treat-
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ment for a wide range of presenting problems. In 2020, Cassiello-Robbins, Southward, Tirpak, and Sauer- Zavala systematically reviewed 77 treatment outcome studies using the UP across 11 different countries and with numerous adaptations. In these studies, the UP was delivered in a variety of formats (i.e., group, indi- vidual, digital), across several different clinical settings (i.e., outpatient, intensive outpatient, inpatient) and for a wide range of diagnostic presentations. Overall, the authors concluded that the UP is acceptable to both patients and therapists and can be flexibly applied to a range of DSM-IV and DSM-5 diagnoses, as well as nondiagnosable problems such as nonsuicidal self-inju- ry, subclinical presentations, and sexual minority stress. However, they also noted that as the majority of stud- ies focused on patients with primary anxiety disorders or closely related conditions (i.e., OCD); thus, findings outside of anxiety and depressive disorders should be considered more preliminary. Sakiris and Berle (2019) conducted a meta-analysis examining the efficacy of the UP across a subset of 15 outcome studies (N = 1,244) described in the review by Cassiello-Robbins et al. (2020). Consistent with Cassiello-Robbins and col- leagues’ conclusions, the UP was associated with large effect size improvements across anxiety and depressive disorders, OCD, and borderline personality disorder. In addition, findings suggest that the UP led to increased use of adaptive and decreased use of maladaptive emo- tion regulation strategies and improvements in func- tioning and quality of life. This meta-analytic review included a number of randomized controlled trials, in- cluding one of the largest trials of the UP to date (N = 223) in which we compared effectiveness of the UP to established single-disorder protocols for panic disorder, social anxiety disorder, OCD, and GAD (Barlow et al., 2017). In that particular study, relative to the single- disorder protocols, the UP was associated with lower rates of attrition and led to similar improvements across a range of outcomes, including diagnostic severity, anx- iety and depressive symptoms, work/social adjustment, hope, quality of life, positive affect, and number of co- morbid disorders (Barlow et al., 2017; Gallagher et al., 2020; Steele et al., 2018; Wilner Tirpak et al., 2019), both at the end of treatment and at 6-month follow- up. These data support the efficacy of the UP when applied in a variety of populations and symptoms. A full explanation of this protocol and a description of its application with a patient with a complex, yet common, presentation follows.
TREATMENT VARIABLES
Setting
The UP has been administered in a number of different settings, including medical centers, inpatient units, and even homeless shelters, but the most common venue is an outpatient setting. Our own outpatient setting is the Center for Anxiety and Related Disorders (CARD) at Boston University. Our clinic receives over 600 new admissions per year, with many patients being offered treatment after their initial intake assessments. CARD, in addition to housing staff psychologists and psychia- trists, is also a training center for doctoral students and psychiatric residents. At any given time, numer- ous National Institutes of Health (NIH)-funded treat- ment and research studies are ongoing at the Center. Regarding diagnostic breakdown of treatment-seeking patients, the most common diagnosis assigned is GAD, followed by social phobia, PD/A, specific phobia, OCD, and PTSD, but the full range of “neurotic spectrum” disorders is assessed and treated. A small percentage of patients are assigned “coprincipal diagnoses,” which re- fers to cases in which two separate diagnoses are judged to be of equal severity.
Prior to the intake evaluation, each patient is mailed a packet of questionnaires to complete and bring to the assessment, which are scored and interpreted sub- sequent to the interview. The majority of the intake appointment comprises administration of the Anxiety Disorders Interview Schedule for DSM-5 (ADIS-5; Brown, Di Nardo, & Barlow, 2014). Following comple- tion of the entire assessment process, consensus diagno- ses are determined during a weekly staff meeting, after which the patient is provided diagnostic feedback and treatment recommendations. Based on the information from the interview, the patient may be offered one of several treatment options at the Center, referral to a clinical trial if the patient qualifies where treatment is always free of charge, or a referral in the community.
Format
Treatment with the UP is typically conducted in an in- dividual format, although it has been successfully con- ducted in a group format with patients with mixed prin- cipal emotional disorder diagnoses (Bullis et al., 2015; de Ornelas Maia, Nardi, & Cardoso, 2015; Reinholt et al., 2017). The treatment described in this chapter re- flects the individual treatment protocol, which allows
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for greater attention to the description and application of treatment components during each session. How- ever, when administered in a group setting, patients are easily able to see the commonalities among their diverse presenting complaints, and this understanding often creates a strong bond among group members; therefore, it may be useful to adapt the protocol for group treat- ment as we have done at CARD.
Therapist Variables
The UP has been administered by therapists with vary- ing degrees of clinical experience and expertise with the protocol. To our knowledge, both junior therapists (even therapists who have never had experience with cognitive-behavioral treatments) and senior therapists (i.e., therapists with at least 4 or more years of treat- ment experience) have been able to adapt to the UP without significant difficulty. Certainly, a background in cognitive-behavioral techniques may be helpful when utilizing the protocol (e.g., facilitating cognitive reappraisal, and designing and conducting exposures). Evidence suggests some benefit to therapist experience, at least when treating PD/A with a highly structured CBT protocol (Huppert et al., 2001).
The UP comprises five core modules that target shared mechanisms associated with neuroticism and resulting emotion dysregulation, specifically, negative evaluation and avoidance of intense emotional experi- ence (Sauer-Zavala et al., 2012) underlying all anxiety, depressive, and related disorders (Barlow, Sauer-Zavala, et al., 2014). Across these core modules, and the proto- col more generally, treatment exercises focus on elicit- ing and changing responses to a variety of emotions and emotional cues. Perhaps one of the most challenging aspects for the therapist is to be able to create and utilize emotion-provoking exposures effectively, which begin early in treatment and continue throughout its course. Most importantly, the therapist must have a sense of when a patient is avoiding the process of experiencing, expressing, or accepting emotions, and this is often sig- naled by very subtle behavioral cues, such as avoiding eye contact, changing the topic of discussion, arriving late for a session, and not completing (or “overdoing”) homework assignments. Each of these behaviors rep- resents attempts to control uncomfortable emotions through either direct avoidance or overcontrol. It is es- sential that the therapist be able to recognize and ad- dress such behaviors when they occur, thereby allowing
the opportunity for an effective emotion exposure and discussion of avoidance to facilitate emotional process- ing.
A second challenge for the therapist is to be able to tolerate and experience the expression of emotion by the patient. It is common for less experienced therapists to quickly “rationalize away” the patient’s emotional reac- tions; however, this only feeds into the cycle of emo- tions and avoidance. At every step, the therapist should encourage the expression and acceptance of emotion, while guiding the patient in how to “examine” it, with- out letting the emotion “take over.” In such cases, mod- eling from a senior therapist and/or extensive supervi- sion may be helpful instruction for less experienced therapists.
Client Variables
As previously mentioned, the rate of comorbidity among patients with a principal anxiety or mood dis- order is approximately 55% (Brown, Campbell, et al., 2001), depending on the principal diagnosis. In most CBT protocols, comorbid diagnoses are never a focus of treatment, although successful treatment of a principal anxiety disorder often results in decreases in comorbid- ity (e.g., Allen et al., 2010; Brown, Antony, & Barlow, 1995; Davis, Barlow, & Smith, 2010). In a recent study by our research group, the UP and single-disorder pro- tocols were equally efficacious in reducing symptoms of comorbid emotional disorders immediately follow- ing treatment (Steele et al., 2018). One advantage of a unified treatment approach is that symptoms related to comorbid diagnoses can be discussed in treatment ses- sions and may even be the focus of an emotion expo- sure. For example, a patient with GAD who experiences chronic worry about daily matters may also feel anxious in social situations. Therefore, that patient’s in-session emotion exposure might comprise a conversation with a stranger or giving a speech to a small group of people. Contrary to traditional protocols, the experience of any emotion that is the target of treatment may be particu- larly beneficial for patients with significant comorbid- ity or for those who would like to address multiple con- cerns during the course of treatment.
Concurrent Drug Treatment
Many patients who present for treatment are also tak- ing some form of psychoactive medication. At CARD,
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patients are required to have stabilized on the dosage of medication prior to the intake interview, so that the therapist has a clear picture of actual symptoms (as op- posed to symptoms that may be caused by the initial addition or removal of a medication). Whereas concur- rent use of medications such as selective serotonin reup- take inhibitors (SSRIs) and serotonin–norepinephrine reuptake inhibitors (SNRIs) does not appear to have a negative impact on treatment outcome initially, once the medications are removed, evidence suggests that patients who received medication alone or CBT in ad- dition to medication are more likely to relapse (e.g., Barlow, Gorman, Shear, & Woods, 2000; Heimberg et al., 1998; Liebowitz et al., 1999). The exact mecha- nisms underlying the return of symptoms are unclear, although some authors have suggested that patients may attribute the success of the treatment to the use of medication and, once it is withdrawn, no longer believe they have the ability to manage their symptoms. How- ever, in an investigation using data from a multisite comparative study for the treatment of panic disorder, results indicated that patients who received CBT plus pill placebo were equally likely to believe they had re- ceived medication as patients who had actually received the medication (Raffa et al., 2008). Yet those in the CBT plus placebo condition were less likely to relapse compared to those who had received either CBT plus medication or medication alone. Therefore, it appears unlikely that the higher relapse rates in the medication conditions were due solely to this “attribution hypoth- esis.” One other possible explanation for greater rates of relapse in patients receiving psychopharmacological treatment is that the medication provides an unintend- ed “protective” effect against increased physiological arousal and anxiety. Since eliciting anxiety and panic is a core component of CBT protocols, patients taking medication (1) may have experienced greater physical sensations when the medication was removed and/or (2) were never able fully to confront the physiological arousal and panic during the course of treatment. How- ever, these hypotheses have yet to be fully investigated.
One additional consideration frequently raised is the use of benzodiazepines on a prn (“as-needed”) basis during the course of treatment. Following conceptions outlined in the UP, any strategy used to reduce the intensity of emotions in the moment is considered an emotional avoidance strategy, and ultimately contrib- utes to increasing levels of anxiety and emotional reac- tivity. Therefore, the use of benzodiazepines (or other fast-acting medications) is discouraged, particularly if
the medications are carried with the person as a “safety signal.”
ASSESSMENT
Case Study
“Marianne” was a 43-year-old, single woman who had been unemployed for 8 months. She previously worked as a supervisor for a large biotech company but was laid off due to significant changes in the company and had been unable to find work since. Marianne came to our Center seeking help for not only the recent significant emotional distress she was experiencing but also a life- long history of depression and anxiety that she saw as interfering with her career and relationships, particular- ly romantic relationships, over the course of her life. Al- though she had never sought treatment previously, the recent unexpected loss of her job intensified her feelings of both depression and anxiety. She recently suffered from an unexpected panic attack on a bus, which she had never experienced before. Marianne then realized she could no longer ignore her symptoms.
During her intake interview, Marianne stated that she had been feeling increasingly depressed over the last several months. She described feeling very lethar- gic and having trouble motivating herself to look and apply for new jobs. This was due, in part, to her dif- ficulty concentrating on tasks, which was necessary for both reviewing job descriptions and completing appli- cations. She also found it hard to watch television or read books, as she had trouble staying focused on the information and felt very “restless.” Marianne reported that she spent a lot of time inside her apartment and was avoiding activities she previously enjoyed, such as spending time with her two close friends and garden- ing. This change was particularly significant for Mari- anne, as she did not have an extensive social circle and was distant from her family; her two friends were her primary sources of social support. Similarly, gardening had been an activity that always boosted her mood, but she had not felt motivated to tend to her garden. She felt guilty about avoiding these activities, although she was unable to push herself to be more active. Marianne also reported that she slept late into the morning be- cause she had trouble falling asleep at night. Waking up late further exacerbated her feelings of worthlessness, thereby creating a continuous cycle of disrupted sleep and low mood. Marianne stated that symptoms of de- pression had been a part of her life for as long as she
Emotional Disorders 225
could remember, although she could never recall feeling as badly as she did now. She had experienced chronic feelings of hopelessness and low-self-esteem, as well as low energy since childhood. She attributed her experi- ence of lifelong depression to a dysfunctional and cha- otic family environment growing up. Her father strug- gled with alcoholism, and one of her sisters was born with a serious heart condition that required significant care and management throughout her childhood. Her parents were rarely emotionally available for Marianne, and Marianne learned to suppress her needs so as to not create additional stress for her parents. Additionally, her father’s alcoholism created anxiety due to his unpredict- able moods. When drinking alcohol, he could become angry and verbally lash out at Marianne and her sister, although he was never physically violent.
Marianne also described a lifelong history of anxi- ety and worry that accompanied her feelings of depres- sion. She worried about the health and relationships of her family members, as well as her future. In school, she was an excellent student but stated she was often paralyzed with anxiety about upcoming tests or assign- ments. Currently, Marianne avoided reading newspa- pers or online news stories, as it would further trigger her worries about climate change and the “state of the world.” Unable to stop worrying, Marianne found that avoiding triggers was her only strategy for managing anxiety. She stated she was restless, although also fa- tigued much of the time. She also had chronic muscle tension. Marianne described worrying so frequently, particularly in the last 8 months, that tasks easily be- came overwhelming, which interfered with taking the steps to find a new job. She also reported interference in social relationships due to worry and anxiety because many of her friends were highly successful, which left Marianne worrying that they did not want to be friends with her anymore because she was not “good enough” for them.
Last, Marianne also described experiencing frequent headaches, and occasionally migraine headaches, in the last several years. She stated that on most days, she woke up with a mild headache that would get progres- sively worse throughout the day, making it difficult to concentrate on what she was doing. She stated the pain would be worse on days near the start of her menstrual cycle, and she had not been able to sufficiently treat her symptoms with medications prescribed by a neurologist she was seeing. The headaches were present 90% of the days and were causing her to further avoid activities and friends.
Objective assessment of Marianne’s emotional state via self-report questionnaires resulted in a score of 53 on the Beck Depression Inventory–II (BDI-II; Beck, Steer, & Brown, 1996), reflecting severe depression and a score of 65 on the Penn State Worry Question- naire (PSWQ; Meyer, Miller, Metzger, & Borkovec, 1990), reflecting moderate levels of worry. Her scores of 18 on the Overall Depression Severity and Impair- ment Scale (ODSIS; Bentley, Gallagher, Carl, & Bar- low, 2014) and 12 on the Overall Anxiety Severity and Impairment Scale (OASIS; Campbell-Sills et al., 2009; Norman, Cissell, Means-Christensen, & Stein, 2006) were consistent with these other measures, suggesting severe levels of depression and moderate-to-severe lev- els of anxiety, respectively. A diagnostic interview using the Anxiety and Related Disorders Interview Schedule for DSM-5—Lifetime Version (ADIS-5L; Brown & Barlow, 2014) revealed a principal diagnosis of major depressive disorder (MDD), single episode, severe at a clinical severity rating (CSR; described below) of 7, on a 0- to 8-point scale (see below) and additional diagnosis of persistent depressive disorder, early onset (CSR = 5). Marianne was not given a separate diagnosis of GAD, as the symptoms of anxiety and worry had been present for as long as the persistent depressive disorder and were therefore subsumed under that diagnosis.
Interviews
A number of structured and semistructured clinical in- terviews may be appropriate for diagnosing emotional disorders. The Structured Clinical Interview for DSM-5 (SCID-5; First, Williams, Karg, & Spitzer, 2016) is widely used and assesses diagnoses. Because this inter- view is highly structured and focuses only on current symptom count, it achieves a high degree of interrater reliability for many diagnoses. However, this interview does not include dimensional ratings of frequency and severity of symptoms, so it may be less useful for more detailed profiling of emotional disorders.
The ADIS-5 (Brown et al., 2014), a semistructured, diagnostic clinical interview, focuses on DSM diagno- ses of anxiety, OCD and related disorders, and trauma- and stressor-related disorders and their accompanying mood states, as well as somatic symptoms and dissocia- tive disorders, and substance and addictive disorders. The information derived from the interview using the ADIS allows clinicians to determine differential diag- noses and gain a clear understanding of the level and severity of each diagnosis. Principal and additional di-
226 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
agnoses are assigned a CSR on a scale from 0 (No symp- toms) to 8 (Extremely severe symptoms), with a rating of 4 or above (Definitely disturbing/disabling) passing the clinical threshold for DSM diagnostic criteria. Inqui- ries about suicidal ideation are part of this interview. A previous version of the ADIS based on DSM-IV criteria has demonstrated excellent to acceptable interrater reli- ability for the anxiety and mood disorders (Brown, Di Nardo, Lehman, & Campbell, 2001).
Two additional clinician-rated measures that provide a wider range of scores are the (1) Structured Interview Guide for the Hamilton Anxiety Rating Scale (SIGH- A; Shear, Vander Bilt, & Rucci, 2001) and the (2) Struc- tured Interview Guide for the Hamilton Depression Rating Scale (SIGH-D; Williams, 1988). The SIGH-A was developed to create a structured format for admin- istering the Hamilton Anxiety Rating Scale (HARS; Hamilton, 1959). Respondents are asked to indicate the presence and severity of a number of symptoms that may have been present over the past week, including anxious mood, tension, sleep problems, irritability, and so forth. The rater is also asked to rate the interview behavior of the patient. The SIGH-A includes specific instructions on administration and anchor points for assigning severity ratings. This measure demonstrated good interrater and test–retest reliability (Shear et al., 2001). In addition, scores are similar to (although con- sistently higher than) the HARS.
Similar to the SIGH-A, the SIGH-D was developed to provide more specific instructions for administra- tion and scoring of the Hamilton Depression Rating Scale (HDRS; Hamilton, 1960). Again, patients are questioned about the presence and severity of a range of depressive symptoms over the past week, including depressed mood, suicidal ideation, fatigue, feelings of hopelessness, weight loss, and so forth. The SIGH-D also demonstrated good interrater and test–retest reli- ability, and produces scores similar to the HDRS (Wil- liams, 1988).
Medical Evaluations
Medical evaluations are generally recommended prior to assignment of diagnoses and initiation of treatment to rule out organic causes for symptoms of emotional disorders. Some conditions, such as hypothyroidism, hyperthyroidism, hypoglycemia, mitral valve prolapse, or alcohol or substance withdrawal, may elicit symp- toms similar to those associated with GAD or PD/A. Although the diagnosis of such medical conditions does
not preclude the need for a psychological treatment, it is generally recommended that such conditions be evalu- ated medically, because an alternative treatment may be clinically indicated.
Self‑Monitoring
Self-monitoring forms are an important part of the treatment protocol for several reasons. First, the thera- pist is able to discuss specific situations or events that occurred over the past week and may have contributed to emotional reactions. Such records can facilitate dis- cussions of concepts presented during the treatment sessions and help the therapist integrate the general treatment components into the patient’s specific symp- toms. Second, some evidence suggests that patients’ retrospective recall of past episodes of anxiety may be inflated, particularly when recalling panic attacks (Margraf, Taylor, Ehlers, Roth, & Agras, 1987; Rapee, Craske, & Barlow, 1990). Self-monitoring forms allow for a prospective, and possibly more accurate, account of anxiety episodes and may therefore be more useful therapeutically. In addition, consistent with the themes outlined in the UP, practicing awareness of emotions in the present moment is believed to be an important com- ponent of changing maladaptive patterns of emotional responding. The very nature of self-monitoring requires patients to disengage, even briefly, from the habitual anxious process to write down concrete thoughts, feel- ings, and behaviors, helping them to begin to adopt a more objective stance toward their own emotional ex- periences. Developing this skill ultimately aids patients in beginning to change emotional reactions and result- ing behaviors.
Treatment forms used in the UP include self- monitoring forms for tracking emotional experiences, automatic appraisals, and emotion avoidance, as well as forms for conducting interoceptive and situationally based emotion exposure. Figure 6.1 illustrates the Fol- lowing Your ARC Form, which was designed to help patients track their emotional experiences during the initial phases of treatment (see description of the ARC below). As new skills are introduced for responding to emotions in a more adaptive manner, other self- monitoring forms are also used. For instance, patients are asked to monitor situations, identify emotional behaviors and alternative actions, as well as the short- and long-term consequences of alternative action on the Countering Emotional Behaviors Form (see Figure 6.2).
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Emotional Disorders 229
Several problems may arise with the introduction and completion of self-monitoring forms. First, some patients may not be compliant with completion of monitoring forms and homework assignments, which is an important issue to be addressed in the therapy ses- sion. Adopting a motivation enhancement approach, eliciting reasons underlying the patient’s ambivalence regarding completing the homework or monitoring can be a valuable technique (i.e., eliciting reasons why the patient might not wish to complete the homework and perceived benefits to not completing it). This process is crucial, as it allows the therapist to identify maladaptive cognitive appraisals and emotional reasons contributing to the lack of completion of monitoring forms. Once such reasons are identified, therapeutic strategies such as cognitive reappraisal may also be used to increase patients’ willingness to complete homework forms. Furthermore, selectively reflecting the benefits of com- pleting the homework and the costs associated with noncompliance can help to build motivation to com- plete homework forms. In some cases, especially when patient self-efficacy for completion is low, completion of homework forms themselves may become an emo- tion exposure, and progress toward this goal should be reinforced accordingly.
Another common problem with the completion of self-monitoring may be the tendency for some patients (particularly those with more obsessive or “perfection- istic” features, commonly seen in GAD and OCD) to “overdo” the homework forms; that is, the patient may write an extremely long and involved description of a situation and his/her reactions to it. This is common with patients who feel a need to “unload” every piece of information about the event. Although the patient is doing the homework, his/her overengagement may also be facilitating the anxious/worry process. If this becomes evident, the therapist may want to discuss the tendency to overengage in the homework as an emo- tional behavior and encourage monitoring situations and events using one- or two-word descriptions, or even implement a time limit to help ensure that patients do not spend lengthy periods of time generating their de- scriptions.
Questionnaires
In our research trials, we employ a number of self- report questionnaires over the course of treatment. We describe most of them here, realizing that for purely clinical purposes only a subset would be needed. Two
general (diagnosis-nonspecific) questionnaires designed to measure symptoms and impairment associated with those symptoms are administered weekly prior to ses- sion to track symptoms and impairment across the course of treatment. A larger questionnaire battery is administered pre-, mid-, and posttreatment, in order to gain a more comprehensive picture of patients’ present- ing concerns, overall functioning, and quality of life. This battery comprises general questionnaires (mea- sures designed to assess a range of symptoms associated with anxiety and mood disorders, as well as disorder- specific measures designed to track symptoms associ- ated with specific disorders).
Weekly General Measures
The OASIS (Campbell-Sills et al., 2009; Norman et al., 2006), a brief, five-item questionnaire developed as a continuous measure of anxiety-related symptom se- verity and impairment, can be used across anxiety dis- orders, with multiple anxiety disorders, and with sub- threshold anxiety symptoms. This measure has good internal consistency, excellent test–retest reliability, and convergent and divergent validity (Campbell-Sills et al., 2009; Norman et al., 2006). The ODSIS (Bentley et al., 2014), a direct adaptation of the OASIS, is modified to be applicable for depression. It is a brief, five-item questionnaire that assesses dimensional depression- related symptom severity and impairment that can be used across depressive disorders, with varied comorbid presentations, and with subthreshold depressive symp- toms. Both measures focus on severity of and impair- ment associated with particular symptoms over the past week, offering a general, diagnosis-nonspecific measure designed to track changes as they occur over the course of treatment.
Optional General Measures
In the Positive and Negative Affect Schedule—Trait version (PANAS; Watson, Clark, & Tellegen, 1988), a brief, reliable, and valid measure of positive and nega- tive affect, individuals rate how frequently they ex- perience 20 feeling or emotion words in general. The PANAS assesses core negative affect and deficits in positive affect in those disorders with this characteristic (i.e., agoraphobia, social anxiety disorder, depression) and is useful in determining changes in positive and negative affect over the course of treatment. In an effort to establish degree of interference from symptoms in
230 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
various domains of living, the Work and Social Adjust- ment Scale (WSAS; Hafner & Marks, 1976) includes five items that ask participants to rate the degree of interference caused by their symptoms in work, home management, private leisure, social leisure, and fam- ily relationships. The WSAS, a descriptive measure of subjective interference in various domains of living, has been successfully used in previous studies (e.g., Brown & Barlow, 1995).
Quality of Life and Well‑Being Measures
The Quality of Life and Enjoyment Satisfaction Ques- tionnaire (QLESQ; Endicott, Nee, Harrison, & Blu- menthal, 1993), a 14-item measure that assesses enjoy- ment and satisfaction across different life areas in the past week, is widely used and has been validated for use in clinical populations and shown to be sensitive to change. The Mental Health Continuum—Short Form (MHC-SF; Keyes, 2005, 2006; Keyes et al., 2008; Lamers, Westerhof, Bohlmeijer, ten Klooster, & Keyes, 2011; Westerhof & Keyes, 2009) is a 14-item measure designed to assess social, emotional, and psychological well-being. The measure has shown excellent internal consistency and discriminant validity in both adoles- cents and adults in the United States, the Netherlands, and South Africa (Keyes, 2005, 2006; Keyes et al., 2008; Lamers et al., 2011; Westerhof & Keyes, 2009).
Diagnosis‑Specific Measures
In addition to the general (diagnosis nonspecific) mea- sures, it is important to assess symptoms specific to the individual’s specific diagnostic presenting concerns. We use the following measures that assess symptom sever- ity over the past week and can be administered both as self-report and clinician-rated measures, increas- ing their clinical utility. The Yale–Brown Obsessive– Compulsive Scale–II (Y-BOCS-II; Storch et al., 2010) is a revised version of the Y-BOCS (Goodman et al., 1989), designed to assess the presence and severity of OCD symptoms.
The Panic Disorder Severity Scale (PDSS; Shear et al., 1997), a seven-item scale, provides ratings of the core features of panic disorder (panic frequency, dis- tress during panic, anticipatory anxiety, panic-related avoidance of situations and sensations) and the degree of work and social impairment/interference due to PD/A.
The Liebowitz Social Anxiety Scale (LSAS; Liebow- itz, 1987) is a widely used 24-item scale designed to as- sess the range of social interaction and performance sit- uations that patients with social anxiety may fear and/ or avoid (Heimberg et al., 1999; Safren et al., 1999).
The Generalized Anxiety Disorder Severity Scale (GADSS; Shear, Belnap, Mazumdar, Houck, & Roll- man, 2006) is a six-item assessment that evaluates the core features of GAD.
The PTSD Symptom Scale (PSS; Foa, Riggs, Dancu, & Rothbaum, 1993), a 17-item measure designed to as- sess DSM-IV symptoms of PTSD, with each item cor- responding to the symptoms of PTSD, comprises one brief question that is rated from 0 (Not at all) to 3 (5 or more times per week/Very much). This measure yields a total PTSD severity score, as well as Reexperiencing, Avoidance, and Arousal subscores (Foa & Tolin, 2000).
Functional Analysis
Regardless of the diagnosis, a functional understand- ing of the processes that contribute to and maintain an individual’s psychopathology provides an essential foundation for case conceptualization and personaliza- tion of the intervention. Several components are impor- tant to consider when diagnosing a patient based on a functional analysis. These include a close examination of symptom topography (including duration of illness, physical sensations, level of distress, and interference from symptoms), triggers (situations, physical symp- toms, places, thoughts, etc.), cognitions (beliefs about symptoms and misappraisals), behavioral responses to emotions (including avoidance of situations, places, people, or triggers, as well as escape behaviors), and the consequences of behavioral reactions (limiting qual- ity of life, reduced “comfort zone,” etc.). The UP Case Conceptualization Worksheet is presented in Figure 6.3; for a detailed description of transdiagnostic as- sessment and case conceptualization, see Boettcher and Conklin (2018).
Marianne, at the diagnostic level, met criteria for what is often referred to as “double depression,” in that she experienced persistent depressive disorder her whole life but now was also experiencing a major depressive episode. Her primary concern involved significant feelings of depression, fatigue, trouble concentrating, and anhedonia, and Marianne clearly met criteria for MDD, single episode. However, feelings of low self- esteem, hopelessness, and fatigue had also been present
Emotional Disorders 231
FIGURE 6.3. UP Case Conceptualization Worksheet. Reprinted with permission from Oxford University Press.
Patient:_______________
PRESENTING PROBLEMS:
STRONG UNCOMFORTABLE EMOTIONS:
AVERSIVE REACTIONS:
AVOIDANT COPING
SITUATIONAL AVOIDANCE/ESCAPE
SUBTLE BEHAVIORAL AVOIDANCE:
COGNITIVE AVOIDANCE:
SAFETY SIGNALS:
TREATMENT PLAN: FOCUS/APPLICATION OF CORE MODULES
MODULE 3:
MODULE 4:
MODULE 5:
MODULE 6:
MODULE 7:
232 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
since childhood, although Marianne was able to cope with the symptoms despite the significant distress and interference in her relationships. Thus, a diagnosis of persistent depressive disorder was also warranted. Mari- anne also presented with significant anxiety and un- controllable worry about her family and their health, the state of the world, and her relationships. These wor- ries, although clearly significant, were only experienced during the course of the persistent depressive disorder. Thus, even though Marianne met diagnostic criteria for GAD, an additional diagnosis was not assigned.
Whereas Marianne’s symptoms merited the assign- ment of multiple co-occurring disorders, it is impor- tant to note that at the phenomenological level, these diagnosis-specific symptoms shared significant overlap. This was an important consideration for treatment, and it provided a strong argument for a unified, transdiag- nostic approach. For example, Marianne’s low self-es- teem, driven by her depressogenic ruminations, resulted in significant anxiety and worry when she confronted situations in which she was being evaluated by others. This anxiety focused on negative evaluation in turn in- creased Marianne’s negative beliefs about herself and her life, then fueled her emotional behaviors, for example, isolating herself, which was an attempt to avoid feel- ing worse about herself. Without any social contact or experiences outside her apartment, she became heavily focused on physical symptoms, particularly headaches, which then created anxiety and additional obstacles to improve her functioning (i.e., applying for jobs). By avoiding job applications and other anxiety-provoking activities Marianne unintentionally reinforced the neg- ative belief that she was incompetent and would not be able to make changes in her life. Marianne attributed this negative cycle to her experiences growing up, when her inability to effect change in her family dynamics, particularly with her father, created a sense that she had little ability to modify her circumstances. Thus, all of these beliefs, behaviors, and physiological responses were interacting in Marianne’s emotional experiences, regardless of their specific diagnostic classification, and affecting her ability to function in an adaptive way. Treatment of Marianne’s symptoms with the UP, which focuses on how the interactions of thoughts, feelings, and behaviors at any given moment influence overall emotional experiences and subsequent actions, allowed us to target Marianne’s phenomenological patterns of dysfunction directly rather than focus on one diagno- sis-specific cluster of symptoms at a time.
COMPONENTS OF TREATMENT
The structure of the UP outlines five core treatment modules and three additional modules, designed to be delivered in 12–18, 50- to 60-minute individual treat- ment sessions, held on a weekly basis. Final sessions may be held every other week to allow patients to con- solidate gains and to provide somewhat of a “taper” off the weekly therapy. This format for the final sessions is not a requirement, though, and it may be more ben- eficial for the patient to continue to have weekly ses- sions if he/she might potentially have trouble using the treatment concepts consistently without the weekly re- inforcement of sessions. Therefore, spacing of the final sessions is determined by the therapist, who takes into consideration the patient’s progress and any anticipated difficulties after treatment.
The five core treatment modules designed to target aspects of emotion processing and regulation are as follows: (1) Mindful Emotion Awareness (Module 3); (2) Cognitive Flexibility (Module 4); (3) Countering Emotional Behaviors (Module 5); (4) Understanding and Confronting Physical Sensations (Module 6); and (5) Emotion Exposures (Module 7). Preceding these core components is a module focused on enhancing motivation and readiness for change and treatment en- gagement (Module 1—Setting Goals and Maintaining Motivation), as well as an introductory module pro- viding psychoeducation about the nature of emotions and a framework for understanding emotional experi- ences (Module 2—Understanding Emotions). A final module reviews progress over treatment and develops relapse prevention strategies (Module 8—Recognizing Accomplishments and Looking to the Future). This treatment, which takes place in the context of provok- ing emotional expression (emotion exposure) through situational, internal, and somatic (interoceptive) cues, as well as through standard mood induction exercises, differs from patient to patient only in the situational cues and exercises utilized. In addition, “exposure” is not conceptualized as a mechanism of action. Rather, successfully provoking emotions creates a setting condi- tion to implement the essential treatment components. Emotion exposures begin with general stimuli (e.g., mood induction and interoceptive provocation) and are later tailored to address each patient’s particular con- cerns and symptoms. Although each session addresses a specific component of the protocol, the expectation is that patients then “carry through” the strategies they
Emotional Disorders 233
learn to future sessions (e.g., patients learn cognitive reappraisal strategies in Module 4 but are expected to continue to use this strategy throughout the remainder of treatment).
Module 1: Setting Goals and Maintaining Motivation
In this initial treatment module, which is grounded in the principles and therapeutic techniques utilized in motivational interviewing (MI; Miller & Rollnick, 2013), therapists work to increase the patient’s readi- ness and motivation for behavior change, and to foster a sense of self-efficacy, or the patient’s belief in his/her ability to change. This module was included in the pro- tocol in response to research by Westra and colleagues (Westra, Arkowitz, & Dozois, 2009; Westra & Dozois, 2006) suggesting that MI may enhance the efficacy of CBT for anxiety disorders. This module utilizes two specific motivational exercises: (1) a decisional balance exercise, in which the therapist works with the patient to identify and weigh the pros and cons of changing versus staying the same; and (2) a treatment goal-setting exer- cise that helps patients more clearly articulate achiev- able and concrete goals for treatment. This module, and the principles and techniques contained therein, are primarily used to help “set the stage” for subsequent learning that takes in the core modules. However, the principles can also be applied throughout the course of treatment to enhance treatment engagement and main- tain patient motivation for behavior change.
Module 2: Understanding Emotions
Following the initial motivation enhancement session, patients are provided with psychoeducation about the nature and function of emotions, including anxiety, anger, sadness, shame/guilt, and fear. In this module (which typically occurs over the course of one to two sessions), patients are provided information about the cognitive, physiological, and behavioral sequelae of emotional reactions and how these three components interact. It is important that the patient begin to con- sider that his/her reactions are functional and serve the purpose of providing information about the environ- ment, in addition to protection from harm. This three- component model is then applied to a recent situation or event that the patient experienced, so that he/she may better understand the aspects of each component and how they interact. Patients also learn how to care-
fully monitor and track their emotional responses and, as a result, are expected to develop greater awareness of their own patterns of emotional responding, including potential maintaining factors (e.g., common triggers and/or environmental contingencies).
As noted earlier, the UP uses the acronym ARC to describe the sequence of events around emotions. Emotions are always triggered by an event, situation, or experience known as an antecedent (the A in the ARC). Often there are multiple antecedents, and may include recent and distal events. One’s response to the emotional experience (the R of ARC) corresponds to all cognitions, somatic sensations, and behaviors from the three-component model. Finally, short- and long-term outcomes of emotional responding are referred to as consequences, or the C of the ARC. During this expla- nation, the therapist clearly works through an example with the patient.
Another important aspect of psychoeducation is the concept of negative reinforcement. This involves a detailed discussion of how the patient’s behavioral re- sponse to an emotional episode (usually escape or some form of emotional avoidance) is problematic, because it reduces the emotion in the short term (i.e., by removing the person from the emotional stimulus) but reinforces the cycle of emotions in the long term (i.e., by teach- ing the person that escape/avoidance is the only way to manage these feelings in the future). It is extremely important that the patient understand the connection between behavioral responses and reinforcement of emotion, so that he/she is better able to appreciate the purpose and function of emotion exposures introduced in future sessions.
Module 3: Mindful Emotion Awareness
The first core module (which typically occurs over the course of one to two treatment sessions) is designed to help patients further identify how they are reacting and responding to their emotions by promoting a more non- judgmental, present-focused approach to the experience of emotions. Often, patients report feeling that their emotions are confusing, or that they seem to just hap- pen “automatically” and/or in such way that they are outside of the patient’s immediate awareness (i.e., “un- consciously”). Through this module, patients learn to become more aware of the interaction among thoughts, feelings, and behaviors, and to view their emotions in a more objective and present-focused manner. This
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occurs within the specific context of the situation in which the emotional experience is unfolding. The focus on present-moment experiences is important and is be- lieved to put the patient in a better position to more clearly identify patterns of emotional responding and/ or the emotion regulation strategies being employed in the particular situation. In turn, this renders the patient better able to modify the emotional response adaptively to make it more consistent or compatible with ongoing situational or motivational demands. Furthermore, the therapist introduces the idea that it is not the emotions per se that are problematic, but rather how the patient reacts to the emotions. As these reactions tend to be judgment-laden (e.g., seeing anxiety as a sign of one’s inability to cope an indication of weakness, or a sign of failure) and are often not based on information from the present-moment context, they can prevent the pro- cessing of potentially corrective information that would allow for a change in the emotional response. It is ex- pected that as patients develop a more nonjudgmental stance toward their emotions, they are better able to identify the specific thoughts, physical sensations, and behaviors that may be contributing to their distress, and thus be in a better position to implement strate- gies for adaptively altering their emotional response. Mindful emotion awareness also allows for the pos- sibility of attending to positive emotions, should they arise. These skills are developed through the practice of a brief mindfulness meditation, emotion induction exercises, and a “three-point check” that utilizes emo- tion awareness in the context of an emotion-provoking situation. Emotion awareness thereby also serves to fa- cilitate extinction of reactivity to and distress associated with emotion experiences.
Module 4: Cognitive Flexibility
Cognitive therapy, initially developed by Aaron T. Beck to treat depression (Beck, 1967; Beck, Rush, Shaw, & Emery, 1979; also discussed in depth in Young, Ward- Ciesielski, Rygh, Weinberger, & Beck, Chapter 7, this volume), has become a fundamental part of psychologi- cal treatments. Individuals with emotional disorders are likely to have appraisals and interpretations of external events that are characterized by cognitive biases, such as the tendency to overestimate the likelihood of the occurrence of negative events and to underestimate the ability to cope with these events. Thus, the aim of cog- nitive therapy is to evaluate objectively the likelihood of these negative appraisals and to incorporate more
realistic, evidence-based appraisals of the outcome of a situation. On the surface, this technique may appear to be a way to suppress or control negative thoughts by “rationalizing” them, and occasionally, this is how cog- nitive therapy is incorrectly used, as noted by Hayes, Strosahl, and Wilson (1999). However, this strategy can also be conceptualized from an emotion regulation per- spective, especially if reappraisals are considered one of many possible interpretations of a situation.
The primary aim of this module is to foster greater flexibility in thinking (this module is typically admin- istered in one or two sessions). This is accomplished first by helping patients develop an understanding of how they interpret or appraise situations, and how their appraisals influence patterns of emotional responding, then by teaching them to generate numerous alternative attributions and appraisals when experiencing strong emotional experiences. As their initial interpretations are typically more negative or anxious, patients are encouraged to be more flexible in their thinking (i.e., to generate alternative appraisals) and are taught reap- praisal strategies.
As adapted in our usage, the UP focuses on correct- ing two fundamental misappraisals often found in in- dividuals with emotional disorders: the probability of a negative event happening (probability overestimation) and the consequences if the negative event does happen (catastrophizing) (Barlow & Craske, 2007; Craske & Barlow, 2006). Although a number of other misapprais- als are noted in other, traditional CBT protocols, most misappraisals can be condensed into one of the two ap- praisals listed here.
Module 5: Countering Emotional Behaviors
Module 5 generally comprises one to two sessions. This module focuses on the behavioral component of emo- tion. Specifically, patients are taught skills to evaluate and prepare to change “emotional behaviors,” which are behaviors that occur in anticipation of or in response to emotion. Emotional behaviors fall into two general categories: behaviors that prevent the full experience of emotion (avoidance) or as behaviors driven by the emotion itself (emotion-driven behaviors [EDBs]). The concept of emotion avoidance is likely to be particu- larly important for patients who do not physically avoid or escape situations but still experience high levels of anxiety without much relief. The therapist should con- vey that even if the person stays physically in the situ- ation, he/she is likely to engage in a number of other
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subtle behaviors to prevent full emotional arousal. Any technique or strategy the patient uses to reduce or to down-regulate emotions, or any behavior that occurs in response to an emotion, may be conceptualized as an emotional behavior, and it is essential that emotion- al behaviors be identified and eliminated as much as possible prior to engagement in emotion exposures, to allow for full emotional processing. Therefore, a very detailed description of individual emotional behaviors must be obtained for each patient. Common examples of emotional behaviors associated with different emo- tions are presented in Figure 6.4.
Within the emotional behaviors, we have identified four general categories of emotional behaviors that serve as avoidance strategies: (1) overt avoidance, (2) subtle behavioral avoidance, (3) cognitive avoidance, and (4) safety signals. Overt avoidance refers to directly avoiding a situation, task, person, or place because of the anticipated emotion it will trigger. Subtle behavioral avoidance strategies may include a number of differ- ent behaviors, with certain behaviors occurring more frequently with particular disorders. For example, the avoidance of caffeine in panic disorder or social phobia (prior to a social engagement) is an attempt to keep physiological symptoms from becoming strong in anx- iety-provoking situations. Patients with social phobia may also avoid eye contact or wear sunglasses when in- teracting in social settings. Individuals with GAD may excessively plan, prepare, or write “to do” lists in an at- tempt to control potentially negative outcomes. At the same time, procrastination is also a form of subtle be- havioral avoidance, if a particular task or project seems too emotionally arousing or distressing for the patient. It is very important to conduct a functional analysis of the subtle behaviors to determine which ones are avoid- ance strategies, that is, behaviors that serve to reduce or avoid emotional experience, and which are functional responses to situations. And, notably, what may be an avoidance strategy for one person may be a functional response for another. Cognitive avoidance strategies are typically more difficult to identify, because they tend to occur outside of the patient’s awareness. Some of these strategies include distraction, “tuning out,” and mentally checking lists or reviewing past conversations. However, data also suggest that worry and rumination actually function as a way to down-regulate and avoid emotions (e.g., Borkovec, 1994). The function of worry is to enable the person to prepare for a possible threat. However, when someone experiences chronic worry and associated anxiety, his/her attention is focused on
the future as opposed to the present moment. Research has shown that when confronted with an emotionally arousing event, chronic worriers do not experience the full emotional impact of that event because (1) they have been “bracing” themselves for something bad to happen, and (2) their focus has already shifted to other, future negative outcomes (Borkovec, Hazlett- Stevens, & Diaz, 1999). Therefore, the worry functions as a cognitive avoidance strategy and only serves as a maladaptive attempt to gain control over seemingly uncontrollable future events. Obsessions, common to individuals with OCD, may also function in a similar manner.
Safety signals are most common to patients with PD/A, although may also be present in individuals with GAD, OCD, or other emotional disorders. Safety sig- nals include any object that the patient carries to feel more safe or “comfortable,” particularly if he/she is en- tering an emotionally arousing situation. Safety signals can range from actual medication (e.g., benzodiaze- pines for reducing physiological arousal or medications for gastrointestinal distress) to empty medication bot- tles, to “lucky” objects (a talisman, teddy bear, “lucky” pen, etc.). Regardless of the object itself, if its function is to help the patient reduce emotional arousal in the moment, then it also is problematic, because it feeds into the cycle of negative reinforcement.
In addition to changing patterns of avoidance, this module also focuses on helping patients identify and subsequently change EDBs. Data and hypotheses from emotion science suggest that the most efficient and effective way to change emotions is by changing the behavior the emotion is driving (Barlow, 1988; Izard, 1971); thus, it is conceivable that the mechanism of change during an exposure is to prevent the action ten- dency associated with a particular emotional experience. Over the past several decades, research has focused on these action tendencies, and changing action tenden- cies has become an important treatment component for anxiety, as well as other emotional disorders (Bar- low, 1988; Linehan, 1993). For example, Beck and col- leagues (1979) based a large part of their treatment for depression on changing the action tendencies of their patients to behave in a “passive, retarded, and apathetic manner” (p. 312). More recently, behavioral activation strategies have become a central feature of newer treat- ments for depression (Dimidjian et al., 2006; Jacobson, Martell, & Dimidjian, 2001); for a more in-depth dis- cussion, see Dimidjian, Martell, Herman-Dunn, and Hubley (Chapter 9, this volume).
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Emotion Emotional Behavior Type
Anxiety Walk instead of taking public transit Overt Avoid talking to attractive individuals Overt Text at parties to avoid small talk Subtle behavioral Say “I don’t know” Subtle behavioral Listen to music when walking Cognitive Worry about tomorrow’s to-do list Cognitive Engage in checking behavior (locks, stove, etc.) EDB Ask for reassurance EDB
Sadness Decline offers to see friends Overt Avoid physical exercise Overt Speak in a low tone of voice Subtle behavioral Make minimal eye contact Subtle behavioral Watch television Cognitive Sleep excessively Cognitive Think about all the things you’ve done wrong EDB Engage in self-injurious behaviors EDB
Anger Refuse to drive during rush hour Overt Avoid talking to provoking people Overt Make snide comments Subtle behavioral Make deprecating jokes Subtle behavioral Silently curse Cognitive Ruminate Cognitive Insult someone EDB Yell or hit someone EDB
Guilt Not say “no” to tasks Overt Not express one’s opinion Overt Fidget Subtle behavioral Speak quietly Subtle behavioral Worry Cognitive Ruminate Cognitive Overapologize EDB Do “extra” things to “make up for doing something wrong” EDB
Happiness Avoid pleasurable activities Overt Avoid contact with enjoyable people Overt Make comments that undercut the enjoyment of a situation Subtle behavioral Remind oneself that the good feelings can’t last Subtle behavioral Worry Cognitive Ruminate Cognitive Do something that makes one feel bad EDB Overengage in pleasurable activities to try to “hold on” to the good feelings EDB
FIGURE 6.4. Examples of emotional behaviors. Reprinted with permission from Oxford University Press.
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Whereas the function of emotional avoidance strat- egies is to down-regulate or suppress emotions, EDBs include a specific set of “reactive” behaviors associated with each emotion. For example, the EDB for a panic attack is escape (fight or flight), whereas that for anxi- ety is hypervigilance. Similarly, the emotion of anger elicits an EDB of attacking–defending, and the EDB for sadness is cognitive, emotional, and physical slow- ing and withdrawal. It is important to note, however, that the therapist must focus on helping the patient engage in alternative actions for all emotional behav- iors, from changing EDBs to preventing all types of avoidance. For example, a patient with social phobia may be able to maintain eye contact and fully engage in social situations but escape the situation when his/ her anxiety rises to the level of panic. On the contrary, this same patient may be able to stay in the situation as long as needed, but he may be distracting him/herself the whole time or avoiding conversations with people. Clearly, both scenarios are problematic, because the pa- tient is preventing him/herself from learning that he/ she can experience emotions at their fullest without leaving the situation.
After reviewing and identifying emotional behaviors in session, patients identify several emotional behaviors they might engage in, then generate possible alternative actions to these emotional behaviors. An alternative ac- tion is any behavior that is different than the emotional behavior. The potential short- and long-term conse- quences of engaging in the alternative actions are also highlighted and reviewed in session.
Module 6: Understanding and Confronting Physical Sensations
This module (typically one session) was designed to increase patients’ awareness of the role of physical sen- sations as a core component of emotional experiences and to promote increased tolerance of these sensations. In this module, patients are asked to engage in a se- ries of interoceptive exposure (IE) exercises designed to induce physical sensations analogous to those typically associated with naturally occurring feelings of anxiety and emotional distress (e.g., shortness of breath, heart palpitations, dizziness), which themselves often become cues for anxiety through interoceptive conditioning (Barlow, 2002). Examples of IE exercises include hy- perventilation, spinning (while standing and/or in a chair), running in place, and breathing through a thin straw). The use of IE has largely been confined to the
treatment of PD/A, and has been shown to be effec- tive in reducing panic attack frequency and the fear of physical sensations that occur as a primary feature of the disorder (e.g., Barlow et al., 2000; Craske, Rowe, Lewin, & Noriega-Dimitri, 1997). However, given the fact that heightened physiological arousal and sensitiv- ity to physical sensations are observed in other emotion- al disorders, IEs are applied across diagnoses, regardless of whether the physical sensations represent a specific focus of the patient’s anxiety.
Module 7: Emotion Exposures
In this final core module, treatment concepts are prac- ticed and extended during in-session emotion expo- sures created by the therapist and individually tailored to the patient’s presenting symptoms (this module is the longest; typically lasting four to six sessions). Through exposure to both internal and external cues, patients ul- timately increase their tolerance of intense and uncom- fortable emotional experiences. In-session exposures can range from an imaginal exposure to a past emo- tional event (for PTSD or GAD), a conversation with a stranger (for social phobia), going into a dirty bathroom (for OCD), or watching a sad movie or movie clip (for MDD or persistent depressive disorder). Furthermore, for some patients, continued engagement in IEs may be indicated to promote greater tolerance of uncomfort- able physical sensations. The goal of the exposures is gradually to introduce situations and experiences that serve as external triggers for emotional experiences. By eliciting the emotions that patients have been avoiding, they have the opportunity to practice the techniques learned in treatment (present-focused awareness, cogni- tive reappraisal, and engaging in alternative action). In this sense, exposure to the emotion itself is the neces- sary mechanism of action for change. Thus, the actual situational context of the exposure becomes less impor- tant. Therapists must be creative in the design of the exposure to maximize the emotion provocation for each patient.
Module 8: Recognizing Accomplishments and Looking to the Future
Treatment concludes with a general review of treatment principles and a discussion of the patient’s progress (usu- ally one session). In this module, therapist and patient identify specific strategies for maintaining and extend- ing treatment gains and for responding to future dif-
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ficulties that may arise. For instance, it is emphasized that a return of anxiety and/or mood difficulties does not reflect relapse and, instead, may be a more natural fluctuation of emotions that can be addressed using the skills developed in treatment.
DETAILED DESCRIPTION OF PROTOCOL
The following session descriptions and accompanying transcripts are from the case of “Marianne,” described earlier, treated by one of the authors (L. A. P.).
Session 1: Functional Assessment and Introduction to Treatment
During the introductory session, the goals of the treat- ment program are identified and reviewed. The UP aims to help clients become aware of and better under- stand emotional experiences and reactions, and to coun- ter maladaptive responses to uncomfortable emotions. Modifying maladaptive responses can help reduce the intensity and frequency of uncomfortable emotions, while still allowing clients to experience them in an adaptive way. It is also important to emphasize that modifying these responses can be challenging, and that change often does not occur in a linear fashion.
Following this introduction to treatment is a detailed review of the presenting complaint. In this review, the therapist focuses on the emotions that result in the most distress and/or interference in the patient’s life, the situ- ations and contexts in which those emotions occur, and how the patient has attempted to manage these emo- tions. Below, Marianne describes how depression has interfered with finding a new job:
THERAPIST: Marianne, you have said that feelings of depression have made it difficult for you to find a new job. Can you tell me more about that?
MARIANNE: Well, when I lost my previous job, I just felt so awful about myself. Even though I knew it didn’t really have much to do with my performance. And since then, I just feel like I’m such a loser. Whenever I think about looking for a new job, I just don’t want to do it.
THERAPIST: Why is that? MARIANNE: Every time I see a job listing that would be
relevant to my qualifications, I automatically think, “They would never want me. I’m not smart enough,
I am not very organized, and I’m just completely in- competent.” Even just thinking about this now gives me a pit in my stomach.
THERAPIST: And so, what do you do when you feel this way?
MARIANNE: I just go lie down in bed usually. Some- times I will try to watch TV if I’m able to concen- trate. But it’s really hard to do anything! I don’t want to keep looking for jobs, but then I just sit there and feel miserable. Then I start thinking about how I’m feeling, and my headache gets worse. After that, I’m useless for the rest of the day.
THERAPIST: So, it sounds like the stress of looking for a new job has also been making your physical symp- toms worse, particularly headaches?
MARIANNE: Yes. THERAPIST: Have you found any strategy that has
helped you? MARIANNE: Not really. I’m just completely paralyzed.
I can’t escape feeling badly, no matter what I do.
Note that in this early exchange, the therapist has already obtained important information about the pa- tient’s emotional experiences and the ways she copes with uncomfortable emotions. In this case, Marianne is experiencing very low self-esteem and intense self- criticism whenever she begins the process of looking for a job. The therapist is able to gather information about some of Marianne’s negative automatic apprais- als (e.g., Marianne’s belief that she is incompetent and not smart), anxiety-related physical sensations (e.g., a “pit” in her stomach and headaches), and maladaptive behaviors (e.g., worry, rumination, avoidance, procras- tination). The therapist is also able to elicit information about whether the patient’s current ways of responding to uncomfortable emotions are actually helpful. In this case, Marianne is aware that avoidance of looking for a job is not a solution to her difficulties, but she is so para- lyzed by emotion that she does not know what else to do.
Although the therapist spends a significant portion of the session reviewing Marianne’s presenting com- plaints and gathering additional information about her responses to emotions, this process will continue across the first several treatment sessions. As the thera- pist obtains more details about strategies (adaptive or maladaptive) for managing emotions, emotional or situational avoidance, and engagement in EDBs, this is then integrated into the patient’s UP Case Concep-
Emotional Disorders 239
tualization Worksheet, and the treatment plan may be adjusted accordingly.
Module 1: Setting Goals and Maintaining Motivation
This module focuses on achieving the goals of prepar- ing and developing each patient’s willingness to make identified behavioral changes, based on the MI princi- pals and techniques developed by Miller and Rollnick (2013). Specifically, the principles of (1) expressing empathy, (2) developing discrepancy, (3) rolling with resistance, and (4) supporting self-efficacy are used in this module and throughout the course of treatment to support behavior change. In this module, the therapist explores motivational issues with the patient through exercises designed to build motivation (through the Decisional Balance Worksheet) and to enhance self- efficacy (using the Treatment Goals Form). The aim of these exercises is both to highlight potential obstacles to change and to identify the patient’s top problems and specific, concrete goals, respectively.
THERAPIST: Let’s take a look at your Treatment Goals Form. We filled out some of this in our last session, and you were going to keep working on it at home. I remember we specifically talked about your top problems last time, which you identified as “I can’t find a job” and “I don’t have many friends.” What concrete goals did you identify for the problem of “I can’t find a job”?
MARIANNE: Well, one goal is to actively look for jobs. This could mean looking on the internet or reaching out to previous co-workers. Another goal would be to actually apply to jobs that seem to match my skills.
THERAPIST: That’s great! Those are two good goals to help you work toward this top problem. What steps did you come up with for each?
MARIANNE: For the goal of looking for jobs, one pos- sibility would be to reach out to previous coworkers and bosses to let them know I’m on the job market, but I’ll need to update my resumé. I guess that could be another step, too. I can also look on the Internet. But I already know I should be doing that—it’s just that I can’t do it!
THERAPIST: Absolutely. If you could just do these steps on your own, you would have done them! But it’s still helpful for us to write them down so that we can refer back to them later on in treatment and to make sure
you and I are on the same page about what you are working toward. That way, I can better help you get there. What are the concrete goals you had for your other top problem of “I don’t have many friends.”
MARIANNE: I don’t know. I really couldn’t come up with anything. Maybe a goal of having more friends?
THERAPIST: Yes, it does sound like having more friends is the outcome you want, but let’s try to stay focused on something clear and concrete that has to do with your own behavior. How about a goal of developing closer relationships with the friends you have?
MARIANNE: Yes, I suppose that would be a good goal. And maybe another goal would be to work on meet- ing new people.
THERAPIST: That’s great. What are some steps for each of those goals? Remember, you’re not expected to be able to take those steps right now.
MARIANNE: One step for trying to have closer relation- ships with my existing friends would be to actually participate in their weekly potluck dinners. I don’t like to go to those, because everyone always asks whether I’ve found a new job. But I think they do have a lot of fun at those dinners and maybe they would bring us closer.
THERAPIST: OK, that’s a good step for that goal. What about for the other goal of meeting new people?
MARIANNE: I suppose I could join some sort of club or group activity of some kind.
THERAPIST: That’s a very good idea. OK, now that you have the hang of this, can you work on some addi- tional steps for these goals over the next week?
MARIANNE: Yeah, I could do that.
Module 2: Understanding Emotions
Understanding Your Emotions: What Is an Emotion?
The therapist begins this module by providing psycho- education about the nature of emotions and how they become disordered. It is important to highlight the functional, adaptive nature of emotions at the onset of this discussion for two reasons: (1) so the patient can understand why he/she would not simply want to elimi- nate emotions and (2) to explore the potentially impor- tant information provided by adaptive emotions.
Next, the three-component model of emotional ex- periences is described as a framework for examining emotions by dividing them into components (cognitive,
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physiological, and behavioral), thereby making them more manageable. The therapist guides the patient in identifying each component in a relevant personal ex- ample and presents the model as the structural basis for treatment. Each component is addressed over the course of treatment as contributing to the overall emo- tion and interacting with the other components. For homework in this section of the module, the patient is asked to complete a three-component model example in which he/she is asked to break down an emotion from the week into the three-component model presented in session, by recording the thoughts, behaviors, and physiological sensations specific to that example.
THERAPIST: When they are functioning in an adaptive way, emotions give us some really helpful informa- tion about the environment. Anxiety lets us know when there could be a possible threat—it makes us “hypervigilant” (or hyperaware) of our surround- ings. This is good, because then we can be prepared if we might be in a dangerous situation. Anger lets us know when we’ve been wronged in some way and encourages us to either get back something that was taken from us by attacking or to defend ourselves. So, when functioning adaptively, all of our emotions are really important to our survival, and that’s why we would not want to get rid of them. But it’s pos- sible for our emotions to start becoming maladap- tive, meaning they are happening too frequently or intensely or in situations that don’t warrant the emo- tion. Because an emotion can also trigger all sorts of associated thoughts, memories, physical sensations, and behaviors, often from other experiences in our lives, we can get overwhelmed and caught up in our emotional responses. It feels like something we can’t cope with, that we have to get away from. So, the sadness you feel about losing your job isn’t function- ing as a helpful way to let you know that you’ve lost something that is important to you and motivating you to change the situation, which is, at its core, the adaptive function of sadness. Instead, the sadness can trigger anxiety and become paralyzing, not let- ting you take the right steps to move forward.
MARIANNE: I guess that’s true, but I don’t feel very sad about losing that particular job. It was OK, but I was thinking of leaving it in a year or two anyway.
THERAPIST: Yes, but I wonder if there is sadness about something else? Maybe not the loss of this specific job, but maybe you felt a sense of rejection? The rea-
son I say that is because I think anyone would feel that to some degree in this situation. It’s natural and adaptive to want to be accepted by others, so feeling rejected can make us sad. But for you, that feeling of rejection and sadness might be associated with many other thoughts and feelings from your life experienc- es, so it quickly becomes overwhelming and intoler- able. So, to help us better understand exactly what’s going on, we need to break down these emotional experiences into their component parts to help make them less overwhelming, and to help us identify how an emotion like sadness goes from something adaptive and useful to something that makes you “paralyzed.” As I mentioned, emotional experiences are made up of three main parts: thoughts, physi- cal sensations, and behaviors. What we need to do is help you recognize each of these parts, to make you a better observer of your emotional experiences. Then, throughout treatment, we’ll take a closer look at each of these components individually, to see how specific thoughts, feelings or physical sensations, and behav- iors might be influencing your overall experience and causing the experience to go from something helpful and useful to something uncomfortable and unwanted.
Understanding Your Emotions: Following the ARC
An important step to gaining greater understanding of emotional experiences involves more closely monitoring when, where, and why the emotions are occurring. This is done through illustration of the ARC of emotions. In this illustration, it is critical that the therapist clearly work through an example with the patient, particu- larly short- and long-term consequences of emotional responding. Consequences are often negative, but it is important that the therapist point out potential positive consequences of emotional responding (e.g., reduction in anxiety after escaping a difficult situation), as this process of negative reinforcement is usually maintain- ing the cycle of emotions. The positive experiences are typically short term, and negative outcomes are usually experienced in the longer term.
Expanding on this discussion, the therapist now in- troduces the concept of learned behaviors, essentially focusing on how the patient has learned responses to emotions that are usually an attempt to manage or con- trol the emotions and may briefly lead to feeling better, but often end up leading the patient to feeling worse. Habitually responding to emotions prevents any new
Emotional Disorders 241
learning from taking place (i.e., that a situation is not as dangerous as it appears during the experience of a panic attack) and disables the patient from developing a way of coping. It also undermines the patient’s sense of self- efficacy for dealing with negative emotions. This entire process is what makes adaptive emotions and emotional responses maladaptive. Yet knowing that the habitual responses provide some relief, even minimally, can help the patient understand why he/she continues to engage in the behaviors.
Module 3: Mindful Emotion Awareness
The goal of this module is to introduce the patient to the concept of mindful emotion awareness and begin developing a regular practice of this skill. The thera- pist must convey that the mindful emotion awareness skill is different than the patient’s current awareness of his/her emotions. This skill allows the patient to see an emotion from an objective and nonjudgmental perspec- tive in order to better identify and alter maladaptive thoughts and behaviors, and process the emotion more fully instead of avoiding it. During this introduction, the therapist reviews the concept of nonjudgmental emo- tion awareness. The therapist discusses how it is easy to judge and critique emotional experiences, either by tell- ing oneself that one “should” or “shouldn’t” be feeling certain emotions or by holding on to beliefs that cer- tain thoughts or emotions are “bad” or “harmful.” Both of these approaches are associated with being anxious about emotions, which makes the patient want to sup- press or avoid those emotional experiences. As discussed in the previous module and in more detail in Module 5, trying to control emotions in this way is precisely what leads to emotions becoming increasingly maladaptive. Nonjudgmental emotion awareness focuses on accep- tance of emotions as they come and go, regardless of the quality or intensity of the emotion. It’s taking a “hands-off” approach to emotional experiences in an effort to interrupt the cycle of emotional avoidance and maladaptive emotions. The therapist must also com- municate to the patient that this is not an endorsement of “giving up” or accepting that he/she will always feel depressed or anxious. Rather, it is an effort to gain more control and confidence by observing emotions instead of reacting to them.
The next component of mindful emotion awareness is present-focused emotion awareness, which is the skill of repeatedly bringing attention back to the present mo- ment and to what is happening in the “here and now” as
opposed to allowing thoughts to focus on past experi- ences or future concerns. Learning to stay in the pres- ent moment can also be very helpful for determining the most adaptive responses to a situation, as well as make it more manageable. Also, focusing on the pres- ent moment can be helpful for connecting with positive emotions, with which many patients may struggle. This new approach to emotions is likely very different from how the patient typically experiences emotions, so de- veloping this skill takes practice.
When practicing mindful emotion awareness, it is important that the therapist remind the patient of sev- eral points. First, this type of practice may feel awk- ward or uncomfortable at first. The goal is not to be “perfect” at the exercise; rather, the patient should focus on becoming an objective observer of emotional experience and start developing the ability to pay at- tention mindfully and in the moment. It is also natu- ral for patients to judge or criticize their experiences during this practice, possibly because they find it dif- ficult to stay focused or remain calm. The mind being judgmental is a natural process, and the value of the exercise comes from the simple act of practicing it, not from feeling calm or staying focused. The goal is the behavior of practicing, not having a specific experience during the practice.
Mindful Emotion Awareness Meditation
Developing the skill of mindful emotion awareness typically begins with the practice of a formal medita- tion exercise. In session, the therapist can read the script detailed in the protocol. The patient may choose to au- dio-record this reading or read the script at home and audio-record it for practice during the week.
Mindful Mood Induction
After the patient has had a chance to practice the mind- ful emotion awareness skill during a formal medita- tion, the next practice involves using the skill to notice slightly stronger emotional experiences. It is often help- ful to have the patient identify a salient piece of music to listen to in session; otherwise, the therapist can select a piece of music. At the conclusion of the music, the therapist helps the patient elicit thoughts, feelings, or other reactions, and practice discussing this experience in an objective and nonjudgmental way. The following excerpt describes Marianne’s reaction to listening to a piece of music:
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THERAPIST: What did you notice when you were listen- ing to the music?
MARIANNE: I noticed that I thought of a friend I had when I was in college. I remembered what it was like to spend time together. Then I thought of all the job applications I should be working on right now and how successful my friends are. I couldn’t stay focused on the music.
THERAPIST: It sounds like you were able to notice a number of different thoughts during this exercise, and your mind seemed to jump from one topic to another. Since the goal of this exercise is to practice observing, just noticing your thoughts have taken you somewhere else, even after it has already hap- pened, counts. What about physical sensations—did you notice any of those?
MARIANNE: No, I didn’t notice any physical sensa- tions. I just felt how I usually feel.
THERAPIST: I was observing you a bit, and I did notice that, at one point, both your fists were clenched. Did you notice that?
MARIANNE: No, I didn’t realize that. But now that you say it, I also notice that my jaw feels tight and hurts.
THERAPIST: And what about behaviors? Did you notice any behaviors, or any urges to do something?
MARIANNE: Well, I noticed a couple of times just feeling uncomfortable and sort of wanting to move around.
THERAPIST: And what about the music itself? Were you able to notice the music itself?
MARIANNE: I think I was more lost in my head. But there was one moment where I thought of my sister. Some parts of the music reminded me of some songs she liked.
THERAPIST: This is what our emotions can do. An emotion can trigger all sorts of associated thoughts, feelings, and behaviors that may have very little to do with what is happening “in the room,” yet the initial- ly triggered emotion itself is connected to something occurring in the present moment, just like the music you were listening to, which was really just sounds happening in the present moment. Getting better at observing our reactions to the trigger (in this case, the music), can help us to see how many of our asso- ciated thoughts, feelings, and behaviors actually “fit” with the current context, and how many of them are
just associations, which may or may not fit the cur- rent context at all.
Anchoring in the Present
Informal mindful emotion awareness practice is also a useful skill for the patient to practice, as this can be used at any time. The therapist can help the patient find a “cue” (e.g., the breath) to shift focus to the pres- ent moment, particularly in times of distress. The goal of this more informal practice is repeatedly to pair the patient’s chosen cue with a shift in attention and aware- ness to the present moment, by focusing on a sight, sound, or other sensation, so that engaging this cue will eventually be automatically paired with present- moment awareness. It is important for the therapist to note that the breath (or other cue) should not be used as distraction—it should only be used as a cue to re- mind the patient to be mindful of the present moment. Eventually, once the patient has successfully associated this cue with refocusing on the present moment, the patient can learn to follow this with a brief “three-point check” of thoughts, physical sensations, and behaviors. By observing what is occurring in the moment within these three domains, the patient can begin to identify how responses in any of these domains may be affecting the overall emotional experience, to compare what is happening in these domains with information from the current context, and ultimately to identify and alter any maladaptive patterns of responding.
Module 4: Cognitive Flexibility
Cognitive appraisal first involves discussing the concept that interpretations depend, in large part, on which of the numerous aspects (or stimuli) a person chooses to focus on in any given situation. Focusing only on limit- ed or specific aspects of a situation is critical for our sur- vival. We would be overwhelmed by information if we focused on all stimuli wherever we went. This process helps us quickly evaluate situations for risk and danger, allows us to estimate what might happen in the future, and usually happens outside of awareness. Importantly, the information we focus on and what we perceive as risky or dangerous tends to be the result of learned as- sociations between specific information or stimuli and the affective or threat value of those stimuli. For exam- ple, if negative evaluation by others has been associated with threat in the past, an increase in vigilance for nega-
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tive evaluation may result. Importantly, appraisals can have a powerful impact on our feelings or mood states, and vice versa. The therapist can illustrate this concept by inquiring how appraisals might vary depending on whether the patient was feeling joyful, sad, or angry.
An in-session exercise is used to demonstrate the many possible different appraisals that can be gener- ated from a situation. The therapist shows the patient an “ambiguous” picture to which many cognitive ap- praisals can be assigned, instructs the patient to look at the picture for approximately 30 seconds, then elicits both the patient’s initial appraisal and at least two or three alternative appraisals. Additionally, the patient is asked what specifically may have contributed to the au- tomatic appraisal (e.g., memories of similar situations, specific details in the picture). This exercise is used to demonstrate the way that situations can be interpreted in many ways, if all available information is considered.
Automatic appraisals, interpretations of situations that happen very quickly, are often negative or pes- simistic in nature. Core automatic appraisals (e.g., “I am a failure”) are appraisals that may be driving many emotional responses. It is helpful if the therapist can identify one or more core automatic appraisals by using the downward arrow technique instead of focusing only on surface-level appraisals related to a specific situation.
Automatic appraisals can lead to a habitual and pow- erful heuristic that begins to exclude other, possibly more appropriate or realistic appraisals of a situation or event. These automatic appraisals are called “thinking traps,” because, over time, a patient may get “stuck” in this way of thinking. As described earlier, two common thinking traps, probability overestimation (jumping to conclusions), or the tendency to assume a high likeli- hood of the occurrence of a negative event, and cata- strophizing (thinking the worst), or assuming that the consequences of an event will be beyond one’s ability to cope, are presented as two cognitive biases common to all emotional disorders. The therapist guides the patient in beginning to identify these biases in the context of his/her experience. Below, the therapist discusses both of these cognitive biases based on a recent situation in which Marianne felt rejected by a friend.
THERAPIST: Tell me what happened when you felt like your friend was ignoring you.
MARIANNE: Well, I had tentatively made plans with my friend Carly to go to the movies. This is pretty
unusual for me, because I hardly ever want to go out, but there was a movie playing locally and Carly asked me to go.
THERAPIST: And what happened next? MARIANNE: I hadn’t talked to her for a while, so on the
day we were supposed to go, I texted her and asked her if we were still going. She didn’t get back to me until several hours later and said she was too busy with work, and asked if we could reschedule.
THERAPIST: Can you remember any of your thoughts at the time?
MARIANNE: Yeah, I remember thinking that it’s pretty clear she doesn’t want to spend time with me any- more. I haven’t been a good friend and, like all my relationships, I really screwed this up.
THERAPIST: You mentioned that you thought she didn’t want to spend time with you anymore—is this what she said?
MARIANNE: No, not exactly. But she canceled at the last minute with the excuse that she was busy with work.
THERAPIST: So you don’t think she was busy with work?
MARIANNE: Well, I don’t know. She did just start a new job and has some pretty crazy hours, but it still felt bad. Like I said, I always mess up my relation- ships.
THERAPIST: And what about the other people in your group of friends?
MARIANNE: Well, I don’t have a big group of friends— really just one or two other good friends. But I haven’t seen them in a while. In my group of coworkers from my previous job, we’re still friends but we don’t hang out very much.
THERAPIST: OK, so it sounds like you still have those relationships, but they’re not as close as you want them to be? Is that the same as “messing them up”?
MARIANNE: I guess not. THERAPIST: What evidence did you have to suggest
that you “mess up” your relationships? MARIANNE: Well, I mean, my dad and I don’t have
a great relationship. We’re not close at all, and we argue when we see each other.
THERAPIST: Yes, I remember you telling me that your relationship with your dad has been hard, often be-
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cause he is under the influence of alcohol and loses his temper. So, given this evidence, do you know for certain that you “mess up” all your relationships?
MARIANNE: Well, not for certain. THERAPIST: Exactly, because even though not all your
relationships are how you would like them to be, we don’t know for sure that it is you who caused that. In fact, it sounds like your friendships are good but maybe not as close as you want them to be, and your difficult relationship with your dad might at least in part be due to his alcohol use. So one possibility is that you caused all these problems in your relation- ships, but can you think of any other possibilities? If you were talking to someone who was expressing the same concerns as you, what would you say?
MARIANNE: I guess I would say that it’s not all your fault. Your friendships aren’t too bad, and your dad acts in a way that makes it hard for anyone to get along with him.
THERAPIST: So, how likely do you think that it is that you are the one who messed up all your relationships?
MARIANNE: I guess not very likely. A bunch of them aren’t even really messed up.
THERAPIST: But for you, at that moment when you felt your friend rejected you, how much did it feel like you ruined your relationships, on a scale of 0% meaning not at all to 100% meaning you’re absolutely certain.
MARIANNE: At that moment? I was convinced com- pletely. 100%.
THERAPIST: And sitting here now, how likely do you actually think it is that you ruined your relation- ships, using the same percentage scale?
MARIANNE: I don’t know, maybe 10%? THERAPIST: And at the time, what emotions were you
experiencing? MARIANNE: Sadness, shame, and maybe a little bit of
anger. THERAPIST: Can you remember any physical sensa-
tions? MARIANNE: My stomach dropped, and I remember
feeling a little nauseous. THERAPIST: So when you were experiencing sadness,
shame, and anger, and all of the associated physical sensations, the thoughts that came with that were that you had done something terribly wrong. And at the time, these thoughts felt like they were true.
Now, sitting here, without the experience of those emotions or the associated physical symptoms, how likely do those thoughts feel?
MARIANNE: Well, sitting here now, I can see how I might have jumped to conclusions a bit. And maybe catastrophized the situation, too.
The therapist discusses the importance of monitor- ing and recording automatic appraisals, in order to in- crease the patient’s awareness that these interpretations are occurring, and reminds the patient that using the present-focused awareness skills learned in the previ- ous module can help aid in this process—by anchoring in the present moment using the patient’s chosen cue (i.e., taking a deep breath and focusing attention on a sound or sensation occurring in the present moment), the patient can use the “three-point check” to observe what thoughts are occurring at that moment. The goal is to notice the thoughts, then, using information from the current situation, consider other possible interpreta- tions of what is occurring within the current context. In this way, the patient can more flexibly apply informa- tion from learned associations (i.e., memory) and infor- mation from the current context toward more adaptive appraisals.
As the patient begins to record automatic thoughts, the therapist can help him/her begin to identify pat- terns in the nature of those thoughts. The therapist provides guidance on identifying thinking traps and tries to focus the patient’s attention on the “core” ap- praisal through the use of “downward arrow” Socratic questioning. The excerpt below is from a discussion of Marianne’s fears of not being qualified to find another job.
THERAPIST: You’ve talked about how you are concerned that you are not qualified to find another job. What specifically concerns you about your qualifications?
MARIANNE: I just don’t have as much experience as some other people. I was only in management for a few years, and then my company let me go. I clearly wasn’t as valuable as some other people, so I must not have what it takes to have a good job like that.
THERAPIST: And what concerns you about not “having what it takes”?
MARIANNE: Well, I just think that I don’t have the skills and inherent abilities to be successful at a good job. I’ll just be stuck in a dead-end position for the rest of my life.
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THERAPIST: And then what will happen? MARIANNE: I won’t be successful, and I’ll be unhappy
forever. THERAPIST: And what does that mean? MARIANNE: That I’m just useless. That there is some-
thing really wrong with me that I won’t ever be able to change.
THERAPIST: Now that is what we want, the real core of it, what is driving this interpretation. A lot of these negative, self-critical thoughts you’ve recorded often do come down to the belief that there is something wrong with you. So you think, “If I lose my one job, that means my life will be miserable and will be an in- dicator that there is something wrong with me” or “If I do something to make a friend dislike me, it means I will never be able to have friends and will be proof that there is something wrong with me.” Of course, anyone would be constantly feeling badly if every time something did not go as planned or expected, it would be an indicator of his/her inherent deficiencies.
As demonstrated earlier, the therapist then engages the patient in a more detailed discussion of this core belief, focusing on flexible thinking. Countering prob- ability overestimation and decatastrophizing strategies are presented as a way to generate alternative thoughts and to place less focus on the core appraisal. Counter- ing probability estimation involves drawing on past evidence to examine how realistic the patient’s estima- tion is when experiencing an emotion. The therapist guides the patient in making concrete estimations and comparing the original estimation to a more realistic one. Decatastrophizing involves helping the patient to identify his/her ability to cope with the feared situation using past evidence and specific examples (e.g., similar experiences in the past). It is important to communicate that these strategies do not eliminate negative thoughts, but they provide greater flexibility and allow the pa- tient to gain perspective on the feared situations, using more accurate information as a guide rather than being caught up in overlearned automatic appraisals.
Module 5: Countering Emotional Behaviors
Emotional Behaviors
The therapist now introduces the concept of emotion- al behaviors, which are behaviors people engage in to manage emotions. As reviewed earlier, while engaging
in these responses can be harmful in the long term, they typically provide some short-term relief, which is why the behaviors are maintained. Types of emotional be- haviors, including overt avoidance (e.g., not going to an event), subtle behavioral avoidance (e.g., avoiding eye contact), cognitive avoidance (e.g., distraction), safety signals (e.g., carrying a water bottle), and EDBs (e.g., escape), are introduced. It is important that the patient understand why and how engaging in emotional behav- iors is problematic. The therapist explains that unhelp- ful emotional behaviors actually (1) prevent habituation to a feared stimulus, so that fear levels are maintained at a high or constant level while in contact with the stimu- lus; (2) interfere with the process of extinction, so that the conditioned association between the cue and fearful response is maintained instead of weakened; (3) prevent the patient from developing a sense of control or self-ef- ficacy in managing the fear, because positive outcomes are attributed to the avoidance strategy; and (4) actually signal to the person that the situation, context, or stimu- lus is dangerous and should be avoided. The therapist asks the patient to generate personally relevant examples of emotional behaviors and discusses how those strate- gies have maintained the cycle of emotions.
THERAPIST: We’re going to shift our focus now and look at how behavioral responses to emotions, what we call “emotional behaviors,” contribute to your emotional experiences. First, let’s talk about overt avoidance. Sometimes you might avoid doing things, like activities, because you anticipate the activity will make you feel uncomfortable. For example, you mentioned that sometimes your friends invite you to go out with them—either to dinner or for other so- cial activities—which triggers thoughts that you are not as successful and not as “good” as they are. Is that right?
MARIANNE: Yes, exactly. It’s really hard to spend time with them, because they start talking about all the great stuff they’re doing, like how their jobs and re- lationships are going so well. And then I just think of my own situation, and I feel terrible about myself.
THERAPIST: So then you avoid going out with them so you’re not confronted with these negative feelings about yourself. This is a good example of one of the ways we try to avoid uncomfortable emotions. There are also some behaviors that can be more subtle, things we aren’t even aware we are doing as an avoid- ance strategy, and this is called “subtle behavioral
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avoidance.” For example, someone who has panic at- tacks might avoid caffeine so he/she doesn’t have to feel the physical sensations of increased arousal. Can you think of any examples of more subtle ways you may be avoiding uncomfortable emotions?
MARIANNE: I guess that when I do spend time with them, I usually avoid talking about myself. I try to change the subject, because I don’t want to have to explain how bad things are for me.
THERAPIST: So you’re trying to avoid feeling even worse about yourself by not talking about your situation?
MARIANNE: Yes, exactly. I’m also trying to avoid feel- ing embarrassed in front of my friends.
THERAPIST: So you can see that we have subtle and more overt ways of avoiding uncomfortable emo- tions, but the question is, does it make the problem go away?
MARIANNE: Not really. When I don’t go out with my friends, I feel bad about not being a good friend. Plus I sit at home with nothing to do. If I do go out and I avoid talking about myself, I end up not feeling very close to any of them.
THERAPIST: So you can see that avoidance might make the problem go away in the short term, but in the long term, this strategy is not particularly helpful and may even make the situation worse. In fact, these avoidance behaviors can strengthen the association of fear and anxiety with these situations—the more you avoid seeing or talking with your friends, the harder and harder it gets!
Next, in-session exercises to demonstrate the effects of emotional avoidance are conducted. The first exer- cise involves asking the patient directly to suppress a memory of when he/she felt very embarrassed. Mari- anne, for example, had been actively trying not to think about a recent e-mail she sent to her former boss, asking if he would serve as a reference for a job application. She was worried that he would respond negatively to her e- mail and decline to serve as a reference. Marianne was asked to think about this memory of sending the e-mail for 30 seconds, then to think of anything other than the e-mail for 30 seconds. Predictably, Marianne found it extremely difficult to prevent ruminations about her boss’s potential responses from coming into her mind. Thus, this exercise presents a poignant and personally relevant demonstration of the futility of active attempts to avoid distressing topics or situations.
Of note, emotional behaviors can sometimes be dif- ficult to identify, and specific behaviors (e.g., escape, distraction) are not always considered unhelpful emo- tional behaviors. Rather, it depends on the function of the behavior for each patient. For example, patients may force themselves to stay in a situation when feel- ing angry, so that they do not feel as though they are “giving in.” In this situation, the emotional behavior is staying in the situation—it gives a feeling of control in the short-term but fuels anger in the long-term. So, es- caping may actually be a helpful way of responding. In the case of Marianne, even though distraction is often considered an unhelpful emotional behavior, it can ac- tually be adaptive and helpful if distraction allows her to prevent herself from getting “stuck” and ruminating about her inadequacies.
Alternative Action
The concept of alternative action is introduced next. Alternative action means engaging in any behavior other than the emotional behaviors, so that emotions that are typically avoided are instead experienced to the fullest. Doing alternative action instead of emotional behaviors provides new information about a situation and also strengthen the patient’s ability to cope with distress. Over time, the patient also begins feeling differently about the situation. In the transcript below, Marianne describes some examples of what alternative action could be for her.
THERAPIST: You mentioned that in the evenings, you often avoid activities because you have a headache. Can you tell me what that is like and what you are doing during that time?
MARIANNE: Yeah, often my head starts to hurt around 4:00 to 5:00 P.M. I feel a little tingling and then I just feel this immense pressure all over my head. At that point, I just feel like I need to lie down. So I usually just lie down in my bed for a while.
THERAPIST: And how do you feel, right when you de- cide to not go out and to lie down instead?
MARIANNE: I feel a bit of relief. Like I said, it’s hard for me to go out, and when I have a headache, it’s extra hard.
THERAPIST: So it sounds like you engage in overt avoid- ance when you feel a headache coming on?
MARIANNE: Yeah, I guess. But I’m just worried that if I
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do go out, my headache will get worse and I won’t be able to get home easily, and then I’ll feel really bad.
THERAPIST: So, do you end up feeling better staying at home and lying down?
MARIANNE: I mean, probably not. I end up just staring at my room, trying to sleep, and thinking about how I’ll never be able to do anything with my life. I guess I do feel pretty bad.
THERAPIST: OK, so let’s try to think of some alterna- tive actions you could do instead of lying down. Re- member, it won’t necessarily feel good right away to change your behavior, but it might help you feel a bit more empowered, even if your headache doesn’t go away. What else could you do?
MARIANNE: I could go out, even if just for a few min- utes.
THERAPIST: Yes, that’s right! Going out of your house doesn’t have to be for hours at a time. Even going out for a few minutes would be an alternative action that would start to break the cycle of emotional behav- iors. What else could you do?
MARIANNE: I could stay at home but not lie down. I could do something quiet, like make a nice dinner, or listen to music in my living room.
THERAPIST: Those are great examples! Alternative ac- tion isn’t just one behavior. It can be many different behaviors that are not the emotional behavior in that situation.
Module 6: Understanding and Confronting Physical Sensations
Module 6 introduces the first opportunity to engage in an exposure that focuses on eliciting physical sen- sations that often trigger strong emotional reactions, and to begin to build the patient’s awareness of the contribution of physical sensations to emotional expe- riences. Following an introduction to the rationale for provoking physical sensations, the therapist and patient work through a list of exercises designed to elicit emo- tion through physical activation, known as a Physical Sensation Test. Some examples include hyperventilat- ing, spinning, and running in place. In addition, any exercises that may be particularly relevant to the patient may be added. For example, in patients with depres- sion, a sense of “heaviness” can be induced by having the patient wear wrist or ankle weights while walking around, wearing a heavy backpack, or lying down with
a weight on his/her chest. Prior to each exercise, the therapist demonstrates the exercise and, following the patient’s completion of the exercise, asks the patient to rate the level of distress and similarity to physical sensa- tions typically experiences during an emotion, each on a scale of 0 (None) to 10 (Extreme).
THERAPIST: So today we’ll do a number of exercises to induce some of these physical sensations that are often present when you experience anxiety or other emotions, and look at the level of your distress, and how similar the sensations are to your typical experi- ence of uncomfortable emotions. The first one I’m going to ask you to do is the hyperventilation exer- cise. ( following the exercise) What sensations do you notice?
MARIANNE: I noticed that my heart started beating faster and I felt a bit dizzy. I found it pretty unpleas- ant.
THERAPIST: So you are having thoughts and judgments about the sensations, which we would expect. In terms of the sensations themselves, how would you rate your level of distress about those sensations?
MARIANNE: Maybe a 3? THERAPIST: And similarity? MARIANNE: Well, I don’t usually get dizzy, so not very
similar. Maybe a 2.
Next, the therapist begins another exercise. The dis- cussion below follows Marianne’s experience of breath- ing through a thin straw.
THERAPIST: How would you rate your distress this time?
MARIANNE: That was really scary and really intense. I would say a 9.
THERAPIST: What did you notice was different with this exercise?
MARIANNE: I don’t know. I just felt really trapped when I was trying to breathe through the thin straw. It might sound weird, but I just felt like I couldn’t get away. And then I started having all these negative thoughts about myself. I felt scared and sad.
THERAPIST: That is very interesting. So the sensations triggered other emotions and negative thoughts?
MARIANNE: Yes, definitely. I didn’t realize I would have that reaction.
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THERAPIST: OK, let’s try another exercise. This time, I want you to lie down on the floor here. I have a heavy book that I’m going to give you to place on your chest for as long as you can or until I tell you to stop.
MARIANNE: ( following the exercise) Wow, that was harder than I thought. The feeling I had was really similar to the heaviness I sometimes feel in my chest when I feel really depressed.
THERAPIST: So how would you rate the similarity on the 0–10 scale?
MARIANNE: I would say maybe an 8. THERAPIST: And how about the level of distress you
felt? MARIANNE: It was pretty high. I would rate that at a
9. That sensation just triggered a really strong feeling of hopelessness.
THERAPIST: That’s really interesting, and it’s great that we were able to trigger that emotional response by eliciting that physical sensation of heaviness. Do you notice how this was different from the other exercise?
MARIANNE: Yeah, exactly. They were both really un- comfortable but in completely different ways.
Following the completion of all the chosen exercises, therapist and patient choose the most relevant exercises to engage in regularly over the next week. The patient is asked to complete one exercise several times a day, until the associated distress decreases. This repeated exposure helps facilitate learning of new information about the dangerousness (or lack thereof) of physical sensations and may help diminish future distress when physical symptoms do occur.
Module 7: Emotion Exposures
This treatment module allows application of all the skills learned thus far to actual situations, events, or activities that trigger strong levels of emotions that the patient has previously avoided. The therapist begins with a discussion about the rationale for emotion ex- posures. Although this module in the treatment pro- gram is often the most challenging, it is the best op- portunity to make lasting behavioral and emotional changes. Emotion exposures serve three critical goals: (1) Interpretations and appraisals about the dangerous- ness of situations (internal or external) are modified and
replaced with newer, more adaptive interpretations and appraisals; (2) avoidance and related impairment is re- versed; and (3) emotional behaviors are recognized and modified. These all work toward achieving the primary goal of extinguishing anxious and distressing reactions to the experience of intense emotions.
In addition to engaging in emotion exposures for homework, an important part of this module is practic- ing emotion exposures in session. This is critical, be- cause the therapist can often challenge the patient to engage in more difficult exposures in session and will be able to note any use of emotional behaviors that may be outside the patient’s awareness. The particular in- session exposure tasks vary from patient to patient, and it is important that the therapist be able to generate a number of different possible tasks in which to engage. Once the task has been identified, the therapist can dis- cuss any anxious or negative automatic appraisals oc- curring and help the patient consider other possibilities. The therapist should also remind the patient to use the skills of present-focused awareness and try to prevent any emotional behaviors that would interfere with the exposure. At the end of each session, the therapist helps the patient choose several emotion exposures to engage in outside of session for homework.
For Marianne, several different exposures were de- signed to target her intense self-criticism and depres- sion. Examples included spending 15 minutes looking at job websites, scheduling social activities with friends, taking a walk around the block every day, gardening for at least 15 minutes one time per week, not canceling plans due to headache, and watching a sad movie and then engaging in an activity.
Described in the discussion below, an exposure near the top of Marianne’s hierarchy was to actually apply for a job. This would require her to engage in a num- ber of challenging situations. First, she would have to search for and identify a potential job that fit with her qualifications. However, for the purposes of the expo- sure, if she could not find an advertisement for a job that was directly relevant to her experience, it would still be useful to apply for any job. Second, she would have to write a cover letter detailing her experience and why she is a good fit for the job. Third, she would need to submit the application, which, due to its very nature, would lead to having another person evaluate her. The following is a review of this exposure at the following session.
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THERAPIST: Wow, this was a really challenging ex- posure. Let’s start from the beginning, when you searched for the job. Do you remember what you were experiencing just before you started that search on the Internet?
MARIANNE: Well, I did the actual search about a week ago. I felt a pit in my stomach and a real sense of dread. I felt tired and heavy.
THERAPIST: So, a lot of physical sensations associated with both depression and anxiety. What about when you actually submitted the application yesterday?
MARIANNE: It was the same feeling but just way worse. I was even shaking a little bit. I put off this exposure until yesterday, but then I knew I had to do it.
THERAPIST: Good! So you noticed some emotional behaviors but were eventually able to engage in al- ternative action by submitting the application. What types of thoughts were you having?
MARIANNE: I just kept thinking “There is no way I can do this.” I’ve thought about applying so many times, but I just have never been able to do it. And I also had the usual thoughts—“I’m useless, they will never hire me”—that kind of stuff.
THERAPIST: So, what happened when you filled out the application?
MARIANNE: I was just really nervous. It was hard to stay focused, and I kept getting up to get water. It helped that we had done some exposures before about what I would say in my application.
THERAPIST: That’s great. What did you take away from this experience?
MARIANNE: Well, it was really, really hard. But one thing I did think of is that I felt pretty much the same way when I first started searching for jobs a week ago, and compared to submitting the applica- tion, that seems so easy now!
THERAPIST: Did your automatic thought of “I can’t do this” come true?
MARIANNE: Well, no, I guess. I mean, I did it. I guess there is something to be said for that. But I still don’t know if they will hire me.
THERAPIST: That’s true. Sometimes our fears about what will happen in the future cannot be fully exam- ined, because it hasn’t happened yet. But what is your fear if you don’t get called for an interview?
MARIANNE: That I will fall back into a deep, deep de- pression.
THERAPIST: And if that did happen, how would you cope with it?
MARIANNE: I guess I would just keep doing what I’m doing. I’ve learned a lot of new skills I didn’t know before, and my friendships are getting a bit better, so I have a little more support. I guess if I was able to survive it once, I can survive it again.
This exposure was an important step for Marianne to start to reverse the cycle of emotional behaviors and introduce some flexibility in her responses to emotional situations. However, Marianne continued to maintain the core belief that she was “useless” and “incompe- tent.” Additional exposures were designed to target these beliefs directly.
THERAPIST: You seem like you have been making some important changes in your behaviors over last few weeks, would you agree?
MARIANNE: Yes, I agree that I have been trying to do that. But I still walk around and think that I’m to- tally worthless and useless.
THERAPIST: Yes, I’ve wondered about that. Can you tell me a little bit more about what your experience has been?
MARIANNE: Well, I’ve been able to force myself to do some of these exposures, but I’m just pushing myself through it. I still feel really badly about myself most of the time.
THERAPIST: I wonder how that affects your behav- ior during the exposures? Do you think getting stuck in that core belief is causing you to make subtle changes in how you are behaving during these ex- posures?
MARIANNE: I’m not sure. I notice I do get distracted when I start thinking about how useless I am.
THERAPIST: OK, that’s a great example. So, the emo- tional behavior would be getting distracted. What would the alternative action be?
MARIANNE: I guess staying involved in whatever ex- posure I’m doing? Using emotional awareness to ground in the present?
THERAPIST: Yes, that’s great. What other emotional be- haviors might you be doing in these situations?
250 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
MARIANNE: I think it’s possible that I hunch over, and I probably look like I’m worried. People have told me that before.
THERAPIST: Yes, body posture and facial expressions are also emotional behaviors. What would alterna- tives to these emotional behaviors be?
MARIANNE: I could try sitting up straight. And maybe trying to smile? But that seems really hard!
THERAPIST: Yes, I do think it will be challenging. These are some very ingrained emotional behaviors associated with anxiety and depression. And, this may be the best way to start to reverse this cycle— let’s give it a shot!
In future sessions, the therapist revisits the patient’s continuing need for emotional exposures. If the thera- pist determines that the patient would benefit from ad- ditional emotion exposures, they can be continued both in session and for homework at this time. Additionally, the therapist can focus on any events or emotional reac- tions over the past week that can be processed in ses- sion. Obstacles to exposure completion and reactions to exposures are discussed in session.
Module 8: Recognizing Accomplishments and Looking to the Future
In the final module of treatment, the therapist reviews both the major concepts presented in treatment and the patient’s progress. The therapist introduces the UP Skills Action Plan, which consists of using the “three- point check” learned earlier, then briefly reviewing all the skills learned in treatment, including cognitive flex- ibility, awareness and tolerance of physical sensations, and modifying emotional behaviors. Progress made over the course of treatment can be reviewed by exam- ining scores on the OASIS and ODSIS forms, as well as having the patient complete the Progress Evaluation. Using these measures, the therapist can highlight both areas of improvement and those in need of continued practice. Reasons for lack of improvement (e.g., initial error in conceptualization, lack of understanding treat- ment principles, unrealistic goals, and lack of motiva- tion) should also be reviewed. The therapist then dis- cusses the inevitability of future stressors and potential reoccurrence of symptoms. The continuation of infor- mal emotion exposures and use of skills learned are en- couraged and detailed in the Practice Plan, which the
patient and therapist can work on together in session to help identify concrete skills that will require ongoing practice. The therapist may further assist the patient in staying committed to treatment by establishing long- term goals for the patient.
CASE OUTCOME AND CONCLUSION
Marianne’s symptoms were assessed at pre- and post- treatment using a battery of self-report questionnaires, as described earlier. During treatment, Marianne’s BDI-II score decreased from 53 at pretreatment to 18 at posttreatment. Her PSWQ score decreased from 65 to 29. Her ODSIS and OASIS scores decreased from 18 and 12 to 9 and 4, respectively. Functionally, Marianne was able to meet many of her treatment goals over the course of treatment. For example, she was able to suc- cessfully apply for a job, a task at the top of her emotion exposure hierarchy that had previously been causing significant anxiety and reinforcing her negative be- liefs about herself. By approaching this task, Marianne gained a greater sense of confidence in her ability to use the skills learned in treatment and to cope through difficult situations. She significantly increased her so- cial interactions with friends, which increased her self- confidence and sense of self-worth, and she challenged her belief that she was “messing up” all of her friend- ships. She gained control of her headache symptoms and no longer engaged in avoidance behaviors related to her symptoms. At the time of termination, Marianne had not yet been hired for a job, but she expressed a sense of hopefulness with regard to several prospective employers. She was in contact with previous cowork- ers, both socially and professionally. Marianne did not participate in an independent posttreatment clinical in- terview; however, her clinician (L. A. P.) estimated that her CSR for MDD was now at a 3, which is considered subclinical. The diagnosis of persistent depressive disor- der remained at a 4, which is considered just above clin- ical severity with moderate symptoms. Additionally, she reported fewer headaches, although she noted that they were still frequent enough to cause some interference in her activities.
Marianne returned to our Center for a follow-up assessment 6 months posttreatment that comprised re- administration of the ADIS-5 and self-report question- naires. At follow-up, Marianne had improved signifi- cantly even from posttreatment. During her interview,
Emotional Disorders 251
Marianne reported that she had recently been hired at a start-up biotech company. She had also started dating, and despite having some anxiety about meeting people, she felt positively about the process. Clinician ratings using the ADIS-5 seemed largely to coincide with Mari- anne’s self-report. Having not experienced clinical lev- els of depression or anxiety for more than 5 months, the diagnosis of persistent depressive disorder was now con- sidered in partial remission with subclinical symptoms (CSR = 3). Symptoms of MDD were no longer evident, and residual depressive symptoms were captured in the persistent depressive disorder diagnosis.
With regard to self-report questionnaires, Mari- anne’s BDI-II score was now 10, and her score on the PSWQ was 20, reflective of a mild amount of anxi- ety and worry. Her ODSIS score was now 9, and her OASIS score remained at a 4. These questionnaires re- flected her report of substantially improved symptoms, both on long- and short-term levels. Although she still experienced residual symptoms of depression, she was able to successfully manage them, so that they no lon- ger caused significant interference in her life.
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One of the most important developments in psychological approaches to emotional problems has been the success of cognitive therapy for depression. Evidence for the powerful efficacy of this ap- proach has increased steadily over the years, particularly in regard to successful long-term outcome. Employing a variety of well-specified cognitive and behavioral techniques, cognitive therapy is also distinguished by the detailed structure of each session, with its specific agendas, and the very de- liberate and obviously effective therapeutic style of interacting with the patient through a series of questions (Socratic style). Moreover, the authors underscore very clearly the importance of a col- laborative relationship between therapist and patient, and outline specific techniques to achieve this collaborative state, so that patient and therapist become an investigative team. In this chapter, the authors cover not only traditional cognitive therapy but also an expansion of cognitive therapy called “schema-focused” therapy. This approach concentrates on identifying and modifying early maladaptive or “core” schemas thought to develop during childhood in more severely depressed and treatment-resistant patients, often with comorbid personality disorders that may make the patient vul- nerable to relapse. Detailed explication of this expanded treatment will be invaluable to experienced cognitive therapists, as well as to those becoming acquainted with cognitive therapy for depression for the first time. Two compelling cases—“Denise,” treated with traditional cognitive therapy, and “Barbara,” treated with schema-focused therapy—illustrate each approach. —D. H. B.
Depression is one of the most common disorders en- countered by mental health professionals. Research
from the National Epidemiologic Survey on Alcohol and Related Conditions–III (NESARC-III; Hasin et al., 2018), the Centers for Disease Control and Preven- tion (CDC; 2010), the Substance Abuse and Mental Health Services Administration (SAMHSA; 2008; 2019), and the World Health Organization (WHO; 2017, 2020) indicate the following:
• The lifetime prevalence estimate for major de- pressive disorder in adults in the United States is 20.6% (Hasin et al., 2018).
• The 12-month prevalence estimate for major de- pressive disorder in the United States is 10.4% (Hasin et al., 2018).
• Across countries and cultures, the lifetime preva- lence estimates for major depressive disorder are 14.6% in high-income and 11.1% in low- to mid- dle-income countries; the 12-month prevalence estimates are 5.5% in high-income and 5.9% low- to middle-income countries (Kessler & Bromet, 2013). Additionally, the number of people living with depression worldwide increased by 18.4% be- tween 2005 and 2015 (WHO, 2017).
• Among adults ages 18 or older, major depressive
C H A P T E R 7
Cognitive Therapy for Depression
Jeffrey E. Young Erin F. Ward‑Ciesielski Jayne L. Rygh Arthur D. Weinberger Aaron T. Beck
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episodes in the United States are associated with higher rates of substance dependence or abuse (21.5%) compared to those without major depres sive episodes (8.2%; SAMHSA, 2008) and youth ages 12–17 exhibit a similar pattern, in which substance use is more common among those with versus those without major depressive episodes (32.7% vs. 14.0%; SAMHSA, 2019).
• Depression increases the risk of heart attacks and is more common in those with chronic conditions such as obesity, diabetes, cardiovascular disease, cancer, asthma, and arthritis (Chapman, Perry, & Strine, 2005; Strine et al., 2008).
• Major depressive disorder in the United States is associated with 27.2 lost workdays and bipolar dis order (I or II) with 65.5 lost workdays for each ill worker per year (Kessler et al., 2006).
• Major depressive disorder is the leading cause of disability in the United States for people ages 15–44 (Friedrich, 2017), and is a major contribu tor to the global burden of disease (GBD) (WHO, 2020; GBD 2017 Disease and Injury Incidence and Prevalence Collaborators, 2018).
The high risk of relapse (Forte et al., 2015), high resource utilization (e.g., Howland, 1993; Tusa et al., 2019), and loss of human capital (Berndt et al., 2000) associated with depression reveal the seriousness of the problem. The WHO (2004) projects that depression will be among the top three causes of the total number of years of life lost to illness, disability, or premature death by 2030. As these reports indicate, depression is widespread, debilitating, costly, and potentially devas tating.
No amount of data can adequately capture or convey the personal pain and suffering experienced in depres sion. Many depressed people do not get professional help (e.g., Kohn, Saxena, Levav, & Saraceno, 2004; Wang et al., 2005), and although the number seeking help continues to increase, undertreatment remains a se rious problem (Olfson, Blanco, & Marcus, 2016; Wang et al., 2005). The cost and/or lack of sufficient coverage by health insurance companies, concerns about confi dentiality, continued social stigma, low perceived need for help or the desire to handle the problem alone, and the lack of information regarding where to go and what type of services to obtain are still obstacles to receiving appropriate and adequate mental health services (Moj tabai et al., 2011; SAMHSA, 2008). Obtaining the right type of help can be at once inhibiting and over
whelming, especially to those already impaired. The following quote remains relevant today:
Americans who do seek treatment for depressive symp toms must decide where to seek which treatment and from what type of practitioner. . . . The clinician must select a somatic, psychological, or combination of treatment, at a given dose and/or schedule of appointments. . . . Throughout this procedure, the patient decides to what extent he/she will comply with the recommendations, for how long, against recognized and unrecognized econom ic, practical, physical, and emotional costs. . . . Sadly, the lack of information as well as the continued social stigma of psychiatric illness and treatment influence de cisionmaking. Simultaneously, the decisions occur in an environment filled with social, political, and economic debate, and tension among policy makers, thirdparty payers, and clinicians, as well as among different types of practitioner guilds. (Jarrett, 1995, p. 435)
When care is provided, it is frequently inadequate or minimally adequate (Wang et al., 2005), which can leave depressed individuals feeling frustrated, hopeless, or anxious (Mago, Fagiolini, Weiller, & Weiss, 2018). Evidencedbased treatments have not been widely ad opted in clinical practice (Wiltsey Stirman et al., 2012), reflecting a public health crisis (Keller & Boland, 1998). The need for delivery of treatments with proven and rapid efficacy remains paramount.
One of the major developments in the treatment of depression has been the emergence of cognitive therapy, which has expanded exponentially since A. T. Beck’s publication of a detailed treatment manual for depres sion in 1979 (Beck, 1967, 1976; Beck, Rush, Shaw, & Emery, 1979). The work of Beck and his colleagues led to a paradigm shift within psychotherapy (Salkov skis, 1996). Due in part to Beck’s development of testable hypotheses and clinical protocols, cognitive therapy has received an enormous amount of professional attention (Hollon, 1998; McGinn & Young, 1996; Rehm, 1990). Of all the cognitivebehavioral treatment approaches to depression, Beck’s paradigm (Beck, 1967; Beck et al., 1979) has received the greatest amount of empiri cal study, validation, and clinical application (Barlow & Hofmann, 1997; de Oliveira, 1998; Dobson, 2016; Dobson & Pusch, 1993; Hollon, 1998; Hollon, Thase, & Markowitz, 2002; Jarrett & Thase, 2010; Rehm, 1990; Roberts & Hartlage, 1996; Scott, 1996; Vittengl, Clark, Dunn, & Jarrett, 2007). Cognitive therapy has become the treatment of choice for many disorders (e.g., Clark & Beck, 2010; Newman, Leahy, Beck, Reilly
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Harrington, & Gyulai, 2002). There are many excel lent books for practitioners who teach cognitive therapy procedures (e.g., J. S. Beck, 2021), as well as workbooks and/or guides for clients (e.g., Fox & Sokol, 2011; Gil son, Freeman, Yates, & Freeman, 2009; Leahy, 2011; Wright & McCray, 2011).
Along with this attention, however, has come confu sion about what is actually meant by the term cogni- tive therapy. The actual cognitive therapeutic strategies employed in “cognitive” treatments may differ in many ways from one another and from those explicitly pre scribed by Beck and colleagues (1979) in their manual for cognitive therapy of depression. Thus, the reader should be aware that common use of the term cognitive therapy does not necessarily imply uniformity in proce dures. The therapy described by Beck and colleagues involves the use of both cognitive and behavioral tech niques, and can therefore be accurately labeled cogni- tive-behavioral; however, in the literature, both terms have been applied in describing Beck and colleagues’ procedures, with some articles utilizing the term cogni- tive therapy (Sacco & Beck, 1995, p. 345).
RESEARCH ON TREATMENT OF THE ACUTE PHASE
Outcome research has found cognitive therapy to be effective with clinical populations in numerous con trolled trials (see reviews by Beck & Alford, 2009; Dobson, 2016; Hollon & Shelton, 2001). Although some early studies (Blackburn, Bishop, Glen, Whal ley, & Christie, 1981; Rush, Beck, Kovacs, & Hollon, 1977) suggested that cognitive therapy may be superior to drug treatment for depression at termination, Me terissian and Bradwejn (1989) noted that psychophar macological interventions often were not adequately implemented. In research in which interventions were adequate, cognitive therapy generally was shown to be equivalent in efficacy to antidepressant medica tions, including tricyclic antidepressants (TCAs) and selective serotonin reuptake inhibitors (SSRIs) in the treatment of outpatients with nonbipolar depression (DeRubeis et al., 2005; Hollon et al., 1992; Murphy, Simmons, Wetzel, & Lustman, 1984) and a mono amine oxidase inhibitor (MAOI) in the treatment of outpatients with atypical depression (Jarrett et al., 1999). Furthermore, Cuijpers and colleagues (2013) found no significant overall differences between cog nitivebehavioral therapy (CBT) and pharmacotherapy
across 20 trials. And in a recent metaanalysis of in dividual patientlevel data from trials comparing CBT to antidepressants (Weitz et al., 2015), although scores on a clinician administered depression measure (i.e., Hamilton Rating Scale for Depression) were signifi cantly more affected by antidepressants than by CBT, there were no differences in rates of response to treat ment or remission between treatments.
Although some reviews have reported that combined psychotherapy and pharmacotherapy is superior to ei ther treatment alone for depressed outpatients (e.g., Friedman et al., 2004; Pampallona, Bollini, Tibalbi, Kupelnick, & Munizza, 2004), several researchers have not found this effect in trials comparing combined CBT and medications to their component parts (Biggs & Rush, 1999; Evans et al., 1992; Hollon, Shelton, & Loosen, 1991; Scott, 1996; Shaw & Segal, 1999). No tably, in their metaanalysis, Cuijpers and colleagues (2013) found that CBT plus pharmacotherapy signifi cantly outperformed pharmacotherapy alone across the 11 relevant trials included. The increment in efficacy appears to be modest in the acute phase of treatment at best, with increases in efficacy from 10 to 20% (Conte, Plutchik, Wild, & Karasu, 1986). Specific studies re garding treatment with depressed inpatients also sug gest beneficial results when CBT is combined with medication (Cuijpers et al., 2011; Stuart & Bowers, 1995; Wright, 1996). Although cognitive therapy ap pears to be a useful adjunct to standard care with in patients, it remains unclear whether cognitive therapy alone is sufficient (Boschloo et al., 2019; Cuijpers et al., 2011; Hollon et al., 2002).
Although many studies comparing CBT to pharma cotherapy have not included pillplacebo conditions, the studies by Jarrett and colleagues (1999) and De Rubeis and colleagues (2005) found the active treat ments superior to pillplacebo. Importantly, only two studies that included a pillplacebo found cognitive therapy to be less effective than psychopharmacologi cal intervention. The first was the National Institute of Mental Health (NIMH) Treatment of Depression Collaborative Research Program (TDCRP) with mod erate to severe depression in adults. The second was the multisite Treatment for Adolescents with Depression Study (TADS) for reduction of depressive symptoms in adolescents.
The NIMH TDCRP was the first major study to include a pillplacebo condition. The initial results of the TDCRP (Elkin et al., 1989) suggested lower rates of improvement with CBT than did earlier studies. It
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also appeared that with more severely depressed patient groups, interpersonal psychotherapy and antidepressant drugs might be superior to CBT. The high visibility and prestige of the NIMH TDCRP study generated a great deal of debate (Hollon, DeRubeis, & Evans, 1996; Wolpe, 1993), because it appeared that the benefits of CBT in the acute treatment phase might have been overestimated in previous studies. However, on later ex- amination of the data, Elkin, Gibbons, Shea, and Shaw (1996) acknowledged Jacobson and Hollon’s (1996) ob- servation that the outcome results varied across sites, with cognitive therapy performing as well as medication at one of the three sites with severely depressed clients. Jacobson and Hollon noted that the best results were obtained at the site with the most experienced thera- pists. Hollon and colleagues (2002, p. 62) “suspect that the explanation is not that cognitive therapy cannot be effective with such patients, but that the therapist’s ex- pertise makes a greater difference the more difficult the depression is to treat.” Additionally, a study by Albon and Jones (2003) raised the question of the distinctive- ness of the two types of psychotherapy treatments in the TDCRP. Albon and Jones, expert therapists in CBT and interpersonal psychotherapy, respectively, devel- oped prototypes of ideal regimens of their own respec- tive treatments. Then, actual transcripts of treatment sessions from the TDCRP were compared to these ex- pert prototypes. Albon and Jones found that both CBT and interpersonal psychotherapy sessions conformed most closely to the cognitive-behavioral prototype, and that closer adherence to the cognitive-behavioral pro- totype produced more positive correlations with out- come measures across both types of treatment. Perhaps this is why Quilty, McBride, and Bagby (2008) found equivalent outcomes with interpersonal psychotherapy, CBT, and pharmacotherapy, and Peeters and colleagues (2013) found similar remission rates with CBT, inter- personal psychotherapy, and both treatments combined with medication. Similarly, Luty and colleagues (2007) found interpersonal psychotherapy and CBT equally effective overall but (in contrast to the NIMH TDCRP study) they found CBT to be more effective with se- vere depression. This is further supported by a recent meta-analysis of CBT for unipolar depression, in which Johnsen and Friborg (2015) found that experienced providers achieved better results than less experienced therapists.
In further analysis of the same dataset used in the Luty and colleagues (2007) study, Joyce and colleagues (2007) found that comorbidity of personality and major
depressive disorders adversely affected the treatment re- sponse to interpersonal psychotherapy but not CBT. Bellino, Zizza, Rinaldi, and Bogetto (2007) found in- terpersonal psychotherapy and CBT (each combined with fluoxetine) equally effective in the treatment of depression in patients with borderline personality and major depressive disorders. Fournier and colleagues (2008) found that at 16 weeks of treatment, CBT was more effective in reducing depression than medication (paroxetine) for patients with moderate to severe de- pression and no personality disorder, but less effective for those with a personality disorder. This study did not include patients with borderline, schizotypal, or antiso- cial personality disorders. The efficacy of CBT (alone or as an adjunct to psychopharmacological treatment) with coexisting major depressive and personality disor- ders is still not clear.
The second pill-placebo study, the multisite TADS (2004) for reduction of depressive symptoms in adoles- cents, found that the combination of medication (fluox- etine) and CBT produced the most positive outcome, that medication alone was superior to pill-placebo, but CBT alone did not significantly differ from pill- placebo. These findings were based on 12-week out- come measures. Analyses (TADS, 2007) on data from outcome measures at Weeks 18, 24, and 36, however, indicated that by Week 36 the effectiveness of CBT sig- nificantly increased and was equivalent to medication, and that the combination of medication and CBT was slightly more effective than CBT or medication alone.
Some writers have argued that the major psychother- apies are essentially equivalent in effectiveness, regard- less of the disorder studied. To test this hypothesis, a meta-analysis examined whether CBT was superior to other forms of psychotherapy across a range of disor- ders (Tolin, 2010). The results showed that, across all disorders included in the study, CBT was superior to psy- chodynamic therapy, although not to interpersonal or supportive therapies, at posttreatment and at follow-up. However, the analysis revealed that CBT was signifi- cantly superior to the alternative therapies studied for depressive and anxiety disorders. Tolin (2010) conclud- ed that “these results argue against previous claims of treatment equivalence and suggest that CBT should be considered a first-line psychosocial treatment of choice, at least for patients with anxiety and depressive disor- ders” (p. 710).
CBT for depression has also demonstrated consid- erable effects for children and adolescents, not just for adults. Spirito, Esposito-Smythers, Wolff, and Uhl
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(2011) completed a review of outcome studies regard- ing CBT for adolescent depression and suicidality. They summarized the data regarding depression by concluding that “CBT for adolescent depression has re- ceived considerable support in the research literature. Individual and group CBT, with and without a parent component, appears to be well established and/or ef- ficacious for the majority of participants” (p. 195). This is consistent with a more recent meta-regression analysis of CBT for child and adolescent depression (Oud et al., 2019) that demonstrated reduced depressive symptoms at posttreatment and at follow-up in CBT compared to inactive control conditions. Regarding CBT and sui- cidality in adolescents, Spirito and colleagues (2011) concluded that
the majority of studies of CBT for depressed adolescents have found a reduction in suicidal ideation regardless of CBT format (i.e., individual, group). It should be noted that reductions in suicidality have also been found in response to family therapy, supportive therapy, and pharmacotherapy. Nonetheless, while various forms of therapy resulted in comparable reductions in adolescent suicidality, CBT has shown the most promise in concur- rently reducing MDD diagnoses/symptoms and suicidal ideation. (p. 196)
Notably, a recent meta-analysis of posttreatment follow-up outcomes (Rith-Najarian et al., 2019) found large effect size gains from pre- to posttreatment that were maintained for up to 2 years for adolescents across CBT treatments for depression, anxiety, and traumatic stress.
A recent development in the treatment outcome literature is the availability of large numbers of CBT trials that enable robust meta-analytic procedures. For example, a meta-analysis by Cuijpers and colleagues (2013) included 115 randomized trials comparing CBT to a control group or another active treatment for adult depression. Although they found that CBT outper- formed comparison treatments overall, they cautioned that higher study quality was associated with smaller effect sizes in favor of CBT. This suggests that the mean effects of CBT may be overestimated. With few excep- tions, they found no differences between cognitive therapy and either medication or psychotherapy com- parison conditions, and the differences observed must be interpreted with caution because they involved a small number of studies. Additionally, in a recent meta- analysis (Johnsen & Friborg, 2015) of 70 CBT trials be- tween 1977 and 2014, the authors found that the effects
of CBT as documented in the research literature have decreased over time. These and other large-scale analy- ses provide important information about the areas in which CBT has room to further develop and improve.
In attempts to make traditional cognitive therapy more accessible and/or affordable for the general pub- lic, Internet-based (ICBT) and group (CBGT) CBT have been explored. In reviews of rapidly accumulating data on ICBT (e.g., Baumeister, Reichler, Munzinger, & Lin, 2014; Cowpertwait & Clarke, 2013; Johans- son & Andersson, 2012; Karyotaki et al., 2017; König- bauer, Letsch, Doebler, Ebert, & Baumeister, 2017), researchers have highlighted mounting support for the effectiveness of ICBT; particularly, guided ICBT (structured self-help materials with therapist contact via e-mail) outperforms unguided ICBT (no therapist contact). Research also indicates that guided ICBT is comparable to face-to-face therapy in effectiveness and that tailored treatments (which include additional spe- cific techniques for coexisting diagnoses) are superior to nontailored treatments (same material for all patients) with severe depression (Johansson & Anderson, 2012).
Regarding CBGT, a recent meta-analysis (Moore, Carr, & Hartnett, 2017) found large, significant effect sizes when comparing CBGT to treatment-as-usual and wait-list control conditions, and medium effects for ac- tive control groups. Another meta-analysis (Feng et al., 2012) also examined treatment characteristics associ- ated with outcomes and revealed that CBGT was more effective with mild to moderate depression. The effect decreased as depression severity increased. Additional notable findings from that review include: the optimal length of session was 60–90 minutes, take-home as- signments improved results, and higher turnover rates were related to poorer outcomes.
RESEARCH ON RELAPSE PREVENTION1
Even though the vast majority of patients recover from an episode of depression, they nevertheless remain vul- nerable to future depression.
Recurrence is a major problem for many individuals suffering from depression: At least 50% of individuals who suffer from one depressive episode have another within 10 years. Those experiencing two episodes have a 90% chance of suffering a third, while individuals with three or more lifetime episodes have relapse rates of 40% within 15 weeks of recovery from an episode (Kupfer, Frank, & Wamhoff, 1996, p. 293).
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Other investigators have found that 21% of adults with a major depressive episode have a new episode dur- ing a 3-year follow-up period (Hoertel et al., 2017), and 85% of patients with unipolar depression are likely to experience recurrences (Keller & Boland, 1998, p. 350). Wang (2004), through a 6-year follow-up, found that 49.8% of those treated for major depression developed subsequent major depressive episodes. As these num- bers clearly show, there is an urgent need for treatments capable of minimizing and preventing relapse.
What we consider a very exciting finding in the treatment of depression with cognitive therapy is the consistent observation (Paykel, 2007) that patients treated with cognitive therapy alone or with a combina- tion of cognitive therapy and medication fare far better in terms of relapse than do patients treated with medi- cation alone (when both treatments are stopped at ter- mination). Despite differences in sample characteristics and methodologies across studies, cognitive therapy ap- pears to have important prophylactic properties. After a 1-year follow-up, numerous studies have reported lower relapse rates for patients treated with cognitive therapy than for patients treated with antidepressants. Simons, Murphy, Levine, and Wetzel (1986) found relapse rates of 12% with cognitive therapy versus 66% with anti- depressants; Bowers (1990) found relapse rates of 20% with cognitive therapy versus 80% with antidepres- sants; Shea and colleagues (1992) reported 9% relapse with cognitive therapy versus 28% with antidepres- sants; Hollon and colleagues (2005) reported rates of 31% relapse with cognitive therapy versus 76% with an- tidepressants. Results from an extensive meta-analysis revealed that “on average, only 29.5% of the patients treated with cognitive therapy relapsed versus 60% of those treated with antidepressants” (Gloaguen, Cot- traux, Cucherat, & Blackburn, 1998, p. 68). This was also reported in a more recent meta-analysis, in which participants who received psychotherapy (including primarily CBT interventions) alone or in combination with another treatment had a lower likelihood of anoth- er depressive episode over more than 4 years of follow- up (Steinert, Hofmann, Kruse, & Leichsenring, 2014). The prophylactic benefits of cognitive therapy are all the more significant because “there is no evidence that pharmacotherapy confers any protection against the re- turn of symptoms after treatment has been terminated.2 Since the majority of depressed individuals will experi- ence multiple episodes, the capacity of an intervention to prevent the return of symptoms after treatment may
be at least as important as its ability to treat the current episode” (Evans et al., 1992, p. 802).
A related concern—and one of the most salient (but not exclusively associated) with psychotropic agents— is the presence of residual symptoms after treatment: “Treatment of depression by pharmacological means is likely to leave a substantial amount of residual symp- toms in most patients” (Fava, Rafanelli, Grandi, Conti, & Belluardo, 1998b, p. 820). Inevitably, patients who improve on antidepressants continue to manifest some of the symptoms of depression and, as numerous in- vestigators have concluded, unless patients achieve full recovery, residual symptoms increase the risk of relapse (Evans et al., 1992; Fava et al., 1998b; Hardeveld, Spij- ker, de Graaf, Nolen, & Beekman, 2010; Keller & Bo- land, 1998; Rush et al., 2006).
A group of investigators who were concerned about the risk of relapse associated with residual symptoms looked at the lingering symptoms after treatment with fluoxetine (Prozac). Nierenberg et al. (1999) found that
even among subjects who are considered full responders to fluoxetine 20 mg for 5 weeks, more than 80% had 1 or more residual DSM-III-R symptoms of major depressive disorder, more than 30% had 3 or more symptoms, and 10.2% met formal criteria for either minor or subsyndro- mal depression. . . . These findings imply that minimal depressive symptoms are prodromal and increase the risk of developing an initial full-blown episode of major de- pression. (pp. 224–225)
Cognitive therapy has been found to be effective in reducing both residual symptoms and relapse after the termination of medication: “Short-term CBT after suc- cessful antidepressant drug therapy had a substantial effect on relapse rate after discontinuation of antide- pressant drugs. Patients who received CBT reported a substantially lower relapse rate (25%) during the 2-year follow-up than those assigned to [clinical manage- ment] (80%)” (Fava et al., 1998b, p. 818). The protec- tive benefits of cognitive therapy were still noticeable in a 4-year follow-up study, although the benefits faded after a 6-year period (Fava, Rafanelli, Grandi, Canes- trari, & Morphy, 1998a). In another study, Williams (1997) found that only 5% of the “CBT treated and re- covered” group sought additional treatment compared with 39% of the antidepressant group. Paykel and col- leagues (1999) found significantly lower cumulative relapse rates at 68 weeks in patients who received 16 sessions of CBT following a partial response to pharma-
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cotherapy. Bockting and colleagues (2005) compared treatment as usual (TAU) that included continuation of medication with TAU augmented with brief cognitive therapy and found relapse significantly reduced in pa- tients with five or more previous episodes of depression. The relapse rates were 72% for TAU versus 46% for TAU augmented with brief cognitive therapy. Further- more, in a 10-year follow-up of this trial, Bockting and colleagues (2015) reported sustained effects of cogni- tive therapy as evidenced by significantly longer time to first depression relapse compared to TAU.
A preventive strategy used by psychiatrists to deal with high relapse rates associated with antidepressant medication is “continuation medication” or “continu- ation phase treatment,” which is long-term (and in many cases lifelong) maintenance treatment (Evans et al., 1992; Fava et al., 1998b; Rush, Aaronson, & De- myttenaere, 2019)—usually at the same dosage pro- vided during the acute phase of treatment. The research comparing relapse rates in patients continuing medica- tion over the long term versus those treated and then withdrawn from cognitive therapy does not suggest a significant advantage to this practice. For example, De- Rubeis and colleagues (2005) found that both groups had equivalent relapse rates (40%); Hollon and col- leagues (2005) found that 31% relapsed when treated and then withdrawn from cognitive therapy compared to 47% who relapsed when treated with continuation medication. Fournier and colleagues (2008) found that patients with both major depression and a personality disorder who responded positively to 16 weeks of CBT, with three optional booster sessions over a 12-month period, showed superior sustained improvement with CBT compared to pharmacotherapy withdrawal, and equivalent improvement to pharmacotherapy with con- tinuation over those 12 months. Dobson and colleagues (2008) followed patients who responded to a treatment of CBT, behavioral activation, or pharmacotherapy for acute depression. During a 2-year follow-up, psy- chotherapy patients received no further treatment and pharmacotherapy patients received either continuation pharmacotherapy or continuation pill-placebo. They found that CBT provided the strongest protection; both psychotherapies were equivalent to pharmacother- apy with continuation; and both psychotherapies were superior to continuation pill-placebo. In a particularly long-term (up to 12 years) follow-up study of depressed patients, Peselow, Tobia, Karamians, Pizano, and IsHak (2015) found that 76.5% of patients who initially
responded to treatment with an SSRI had a depressive episode recurrence. In those who received concomitant CBT during the maintenance phase, 58.8% had a re- currence, while 81.9% without CBT had a recurrence.
An additional research area focuses on providing treatment after a standard course of CBT or medica- tions to increase treatment gains and/or prevent remis- sion of depression. Recently, Dunlop and colleagues (2019) evaluated the addition of CBT or antidepres- sant combination treatment to patients who had not achieved remission with 12 weeks of the other treat- ment. They found that patients who did not achieve remission with CBT who then received concurrent antidepressant treatment evidenced greater response rates over an additional 12 weeks than did patients who originally did not respond to antidepressants and were given concurrent CBT. By contrast, in their meta-anal- ysis of interventions delivered after remission to prevent relapse, Biescheuvel-Leliefeld and colleagues (2015) found that cognitive therapy interventions significantly outperformed TAU but not antidepressants. Taken to- gether, these results suggest a complex relationship be- tween the order in which treatments are provided and the long-term effects of each one.
Some researchers have pointed out the tautological nature of the relapse solution of continuing medica- tions indefinitely: “Drug treatment results in a higher relapse rate than cognitive-behavioral therapy; there- fore patients should be maintained on drugs to prevent relapse” (Antonuccio, Danton, & DeNelsky, 1995, p. 578). Although drugs are still the initial and most frequently prescribed form of treatment for major de- pression in the United States (Antonuccio et al., 1995; Purgato et al., 2014), and the most commonly used method to maintain treatment gains (Geddes et al., 2003), three important points need to be considered: premature termination, iatrogenic effects of pharmaco- therapy, and cost-effectiveness.
Research has shown that “a sizeable group of patients either chooses not to continue long-term pharmaco- therapy in the absence of any depressive symptoms, cannot take medication due to a medical condition that precludes the use of antidepressants, or suffer from side effects that are intolerable to them” (Spanier, Frank, McEachran, Grochocinski, & Kupfer, 1999, p. 250). Although the newer “first-line” medications are more tolerable than older medications, 70% of patients con- tinue to experience significant depressive symptoms with one of these medications (Kato & Chang, 2013),
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and up to 50% discontinue trials due to unwanted side effects (Connolly & Thase, 2012). Thase (2011) has noted that various combinations of antidepressants are widely prescribed as the result of problems with insuf- ficient or no response, even though properly controlled and adequately powered clinical trials have not yet been conducted on such combinations.
Regarding iatrogenic effects, one group of research- ers concluded that
there is much evidence that antidepressant medications are not benign treatments. . . . Many antidepressants are cardiotoxic, have dangerous side effects, and are often used in suicide attempts. . . . [They also] result in relatively poorer compliance than psychotherapy, have a higher dropout rate, and result in as much as a 60% non- response rate with some patient populations. (Antonuc- cio et al., 1995, p. 581)
We should note that psychotherapy also may have un- intended and undesirable side effects (Mohr, 1995), but very little is known about negative effects associated with cognitive therapy.
The third consideration is the cost-effectiveness of treatment. The research on this topic is relatively lim- ited but has begun to receive more attention in recent years. Antonuccio, Thomas, and Danton (1997) con- ducted a cost-effectiveness analysis on several outcome studies on depression and found that over a 2-year pe- riod, the cost of fluoxetine alone was 33% higher than individual CBT, and that the cost of the combined treatment of fluoxetine with CBT was 23% higher than CBT alone. In an Australian study, Vos, Corry, Haby, Carter, and Andrews (2005) examined the costs and benefits of CBT and drugs in the episodic and main- tenance treatment of depression. They found mainte- nance treatment with SSRIs to be the most expensive option, nearly double that of bibliotherapy, group CBT, individual CBT, and TCAs. Scott, Palmer, Paykel, Teas- dale, and Hayhurst (2003) compared the cost-effective- ness of relapse prevention in depression by comparing CBT as an adjunctive treatment to antidepressants and clinical management, and with antidepressants and clinical management alone, over a 17-month period. They found the addition of CBT was more expensive but also more effective in reducing cumulative relapse rates (relapse rates were 29% with adjunctive CBT vs. 47% without adjunctive CBT). Importantly, they noted that the costs associated with adjunctive CBT in their study were a “worst-case” scenario, because the follow-
up extended only 17 months; other research (as noted in the previous section) has demonstrated maintenance of gains and lowered relapse rates up to 6 years with CBT. Although Dobson and colleagues (2008) did not conduct a formal statistical comparison of costs among treatment conditions, they noted that the “cumula- tive cost of continued medications proved to be more expensive by the end of the first year of follow-up in this study” (p. 471). Scott and colleagues (2003) argued that the incrementally adjusted costs over time to re- lapse should be considered in decision making on the value of various treatments. Koeser, Donisi, Goldberg, and McCrone (2015) conducted an analysis comparing the cost-effectiveness of CBT to pharmacological treat- ment and combined treatment in the United Kingdom across 11 trials. They found that CBT alone was most cost-effective, followed by pharmacotherapy alone. Ad- ditionally, in a systematic review that included seven RCTs of CBT compared to pharmacotherapy, Karyo- taki, Tordrup, Buntrock, Bertollini, and Cuijpers (2017) concluded CBT was more cost-effective than pharmacotherapy. These findings suggest that CBT, either alone or in combination with drugs, can enhance cost-effectiveness, particularly when higher short-term costs of combined treatments are balanced against bet- ter outcomes and lower marginal costs in the long term.
What is the optimum frequency and duration of ses- sions for cognitive therapy to be effective, both at termi- nation and at long-term follow-up? According to Sacco and Beck (1995, p. 332),
General guidelines suggest 15 to 25 (50-minute) sessions at weekly intervals, with more seriously depressed clients usually requiring twice-weekly meetings for the initial 4–5 weeks. To avoid an abrupt termination, a “tapering off” process is recommended, with the last few sessions occurring once every 2 weeks. After termination, some clients may also need a few booster sessions (four or five are common).
Some writers have noted that longer courses of treat- ment may be necessary for full and more lasting recov- ery (Elkin et al., 1996; Thase, 1992). Research by Jar- rett and colleagues (2001) suggests that relapse rates in high-risk patients with an early age of onset or unstable remission might possibly be reduced further with “con- tinuation-phase cognitive therapy” (C-CT), which con- sists of 10 sessions (biweekly during the first 2 months and once a month for the following 6 months) follow- ing the acute phase of treatment. The focus in the con-
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tinuation phase is on relapse prevention and the gen- eralization of skills (across responses, settings, stimuli, and times). This strategy is supported by studies (Jar- rett et al., 2001; Vittengl et al., 2007; Vittengl, Clark, & Jarrett, 2009) aimed at preventing relapse in responders to a variety of treatment modalities (pharmacotherapy, interpersonal psychotherapy, and/or CBT) for the acute phase of depression. In two trials comparing C-CT to fluoxetine and a pill-placebo control (Jarrett, Min- hajuddin, Gershenfeld, Friedman, & Thase, 2013; Vit- tengl, Clark, Thase, & Jarrett, 2014), C-CT and fluox- etine exhibited similar effects on relapse over 8 months and 2 years of follow-up. As a result of these and other studies (Jarrett & Thase, 2010; Jarrett, Vittengl, & Clark, 2008; Vittengl, Clark, Thase, & Jarrett, 2017), researchers have suggested using scores on a variety of measures (Hamilton Rating Scale for Depression, Beck Depression Inventory [BDI], Inventory for Depressive Symptomatology, and the Longitudinal Interval Fol- low-Up Evaluation) to help cognitive therapists decide how many more sessions may be needed to help avoid relapse or recurrence.
Another alternative for relapse prevention is mind- fulness-based cognitive therapy (MBCT), developed by Teasdale, Segal, and Williams (1995). MBCT draws from acceptance and meditation strategies that are also central to dialectical behavior therapy for borderline personality (Linehan, 1993a, 1993b). “MBCT aims at developing participants’ awareness of, and changing their relationship to, unwanted thoughts, feelings, and body sensations, so that participants no longer avoid them or react to them in an automatic way but rather respond to them in an intentional and skillful manner” (Ma & Teasdale, 2004, p. 32). Teasdale and colleagues (Ma & Teasdale, 2004; Teasdale, 1997a, 1997b; Teas- dale et al., 1995, 2002) have argued that the primary mechanism of therapeutic change in cognitive therapy is in distancing or decentering from cognition rather than changing the content of thought. Two studies con- ducted on MBCT found that TAU followed by MBCT, in comparison with TAU alone, significantly reduced relapse in patients with three or more episodes of depres- sion. In the first study, 66% relapsed with TAU alone versus 37% with TAU followed by MBCT (Teasdale et al., 2000); in the second study, 78% relapsed with TAU alone versus 36% with TAU followed by MBCT (Ma & Teasdale, 2004). Encouragingly, Mathew, Whitford, Kenny, and Denson (2010) and Munshi, Eisendrath, and Delucchi (2013) also reported maintained treat- ment gains over 2- and nearly 5-year follow-up peri-
ods, respectively. While Mathew et al. (2010) noted a weakening of effects over time that appeared to be related to the amount of formal MBCT practice, Mun- shi and colleagues (2013) found no association between amount of practice and depression outcomes. Notably, Williams and colleagues (2014) compared 8-week treat- ment of MBCT plus TAU, psychoeducation plus TAU, and TAU alone. They found no differences between conditions on risk of relapse over a 12-month follow-up period. Additionally, Kuyken and colleagues (2016), in an individual patient data meta-analysis that included nine studies, found that patients who received MBCT had a significantly reduced risk of relapse over 5 years of follow-up relative to comparison conditions, and there was some evidence of a larger effect for patients who had greater pretreatment depression severity.
Although prior researchers (Segal, Williams, & Teasdale, 2002) presumed that the difficulty con- centrating and negative thinking during a depressive episode would preclude training in attentional control skills with MBCT, van Aalderen and colleagues (2012) found that MBCT plus TAU, compared to TAU alone, showed equivalent gains in effectiveness for patients in remission as for those currently depressed. Mani- cavasagar, Perich, and Parker (2012) also examined the effectiveness of MBCT in reducing current depres- sion. They compared CBGT and MBCT, and found equivalent improvements in depression. Interestingly, they found no significant differences between the two conditions in mindfulness or rumination scores. The potential for lower costs associated with treatments that can be implemented in a group format suggests that they may be attractive for not only relapse prevention but also recurrent depression.
RESEARCH ON CHRONIC DEPRESSION
As the previous data demonstrate, CBT has been shown to be an effective treatment across a wide range of de- pressed populations. Nevertheless, many depressed patients still do not respond to treatment (Solomonov & Barber, 2016). Depression that is resistant to cur- rent treatments remains a major public health problem. Between 40 and 50% of patients may not complete or respond to CBT treatment for acute depression (De- Rubeis et al., 2005; Jarrett & Thase, 2010), and 50% of patients do not achieve full remission in depressive symptoms after two trials of medication (Mathys & Mitchell, 2011; Rush et al., 2006; Trivedi et al., 2006).
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Negt and colleagues (2016) note from current research that around 30% of depressions are chronic and that 47% of outpatient mental health patients suffer from chronic depression.
McCullough (2003) proposed, on the basis of ex- isting research, that there are qualitative differences between chronic and nonchronic forms of depression, and that they require different treatment strategies. According to McCullough, research “shows that the chronic disorders, when compared with acute/episodic major depression (both single and recurrent episodes with interepisode full recovery), differ significantly in terms of age of onset, clinical course patterns, devel- opmental history, modal Axis II comorbidity profiles, characteristic response-to-treatment rates, predictable relapse percentages, and need for long-term treat- ment” (p. 243). He noted that these differences largely have not been addressed in the treatment literature; consequently, therapeutic work by psychologists, psy- chiatrists, and social workers has been conducted as if patients with depression are an undifferentiated popu- lation. Young, Klosko, and Weishaar (2003) noted that although traditional CBT is highly effective for many patients, there remains a significant number who either are not helped or continue to experience emotional dis- tress and impaired functioning, particularly those with significant character pathology. For those with chronic problems, a more extensive treatment approach may be required.
Before discussing specific treatments for chronic de- pression, we describe the general characteristics of this population. An early age of onset (usually in midadoles- cence, before age 20) in the form of dysthymia tends to differentiate between the chronic and nonchronic forms of depression in 70–75% of clinical populations (Keller & Boland, 1998; Keller & Hanks, 1995; McCullough, 2000). Early life trauma or adverse family relations (loss of a parent in childhood; sexual, physical, and/or verbal abuse; neglect; and overprotection) are more evident in those with chronic depression (Chapman et al., 2004; Cong et al., 2012; Dube et al., 2001; Heim & Nem- eroff, 2001; Kendler et al., 1995; Lizardi et al., 1995; Randolph & Dykman, 1998; Sachs-Ericsson, Verona, Joiner, & Preacher, 2006). In patients with early-onset dysthymia who experience chronic stress, those with the addition of an adverse family history evidence an increase in depression severity over time, compared to those without such adverse family histories but with familial loadings for dysthymic disorder (Dougherty, Klein, & Davila, 2004). There is a higher prevalence of
comorbid disorders, particularly personality disorders (Garyfallos et al., 1999; Pepper et al., 1995). Cluster C personality disorders are associated with chronic de- pression (Hayden & Klein, 2001).
Five potentially promising treatments that expand on CBT have been developed that can address chron- ic depression. These treatments are Harley, Sprich, Safren, Jacob, and Fava’s (2008) application of Line- han’s (1993b) dialectical behavior therapy (DBT) skills training, applications (Barnhofer et al., 2009; Eisen- drath, Chartier, & McLane, 2011), Segal and col- leagues’ (2002) MBCT, Wells and colleagues’ (2012) metacognitive therapy (MCT), McCullough’s (2000) cognitive-behavioral analysis system of psychotherapy (CBASP), and Young and colleagues’ (2003) schema therapy (ST).
Harley and colleagues (2008) have provided prelimi- nary evidence that DBT skills training conducted in groups may be an effective alternative for treatment- resistant depression. Patients who had not achieved re- mission with antidepressant medication were assigned to either a 16-session, once-weekly DBT skills training condition (mindfulness, interpersonal effectiveness, emotion regulation, and distress tolerance) or a wait-list condition. They found significantly greater improve- ment (with large effect sizes on the Hamilton Rating Scale for Depression and the BDI) in depressive symp- toms in the DBT skills training group. Feldman, Har- ley, Kerrigan, Jacobo, and Fava (2009) hypothesized that DBT skills training helps patients process their emotional experience in a way that reduces rather than exacerbates their depressive symptoms.
Another preliminary study (Barnhofer et al., 2009) and one case study (Eisendrath et al., 2011) successfully used MBCT to treat chronic depression. Barnhofer and colleagues (2009) compared MBCT plus TAU and TAU alone, and found significantly greater improve- ment in the MBCT plus TAU group. Eisendrath and colleagues (2011) successfully treated a patient with a modified version of MCBT. They added exercises and metaphors from acceptance and commitment therapy (ACT; Luoma, Hayes, & Walser, 2007; Zettle, 2007), and focused on current depression in their MCBT treatment. Building on these results, Meadows and col- leagues (2014) conducted a randomized trial of MBCT plus depression relapse active monitoring (DRAM) compared to DRAM alone. They found participants who received MBCT had fewer days with depression and fewer participants relapsed both 1 and 2 years post- treatment. These are intriguing initial results, especial-
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ly since these treatments are of relatively short duration and conducive to a group format.
Wells and colleagues (2012) also conducted a pre- liminary study in which they used MCT to treat pa- tients with treatment-resistant depression. Attentional control, rumination, worry, and metacognitive beliefs were targeted in eight treatment sessions. They found significant improvements both posttreatment and at 12-month follow-up. Dammen, Papageorgiou, and Wells (2015) followed up on these results with a small open trial of MCT delivered in a group format over 10 weeks. All 11 patients were classified as recovered, based on depression symptoms, and improvements were maintained at a 6-month follow-up assessment. Finally, Papageorgiou and Wells (2015) evaluated 12-session group MCT and observed improvements in depres- sion that were maintained at a 6-month follow-up. This treatment will be of further interest if the positive re- sults can be replicated in a randomized controlled trial.
McCullough’s (2000) CBASP is an integrative, time- limited treatment that contains elements of cognitive, behavioral, interpersonal, and psychodynamic psycho- therapies. McCullough (2003) states:
Treatment begins with a cognitive-emotionally retarded adult child who brings a negative “snapshot” view of the world to the session. The chronic patient functions, at least in the social–interpersonal arena, with the struc- tural mindset of a 4–6 year old preoperational (Piaget) child. . . . The patient must be taught to function formal- ly, to perceive that his or her behavior has consequences, be taught to generate authentic empathy, and to learn to assert himself or herself effectively. Psychotherapy begins with an “adult child” who must be assisted to mature de- velopmentally in the cognitive–emotive sphere. (pp. 247, 248)
Change is brought about through a contingency program that relies on negative reinforcement. First, contingencies between behaviors and consequences are exposed. Then, as the result of positive changes in be- havior, discomfort and distress are reduced or eliminat- ed. Three techniques are used to bring about change: situational analysis, interpersonal discrimination exer- cise, and behavioral skill training/rehearsal. Two initial studies used CBASP with chronically depressed out- patients. The first (Keller et al., 2000) compared the effects of CBASP alone, Serzone (nefazodone) alone, and combined treatment after a 12-week acute phase of treatment. The overall response rate was 48% for both monotherapies, compared with 73% for the combined
treatment. Among the 76% (519 out of 681) completers of the study, 52% responded to CBASP, 55% respond- ed to Serzone, and 85% responded to combined treat- ments. The second (Klein et al., 2004), a 1-year follow- up to this initial study, examined relapse and depressive symptoms over time in the CBASP responders by com- paring the effects of continuation CBASP therapy (16 sessions over 52 weeks) with assessment only. There were significantly fewer relapses and depressive symp- toms for those in the continuation CBASP therapy. A recent meta-analysis of CBASP for chronic depression (Negt et al., 2016), including these studies and five oth- ers, found superior outcomes for CBASP, particularly in comparison to TAU and interpersonal psychotherapy control conditions.
ST also is an integrative therapy (Young et al., 2003), with elements of cognitive, behavioral, interpersonal, and emotion-focused therapies. Hawke and Povencher (2011) noted that “Young’s schema theory does not at- tempt to compete with traditional Beckian theory, but rather expands on it for treatment-resistant clientele whose psychological problems are thought to be main- tained by complex characterological underpinnings. It does so by placing greater emphasis on the developmen- tal origins of severe psychopathology” (p. 258).
A study by Giesen-Bloo and colleagues (2006) found surprisingly strong and significant results in favor of ST over transference-focused therapy with the chronic disorder of borderline personality. After 3 years of treat- ment (sessions twice per week), 45% of the patients in ST (vs. 24% in transference-focused therapy) complete- ly recovered. One year later, over half (52%) in ST had fully recovered (vs. 29% in transference-focused thera- py) and two-thirds (70%) in ST showed significant im- provement. In addition, patients in ST were significant- ly less likely to drop out of therapy (27% dropped out of ST vs. 50% out of transference-focused therapy). Even stronger results were reported (Farrell, Shaw, & Web- ber, 2009) for group schema-focused therapy (GST; see Farrell & Shaw, 2012) for people with borderline per- sonality disorder. This study compared individual TAU (CBT or psychodynamic) plus adjunct GST with TAU alone. Ninety-four percent receiving TAU plus GST, compared to 16% receiving TAU alone, no longer met criteria for borderline personality disorder at the end of 20 months of treatment. In addition, there was a 0% dropout rate in the TAU plus GST condition compared to 25% in the TAU condition. Given the high degree of similarities between patients with chronic disorders (adverse childhood histories, early-onset depression,
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and a multitude of schemas), we believe that ST is very likely to be an effective treatment for the chronically depressed population as well.
Evidence from case series studies supports this hy- pothesis. For example, Malogiannis and colleagues (2014) conducted a single case series study with 12 pa- tients with chronic depression. Participants completed baseline, introduction, and ST phases. At posttreat- ment, 60% of participants had remitted or responded. More recently, Renner, Arntz, Peeters, Lobbestael, and Huibers (2016) conducted a multiple-baseline case se- ries study with 25 participants with chronic depression. Participants completed a baseline phase, an exploration phase, then up to 65 sessions of ST. Compared to the no-treatment baseline phase, ST had a large and signifi- cant effect on depression. Additionally, a meta-analysis by Körük and Özabaci (2018) included five additional experimental studies of ST provided to participants with depressive disorders and found support for the efficacy of ST. Given the substantial heterogeneity be- tween studies (duration, delivery format), additional experimental studies are needed to continue to evaluate ST with chronically depressed patients.
CURRENT STATUS AND FUTURE RESEARCH ON TREATING DEPRESSION
There is now a considerable body of research on treat- ments for depression. Certainly, there are enough in- consistencies in the literature to warrant continued debate and research regarding the relative merits of dif- ferent treatments for depression. Nevertheless, the over- all efficacy of cognitive therapy for depression is clearly a replicable and robust finding.
Many important, unanswered questions—along with inconsistent research findings—will probably make it impossible for proponents of any single treat- ment to make firm recommendations favoring one treatment for depression over another across disorders and populations. In the spirit of Beck’s emphasis on testable hypotheses and clinical protocols, we hope that, through more sophisticated research studies, it will eventually be possible to better understand which types of depressed patients benefit most from which type of treatment, or combination of treatments, and in what sequence.
The remainder of this chapter is devoted to describ- ing the cognitive model of depression and schema the-
ory, detailing the basic characteristics of cognitive and schema therapies, and demonstrating applications of cognitive and schema therapies to depression in clinical practice.
COGNITIVE MODEL OF DEPRESSION
The cognitive model assumes that cognition, behav- ior, and biochemistry are all important components of depressive disorders. We view them not as com- peting theories of depression but as different levels of analysis. Each treatment approach has its own “focus of convenience.” The pharmacotherapist intervenes at the biochemical level; the cognitive therapist intervenes at the cognitive, affective, and behavioral levels. Our experience suggests that when we change depressive cognitions, we simultaneously change the characteristic mood, behavior, and, as some evidence suggests (e.g., Free, Oei, & Appleton, 1998; Joffe, Segal, & Singer, 1996; Kéri, Szabó, & Kelemen, 2014; Mondin et al., 2015), the biochemistry of depression. Although the exact mechanism of change remains a target of consid- erable investigation, speculation, and debate (Barber & DeRubeis, 1989; Castonguay, Goldfried, Wiser, Raue, & Hayes, 1996; DeRubeis et al., 1990; DeRubeis & Feeley, 1990; Franklin, Carson, & Welch, 2016; Hayes & Strauss, 1998; Oei & Dingle, 2001; Oei & Free, 1995; Shea & Elkin, 1996; Whisman, 1993; Yang et al., 2018), “there are indications that cognitive therapy works by virtue of changing beliefs and information- processing proclivities and that different aspects of cognition play different roles in the process of change” (Hollon et al., 1996, p. 314).
Our focus in this chapter is on the cognitive dis- turbances in depression. Cognitive science research emphasizes the importance of information processing in depressive symptomatology (e.g., Ingram & Holle, 1992; Park et al., 2019). According to these theories, negatively biased cognition is a core process in depres- sion. This process is reflected in the “cognitive triad of depression”: Depressed patients typically have a nega- tive view of themselves, of their environment, and of the future. They view themselves as worthless, inad- equate, unlovable, and deficient. Depressed patients view the environment as overwhelming, as presenting insuperable obstacles that cannot be overcome, and that continually result in failure or loss. Moreover, they view the future as hopeless: Their own efforts will be insuf- ficient to change the unsatisfying course of their lives.
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This negative view of the future often leads to suicidal ideation and actual suicide attempts.
Depressed patients consistently distort their interpre- tations of events, so that they maintain negative views of themselves, their environment, and the future. Beck suggests that much of this distorted cognitive process- ing takes place outside of conscious awareness, in the form of “automatic thoughts,” those thoughts that in- tervene between life events and the patient’s emotional reactions to those events. Automatic thoughts often go unnoticed by the patient because they are out of aware- ness, they are part of a repetitive or habitual way of thinking, and they occur so often. Automatic thoughts are often contrary to what a patient logically and con- sciously knows to be true, and most patients, prior to therapy, cannot stop them through rational thought processes.
This process of cognitive distortion is far more com- mon in depressed patients than in nondepressed indi- viduals. For example, a depressed woman whose hus- band comes home late one night may conclude that he is having an affair with another woman, even though there is no other evidence supporting this conclusion. This example illustrates an “arbitrary inference,” reach- ing a conclusion that is not justified by the available evidence. Other distortions include all-or-nothing thinking, overgeneralization, selective abstraction, and magnification (Beck et al., 1979).
SCHEMA THEORY
According to subsequent developments within the cognitive model, an important predisposing factor for many patients with depression is the presence of sche- mas (Stein & Young, 1992; Young, 1990/1999).3 Beck (1976) emphasized the importance of schemas in de- pression and provided the following definition: “A schema is a cognitive structure for screening, coding, and evaluating the stimuli that impinge on the organ- ism. . . . On the basis of this matrix of schemas, the individual is able to orient himself in relation to time and space and to categorize and interpret experiences in a meaningful way” (p. 233).
Furthermore, Beck, Freeman, and Associates (1990) noted:
In the field of psychopathology, the term “schema” has been applied to structures with a highly personalized idiosyncratic content that are activated during disorders
such as depression, anxiety, panic attacks, and obsessions, and become prepotent. . . . Thus, in clinical depression, for example, the negative schemas are in ascendancy, resulting in a systematic negative bias in the interpreta- tion and recall of experiences as well as in short-term and long-term predictions, whereas the positive schemas be- come less accessible. It is easy for depressed patients to see the negative aspects of an event, but difficult to see the positive. They can recall negative events much more readily than positive ones. They weigh the probabilities of undesirable outcomes more heavily than positive out- comes. (p. 32)
There has also been increasing recognition that “fo- cusing on core schemas is a key to effective short-term therapy” (Freeman & Davison, 1997, p. 8).
Through clinical observation, Young has identi- fied a subset of schemas that he terms early maladap- tive schemas (EMSs): “Early Maladaptive Schemas refer to extremely stable and enduring themes that develop during childhood and are elaborated upon throughout the individual’s lifetime and that are dysfunctional to a significant degree” (Young, 1990/1999, p. 9). The 18 EMSs identified by Young are listed in Figure 7.1.4
According to Young’s (see Young et al., 2003) theory, early schemas5 result from an interaction between the child’s innate temperament and early negative life ex- periences, especially with significant others. Children gradually construct pervasive, maladaptive views of themselves and others that are filtered through, and consistent with, their schemas.
According to Young, EMSs are (1) a priori truths about oneself and/or the environment; (2) self-perpet- uating and resistant to change; (3) dysfunctional; (4) often triggered by some environmental change (e.g., loss of a job or mate); (5) tied to high levels of affect when activated; and (6) as noted earlier, usually result from an interaction of the child’s temperament with dysfunctional developmental experiences with family members, caretakers, and peers (Young, 1990/1999). Young goes on to elaborate that when an EMS is trig- gered, specific early memories, core beliefs, strong emo- tions, and physiological reactions are also activated. (In Young’s model, core beliefs represent the cognitive com- ponent of schemas.6)
EMSs are likely to develop when the environment does not meet the child’s core needs for safety, stability or predictability, love, nurturance and attention, accep- tance and praise, empathy, realistic limits, and valida- tion of feelings and needs. When their core needs are not met, children often internalize attitudes and beliefs
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1. ABANDONMENT/INSTABILITY The perceived instability or unreliability of those available for support and connection. Involves the sense that significant others will not be able to continue providing emotional support, connection, strength, or practical protection because they are emotionally unstable and unpredictable (e.g., angry outbursts), or unreliable or erratically present; because they will die imminently; or because they will abandon the patient in favor of someone better.
2. MISTRUST/ABUSE The expectation that others will hurt, abuse, humiliate, cheat, lie, manipulate, or take advantage. Usually involves the perception that the harm is intentional or the result of unjustified and extreme negligence. May include the sense that one always ends up being cheated relative to others or “getting the short end of the stick.”
3. EMOTIONAL DEPRIVATION Expectation that one’s desire for a normal degree of emotional support will not be adequately met by others. The three major forms of deprivation are as follows:
A. Deprivation of nurturance: Absence of attention, affection, warmth, or companionship. B. Deprivation of empathy: Absence of understanding, listening, self-disclosure, or mutual sharing of
feelings from others. C. Deprivation of protection: Absence of strength, direction, or guidance from others.
4. DEFECTIVENESS/SHAME The feeling that one is defective, bad, unwanted, inferior, or invalid in important respects; or that one would be unlovable to significant others if exposed. May involve hypersensitivity to criticism, rejection, and blame; self-consciousness, comparisons, and insecurity around others; or a sense of shame regarding one’s perceived flaws. These flaws may be private (e.g., selfishness, angry impulses, unacceptable sexual desires) or public (e.g., undesirable physical appearance, social awkwardness).
5. SOCIAL ISOLATION/ALIENATION The feeling that one is isolated from the rest of the world, different from other people, and/or not part of any group or community.
6. DEPENDENCE/INCOMPETENCE Belief that one is unable to handle one’s everyday responsibilities in a competent manner, without considerable help from others (e.g., take care of oneself, solve daily problems, exercise good judgment, tackle new tasks, make good decisions). Often presents as helplessness.
7. VULNERABILITY TO HARM OR ILLNESS Exaggerated fear that imminent catastrophe will strike at any time and that one will be unable to prevent it. Fears focus on one or more of the following: (A) medical catastrophes (e.g., heart attacks, AIDS); (B) emotional catastrophes (e.g., going crazy); (C) external catastrophes (e.g., elevators collapsing, victimized by criminals, airplane crashes, earthquakes).
8. ENMESHMENT/UNDEVELOPED SELF Excessive emotional involvement and closeness with one or more significant others (often parents), at the expense of full individuation or normal social development. Often involves the belief that at least one of the enmeshed individuals cannot survive or be happy without the constant support of the other. May also include feelings of being smothered by, or fused with, others OR insufficient individual identity. Often experienced as a feeling of emptiness and floundering, having no direction, or in extreme cases questioning one’s existence.
(continued)
FIGURE 7.1. Early maladaptive schemas. Copyright © 1999 Jeffrey E. Young. Reprinted by permission.
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9. FAILURE The belief that one has failed, will inevitably fail, or is fundamentally inadequate relative to one’s peers, in areas of achievement (school, career, sports, etc.) Often involves beliefs that one is stupid, inept, untalented. ignorant, lower in status, less successful than others, and so forth.
10. ENTITLEMENT/GRANDIOSITY The belief that one is superior to other people; entitled to special rights and privileges; or not bound by the rules of reciprocity that guide normal social interaction. Often involves insistence that one should be able to do or have whatever one wants regardless of what is realistic, what others consider reasonable, or the cost to others; OR an exaggerated focus on superiority (e.g., being among the most successful, famous, and wealthy) in order to achieve power or control (not primarily for attention or approval). Sometimes includes excessive competitiveness toward, or domination of others: asserting ones power, forcing one’s point of view, or controlling the behavior of others in line with one’s own desires—without empathy or concern for others’ needs or feelings.
11. INSUFFICIENT SELF-CONTROL/SELF-DISCIPLINE Pervasive difficulty or refusal to exercise sufficient self-control and frustration tolerance to achieve one’s personal goals, or to restrain the excessive expression of one’s emotions and impulses. In its milder form, patient presents with an exaggerated emphasis on discomfort avoidance: avoiding pain, conflict, confrontation, responsibility, or overexertion—at the expense of personal fulfillment, commitment, or integrity.
12. SUBJUGATION Excessive surrendering of control to others because one feels coerced—usually to avoid anger, retaliation, or abandonment. There are two major forms of subjugation:
A. Subjugation of needs: Suppression of one’s preferences, decisions, and desires. B. Subjugation of emotion: Suppression of emotional expression, especially anger.
Usually involves the perception that one’s own desires, opinions, and feelings are not valid or important to others. Frequently presents as excessive compliance, combined with hypersensitivity to feeling trapped. Generally leads to a buildup of anger, manifested in maladaptive symptoms (e.g., passive–aggressive behavior, uncontrolled outbursts of temper, psychosomatic symptoms, withdrawal of affection, “acting out,” substance abuse).
13. SELF-SACRIFICE Excessive focus on voluntarily meeting the needs of others in daily situations at the expense of one’s own gratification. The most common reasons are to prevent causing pain to others, to avoid guilt from feeling selfish, or to maintain the connection with others perceived as needy. Often results from an acute sensitivity to the pain of others. Sometimes leads to a sense that one’s own needs are not being adequately met and to resentment of those who are taken care of. (Overlaps with concept of codependency.)
14. APPROVAL SEEKING/RECOGNITION SEEKING Excessive emphasis on gaining approval, recognition or attention from other people or fitting in, at the expense of developing a secure and true sense of self. One’s sense of esteem is dependent primarily on the reactions of others rather than on one’s own natural inclinations. Sometimes includes an overemphasis on status, appearance, social acceptance, money, or achievements—as a means of gaining approval, admiration, or attention (not primarily for power or control). Frequently results in major life decisions that are inauthentic or unsatisfying, or in hypersensitivity to rejection.
(continued)
FIGURE 7.1. (continued)
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that later prove maladaptive. For example, a child who is criticized repeatedly may develop a Failure schema: a sense that no matter what he/she does, his/her perfor- mance will never be good enough.
A schema usually occurs outside of awareness and may remain dormant until a life event (e.g., being fired from a job) activates it. In this example, once the Fail- ure schema has been activated, the patient categorizes, selects, and encodes information in such a way that the schema is maintained. EMSs therefore predispose many depressed patients to distort events in a characteristic fashion, leading to a negative view of themselves, the environment, and the future.
For patients who have a large number of strong and deeply entrenched EMSs, and for patients who cope
with their schemas by rigidly avoiding life situations or by overcompensating for them, we have found that the concept of “schema modes” (Young et al., 2003) is very often invaluable in understanding and changing patients’ thoughts, feelings, and behaviors. Mode work strengthens and develops healthy modes and weakens dysfunctional modes, thereby increasing control over one’s responding.
Young’s concept of a mode is similar to that of an ego state. A mode is defined as “those schemas or schema operations—adaptive or maladaptive—that are cur- rently active for an individual” (Young et al., 2003, p. 271). Modes include whatever an individual is think- ing, feeling, and doing at a given point in time, and may therefore be thought of as states rather than traits. A
15. NEGATIVITY/PESSIMISM A pervasive, lifelong focus on the negative aspects of life (pain, death, loss, disappointment, conflict, guilt, resentment, unsolved problems, potential mistakes, betrayal, things that could go wrong, etc.), while minimizing or neglecting the positive or optimistic aspects. Usually includes an exaggerated expectation—in a wide range of work, financial, or interpersonal situations—that things will eventually go seriously wrong, or that aspects of one’s life that seem to be going well will ultimately fall apart. Usually involves an inordinate fear of making mistakes that might lead to financial collapse, loss, humiliation, or being trapped in a bad situation. Because potential negative outcomes are exaggerated, these patients are frequently characterized by chronic worry, vigilance, complaining, or indecision.
16. EMOTIONAL INHIBITION The excessive inhibition of spontaneous action, feeling, or communication—usually to avoid disapproval by others, feelings of shame, or losing control of one’s impulses. The most common areas of inhibition involve (A) inhibition of anger and aggression; (B) inhibition of positive impulses (e.g., joy, affection, sexual excitement, play); (C) difficulty expressing vulnerability or communicating freely about one’s feelings, needs, etc.; or (D) excessive emphasis on rationality while disregarding emotions.
17. UNRELENTING STANDARDS/HYPERCRITICALNESS The underlying belief that one must strive to meet very high internalized standards of behavior and performance usually to avoid criticism. Typically results in feelings of pressure or difficulty slowing down and in hypercriticalness toward oneself and others. Must involve significant impairment in pleasure, relaxation, health, self-esteem, sense of accomplishment, or satisfying relationships. Unrelenting standards typically present as (A) perfectionism, inordinate attention to detail, or an underestimate of how good one’s own performance is relative to the norm; (B) rigid rules and “shoulds” in many areas of life, including unrealistically high moral, ethical, cultural, or religious precepts; or (C) preoccupation with time and efficiency so that more can be accomplished.
18. PUNITIVENESS The belief that people should be harshly punished for making mistakes. Involves the tendency to be angry, intolerant, punitive, and impatient with those people (including oneself) who do not meet one’s expectations or standards. Usually includes difficulty forgiving mistakes in oneself or others because of a reluctance to consider extenuating circumstances, allow for human imperfection, or empathize with feelings.
FIGURE 7.1. (continued)
Cognitive Therapy for Depression 273
dysfunctional mode is activated when specific maladap- tive schemas have erupted into distressing emotions, avoidance responses, or self-defeating behaviors that take over and control an individual’s functioning at a given point in time. An individual may “flip” from one mode to another; as that shift occurs, an individual’s cognitions, emotions, and coping responses change as well. Young and colleagues have identified four main types of modes: Child modes (Figure 7.2a), Maladap-
tive Coping modes (Figure 7.2b), Dysfunctional Par- ent modes (Figure 7.2c), and the Healthy Adult mode. The Healthy Adult mode is “the healthy, adult part of the self that serves an ‘executive’ function relative to the other modes. The Healthy Adult helps meet the child’s basic emotional needs. Building and strengthening the patient’s Healthy Adult to work with the other modes more effectively is the overarching goal of mode work in ST” (Young et al., 2003, p. 277).
FIGURE 7.2A. Child modes. From Young, Klosko, and Weishaar (2003). Copyright © 2003 The Guilford Press. Reprinted by permission.
Child Mode Description Common associated schemas
Vulnerable Child Experiences dysphoric or anxious affect, especially fear, sadness, and helplessness, when “in touch” with associated schemas.
Abandonment, Mistrust/Abuse, Emotional Deprivation, Defectiveness, Social Isolation, Dependence/Incompetence, Vulnerability to Harm or Illness, Enmeshment/Undeveloped Self, Negativity/Pessimism.
Angry Child Vents anger directly in response to perceived unmet core needs or unfair treatment related to core schemas.
Abandonment, Mistrust/Abuse, Emotional Deprivation, Subjugation (or, at times, any of the schemas associated with the Vulnerable Child).
Impulsive/ Undisciplined Child
Impulsively acts according to immediate desires for pleasure without regard to limits or others’ needs or feelings (not linked to core needs).
Entitlement, Insufficient Self-Control/Self- Discipline.
Happy Child Feels loved, connected, content, satisfied. None. Absence of activated schemas.
FIGURE 7.2B. Maladaptive Coping modes. From Young, Klosko, and Weishaar (2003). Copyright © 2003 The Guilford Press. Reprinted by permission.
Maladaptive Coping Modes
Description
Compliant Surrenderer Adopts a coping style of compliance and dependence.
Detached Protector Adopts a coping style of emotional withdrawal, disconnection, isolation, and behavioral avoidance.
Overcompensator Adopts a coping style of counterattack and control. May overcompensate through semiadaptive means, such as workaholism.
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Research Related to Schema Theory
A large number of research studies have examined the 18 EMSs, as measured by the Young Schema Ques- tionnaire (YSQ; Young, 2005). While the results have varied somewhat across different populations, all 18 EMSs have generally been supported (e.g., Calvete, Orue, & González-Diez, 2013; Lee, Taylor, & Dunn, 1999; Schmidt, 1994; Schmidt, Joiner, Young, & Telch, 1995).
Numerous studies have examined EMSs in de- pressed patients. Hawke and Provencher (2011) provide an excellent review of research on EMSs in both mood (Halvorsen et al., 2009; Halvorsen, Wang, Eisemann, & Waterloo, 2010; Özdin et al., 2018; Riso et al., 2003, 2006; Wang, Halvorsen, Eisemann, & Waterloo, 2010) and anxiety disorders. Elevations across most, if not all, schema domains have been evident when comparing depressed patients with never-ill controls. For example, in a study specifically comparing EMSs in patients with chronic depression, nonchronic depression, and healthy controls, Riso and colleagues (2003) found that both depressed groups scored higher on all schema domains compared to healthy controls. However, the scores in the chronic depression group were highest on schemas in the disconnection and rejection, impaired autonomy and performance, and overvigilance domains, even when researchers controlled for depressive and person- ality disorder symptoms. Hawke and Provencher (2011, p. 261) note: “This suggests that chronic depression is associated more strongly with EMSs than the non- chronic form, and that this association is not simply a function of current depressive or Axis II symptoms.”
Renner, Lobbestael, Peeters, Arntz, and Huibers
(2012) also found EMSs, particularly those in the dis- connection and rejection and impaired autonomy and performance domains, to be related to severity of de- pressive symptoms. They note that, consistent with Beck’s theory, “these findings are consistent with the cognitive model of depression, placing schemas or core beliefs in the domains of failure, loss, and worthlessness at the core of depressive symptoms” (p. 587). In their examination of the robustness of EMSs with evidence- based treatments (CBT and interpersonal psychothera- py, with and without medication) for depression, they found that EMSs remained relatively stable over time (pre- and posttreatment). This finding is consistent with Young and colleagues’ (2003) notion of EMSs as stable, trait-like beliefs that remained even after suc- cessful treatment of Axis I symptoms. According to the schema model, these results should not be surprising, since none of the treatments in this study specifically targeted change in EMSs. A study by Calvete, Orue, and Hankin (2015) also revealed that EMSs did not moderate the effect of stressors on symptoms of depres- sion and anxiety in adolescents, further suggesting the independence, and perhaps stability, of EMS domains.
In another study examining the relationship between EMSs and depression, Eberhart, Auerbach, Bigda- Peyton, and Abela (2011) examined how EMSs and stress impact depressive symptoms by comparing two models of stress: diathesis–stress and stress generation. The diathesis–stress model posits that EMSs only create vulnerability to depression when interacting with high levels of stressors. The stress generation model posits that EMSs are instrumental in creating stressful condi- tions which then increase depression. The results sup-
Dysfunctional Parent Mode
Description Common associated schemas
Punitive/Critical Parent Restricts, criticizes, or punishes the self or others.
Subjugation, Punitiveness, Defectiveness, Mistrust/Abuse (as abuser).
Demanding Parent Sets high expectations and high level of responsibility toward others; pressures the self or others to achieve them.
Unrelenting Standards, Self-Sacrifice.
FIGURE 7.2C. Dysfunctional Parent modes. From Young, Klosko, and Weishaar (2003). Copyright © 2003 The Guilford Press. Reprinted by permission.
Cognitive Therapy for Depression 275
ported the stress generation hypothesis. The researchers noted that
a number of maladaptive schemas in the domains of disconnection and rejection, impaired autonomy and performance, and other-directedness predicted the gen- eration of dependent, interpersonal stressors. These dependent interpersonal stressors, in turn, predicted increases in depressive symptoms. Moreover, there was evidence that these stressors mediated the relationships between maladaptive schemas and depressive symptoms. In particular, mediation effects were observed for subju- gation schemas, failure schemas, and a number of sche- mas related to disconnection and rejection. (p. 96)
This research highlights the importance of targeting EMSs in the treatment of chronic depression.
In the following sections we present information about the general characteristics and nature of cognitive therapy, a discussion of the process of cognitive therapy, then two case examples that illustrate cognitive therapy in action. The patient in the first case has a nonchronic form of depression and is treated with “standard” cog- nitive therapy (as originally outlined in Beck et al.’s [1979] book). The focus of standard cognitive therapy is on changing depressive thinking in the present. The patient in the second case has chronic depression and is treated with both cognitive therapy and ST. The focus of ST, in this case, is on identifying and modifying the patient’s underlying schemas through mode work.
CHARACTERISTICS OF COGNITIVE THERAPY
Cognitive therapy with adult depressed outpatients is usually undertaken in the therapist’s office. It has most frequently been applied in a one-to-one setting. How- ever, group cognitive therapy has also been shown to be successful with many depressed outpatients (Oei, 2008), although it may not be as effective as individ- ual treatment, at least in the short-term (Cuijpers, van Straten, & Warmerdam, 2008; Huntley & Salisbury, 2012). Additionally, computer-assisted cognitive ther- apy for depression appears to show promise (Cowper- twait & Clark, 2013; Eells, Barrett, Wright, & Thase, 2014), although findings across trials have been mixed (So et al., 2013). It is not unusual to involve spouses, partners, parents, and other family members during treatment. For example, they may provide information
that helps patients test the validity of their thinking with respect to how other family members view them. Moreover, couple therapy based on the cognitive model is often very effective in relieving depression related to chronic interpersonal problems (e.g., Beck, 1988; Cohen, O’Leary, & Foran, 2010).
In our clinical experience, a number of therapist characteristics contribute to effective cognitive therapy. First, cognitive therapists ideally should demonstrate the “nonspecific” therapy skills identified by other writ- ers (see, e.g., Truax & Mitchell, 1971): They should be able to communicate warmth, genuineness, sincer- ity, and openness. Second, the most effective cognitive therapists seem to be especially skilled at seeing events from their patients’ perspectives (accurate empathy). They are able to suspend their own personal assump- tions and biases while listening to depressed patients de- scribe their reactions and interpretations. Third, skilled cognitive therapists can reason logically and plan strate- gies; they are not “fuzzy” thinkers. In this respect, they resemble good trial lawyers, who can spot the some- times subtle flaws in another individual’s reasoning and skillfully elicit a more convincing interpretation of the same events. Skilled cognitive therapists plan strategies several steps ahead, anticipating the desired outcome. Fourth, the best practitioners of this approach are ac- tive. They have to be comfortable taking the lead, pro- viding structure and direction to the therapy process.
Although patient characteristics have received some empirical attention (Eifert, Beach, & Wilson, 1998; Padesky, with Greenberger, 2021; Persons, Burns, & Perloff, 1988; Schindler, Hiller, & Witthöft, 2013), we do not yet have adequate knowledge as to which patient characteristics are related to success in cognitive ther- apy. Our experience suggests that patients with major depressive disorder (or milder forms of depression) re- spond well to the cognitive therapy approach described in this chapter. To the extent that the patient was diag- nosed with Axis II personality disorders and/or his/her depression was chronic, the combination of cognitive therapy and ST may be significantly longer in duration and more crucial in obtaining a more complete and last- ing positive response to treatment.
Cognitive therapy can serve an important adjunctive role to pharmacotherapy for bipolar disorders (Ball et al., 2006; Basco & Rush, 1996; Chiang et al., 2017; Craighead, Miklowitz, Vajk, & Frank, 1998; Lam, Hayward, Watkins, Wright, & Sham, 2005), and is ef- fective in treating patients with severe endogenous de-
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pression (Thase, Bowler, & Harden, 1991; Whisman, 1993). Preliminary evidence also suggests that cogni- tive therapy is effective in the treatment of women with postpartum depression (Huang, Zhao, Qiang, & Fan, 2018).
It is advisable to assess patients’ suitability for cogni- tive therapy (Padesky, with Greenberger, 2021; Safran & Segal, 1990; Safran, Segal, Vallis, Shaw, & Samstag, 1993). In our experience, certain patient characteristics are predictive of a more rapid response. “Ideal” cogni- tive therapy patients are appropriately introspective and can reason abstractly; are well organized, good plan- ners, and conscientious about carrying out responsi- bilities; are employed or have a history of employment; are not excessively angry at either themselves or other people; are less dogmatic and rigid in their thinking; can identify a clear precipitating event for the depressive episode; and have close relationships with others. Most patients deviate in some ways from this prototype, and these characteristics are not essential to successful treat- ment. However, patients with more of these attributes often show faster improvement in depressive symptoms through cognitive therapy.
Age is not an obstacle. Many studies have indicated that children and adolescents show significant clini- cal improvement following CBT (Oud et al., 2019; Reinecke, Ryan, & DuBois, 1998). Studies of older pa- tients also show that “various forms of cognitive and behavioral psychotherapy can be as effective in treating geriatric depression as depressions occurring earlier in life” (Futterman, Thompson, Gallagher-Thompson, & Ferris, 1995, p. 511; Francis & Kumar, 2013; Thomas et al., 2018).
COLLABORATION
Basic to cognitive therapy is a collaborative relationship between patient and therapist. When therapist and pa- tient work together, the learning experience is enhanced for both, and the cooperative spirit that is developed contributes greatly to the therapeutic process. Equally important, the collaborative approach helps to ensure compatible goals for treatment, and to prevent misun- derstandings and misinterpretations between patient and therapist. Because of the importance of the col- laborative relationship, we place great emphasis on the interpersonal skills of the therapist, the process of joint selection of problems on which to work, regular feed-
back, and the investigative process we call “collabora- tive empiricism.”
Interpersonal Qualities
Because collaboration requires that the patient trust the therapist, we emphasize those interpersonal qualities that contribute to trust. As noted earlier, warmth, ac- curate empathy, and genuineness are desirable personal qualities for the cognitive therapist, as well as for all psy- chotherapists. It is important that the cognitive thera- pist not seem to be playing the role of therapist. The therapist should be able to communicate both verbally and nonverbally that he/she is sincere, open, concerned, and direct. It is also important that the therapist not seem to be withholding impressions or information, or evading questions. The therapist should be careful not to seem critical or disapproving of the patient’s perspec- tive.
Rapport between patient and therapist is crucial in the treatment of depressed patients. When rapport is optimal, patients perceive the therapist as someone who is tuned in to their feelings and attitudes, who is sym- pathetic and understanding, and with whom they can communicate without having to articulate feelings in detail or qualify statements. When the rapport is good, both patient and therapist feel comfortable and secure.
A confident, professional manner is also important in cognitive therapy. A therapist should convey relaxed confidence in his/her ability to help a depressed patient. Such confidence can help to counteract the patient’s initial hopelessness about the future. Because the cogni- tive therapist must sometimes be directive and impose structure, especially in the early stages of treatment, it is helpful to maintain a clear sense of professionalism.
Joint Determination of Goals for Therapy
The patient and therapist collaboratively work together to set therapeutic goals, determine priorities among them, and create an agenda for each session. Problems to be addressed over the course of therapy include spe- cific depressive symptoms (e.g., hopelessness, crying, and difficulty concentrating) and external problems (e.g., couple difficulties, career issues, child-rearing concerns). Priorities are then jointly determined in accordance with how much distress is generated by a particular problem and how amenable that particular problem is to change. During the agenda-setting por-
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tion of each therapy session (discussed in detail in the next section), therapist and patient together determine the items to be covered in that session. Through this collaborative process, target problems are selected on a weekly basis.
The process of problem selection often presents dif- ficulties for the novice cognitive therapist, including failure to reach agreement on specific problems on which to focus, selection of peripheral concerns, and the tendency to move from problem to problem instead of persistently seeking a satisfactory solution to only one problem at a time. Because the problem selection process entails both structuring and collaboration on the part of the therapist, considerable skill is necessary.
Regular Feedback
Feedback is especially important in therapy with de- pressed patients; it is a crucial ingredient in develop- ing and maintaining the collaborative therapeutic rela- tionship. The cognitive therapist initiates the feedback component early in therapy by eliciting the patient’s thoughts and feelings about many aspects of the ther- apy, such as the handling of a particular problem, the therapist’s manner, and homework assignments. Since many patients misconstrue therapists’ statements and questions, it is only through regular feedback that the therapist can ascertain whether he/she and the patient are on the same “wavelength.” The therapist must also be alert for verbal and nonverbal clues to covert negative reactions.
As part of the regular feedback process, the cognitive therapist shares the rationale for each intervention. This helps to demystify the therapy process and facilitates the patient’s questioning of the validity of a particular approach. In addition, when a patient understands how a particular technique or assignment may help solve a particular problem in the patient’s life, he/she is more likely to participate conscientiously.
Another key element of the feedback process is for the therapist to check regularly to determine whether the patient understands his/her formulations. Patients sometimes agree with a formulation simply out of com- pliance, and depressed patients frequently exhibit both compliance and reluctance to “talk straight” with their therapists for fear of being rejected or criticized, or of making a mistake. Therefore, the therapist must make an extra effort to elicit the patient’s feelings or wishes relevant to compliance (e.g., anxiety about rejection,
wish to please) and be alert for verbal and nonverbal clues that the patient may indeed not understand the explanations.
At the close of each session the cognitive therapist provides a concise summary of what has taken place and asks the patient to abstract and write down the main points from the session. The patient keeps this summary for review during the week. In practice, the therapist uses capsule summaries frequently during a standard therapeutic interview: in preparing the agen- da, in a midpoint recapitulation of the material covered up to that point, and in the final summary of the main points of the interview. Patients generally respond favorably to the elicitation of feedback and presenta- tion of capsule summaries. We have observed that the development of empathy and rapport is facilitated by these techniques.
Collaborative Empiricism
When the collaborative therapeutic relationship has been successfully formed, patient and therapist act as an investigative team. Though we elaborate on the in- vestigative process later, it is appropriate to introduce it in the context of the collaborative relationship. As a team, patient and therapist approach the patient’s auto- matic thoughts and schemas in the same manner that scientists approach questions: Each thought or schema becomes a hypothesis to be tested, and evidence is gath- ered that supports or refutes the hypothesis. Events in the past, circumstances in the present, and possibilities in the future are the data that constitute evidence, and the conclusion to accept or reject the hypothesis is joint- ly reached as patient and therapist subject the evidence to logical analysis. Experiments may also be devised to test the validity of particular cognitions. Cognitive therapists need not persuade patients of illogicality or inconsistency with reality, because patients “discover” their own inconsistencies. This guided discovery pro- cess, a widely accepted educational method, is one of the vital components of cognitive therapy.
THE PROCESS OF COGNITIVE THERAPY
Here we attempt to convey a sense of how cognitive therapy sessions are structured and of the course of treatment. Detailed discussion of particular techniques follows this section.
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The Initial Sessions
A main therapeutic goal of the first few sessions is to produce some symptom relief. Reducing the patient’s suffering helps to increase rapport, collaboration, and confidence in the therapeutic process. Symptom relief, however, should be based on more than rapport, sym- pathy, and implied promise of “cure.” In the first few sessions, the cognitive therapist starts the process of de- fining the patient’s problems and demonstrating some of the strategies that will be used in the therapy to deal with those problems.
Problem definition is a primary goal in the early stag- es of therapy. The therapist collaboratively works with the patient to define the specific problems on which they will focus during therapy sessions. The cognitive therapist does this by obtaining as complete a picture as possible of the patient’s psychological and life situation difficulties. The therapist also seeks details concerning the depth of depression and particular symptomatol- ogy. Cognitive therapists are especially concerned with how patients see their problems.
Once the specific problems have been defined, pa- tient and therapist establish priorities among them. Decisions are made on the basis of amenability to therapeutic change and centrality of the life problem or cognition to the patient’s emotional distress. To help establish priorities effectively, the therapist must see the relationships among particular thoughts, particular life situations, and particular distressing emotions.
Another goal of the initial session is to illustrate the close relationship between cognition and emotion. When the therapist is able to observe the patient’s mood change (e.g., crying), he/she points out the alteration in affect and asks for the patient’s thoughts just before the mood shift. The therapist then labels the negative thought and points out its relationship to the change in mood. He/she initially gears homework assignments toward helping the patient see the close connection be- tween cognition and emotion.
A frequent requirement in the early stage of therapy is to socialize the patient to cognitive therapy. A patient who has previously undertaken analytically oriented or Rogerian therapies may begin cognitive therapy expect- ing a more insight-oriented, nondirective therapeutic approach. The cognitive therapist can facilitate the transition to a more active and structured approach by maintaining a problem-oriented stance, which often entails gently interrupting a patient who tends to specu-
late about the sources of the problems and to seek inter- pretations from the therapist.
Finally, the therapist must communicate the impor- tance of self-help homework assignments during the initial session by stressing that the homework is actu- ally more important than the therapy session itself. The therapist also can enhance motivation by explaining that patients who complete assignments generally im- prove more quickly. The nature and implementation of self-help homework assignments are considered in fur- ther detail in a later section of this chapter.
The Progress of a Typical Therapy Session
Each session begins with the establishment of an agen- da for that session. This ensures optimal use of time in a relatively short-term, problem-solving therapeutic approach. The agenda generally begins with a short synopsis of the patient’s experiences since the last ses- sion, including discussion of the homework assignment. The therapist then asks the patient what he/she wants to work on during the session, and often offers topics to be included.
When a short list of problems and topics has been completed, patient and therapist determine the order in which to cover them and, if necessary, the time to be al- lotted to each topic. There are several issues to consider in establishing priorities, including stage of therapy, severity of depression, likelihood of making progress in solving the problem, and potential pervasiveness of the effect of a particular theme or topic. The cognitive therapist is sensitive to a patient’s occasional desire to talk about something that seems important to him/her at the moment, even if such discussion seems not to be productive in terms of other goals. This kind of flex- ibility characterizes the collaborative therapeutic rela- tionship.
After these preliminary matters have been covered, patient and therapist move on to the one or two prob- lems to be considered during the session. The therapist begins the discussion of a problem by asking the patient a series of questions designed to clarify the nature of the patient’s difficulty. In doing so, the therapist seeks to determine whether early maladaptive schemas, mis- interpretations of events, or unrealistic expectations are involved. The therapist also seeks to discover whether the patient had unrealistic expectations, whether the patient’s behavior was appropriate, and whether all possible solutions to the problem were considered. The
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patient’s responses suggest to the therapist a cognitive- behavioral conceptualization of why the patient is hav- ing difficulty in the area of concern. The therapist by now has discerned the one or two significant thoughts, schemas, images, or behaviors on which to work. When this target problem has been selected, the therapist chooses the cognitive or behavioral techniques to apply and shares their rationale with the patient. The specific techniques used in cognitive therapy are explained in the following sections of this chapter.
At the close of the session, the therapist asks the patient for a summary, often in writing, of the major conclusions drawn during the session. The therapist asks for the patient’s reactions to the session to ascertain whether anything disturbing was said and to forestall any delayed negative reactions following the interview. Finally, the therapist gives a homework assignment de- signed to assist the patient in applying the particular skills and concepts from the session to the problem dur- ing the following week.
Progression of Session Content over Time
Although the structure of cognitive therapy sessions does not change during the course of treatment, the content often changes significantly. The first phase of treatment, symptom reduction, focuses on overcoming hopelessness, identifying problems, setting priorities, socializing the patient to cognitive therapy, establishing a collaborative relationship, demonstrating the relation- ship between cognition and emotion, labeling errors in thinking, and making progress on a target problem. Therapy is initially centered on the patient’s symptoms, with attention given to behavioral and motivational dif- ficulties.
In the second phase, which focuses on chang- ing schemas for relapse prevention and chronic cases, therapist and patient turn from specific thoughts about particular problems to core schemas about the self and others, and to the modes associated with those sche- mas. Therapist and patient explore how the schemas and modes initiate, exacerbate, and maintain many of the patient’s problems. Therapist and patient then work collaboratively to restructure and modify the schemas and modes through a variety of techniques, which even- tually brings about a broader and more pervasive im- provement in life functioning and mood.
Over the course of therapy, the patient assumes in- creased responsibility for identifying problems, com-
ing up with solutions, and implementing the solutions through homework assignments. The therapist increas- ingly assumes the role of advisor or consultant as the patient learns to implement therapeutic techniques without constant support. As the patient becomes a more effective problem solver, the frequency of sessions is reduced, and therapy is eventually discontinued.
The remainder of this chapter is devoted to a detailed description of cognitive- and schema-based treatment strategies.
SYMPTOM REDUCTION
Behavioral Techniques
Behavioral techniques are used throughout the course of cognitive therapy, but they are generally concentrat- ed in the earlier stages of treatment. Behavioral tech- niques are especially necessary for those more severely depressed patients who are passive, anhedonic, socially withdrawn, and unable to concentrate for extended periods of time. By engaging such a patient’s attention and interest, the cognitive therapist tries to induce the patient to counteract withdrawal and become more in- volved in constructive activity. From a variety of be- havioral techniques, the therapist selects those that will help the patient cope more effectively with situational and interpersonal problems. Through homework as- signments, the patient implements specific procedures for dealing with concrete situations or for using time more adaptively.
The cognitive therapist uses behavioral techniques, with the goal of modifying automatic thoughts. For ex- ample, a patient who believes “I can’t get anything done any more” can modify this thought after completing a series of graded tasks designed to increase mastery. The severely depressed patient is caught in a vicious cycle, in which a reduced activity level leads to a negative self-label, which in turn results in even further discour- agement and consequent inactivity. Intervention with behavioral techniques can change this self-destructive pattern.
The most commonly used behavioral techniques in- clude scheduling activities that include both mastery and pleasure exercises, cognitive rehearsal, self-reliance training, role playing, and diversion techniques. The scheduling of activities is frequently used in the early stages of cognitive therapy to counteract loss of moti-
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vation, hopelessness, and excessive rumination. The therapist uses the Weekly Activity Schedule for plan- ning activities hour by hour, day by day (see Figure 7.3). Patients maintain an hourly record of the activities in which they engaged. Activity scheduling also helps patients obtain more pleasure and a greater sense of accomplishment from activities on a daily basis. The patients rate each completed activity (using a 0- to 10- point scale) for both mastery and pleasure. The ratings usually contradict patients’ beliefs that they can no lon- ger accomplish or enjoy anything. To assist some pa- tients in initiating mastery and pleasure activities, the therapist may sometimes find it necessary to subdivide an activity into segments, ranging from the simplest to the most difficult and complex aspects of the activity. We call this the “graded task” approach. The subdivi- sion enables depressed patients to undertake tasks that
were initially impossible, thus providing proof of suc- cess.
Cognitive rehearsal entails asking a patient to picture or imagine each step involved in the accomplishment of a particular task. This technique can be especially help- ful with those patients who have difficulty carrying out a task that requires successive steps for its completion. Sometimes impairment in the ability to concentrate creates difficulties for the patient in focusing attention on the specific task. The imagery evoked by the cogni- tive rehearsal technique helps the patient to focus and the therapist to identify obstacles that make the assign- ment difficult for the particular patient.
Some depressed patients rely on others to take care of most of their daily needs. With self-reliance train- ing, patients learn to assume increased responsibility for routine activities such as showering, making their beds,
FIGURE 7.3. Weekly Activity Schedule.
Note: Grade activities M for mastery and P for pleasure 0–10.
Mon. Tues. Wed. Thurs. Fri. Sat. Sun.
M or
ni ng
6–7
7–8
8–9
9–10
10–11
11–12
A fte
rn oo
n
12–1
1–2
2–3
3–4
4–5
5–6
E ve
ni ng
6–7
7–8
8–9
9–10
10–11
11–12
12–6
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cleaning the house, cooking their own meals, and shop- ping. Self-reliance involves gaining increased control over emotional reactions.
Role playing has many uses in cognitive therapy. First, it may be used to bring out automatic thoughts through the enactment of particular interpersonal situ- ations, such as an encounter with a supervisor at work. Second, through homework assignments, it may also guide the patient in practicing and attending to new cognitive responses in problematic social encounters. A third use of role playing is to rehearse new behaviors. Thus, role playing may be used as part of assertiveness training and is often accompanied by modeling and coaching.
Role reversal, a variation of role playing, can be very effective in helping patients test how other people might view their behavior. This is well illustrated by a patient who had a “humiliating experience” while buying some clothes in a store. After playing the role of the clerk, the patient had to conclude that she had insufficient data for her previous conclusion that she appeared clumsy and inept. Through role reversal, patients begin to view themselves less harshly as “self-sympathy” responses are elicited.
Finally, the therapist may introduce various distrac- tion techniques to assist the patient in learning to re- duce the intensity of painful affects. The patient learns to divert negative thinking through physical activity, social contact, work, play, and visual imagery. Practice with diversion techniques also helps the patient gain further control over emotional reactivity.
Cognitive Techniques
The specific cognitive techniques provide points of entry into the patient’s cognitive organization. The cognitive therapist uses techniques for eliciting and testing automatic thoughts, and identifying schemas to help both therapist and patient understand the patient’s construction of reality. In applying specific cognitive techniques in therapy, it is important that the therapist work within the framework of the cognitive model of depression. Each set of techniques is discussed in turn.
Eliciting Automatic Thoughts
Automatic thoughts are those thoughts that intervene between outside events and the individual’s emotional reactions to them. They often go unnoticed, because they are part of a repetitive pattern of thinking, and because
they occur so often and so quickly. People rarely stop to assess their validity, because they are so believable, famil- iar, and habitual. The patient in cognitive therapy must learn to recognize these automatic thoughts for therapy to proceed effectively. The cognitive therapist and the patient make a joint effort to discover the particular thoughts that precede emotions such as anger, sadness, and anxiety. The therapist uses questioning, imagery, and role playing to elicit automatic thoughts.
The simplest method to uncover automatic thoughts is for therapists to ask patients what thoughts went through their minds in response to particular events. This questioning provides a model for introspective exploration that patients can use on their own, when the therapist is not present, and after the completion of treatment.
Alternatively, when a patient is able to identify those external events and situations that evoke a particular emotional response, the therapist may use imagery by asking the patient to picture the situation in detail. The patient is often able to identify the automatic thoughts connected with actual situations when the image evoked is clear. In this technique, therapists ask patients to relax, close their eyes, and imagine themselves in the distressing situation. Patients describe in detail what is happening as they relive the event.
If a distressing event is an interpersonal one, cogni- tive therapists also can utilize role playing. The therapist plays the role of the other person in the encounter, while the patient plays him/herself. The automatic thoughts can usually be elicited when the patient becomes suf- ficiently engaged in the role play.
In attempting to elicit automatic thoughts, the thera- pist is careful to notice and point out any mood changes that occur during the session, and to ask the patient his/her thoughts just before the shift in mood. Mood changes include any emotional reaction, such as tears or anger. This technique can be especially useful when the patient is first learning to identify automatic thoughts.
Once patients become familiar with the techniques for identifying automatic thoughts, they are asked to keep a Daily Record of Dysfunctional Thoughts (Beck et al., 1979; see Figure 7.4), in which they record the emotions and automatic thoughts that occur in upset- ting situations between therapy sessions. In later ses- sions, patients are taught to develop rational responses to their dysfunctional automatic thoughts and to record them in the appropriate column. Therapist and patient generally review the daily record from the preceding week, near the beginning of the next therapy session.
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In sessions, the therapist also teaches chronic patients to recognize modes. Various affective exercises are then used to bring about change in the underlying schemas associated with those modes.
Eliciting automatic thoughts should be distinguished from the interpretation process of other psychothera- pies. In general, cognitive therapists work only with those automatic thoughts mentioned by patients. Sug- gesting thoughts to patients may undermine collabora- tion and inhibit patients from learning to continue the process on their own. As a last resort, however, when nondirective strategies fail, a cognitive therapist may offer several possible automatic thoughts, then ask the patient whether any of these choices fit.
Even when many efforts to elicit automatic thoughts have been made by the therapist, sometimes the thought remains inaccessible. When this is the case, the cogni- tive therapist tries to ascertain the particular meaning of the event that evoked the emotional reaction. For ex- ample, one patient began to cry whenever she had an argument with her roommate, who was a good friend. Efforts to elicit automatic thoughts proved unsuccess-
ful. Only after the therapist asked a series of questions to determine the meaning of the event did it become clear that the patient associated having an argument or fight with ending the relationship. Through this pro- cess, therapist and patient were able to see the meaning that triggered the crying.
Testing Automatic Thoughts with Nonchronic Patients
When therapist and patient have managed to isolate a key automatic thought, they approach the thought as a testable hypothesis. In this “scientific” approach, which is fundamental to cognitive therapy, the patient learns to think in a way that resembles the investigative pro- cess. Through the procedures of gathering data, evalu- ating evidence, and drawing conclusions, patients learn firsthand that their view of reality can be quite differ- ent from what actually takes place. By designing experi- ments that subject their automatic thoughts to objective analysis, patients learn how to modify their thinking, because they learn the process of empirical thinking. Pa- tients who learn to think this way during treatment are
FIGURE 7.4. Daily Record of Dysfunctional Thoughts.
DATE
SITUATION EMOTION(S) AUTOMATIC THOUGHT(S) RATIONAL RESPONSE OUTCOME Describe:
1. Actual event leading to unpleasant emotion, or
2. Stream of thoughts, daydream, or recollection, leading to unpleasant emotion.
1. Specify sad/ anxious/ angry, etc.
2. Rate degree of emotion, 1–100.
1. Write automatic thought(s) that preceded emotion(s).
2. Rate belief in automatic thought(s), 0–100%.
1. Write rational response to automatic thought(s).
2. Rate belief in rational response, 0–100%.
1. Rerate belief in automatic thought(s), 0–100%.
2. Specify and rate subsequent emotions, 0–100%.
Explanation: When you experience an unpleasant emotion, note the situation that seemed to stimulate the emotion. (If the emotion occurred while you were thinking, daydreaming, etc., please note this.) Then note the automatic thought associated with the emotion. Record the degree to which you believe this thought: 0% = not at all; 100% = completely. In rating degrees of emotion: 1 = a trace; 100 = the most intense possible.
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better able to continue the empirical approach after the end of formal therapy.
The cognitive therapist approaches the testing of au- tomatic thoughts by asking the patient to list evidence from his/her experience for and against the hypothesis. Sometimes, after considering the evidence, the patient immediately rejects the automatic thought, recognizing that it is either distorted or actually false.
When previous experience is not sufficient or appro- priate to test a hypothesis, the therapist asks the patient to design an experiment for that purpose. The patient then makes a prediction and proceeds to gather data. If the data contradict the prediction, the patient can reject the automatic thought. The outcome of the experiment may, of course, confirm the patient’s prediction. It is therefore very important for the therapist not to assume that the patient’s automatic thought is distorted.
Some automatic thoughts do not lend themselves to hypothesis testing through the examination of evidence. In these cases, two options are available: The therapist may either produce evidence from his/her own experi- ence and offer it in the form of a question that reveals the contradiction or ask a question designed to uncover a logical error inherent in the patient’s beliefs. The ther- apist might say, for example, to a male patient who is sure he cannot survive without a close personal relation- ship, “You were alone last year, and you got along fine; what makes you think you can’t make it now?”
In testing automatic thoughts, it is sometimes neces- sary to refine the patient’s use of a word. This is particu- larly true for global labels such as bad, stupid, or selfish. What is needed in this case is an operational definition of the word. To illustrate, a patient at our clinic had the recurring automatic thought, “I’m a failure in math.” Therapist and patient had to narrow down the meaning of the word failure before they could test the thought. They operationalized “failure” in math as “being un- able to achieve a grade of C after investing as much time studying as the average class member.” Now they could examine past evidence and test the validity of the hypothesis. This process can help patients to see the overinclusiveness of their negative self-assessments and the idiosyncratic nature of many automatic thoughts.
Reattribution is another useful technique for help- ing the patient to reject an inappropriate, self-blaming thought. It is a common cognitive pattern in depression to ascribe blame or responsibility for adverse events to oneself. Reattribution can be used when the patient un- realistically attributes adverse occurrences to a personal deficiency, such as lack of ability or effort. Therapist
and patient review the relevant events and apply logic to the available information to make a more realistic assignment of responsibility. The aim of reattribution is not to absolve the patient of all responsibility but to examine the many factors that contribute to adverse events. Through this process, patients gain objectivity, relieve themselves of the burden of self-reproach, and can then search for ways to solve realistic problems or prevent their recurrence.
Another strategy involving reattribution is for thera- pists to demonstrate that patients’ criteria for assigning responsibility to their own unsatisfactory behavior are stricter than criteria they use in evaluating the behavior of others. Cognitive therapists also use reattribution to show patients that some of their thinking or behavior problems can be symptoms of depression (e.g., loss of concentration) and not signs of physical decay.
When a patient is accurate in identifying a realistic life problem or skills deficit, the cognitive therapist can use the technique of generating alternatives, in which therapist and patient actively search for alternative solu- tions. Because a depressed person’s reasoning often be- comes restricted, an effort to reconceptualize the prob- lem can result in the patient seeing a viable solution that he/she may previously have rejected.
It should be noted that all the cognitive techniques outlined here entail the use of questions by the thera- pist. A common error we observe in novice cognitive therapists is an exhortative style. We have found that therapists help patients to change their thinking more effectively by using carefully formed questions. If pa- tients are prompted to work their own way through problems and reach their own conclusions, they learn an effective problem-solving process. We next elaborate on the use of questioning in cognitive therapy.
Questioning
As we have stressed throughout this chapter, question- ing is a major therapeutic device in cognitive therapy. A majority of the therapist’s comments during the therapy session are questions. Single questions can serve several purposes at one time, whereas a carefully designed se- ries of questions can help patients consider a particular issue, decision, or opinion. The cognitive therapist seeks through questioning to elicit what patients are think- ing, instead of telling patients what he/she believes they are thinking.
In the beginning of therapy, questions are employed to obtain a full and detailed picture of a patient’s partic-
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ular difficulties; to obtain background and diagnostic data; to evaluate the patient’s stress tolerance, capacity for introspection, coping methods, and so on; to obtain information about the patient’s external situation and interpersonal context; and to modify vague complaints by working with the patient to arrive at specific target problems on which to work.
As therapy progresses, the therapist uses questioning to explore approaches to problems, to help the patient to weigh advantages and disadvantages of possible so- lutions, to examine the consequences of staying with particular maladaptive behaviors, to elicit automatic thoughts, and to demonstrate EMSs and their con- sequences. In short, the therapist uses questioning in most cognitive therapeutic techniques.
Although questioning is itself a powerful means of identifying and changing automatic thoughts and sche- mas, it is important that the questions be carefully and skillfully posed. If questions are used to “trap” patients into contradicting themselves, patients may come to feel that they are being attacked or manipulated by the therapist. Too many open-ended questions can leave patients wondering what the therapist expects of them. Therapists must carefully time and phrase questions to help patients recognize their thoughts and schemas, and to weigh issues objectively.
Self‑Help Homework Assignments
Rationale
Regular homework assignments are very important in cognitive therapy. When patients systematically apply what they have learned during therapy sessions to their outside lives, they are more likely to make sig- nificant progress in therapy and to be able to maintain their gains after termination of treatment. Burns and Spangler (2000) found that patients who did the most homework showed larger and more significant decreas- es in depression than those who were less compliant. Homework assignments are often the means through which patients gather data, test hypotheses, and begin to modify their thoughts and schemas. In addition, the data provided through homework assignments help to shift the focus of therapy from the subjective and ab- stract to more concrete and objective concerns. When patient and therapist review the previous week’s activi- ties during the agenda-setting portion of the interview, they may do so quickly, and the therapist can draw relationships between what takes place in the session
and specific tasks, thereby avoiding tangents and side issues. Homework assignments further patients’ self- reliance and provide them with methods to continue working on problems after the end of treatment. Cogni- tive therapists emphasize the importance of homework by sharing with patients their rationale for assigning homework in therapy. They are also careful to explain the particular benefits to be derived from each individ- ual assignment.
Assigning and Reviewing Homework
The cognitive therapist designs each assignment for the particular patient. The assignment should be directly related to the content of the therapy session, so that the patient understands its purpose and importance. Each task should be clearly articulated and very specific in nature. Near the end of each session, the assignment is written in duplicate, with one copy going to the thera- pist and the other to the patient.
Some typical homework assignments include reading a book or article about a specific problem, practicing distraction or relaxation techniques, counting auto- matic thoughts on a wrist counter, rating activities for pleasure and mastery on the Weekly Activity Sched- ule, maintaining a Daily Record of Dysfunctional Thoughts, and listening to a tape of the therapy session.
During the therapy session, the therapist asks for the patient’s reactions to homework assignments. For example, the therapist might ask whether the assign- ment is clear and manageable. To determine potential impediments, the therapist may ask the patient to imag- ine taking the steps involved in the assignment. This technique can be especially helpful during the earlier stages of therapy. The patient assumes greater responsi- bility for developing homework assignments as therapy progresses through the middle and later stages.
It is essential that patient and therapist review the previous week’s homework during the therapy session itself. If they do not, the patient may conclude that the homework assignments are not important. During the first part of the therapy sessions, therapist and patient discuss the previous week’s assignment, and the thera- pist summarizes the results.
Difficulties in Completing Homework
When a patient does not complete homework assign- ments, or does them without conviction, the cognitive therapist elicits automatic thoughts, schemas, or behav-
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ioral problems that may help them both understand where the difficulty resides. The therapist does not pre- suppose that the patient is being “resistant” or “passive– aggressive.” When the difficulties have been successful- ly identified, therapist and patient work collaboratively to surmount them. It is, of course, common for patients to have difficulties in completing homework, and here we consider some of the typical problems and ways to counteract them.
When patients do not understand the assignment completely, the therapist should explain it more fully, specifying his/her expectations in detail. Sometimes using the behavioral technique of cognitive rehearsal (described earlier) can be helpful in such situations.
Some patients believe that they are naturally disorga- nized and cannot maintain records and follow through on detailed assignments. Therapists can usually help to invalidate such general beliefs by asking patients about other circumstances in which they make lists—for example, when planning a vacation or shopping trip. Therapists can also ask these patients whether they could complete the assignment if there were a substan- tial reward entailed. This kind of question helps such patients recognize that self-control is not the problem; rather, they do not believe that the reward is great enough. When patients realize that the problem is an attitudinal one, therapist and patient can proceed to enumerate the advantages of completing the assign- ment.
More severely depressed patients may need assistance to structure their time, so that homework becomes a regular activity. This can generally be accomplished by setting a specific time each day for the homework as- signment. If necessary, patient and therapist can set up a reward system to increase motivation to complete the homework. For example, patients can reward themselves for doing the assignment by making a special purchase.
Some patients are afraid of failing the assignments or of doing them inadequately. In these cases, the thera- pist can explain that self-help assignments cannot be “failed”: Doing an assignment partially is more helpful than not doing it at all, and mistakes provide valuable information about problems that still need work. In ad- dition, because performance is not evaluated, patients cannot lose if they view the activity from a more adap- tive perspective.
Sometimes patients believe their problems are too deeply embedded and complex to be resolved through homework assignments. The therapist can explain to these patients that even the most complex undertakings
begin with and comprise small, concrete steps. A writer, for example, may resolve “writer’s blocks” by taking the attitude, “If I can’t write a book, I can at least write a paragraph.” When enough paragraphs have been writ- ten, the result is a book. Therapist and patient can con- sider the advantages and disadvantages of the patient’s belief that problems cannot be solved by doing home- work. Or the therapist can ask the patient to experi- ment before reaching such a conclusion. In instances in which a patient believes that he/she has not made enough progress and that the homework is therefore not helpful, the therapist can detail progress the patient has made or help the patient see that it may take more time before substantial change can be perceived.
When patients seem to resent being given assign- ments, the therapist can encourage them to develop their own assignments. He/she might also offer patients alternative assignments from which to choose, making one of the alternatives noncompliance with homework assignments. If patients choose noncompliance, the therapist can help to examine the consequences of that choice. Still another strategy is to present patients with a consumer model of therapy: Patients have a certain goal (overcoming depression), and the therapist offers a means to achieve that goal; patients are free to use or reject the tools, just as they are free to buy or not to buy in the marketplace.
Some patients believe that they can improve just as readily without homework. In this case, therapists have two options. First, they can offer their own clini- cal experience (which is supported by existing empirical evidence) that most patients who do not actively en- gage with and complete therapeutic homework progress more slowly in therapy. The other option is to set up an experiment for a given period of time, during which pa- tients do not have to complete assignments. At the end of the predetermined period, therapists and patients can evaluate patients’ progress during that time inter- val. Once again, it is important for cognitive therapists to keep an open mind: Some patients do indeed effect significant change without formally completing home- work assignments.
Special Problems
The novice cognitive therapist often errs by staying with the standard method we have outlined here, even if it is not working very well. The cognitive therapist should be flexible enough to adapt to the needs of patients and to the several special problems that commonly arise in
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therapy. We have grouped these special problems into two categories: difficulties in the therapist–patient re- lationship, and problems in which the therapy itself seems not to be working.
Therapist–Patient Relationship Difficulties
The first set of problems concerns the therapist–patient relationship itself. When the therapist first perceives a patient to be dissatisfied, oppositional, angry, or hostile, it is imperative that he/she present these observations to the patient in an empathic manner. It is important that the therapist refrain from responding to the patient simply with an increased and rigid adherence to pre- scribed techniques or the therapeutic rationale. It also is important that the therapist refrain from self-criti- cal statements. Research indicates that such responses have detrimental effects on the therapeutic relationship (Castonguay et al., 1996; Henry et al., 1993; Piper et al., 1999). Instead, research (Castonguay et al., 2004; Hatcher, 2015; Safran, Muran, Samstag, & Stevens, 2002; Safran et al., 2014) indicates that the therapist’s use of metacommunication skills (open discussion about the patient’s negative reaction, exploration of the patient’s experience, recognition and acknowledg- ment of the therapist’s contribution to those negative reactions) is significantly more likely to repair and re- store—and even improve—the therapeutic bond.
It is essential for therapists to be aware that many interventions can be misinterpreted in a negative way by depressed patients. Therapists approach problems of misinterpretation in the same way that they approach other thoughts: They work with patients to gather data and search for alternative accounts of the evidence. Dif- ficulties in the therapist–patient relationship can gener- ally be resolved through dialogue. There are times when a therapist may need to tailor behavior to the particular needs of an individual patient. For instance, a therapist may become freer with appropriate self-disclosure and personal reactions to meet the needs of a patient who persists in seeing the therapist as impersonal. Similarly, the therapist can make a point of checking formula- tions of the patient’s thoughts more frequently to meet the needs of a patient who continues to believe that the therapist does not understand him/her.
It is imperative in situations like these for the thera- pist not to assume that the patient is being stubbornly resistant or irrational. Therapeutic reactance (“a motiva- tional state characterized by the tendency to restore or re-assert one’s ability to engage in freedoms perceived
as lost or threatened”; Arnow et al., 2003, p. 1026) was found to be a positive predictor of treatment outcome in directive therapy with chronically depressed patients. Arnow and colleagues found that treatment was en- hanced when therapists responded in a flexible man- ner to such patient behaviors. Cognitive therapists col- laborate with patients to achieve a better understanding of patients’ responses. The reactions themselves often provide data regarding the kinds of distortions patients make in their other social and personal relationships. Therefore, patients’ responses give therapists the oppor- tunity to work with them on their maladaptive inter- pretations in relationships.
Unsatisfactory Progress
A second set of problems occurs when the therapy ap- pears not to be working, even when the patient con- scientiously completes homework assignments and the collaborative relationship seems successful. Sometimes problems stem from inappropriate expectations on the part of the patient—or unrealistic expectations on the part of the therapist—regarding the rapidity and consistency of change. When therapy seems not to be progressing as quickly as it “should,” both patient and therapist must remember that ups and downs are to be anticipated in the course of treatment. It is important for therapists to keep in mind that some patients sim- ply progress more slowly than others. The therapist or patient, or both, may be minimizing small changes that have indeed been taking place. In this case, the thera- pist can emphasize small gains that have been made and remind the patient that large goals are attained through small steps toward them.
At times, hopelessness can lead patients to invalidate their gains. Therapists should seek to uncover the mal- adaptive automatic thoughts, cognitive distortions, and early schemas that contribute to the pervasive hopeless- ness. In these cases, therapists must work to correct mistaken notions about the process of change and the nature of depression before further progress in therapy can occur.
In some cases in which therapy seems not to be work- ing successfully, it may be that some of the therapeu- tic techniques have not been correctly used. Problems often arise when patients do not really believe the ratio- nal responses or are not able to remember them in times of emotional distress. It is important for a therapist to determine the amount of a patient’s belief in the ratio- nal responses and help him/her use the new responses
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as closely as possible to the moment when the automatic thoughts occur. To the patient who does not fully be- lieve a rational response, the therapist can suggest an experimental stance—taking the new belief and “trying it on for size.” The patient who cannot think of answers because of emotional upset should be told that states of emotional distress make reasoning more difficult, and that thoughts such as “If this doesn’t work, nothing will” can only aggravate the problem. Patients should be assured that they will be able to think of rational responses more readily with practice.
Another problem that derives from the misapplica- tion of cognitive therapy techniques occurs when the therapist uses a particular technique inflexibly. It is often necessary for the therapist to try out several be- havioral or cognitive techniques before finding an ap- proach to which a patient responds well. The cognitive therapist must stay with a particular technique for a while to see whether it works, but he/she must also be willing to try an alternative technique when it becomes apparent that the patient is not improving. To give a specific example, behavioral homework assignments are sometimes more helpful with particular patients, even though the therapist has every reason to predict in ad- vance that cognitive assignments will be more effective.
In some instances in which it appears that little prog- ress is being made in therapy, it turns out that the ther- apist has selected a tangential problem. The cognitive therapist should be alert to this possibility, especially during the early stages of therapy. When there appears to be little or no significant change in depression level, even when the patient seems to have made considerable progress in a problem area, the therapist should con- sider the possibility that the most distressing problem has not yet been uncovered. A typical example of this kind of difficulty is the patient who presents difficulty at work as the major problem, when it turns out that relationship problems are contributing significantly to the work difficulties. The patient my avoid the real issue because it seems too threatening.
Finally, cognitive therapy is not for everyone. If the therapist has tried all available approaches to the prob- lem and has consulted with other cognitive therapists, it may be best to refer the patient to another therapist with either the same or a different orientation.
Regardless of why therapy is not progressing satisfac- torily, cognitive therapists should attend to their own af- fect and cognitions. They must maintain a disciplined, problem-solving stance. If the cognitive therapist finds him/herself unduly influenced by a patient’s despair or
begins to notice that his/her own schemas are triggered by therapeutic interactions, then he/she should seek su- pervision. Hopelessness in patients or therapists is an obstacle to problem solving. If therapists can effectively counteract their own negative self-assessments and other dysfunctional thoughts, then they will be better able to concentrate on helping patients find solutions to their problems.
Case Study: Nonchronic Depression
In the case study that follows, we describe the course of treatment for a nonchronically depressed woman, “De- nise,” seen at our Center. Through the case study, we illustrate many of the concepts described earlier in this chapter, including elicitation of automatic thoughts, the cognitive triad of depression, collaborative empiricism, structuring a session, and feedback.
Assessment and Presenting Problems
At the initial evaluation, Denise, a 59-year-old widow, reported that she had lived alone for the last year. De- nise’s husband had been diagnosed with brain cancer 3 years earlier and had died approximately 1 year earlier. She had two grown, unmarried children (ages 27 and 25 years) who were pursuing careers in other parts of the country. Denise had an undergraduate degree and had worked until age 30 but stopped after marrying. She described her major problems as depression (over the last year and a half), difficulty coping with daily life, and loneliness. She reported one prior episode of major depression around age 25, following the death of her father.
Denise said she had become increasingly socially isolated with the onset of her husband’s illness (brain cancer). She reported having had normal friendships as a child, teenager, and young adult. She and her husband had led a relatively quiet life together, with a focus on raising their children and their respective work. When they had free time, they had enjoyed intellectual and cultural activities together (museums, lectures, con- certs, and fine restaurants). The few close friends with whom they socialized had retired to Florida and Ari- zona during the time of the husband’s illness.
Denise was diagnosed with a major depressive disor- der, recurrent. Her test scores verified the diagnosis of depression. Denise’s BDI-II score was 28, placing her in the moderate to severe range of depression. Her most prominent depressive symptoms included loss of plea-
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sure, irritability, social withdrawal, inability to make decisions, fatigue, guilt, difficulty motivating herself to perform daily functions, and loneliness.
Session I
The session began with Denise describing the “sad feel- ings” she was having. The therapist almost immediately started to elicit Denise’s automatic thoughts during these periods.
THERAPIST: What kind of thoughts went through your mind when you had these sad feelings this past week?
DENISE: Well, I guess I’m thinking what’s the point of all this. My life is over. It’s just not the same. I have thoughts like “What am I going to do?” Some- times I feel mad at him, you know, my husband. How could he leave me? . . . Isn’t that terrible of me? What’s wrong with me? How can I be mad at him? He didn’t want to die a horrible death. I should have done more. I should have made him go to the doc- tor when he first started getting headaches. . . . Oh, what’s the use?
THERAPIST: It sounds like you are feeling quite bad right now. Is that right?
DENISE: Yes. THERAPIST: Keep telling me what’s going through your
mind right now. DENISE: I can’t change anything. It’s over. I don’t
know. . . . It all seems so bleak and hopeless. What do I have to look forward to . . . sickness and then death?
THERAPIST: So one of the thoughts is that you can’t change things, and that it’s not going to get any bet- ter?
DENISE: Yes. THERAPIST: And sometimes you believe that complete-
ly? DENISE: Yeah, I believe it, sometimes. THERAPIST: Right now, do you believe it? DENISE: I believe it—yes. THERAPIST: Right now you believe that you can’t
change things and it’s not going to get better? DENISE: Well, there is a glimmer of hope, but it’s most-
ly . . . THERAPIST: Is there anything that you kind of look
forward to in terms of your own life from here on?
DENISE: Well, what I look forward to . . . I enjoy seeing my kids, but they are so busy right now. My son is a lawyer and my daughter is in medical school. So, they are very busy. They don’t have time to spend with me.
By inquiring about Denise’s automatic thoughts, the therapist began to understand her perspective—that she would go on forever, mostly alone. This illustrates the hopelessness about the future that is characteristic of most depressed patients. A second advantage to this line of inquiry is that the therapist introduced Denise to the idea of looking at her own thoughts, which is central to cognitive therapy.
As the session continued, the therapist probed De- nise’s perspective regarding her daily life. The therapist chose to focus on her inactivity and withdrawal. This is frequently the first therapeutic goal in working with a severely depressed patient.
In the sequence that follows, the therapist guided Denise to examine the advantages and disadvantages of staying in her house all day.
DENISE: Usually, I don’t want to leave my house. I want to stay there and just keep the shades closed; you know, I don’t want to do anything. I just want to keep everything out, keep everything away from me.
THERAPIST: Now, do you feel better when you stay in the house all day trying to shut everything out?
DENISE: Sort of . . . THERAPIST: What do you mean? DENISE: Well, I can watch TV all day and just lose my-
self in these silly shows. I feel better when I see other people and their problems on these shows. It makes me feel less lonely and like my problems aren’t so bad.
THERAPIST: And so how much time do you spend doing that?
DENISE: Now, lately? . . . Most of the time. Staying inside and watching TV feels safe, sort of secure, ev- erything . . . like my loneliness, feels more distant.
THERAPIST: Now, after you have spent some time like this, how do you feel about yourself?
DENISE: Afterwards? I usually try not to pay much at- tention to how I’m feeling.
THERAPIST: But when you do, how do you feel? DENISE: I feel bad. I feel bad for wasting the day. I don’t
get to things that I need to take care of . . . like my
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bills, like cleaning, like taking a shower. I usually end up feeling kind of pathetic . . . and guilty.
THERAPIST: On the one hand, you seem to feel soothed and on the other hand, afterwards, you’re a bit criti- cal of yourself?
Note that the therapist did not try to debate or exhort Denise to get out of the house or become involved with necessary daily tasks. Rather, through questioning, the therapist encouraged her to examine more closely her assumption that she was really better off watching TV all day in her house. This is the process we call “col- laborative empiricism.” By the second session, Denise had reexamined her hypothesis about watching TV and remaining in the house all day.
DENISE: About watching TV in the house versus get- ting out, I thought about that the other day. I re- member telling you that it made me feel better to stay there. When I paid attention to what I really felt, it didn’t make me feel better. It just kind of blocked out feeling bad, but I didn’t feel better.
THERAPIST: It is funny then that when you talked about it, your recollection of the experience was more positive than it actually was, but that sometimes hap- pens with people. It happens to me, too. I think that something is good that’s not so hot when I actually check it out.
We now return to the first session. After some prob- ing by the therapist, Denise mentions that it sometimes feels like cognitive therapy “is my last hope.” The thera- pist uses this as an opportunity to explore her hopeless- ness and suicidal thinking.
THERAPIST: What was going through your mind when you said, “This is my last hope”? Did you have some kind of vision in your mind?
DENISE: Yeah, that if this doesn’t work, I feel like I couldn’t take living like this the rest of my life.
THERAPIST: If it doesn’t work out, then what? DENISE: Well, I don’t really care what happens to
me . . . THERAPIST: Did you have something more concrete in
mind? DENISE: Well, right this minute, I don’t think I could
commit suicide, but if I keep feeling this way for a long time, maybe I could. I don’t know, though—
I’ve thought about suicide before, but I have never really thought about how I would do it. I know cer- tain things stop me, like my kids. I think it would really hurt them and some other people, too, like my mother. My mom is in good health now, but she may need me someday. . . . Yeah, those are the two things that stop me, my children, and my mother.
THERAPIST: Now those are the reasons for not commit- ting suicide. Now what are some of the reasons why you might want to, do you think?
DENISE: Because sometimes it just feels so empty and hopeless. There’s nothing to look forward to—every day is the same. My life is such a waste, so why not just end it?
The therapist wanted Denise to feel as free as possible to discuss suicidal thoughts; thus, he tried hard to un- derstand both the reasons for her hopelessness and the deterrents to suicide. After determining that she had no imminent plans to make an attempt, the therapist said that he would work with her to make some changes. He then asked her to select a small problem that they could work on together.
THERAPIST: Now are there any small things that you could do that would affect your life right away?
DENISE: I don’t know. Well, I guess just calling my friend Diane in Florida. She called about a month ago and then again last week. Both times I told her I was busy and would call her back, but I haven’t. I’ve felt so down. I have nothing to say to her.
THERAPIST: Well, when she lived in the area, what kinds of things did you talk about?
DENISE: We have kids about the same age, so we would talk about our kids. We both like to read and we used to go to a book club together—so we would talk about the books we were reading. Both of us liked art. We used to attend lectures at the museum during the week, so we would talk about art and the lectures. We would spend time making plans to do things together in our free time. It always was very interesting when I spent time and with her. We had so much in common. I do miss her.
THERAPIST: It sounds like you used to be involved in a number of interesting activities. What about now?
DENISE: After my husband got sick and then my friends moved, I just stopped. I haven’t done any of those things in quite a while.
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THERAPIST: What do you think about attending a lec- ture series now?
DENISE: I don’t know. THERAPIST: Well, what do you think about that idea? DENISE: It’s an OK idea, but it just seems like too
much. I don’t think I’ll enjoy it . . . the way I feel . . . I don’t know.
THERAPIST: Would you be willing to test out that thought that you won’t be able to enjoy it now?
DENISE: I don’t know . . . I guess so. THERAPIST: Is that a “yes”? DENISE: Yes, but I don’t see how I’m going to get myself
to do it. THERAPIST: Well, how would you go about finding out
about a lecture series? DENISE: You look online at the museum’s website to see
what’s available. THERAPIST: OK. Do you have a computer? DENISE: Yes. THERAPIST: Is it working? DENISE: Yes. THERAPIST: How do you feel about doing that? DENISE: I guess I could do that. . . . I’m so pathetic, I
know what to do. I don’t need you to spell it out for me. Why didn’t I just do this before?
THERAPIST: Well, you probably had good reasons for not doing it before. Probably you were just so caught up in the hopelessness.
DENISE: I guess so. THERAPIST: When you are hopeless you tend to deny,
as it were, or cut off possible options or solutions. DENISE: Right. THERAPIST: When you get caught up in hopelessness
then, there is nothing you can do. Is that what you think?
DENISE: Yeah. THERAPIST: So, then, rather than be down on your-
self because you haven’t looked this up online before, why don’t we carry you right through?
This excerpt illustrates the process of graded tasks that is so important in the early stages of therapy with a depressed patient. The therapist asked the patient a se- ries of questions to break down the process of attending
a lecture series into smaller steps. Denise realized that she had known all along what to do, but, as the thera- pist pointed out, her hopelessness prevented her from seeing the options.
DENISE: Taking this step is going to be hard for me. THERAPIST: First steps are harder for everybody, but
that’s why there is an old expression: “A journey of a thousand miles starts with the first step.”
DENISE: That’s very true. THERAPIST: It’s the first step that is so very important,
and then you can ready yourself for the second step, and then the third step, and so on. Eventually, you build up some momentum, and each step begins to follow more naturally. But first, all you have to do is take one small step. You don’t have to take giant steps.
DENISE: Well, yeah, I can see that. I guess I was think- ing every step was just as hard as the first. Maybe it will get easier.
In the second session, Denise reported success.
DENISE: I checked online about the lecture series and I surprised myself. One actually sounded interesting, and I’m thinking that I might just register for it on- line. I really didn’t think any of those feelings were still there. I’m kind of looking forward to that next step.
At the end of the first session, the therapist helped Denise fill out the Weekly Activity Schedule for the coming week. The activities were quite simple, such as getting up and taking a shower, fixing meals, going out shopping, and checking out the lecture series online. Finally, the therapist asked Denise for feedback about the session and about her hopelessness.
THERAPIST: Do you have any reactions? DENISE: I’m still feeling down, but I’m also feeling a
little better. It’s interesting that just the idea of look- ing at what lectures might be available is making me feel a little lighter. I even had the thought of calling Diane to talk over the options. . . . Is this a sign of better things to come?
THERAPIST: What do you think? DENISE: Maybe.
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Session 2
In the second session, the therapist began by collabo- rating with Denise to set an agenda. Denise wanted to discuss the fact that she had not been attending to her bills or to her housework and was still spending a good part of the day alone in front of the TV; the therapist utilized this as an opportunity to discuss the issue of activity versus inactivity on the agenda. They then re- viewed the previous homework. Denise had carried out all the scheduled activities and had also listed some of her negative thoughts in between sessions. Her BDI- II score had dropped somewhat. (Patients routinely fill out the BDI-II before each session, so that both patient and therapist can monitor the progress of treatment.)
Denise then shared her list of negative thoughts with the therapist. One concern was that she had expressed angry feelings about her husband during the first ses- sion.
DENISE: I don’t like revealing things about myself, but you told me to write down my thoughts. So here it is. When I went to bed the night after of our first ses- sion, I thought about what I said to you, you know, about being angry at my husband. I was thinking that you probably think I am this really harsh and cold person. I mean, here my husband died this hor- rible death and I have this hard, insensitive reaction. I started thinking that now you probably feel really negatively toward me because of that statement and that you don’t want to work with me.
THERAPIST: I’m really glad you’re telling me these thoughts. Let me start by asking you who is having these negative thoughts?
DENISE: You? Well, no. Actually, it’s me. THERAPIST: Right. Do you think that someone like me
might have another reaction to what you said? DENISE: I don’t know. I mean it is pretty harsh being
angry at someone who had no control over what was happening.
The therapist then offered Denise an alternative per- spective:
THERAPIST: Do you think that someone might react to your statements with empathy?
DENISE: How could they? THERAPIST: I imagine it would be very upsetting and
annoying to have lost both your husband and your friends—all around the same time. Even though you love and care about all of them, feeling angry is un- derstandable. It sounds like a basic human reaction to some very difficult life events.
DENISE: Yeah, I guess that does make sense. Thanks.
This illustrates how a cognitive therapist can utilize events during the session to teach a patient to identify automatic thoughts and to consider alternative interpre- tations. In addition, the therapist provides a summary of a key theme he identified from listening to Denise’s automatic thoughts about her husband and about ther- apy. The theme was her fear of being harshly judged and potentially punished for her statement (Punitive- ness schema). Cognitive therapists often identify and begin to correct EMSs during the first phase of treat- ment. More intensive work on changing schemas in a later phase of treatment may be required to inoculate against relapse. We elaborate on this process in the next section of this chapter.
In the segment that follows, the therapist explained how he arrived at the conclusion that punitiveness was an important schema for Denise.
THERAPIST: When you said that you thought I would have a negative opinion about you and not want to work with you because you said you felt angry at your husband, it sounded as though you were really concerned that you would be harshly judged and punished for your statements.
DENISE: Yes, that’s right. THERAPIST: I don’t want to make too much out of
this at the moment, but you also said that after your friends had moved, you felt angry at them and judg- mental of their decision. Even though you knew that each set of friends had to move for specific finan- cial or health reasons and had been in the process of completing their moves over several years, part of you still felt very angry with them. You mentioned that you strongly believe that friends should be there for each other, especially in times of great need, and if a friend lets another friend down, that relationship should end. Is that right?
DENISE: Right. THERAPIST: So, here, you largely have withdrawn from
these important relationships and now you’re feeling quite lonely. The thought of talking to these friends
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again brings fears that they will now be angry and punitive with you for your reaction to them. You’re caught in a no-win situation. Is that right?
DENISE: Yes, that sounds right. THERAPIST: So one of the things that can really grab
hold of you—and make you feel terrible—is this no- tion that people, including yourself, should behave in specific ways, and if they or you don’t behave the “right” way, then harsh punishment should result. Is that correct?
DENISE: Yes, that sounds right. But hearing you say it makes me realize that it doesn’t really sound right.
THERAPIST: What do you mean? DENISE: It’s too extreme. It’s too harsh. People are
human and they have limitations, and they make mistakes sometimes.
THERAPIST: It’s good that you are starting to notice and evaluate these thoughts rather than just responding to them automatically. What this tells us is that you have to be alert for whenever you have the sense that either you or others should be strongly punished for not behaving in a specified way. The idea that people should not be cut a break, even under very difficult circumstances, may not work very well in real life with real people. You mentioned that both friends told you they felt terrible about leaving you at this time, and both have called you regularly since leav- ing the area. Do you think that if you begin to re- spond to and return their calls, they might react dif- ferently—in the same way that I reacted differently from what you expected?
DENISE: Yes, that is very likely.
About halfway through the session, the therapist asked the patient for feedback thus far.
THERAPIST: Now, at this point, is there anything that we have discussed today that bothered you?
DENISE: That bothered me? THERAPIST: Yeah. DENISE: I feel like I’m a bit of a freak. THERAPIST: That is important. Can you . . . DENISE: Well, I’m trying not to feel that way, but I do. THERAPIST: Well, if you are, you are. Why don’t you
just let yourself feel like a freak and tell me about it? DENISE: Well, I’m feeling like I’m just so different from
everyone else. Other people don’t seem to have my problems. They’re still happily married and carrying on with life. I just feel so different from everyone.
This comment led to identification of a third theme, the Social Isolation/Alienation schema. Denise had been viewing herself as increasingly different for the past couple of years. By this point, however, she was beginning to catch on to the idea of answering her thoughts more rationally. After the therapist pointed out the negative thought in the preceding excerpt, the patient volunteered:
DENISE: I know what to do with the thought “I’m a freak.”
THERAPIST: What are you going to do with it right this minute?
DENISE: I am going to say to myself, “I’m not so differ- ent from other people. Other people have lost their mates. I’m not the only one. I’m just the first one in my group of friends. Eventually, they will all have the same situation as me. It’s just a part of life.” Seeing you for help doesn’t mean I’m a freak. You probably see lots of people and help them with problems like mine.
THERAPIST: Right.
The same automatic thoughts arose later in the ses- sion, when Denise noticed the therapist’s wedding ring. In the following extended excerpt, the therapist helped her set up an experiment to test the thought “I’m so dif- ferent from him.”
THERAPIST: OK, now let’s just do an experiment and see if you yourself can respond to the automatic thought, and let’s see what happens to your feeling. See if responding rationally makes you feel worse or better.
DENISE: OK. THERAPIST: OK. “I’m so different from him.” What is
the rational answer to that? A realistic answer? DENISE: You are wearing a wedding ring and that is dif-
ferent from me, because I’m alone, without a mate. THERAPIST: Yes. And? DENISE: And? . . . I don’t really know much about you,
other than you’re married. I guess from what I do know, that information could also be viewed as a
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similarity. We both have gotten married and know what it’s like to be married. I assume that you’ve never lost a mate, but maybe that is not true. You may have lost a mate as well.
THERAPIST: So, is it that you’re different or that I’m different? Or is it that we just have different situa- tions with respect to our mates at this point in time?
DENISE: We just have different situations right now.
The preceding exchange demonstrates the use of re- attribution. At first, Denise interpreted the therapist’s ring as evidence that they were very different. As a re- sult of the guided discovery approach, she reattributed the difference to one of two factors: that either she or the therapist was different or that the situation with re- spect to mates was different for each. At the end of the experiment, Denise expressed satisfaction that she was finally recognizing this tendency to distort her apprais- als.
DENISE: Right now, I feel glad. I’m feeling a little better that at least somebody is pointing these things out to me. I never realized I was so judgmental of myself and other people, and that I’m assuming I’m so dif- ferent from everyone.
THERAPIST: So you feel good that you have made this observation about yourself?
DENISE: Yes.
After summarizing the main points of the second session, the therapist assigned homework for the com- ing week: to fill out the Daily Record of Dysfunctional Thoughts (see Figure 7.4) and the Weekly Activity Schedule (with mastery and pleasure ratings; see Figure 7.3).
Session 3
By the beginning of the third session, Denise’s mood had visibly improved. She had registered for a lecture series at the museum and was looking forward to at- tending the first lecture. She also had called her friend Diane, with very positive results. She was catching neg- ative and punitive thoughts toward others and herself and challenging these thoughts. The primary agenda item Denise chose to work on was “how I back away from other people,” an aspect of her Unrelenting Stan- dards, Punitiveness, and Social Isolation/Alienation schemas.
DENISE: I want to stop withdrawing from people. I want to be more accepting and engaged with others.
THERAPIST: What holds you back? DENISE: I guess I believe that I have to be a bit removed
and strict in relation to others or they’ll just behave in whatever way they want. People have to know my rules and abide by them if they want to have a rela- tionship with me.
The therapist continued probing to understand why Denise believed she had to have others adhere to such a strict set of rules to have a relationship. As the discus- sion progressed, it became obvious that, in the abstract, she could see that such hard-and-fast rules were not necessarily conducive to having a good relationship— in fact, such rules sometimes put others off. But in real- life situations, Denise never felt she was wrong.
The therapist’s next task was to help Denise bring her rational thinking to bear on her distorted think- ing in the context of a concrete event. At the therapist’s request, Denise then described a conversation with her friend Diane, and how her intolerance for Diane’s deviation from her rules created distance. Denise had wanted Diane and her husband to come for a visit the following summer. Diane, however, told her that their dog had been quite sick, and that if the dog was still alive, she could not leave it. Denise thought this was ridiculous. She believed a relationship with a pet should never take precedence over a human relationship. This occurred when Denise actually had wanted and hoped to get closer to Diane again. The therapist helped her use logic to evaluate her maladaptive schema.
THERAPIST: You had the thought “I’m right to set the record straight with her. She can’t put me in second place to her dog. She can’t do that without consequence.” It seems likely that you believed that thought, and that you believed the thought was right. And since you believed that thought was right, you then felt you had to withdraw your affection from her if she didn’t abide by your wishes.
DENISE: Right. THERAPIST: Now, let’s look at it. Do you think that
thought is correct? DENISE: Well, yes, it’s insulting. THERAPIST: What’s insulting? DENISE: She’s putting her dog in a higher priority posi-
tion.
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THERAPIST: Have you ever had a pet? DENISE: No. THERAPIST: Do you think that maybe Diane feels like
her dog is a part of her family? DENISE: I never thought of it that way. THERAPIST: If you look at the situation from that per-
spective, how do you feel? DENISE: I feel like I’m being a little insensitive. . . .
That’s not right. I’m not allowing for any other per- spective. I’ve never had a pet, so I don’t really know what it’s like to have a pet. It’s not right for me to be so judgmental of Diane. I need to be more under- standing. I wasn’t very caring. I am actually behav- ing in a way that goes directly against my deepest values.
THERAPIST: So, according to your own values, was this right?
DENISE: No, it’s not right. I wasn’t respecting her feel- ings. I was just demanding that she respect mine. That wasn’t right.
THERAPIST: OK, now this is one of the problems. If you want to get over this sense that you should never give in or bend your rules for others, one of the things you can do is look for this thought, “I’m right and you should have a negative consequence for your ‘wrong’ decision”—and refer back to this conversation we are having now and decide for your- self whether, indeed, you were right. Now, if every time you approach a conflict in a relationship and allow for the possibility that you might not fully un- derstand, but really think underneath, “But I know I’m right,” you are going to feel put out, and then you are not going to want to engage with that per- son. Is that right?
DENISE: Yeah, that sounds right. THERAPIST: So we have to decide here and now. Do
you indeed think that you are right to suspend your initial negative judgment to leave open the possibility of reevaluating your reaction to her behavior?
DENISE: Yes. THERAPIST: Now, the next time you get the thought
“I’m right and I’m going to make sure this other person knows it,” how are you going to answer that thought?
DENISE: If I’m right? But I’m not necessarily right. I need to consider the other person’s perspective. I
need to try to understand them and then see if what I’m thinking fits.
THERAPIST: Now are you saying that because that is the correct answer, or because you really believe it?
DENISE: No, I really believe it.
The therapist followed this discussion with a tech- nique called “point–counterpoint” to help Denise prac- tice rational responses to her automatic thoughts even more intensively. In this excerpt, the therapist expressed Denise’s own negative thinking as Denise tried to de- fend herself more rationally.
THERAPIST: Now I am going to be like the prosecut- ing attorney, and I’ll say, “Now I understand you let your friend violate one of your rules of friendship. Is that true?”
DENISE: Yes. THERAPIST: “Now it seems to me that that was a very
bad thing for you to do.” DENISE: No, it wasn’t. THERAPIST: “You don’t think it was?” DENISE: No, I should try to understand her perspec-
tive. THERAPIST: “Well, you can sit there and say you should
be more understanding, but I thought you said be- fore that you wanted people to respect you.”
DENISE: I do, but I also need to respect others. THERAPIST: “I know, but now you are saying that you
are going to let her get away with this. What’s next?” DENISE: What’s next can only be a better understand-
ing of one another. We’ll feel closer. THERAPIST: “But how can you feel closer if she’s not
respecting your rules of friendship?” DENISE: Maybe my rules are not appropriate in this
situation. I need to learn to be more understanding, flexible, and tolerant of some deviations from my rules.
THERAPIST: “But then you’ll lose control of the situa- tion.”
DENISE: No, that’s an exaggeration. I don’t need to con- trol the whole situation. I can still decide what makes sense. I am still in control of what’s important.
THERAPIST: “How can that be?” DENISE: Because I can respect myself and respect my
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friend as well. I don’t have to turn everything into an either–or situation to try to make her see and do it my way. That just makes it difficult for her to get along with me, and I’ll lose out on the relationship in the long run if I keep on insisting that she either do it my way or we do nothing.
Finally, the therapist returned to the schema and asked the patient how much she believed the new per- spective.
THERAPIST: If you’re flexible, you’ll lose control. Now do you believe that?
DENISE: No. THERAPIST: Do you believe it partially? DENISE: No. In fact, I’m more likely to lose control of
any possibility of getting what I want if I’m so in- flexible. It’s like I lose sight of the importance of the relationship when I get so stuck on thinking that I have to be in control and that the other person has to do it my way.
THERAPIST: OK, so right now, how much do you be- lieve that?
DENISE: Completely. THERAPIST: 100%? DENISE: Yes. THERAPIST: You are sure 100%, not 90 or 80%? DENISE: No, 100%.
For the remainder of Session 3, Denise and the therapist reviewed other instances in which she noticed that her standards were not flexible and felt the urge to be punitive when her rules were not met. The session ended with a summary of the main issues raised in the first three sessions.
Summary of Initial Sessions
In the first three sessions, the therapist laid the ground- work for the remainder of treatment. He began im- mediately by teaching Denise to identify her negative automatic thoughts. By doing this, the therapist began to understand her feelings of hopelessness and to ex- plore her isolation. By identifying her thoughts in a variety of specific situations, he was able to deduce sev- eral key schemas that later proved central to Denise’s thinking: (1) Unrelenting Standards, (2) Punitiveness,
and (3) Social Isolation/Alienation. All appeared to be contributing to Denise’s social isolation and depression. The therapist made especially skillful use of Denise’s thoughts during the second therapy session to help her see that she was distorting evidence about the therapeu- tic interaction and coming to the inaccurate conclusion that the therapist would be judgmental and punitive with her, and withdraw positive feelings for her, in the same way that Denise tends to respond to others.
Beyond identifying thoughts and distortions, the therapist guided Denise to take concrete steps to over- come her inactivity and withdrawal. He asked her to weigh the advantages and disadvantages of staying in the house all day watching TV; he broke down the task of attending a lecture series at the museum into small, manageable steps; and he worked with her to develop an activity schedule to follow during the week.
Finally, the therapist employed a variety of strategies to demonstrate to Denise that she could test the valid- ity of her thoughts, develop rational responses, and feel better. For example, during the course of the three ses- sions, the therapist set up an experiment, used reattri- bution, offered alternative perspectives, and practiced the point–counterpoint technique.
One final point we want to emphasize is that the pri- mary therapeutic mode was questioning. Most of the therapist’s comments were in the form of questions. This helped Denise to evaluate her own thoughts out- side of the session and prevented her from feeling at- tacked by the therapist.
By the end of these initial sessions, Denise reported being more optimistic that her life could change.
Later Sessions
Denise continued to fill out the Daily Record of Dys- functional Thoughts and gathered evidence that she could relax her standards and be more tolerant of oth- ers’ viewpoints and foibles. She discovered that she felt happier, both with herself and with others, as a result.
The therapist set up several experiments with Denise to test a series of beliefs: that her friends would become punitive with her when she did not behave perfectly, and that her relationships would become unpleasant and undesirable if she relaxed any of her rigid standards regarding how others should behave in relationships.
Through graded tasks, Denise counteracted her ten- dency to withdraw by gradually approaching new and sometimes unfamiliar situations. When she noticed herself imposing her standards of behavior on others,
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or noticed in herself the urge to become punitive, De- nise practiced more open and accepting behaviors (by asking open-ended questions that reflected back her understanding of others’ responses, and by inhibiting harsh and judgmental statements). She practiced tol- erating the discomfort associated with these new be- haviors until they began to feel more comfortable and natural.
When Denise terminated therapy, her BDI-II score was in the normal range. The symptom reduction phase of treatment was successfully completed in 20 sessions.
The next section describes and includes a case ex- ample of ST for chronic depression.
ST FOR CHRONIC DEPRESSION
ST, developed by Young (1990/1999; Young et al., 2003), can be used with patients who present with re- current depressive episodes, dysthymic disorder, early onset of depression, early life trauma or adverse family relations (e.g., the loss of a parent in childhood; sexual, physical or verbal abuse, neglect, and overprotection), comorbid personality disorders, or a large number of EMSs (identified with the YSQ [Young, 2005]). Young and Klosko (1994) have published a self-help book to help patients better understand their schemas.
Beck and colleagues (1990) have noted that
schemas are difficult to alter. They are held firmly in place by behavioral, cognitive, and affective elements. The therapeutic approach must take a tripartite ap- proach. To take a strictly cognitive approach and try to argue patients out of their distortions will not work. Having the patients abreact within the session to fan- tasies or recollections will not be successful by itself. A therapeutic program that addresses all three areas is es- sential. A patient’s cognitive distortions serve as signposts that point to the schema. (p. 10)
As a result, ST represents a significant expansion of traditional CBT. It places more emphasis on early de- velopmental patterns and origins, long-term interper- sonal difficulties, the patient–therapist relationship, and emotion-focused or experiential exercises.
Case Study: Chronic Depression
The second case study demonstrates the use of ST with a chronically depressed patient, “Barbara.”
History and Presenting Problems
Barbara was an extremely attractive 46-year-old woman who had been married for the past 20 years to George, a functional alcoholic working on Wall Street in invest- ment banking. It was the first marriage for both, but it had been extremely rocky throughout. Barbara had wanted children in the marriage but had been unable to conceive naturally. Although fertility treatments and adoption had been discussed, Barbara reported that George resisted following through on these options, because he questioned her ability to be an adequate par- ent.
At the beginning of George and Barbara’s relation- ship, Barbara reported extremely strong sexual chem- istry. However, she stated that the chemistry had been erratic and often disappeared for long periods over the course of their relationship. She said that she had only felt real happiness with George in the first few months of the relationship, when he was extremely generous and attentive. Her decision to marry George was based on a feeling that they were meant for each other. They initially met at a high-end bar, where Barbara had worked as a cocktail waitress. Once their relationship was established, however, George continued to spend most of his free time in cocktail lounges without her, as she did not like to drink.
At the time she came in for her first interview, Bar- bara was spending most of her time in bed or watch- ing TV. She rarely left the house except to go shopping. Outings with her mom or friends “to lift her spirits” often culminated in shopping sprees, followed by ex- tended verbal berating by George, drunk upon his re- turn home from the bar, because of what he perceived as her lack of taste, judgment, and intelligence regard- ing purchases. Barbara entered treatment because her husband told her that she “was driving him crazy with all her ridiculous behavior” and that she should “go get fixed.” Barbara acknowledged feeling very depressed. She stated that this latest episode of depression started after a particularly upsetting fight with her husband over adopting a child.
Barbara reported having mild to moderate depres- sion most of her life, interspersed with multiple episodes of major depression. She first became aware of feeling moderately depressed around age 11. An only child, she initially described her childhood family as “fine.” Bar- bara described her mother as extremely attentive and devoted, a “very good mother who did everything for me.” Barbara stated that her mother lived for her, but
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she also remembered her mother occasionally falling into depressions. As early as age 6, she recalled that her mother was emotionally unavailable when depressed.
Barbara described her father as a workaholic who was almost never home. When he did come home, he was remote, preferring the solitude of his study over in- teracting with Barbara and her mother. If, as a child, Barbara tried to engage him, he would upbraid her by calling her “an annoying simpleton” and demand that she leave him alone.
Barbara described her first major depressive episode, which occurred around age 16, after a breakup with her first serious boyfriend. Later episodes were triggered by other breakups and the fertility problems.
Barbara scored 29 on the BDI-II, placing her in the severe range of depression. She also completed the third edition of the YSQ (Long Form; Young, 2005), and received very high scores on the Emotional De- privation, Defectiveness, Abandonment, Dependence/ Incompetence, Entitlement, Failure, Subjugation, Ap- proval Seeking, and Negativity/Pessimism schemas. Her Schema Mode Questionnaire (Young et al., 2008) indicated that she primarily functioned in the follow- ing modes: Detached Protector, Compliant Surrender, Punitive Parent, and Vulnerable Child.
At Barbara’s initial consultation, the therapist con- ducted additional assessment work through imagery (a standard assessment procedure for ST). During this assessment, Barbara was instructed: “Close your eyes and let your mind float to your earliest memories of your mother.” Barbara reported painful recollections of being 6 years old with her mother in bed, depressed and emotionally unavailable. She reported feeling very scared and lost at these times. The same imagery ex- ercise was utilized in a subsequent session in which Barbara was asked to retrieve an early memory of her father. In this image, Barbara’s father displayed intoler- ant, demeaning, and rejecting behavior toward her as a child. During the exercise, she reported feeling unac- ceptable, ashamed of herself, and unwanted by him.
On the Multimodal Life History Inventory (Lazarus & Lazarus, 1991), a 15-page assessment tool covering a wide range of issues dealing with feelings, thoughts, behaviors, and a variety of other psychotherapeutic is- sues, Barbara reported her main problems as depression, being unhappy with herself, feeling empty and unloved, and feeling unappreciated. She also listed the follow- ing behaviors as applicable: procrastination, with- drawal, concentration difficulties, sleep disturbance, crying, and occasional outbursts of temper. She further
indicated that she often felt sad, depressed, unhappy, hopeless, useless, and lonely. She endorsed the follow- ing statements: “I don’t know what to do with my life,” “Life is empty, a waste,” and “There is nothing to look forward to.”
Based on the initial interview, Barbara was diag- nosed with major depressive disorder, recurrent episode on Axis I, and dependent personality disorder on Axis II, based on DSM-IV-TR (American Psychiatric Asso- ciation, 2000).
Schema Mode Work
This section demonstrates the use of schema mode work—an important component of the ST approach— with Barbara.
The therapist shifted to ST because Barbara’s depres- sion was not lifting with standard cognitive therapy. Although Barbara had learned how to challenge her automatic thoughts, identified and challenged her core beliefs with rational responses, and followed through on graded behavioral assignments to test her thoughts and beliefs, she never emotionally accepted the rational viewpoint, despite much concrete evidence. Barbara remained convinced that she was worthless, useless, and hopeless. Her EMSs continued to be stubbornly entrenched. The therapist decided that the next step would be to introduce emotion-focused exercises to access Barbara’s schemas on a deeper emotional level, utilizing the schema mode approach.
There are seven general steps in schema mode work: (1) Increase awareness of modes by identifying and la- beling modes with the patient; (2) explore the origins of modes in childhood and adolescence, and discuss their adaptive value; (3) link current problems and symptoms to the patient’s maladaptive modes; (4) uncover the ad- vantages and disadvantages of each mode; (5) use im- agery to access the Vulnerable Child mode; (6) conduct dialogues between modes; and (7) generalize the results from mode work in session to the patient’s life outside of sessions. The following sections illustrate each step of mode work in helping Barbara.
Step 1: Increase Awareness of Modes by Identifying and Labeling Modes with the Patient
This first step helps both therapist and patient concep- tualize the problems in terms of different parts of the self or modes. From the Schema Mode Questionnaire, the therapist already was aware that Barbara primarily
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functioned in the Detached Protector, Compliant Sur- renderer, Punitive Parent, and Vulnerable Child modes. The session reveals how the therapist queries the pa- tient, so that she can begin to recognize and differenti- ate these parts within herself.
Throughout this section, the patient is encouraged to label modes with terms that feel right—rather than simply applying generic terms from the Schema Mode Questionnaire. Patients are encouraged to find terms that best capture the thoughts, emotions, and/or be- haviors associated with each mode. A primary goal with this first step is to help the patient observe these parts, and decenter him/herself from them. This step begins the process of interrupting the automaticity of the modes.
THERAPIST: I’m noticing in our sessions that some- times you seem very sad and upset and critical of yourself, and other times you seem a bit distracted from what you’re feeling, like when you were telling me about the great pair of shoes that you found on your shopping trip.
BARBARA: Yeah, I guess that’s true. Talking about my purchases makes me feel better.
THERAPIST: When you say “better,” what do you mean? BARBARA: I feel good. THERAPIST: Like happy, peaceful, and content? BARBARA: I feel pleasure. THERAPIST: In what way is it pleasurable? BARBARA: I feel pleasure when I look at pretty things
with my mom or my friends, and I like buying those things. It takes my mind off of everything else.
THERAPIST: Like you’re temporarily distracted from other feelings?
BARBARA: Yeah, that’s right. THERAPIST: What are those other feelings? BARBARA: Just feeling real bad. I can’t stand those feel-
ings. THERAPIST: So, sometimes there is this one part of you
that just wants distance from this other part of you that feels bad?
BARBARA: Yes. THERAPIST: Are there other things you do besides
shopping that help you distance from bad feelings? BARBARA: Well, yeah, I sleep a lot.
THERAPIST: Anything else? BARBARA: I watch TV, but TV doesn’t always work. THERAPIST: This part of you that wants distance from
feeling bad—what could we call that part of you? BARBARA: That part of me? I don’t know. I don’t know
what to call it. THERAPIST: What does it feel like? BARBARA: It feels like I’m escaping. THERAPIST: OK. So should we call that part “the Es-
capist”? BARBARA: I guess so. . . . That sounds right. THERAPIST: And the part of you that you’ve escaped
from—can you tell me more about that part of you? BARBARA: That part feels bad . . . really bad and ter-
rible. THERAPIST: Let me hear that part speak about those
feelings. BARBARA: I’m just a bad person. (Starts to cry.) . . . I’m
a useless good for nothing. I feel so hopeless. I don’t know what to do. I can’t figure anything out. I’m such a zero, such a failure. . . . Do we really have to talk about this?
THERAPIST: Barbara, I know that it feels bad to be in touch with this part of yourself, but if you can hang in there for just a bit, it will help me to understand why you’re feeling so bad. Do you know what this part of you wants?
BARBARA: I want to feel good. THERAPIST: What do you think would help you feel
better? BARBARA: I don’t know. I really don’t know. I just want
you to fix me. My husband is right. I am a ridiculous person.
THERAPIST: It sounds like there is one part of you that feels really awful. It sounds like this part is listening and taking in what your husband says about you— that “you’re ridiculous.” I want you to hold back on agreeing with your husband, and I want to hear more about this part of you that feels awful—the part of you who wants everything fixed. That part . . . do you feel it?
BARBARA: Yes, I feel it. THERAPIST: Tell me more. What are the things you
want to fix?
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BARBARA: I don’t know. I just want to feel good about myself, proud of myself, but I just don’t. I want to have a child, but my husband doesn’t think I can handle it. He’s probably right. I need so much help with just everyday living. I don’t know how to handle anything.
THERAPIST: So this part of you, this part that feels awful and helpless but also wants to feel better, what could we call this part?
BARBARA: I don’t know. What do you think? THERAPIST: Well, what does it feel like? BARBARA: It feels helpless—ashamed and helpless. THERAPIST: How old do you feel when you’re in touch
with this part of yourself? BARBARA: I feel young, very young. Therapist: Do you want to call that part “Ashamed Lit-
tle Barbara” [Vulnerable Child mode with associated EMSs of Defectiveness, Dependence/Incompetence, and Enmeshment/Undeveloped Self]?
BARBARA: Sure. THERAPIST: OK. And now this other part—the one
that is agreeing with your husband and calling your- self ridiculous . . .
BARBARA: Well, I am ridiculous and silly. I can’t cope with anything.
THERAPIST: Before you agree with that part, I want you to just notice how that part sounds. How does that part sound to you? Does it sound critical?
BARBARA: Yes, but I deserve it. I’m so useless. THERAPIST: It sounds like you are having a hard time
just listening to that part without automatically agreeing with it?
BARBARA: Yeah, I guess that’s true. THERAPIST: So, what do you want to call that part? BARBARA: I don’t know. . . . But . . . you’re not going to
tell me what to call it, are you? THERAPIST: Right. BARBARA: OK. I guess “the Critic” [Punitive Parent
mode with associated EMSs of Defectiveness and Subjugation].
In this part of the session, the therapist has helped Barbara begin to recognize and label the modes: the De- tached Protector as “the Escapist,” the Punitive Parent
as “the Critic,” and the Vulnerable Child as “Ashamed Little Barbara.” Although not fully illustrated here, the therapist also used a similar sequence of questions to help Barbara identify other modes. From this portion of the session, it is clear that “the Critic” (Punitive Parent mode) is generating a tremendous amount of negative affect in Barbara. Barbara’s only apparent way to cope with the onslaught of punitive statements from this mode is “the Escapist” (Detached Protector mode), in which she sleeps away much of her life. Otherwise, Bar- bara’s primary experience of herself rests with “Ashamed Little Barbara” (the Vulnerable Child mode), where she feels defective, useless, hopeless, and helpless.
Step 2: Explore Origins of Modes in Childhood and/or Adolescence
This section illustrates how the therapist helps Barbara recognize the origins of these modes. In addition, the therapist assesses the strength of her Healthy Parent mode.
THERAPIST: Does “the Critic” sound like anyone else you know or have known in your life?
BARBARA: Yes, it sounds like George. THERAPIST: Anyone else? BARBARA: Yeah, it also sounds like my dad . . . just like
my dad. THERAPIST: In what way? BARBARA: My dad used to talk like that to me . . .
whenever I tried to get his attention. THERAPIST: How old were you? BARBARA: Young, very young . . . 3 or 4 . . . as far back
as I remember. THERAPIST: Can you close your eyes and try to let
yourself feel like that young child again with your dad?
BARBARA: (Closes her eyes.) THERAPIST: Tell me what’s happening. BARBARA: He’s yelling at me because I pulled on his
coat jacket. THERAPIST: Let me hear what he’s saying to you. BARBARA: “Stop it, you little pest. You’re such a simple-
ton. Can’t you find anything better to do than pull on my coat? Get out of here!”
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THERAPIST: And how are you feeling as he is yelling these things at you?
BARBARA: I feel stupid, like I’m a jerk. I’m nothing—a useless pest, an annoyance.
THERAPIST: Does it feel like he’s right, or are you angry at him?
BARBARA: No. I don’t feel angry. I just feel bad (starts to cry)—I’m just bad.
THERAPIST: So there is part of you agreeing with him, punishing yourself—like your dad—thinking you’re bad.
BARBARA: Yeah. THERAPIST: And where is your mom? BARBARA: She’s telling me to shush and leave him
alone. She says he’s tired from working so hard all day.
THERAPIST: And what are you thinking and feeling when she says this?
BARBARA: I’m thinking that I’m a terrible person. THERAPIST: So, you’re getting the message that you are
the problem from both of your parents. It feels like both parents are saying you deserve this harsh treat- ment, and there is a part of you that believes them— you deserve to be punished because you’ve bothered your father. Is that right?
BARBARA: Yes, that’s right. THERAPIST: So there is also this punishing part of you,
this part that accepts that message from your par- ents—this punitive message that you’re bad and a problem, a pest.
BARBARA: Yes. THERAPIST: What is your mom doing? BARBARA: After a while, she takes me out. She sees I’m
sad and wants me to feel better. She tries to make me feel better by giving me something, like a toy, or something to eat. A lot of times she takes me out shopping and buys me something special.
THERAPIST: And how do you feel when she does this? BARBARA: I feel a little better while we are out . . . but
later, I feel bad. I still feel shame because I’m so bad and useless.
THERAPIST: So there is still the “Ashamed Little Bar- bara” underneath?
BARBARA: Yes. That is it.
THERAPIST: If you could have rewritten the script for your family, a family with ideal parents, what would you have happen?
BARBARA: I have no idea. They weren’t bad. They were doing their best.
THERAPIST: Yes, but what if you had had a daddy who was excited to see you at the end of his work day . . . a daddy who enjoyed coming home to his family . . . who found pleasure in talking with you and getting to know you, and played with you?
BARBARA: You mean . . . a daddy who loved me? THERAPIST: Yes. I mean a daddy who was able to show
you his love through all sorts of actions. BARBARA: Wow . . . that would have been so different. THERAPIST: Do you feel any angry feelings at him now
as you think about how he spoke to you—this very young child simply trying to get his attention?
BARBARA: No, I was in his way. He worked hard. I had to leave him alone.
THERAPIST: What you just said—does that sound like anyone you know?
BARBARA: Yes. It sounds like my mother. THERAPIST: And what do you think of that now? BARBARA: Well. She was just trying to keep the peace
and fill in for him. THERAPIST: But what about you, this sweet innocent
little child simply wanting what all children want— love and attention from her father?
BARBARA: It’s sad. I feel sad for me. THERAPIST: Right. It is sad for you. You are a child
doing what all children do—children try to get their parents’ attention; children want to know they are loved, valued, appreciated. You were no different from any other child, but what is happening here?
BARBARA: (Cries.) THERAPIST: No one’s calling your dad on his horrible
behavior toward you. Everyone’s accommodating him and speaking to you as if you are the problem, when all that you are doing is what every young child does. And yet your father and your mother are re- sponding as if you are the problem.
BARBARA: Yeah. You’re right. Why did they do that? THERAPIST: Do you think there was something wrong
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with you, or do you think there was something wrong with the way they were behaving with you?
BARBARA: The way they were behaving with me. . . . It’s a problem with the way they treated me.
THERAPIST: Right. They are the ones who should feel shame about their behavior. There was nothing shameful about you or your behavior.
In the preceding section, the therapist helps Barbara to realize the origin of “the Critic,” the part of herself that has accepted her “Punitive Parent” message that she was the problem. The therapist’s questions and comments also help Barbara realize that the problem was actually her parents’ behavior toward her rather than an inherent defect in herself.
The therapist now turns Barbara’s attention to the origin of “the Escapist” mode—the part that was seek- ing relief from these terrible feelings about herself as a child. The therapist also helps Barbara become more aware that “the Escapist” was only able to provide short- term relief.
THERAPIST: Now when you had this bad feeling about yourself as a child, the “Ashamed Little Barbara” feeling, how did you cope with that feeling? What did you do?
BARBARA: A lot of the time, I did nothing. I just sat on my bed in my room daydreaming, wishing ev- erything could be different. I would fantasize being a star, a beautiful person that everyone adored. Peo- ple would dote on me and give me expensive gifts and clothes that made me look even more beautiful. Sometimes when my mom would take me out and buy me things, it kind of felt like she was making this dream come true.
THERAPIST: Is that “the Escapist” part of you trying to help you feel better?
BARBARA: Yes, it definitely is. THERAPIST: And then what would happen? BARBARA: I would feel better, especially as I got older
and I got a lot of attention from the way I looked, but eventually my dad always would start yelling again. I remember him yelling at my mom for “spending too much money” simply to turn me into “a pretty Bimbo.”
THERAPIST: So the efforts to feel better eventually backfired.
BARBARA: Right. I never felt very good for long. I never felt good inside.
Step 3: Link Current Problems and Symptoms to Maladaptive Modes
In this section, the therapist asks Barbara questions that help her to recognize how these modes that developed in childhood are still operating in the present. Barbara begins to connect these modes with why she is feeling so depressed, and she begins to see the repetitive pat- terns in her life.
THERAPIST: Let’s look at what is happening now in your life. Do you recognize any relationship between what we have been talking about—these different parts of you—and how you are thinking and feeling about yourself and coping with your life now?
BARBARA: Yeah, I’m still trying to feel good—or just not feel—by being “the Escapist.” When I go on these shopping sprees and let my mom and my friends dress me up, it still doesn’t work any better than it ever did. And sleeping all the time doesn’t work either.
THERAPIST: What do you mean? BARBARA: Well, I only feel good for a short while.
Then, instead of my dad coming home, now I’m coming home to George or he’s coming home to me. George is just as mean and unavailable as my dad.
THERAPIST: And then what happens? BARBARA: I start to feel really bad again, really de-
pressed. I feel like I’m not worth spending time with, like I’m boring and useless. I’m saying all sorts of bad things about myself, and I agree with every- thing George says about me. I’m my worst “Critic.” In the end, I still feel like the same old “Ashamed Little Barbara” inside who never ever really feels bet- ter. Then, I just want to go to sleep to get away from it all. I’m finally starting to see it more clearly, going around and around the same old circle—nothing has changed and nothing changes. I’ve been miserable my whole life.
THERAPIST: But there is one very important change. BARBARA: What is that? THERAPIST: You’re starting to see and understand
what’s been happening for a long time instead of just being on the treadmill without any awareness.
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Step 4: Uncover Advantages and Disadvantages of Each Mode
The therapist now begins to ask Barbara questions re- garding the advantages and disadvantages of listening and acting on these different parts of herself. This helps Barbara to gain more distance from the modes and in- creases her awareness of a choice in how she responds.
THERAPIST: When these different parts of yourself or modes developed, they served a purpose. Why don’t we talk about each of them and explore their advan- tages and disadvantages, both in the past and pres- ent? Let’s start with “the Escapist.”
BARBARA: Well, that part lets me feel good—or at least not feel bad.
THERAPIST: For how long? BARBARA: For a while. THERAPIST: And in the long run? Does that part help
you feel better? BARBARA: No, not really. I can’t really escape feeling
bad. I can’t say I feel any better in the long run. THERAPIST: So, is there any advantage to this part of
you—“the Escapist”? BARBARA: I’m mixed about it. THERAPIST: Sure. I can understand that. If you don’t
know of any other way to feel better, any relief is bet- ter than no relief at all.
BARBARA: Yeah. THERAPIST: But sometimes it’s good to let yourself feel
bad, because when you let yourself stay in touch with your feelings, you often can begin to recognize what feels better in the long run . . . like finding activities that are truly interesting to you, or that give you a sense of accomplishment and purpose, or that bring out a feeling of deep enjoyment.
BARBARA: That makes sense, but I have no idea how to find those things.
THERAPIST: Well, that is something we can work on together.
BARBARA: That sounds good. THERAPIST: And what about “the Critic”? Is there any
advantage to listening to “the Critic”? BARBARA: That part tells me what’s wrong with me. THERAPIST: And what does “the Critic” say is wrong
with you?
BARBARA: That I’m stupid and silly, useless and an- noying.
THERAPIST: Do you think “the Critic” is right? BARBARA: Of course. THERAPIST: But if you put the words of “the Critic”
back in your dad’s mouth and listen to him speak to little 3-year-old Barbara as she excitedly greets him coming home from work, what do you think?
BARBARA: When you put it that way, I think he’s a jerk. I mean, what does he think he is doing to this poor little girl? What’s wrong with him?
THERAPIST: Right. So is there any advantage to listen- ing to these critical words?
BARBARA: No . . . no, definitely not. THERAPIST: Are there any disadvantages of listening to
“the Critic”? BARBARA: Yes. It’s getting clearer now why that part is
making me feel so bad. I have to stop listening to that part. When I accept what my dad said as the truth, I feel bad, really bad, about myself.
THERAPIST: You mean it brings up that “Ashamed Lit- tle Barbara” feeling?
BARBARA: Yes. THERAPIST: And what about her? What does she need? BARBARA: She needs to feel good about herself. She
needs to hear good things about herself. She needs someone to listen to her and pay attention to her—to love her.
THERAPIST: I agree.
Step 5: Use Imagery to Access the Vulnerable Child Mode
The therapist now begins to engage Barbara in the Vul- nerable Child mode. By accessing this mode, therapist and patient can begin to work on the core schemas that are part of “Ashamed Little Barbara.”
THERAPIST: I know it’s sometimes unpleasant to let yourself be in touch with “Ashamed Little Barbara,” but would you be willing to go there, so that we can get to know that part of you to find out what you need to truly feel better and to find out what is get- ting in the way?
BARBARA: I guess . . . (Closes her eyes.)
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THERAPIST: Tell me what you are feeling and thinking right now.
BARBARA: It’s the same old feelings—I feel bad . . . and useless. (Visibly begins to look upset, then opens her eyes.)
THERAPIST: Can you go back there to “Ashamed Little Barbara,” can you let yourself feel her?
BARBARA: OK. (Closes her eyes again.) THERAPIST: Where are you? What are you doing? BARBARA: I’m sitting on my bed in my room. My
daddy just told me to go away. THERAPIST: And how are you feeling? BARBARA: Awful. THERAPIST: And what do you want? BARBARA: I want my mommy to come in and make
me feel better. THERAPIST: Where is she? BARBARA: She’s in her room, lying on her bed. She
doesn’t feel good either. THERAPIST: If you could bring in a healthy mommy to
be with you right now, what would she say to you? Let me hear her speak to Little Barbara.
BARBARA: “You know he’s just tired from work. If you just leave him alone, everything will be all right.”
THERAPIST: Let me hear what Little Barbara thinks about this?
BARBARA: That doesn’t help much. I still feel upset and bad.
THERAPIST: How about if I come in to help? BARBARA: OK. THERAPIST: You are such a loving little girl. So many
fathers would relish coming home to such a greeting from their little girl. Something is wrong with your daddy. Why doesn’t he recognize that you’re offering him something that is precious—so special? . . . How does little Barbara feel as she hears this?
BARBARA: Better. THERAPIST: Let me talk to your father now. BARBARA: OK. THERAPIST: “How can you speak to your daughter that
way? She’s done nothing but welcome you home with joy and love. And look at how you are responding. Your response to her is completely inappropriate. You are so closed off and removed from everything.
What is going on with you? Why can’t you see that you have a beautiful, creative, and loving daughter? Barbara does not deserve this type of treatment. I’m not going to stand for this and let you hurt her any- more.” . . . How does little Barbara feel as she hears this?
BARBARA: A lot better. I wish my mom had spoken to my dad that way. But you know, if you really tried to say anything like that to him, he wouldn’t listen. He never listened to my mom. He’d probably just say something mean to you and then shut the door.
THERAPIST: OK. Well if that happened, what would you want to happen next?
BARBARA: I don’t know. THERAPIST: Let me step in again and say this to him
through the door. “Whether or not you choose to listen, there is a limit, a limit as to how long we will stay here for you. If you choose not to be here for us, we will not stay here for you.”
BARBARA: I don’t think he’ll change. THERAPIST: Then you and I, together, will leave him
and create a better life. BARBARA: Is that really possible? THERAPIST: Do you want to make it happen? BARBARA: Yes, but what about him? He’ll be so lonely. THERAPIST: Who will be lonely? BARBARA: He will, unless we stay. THERAPIST: But if you stay, who will be lonely then? BARBARA: Me. THERAPIST: Do you want to continue to be there for
someone who chooses not to be there for you? BARBARA: Well, no—no, that isn’t right. THERAPIST: So what do you want to do? BARBARA: I want to leave.
In this part of the session, the therapist has taken on the “Healthy Parent” mode for Barbara, because she does not have a strong template for this mode. This is one example of what is meant by “limited reparenting.” In this role, the therapist temporarily steps in to support the client in relation to unmet basic needs for safety; stability or predictability; love, nurturance, and atten- tion; acceptance and praise; empathy; realistic limits; and validation of feelings and needs. The therapist also counters and challenges any unreasonable messages
304 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
or beliefs that such needs should remain unfulfilled. As she begins to feel safer and more protected by the “Healthy Parent” through this work, “Little Barbara” no longer feels so ashamed of herself.
Step 6: Conduct Dialogues between Modes
Once patients begin to internalize the Healthy Parent mode demonstrated by the therapist, their own Healthy Adult mode becomes stronger. The patient’s Healthy Adult mode can now actively challenge and combat the Punitive Parent mode, thereby supporting, protecting, and healing the Vulnerable Child, with the help of the therapist.
The therapist now addresses the Escapist, or De- tached Protector, mode. In the segment that follows, the therapist sets up a dialogue between the Vulnerable Child and Escapist modes.
THERAPIST: How about having “Little Barbara” talk with “the Escapist” about things that she really en- joys?
BARBARA: OK . . . but how do we do that? THERAPIST: First, I want you to sit on this side of the
couch. When you’re on this side of the couch, I want you to let yourself get in touch with and speak for “Little Barbara.” Have “Little Barbara” talk about all those things that interest her—those things that interest and excite her and help her feel alive. And then, I want you to get up and sit on the other side of the couch. When you’re on this side of the couch, I want you to let yourself get in touch with and speak for “the Escapist.” We’ll go back and forth between those two parts of yourself to see what comes out. I’ll help out “Little Barbara” if she needs me.
BARBARA: [as “Little Barbara”] You know, I once made a dress at school, and I noticed that I really liked sew- ing. It was a really simple pattern, nothing special, but I had so much fun making it. I think I might want to take a class to try sewing again.
[as “the Escapist”] Why do you want to do that? If it doesn’t turn out, you’ll just feel bad about yourself. People might think you’re ridiculous at this age, try- ing to learn to sew. Why take the chance that you’ll feel bad or stupid? Why don’t you just lie down and forget about it?
[as “Little Barbara”] But I might like it. If I don’t start trying the things that I think I might enjoy, I’ll never
know what I like or what makes me happy. . . . If I keep listening to you, I’ll do nothing but sleep away the rest of my life. I want to have a life.
[as “the Escapist”] I don’t know if it’s worth the risk of feeling bad.
[as “Little Barbara”] Even if I feel bad at first, it will only be temporary. Either I’ll get good at sewing or I can find something else that I’m good at. I’ll eventu- ally find something if I just keep at it.
[as “the Escapist”] Well OK, suit yourself. [as “Little Barbara”] I will.
At this point, the therapist is focused on helping Bar- bara discover what gives her an inner sense of joy and accomplishment. This task is difficult for Barbara, be- cause she spent so many of her early years dependent on her mother, not developing any special skills or talents, and surrendering to what others wanted her to be. Nev- ertheless, as the previous segment illustrates, Barbara has begun to recognize the importance of trying out new activities that interest her, in spite of the temporary discomfort she may feel about the possibility of failing and feeling stupid again. The final step in therapy is to take these lessons she has learned in the sessions and integrate them into her everyday life experiences.
Step 7: Generalize Results from Mode Work to Real Life
Barbara decided to enroll in one sewing class and sur- prised herself by doing quite well. She then decided to take two more classes—a more advanced sewing class and a course in costume design. Following these classes, she started to volunteer for a local theater group, work- ing on costumes. Barbara received much attention, praise, and appreciation from her teachers and theater friends. At this point in treatment, Barbara commented to her therapist, “You know, I think this is the first time I have ever really felt good and proud of myself.”
As Barbara’s confidence and her network of friends grew, she became less accepting and less tolerant of George’s neglectful and demeaning behaviors toward her. She also became increasingly annoyed with her mother’s pattern of excusing George’s behavior for the sake of “being financially comfortable.” This was in stark contrast to Barbara’s unquestioning acceptance of her relationship with George at the beginning of treat- ment.
As she began to see parallels between how she felt with George and how she felt as a child with her parents,
Cognitive Therapy for Depression 305
Barbara began to question whether this was a healthy marriage for her. She recognized that many of George’s behaviors were damaging to her, just as her parents’ behaviors had been. Although Barbara still wanted to adopt a child, she began questioning George’s ability to be a good parent.
The following vignette from a later session in Bar- bara’s treatment illustrates how much healthier and as- sertive she has become in relation to George:
BARBARA: I’m noticing that when George speaks to me in such a condescending tone, I feel like a little girl with my father again. I don’t want this. I want to be treated with love and respect, and as an equal. It isn’t right for me to accept his behavior—being ignored and demeaned by someone who is supposed to love me.
THERAPIST: So what do you want to do? BARBARA: I think I’m ready to confront George about
his drinking and abusive behavior. I can’t even imag- ine adopting a child and bringing that child into our home if he continues to behave this way.
THERAPIST: What do you want to happen? BARBARA: I want him to stop drinking and start treat-
ing me with love and respect. THERAPIST: And if he doesn’t? Then what? BARBARA: I guess I’ll leave him and seek a divorce. THERAPIST: And how will that be for you—in the
worst case scenario you might imagine? BARBARA: In the worst case . . . you know, I think
I’ll be OK. I mean, I have my own life now. I have my own friends. And I have you, if things really get rough.
THERAPIST: I’ll be here for you whenever you need my support.
BARBARA: Yeah, I think I’ll be OK.
At this point in treatment, Barbara has fully incorpo- rated the Healthy Adult mode and has healed the most damaging schemas that had been part of her Vulner- able Child mode. Along with these changes, Barbara’s depression went into full remission. Soon after this ses- sion, Barbara confronted her husband. Despite couple therapy, George refused to make any changes, and Bar- bara filed for divorce.
Barbara did experience one relapse of major depres- sion as her divorce was finalized. “Ashamed Little Bar-
bara” and “the Escapist” temporarily returned during this period. Barbara, however, was able to recognize the reappearance of the Punitive Parent mode and suc- cessfully overcame it with her now stronger Healthy Adult mode. She was able to empathize with and for- give herself, and to mourn the lost opportunity to have her own family. She decided to go back to school and succeeded in becoming a certified teacher at the high school level, teaching costume design and drama in the theater department. She also developed a lasting relationship with a caring, emotionally available man who shared her passion for theater. Barbara’s chronic depression lifted, and she has, for the most part, been symptom free since.
CONCLUSION
Evidence demonstrating the efficacy of cognitive ther- apy in the treatment of unipolar and bipolar depression continues to mount. Adolescents, adults, and geriatric patients have all been shown to benefit from cognitive therapy.
Cognitive therapy helps patients understand the relationships among their thoughts, behaviors, and feelings. Cognitions are “put to the test” by examin- ing evidence, setting up in vivo experiments, weighing advantages and disadvantages, trying graded tasks, and employing other intervention strategies. Through this process, patients begin to view themselves and their problems more realistically, to feel better, to change their maladaptive behavior patterns, and to take steps to solve real-life difficulties. These changes take place as a direct result of carefully planned, self-help homework assignments—one of the hallmarks of cognitive treat- ment. Cognitive therapy reduces symptoms by helping patients to identify and modify automatic thoughts, and the behaviors associated with them.
An expansion of cognitive therapy called schema therapy (ST) has been developed to deal with the deep- er psychological structures that predispose patients to chronic depression. After utilizing interventions aimed at initial symptom reduction, a great deal of subsequent attention and effort are directed toward identifying and modifying the underlying schemas and modes that often predispose individuals to chronic depression.
Following a thorough assessment, an extensive change component is implemented. During this phase of treatment, patients come to understand their own schemas and modes, their developmental origins, and
306 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
how these dysfunctional schema patterns are triggered, reinforced, and maintained.
Throughout the treatment, cognitive therapists maintain a collaborative alliance with their patients. They are very active in structuring sessions, yet go to considerable lengths to help patients reach conclusions on their own. Cognitive therapists serve as guides, help- ing patients maneuver through a labyrinth of dysfunc- tional cognitions and life patterns. As a result, patients develop the psychological tools they need to become more proactive in making the cognitive, affective, in- terpersonal, and behavioral changes that serve to mini- mize future episodes of depression.
NOTES
1. Some researchers have found it useful to differentiate be- tween relapse (the return of symptoms within 6 months after termination of treatment) and recurrence (a whole new epi- sode of depression, occurring at least 12 months after treat- ment has ended; Gelder, 1994; see also Overholser, 1998). However, this distinction has not been uniformly incorpo- rated into the literature.
2. Reported relapse rates for patients treated with medication have varied depending on the definition of relapse, the dura- tion of the follow-up period, and the severity of depression within the patient population (Williams, 1997). Because of these differences, some of the estimates have ranged from 34 to 92% (Frank, 1996; Overholser, 1998; Versiani, 1998; Williams, 1997), though lower rates have also been reported (Keller & Boland, 1998).
3. The book by Young (1990/1999) cited here and throughout the chapter, Cognitive Therapy for Personality Disorders: A Schema-Focused Approach, refers to the third edition. How- ever, the ideas expressed were developed in 1990, for the original edition. Similarly, the Young Schema Question- naire was developed in 1990, then reprinted in the third edi- tion.
4. Currently, the concept of a schema domain is not a com- ponent of schema theory. Although early factor-analytic re- search supported the grouping of 18 EMSs into five broader domains, later studies have been inconsistent regarding how schemas cluster together, and some domains have not been supported at all. Nevertheless, we have included research studies that focus on these five domains, because the find- ings do shed light on the relationship between schemas and other constructs. We are in the process of reviewing all of the research available so that we can reexamine the question of how schemas cluster together.
5. For the remainder of the chapter, we use the term schemas to refer specifically to Young’s “early maladaptive schemas.”
6. Many cognitive therapists also focus on “underlying as- sumptions,” which represent cognitions that are “deeper” than automatic thoughts but less central than schemas or core beliefs. Underlying assumptions are considered condi- tional beliefs, whereas most schemas are unconditional. In our own work, we have not found this distinction to be nec- essary in working with most patients. Thus, conditional and unconditional beliefs that are enduring and pervasive can be merged into the broader construct of a schema.
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Much evidence has emerged over the past several decades (Ravitz et al., 2019) supporting the clini- cal effectiveness of interpersonal psychotherapy (IPT) for treating a variety of diagnoses, particularly major depression. A substantial advantage of IPT is the relative ease with which clinicians can learn to administer this protocol with integrity. This chapter illustrates the process of IPT in some detail with the treatment of “Sara,” who was suffering from a major depressive episode associated with grief following the death of her baby girl in utero at 27 weeks’ gestation 2 months earlier. The first author, Kathryn L. Bleiberg, an international authority on IPT training, was the therapist. Although IPT is relatively easy to comprehend, the twists and turns encountered in administering IPT (or any psycho- therapy) are evident in this chapter. Here the therapist skillfully focuses on both resolving grief and ad- dressing the patient’s social isolation and conflicts with her husband over emotional reactions to the loss. Also notable about IPT is the finding that the treatment is more successful when administered with fidelity to the goals of IPT and adherence to the protocol. The power of a therapist and patient working well together and staying on task provides some good evidence for the specific effects of an interpersonal focus to psychotherapy. —D. H. B.
interpersonal psychotherapy (IPT), a time-limited, diagnosis-targeted, pragmatic, empirically supported,
manualized treatment, was originally developed to treat outpatients with major depression (Weissman, Markowitz, & Klerman, 2000). IPT focuses on cur- rent or recent life events, interpersonal difficulties, and symptoms. Through use of the medical model, linking mood symptoms to recent life events, and normalizing emotions in an interpersonal context, the IPT therapist helps the patient to feel understood. IPT aids recovery from depression by relieving depressive symptoms, by helping the patient to develop more effective strategies for dealing with current interpersonal problems related to the onset of symptoms, and by mobilizing social sup- port (Bleiberg & Markowitz, 2007). IPT’s success as
an individual treatment for major depression has led to its adaptation for subpopulations of patients with mood disorders, including depressed older patients (Reynolds et al., 2006, 2010; Sholomskas, Chevron, Prusoff, & Berry, 1983), depressed adolescents (Mufson, Moreau, & Weissman, 1993; Mufson, Weissman, Moreau, & Garfinkel, 1999; Mufson et al., 2004), depressed HIV- positive patients (Markowitz, Klerman, Perry, Clough- erty, & Mayers, 1992; Markowitz, Kocsis, et al., 1998; Ransom et al., 2008; Heckman et al., 2017), patients with antepartum (Spinelli & Endicott, 2003; Swartz et al., 2008) and postpartum depression (O’Hara, Stuart, Gorman, & Wenzel, 2000), dysthymic disorder ( Markowitz, 1998), and bipolar disorder (Frank, 2005; Frank et al., 2005; Swartz, Frank, & Cheng, 2012).
C H A P T E R 8
interpersonal Psychotherapy for Depression
Kathryn L. Bleiberg John C. Markowitz
318 CliniCal Handbook of PsyCHologiCal disorders
IPT has been adapted for posttraumatic stress disor- der ( Bleiberg & Markowitz, 2005; Markowitz, Milrod, Bleiberg, & Marshall, 2009; Markowitz et al., 2015), social phobia (Lipsitz, Fyer, Markowitz, & Cherry, 1999; Markowitz, Lipsitz, & Milrod, 2014), bulimia nervosa (Fairburn, Jones, Peveler, Hope, & O’Connor, 1993; Fairburn et al., 1995), binge-eating disorder (Wilfley, 2008; Wilson, Wilfley, Agras, & Bryson, 2010), and borderline personality disorder (Markowitz, Skodol, & Bleiberg, 2006). In addition to its adaptation to treat patients with different diagnoses, IPT has been increasingly practiced and studied among patients from different cultures (Markowitz & Weissman, 2012a). It is been adapted to treat patients in varied settings, in- cluding urban and rural areas in developed and devel- oping countries (Ravitz et al., 2019; Weissman, 2020). The coronavirus disease 2019 (COVID-19) pandemic has forced mental health professionals practically over- night to provide psychotherapy remotely. Fortunately, IPT has been adapted and tested for various formats, including telephone and video, over the past 20 years (Dennis, Grigoriadis, Zupancic, Kiss, & Ravitz, 2020; Heckman et al., 2017; Neugebauer et al., 2007; Ravitz et al., 2019). Furthermore, IPT’s demonstrated efficacy in the treatment of major depression, PTSD, and other disorders has led to its incorporation into national treat- ment guidelines (American Psychiatric Association, 2010; Cuijpers et al., 2011; Curry et al., 2019; Weiss- man, 2020).
This chapter describes the principles, characteristics, and techniques of individual IPT for major depression and illustrates how a clinician implements IPT tech- niques based on an actual patient.
MAJOR DEPRESSION
Major depressive disorder (MDD), the most common depressive illness, affects millions of Americans each year. The Global Burden of Disease (GBD) Study 2017 found that depression is the third leading cause of dis- ability among women and the fifth leading cause of disability among men worldwide (GBD 2017 Disease and Injury Incidence and Prevalence Collaborators, 2018). Additionally, the number of new cases increased by nearly 50%, from 172 million in 1990 to 258 mil- lion in 2017 (Lin et al., 2019), suggesting that depres- sion is being increasingly identified and diagnosed. The 2012–2013 National Epidemiologic Survey on Alcohol
and Related Conditions–III (NESARC-III) revealed a 20.6% lifetime prevalence of MDD among adults age 18 and older, 26.1% for women and 14.7% for men (Hasin et al., 2018). The National Institute of Men- tal Health (NIMH) reports that in the United States the annual prevalence of MDD is 7.1% among adults age 18 and older, and 13.3% among adolescents ages 12–17, with the majority of cases of MDD associated with substantial symptom severity and impairment in functioning (NIMH, 2019). National and internation- al studies have consistently found higher prevalence of MDD in women than in men; women are twice as like- ly as men to experience an episode of MDD. Both the NIMH and the World Health Organization (WHO) recommend IPT as a first-line treatment for depression (NIMH, 2019; WHO, 2020a). Furthermore, the U.S. Preventive Services Task Force recently recommended IPT for the prevention and treatment of depression dur- ing pregnancy (Curry et al., 2019; Weissman, 2020).
A major depressive episode comprises a period of at least 2 weeks during which a person experiences de- pressed mood and/or anhedonia and a variety of cogni- tive, somatic, and interpersonal symptoms. Common symptoms include sleep and appetite disturbance; dif- ficulty concentrating and making decisions; low energy and motivation; and feelings of helplessness, hopeless- ness and worthlessness, and suicidality. For additional criteria, see the fifth edition of the Diagnostic and Sta- tistical Manual of Mental Disorders (DSM-5; American Psychiatric Association, 2013), and the 11th revision of the International Classification of Diseases (ICD-11; WHO, 2020b).
THE DEVELOPMENT OF IPT
Klerman, Weissman, and colleagues developed IPT in the 1970s as a treatment arm for a pharmacotherapy study of depression (Markowitz & Weissman, 2012b). Being researchers, they developed a psychotherapy based on empirical data. Post-World War II research on psychosocial life events and the development of mental disorders had shown relationships between de- pression and complicated bereavement (death of a sig- nificant other), role disputes (bad relationships), role transitions (e.g., losing or getting a new job, or any meaningful life change), and interpersonal deficits (so- cial isolation). Stressful life events can trigger depres- sive episodes in vulnerable individuals, and depres-
Interpersonal Psychotherapy for Depression 319
sive episodes compromise interpersonal functioning, making it difficult to manage stressful life events and often triggering further negative life events (Bleiberg & Markowitz, 2007).
IPT was also built on the interpersonal theory of Adolph Meyer (1957) and Harry Stack Sullivan (1953), and on the attachment theory of John Bowlby (1973). The interpersonalists broadened the scope of psychia- try by emphasizing social, cultural, and interpersonal factors. Sullivan stressed the role of interpersonal rela- tionships in the development of mental illness and the use of interpersonal relationships to understand, assess, and treat mental illness. Sullivan also indicated that life events and relationships occurring after early childhood influenced psychopathology, in contradistinction to the then current focus on pre-Oedipal life events.
Bowlby (1973) posited that the disruption of secure attachments can contribute to the onset of depression, and that psychiatric disorders result from difficulties in forming and maintaining secure attachments. In- deed, social supports protect against depression. In psy- chiatry, the idea that mental illness was influenced by current life events and not (simply) due to early child- hood experiences was novel in an era divided between psychoanalytic and biological approaches (Klerman, Weissman, Rounsaville, & Chevron, 1984).
PRINCIPLES OF IPT: THE IPT MODEL OF DEPRESSION
Two basic principles of IPT explain the patient’s depres- sion and situation. These principles are simple enough to grasp, even for a very depressed patient with poor concentration. First, the IPT therapist defines depres- sion as a medical illness and explains that the patient has a common illness with a discrete and predictable set of symptoms, thus making the symptoms seem less overwhelming and more manageable. The IPT thera- pist assumes that the etiology of depression is complex and multidetermined: The etiology may comprise biol- ogy, life experiences, and family history, among other factors. The IPT therapist emphasizes that depression is a medical illness that is treatable and not the patient’s fault. Explaining that depression is treatable inspires in patients the hope that they can feel better. Hopeless- ness, a potentially deadly depressive symptom, distorts the generally good prognosis of the illness. Depressed patients often see their symptoms and consequent dif-
ficulties in functioning as reflections of a personal fail- ure, character flaw, or weakness.
Defining depression as a blameless illness helps to combat the depressed patient’s guilt and self-criticism. The therapist diagnoses depression using DSM-5 or the ICD-11 criteria and assesses symptoms using rat- ing scales such as the Hamilton Depression Rating Scale (HDRS; Hamilton, 1960) or the Beck Depression Inventory–II (BDI-II; Beck, Steer, & Brown, 1996). IPT’s use of the medical model to define depression distinguishes it from other psychotherapies and makes it highly compatible with antidepressant medication in combination treatment.
The second IPT principle is that the patient’s de- pression is connected to a current or recent life event. Stressful life events can precipitate depressive episodes in vulnerable individuals and, conversely, depression can make it difficult for individuals to manage stress- ful life events. IPT focuses on helping the patient to solve an interpersonal problem in her life,1 a problem area—complicated bereavement, a role dispute, a role transition, or interpersonal deficits—connected to the patient’s current depressive episode. By solving an in- terpersonal crisis, the patient improves her life situa- tion, often gains new social skills, and simultaneously relieves depressive symptoms.
CHARACTERISTICS OF IPT
Several characteristics define IPT, sometimes distin- guishing it from other psychotherapies.
• IPT is time-limited and focused. Acute treatment at the start is set at 9, 12, or 16 weekly sessions. Some studies have included continuation and maintenance phases with biweekly and monthly sessions. IPT’s time limit provides hope for patients that their symptoms and life situation can rapidly improve; the time limit encourages patients to stay focused in treatment. It also pressures both patient and therapist to work hard and efficiently within the therapeutic window of op- portunity. Therapist and patient agree to focus on one, or at most two, problem areas at the beginning of treatment.
• IPT is empirically grounded. Because IPT has shown repeated efficacy in research studies, therapists can offer and deliver the treatment with confidence and
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optimism, and patients can feel hopeful about the treat- ment they are receiving.
• IPT is diagnosis-targeted. IPT focuses on a specific diagnosis, its symptoms, and how symptoms interfere and interact with social functioning. IPT is not intend- ed for all patients, but it has been tested in a series of randomized controlled trials to determine its efficacy.
• IPT has a “here-and-now” focus. IPT focuses on the present and on improving the patient’s situation for the future—not on what happened in the patient’s past. The IPT therapist relates current symptoms and interpersonal difficulties to recent or current life events. Although past depressive episodes and relationships are reviewed and relationship patterns are identified, treat- ment focuses on current relationships—building social supports and resolving disputes—and social function- ing.
• IPT focuses on interpersonal problems. The IPT therapist may recognize intrapsychic defenses but does not see the patient’s current difficulties as a function of internal conflict. Instead, the therapist focuses on inter- personal relationships and functioning.
• IPT focuses on the interrelationship between mood and current life events. The IPT therapist emphasizes that stressful life events can trigger episodes of major depression and, reciprocally, that depression compro- mises psychosocial functioning. This makes it difficult to manage life stressors, leading to further negative life events.
• IPT emphasizes eliciting affect. Depressed patients often have difficulty understanding, identifying, artic- ulating, and tolerating what they are feeling. Whereas patients with depression tend to report feeling “bad,” they often have difficulty identifying negative feelings more specifically, such as anger, hurt, shame, rejec- tion, disappointment. Furthermore, depressed patients who do recognize such negative affects tend to feel ashamed of having such “bad” emotions. The IPT therapist helps the patient to better identify what she is feeling, validates emotions such as anger and disap- pointment as normal and useful interpersonal signals, and helps the patient to use such emotion as a guide (Markowitz & Milrod, 2011). Patients in IPT learn to manage their feelings better and to use them in decid- ing how to behave and what to say in interpersonal encounters.
IPT COMPARED WITH OTHER PSYCHOTHERAPIES
Although IPT has a distinct rationale and is distinguish- able from other psychotherapies (Amole et al., 2017; Hill, O’Grady, & Elkin, 1992; Weissman et al., 2000), it is an eclectic psychotherapy that uses techniques seen in other treatment approaches. IPT includes the so-called “common” factors of psychotherapy (Frank, 1971). IPT shares the “here and now” diagnostic focus, time limit, and active approach with cognitive-behavioral therapy (CBT). IPT and CBT both include role playing and skills building. However, IPT is much less structured and assigns no formal homework, although the IPT therapist does encourage activity between sessions to improve mood and as it relates to resolving the interper- sonal problem area. Whereas the CBT therapist defines depression as a consequence of dysfunctional thought patterns and attributes the patient’s difficulties to them, the IPT therapist emphasizes that depression is a medi- cal illness and relates difficulties to feeling depressed in connection with recent life events. IPT emphasizes elic- iting affect rather than (“hot,” affectively charged) au- tomatic thoughts. IPT addresses interpersonal issues in a manner similar to that in marital therapy. Much like a supportive therapist, IPT therapists provide support and encouragement (Bleiberg & Markowitz, 2007).
IPT has been termed a “psychodynamic” psychother- apy on occasion, but it is not (Markowitz, Svartberg, & Swartz, 1998). IPT employs the medical model of de- pressive illness, whereas psychodynamic psychotherapy uses a conflict-based approach. The IPT therapist does not address unconscious processes, or explore or inter- pret the transference, but instead focuses on current re- lationships outside of the treatment room. Childhood experiences are recognized but not emphasized. The IPT therapist relates current symptoms and interper- sonal problems to recent life events, not to childhood experiences. IPT acknowledges the influence of past experiences on present difficulties, but only to identify patterns of interpersonal behavior and to empathize with the patient’s struggle. Unlike psychodynamic treatment, the goal in IPT is to reduce symptoms and improve social functioning, not to change character or personality. Like the psychodynamic psychotherapist, however, the IPT therapist emphasizes facilitating af- fect in the treatment room and helping patients be- come aware of feelings they may not have been aware of previously (Markowitz & Milrod, 2011; Weissman et al., 2000). IPT and psychodynamic therapy overlap
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in their use of mentalizing (Markowitz, Milrod, Luy- tens, & Holmqvist, 2019) and may even share neural substrates with other affect-focused psychotherapies (Suarez-Jimenez et al., 2020).
THE IPT THERAPIST
The IPT therapist conducts office treatment in an aca- demic, hospital, or private practice setting. The thera- pist typically does not consult with the patient’s family or friends.
The IPT therapist takes a non-neutral, active stance, providing psychoeducation about depression, empha- sizing the IPT rationale, teaching social skills, and instilling hope. A somewhat directive approach is es- sential for adhering to the time limit and keeping the treatment focused on the interpersonal problem area. Taking an active stance may be challenging for thera- pists with psychodynamic orientations, who are used to taking a neutral stance and offering little guidance in the session.
On the other hand, the IPT therapist does not want to reinforce the passivity and dependency that charac- terize depression. A therapist who solves all problems may reinforce the patient’s sense of inadequacy. Hence, the IPT therapist encourages the patient to come up with ideas, explore options, and test them out between sessions. Hence, the patient deserves (and receives) credit for making the life changes that lead to improve- ment in treatment.
The IPT therapist needs to be supportive, enthusi- astic, and optimistic—without trivializing or failing to acknowledge the patient’s distress—to instill hope that the depression will decrease, and changes will be forthcoming, and to encourage and inspire the patient to make changes. The structure of the IPT manual (Weissman, Markowitz, & Klerman, 2018) and the empirical validation of IPT in randomized controlled studies help to bolster therapist confidence. The IPT therapist congratulates the patient on her progress in treatment and efforts to make changes.
Given the emphasis on helping the patient to iden- tify and express feelings, the IPT therapist needs to feel comfortable encouraging expression of affect and toler- ating intense negative affects. The therapist can show by example that feelings are indeed potent, but they are only feelings that can be understood and used in an interpersonal context, and will pass, if tolerated.
THE IPT PATIENT
Research has demonstrated that a wide range of patients with major depression are good candidates for IPT. IPT has been validated with minor modifications as a treatment for adolescent, adult, peripartum, and geriat- ric depression. The patient should ideally report some recent life stressor and have some social contacts. Pa- tients with depression who report no recent life events, are socially isolated, and lack basic social skills tend to do least well in IPT. IPT is not intended for delusional depression, which requires antidepressant and antipsy- chotic pharmacotherapy or electroconvulsive therapy. Patients with comorbid moderate or severe personality disorder may be less likely to respond to short-term psy- chotherapy (Weissman et al., 2018). Accordingly, the adaptation of IPT for borderline personality disorder allows up to 32 weeks of treatment (Markowitz et al., 2006).
THE FOUR INTERPERSONAL PROBLEM AREAS
Treatment focuses on solving one of the four interper- sonal problem areas related to the onset or maintenance of the patient’s current depressive episode. The IPT therapist follows strategies specific to each problem area.
Grief
This problem area addresses a patient’s complicated bereavement following the death of a significant other. The therapist facilitates the mourning process, encour- ages catharsis, and ultimately helps the patient to form new relationships and find new activities to compensate for the loss. The therapist explores the relationship and the associated feelings the patient had with the loved one. Patients with complicated bereavement often have had a conflicted relationship with the deceased, report- ing unresolved feelings about and anger toward the person, and feeling guilty or uncomfortable with such feelings. Patients may feel guilty about what they did or did not say to or do for the deceased. The therapist encourages exploration of these feelings and validates and normalizes negative feelings, allowing the patient to let go of the guilt she experiences.
The release of negative affects in the therapy office can diminish the intensity of such feelings. The thera-
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pist also explores positive feelings the patient had for the lost person and sympathizes with the loss. Finally, the therapist helps the patient explore options for form- ing new relationships and finding new activities to help to substitute for the lost relationship and give the pa- tient a new sense of direction. The loss may provide op- portunities to meet people and engage in activities the patient might not otherwise have encountered.
Role Disputes
A role dispute is a conflict with a significant other: a spouse, friend, parent, relative, employer, coworker, or close friend. Therapist and patient explore the relation- ship, the nature of the dispute, and options to resolve it. Depressed patients tend to put other people’s needs ahead of their own. They have difficulty asserting themselves, confronting others, and getting angry ef- fectively, which makes it difficult for them to manage interpersonal conflicts. The therapist blames the de- pression and explains: “It’s not your fault. You can learn how to assert and defend yourself.”
The therapist validates the patient’s feelings in the relationship: recognizing anger as a natural response to someone bothering her, for example. The next question is how to express such feelings. The therapist helps the patient to conceive ways to communicate thoughts and feelings more effectively and role-plays potential inter- actions with her. If, after exploring and attempting to implement options to resolve the dispute, the conflict has reached an impasse, the therapist helps the patient to consider ways either to live with the impasse or end the relationship.
Role Transitions
A role transition is a change in life status, such as begin- ning or ending a relationship, starting or losing a job, a geographic move, graduation or retirement, becoming a parent, or receiving the diagnosis of a medical illness. The therapist helps the patient to mourn the loss of the old role, to explore positive and negative aspects of the new role, and to determine what positive aspects of the old role, if any, she can retain. Ultimately, the thera- pist helps the patient adjust to and gain a sense of mas- tery over the new role. Even if a new role is wanted or positive, the role may be accompanied by unanticipated loss. For example, getting married may mean spending less time with one’s family of origin due to having to
see the spouse’s family. Moving to a new, larger house in a nicer neighborhood may disrupt relationships with friends in the old neighborhood. If a new role is unde- sired, a patient may discover unseen benefits in therapy. A patient who has lost a job may come to see the loss as an opportunity to pursue a better job.
Interpersonal Deficits
Interpersonal deficits, the least developed of the four problem areas, is the focus of IPT for major depres- sion only when a patient reports no recent life events and therefore lacks any of the first three problem areas. Patients in this category tend to be socially isolated, and to have few social supports and a history of dif- ficulty forming and sustaining relationships or finding relationships unfulfilling. The goal of treatment in in- terpersonal deficits is to reduce the patient’s isolation, improving social support. Because the patient lacks current relationships, treatment focuses on patterns in past relationships and starting to form new ones. The therapist reviews past significant relationships, explor- ing positive and negative aspects and identifying recur- rent problems. The therapist helps the patient to explore options for meeting people and participating in activi- ties that she used to enjoy.
Unlike the other problem areas, treatment for in- terpersonal deficits may focus on the relationship with the therapist. In the absence of other relationships and recognizing that the patient is likely to feel uncomfort- able in the therapy as in all situations, the therapist en- courages the patient to discuss her feelings about the therapist and work on interpersonal problems that arise in their relationship. Ideally, the relationship with the therapist serves as model for the patient to form other relationships. Inasmuch as IPT usually focuses on a life event, it is not surprising that patients who lack such life events have been shown to respond least well to IPT. It is important to identify patients who have underly- ing dysthymic disorder, because such patients often de- scribe few recent life events. There is an IPT protocol adapted to the treatment of patients who are dysthymic (Markowitz, 1998; Weissman et al., 2018).
THE PROCESS OF IPT TREATMENT
Acute IPT treatment comprises initial, middle, and termination phases. IPT techniques help the patient
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to pursue the treatment goals for the focal interper- sonal problem area. This section leads into a case ex- ample illustrating the implementation of these tech- niques.
The Initial Phase (Sessions 1–3)
Tasks of the initial IPT sessions include eliciting the patient’s chief complaint; reviewing her symptoms and establishing a diagnosis; determining the interpersonal context for the current depressive episode; forming a therapeutic alliance; and setting the treatment frame, including the goals and strategies. Although these tasks are common to other psychotherapeutic interventions, the techniques and process for accomplishing them are specific to IPT.
Diagnosing Major Depression
To diagnose MDD, the therapist reviews current symptoms of depression using either DSM-5 or ICD- 11 criteria, inquiring about each symptom and about any past history of depression. The therapist may ad- minister a symptom severity scale such as the HDRS (Hamilton, 1960) or the BDI-II (Beck et al., 1996) and repeat the instrument every few weeks to monitor the patient’s progress. The therapist rules out other diag- noses, such as bipolar illness, depression due to general medical condition or substance use, and other psychi- atric disorders. If the patient meets MDD criteria, the therapist tells her, describing explicitly the symptoms she reported.
“You have an illness called major depression. The symptoms you describe having had for the past couple of months—feeling down most of the time, having difficulty enjoying things, feeling like you have to push yourself to get things done, difficulty sleeping, loss of appetite, trouble concentrating, and feeling very self-critical and down on yourself and pessimistic about your future—are all symptoms of depression. Depression is a treatable illness. It is not your fault that you feel this way and have had dif- ficulty functioning, any more than it would be your fault if you had asthma, or high blood pressure, or any other medical problem. And although you’re feeling hopeless, that’s just a depressive symptom. Your prognosis with treatment is quite good. You have an excellent chance of feeling better.”
In the initial phase, and as needed throughout treat- ment, the therapist provides psychoeducation about depression and how it affects social functioning. The therapist helps the patient to identify and understand her depressive symptoms and how better to manage them, and to distinguish between the illness and pre- morbid strengths and capabilities. The therapist de- termines the need for medication based on symptom severity, past response to medications, and patient pref- erence.
The “Sick Role”
The IPT therapist gives the patient the “sick role” (Par- sons, 1951), a temporary status intended to help the patient recognize that she suffers from an illness that comprises a distinct set of symptoms that compromise functioning. Assuming the sick role relieves the patient of self-blame and exempts her from responsibilities that the depression compromises until she recovers. The therapist educates the patient about how depression can impair social functioning and how to explain the ill- ness to family and friends to gain support. The sick role also gives the patient the responsibility of working on improving her symptoms in treatment.
The Interpersonal Inventory
In IPT, the psychiatric history includes the “interper- sonal inventory,” a thorough review of the patient’s past and current social functioning, close relationships, relationship patterns, expectations of others within re- lationships, and the perceived expectations that others have of the patient. The interpersonal inventory should give the therapist a sense of how the patient interacts with other people. It should illuminate how relation- ships may have contributed to the current depressive ep- isode and, conversely, how depressive symptoms may be affecting current relationships. Furthermore, the inter- personal inventory assesses actual and potential social support. To glean this information, the IPT therapist asks detailed questions about the patient’s past and cur- rent relationships. An inquiry about current relation- ships might include the following questions: “Who is in your life currently?’; “Are you in a relationship?”; “Girl- friend/boyfriend?”; “What is your relationship like with him/her?”; “What do you like about him/her?”; “What don’t you like?”; “Do you argue?”; “What do you argue about?”; “What happens when you argue—what do you
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do/say?”; “What do you expect of him/her?”; “What do you think he/she expects of you?”
Identification of Interpersonal Problem Areas
The primary goal of the interpersonal inventory is to determine which interpersonal issues are most related to the patient’s current depressive episode. The therapist should identify major interpersonal problem areas that can become the treatment focus. The therapist inquires about any life changes that occurred around the onset of current depressive symptoms: “What was going on in your life when you became depressed?” The therapist explores different areas in the patient’s life: home, work, relationships with significant others, family members, and friends. The therapist should pick one problem area on which to focus, or at most two; too many treatment foci yield an unfocused treatment. The therapist relates the depression to a problem area and presents this to the patient in a formulation (Markowitz & Swartz, 2007):
“It seems from what you have been telling me that the main problem has been your difficulty in get- ting along with your husband. Although the causes of depression are complex and not fully known, we do know that conflicts with significant others can be related to depression. Furthermore, depression can make it difficult to handle conflicts with other peo- ple. I suggest that we meet for the next 12 weeks to figure out how you can better deal with the problems with your husband you’ve described. In IPT, we call that conflict a ‘role dispute.’ As you solve your role dispute, both your life and your depression should improve. Does this make sense to you?”
Only with the patient’s explicit agreement to work on the chosen interpersonal problem area does the thera- pist proceed to the middle phase of treatment. The pa- tient’s agreement on the focus allows the therapist to bring her back to this theme thereafter, maintaining a thematic flow for the treatment.
Explanation of the Treatment Contract and the IPT Approach
Besides agreeing on a treatment focus in the initial sessions, the therapist and patient come to an under- standing about other aspects of treatment. The thera- pist discusses practical issues, including the time limit, the length and frequency of sessions, termination date,
appointment time, fee, and so forth. The therapist explains that IPT is one of several empirically sup- ported antidepressant treatments and briefly describes the basic IPT principles. The therapist emphasizes the “here and now,” and the social and interpersonal focus of the treatment, explaining:
“We’ll work together to try to understand how cur- rent stresses and relationships may be affecting your mood. We will work on helping you to better man- age these stresses and the problems you may be hav- ing in relationships. We’ll explore what you want and need in your relationships and help you figure out how to get what you want and need.
“I’ll be interested in hearing each week about what’s going on in your relationships with other peo- ple, how those interactions make you feel, and also how your feelings influence what happens with other people.”
The therapist encourages the patient to bring up any discomforts she has about the sessions: “If anything bothers you, please bring it up. I don’t intend to do any- thing to make you uncomfortable, but if you feel that way, please tell me so that we can address the issue. It’s just the sort of interpersonal tension that we need to focus on in your outside life as well.”
The Middle Phase (Sessions 4–9)
Having made the treatment contract and chosen an interpersonal problem area as the treatment focus, the therapist proceeds to the middle phase of sessions, in which the goal is to work on resolving the focal problem area.
Each session begins with the question “How have you been feeling since we last met?” This question elic- its an interval history of mood, events, and interperson- al interactions that transpired between sessions. It keeps the patient focused on current mood and situation. The patient is likely to respond by describing a mood (“I felt really down”) or an event (“My husband and I had a huge fight”). After further inquiry, the therapist links the patient’s mood to a recent event, or an event to her mood (“No wonder you felt depressed after the fight you had with your husband!”).
Inquiring about emotionally laden interpersonal in- teractions, the therapist uses communication analysis— the reconstruction and evaluation of affectively charged interactions—to help the patient understand how she
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felt in the situation and what she might have done to communicate more effectively. The therapist explores the patient’s wishes and options, helping her to decide what she wants and exploring the options for achieving it: “What did you want to happen in that situation? . . . What could you have done to get what you wanted in that situation? What other options do you have?”
Depressed patients often have difficulty seeing that they have options, and their tendency to discount their own needs as less important than others’ needs contrib- utes to difficulty in asserting themselves. The therapist empathically explains this to the patient, blaming the depressive syndrome for the patient’s difficulties where appropriate. To help the patient choose which options to pursue, the therapist uses decision analysis. The case example that follows elaborates these techniques.
The therapist and patient role-play potential interac- tions to prepare her for interpersonal interactions in real life. Rather than supplying words for the patient dur- ing role play, the therapist encourages her to come up with her own words. This empowers the patient, foster- ing her independence from the therapist. The therapist points out that the patient is able to figure out what to say and do in interpersonal interactions, despite the depressive symptom of helplessness. The therapist asks the patient how she felt during role play, whether the content and tone of voice felt comfortable, and how she imagines it will feel to say the words in reality. When a patient communicates effectively during role play— and, ultimately, in real life—the therapist reinforces the adaptive behavior with congratulations and encourage- ment. Real-life successes not only improve mood but also inspire patients to try to assert themselves in sub- sequent situations.
Depressed patients withdraw socially and tend to lose interest in activities they previously found pleasurable. The therapist encourages the patient to resume social activity and to explore options for new activities and opportunities to form new relationships, if applicable. The therapist empathizes with the patient’s difficulty in pushing herself to engage with others, but stresses that, once engaged, she will likely feel better. Indeed, the IPT therapist asks the patient to take risks—both in asserting herself with others and in pushing herself to reengage in social activities. The therapist explicitly acknowledges that he/she is asking the patient to take risks, yet assures her that these risks will likely lead to improvement of her mood and life situation. The thera- pist will be there to discuss anything that goes right or wrong.
The Termination Phase (Sessions 10–12)
In the final sessions, the therapist reviews the patient’s progress in symptom improvement and the extent to which the patient has resolved the focal problem area. By reviewing why the patient is better, through the actions she has taken to resolve the interpersonal focus, the thera- pist reinforces the patient’s growing self-esteem by point- ing out that the patient’s actions have led to her gains. The therapist congratulates the patient on her progress and hard work and expresses optimism that the patient can maintain that progress independent of the therapist.
The therapist addresses nonresponse in patients whose moods and life situations do not or only partially improve. The therapist explains that it is the treatment that failed—not the patient. The therapist communi- cates hope by emphasizing that depression is treatable and many other effective treatments exist, and encour- aging her to explore alternative treatments.
The therapist explores the patient’s feelings about the treatment and termination, acknowledging not only his/her own sadness to be ending their relationship but also happiness about the patient’s improvement and confidence that she will be able to maintain the prog- ress she made in treatment. Should symptoms recur, the patient has gained tools to manage symptoms of depres- sion on her own. Furthermore, the patient can return to IPT for “booster” sessions as needed.
Using the IPT medical model, the therapist provides psychoeducation about relapse and recurrence of major depression, preparing the patient about potential for relapse. Patients who have experienced one or more epi- sodes of major depression unfortunately remain vulner- able to future episodes. Explaining this, the therapist advises that given the link between stressful life events and mood, the patient can anticipate that she may have difficulty with future stressful life events. Fortunately, the patient can use the coping skills gained in treatment to ward off symptoms. If the patient has improved in IPT but has either significant residual symptoms or a history of multiple episodes, therapist and patient may contract for continuation or maintenance IPT, which has demonstrated efficacy in forestalling relapse (Frank et al., 2007).
CASE STUDY
This case demonstrates how a clinician (K. L. B.) im- plemented IPT for major depression in a 12-week acute
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treatment, illustrating how one works with the problem area of grief. In IPT, grief (complicated bereavement) is considered a focal problem area when the depressive onset is temporally related to the death of a significant other and the patient is experiencing an abnormal grief reaction (Weissman et al., 2018). Although cases that focus on grief usually address complicated bereavement related to the death of a person who has actually lived, the following case involves complicated bereavement related to a stillbirth (Bleiberg, 2012). Please note that any identifying information about an actual patient has been disguised.
Background Information
“Sara,” a 35-year-old, married, childless woman, was referred for treatment of major depression 2 months after the death of her baby girl in utero at 27 weeks’ ges- tation. Her doctor considered a bacterial infection the most likely cause of the stillbirth. Sara’s chief complaint was “I feel like I should be over it.”
At 27 weeks, after not having felt the baby move for several hours, Sara called her doctor, who told her to come to the hospital. The doctor found no heartbeat and told Sara that he needed to deliver the fetus. Sara recalled feeling shocked, numb, and unable to cry at first. She was given medication to induce labor and an epidural, and delivered the baby vaginally. Despite ef- forts to revive her, the baby girl was pronounced dead shortly after delivery. Sara said that she wanted to hold her and was given the baby to hold, swaddled in a white-and-pink blanket. She recalled that she and her husband had cried uncontrollably while taking turns holding the baby, and for a long time after giving the baby back to the doctor. She remembered that the baby was “very cute” and looked like her husband. She was given pictures of the baby and footprints to take home. Sara and her husband decided not to hold a funeral or memorial service.
Sara reported that since the stillbirth 2 months ear- lier, she had been feeling sad and irritable most of the day, nearly every day, and unable to enjoy previous pleasures such as reading fiction, cooking, going to the movies, and exercise. She worked as an inpatient nurse in a New York City hospital, and prior to the stillbirth had very much enjoyed her work. She now felt unable to enjoy work because of her mood, and she feared having to talk about her loss with coworkers who knew she had been pregnant. Crying frequently, socially withdrawn, she had low energy and difficulty concentrating, ex-
perienced decreased appetite, and felt very bad about herself. She denied ever having thoughts of suicide or feeling that life was not worth living.
Sara reported that despite trying not to think about the baby’s death, she nonetheless was frequently both- ered by thoughts about the baby, often wondering what her life would have been like had she survived. Sara had returned to work 3 weeks after the stillbirth, hoping that work would distract her and help her “get over” her loss. She reported feeling very angry at and avoid- ing other pregnant women, including close friends and women with newborns, in addition to other reminders of her pregnancy. She felt angry at having had to go through pregnancy, labor, and delivery without gaining the pleasure of having a child.
Sara was plagued by inappropriate guilt. She felt guilty, because she feared that she had done something to cause her loss, despite the doctor telling her that she could have done nothing to prevent it. He explained that when bacterial infections cause fetal death, they often cause no symptoms in the mother and go undi- agnosed until they cause serious complications. Never- theless, Sara felt that she should have recognized the infection, and she felt guilty about having waited until age 35 to try to conceive. She felt like a failure for hav- ing had a stillbirth. Sara felt guilty that she had disap- pointed and upset her husband by losing the baby, and she did not want to burden him with her feelings about the loss.
Sara had never sought treatment prior to her current evaluation. She described one prior episode of major depression in her late 20s, lasting 4–6 weeks, precipi- tated by a breakup with a boyfriend of several years, but reported feeling much worse since losing the baby. She reported that her mother had been treated for depres- sion with antidepressant medication with good results.
Sara was an attractive woman of average height and weight who looked her stated age. She was casually but neatly dressed in jeans and a large sweater. Sara’s move- ments were slightly slowed; her speech was fluent. Her mood was depressed and anxious, and her affect con- gruent and tearful. She denied current or past suicidal ideation and any history of substance abuse or psychot- ic symptoms. She denied current or past medical condi- tions, including thyroid dysfunction. She reported no known prior pregnancies, pregnancy losses, or fertility issues prior to the stillbirth. In fact, she had conceived after just a couple of months of trying to get pregnant.
Sara was good candidate for IPT: She met criteria for major depression and had experienced a recent life event
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proximate to the onset of her symptoms. Furthermore, IPT could address the interpersonal problems she was experiencing related to the onset of her symptoms. Sara was also a potential candidate for CBT, pharmacother- apy, or (evidence-based antidepressant) psychotherapy combined with medication. She was uninterested in doing written homework and resistant to taking medi- cation, because she was hoping to conceive again in the near future.
IPT Treatment with Sara
Initial Phase (Sessions 1–3)
Therapy with Sara followed the IPT acute treatment format. In the first three sessions, the therapist obtained a thorough psychiatric history and set the treatment framework. In the first session, she obtained a chief complaint and a history of Sara’s present illness. Be- cause treatment occurred prior to the release of DSM-5, the therapist used DSM-IV-TR (American Psychiatric Association, 2000) criteria to determine that Sara met criteria for major depressive disorder. She administered the HDRS to assess the severity of Sara’s symptoms.
The therapist offered Sara empathy for her preg- nancy loss, saying: “I am so sorry. You’ve suffered a ter- rible loss. No wonder you have been feeling so badly and having such a difficult time.” The therapist gave Sara her diagnosis of major depression, reviewed her specific symptoms, gave her the “sick role,” and offered her hope:
“The symptoms you’ve described having in the past couple of months—depressed mood, not being able to enjoy things and your loss of interest in things, feeling very badly about yourself and guilty, your difficulty eating and sleeping, and difficulty con- centrating—are all symptoms of major depression. Major depression is an illness that is treatable. It is not your fault that you have been feeling this way. And you have a very good chance of recovering.”
The therapist explained that Sara’s HDRS score of 24 indicated moderately severe depression and that she would readminister the HDRS at regular intervals to monitor Sara’s progress. Given the severity of Sara’s symptoms, her willingness to participate in psychother- apy, and her reluctance to take medication in anticipa- tion of trying to conceive again, the therapist did not think medication was needed.
The therapist described IPT and the treatment ra- tionale:
THERAPIST: I am trained in interpersonal psycho- therapy, which I think could be helpful to you. In- terpersonal psychotherapy, or IPT, is a time-limited treatment that focuses on how recent life events and stresses—such as losing a baby—affect your mood, and how mood symptoms make it difficult to handle current life events and stresses, particularly problems in relationships. Although we will take the first few sessions to review your history, our sessions will focus on the here and now, on your current difficulties and relationships and how to solve them, not on the past. Does this make sense to you?
SARA: Yes. THERAPIST: Often, people respond to IPT treatment
in 12 weekly sessions. I propose that we meet once a week for a 50-minute session for the next 12 weeks. If it’s helpful, at the end of the 12 sessions, we can discuss whether it might be useful to have additional sessions to work on issues and maintain your prog- ress. How does that sound to you?
SARA: It sounds good. I hope I can feel better in 12 weeks.
THERAPIST: You can feel better in 12 weeks. IPT has been shown in numerous research studies to effec- tively treat symptoms like the ones you have de- scribed.
After the first session, Sara felt somewhat more hope- ful but stated that she did not like the idea that she had a diagnosis of major depression. Although she could understand that there was a relationship between her stillbirth and her mood, Sara still felt she should be feel- ing better after 2 months and did not want to think of herself as depressed, like her mother, and in need of help. Sara stated that she was always the “strong one,” used to functioning at a very high level. The therapist was not surprised by Sara’s initial skepticism, as it can take time for patients to accept the medical model. Fur- thermore, patients with depression often feel uncom- fortable about seeking help because they fear burdening others, and hopeless about their prognosis. Neverthe- less, they agreed to work together for 12 weeks, then decide whether further sessions were needed.
In obtaining Sara’s psychiatric history, the therapist conducted an interpersonal inventory, carefully review-
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ing Sara’s past and current social functioning and close relationships. She started the inventory by asking about Sara’s family: “Where did you grow up?”; “Who was in your family?”; “How would you describe your relation- ship with your mother?”; “With your brother?”
Sara had grown up in Canada with her parents, now in their early 60s, and her younger brother, now age 33, all of whom still lived near her hometown of Toronto. Her father had worked a lot while Sara was growing up, and although she was fond of him, she did not feel so close to him. Sara felt closer to her mother, spoke with her weekly, but was easily irritated by her. It bothered Sara that her mother was not assertive and was inter- mittently depressed. She spoke weekly with her brother, who lived with his wife and 2-year-old son. She de- scribed her relationship with her brother as fairly close. She reported less contact with him since the stillbirth because she felt jealous that he had a child. When they did speak, Sara avoided asking about her nephew.
After exploring Sara’s relationships with family members, the therapist asked about other important people in her life and about her relationship with her husband. At age 33, Sara met her husband, Steve, who was 1 year her junior. She described Steve as warm and charming, and reported that he took great care of her. She felt she did not “deserve him” because he was “such a good guy.” She described her previous boyfriends as less emotionally available and “not very nice.” Both Sara and Steve had originally came from Canada but met in New York City, where mutual friends introduced them. Sara had moved to New York in her early 20s, whereas her husband had moved there 2 years before they met.
Since the stillbirth, Sara felt distant from Steve and argued with him about “little things.” She reported feeling guilty that she had let him down by losing the baby and feared that he blamed her for the baby’s death. She did not want to burden him further by sharing her distress about the loss. She also felt that Steve would not be able to understand her fears about trying to conceive again.
Sara reported having a few close girlfriends who lived in the tristate area and, until the pregnancy loss, had spoken with them about once per week. She had sev- eral work friends with whom she had chatted almost daily until the loss. She described herself as “indepen- dent,” “outgoing,” and “not one to lean on other peo- ple” prior to becoming depressed. Rather, her friends turned to her when they had problems. Sara said that before the depression, her friends would describe her
as hardworking and energetic. She rarely argued with friends, because she felt “uncomfortable” with conflict. She avoided confronting friends and coworkers when she disagreed or felt angry with them.
The therapist asked Sara if there was anyone to whom she had turned for comfort after her loss, be- cause it is important to have someone to confide in after such a terrible loss or any stressful experience. Sara replied that she had been avoiding her friends and family. She had felt uncomfortable talking to friends, family, and coworkers about her pregnancy when she was pregnant, because she did not like being the center of attention and felt guilty that she did not enjoy the first trimester of her pregnancy. She felt even more un- comfortable discussing her pregnancy loss. Her parents and in-laws came to see Sara and her husband after the stillbirth, but she felt unable to talk with them about what had happened and how she was feeling. Her co- workers knew that she had been pregnant, and Sara felt obligated to say something to them about what had happened. The therapist noted that it sounded like Sara could trust no one with her feelings about the stillbirth. Sara did not want to reach out to family or friends, or let them know how bad she felt; she ex- plained: “I don’t want to bother people with my prob- lems. I don’t want to be weak.”
The therapist reframed Sara’s difficulty in reaching out to others, using the medical model to explain how depression affects social functioning:
THERAPIST: You are not weak—you are depressed—and that’s not your fault. People with depression tend to minimize their own needs and avoid seeking help from their friends, as you have, because they fear being a burden. However, it’s not only appropriate to seek support from others but it also can be really help- ful to get their support. In fact, support from others has been shown to help in recovery from depression. I appreciate your dilemma. Your depression makes you feel uncomfortable seeking support, yet support from others has been shown to reduce depression and protect people from becoming depressed. Does this make sense to you?
SARA: Yes, but I also don’t want to hear what they have to say. It just makes me more upset. They don’t un- derstand what I have been through.
THERAPIST: What kinds of things have people said to you?
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Sara replied that it bothered her when people said things like “You’ll get pregnant again” or “I know someone who also lost a baby.” These statements made her feel angry. She felt that others could not understand what she had experienced. One close friend had recently given birth to her first child, and Sara had avoided call- ing or seeing her. It felt unfair that her friend had a baby when she did not. A coworker had been pregnant at the same time but had a relatively easy pregnancy. Sara felt that her coworker was not sympathetic to her physical discomfort during pregnancy.
By the end of the first phase of treatment, the thera- pist had connected Sara’s major depressive episode to her interpersonal situation in a formulation centered on an IPT focal problem area. Sara’s chief complaint re- flected that she was still grieving the loss of her baby and unable to resume her normal level of functioning. Her situation was a clear example of the grief problem area: Sara was suffering from complicated bereavement. While it is normal to grieve for months after losing a loved one, the severity of Sara’s depressive symptoms— especially the excessive guilt, low self-esteem, and social isolation—and her avoidance of thoughts, feelings, and reminders of the baby and the baby’s death, reflected an abnormal grief reaction. She had not sought emotional support after the stillbirth and had not really mourned the loss of her baby. In fact, people often develop com- plicated bereavement when they lack or have not used their social network to help them mourn the loss of their loved one.
The therapist presented this formulation to Sara:
THERAPIST: From what you are telling me, it’s clear that the loss of your baby triggered your current de- pression. You have suffered a terrible loss and you are having trouble grieving. No wonder you are having such a hard time. This is not your fault. Furthermore, your loss and your depression have affected your re- lationships with people in your life, like your hus- band, your friends and coworkers, and you’re having difficulty expressing your feelings to them. Grief is one of the problem areas that IPT has been shown to treat. I suggest that we focus our sessions on han- dling your grief over this terrible event, on helping you to mourn the loss and to improve your relation- ships that have been affected by your loss. How does this sound to you?
SARA: It sounds good.
With Sara’s explicit agreement about the treatment focus, the therapist began the middle phase of treat- ment.
Middle Phase (Sessions 4–9)
During the middle phase, therapist and patient worked on resolving Sara’s interpersonal problem area. The IPT strategy for grief is to help the patient to tolerate and manage the affect of loss, and to gather social support to help the patient through mourning. The therapist helps the patient to use existing social supports, to re- establish interests and relationships, and to form new relationships and explore new activities to compensate for the loss (Weissman et al., 2018).
The therapist continued psychoeducation about complicated bereavement and how depression affects social functioning, and repeatedly linked Sara’s depres- sion to the identified problem area. She began each ses- sion with the opening question, “How have things been since we last met?” This question elicited affect and a history of Sara’s mood and events between sessions, and kept Sara focused on her current mood and life events.
To facilitate the mourning process, the therapist encouraged Sara to think about the loss. In fact, this process had begun during the initial phase, while the therapist took a history of the events related to the onset of Sara’s depression. The therapist asked Sara to describe the events prior, during, and after the baby’s death—often a source of patient guilt—and explored Sara’s feelings associated with these events. In helping a patient mourn the loss of a loved one, the IPT therapist asks the patient to describe her feelings about the death and about the person who died. The therapist explores what the patient and the deceased did together, what the patient liked and did not like about the person, and what the patient wished they had done together but did not have a chance to do. The therapist asks the patient to describe how the deceased died and how she learned about the death, and explores the patient’s related feel- ings. Because Sara’s baby died in utero, the therapist modified this inquiry by encouraging Sara to talk about her experience of being pregnant, about the baby, and what she imagined the baby would be like. The thera- pist asked Sara what she liked about carrying the baby, what she did not like, and what she had hoped to do with the baby.
Sara tearfully described having had mixed feel- ings about her pregnancy. She reported that she and
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Steve started trying to conceive 6 months after getting married and, to her surprise, she got pregnant after 2 months. When she discovered she was pregnant, Sara felt really happy but scared about becoming a parent. She questioned whether she was “ready.” Sara reported that she made a great effort to practice good prenatal care: She ate healthy, pregnancy-safe foods, took prena- tal vitamins, and started prenatal yoga classes. Practic- ing good prenatal care made her feel good, “as if I was already a mom taking care of my baby.”
Sara quickly began to experience terrible fatigue and unrelenting nausea, which lasted for the first 12 weeks of the pregnancy. She described feeling as if she had been “taken over” by the pregnancy. She complained that she loved to cook but did not want to cook, because she felt so sick. Despite the nausea, she ensured that she got the nutrients the baby needed. The fatigue and nau- sea were so debilitating that Sara could no longer meet the physical demands of her job as a nurse. As a result, she was unable to hide her pregnancy from her cowork- ers; she told her supervisor, who was happy to accom- modate Sara by giving her more administrative respon- sibilities in lieu of patient care until she felt better. Sara resented having to give up clinical work with patients, which was the part of her job she enjoyed. She felt self- conscious about her symptoms and very guilty that her coworkers had to absorb her patient load, despite their being very supportive. It bothered her that others ide- alized pregnancy, whereas she found it so unpleasant. At the same time, she felt guilty and selfish that she had complained about the pregnancy: Sara felt that she should have just been grateful she was pregnant.
The therapist empathized with Sara’s discomfort during her first trimester and validated her need to complain:
THERAPIST: The first trimester of pregnancy can be re- ally difficult and disruptive. Give yourself a break! It can be hard to appreciate being pregnant when you are feeling so terrible. It sounds like you did appreci- ate being pregnant—you made a great effort to take care of yourself. You watched your diet carefully and rearranged your work situation.
SARA: I don’t know . . . I guess that’s true.
When the exhaustion and nausea subsided in her sec- ond trimester, Sara began to feel more optimistic and excited about having a child. Seeing sonograms made
the baby seem “more real” and helped Sara feel con- nected to the baby. At Week 16, Sara learned that the baby was a girl. Excited, she immediately began con- sidering names and envisioning what the baby would look like. Sara imagined her as a combination of herself and her husband, with blue eyes and blond, curly hair. She thought the baby would be a kind person, like her husband. She imagined walking the baby to the park in a stroller and playing with her. At Week 20, Sara began to feel the baby move, which she very much enjoyed. When the baby moved, Sara would stop whatever she was doing to watch and feel her abdomen. She de- scribed feeling the movements as “some of the happiest moments in my life.” Neither she nor her husband had thought of a name for the baby, but referred to her as “Sweetie” in utero.
For weeks after the stillbirth, Sara struggled with physical reminders of the baby. After the delivery, she had leaky breasts for a few days and vaginal bleeding for several weeks. She reported that she still looked preg- nant for weeks after delivering the baby, as her uterus slowly returned to its prepregnancy size. At the time of her initial evaluation, Sara reported that she still had to lose 5 pounds to return to her prepregnancy weight. Sara missed being pregnant and described feeling “empty” and “alone” without the baby inside her. She was eager and ready to be a parent, yet she felt fright- ened about conceiving again because she feared losing another baby.
A couple of weeks after the stillbirth, Sara’s doc- tor determined that an undetected bacterial infection caused the stillbirth. The doctor explained that there was nothing Sara or her husband could have done to prevent the loss, and that this kind of loss was very rare. Despite her doctor’s explanation, Sara blamed herself for her baby’s death and feared that her husband blamed her too, although he repeatedly denied this. The thera- pist explored Sara’s guilt further:
THERAPIST: What could you have done to prevent your baby’s death?
SARA: (tearfully) I don’t know. . . . I should have been able to do something.
The therapist offered Sara empathy and support, and related her guilt to depression:
THERAPIST: It would be great if there were something
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you could have done to prevent this tragedy, but there is generally nothing parents can do to prevent a pregnancy loss. It sounds like you did everything you could—you took very good care of yourself. You are struggling with inappropriate and excessive guilt— a symptom of depression. You are blaming yourself for something you didn’t do. Perhaps when you find yourself feeling guilty, you can try to label this as a symptom of depression.
SARA: Yes. I guess I can try.
Talking about the pregnancy, the baby, and the ba- by’s death, and exploring related feelings enabled Sara to develop a more balanced and realistic perception of her relationship with the baby and her role in the baby’s death. She realized that she had not taken her pregnancy for granted. In fact, she had done everything she could to manage a difficult first trimester and take care of her baby. In addition, her experience with the pregnancy and the baby made Sara realize that despite her initial anxiety, she was ready and excited to become a parent. By the end of the first month of treatment, Sara’s mood was somewhat improved and her HDRS score had fallen to 18. She was less self-critical and more hopeful.
An important part of treating grief is facilitating the expression of affect related to the loss of the loved one. The therapist explored Sara’s feelings as she spoke about the baby and her loss, giving Sara time to artic- ulate what she was feeling and to cry. Although IPT therapists generally take an active stance, when facili- tating the expression of painful feelings, it is important to allow for silences. By listening silently, the therapist showed that she could tolerate Sara’s painful feelings, and that catharsis was an important part of mourning her loss. Sara was able to express not only feelings she had been avoiding but also feelings of which she had previously been unaware.
Sara had avoided looking at the pictures and foot- prints of the baby from the hospital, which had been stored in a box under her bed. She and the therapist explored what it would be like for her to look at these items. Sara feared it would be scary, and that she would feel really bad. The therapist gently encouraged Sara to take a risk and look, because it might make her feel better to experience the feelings she had been avoiding: “Your feelings are not going to hurt you. You might ac- tually feel better if you allow yourself to let out some
of the feelings you have been trying to keep inside. I know I am asking you to take a risk, but you might be pleasantly surprised.”
Between sessions, Sara looked at the pictures and the footprints. The therapist asked what it was like for her.
SARA: I cried a lot. She was so cute. It wasn’t as hard as I thought it would be. It felt like a release. I was surprised that I felt a little better afterwards.
THERAPIST: I am so glad you took a risk and looked. It sounds like it made you feel better.
In fact, every few weeks before the end of treatment, Sara looked at the pictures and the footprints. She ex- plained that the pictures were sort of comforting, be- cause they made her feel a connection to her baby.
In addition to encouraging catharsis, the therapist encouraged Sara to work on her interpersonal interac- tions, to reconnect with the people in her life, and to consider opportunities to form new relationships and start new activities to compensate for the loss. The ther- apist explained that when depressed, people tend to iso- late themselves and stop engaging in previously pleasur- able activities, both of which can perpetuate depression. Sara reported not wanting to talk to people, because she feared that she would have to talk about the loss, or that things people said would make her feel worse. In fact, as Sara and the therapist discussed, she could guide the conversation in a way that made her feel comfortable. They explored and role-played options for maintaining control of such conversations. Furthermore, Sara could tell people what would be helpful to her. The therapist explained:
“People with depression often have difficulty assert- ing their needs. If you communicate your needs to others—like your husband, friends, coworkers, and your family—you might improve those relationships and your mood. The people in your life may not know what you need. If you tell them, you might not only get support from them, but you might enjoy their company again and feel better.”
Using communication analysis, the therapist asked Sara to recount arguments and unpleasant interactions with others: what she was feeling during the interac- tion, what she said or did, and what the other person said or did. They explored what Sara wished other
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people would say or do, what options she had for asking them to do these things, and they role-played Sara ask- ing for what she wanted. Sara reported that she hated running into people who knew she had been pregnant but did not know about the stillbirth. In fact, she avoid- ed going places, because she feared having to answer questions about the stillbirth. Sara and the therapist explored these interactions and how Sara could handle them more effectively:
THERAPIST: What kinds of things have people asked, or what are you afraid they will ask?
SARA: People have asked, “How’s your baby?” or “Weren’t you pregnant?”
THERAPIST: How does that make you feel? SARA: Awful! THERAPIST: How do you handle it? SARA: I don’t know. . . . Sometimes I say, “It didn’t
work out” or “My baby died.” THERAPIST: That sounds good. How does it feel for
you to say that? SARA: It feels OK, but then they want to know what
happened and say stupid things like “At least you know you can get pregnant” or “You can have an- other one.”
THERAPIST: What would you like them to say or do? SARA: I would like them to just say, “I’m sorry,” and not
ask any questions. I don’t want to talk about what happened.
THERAPIST: How could you convey that? SARA: I guess I could say, “I’m sorry, but I’d rather not
talk about it.” THERAPIST: How does that sound? How did it feel to
say that? SARA: It felt OK. Don’t you think that is rude to say
that? THERAPIST: No. You said it politely, and it’s appropri-
ate for you to assert your needs. It is an uncomfort- able situation for both you and the person who asked the question. If you are polite and direct with people, they are likely to understand. But why not try it and see?
Sara reported that she had avoided returning calls from old friends. She explained that she felt uncomfort- able seeing her friends who had babies, because it would
remind her of the baby she had lost. Sara also did not want to have to talk about the loss. She did not want to tell them how she felt, because she feared hurting their feelings. Sara and the therapist role-played Sara telling her friends about her discomfort and explaining that she did not want to offend them. Role play helped Sara feel prepared and less anxious about going to work, walking around her neighborhood, and talking to old friends. As a result, she gradually starting going out more and began returning phone calls. She returned to the yoga studio, where she had taken prenatal yoga, and started taking regular yoga classes, which helped her mood and provided an opportunity to be among other people. By midtreatment, Sara’s HDRS had fallen to 13, consistent with mild depression.
Since the stillbirth, Sara had been bickering with her husband Steve “over stupid things” and felt “distant from him.” The therapist asked her to describe a recent incident. Sara said that Steve came home from work and told her that his friend’s wife had just had a baby. She felt it was insensitive for him to tell her about other people’s positive pregnancy experiences. It bothered her that Steve did not seem as uncomfortable as she was with this information, and that he no longer seemed as upset as she about the loss. The interaction made her feel “alone.” She had responded to him by saying, “That’s nice,” then leaving the room and ruminating for the rest of the evening about his insensitivity.
Sara reported that they often had similar interac- tions. The therapist once again related Sara’s difficulty expressing her anger toward her husband to depression, and noted that keeping her feelings inside might actu- ally be making Sara feel worse. They explored inter- personal options for handling this situation in a way that might make Sara feel better. The therapist helped Sara to explore what her husband’s intentions might have been in the situation she described. She wondered whether he was trying to make her feel better, because his friend’s wife had experienced several miscarriages. They role-played Sara telling her husband how she felt. Subsequently, when Sara was able to express her feel- ings to him, she learned that Steve was, in fact, tell- ing her these stories to give her hope. Furthermore, her husband revealed that he was still upset about the loss of their baby but did not want to upset her by sharing his feelings. Sara was relieved that she and Steve were “on the same page,” and felt good that she was able to feel close to him again. They subsequently were able to share more of their mixed feelings about the pregnancy experience.
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Termination Phase (Sessions 10–12)
During the final sessions, the therapist and Sara re- viewed the progress she had made. She reported that her mood was much improved. Her HDRS was now a 5, consistent with euthymia and remission. Sara’s affect was brighter, and she was less preoccupied with the loss of her baby: “I still get upset when I think about my baby, but I don’t get as upset. It doesn’t ruin my en- tire day. I am actually able to enjoy things again.” Fur- thermore, Sara no longer blamed herself for her baby’s death. She felt good about her ability to communicate her feelings more effectively with her husband, friends, and others, and to enjoy socializing and other activities again.
The therapist congratulated Sara on her hard work and achievements, and told her how happy she was that Sara felt so much better. They discussed the po- tential for relapse and how Sara could maintain her progress. Given Sara’s history of depression, the thera- pist explained that Sara was, unfortunately, vulnerable to future episodes; however, Sara could anticipate that she would be vulnerable in the setting of stressful life events—role disputes, role transitions, deaths—and use the coping skills she had learned during their work to- gether. Sara anticipated trying to conceive again and, she hoped, getting pregnant again—both role transi- tions. The therapist explored with Sara ways that she could take care of herself during this potentially stress- ful time. They discussed Sara’s reaching out to others for support, communicating with her husband about how she was feeling, and forgiving herself if she found herself having a hard time.
In the final session, Sara told the therapist that she had reread her diary entries from the days before begin- ning treatment and could not believe how far she had come, that her pregnancy loss had forced her to seek treatment for depression that she now realized had been a lifelong problem; in retrospect, she had suffered nu- merous episodes of mild to moderate depression. Sara admitted that she initially had felt very resistant to the medical model. Defining depression as a medical illness ultimately relieved Sara of her shame and guilt about her difficulty in functioning. Furthermore, being able to see depression as a set of discrete symptoms made it seem more manageable. Sara reported that she was getting along better with her mother; now that she understood depression, she felt more sympathy for her mother’s struggle with depression. She was grateful for the opportunity to learn coping skills that she felt con-
fident about maintaining. In addition, Sara said that she would not hesitate to seek treatment in the future should she find herself becoming depressed again.
The therapist’s frequent encouragement, the time limit, and the brief duration of IPT helped keep Sara motivated. Sara said that she appreciated the opportu- nity to talk about her feelings about her pregnancy, her baby, and her baby’s death, and that she felt the thera- pist understood and supported her. She recognized that her feelings, while powerful, made sense in context and had subsided with discussion. Sara confessed that she appreciated the therapist “pushing” her to reconnect with others. She had not thought she could handle so- cializing with others, but was pleasantly surprised.
Although each patient is unique, Sara’s therapy re- sembled other IPT treatments for major depression and is a good example of working with the problem area of grief. The exploration and normalization of affect, communication analysis, exploration of options, use of role play, encouragement to take social risks, and other techniques employed in Sara’s treatment are character- istic of working with interpersonal difficulties related to any of the four IPT problem areas.
COMMON PROBLEMS THAT ARISE DURING TREATMENT
The problems that typically arise during IPT treatment for major depression are (1) those inherent to working with depressed patients and (2) those related to the ther- apeutic frame. Although these problems are not unique to IPT, how the therapist views and treats these issues distinguishes IPT from other psychotherapies. In keep- ing with important IPT themes, the therapist attributes problems to depression, and to the patient’s difficulties handling interpersonal interactions and communicat- ing effectively outside of the treatment. The therapist continues to maintain an optimistic, supportive, and nonjudgmental stance and avoids transference interpre- tations.
For example, patients with major depression super- imposed on dysthymic disorder (“double depression”) and their therapists are often discouraged by the chro- nicity of their depression. In these cases, the therapist should remain hopeful and optimistic. Some depressed patients feel that their depression is incurable, despite reassurances from the therapist. In these cases, the IPT therapist employs the medical model, labeling the hopelessness as a depressive symptom, and emphasizes
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that patients need not believe the hopelessness, since depression is treatable. Depressed patients often view seeking treatment as a personal failure. The IPT thera- pist frames seeking treatment as the appropriate and smart way to treat a medical illness, and a positive step toward gaining mastery over their problems (Weissman et al., 2018).
The most serious problem to arise in any treatment for depression is suicidality. As in any treatment, the therapist determines whether hospitalization is nec- essary, based on the seriousness of the intent and the availability of the patient’s social supports. The thera- pist is as available as possible to the patient and sched- ules extra sessions as needed. The therapist assesses the circumstances in which the suicidal ideation developed, what the patient hoped to accomplish by ending her life, and reviews how the patient imagines others would react to her suicide. The therapist helps the patient ex- plore alternative ways of expressing what she intended to communicate by committing suicide. The therapist provides psychoeducation about suicide, explaining that it is the most deadly symptom of depression, and that therapist and patient have to work together to keep the patient alive long enough to get through successful treatment—at which point the patient will again want to live. Augmenting the therapy with medication treat- ment should be considered for severely suicidal patients. The therapist remains optimistic that the patient’s de- pression will improve, and that she will no longer feel that life is not worth living (Weissman et al., 2018).
Problems may arise in the relationship with the therapist. For example, a patient who has poor social supports may come to view the therapeutic relationship as a substitute for relationships outside of the therapy. Because IPT focuses on relationships outside of the treatment, the therapist gently refocuses the patient to outside relationships. Whereas the therapist notes that the patient’s ability to connect within the treatment re- lationship reflects her ability to form intimate relation- ships, he/she clarifies that they are not friends or family and emphasizes the importance of the patient’s life out- side of the treatment. The therapist helps the patient ex- plore options for connecting with others in ways similar to the way she connected with the therapist (Weissman et al., 2018).
Arriving late and missing sessions are also considered to be symptomatic of depression. The therapist calls attention to and empathizes with the fact that the pa- tient has missed or is late to a session, and notes that difficulty getting to sessions may reflect functioning
that is characteristic of depression. It is likely that the patient is late to appointments outside of the therapy. The therapist can remind the patient of the time limit of IPT to motivate her to come to sessions. In the event that the patient misses or comes late to sessions because she is uncomfortable with the material being discussed in session, or because she has some other negative feel- ing about the treatment or the therapist, the therapist empathizes with the patient’s feelings and helps her to explore ways to express these feelings directly.
When a patient is silent to the extent of refrain- ing from sharing thoughts and feelings, or when she changes or avoids subjects, or has problems with self- disclosure, the therapist notes this behavior and ex- plores the patient’s feelings related to the behavior. These behaviors are particularly problematic in a time- limited, focused treatment such as IPT, because they make it difficult to work on the chosen problem area. The patient may feel uncomfortable and ashamed to share her thoughts and feelings with the therapist. The therapist assures the patient that there is little that can surprise him/her, and that the patient does not have to talk about everything.
PREDICTORS OF RESPONSE
Although there is strong evidence that IPT is an ef- ficacious treatment for major depression and other disorders, there are fewer data on factors that predict response to IPT. Comparative treatment studies involv- ing IPT suggest some clinical predictors of response. In the multisite NIMH Treatment of Depression Collab- orative Research Program (TDCRP; Elkin et al., 1989), 250 outpatients with major depression were randomly assigned to 16 weeks of imipramine (IMI), IPT, CBT, or placebo. The TDCRP dataset has been examined for predictors of response by several researchers. Sotsky and colleagues (1991) found that TDCRP subjects with low baseline social dysfunction responded well to IPT, whereas those with interpersonal deficits responded less well. These findings support the idea that IPT works least well for patients with few or no social contacts, who report no recent life events, and whose treatment therefore focuses by default on the IPT problem area of interpersonal deficits. High initial symptom sever- ity and impaired functioning predicted superior re- sponse to IPT and to IMI compared to CBT (Sotsky et al., 1991; Weissman et al., 2018). In another analysis, TDCRP subjects with symptoms of atypical depres-
Interpersonal Psychotherapy for Depression 335
sion, such as mood reactivity and reversed neuroveg- etative symptoms, responded better to IPT and CBT than to IMI or to placebo (Stewart, Garfinkel, Nunes, Donovan, & Klein, 1998).
Barber and Muenz (1996) found that among patients who completed treatment in the TDCRP study, IPT had greater efficacy than CBT for patients with obses- sive–compulsive personality disorder, whereas CBT was better for patients with avoidant personality disorder, as measured by the HDRS. However, another study ex- amining the relationship between personality traits and outcome in the same dataset found no significant dif- ferences among personality traits (Blatt, Quinlan, Pil- konis, & Shea, 1995; Weissman et al., 2018).
In another study, Thase and colleagues (1997) found that among 91 patients with depression, patients who had abnormal electroencephalographic (EEG) sleep profiles had significantly poorer response to IPT than did patients with normal profiles. In this study, un- like the Sotsky and colleagues (1991) report, symptom severity did not significantly predict response to IPT (Weissman et al., 2018). Additional potential predictors of response appear in an earlier section in this chapter describing Sara.
CONCLUSION
IPT is a time-limited, diagnosis-targeted, manualized treatment with demonstrated efficacy for patients with major depression and other mood disorders. It has been adapted for the treatment of anxiety disorders, eating disorders, and, most recently, personality disorders. Al- though there is substantial evidence of IPT’s efficacy for the treatment major depression and other mood and psychiatric disorders, further evidence of predictors of response to IPT is warranted. This chapter has focused on the original IPT protocol: IPT as an individual treatment for major depression.
IPT employs the medical model and focuses on current or recent life events, interpersonal difficulties, and symptoms. IPT emphasizes the interrelationship between mood and life events: Negative or stressful life events affect mood and, conversely, mood symp- toms affect how people manage negative or stressful life events. Treatment with IPT focuses on one of four interpersonal problem areas—grief, role disputes, role transitions, and interpersonal deficits. The therapist helps patients recover from depression by helping them to resolve the chosen interpersonal problem area, which
relieves depressive symptoms. The IPT therapist takes an active, optimistic, and supportive stance.
The case of Sara demonstrates the techniques used and the process of treatment with IPT. IPT, an eclectic treatment with proven efficacy, uses techniques em- ployed by other psychotherapies. The combination of IPT’s main principles, techniques, strategies, and thera- pist and patient characteristics distinguishes it from other antidepressant treatments.
For further information about IPT and its adapta- tions, readers may consult The Guide to Interpersonal Psychotherapy by Weissman and colleagues (2018) and the Casebook of Interpersonal Psychotherapy (Markowitz & Weissman, 2012a).
NOTE
1. For stylistic simplicity, patients are referred to in the femi- nine. Indeed, most depressed patients are women.
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The behavioral activation (BA) approach to treating depression has received very strong empirical support in recent decades, with results as good or better than cognitive therapy and antidepressant medications, even for the most severe cases of depression. Seemingly counterintuitive at first blush, this treatment does not focus on the notion of “just do it” but takes a comprehensive look at contin- gent relationships in the patient’s life across the full range of behavior, cognition, and affect that may be maintaining the depression. As such, this idiographic approach does not prescribe a set number of sessions to accomplish certain goals but is very adaptable to the individual with depression. In the detailed and very human description of the treatment of “Mark,” readers will also note a very up- to-date focus on the role of rumination in depression (or worry in anxiety) as a fundamentally avoid- ant technique. The illustration of creative therapeutic strategies for activating patients, and the very adaptable and flexible nature of BA, will be of interest to all therapists treating depression, since it may be one of the easiest to learn and most disseminable of evidence-based psychological treatments for depression. —D. H. B.
behavioral activation (BA) is a structured, brief psy- chosocial approach that aims to alleviate depression
and prevent future relapse by focusing directly on be- havior change. BA is based on the premise that prob- lems in vulnerable individuals’ lives, and their behav- ioral responses to such problems, reduce their ability to experience positive reward from their environment. The treatment aims to increase activation systemati- cally in ways that help clients to experience greater con- tact with sources of reward in their lives and to solve life problems. The treatment procedures focus directly on activation, and on processes that inhibit activation, such as escape and avoidance behaviors and ruminative thinking, to increase experiences that are pleasurable or productive and improve life context. We believe that BA is an important treatment for depression for two
main reasons. First, its efficacy is supported by a robust evidence base; second, it is based on simple and easily grasped underlying principles and utilizes a small set of straightforward procedures.
BEHAVIORAL MODELS OF DEPRESSION
Basic Concepts
The central premise in virtually all behavioral models is the assumption that depression is associated with par- ticular behavior–environment relationships that evolve over time in a person’s life. “Behavior” is a very broad construct in these models and includes everything from taking a walk to grieving over the loss of a loved one. Behaviors can be fairly circumscribed (e.g., lying on
C H A P T E R 9
behavioral Activation for Depression
Sona Dimidjian Christopher R. Martell Ruth Herman‑Dunn Samuel Hubley
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the couch watching television after dinner) or they can be part of a more general repertoire (e.g., avoidance of asserting one’s own needs and desires in interpersonal conflict).
“Environment” is also a broad construct that can best be thought of as the settings in which behaviors currently occur, as well as those in which behaviors have evolved over time. The temporal nature of envi- ronments is crucial for understanding behavioral ap- proaches to depression. Often, behavior that appears to serve no function in a person’s current environment has served a very important function in the past. Thus, when practitioners wonder why a depressed person is engaging in a particular set of behaviors, such as re- maining in an unsatisfying job, it is often necessary to consider how particular repertoires have evolved over time (e.g., avoiding potential losses).
Finally, all behavioral models of depression empha- size the importance of contingent relationships between behaviors and the environments in which they occur. Contingent relationships are “if–then” relationships be- tween human activities and their (often interpersonal) environmental consequences. For example, practitio- ners working within a behavioral framework are proba- bly less interested in the fact that a depressed client stays in bed each morning worrying, for example, about the future of a troubled marriage, than they are about the consequences of this behavior. What happens as a re- sult? Does the client become more or less depressed? By staying in bed, does the client avoid something aversive, such as confronting a spouse about an issue in the rela- tionship, or going to work and facing a pile of uncom- pleted tasks? Understanding contingent relationships is a central feature of behavioral models of depression and a requisite skill of BA therapists.
Behavioral Roots of BA
These general behavioral concepts were developed and refined into specific conceptual frameworks and treat- ments for depression by Ferster (1973, 1981) and Le- winsohn and colleagues (Lewinsohn, 1974; Lewinsohn, Antonuccio, Steinmetz-Breckenridge, & Teri, 1984; Lewinsohn, Biglan, & Zeiss, 1976). Ferster’s primary assumption was that depression is the result of a learn- ing history in which the actions of the individual do not result in positive reward from the environment, or in which the actions are reinforced because they allow the individual to escape from an aversive condition. Over time, behavior that would typically produce positive
consequences ceases to do so. For example, for a vari- ety of different reasons, a person’s efforts to form close relationships with others might gradually fade away be- cause they are not followed by positive reinforcement (e.g., reciprocal efforts from others).
Ferster (1973, 1981) reasoned that this decrease in response-contingent positive reinforcement produces two additional consequences that facilitate depression. First, when people’s efforts do not result in reward, they often become more focused on responding to their own internal state than to potential sources of positive re- inforcement in the external environment. This is the classic “turning inward” that is often seen in depres- sion, and this makes sense from a behavioral perspec- tive; when individuals learn that their own behavior is an unreliable predictor of positive consequences in their environment, they naturally spend less time attending to contingencies in that environment.
The second consequence of decreased rates of positive reinforcement that Ferster (1973, 1981) observed was a narrowing of individuals’ repertoires of adaptive be- haviors. This makes logical sense as well, because fewer and fewer behaviors are being maintained by positive reinforcement. Individuals may adopt extremely passive repertoires (e.g., “doing nothing”) because their active attempts to become engaged in life are not rewarded.
Finally, Ferster (1973, 1981) observed that increases in aversive consequences following behavior typically lead depressed individuals to become preoccupied with escape and avoidance. In effect, more energy is expend- ed attempting to avoid or escape from anticipated aver- sive consequences than attempting to contact potential positive reinforcers in the environment.
Lewinsohn’s (1974) early behavioral model of depres- sion was very compatible with many of the ideas pro- posed by Ferster’s (1973) behavioral analysis of depres- sion. Lewinsohn and colleagues similarly emphasized the importance of response-contingent reinforcement and conceptualized that its rate was influenced by three factors: the number of potentially reinforcing events for an individual; the availability of reinforcement in the environment; and the instrumental behavior of the individual required to elicit the reinforcement. Lewinsohn also identified social avoidance as a core part of his model. Importantly, Lewinsohn, Sullivan, and Grosscup (1980) developed the first stand-alone behaviorally oriented treatment for depression. Later, Lewinsohn, Hoberman, Teri, and Hautzinger (1985) proposed an integrated model that was intended to ex- plain the interactive and complex nature of depression,
Behavioral Activation for Depression 341
including dispositional factors such as cognition, with environmental factors. This model did not overempha- size or give precedence to either cognitive factors or en- vironmental factors in the etiology and maintenance of depression; rather it attempted to account for the com- plexity of depression. Research initiated in Lewinsohn’s laboratory has continued through the work of former students and colleagues across diverse settings and populations (Dimidjian, Barrera, Martell, Muñoz, & Lewinsohn, 2011).
Beck, Rush, Shaw, and Emery (1979) also pioneered early work on BA. They incorporated BA strategies as a core component of cognitive therapy (CT) for depres- sion. In so doing, Beck and colleagues formalized and widely disseminated some of the principal BA strate- gies, while emphasizing the importance of cognition in etiology and treatment of depression.
Contemporary BA
The work of Ferster, Lewinsohn, and Beck strongly in- fluenced the development of contemporary BA in im- portant ways. They were a direct influence on Jacobson and colleagues’ initial research and clinical development of BA (Jacobson, Martell, & Dimidjian, 2001; Mar- tell, Addis, & Jacobson, 2001; Martell, Dimidjian, & Herman-Dunn, 2010). Their work similarly informed the context of other investigators, such as the team of Lejuez, Hopko, LePage, Hopko, and McNeil (2001; Lejuez, Hopko, Acierno, Daughters, & Pagoto, 2011), who articulated a BA approach that is convergent in both theory and clinical emphasis on targeting behav- ior change. This approach, BA treatment for depression, has been supported in multiple studies by their group (e.g., Hopko, Lejuez, LePage, Hopko, & McNeil, 2003).
With respect to a conceptual model of depression, the current conceptualization draws heavily on the work of Ferster (1973, 1981) and Lewinsohn (1974) in emphasizing the central importance of context and activity in understanding depression. While acknowl- edging that genetic, biological, and other distal factors may be causally related to depression, the current be- havioral conceptualization focuses on the aspects of a person’s life context that may have triggered depression, and particular ways of responding to this context that may be maintaining depression. Specifically, the model assumes that one reason people get depressed is because changes in the context of their lives provide low lev- els of positive reinforcement and high levels of aversive control. Lives that are “less rewarding” can lead to feel-
ings of sadness and depressed mood. And when people get depressed, they often pull away from the world in important ways, and the basic routines of their lives are disrupted. Both of these processes can increase de- pressed mood and make it difficult to solve problems effectively in one’s life. In fact, these processes are con- ceptualized as “secondary problem behaviors,” because they frequently prevent people from (1) connecting with aspects of their lives that may provide some im- provement in mood and (2) solving problems that may help to decrease stress and improve life context.
The BA approach to therapy addresses both of the factors that may be contributing to depression: those aspects of one’s life that need to be changed to reduce depression and the ways withdrawal from the world may be maintaining or increasing depression. BA ac- complishes these aims through guided activation, which is the use of a series of behavior change strategies that the therapist and client develop together on the basis of a careful examination of what activities will be reinforc- ing for a given client and help to disrupt the relation- ships that are maintaining the depression. The point of BA is not to engage in increased activation at random or activities that are “generally” thought to be pleasing or to improve mood (e.g., taking a walk); in contrast, activation strategies are highly individualized and “cus- tom tailored.” The role of the BA therapist is to act as a “coach,” while the client implements the activation strategies, providing expert help in setting achievable goals, breaking difficult tasks down into manageable units, troubleshooting problems that arise, and main- taining motivation during the process of change.
EMPIRICAL CONTEXT
The first study to revitalize interest in a purely behav- ioral approach to treating depression was conducted by Jacobson and colleagues (1996), who proposed a simple but provocative question: Could the behavioral component of CT account for the efficacy that CT has demonstrated in previous clinical trials? Adults with major depression were randomly assigned to one of three treatment conditions, including BA only, BA plus interventions designed to modify automatic thoughts, and the full CT package. Results suggested that BA was comparable to the full CT package in both acute effica- cy (Jacobson et al., 1996) and prevention of relapse over a 2-year follow-up period (Gortner, Gollan, Dobson, & Jacobson, 1998).
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On the basis of these findings, BA was developed into a more fully articulated behavioral intervention that included the behavioral aspects of CT and in- corporated the early behavioral work of Ferster (1973, 1981) and Lewinsohn (1974), as described earlier. This expanded BA model has been articulated in published reports (Jacobson et al., 2001; Martell et al., 2001, 2010) and in a patient-oriented self-help manual (Addis & Martell, 2004). BA was further tested in a random- ized, placebo-controlled clinical trial (N = 241) that compared its acute and long-term efficacy to both CT and antidepressant medication (ADM). Among more severely depressed patients, the performance of BA was comparable to the current standard of care, ADM, and demonstrated better retention; and both BA and ADM were superior to CT (Dimidjian et al., 2006). Moreover, follow-up results indicate that BA appears to have promising enduring effects (Dobson et al., 2008). Finally, BA may demonstrate an important cost-effec- tiveness advantage compared to continuing patients on medication.
These results were consistent with a range of other studies suggesting that activation interventions are par- ticularly important components of cognitive-behavioral treatments. In a classic study, Zeiss, Lewinsohn, and Muñoz (1979) reported comparable outcomes for de- pressed patients who received treatment focused on interpersonal skills, pleasant activities, or cognitive change. In addition, in a study with depressed older adults, Scogin, Jamison, and Gochneaur (1989) found no differences in outcome between a cognitive biblio- therapy treatment and a behavioral bibliotherapy treat- ment among mildly and moderately depressed older adults. The importance of behavioral strategies has also been reported in other studies across multiple di- agnostic categories (e.g., Borkovec, Newman, Pincus, & Lytle, 2002; Foa, Rothbaum, & Furr, 2003; Gloag- uen, Cottraux, Cucherat, & Blackburn, 1998). Other process-oriented research has similarly emphasized the importance of BA components of CT (Bennett-Levy et al., 2004) and has suggested the possibility of negative outcomes when therapists work on changing clients’ thoughts about interpersonal relationships as opposed to changing actual interpersonal relationships (Hayes, Castonguay, & Goldfried, 1996).
In addition, Ferster’s early focus on avoidance has also been underscored by contemporary behavior thera- pists. Specifically, Linehan (1993) incorporated the use of “opposite action” for sadness as a means to target
depression in dialectical behavior therapy. Hayes and colleagues (1996) emphasized the role of experiential avoidance in the development of a wide range of psy- chopathologies and in the conceptualization of accep- tance and commitment therapy (ACT; Hayes, Strosahl, & Wilson, 1999). A study on an early precursor to ACT found significant treatment benefits for depressed cli- ents in comparison to standard CT (Zettle & Rains, 1989).
Some studies also suggest that patient activation is an important element of the change process. In a sub- stance use treatment study in which one condition was augmented with BA interventions, pre- to posttreat- ment increases in environmental reward were associat- ed with reductions in depressive and anxiety symptoms for such patients, but not for those receiving substance use treatment only (Daughters et al., 2008). In a study of cognitive-behavioral therapy (CBT) for depression, increases from baseline in activation predicted post- treatment depression improvement (Christopher, Jacob, Neuhaus, Neary, & Fiola, 2009). Hoyer, Hoefler, and Wuellhorst (2020) also found that increases in behav- ioral activity and reduced depressed mood predict each other across time in a preliminary study. Maitland, Neilson, Muñoz, Ybanez, Murray (2019) found sup- port for the behavioral model of depression, specifi- cally, that an enriched environment (i.e., contact with environmental rewards) was correlated with improve- ments in depression, and Santos and colleagues (2019) showed that increased activation was associated with improved depression scores in a residential treatment setting. In Japan, Yamamoto, Hikida, Shudo, and Sakai (2019) conducted a mediation analysis and con- cluded that there was a direct relationship between ac- tivation and avoidance on depression and that positive reinforcement partially mediated the influence of the two on depression.
Continued enthusiasm for BA is also fueled by the broad dissemination potential of a straightforward, par- simonious intervention such as BA. The application of BA in novel settings and with diverse populations is a focus of much recent research (see below for detailed discussion of settings and client variables). Teletherapy and videoconferencing technology have been shown to be effective for adolescent and late-life depression (Laz- zari, Egan, & Rees, 2011; Quijano et al., 2007), as well as computerized adaptations of BA delivered via the Internet (Acierno et al., 2012; Spates, Kalata, Ozeki, Stanton, & Peters, 2012; Spek et al., 2007, 2008; Van
Behavioral Activation for Depression 343
Voorhees et al., 2009; Warmerdam, Van Straten, Twisk, Riper, & Cuijpers, 2008). This became particularly important as therapists were thrust into the world of online treatment during periods of isolation during the COVID-19 pandemic. Finally, novel training methods are also being enhanced with technology, including digital BA training (Hubley, Woodcock, Dimeff, & Dimidjian, 2015).
In summary, research on BA provides a strong foun- dation for clinical application with depressed patients and for extension to other populations (Dimidjian et al., 2011). These conclusions are consistent with other meta-analyses that incorporate clinical trial data from multiple studies (Cuijpers, van Straten, & Warmerdam, 2007; Ekers, Richards, & Gilbody, 2008; Mazzuc- chelli, Kane, & Rees, 2009), including a recent meta- analysis of 88 studies, which concluded that BA out- performed inactive control conditions in improvement in depression, anxiety, and activation, although there was not a significant difference between BA and other active control conditions (Stein, Carl, Cuijpers, Karyo- taki, & Smits, 2020). BA also has been represented in influential treatment guidelines (e.g., National Institute for Health and Care Excellence, 2009).
ASSESSING DIAGNOSTIC, CLINICAL, AND FUNCTIONAL DOMAINS
The application of BA is based on a comprehensive di- agnostic, clinical, and functional assessment. Some of these assessment activities are completed as a precur- sor to the initiation of therapy, and others are ongoing throughout the course of therapy.
In our treatment outcome research, we have used a number of structured diagnostic interview instruments to assess Diagnostic and Statistical Manual of Mental Disorders (DSM) diagnoses, including the Structured Clinical Interview for DSM-IV Axis I Disorders (SCID- I; First, Spitzer, Gibbon, & Williams, 1997; First, Wil- liams, Karg, & Spitzer, 2016; Tolin et al., 2018), and the Structured Clinical Interview for DSM-IV Axis II Personality Disorders (SCID-II; First, Spitzer, Gib- bons, Williams, & Benjamin, 1996). In addition, we have used measures of depressive severity, including the clinician-administered Hamilton Depression Rating Scale (HDRS; Hamilton, 1960), the client self-reported Beck Depression Inventory–II (BDI-II; Beck, Steer, & Brown, 1996), and the nine-item Patient Health Ques-
tionnaire Depression Scale (PHQ-9; Kroenke, Spitzer, & Williams, 2001).
In routine clinical practice, we recommend conduct- ing a baseline diagnostic interview and ongoing use of a measure to assess depressive severity. Typically, the most easily administered measure is a self-report mea- sure (e.g., Patient Health Questionnaire–9 [PHQ-9]; Kroenke, Spitzer, & Williams, 2001). Also, a number of self-report instruments may serve as useful assessment measures of patient activity level and of the reward available in a client’s environment. The Behavioral Ac- tivation for Depression Scale (BADS; Kanter, Mulick, Busch, Berlin, & Martell, 2007; Kanter, Rusch, Busch, & Sedivy, 2009), a 29-item measure of client activa- tion, has been used in several studies (e.g., Weinstock, Munroe, & Miller, 2011) to measure changes in levels of activation and avoidance over the course of BA. The BADS has been validated in European Spanish (Bar- raca, Pérez-Álvarez, & Lozano Bleda, 2011), Persian (Mohammadi & Amiri, 2010), and Dutch (Raes, Hoes, Van Gucht, & Kanter, 2010).
In addition, self-report questionnaires have been de- veloped to measure the construct of response-contingent positive reinforcement, including the Environmental Reward Observation Scale (EROS; Armento & Hopko, 2007; Valderrama-Diaz, Bianchi-Salguero, & Villalba- Garzon, 2016) and the Reward Probability Index (RPI; Carvalho et al., 2011; Wagener & Blairy, 2015). Both of these measures are brief, and studies indicate promising psychometric properties. Clinicians who want a nomo- thetic measure of pleasurable activities to augment the idiographic behavioral assessment (described in more detail below) can use the Pleasant Events Schedule ( Lewinsohn & Graf, 1973). These measures may prove to be useful clinical tools that can be administered pe- riodically throughout the course of treatment to assess change in activity and reward. For a full discussion of measures available and issues related to measuring the BA model, see Manos, Kanter, and Busch (2010).
Because functional capacity is such a key component of BA treatment, it is important to gather detailed in- formation about the impact of the client’s depression on functional status across multiple life domains, includ- ing work, family, social activity, and so forth. These domains can be assessed using clinical interview or standard assessment instruments (e.g., the Social Ad- justment Scale [Weissman & Bothwell, 1976] and the Medical Outcomes Study 36-Item Short Form Health Survey [Ware & Sherbourne, 1992]).
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COURSE OF TREATMENT
BA is a theory-driven as opposed to a protocol-driven treatment and, as such, is highly idiographic in its appli- cation. Treatment does not follow a required session-by- session format; however, it does follow a general course over time. This general course comprises the following activities, which are described in greater detail below:
• Orienting to treatment • Developing treatment goals • Individualizing activation and engagement targets • Repeatedly applying and troubleshooting activa-
tion and engagement strategies • Reviewing and consolidating treatment gains
Orienting to Treatment
BA begins with orienting the client to the treatment, a process that is typically the focus of the first two ses- sions. The primary tasks to accomplish during this initial phase of treatment include discussing the BA model of depression and primary treatment strategies, and providing information about the structure of treat- ment, and the roles and responsibilities of the client and therapist.
The presentation of the treatment model includes describing the behavioral approach to depression and the process of change during treatment, discussing the specific ways the model fits with the client’s experienc- es, and encouraging and responding to questions and concerns about the model. The model is presented both verbally during the first session and in a brief, written description that is given to the client at the end of the first session. In addition, many clients find the illustra- tion provided in Figure 9.1 to be a helpful adjunct when orienting to the model. A detailed transcript illustrating the presentation of the treatment rationale is included in the case study below, and the key points to address are summarized in Table 9.1.
During the second session, therapist and client again discuss the treatment model and the client’s reactions, including questions that may have arisen following the first session. It is essential that the therapist obtain “buy in” from the client with the basic elements of the treat- ment model. Therapy works best if the client accepts and buys into the rationale for treatment and the case conceptualization (Addis & Carpenter, 2000) and cli- ent’s positive expectations for treatment predict success- ful outcomes (Constantino, Vîslă, Coyne, & Boswell, 2018). The therapist is advised to guard against mov- ing too quickly if the client does not express agreement
FIGURE 9.1. The behavioral activation treatment model.
What is the context? How do you feel? What do you do (or not do)?
Have any problems started, continued, or worsened?
Behavioral Activation for Depression 345
with the key tenets of the model. Thus, during the ini- tial sessions, it is essential that the therapist encourage the client to ask questions and elicit the client’s poten- tial doubts and concerns.
For instance, some clients may find it difficult to ac- cept the idea that changing behavior directly is an ef- fective way to work with depression. Often, clients are strongly committed to a biological explanation for their depression. It is not advisable for therapists to debate this position; instead, therapists can explain that there are many sources of vulnerability to depression, and that one of the effective ways to change depression is by changing what one does. At times, clients also may think that the emphasis on behavioral change means that all they need to do is exercise more, go to a few more movies, or take a few more walks, and their de- pression will remit. If clients understand BA in this way, then it is not surprising when they feel that the treatment invalidates their degree of distress and the difficulty they face in overcoming depression. We often find it helpful to talk to clients about two points. First, behavior can have a powerful effect on our moods, and people are often unaware of this link, particularly when they are depressed. For example, subtly shifting the way someone approaches interactions with family members may not rid that person of depression, but it can reduce the severity of depressed mood, thereby setting the stage for other changes that collectively help to reverse the depression. The second point is that behavior change is not easy; if it were, we would all behave exactly as we think we should all the time (and we know this is not the case!). Changing behavior requires knowing what to change, and this can take some serious and sustained “detective work” in therapy. The therapist can again emphasize his/her role as a coach in helping the client to figure out what to change and how to do it.
In addition to presenting and discussing the treat- ment model, it is also important to discuss thoroughly the structure of treatment and the roles of therapist and client. It is necessary to emphasize three key elements: between-session practice, collaboration, and the struc- ture of sessions.
1. It is important early in treatment to highlight the active nature of BA and establish the importance of between-session practice. The therapist sets the tone of therapy and expectations by highlighting that BA is a very action-oriented and problem-focused treatment in which the majority of the “work” of therapy goes on between sessions, as the client implements plans that
TABLE 9.1. 10 Key Points to Address When Presenting the Treatment Model
1. Behavioral activation is based on the idea that the events in your life and how you respond to such events influence how you feel.
2. BA assumes that one reason people get depressed is that their lives are providing too few rewards and too many problems. Sometimes it is possible to identify easily stressors or problems; other times there are no clearly identifiable stressors but there is still not adequate reward from the environment.
3. When one’s life context is difficult, it is common to experience feeling sad, down, discouraged, anxious, fatigued, drained, and so forth.
4. When feeling these ways, it is also common to do (or not do) particular actions. People often pull away from the world around them and find that basic routines in their lives become disrupted.
5. Pulling away from the world when feeling down is natural and understandable. The problem is that it also can initiate downward spirals with how you feel (e.g., the less you do, the worse you feel, and the worse you feel, the less you do).
6. Acting (or not acting) in such ways also can maintain depression by making it hard to solve life problems effectively; this initiates another downward spiral in which what you do or don’t do makes the context of life harder or keeps you from improving it.
7. In this treatment, we will work together to focus on specific things you can do to help shift these downward spirals and help you become more active and engaged in your life.
8. BA is not just about “doing more.” If feeling better were that easy, you would have already done it. We can work together to identify the activities that would be most helpful and the small and manageable steps you can take to get started. You can think of me as a your coach or a consultant in the process of change.
9. Each session will involve developing practical and do-able steps to engage in activities that improve mood and to solve specific life problems. Between sessions, you will work on homework assignments that we develop together; these assignments are an essential part of therapy and will focus on re-connecting or building parts of your life that increase feelings of pleasure or accomplishment and bring you closer to important life goals.
10. Activating and engaging in specific ways can help you experience more reward and effectively solve life problems. When you are active, engaged, and solving problems effectively, it is likely that you will be moving toward important life goals and feeling better.
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therapist and client devise in session. Subsequent ses- sions examine what the client has learned, highlight relevant consequences of activities, and identify barriers and troubleshoot to maximize the likelihood of success on future attempts. The assignment of homework be- gins in the very first session, when the therapist asks the client to read the brief pamphlet that reviews the key ideas of the BA approach (see Martell et al., 2001).
2. It also is important to emphasize that BA is a col- laborative approach to therapy, in which therapist and client work together in the service of the client’s goals.
3. It is also helpful to orient clients to the structured nature of each treatment session. Although the spe- cific foci of each session vary across clients and across time, each session nonetheless follows a similar general outline. Specifically, as in CT for depression (Beck et al., 1979), each session begins with therapist and client setting an agenda in a collaborative fashion. The aim of the agenda is to organize the time effectively and to ensure that sessions address the client’s most important topics and have maximal likelihood of helping the cli- ent reach key goals. Because the goal of treatment is ac- tivation, the more control given to the client in setting the agenda, the better. In addition, given the integral role of homework in BA, the majority of each session is devoted to reviewing homework from the previous ses- sion and assigning homework for the next session. This is simply a structured way to discuss what happened during the week while remaining focused on treatment goals. The end of each session includes asking the cli- ent to reiterate a “take-home message” from the session, verifying that the client has a clear understanding of the assigned homework, and reviewing the time for the next scheduled session and methods to reach the thera- pist, if needed, in the interim.
In attending to each of these specific tasks, the thera- pist establishes his/her credibility as an expert who can help the client and conveys a sense of hope. By estab- lishing at the outset of treatment a strong foundation of collaboration, client and therapist can begin working together toward the client’s goals.
Developing Treatment Goals
The ultimate goal of BA is to help clients modify their behavior to increase contact with sources of positive reinforcement in their lives. Typically, this process in- volves (1) addressing basic avoidance patterns and areas
of routine disruption and (2) addressing short- and long- term goals. A good deal of the therapist’s time in BA is spent helping clients to increase awareness of their escape and avoidance repertoires and to practice ac- tive coping responses. Often, part of this process also involves changing basic routines (e.g., sleeping, eating, and social contact). Thus, short-term goals are set to specify concrete accomplishments that can help clients shift their life situations in a less depressing direction. Often, therapists are uncertain about how to sequence treatment targets; generally, we focus initially on behav- ior change that has the greatest likelihood of success, which may be based on ease of accomplishment or level of importance to client values and priorities. Common examples might include getting the house cleaned, spending time with friends and family, making head- way on a large pile of paperwork on which the client has procrastinated, exercising more frequently, and so on. Often, behaviors necessary for progress on short-term goals can be scheduled and structured in such a way that they substitute for maladaptive avoidant or withdrawal responses. A therapist works with a client to make prog- ress on short-term goals regardless of how the client is feel- ing. In other words, one of the therapist’s primary goals is to help the client change the pattern of having his/ her behavior governed by mood. Rather, the objective is to make progress on goals regardless of how one feels at a particular point in time, under the assumption that progress on life goals is itself antidepressive. This is a crucial point, because clients often judge the success of a particular behavior change based on how it makes them feel in the moment. Thus, it is important for therapists to remain mindful of the consequence of different be- haviors specifically with respect to whether they help clients move toward or achieve treatment goals.
Once the short-term goals relating to avoidance, withdrawal, and routine disruption have been ad- dressed, clients are assisted in addressing larger life cir- cumstances that may be related to depression. Larger life goals are those shifts that take time to accomplish but have the potential to alter a person’s life situation in substantial ways. Common examples include finding a new job, getting out of a distressing relationship, start- ing a new relationship, or moving to a new city or town. BA can be helpful in teaching and encouraging clients to continue to make progress toward these goals even though their actual realization may take some time to accomplish. Essentially, in BA, clients learn basic change strategies that can be used to accomplish short- term and larger life goals.
Behavioral Activation for Depression 347
Individualizing Activation and Engagement Targets
No two people are the same, and no person is exactly the same from situation to situation. In the context of treating depression, this means that the particular acti- vation strategies that work for one person may not work for another, and they may work for the same person sometimes, but not always. Whether activity–environ- ment transactions shift someone’s mood in a positive or negative direction is an empirical question, and one that requires careful attention and assessment to an- swer. Much of the skill of doing competent BA relies on just this kind of careful examination. In BA, this pro- cess is referred to as “functional analysis,” which is the key to individualizing activation targets and the heart of BA. Functional analysis involves identifying for each client the variables that maintain the depression and are most amenable to change. This understanding forms the basis of the case conceptualization and guides the idiographic application of specific activation strategies. In general, the therapist must engage the client in a de- tailed examination of the following:
• What is maintaining the depression? • What is getting in the way of engaging in and en-
joying life? • What behaviors are good candidates for maximiz-
ing change?
This process sounds simple, yet, in practice, it can be complicated given that we all frequently lack awareness of the contingencies that control our behavior. Given this reality, early in treatment, we talk explicitly about the goal (and the challenge!) of identifying these rela- tionships.
Two key steps are involved in identifying the contin- gencies that control behavior. First, therapist and cli- ent must clearly and specifically define the behavior of interest; this includes defining the frequency, duration, intensity, and setting of the behavior. The behaviors of greatest interest are those most closely tied to changes in mood. For clients who are familiar with antidepres- sant treatment, we often explain that we want to iden- tify the ingredients of a behavioral antidepressant that works for them. In order to do so, we need to define specifically the activities that maintain depression (e.g., “down activities”) and those that improve mood and functioning (e.g., “up activities”). For instance, for one client, difficulty completing basic household tasks was maintaining and exacerbating his experience of depres-
sion. It was important to specify the problems of (1) fill- ing and closing bags of household trash, then leaving them in the pantry room rather than taking them to the dumpster behind the house for the past 6 weeks, and (2) receiving bills in the mail and placing them un- opened in a file drawer for the past 4 months. Treat- ment with this client began with a series of graded tasks to accomplish the goal of taking out the trash. This was identified specifically as a potential “up” activity (even though it was, admittedly, not a pleasurable one) and selected as an initial focus because therapist and client decided it was more easily accomplished than address- ing the bills, which the client experienced as more over- whelming.
Second, therapist and client can begin to identify the antecedents and consequences of the behavior, with the goal of specifying variables that elicit or reinforce depression. In terms of the BA model, this is parallel to identifying the links between context and mood, between action and mood, and the downward spirals that can maintain depression over time. Understanding basic behavioral principles can often be of great value in identifying these contingent relationships. What does this mean in practical terms? For depressed clients, a number of contingent relationships are often observed. As we discussed earlier, negative reinforcement con- tingencies are often pervasive. Negative reinforcement means that the likelihood of a behavior occurring is increased by the removal of something from the envi- ronment, typically, an aversive condition. Negative re- inforcement contingencies can be a very adaptive part of human behavior. For instance, putting on a warm coat to avoid getting cold, stopping at stop signs to avoid getting in accidents, and being extra nice to a parent after crashing the car to avoid being punished are all examples of ways that negative reinforcement can serve one well. Unfortunately, however, when an individual becomes depressed, his/her behavioral reper- toires can become dominated by escape and avoidance behaviors that temporarily allow a person to escape from painful feelings or difficult interpersonal situa- tions. In this way, many avoidant and escape behaviors may be understood as secondary coping responses— efforts to cope with the experience of depression that, unfortunately, make it worse. For example, a person might attempt to escape from feelings of hopelessness and fatigue by taking a long nap in the middle of the afternoon. This might, as a consequence, temporarily remove the person from an aversive context, but it can also prevent him/her from taking the steps necessary to
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shift into a less depressive context overall (exercising, applying for jobs, cleaning the house, etc.). Substance abuse, excessive sleeping, watching too much televi- sion, and general inactivity are all common examples of secondary coping responses that can be maintained by negative reinforcement. These types of negative re- inforcement contingencies are often central in prevent- ing people from coming into contact with potentially reinforcing environments that contribute to leading a more adaptive and engaged life. Careful assessment is required to identify whether and how specific negative reinforcement contingencies are active in a client’s life. Positive reinforcement contingencies may also be prob- lematic for clients. In these cases, the likelihood of a be- havior is increased because it is contingently associated with positive consequences. For instance, going to bed early may be positively reinforced by family members offering empathy and support. Some behaviors, such as overeating and substance abuse, can also provide imme- diate positive reinforcement but detract from long-term goals, thereby maintaining the depression.
How do we conduct functional analyses in BA? There exist two primary supports for the BA therapist doing functional analyses: the BA model and activity monitoring. First, the BA model used to orient clients at the outset of treatment can be used throughout treat- ment to guide assessment of specific events that arise in a client’s life to help identify key links between activity and mood. For example, if a client begins to talk in session about feeling troubled by a difficult interaction with her son, the therapist can suggest that they use the model to understand the components of the inter- action. Together, they can discuss and write down spe- cifically what happened (e.g., “My son said that he was failing math”), how the client felt (e.g., “I felt sad about how hard our lives always seem to be and afraid that he would not graduate”), and what the client did (e.g., “I left dinner, went to my room, and thought about how I’m failing as a parent”). These components can then be linked to identify the downward spiral that maintains negative mood (e.g., isolating and ruminating increas- es anxiety and sadness) and the downward spiral that prohibits effective problem solving (e.g., “I didn’t talk directly with him, and he got angry, went out with his friends, and didn’t come home until the middle of the night”). This process of assessment helps to identify tar- gets of activation for that difficult event (e.g., generate and practice alternatives to leaving the interaction and ruminating; identify and implement steps to solving the problem of her son’s poor performance in math). Re-
peated application of the model in sessions and for use as homework between sessions also will help therapist and client identify patterns of maladaptive actions over time and place. Finally, repeated use of the model in such ways teaches the client a method to guide his/her actions long after therapy has ended.
Second, activity monitoring in the context of daily life is the heart of the assessment process in BA. Through detailed and ongoing activity monitoring that the client completes between sessions, therapist and cli- ent can work together to develop an understanding of the questions listed earlier. Given the role of activity monitoring, it is important early in treatment for the therapist to set the stage to explain clearly how to do it, defining both what to monitor and when to do it. Also, therapists must carefully and skillfully review monitor- ing tasks to reinforce the client’s efforts to begin devel- oping activation and engagement assignments.
Therapists may elect to use a number of different formats for activity monitoring, the most basic form of which includes recording both an activity and a mood rating for each hour of the client’s waking day. Ther- apists also may elect to have clients monitor mastery (sense of accomplishment) or pleasure (enjoyment) as- sociated with specific activities. Generally, we advise clients to record enough information about activities that we can begin to identify links between what they were doing and how they were feeling, but not so much information that the task is overly burdensome. It also is helpful to identify at what intervals during the day the client will write down the observations (e.g., morn- ing, lunch, dinner, before bed). If recording for each hour is too taxing for a client, time sampling proce- dures may also be used. In such a procedure, client and therapist agree on a specified number of hours when activities will be monitored during the week between sessions. Time-sampling procedures need to include a variety of situations in which the client functions dur- ing the week. In general, therapists will want to en- courage clients to complete entries at regular intervals throughout the day and are advised to work with clients to develop plans for recording that take advantage of natural cues and rhythms in their lives to facilitate such regular recording.
Therapists can provide clients with a simple weekly Activity Record for monitoring assignments (see Figure 9.2). However, as is often emphasized in BA, the func- tion of the behavior is more important than its form; thus, clients may eschew monitoring on an Activity Record but be comfortable using personal calendars,
Behavioral Activation for Depression 349
FIGURE 9.2. Activity Record (hourly).
Instructions: Record your activity for each hour of the day, and record a mood rating associated with each activity. Use the scale below with the anchors that you and your therapist develop to guide your mood rating. Aim to make entries on your Activity Record at least every 3–4 hours each day.
Monday Tuesday Wednesday Thursday Friday Saturday Sunday
5–6
6–7
7–8
8–9
9–10
10–11
11–12
12–1
1–2
2–3
3–4
4–5
5–6
6–7
7–8
8–9
9–10
10–11
11–12
12–1
1–2
2–3
3–4
4–5
Mood Ratings: 0: Description, with examples of associated activities:
5: Description, with examples of associated activities:
10: Description, with examples of associated activities:
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smartphones, or other idiosyncratic recording meth- ods. Adapting the monitoring assignment to a form that is compatible with the client’s normal daily routine is highly encouraged. For instance, clients who spend a lot of time in their car may keep their records above the visor; others may find it helpful to keep it taped to the refrigerator or bathroom mirror; still others find it use- ful to carry it with them in a pocket, purse, backpack, or briefcase.
When a client has completed an activity monitoring assignment, it is essential for the therapist to review it in detail. Failing to review activity monitoring records may mean missed opportunities to reinforce the client’s behavior and to develop the case conceptualization. Much of competent BA lies in skillfully reviewing a completed Activity Record. What does the competent therapist attend to when reviewing the records? In gen- eral, the therapist will want to keep the case conceptu- alization questions listed earlier in the forefront of his/ her mind when reviewing a completed activity log. The therapist reviews the Activity Record to understand the client’s activities, routines, and life context, and to begin to identify patterns that may be maintaining or exacerbating depressed mood.
Specific questions that therapists can use to guide their review of activity schedules are listed below:
• What would clients be doing if they were not de- pressed (working, managing family responsibili- ties, exercising, socializing, engaging in leisure ac- tivities, eating, sleeping, etc.)?
• Are clients engaging in a wide variety of activities, or have their activities become narrow?
• What is the relationship between specific activities and mood?
• What is the relationship between specific life con- texts/problems and mood?
• In what ways are avoidance and withdrawal main- taining or exacerbating depression? What do cli- ents avoid or from what are they pulling away? In what specific ways?
• Are there routine disruptions? • Where has contact with reinforcers been lost? • Are there deficits in coping skills and strategies?
To answer these questions, it is essential to focus on the parts of the client’s activity and context that change and the parts that are consistent over time. It is not un- common for depressed clients to report that their mood is always low, no matter what they are doing or where
they are doing it. They may describe that they simply feel “blah” all the time or that, perhaps, their mood changes, but such changes are minor or irrelevant. A central premise of BA, however, is that variability is everywhere, though sometimes it is difficult to detect. Moreover, the variability is not random. Instead, varia- tions in behavior and its settings have a direct effect on a person’s mood and, as such, provide critical information about central contingencies. When clients report that they feel depressed “all the time,” it is either because they are inaccurately reporting on their mood retrospec- tively, their behavioral repertoires are extremely narrow (e.g., lying in bed all day long), or they have not learned to discriminate between subtle differences in mood. This last point is a critical one. One of the key tasks for therapists is to help clients understand that their moods are intimately linked to what they are doing, where they are doing it, and the resulting consequences. Treating depression requires making a series of strategic changes in each of these domains, all of which are based on un- derstanding the basic contingent relationships.
Repeatedly Applying and Troubleshooting Activation and Engagement Strategies
Given the idiographic nature of BA, the course of treat- ment may look quite different across a range of clients. Despite this diversity, we discuss below a few straight- forward behavioral methods that are frequently used.
Activity Scheduling and Self‑Monitoring
The major work of therapy in BA occurs between treat- ment sessions. It is uncommon for clients to leave a session without some specific activities with which to experiment during the week. Thus, activity scheduling and monitoring of outcome are standard methods used throughout treatment. At the end of each session, the client should clearly understand the specific activity as- signment and have a clear strategy for implementing it during the week (including a plan for overcoming likely obstacles to implementation).
Specifically scheduling the activity is a useful tool for having the client commit to times when he/she will do the homework. When the assignment is listed in writ- ing on a particular day of the week, at a particular hour, the client has the benefit of an external aid to motivate behavior change (i.e., working from the “outside-in” as opposed to the “inside-out”). Activity scheduling is also used frequently for clients with significant routine
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disruptions. Schedules can be an aid in the effort to develop and follow regular routines for eating, work- ing, sleeping, exercising, and maintaining social con- tact. Depending on the activity, the client may not spe- cifically schedule the time but may instead record its completion on a daily log.
A key part of scheduling activities frequently involves careful attention to contingency management. As social psychologists have long known, “the correlations be- tween intention and behavior are modest . . . the weak intention–behavior relation is largely due to people hav- ing good intentions but failing to act on them” (Goll- witzer, 1999, p. 493). Given this reality, it is essential for BA therapists to consider ways they can help clients structure their environment so as to maximize success with treatment assignments and goals.
One helpful method of contingency management is the use of public commitment to enhance the like- lihood of completing assignments (Locke & Latham, 2002). Often, we explore whether friends, coworkers, or family members are available to be included in ac- tivation plans. For instance, one of our clients learned in treatment that when his depression was more severe, it was essential for him to tell his wife each morning the primary tasks he intended to complete that day. For him, “keeping his word” was an effective reinforcer that helped to increase his activation.
In addition, we work with clients to structure their environments in other ways that will enhance activa- tion. Thus, for a client who works on an exercise plan during the week, putting on her exercise clothes before she leaves work at the end of the day is an essential part of the plan.
Finally, clients may also experiment with the use of arbitrary reinforcers for specific behavior change tasks. Although the emphasis of BA is heavily on increasing contact with natural reinforcers in one’s environment, the selective use of arbitrary reinforcers can at times be helpful. The client we noted earlier planned a special dinner with his wife at the end of a week of adherence with activation tasks; the client who was working on the exercise program bought a new shirt for exercising after she started her new program. Occasionally, thera- pists may suggest the use of aversive contingencies to help promote behavior change; for instance, one cli- ent found it useful to agree to call his therapist if he was going to stay in bed and miss work for the day. We have described to other clients the method of writing donation checks to their least favored charities, which are then cashed if they do not complete scheduled ac-
tivities (Watson & Tharp, 2002). Often, simply the suggestion of an aversive contingency is sufficient to motivate change. For instance, the client who agreed to call his therapist did, in fact, call early one Monday morning; when he was halfway through leaving a mes- sage, he stated, “This is ridiculous. Forget it. I am going to work.” Although the use of aversive contingencies is not a common strategy in BA, it is occasionally used if determined between therapist and client in a collabora- tive fashion.
When clients do activity scheduling, it is also es- sential to build in a monitoring component, such that they record the context and consequences of activation. This provides both information about the specific ac- tivation assignment, and regular and ongoing practice in noticing contingent relationships between activity and mood. The therapist should discuss what the client learned from the activation and self-monitoring tasks in each session. In addition, the therapist needs to provide regular feedback about progress and to highlight areas of improvement or troubleshoot problems that may have arisen.
Treatment requires that the therapist not shy away from asking about homework that is incomplete or not done. Attending to these domains is exactly the job of the BA therapist. Repeated and persistent focus on a small set of activation tasks often occupies a great deal of the course of treatment. Asking about what prevent- ed the completion of homework gives therapist and cli- ent essential information about important barriers and possible examples of avoidance patterns. The purpose of such discussions is not to punish or shame the client, so it is important to approach homework review with a di- rect and nonjudgmental attitude. At the same time, dis- cussing incomplete or partially completed homework may be experienced as aversive by the client, which may help to facilitate his/her doing the homework next time (i.e., through being negatively reinforced by escaping from the therapist’s uncomfortable questioning). If this occurs naturally, it is not a problem and can in fact enhance treatment progress. However, the therapist should never use shame or criticism, however subtly, to enhance homework completion.
Graded Task Assignment
Graded task assignment, which is a core part of CT for depression (Beck et al., 1979), is also a hallmark of BA and a key part of most activity scheduling efforts. Thus, it is important for therapists to help clients break
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down behaviors into specific, achievable units to facili- tate successful behavior change. Knowing how to break down tasks and grade them appropriately in a stepwise progression from simple to complex requires therapists to use a broad array of basic self-management and prob- lem-solving skills. Toward this end, it is also important for therapists to help clients learn the method of grad- ing tasks during therapy, so that they can apply this skill to new contexts and tasks after therapy has ended. In explaining the tool of graded task assignment, it is often important to remind clients that the goal is not to accomplish all parts of the activity; rather, the goals are to get started on important tasks, increase activation, and disrupt avoidance. Therapists can also explain to clients that breaking tasks down helps to ensure success with subtasks, and such success experiences can in turn reinforce and motivate work on successive components of the larger task.
It is very important to break down tasks in such a way that early success is nearly guaranteed. If clients experience difficulty with tasks, therapists may want to revisit explicitly whether the task was broken down and graded sufficiently. Clients also can be asked to envi- sion the steps involved in a given task before attempting it outside of therapy, and to anticipate any obstacles that might arise. If this process suggests that certain com- ponents may be difficult to master, therapist and client can grade that task into smaller and more achievable components.
Avoidance Modification and Problem Solving
This is perhaps one of the most rich and varied aspects of BA. As noted earlier, clients may be addressing avoid- ance of concrete tasks at work or home, avoidance of painful emotions such as grief or fear, avoidance of in- terpersonal conflict, and so forth. The specific methods used to address these areas are tied to the specific nature of the avoidance. For instance, a client who avoids the experience of grief over a lost relationship may be assist- ed in spending time each day reviewing photos of the former partner, reminiscing about times they shared, and so forth. A client who avoids tasks at work may be assisted in breaking down tasks, making specific to-do lists, asking others for help, and so forth. A client who avoids interpersonal conflict may be assisted in practic- ing assertive communication in role plays in sessions, experimenting with discussions with friends, bringing a family member to a therapy session, and so forth. That said, within this broad domain, a number of basic strat- egies may be helpful in planning treatment.
First, when addressing avoidance, start from a col- laborative stance with the client. It is important to un- derstand and to communicate an understanding of the discomfort that a client may experience in a particular situation, which is then followed by some action on the part of the client to end the aversive experience. Thera- pists can emphasize the ways that avoidance may serve an adaptive function in the short term but be problemat- ic in the long term. Given that many avoidant behaviors may be under the control of immediate contingencies, it is often helpful to highlight repeatedly the long-term consequences of particular behaviors. Returning to the BA model to highlight such patterns is often helpful.
Second, basic problem-solving methods are fre- quently used to address avoidance. Although we rarely teach problem-solving steps in a structured and formal manner, addressing avoidance typically involves figur- ing out how to approach and solve problems. Thus, it is essential for therapists to maintain a problem-solving mindset with respect to avoidance and to work with clients to generate a range of options for possible al- ternative coping behaviors. Problem-solving strategies include defining and assessing the problem, generating alternative solutions, managing environmental contin- gencies, and troubleshooting the solution when needed. It should be noted that all of the other basic strategies are also frequently used in the service of avoidance modification and problem solving (activity scheduling and monitoring, graded task assignment, etc.).
Third, to help maintain a consistent focus on avoid- ance, clients may be assisted by several mnemonic de- vices. These devices help to organize a method of exam- ining, “What is the function of a behavior; what are its consequences?” We have used the acronym ACTION to identify the general approach that we ask clients to take (Martell et al., 2001):
• Assess—Is this behavior approach or avoidance? Will it be likely to make me feel better or worse?
• Choose—Either choose to continue this behavior, even if it makes me feel worse, or try a new be- havior.
• Try—Try the behavior chosen. • Integrate—Any new behavior needs to be given a
fair chance, so integrate a new behavior into a rou- tine before assessing whether it has been helpful or not.
• Observe the Results—Pay close attention and monitor the effects of the new behavior.
• Never Give Up—Remember that making changes can often require repeated efforts and attempts.
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When clients demonstrate behavioral patterns char- acterized by avoidance behaviors, therapists may use the acronym of being in a TRAP (Martell et al., 2001):
• Trigger—usually something in the environment (e.g., criticized by employer)
• Response—usually an emotional reaction (e.g., feels shame and sadness)
• Avoidance Pattern—The avoidance behavior(s) used to cope with the emotional response (e.g., leaves work early, complains to partner about dis- pleasure with job)
Therapists then ask the client to get out of the TRAP and back on TRAC; that is, under the same trigger and response conditions, they are asked to experiment with “alternative coping” behaviors.
Engagement Strategies
Research has documented well the frequency and nega- tive consequences of ruminative behavior among people with depression (Nolen-Hoeksema, 2000). The BA ap- proach considers ruminating as a behavior that fre- quently prevents people from engaging fully with their activities and environments. BA therapists are on alert for client reports of ruminating and are also careful to assess whether ruminating is a problem when clients return to sessions reporting that an activation assign- ment “didn’t work.” If, for example, a client reports that she experienced little mood improvement while playing with her son in the park, the therapist will want to ex- amine whether she was only partially engaged with the task of playing, because her mind was focused on why her former partner did not want to continue their rela- tionship, what that meant about her value as a woman, and so forth.
In addressing rumination in BA, we are less inter- ested in the particular content of ruminative thoughts than in the context and consequences of rumination. For instance, in working with a client who frequently ruminated about a job that he regretted having de- clined, the BA therapist asked him to examine the fol- lowing types of questions: “What were you doing while you were thinking about the other job?”; “How engaged were you with the activity of the moment and with your surroundings?”; “What happened during and after your thinking about the other job?” In examining these ques- tions, therapist and client identified greater likelihood of ruminating when he was working on aversive tasks in his current job, about which he felt significant anxiety;
thus, ruminating was negatively reinforced by distract- ing the client from anxiety and decreasing his focus on the aversive tasks. BA therapists may ask clients who ruminate frequently to experiment with “attention to experience” practice, in which they deliberately focus their attention on their current activity and surround- ings. For instance, they may be asked to bring their full awareness to physical sensations (colors, sounds, smells, tastes, physical movements, etc.). These strate- gies are akin to mindfulness practices (Segal, Williams, & Teasdale, 2002) and are also very consistent with the dialectical behavior strategy of “opposite action all the way” (Linehan, 1993).
Reviewing and Consolidating Treatment Gains
As therapist and client agree that there has been suf- ficient improvement and termination seems indicated, remaining sessions should focus on relapse prevention, which largely involves reviewing and consolidating gains the client has made. Toward the end of therapy, it is often wise to focus on anticipating situations in the client’s life that may trigger depressive feelings and behaviors, and to generate plans for coping with such situations. Upcoming life events that can be anticipated as challenges for the client (e.g., the death of a parent, a career change) should be discussed in detail, and the client can draft a self-help plan to activate in the face of the stressor. In addition, it is also very important to review the basic BA model and the methods used in therapy to ensure that the client is leaving with a solid understanding of how to apply these as tools in the fu- ture. For instance, therapists will want to review how to identify links between what one does and how one feels, how to set specific and concrete goals, how to use graded task assignment, and how to identify and target primary avoidance patterns (noticing that one is rumi- nating more at work, noticing that one is starting to fail to return phone calls of friends, etc.).
The Therapy Setting
Initial research on BA primarily focused on the context of outpatient individual psychotherapy settings; how- ever, recent studies have examined application across a broad array of settings and delivery modes. For exam- ple, several groups have found creative ways to transport BA to settings outside of specialty mental health clinics. Several investigators have examined the effectiveness and cost-effectiveness of nonspecialists in the deliv- ery of BA in various settings (Chowdhary et al., 2016;
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Darnell et al., 2019; Ekers, Dawson, & Bailey, 2013; Ekers, Richards, McMillian, Bland, & Gilbdoy, 2011; Patel et al., 2017; Singla, Hollon, Fairburn, Dimidjian, & Patel, 2019). Similarly, Hopko and colleagues (2011) conducted a successful randomized controlled trial (RCT) of BA for depressed cancer patients in oncology clinics. BA has also been utilized in the treatment of antenatal (Dimidjian et al., 2017) and postnatal depres- sion (O’Mahen et al., 2014). Group therapy appears to be a viable format for delivering BA to larger numbers of clients (Houghton, Curran, & Saxon, 2008; Porter, Spates, & Smitham, 2004; Kellett, Simmonds-Buckley, Bliss, & Waller, 2017). There is also growing interest in integrating BA into university settings (e.g., Cullen, Spates, Pagoto, & Doran, 2006; Gawrysiak, Nicholas, & Hopko, 2009; Reynolds, MacPherson, Tull, Baruch, & Lejuez, 2011) or school settings (e.g., Chu et al., 2016).
Treatment duration has ranged from 6- to 24- session formats. Limitations of client resources, insurance reim- bursement, and other factors may necessitate particular treatment durations. In our studies and clinical work, we often schedule brief phone contacts between sessions to reinforce the interpersonal connection to the thera- pist and the importance of completing the between- session assignments, and to provide an opportunity to address questions or problems with the between-session assignments.
Although BA is most often delivered as an individual treatment modality, significant others in clients’ lives are often included in sessions across the course of treat- ment. Decisions about whether to include significant others in treatment follow from the functional analysis; thus, they are determined on an idiographic basis. Con- joint sessions can be helpful in assessing patterns that may be maintaining the client’s depression, providing information and education to the family member about the treatment rationale and approach, and providing opportunities for the client and family member to prac- tice new interpersonal behaviors with the therapist’s di- rect and immediate feedback.
Therapist Qualities
In our experience, a number of structural and stylis- tics qualities are important for BA therapists to bring to their clinical work. Briefly, the structured nature of BA is maintained through the use of agendas to guide session foci; therapists engage clients in the process of collaborative agenda setting at the outset of each ses-
sion. Typically, the agenda includes some review of progress through administration of a depression inven- tory (e.g., PHQ-9), review of homework, discussion of target problems, assignment of new homework, and a session summary. In addition, the structure is guided by a steadfast focus on nurturing activation. From a stylistic standpoint, essential qualities of the BA thera- pist include an emphasis on collaboration or learning together as a team. In so doing, the therapist is mindful of pacing to support active collaboration and of solicit- ing information to ensure that the client understands information presented in session (e.g., specific targets or interventions, the overall BA model, or other “take- home” points from the session). All of the BA strate- gies also require the basic skill of being a good problem solver. Therapists approach most matters that arise in treatment simply as problems to be solved. Thus, thera- pists must be naturally curious about factors that main- tain problems and be skilled at generating a range of more functional alternative behaviors. Toward this end, it is important to be comfortable with a direct, matter- of-fact, and nonjudgmental manner of communication, particularly in the face of challenges such as not doing assigned activation plans or not attending scheduled sessions. Therapists must also balance a genuine sense of empathy and understanding for the suffering and struggles of their clients with an optimistic and dogged commitment to the possibility of change. BA therapists validate the struggles clients experience and seek out oc- casions to encourage progress, even if seemingly mini- mal. Finally, understanding basic behavioral concepts and principles can help therapists conceptualize cases according to a behavioral model of depression and pres- ent a coherent framework to clients.
The acronym ENLIVEN (Dimidjian, 2011) captures the structural and stylistic strategies necessary for the competent BA therapist in an easily remembered mne- monic:
• Establishes and follows agenda • Nurtures activation • Learns together with client • Is nonjudgmental • Validates • Encourages • Naturally expresses warmth
In our treatment outcome research, we have used ongoing clinical supervision and therapist consultation teams to assist therapists in adhering to and refining
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these important therapist qualities. Therapists typically meet together weekly for 1–2 hours. The teams help therapists increase skills with basic treatment strate- gies (conceptualizing treatment plans, doing functional analysis, effectively grading tasks, etc.). In the context of a focus on specific cases and strategies, the team also provides essential reinforcement for the therapist quali- ties of empathy, nonjudgment, problem solving, curi- osity and persistence, and optimism about change. Al- though we have not tested this hypothesis empirically, we strongly suspect that it would be difficult for many therapists to maintain these qualities, particularly in their work with clients struggling with severe, compli- cated, or chronic depression, without the support of an effective consultation team.
Client Variables
Our treatment outcome research suggests that depressed adults can experience acute and enduring clinical ben- efit from a course of BA. Our clinical impressions are that engagement with the basic treatment rationale and willingness to complete homework assignments are both important predictors of outcome in BA. Moreover, it is important to note that we used a number of client characteristics as exclusionary criteria in our treatment research. For instance, if a client were acutely suicidal, such that his/her risk could not be managed on an out- patient basis, then we would refer him/her for more acute and intensive treatment. In addition, if a client had a comorbid diagnostic disorder that was more se- vere and prominent (more interfering and the primary focus of the client), and necessitated another evidence- based treatment (e.g., obsessive–compulsive disorder), then we would also refer him/her to a more specifically appropriate treatment. We also carefully evaluated any potential medical problems that may have contributed to depression and referred clients for appropriate con- current medical treatment, if necessary.
Recent clinical research also highlights the poten- tial of BA as a treatment option for patients across the lifespan, including adolescents (McCauley, Schloredt, Gudmundsen, Martell, & Dimidjian, 2011; Ritschel, Ramirez, Jones, & Craighead, 2011; Ruggiero, Morris, Hopko, & Lejuez, 2007; Van Voorhees et al., 2009). This work is in line with earlier work by Lewinsohn and colleagues (1984) in the development of the Cop- ing with Depression Course for adolescents. This treat- ment program includes activity scheduling, relaxation training, assertiveness and social skills training, and
cognitive restructuring. Admittedly, the inclusion of cognitive restructuring in the Coping with Depression Course places this program in the broader area of CBT rather than specific BA, but the emphasis is on sched- uling pleasant events. Evidence also supports the use of BA with older adults (Acierno et al., 2012; Egede et al., 2015; Meeks, Looney, van Haitsma, & Teri, 2008; Meeks, Teri, van Haitsma, & Looney, 2006; Pizzi et al., 2014; Snarski et al., 2011; Sood, Cisek, Zimmerman, Zaleski, & Fillmore, 2003), ethnically diverse patients (Kanter, Hurtado, Rusch, Busch, & Santiago-Rivera, 2008; Kanter, Santiago-Rivera, Rusch, Busch, & West, 2010), patients with anxiety and borderline symptoms (Hopko, Lejuez, & Hopko, 2004; Hopko, Sanchez, Hopko, Dvir, & Lejuez, 2003), patients with posttrau- matic stress disorder (Etherton & Farley, 2020; Flint, Ferrell, & Engelman, 2020; Jakupcak et al., 2006; Mu- lick & Naugle, 2004; Wagner, Zatzick, Ghesquiere, & Jurkovich, 2007), substance users with elevated depres- sive symptoms (Daughters et al., 2008; MacPherson et al., 2010), patients with schizophrenia (Mairs, Lovell, Campbell, & Keeley, 2011), inpatients (Curran, Law- son, Houghton, & Gournay, 2007; Hopko, Lejuez, et al., 2003), patients with cancer (Armento & Hopko, 2009; Hopko, Bell, Armento, Hunt, & Lejuez, 2005; Hopko et al., 2011) and other medical comorbidities such as obesity (Pagoto, Bodenlos, Schneider, Olendzki, & Spates, 2008) and diabetes (Schneider et al., 2011). Although many of these studies are preliminary, report- ing data from small open-trial designs, the breadth of this work suggests that BA may be adapted as a treat- ment framework for a wide variety of clients struggling with depression and comorbid problems.
CASE STUDY
Background Information
The following section presents the treatment of “Mark,” a 43-year-old man with a long history of depression. Mark was in treatment for 19 sessions across 4 months. The description here is presented to illustrate the imple- mentation of core BA principles and strategies. Earlier sessions are described in greater detail to provide the reader with “how-to” information regarding the pri- mary principles and strategies. Later sessions emphasize a thematic focus for which the same types of principles and strategies are applied. It is important to emphasize at the outset that this case description is not intended to communicate a prescriptive course of treatment, and
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readers are advised against following the sequence of strategies in a lockstep fashion. BA is a highly idio- graphic treatment, in which the choice of specific acti- vation strategies is driven by functional analysis; given this, the reader is encouraged to attend to the ways the therapist conceptualizes Mark’s difficulties and imple- ments treatment strategies over the course of therapy. It is our hope that this detailed illustration will inspire readers to apply the basic principles and core strategies in a flexible and idiographic manner.
Mark sought treatment at the urging of his primary care physician. His recent episode of depression had lasted without remission for 3 years. Mark also had a history of alcohol abuse. His early alcohol abuse had caused significant problems in Mark’s first marriage, which ended in divorce when he was in his early 20s; however, problems with alcohol were not a cause of cur- rent concern. He had been in therapy previously, dur- ing his separation and divorce 4 years earlier. However, Mark described it as unstructured and unfocused, and reported that he stopped going after a few sessions. He lived alone, although he had joint custody of his twin adolescent daughters; Mark and his ex-wife alternated parenting every other week.
Mark reported that he had had periods of depres- sion for “as long as I can remember.” In particular, he recalled his first episode of depression at age 12, shortly after his father abruptly left and severed all contact with Mark and his family. Mark reported that he had believed his parents were happily married and, at that time, blamed himself for his father’s departure. Mark reported that his mother and older siblings never discussed his father. In describing his mood during adolescence and adulthood, he reported, “I have peri- ods when I’m able to function OK. I go to work and all that, but I’m never really happy.” Mark’s primary depressive symptoms included depressed mood, loss of pleasure in nearly all activities, excessive guilt, fa- tigue, difficulty concentrating, and occasional passive thoughts of death.
Mark had had a social network that revolved primar- ily around his former marriage, but he had withdrawn from that network since his separation and divorce. Currently, he spends most of his time alone, with the exception of caring for his daughters. Mark was col- lege educated and worked as an accountant for a local manufacturing company. He also wrote children’s sto- ries and, prior to his most recent episode of depression, was working on a number of stories as a member of a local writer’s group.
Case Conceptualization and Overview of Treatment
Mark’s depression was conceptualized as occurring in the context of his divorce and the changes that ensued following that process; in addition, vulnerabilities re- lated to his family history also formed a context for his current experience. Mark experienced intense grief and anxiety following his divorce, to which he responded with patterns of interpersonal avoidance that in turn were negatively reinforced by reductions in the grief and anxiety. Mark had trouble fully engaging in his sig- nificant relationships and instead avoided intimacy in various ways, both overt (e.g., refusing social contacts) and subtle (e.g., ruminating about mistakes he made in the past, failing to express commitment to the relation- ship and what he thought or felt about various topics on a regular basis). Over the course of treatment, the therapist and Mark hypothesized that avoiding close in- terpersonal connections in his adult life kept Mark de- tached enough that he would not feel subsequent losses as acutely as those he felt as a child. However, these pat- terns of avoidance also maintained Mark’s depression by limiting his experience of reward in many of his cur- rent contexts. Treatment focused initially on increasing activation and addressing many secondary problems and routine disruptions that had become established. Treatment sought to reverse the downward spirals of depression by scheduling and structuring activities. Al- though Mark increased his activation relatively quickly, his mood did not improve significantly. This led to a primary focus on Mark’s rumination and the ways it functioned to avoid intimacy in his relationships, and experimentation with new behaviors designed to move Mark closer to his goal of having a close intimate rela- tionship and feeling better.
Session 1
Session 1 focused on reviewing the results from the assessment process, presenting the treatment model, encouraging questions and feedback, and tailoring the model to Mark’s specific experiences. The review of the assessment process is typically brief; in this part of the session, the aim of the therapist is to ensure that he/ she has a solid understanding of the client’s present- ing problems, relevant history, and previous experience with treatment, if any. The therapist also reviews the basic diagnostic formulation to ensure that the assess- ment outcome matches the client’s subjective experience of his/her current problems. Discussion of the treat-
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ment typically forms the bulk of the early sessions. The following transcript provides an example of the thera- pist presenting the treatment model and responding to frequently asked questions about the etiology of depres- sion. Specifically, the therapist puts forth the idea that depression is treated behaviorally, regardless of etiology.
THERAPIST: Let me tell you a little about the basic model that guides BA. The first idea is that there are often things that happen in people’s lives that make it hard for them to connect with the kinds of expe- riences that would normally help them feel good. These shifts can be clear and easy-to-detect changes like major losses or disruptions in life. And they can also be smaller things, like the kind of things that just bug you a little but they keep happening, or you have a bunch of them happen all around the same pe- riod of time. The most important part is the idea that the effect of these events is that it’s harder to connect with the kinds of experiences that could give you a sense of pleasure or accomplishment in your life, and that could help you feel better. Does that sound like it fits for you?
MARK: I would say that is true for me. Definitely get- ting divorced was a big one. I think that did set things off, but even now, there isn’t much that helps me feel better. Even things that I think should help me feel better don’t do much. I just don’t have the energy at this point.
THERAPIST: Yes, exactly. It’s very normal to feel a whole range of things in the context of such events. Often sadness or grief is central, but so are feelings of fa- tigue and a sense of not having energy or interest in anything. All of these are parts of the experience of depression.
MARK: That describes it. THERAPIST: I’m going to draw that out here on this
form. In the first circle, we can list some of the events we’ve already talked about, like the divorce, sharing custody of your girls, and your move. Those reac- tions of fatigue and low energy that follow are very normal, and we’ll write them in here in the second circle. What we find often happens is that people can respond to these changes by pulling away from their lives even more. This pulling away can happen some- times in obvious ways, like staying in bed or calling in sick to work, or canceling social engagements, and sometimes in more subtle ways, like being focused
more on your thinking than on the activities you are engaged in. Does that make sense for you?
MARK: Yes, absolutely. I do all of those things. THERAPIST: It makes total sense that you would pull
away when you are feeling so down. The problem with pulling away like this is that it tends to keep people stuck in feeling depressed, and the pulling away can become a problem in its own right, so that is the arrow that links what you do and how you feel in a kind of downward spiral. The more you pull away or the more you are caught in your thoughts, the worse you actually feel, the less energy you have.
MARK: Yes. That sums it up. THERAPIST: And, actually, for many people, there is
also a second downward spiral. So the more the first downward spiral is set in motion, it actually can lead to new problems, like your boss gets frustrated with you or your friends stop calling, or it can keep you from solving some of the problems that triggered the depression in the beginning. So the ultimate goal of our work together is to figure out new actions you can take here (pointing to the third circle on the dia- gram) that can help to reverse this downward spiral. We will want to learn together what sorts of activities may have a positive effect on your mood, and then help you activate and engage in those specific ways. And we will figure out how to solve the problems that are creating stress or dissatisfaction in your life. How do you see this fitting with your experience? Do you have questions about what I’ve said? Parts that fit or don’t fit?
MARK: I understand what you are saying, and I think some of it fits, but I guess I don’t understand why I get so depressed. I mean, other people have stress- ful things in their lives and they seem to function. Other people get divorced or have crappy jobs, and they move on. I mean, come on, I’ve been divorced for 4 years now. I think depression runs in my family. My older brother has been depressed forever, and I sometimes wonder if my dad was depressed when he took off. Sometimes, I can’t really identify anything that has happened in my life. I mean, I am never really happy and then, it’s just like a switch goes in my brain and I’m back in that dark hole again. How does that fit with what you are saying?
THERAPIST: That is an excellent question. What I mean as I talk about depression is that some people are more vulnerable than others. And, there are many ways
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that you may be vulnerable to depression—through genetics, biology, or experiences in your history. In fact, we can add some of these things you are talking about now to the first circle as part of the context for you. (Writes in family history.) What this treatment emphasizes is that it’s possible to change depression by making changes in what you do.
MARK: That makes sense to me. One part of what you said definitely fits for me—the part about pulling away more. I definitely do that. Sometimes I don’t talk to another person or get out of bed all weekend. I know it makes it all worse. But I still do it. I don’t seem to be able to do anything else when I feel that way.
As the therapist replies to these very common ques- tions, she seeks to normalize avoidant responses to de- pression. It is essential for the client to experience the therapist as someone who understands and has sincere empathy for his/her struggle. The therapist must com- municate that the client’s behaviors make sense, even though they may not serve the client well in the long term. In this way, the client is more likely to experience the therapist as an ally in the change process as opposed to someone who oversimplifies or “doesn’t get” the challenges of making changes. Additionally, the thera- pist also emphasizes to Mark the importance of guided activity, highlighting her own role as an expert and the importance of careful assessment. She emphasizes the difference between assignments based on a superficial understanding of depression and those that are guided by functional analysis, a key aspect of the treatment, to which the therapist will return many times.
THERAPIST: Those are great observations and are really on target with what I have noticed for a lot of people as well. What many people experience is that when they start to activate and engage, they can actually feel worse initially! The troubling fact about pulling away or avoiding is that it does provide some short- term relief. But in the long term, that downward spi- ral can keep you trapped in depression.
MARK: That makes a ton of sense to me. I just don’t want to do anything. Making a meal makes me tired. I feel irritated by the sound of silverware scratching on plates. It’s kind of crazy, but I just want to crawl in a hole, to turn out a light in my head and make it all go away. Then, I end up feeling worse when I do stay in bed. I used to drink, too. I knew it would
make it worse, and I don’t do it much anymore, but it helped in the moment, even though I knew it didn’t really help. I guess I felt better temporarily and that was enough.
THERAPIST: Yes, exactly. Avoidance is a perfectly natu- ral response. What unfortunately happens, though, is that you are not in touch with all those things that can give you pleasure and a sense of accomplishment, and you are not engaged in solving the problems that create stress in your life.
MARK: That’s the first and second downward spirals you were talking about, right? I get it but it just all feels so overwhelming. Just the thought of it . . .
THERAPIST: Yes, I know. That is where I come in. It’s important to emphasize that this treatment is not just about me saying you should “do more” in gen- eral. Sometimes I tell people that it’s not the Nike approach to therapy, where I tell you each week to “just do it.” You have probably received feedback like that from other people in your life, and you may even say something similar to yourself.
MARK: Yeah, guilty as charged. THERAPIST: My assumption is that if this were easy
to figure out, you would already have done it. It’s a simple treatment but that doesn’t mean it’s easy. The reason that you are here is that it’s not easy, and that is where my expertise comes in. A major part of this treatment is the idea of guided activation. This means that you and I will be working together to identi- fy specific ways in which you can experiment with activation. My expertise lies in figuring out, first, where the places are that would be the most helpful in increasing your activation and engagement, and second, what small and manageable steps you can take to get started. You can think of me as a coach or consultant to you in the process of change. We will work together, as a team, in small steps, all along the way. How does that sound?
MARK: The idea of it sounds good. I guess it’s worth trying.
THERAPIST: I’d like to ask you to read a short pamphlet about this treatment, between now and the next time that we meet. It will provide you with more infor- mation. When we meet next time, we can talk more about how we will put the ideas into practice.
With this initial session, the therapist has begun to teach Mark about the treatment model and is get-
Behavioral Activation for Depression 359
ting him actively involved in and on board with the rationale. The therapist has oriented Mark to their re- spective roles in treatment and has given him this first homework assignment (reading the treatment rationale pamphlet). These critical tasks of the first session set the stage for additional discussion in Session 2.
Session 2
In Session 2, the therapist carefully follows up on a number of the key orienting tasks, which includes en- suring that Mark is on board with the basic treatment model and explaining the structure of the therapy. The therapist attends to these topics in opening the session:
THERAPIST: It’s great to see you today, Mark. MARK: Thanks. It’s good to be back here. THERAPIST: That’s great. You know, when I was think-
ing about our session last time, I realized that there were a couple of points I wanted to emphasize more. One of the important ones is that this is a very col- laborative approach to therapy, and one that is also fairly structured. So each time we meet, we will start out by setting an agenda for the session, and we will do this collaboratively. In fact, over time, you will set the agenda more and more, though I may have more to say about it in the beginning. The idea is that I’m the expert on how to get over depression, and you are the expert on yourself and your life, and what things help or don’t help.
MARK: That sounds reasonable to me. THERAPIST: Great. So in terms of the agenda for today,
I have a couple of things. I’d like to talk more about the treatment approach and your reaction, and more about how we put some of the ideas into practice. Do you have items you want to be sure we address today?
MARK: No, that sounds good. I did read the pamphlet, and it really hit home. It was like they wrote it about me, basically. I thought, “Thank goodness somebody has figured this out.”
THERAPIST: That’s great. I think one of the core ideas of the model is things happen that tend to trigger depressed mood, and then people tend to do things, or not do things, that make the depression worse. For you, my understanding is that the main trigger was your divorce and that occurred in the context of your history of important losses, too, in your family grow- ing up.
MARK: Yeah, both are true. I’ve really pulled back on a lot, like not exercising and not doing things with other people or even with my girls. We used to cook these great dinners together and now it’s like an ef- fort to get organized to order pizza. It’s kind of like that everywhere—at work, too. I’m just managing the minimum and, honestly, a lot of times I’m not even doing that.
THERAPIST: I know. It can be very hard to keep doing the sort of things that will keep you feeling well. And that is where this therapy comes in. From our ses- sion last time and from your reading, what is your understanding of what we are going to be doing in here, and how I am going to be helpful? If you were to tell a friend of yours what we were going to do in this therapy, what would you say?
MARK: I guess I would say that we are going to pin- point the activities that give me some pleasure or help me feel like I’m handling things well. Then, we will figure out how to help me get into the position of being more involved in some of those things.
THERAPIST: Yes, that is a big part of it. Sometimes in people’s lives something that is completely beyond their control triggers depression, and then what I call “secondary” problem behaviors get triggered or made worse. These are the behaviors that involve pulling away or avoiding, as you were saying, like stopping fun activities with your girls or withdrawing at work. And in those cases, we work on the secondary prob- lem behaviors, and that is the core of the therapy. Other times, we also need to address larger problems in your life that may be related to what makes you vulnerable to depression. In those cases, therapy can involve both directly addressing the secondary prob- lem behaviors and working directly on the problems, after we have kind of cleared the path for doing some problem solving by getting you activated and en- gaged.
MARK: That sounds like it’s probably the case for me, because I know I had a lot of problems relating to Diane that were part of our divorce, and those are not any better.
THERAPIST: Yes, we will talk more as we go along about what set off the depression for you. In a global sense, we know now that it was the divorce. But, as we start following your mood and activities day to day, we will see the ways that your mood has ups and downs. We will work together and look at that carefully,
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asking what set that off, how you responded to your mood hitting that point, and whether it would help if you tried something different.
The therapist has now stated twice that generally a contextual event triggers depression, while earlier ac- knowledging that several things can contribute to vul- nerability. This is a subtle but important point, because clients sometimes believe their depression came “out of the blue” or that it is simply “biological” and not modi- fiable by behavioral means. By emphasizing an environ- mental antecedent (e.g., a loss of positive reinforcement), the therapist sets up the idea that rather than depression being completely beyond patients’ control, their de- pressive response makes sense, and more importantly, it is possible to make behavioral changes to regain or establish new reinforcers in their lives. Moreover, the therapist has continued to emphasize the importance of carefully monitoring and assessing the relationships among mood, activity, and context as a key part of de- signing effective behavior change plans. The therapist then builds on this foundation as she moves into the other main focus of Session 2—the initiation of activity monitoring. Here, the therapist explains to Mark why activity monitoring is important, begins to teach him how to complete an Activity Record (see Figure 9.3), and links it directly to some of his recent experiences.
THERAPIST: One of the main tools that we use in this therapy is called an Activity Record. This is one example. (Hands Mark the record.) As you can see, it has blocks for each hour of the day. I’d like you to use this to start recording your activity and your mood. It’s basically a way to keep track of how you are spending your time during the day and how you are feeling. We want to learn what you are doing on an hour-by-hour and day-to-day basis. What things in your life help you feel better, and what things make you feel worse? You and I will review these very carefully together, focusing on how you are spending your time and how you feel. Sometimes the Activity Record tells us right away where changes need to be made, and other times we have to look at it over a couple of weeks.
MARK: OK. THERAPIST: Is there anything you have been doing
since you started to feel more depressed that is differ- ent from what you normally do?
MARK: Yes, exercising less, watching more TV, and just
the amount of time I spend thinking about all this. It’s just crazy.
THERAPIST: It’s not crazy at all, but I agree that it’s not helping you very much. And it’s very difficult, which is why you are here. We can start to figure this out together. It’s great that you are already aware of those patterns, and those are good examples of look- ing concretely at what you are doing. This therapy is about increasing your awareness of how your mood is affected subtly from activity to activity and increas- ing those that tend to be more rewarding. It’s like we are on a detective mission for the “up” and “down” activities in your life, those that are linked with feel- ing improved mood and those are that not.
MARK: Makes sense. So, should I write all this down? Do you really want me to do this every hour?
THERAPIST: Here’s the guideline that I use: I want people to record their activity frequently enough that they are not relying heavily on memory. The problem with memory when you are depressed is that your awareness can be dulled or biased by the depression. So you don’t have to do it every hour. We have to be realistic about the rest of your life! But you may want to experiment with doing it every 3–4 hours. Some- times, people like to do it at breakfast, lunch, dinner, and before bed.
MARK: That might work for me. THERAPIST: Let’s go over what to write down. You put
your activity down for each hour block and then for each hour block you also assign a mood rating from 0 to 10. Let’s look at today as an example. What were you doing in the hours before you came here?
MARK: I was at work. THERAPIST: OK, great. What were you doing at work? MARK: I was teaching a new employee how to use our
computer system. It was really frustrating, because she wasn’t picking it up, and I didn’t have much pa- tience.
THERAPIST: That’s great information to record. Why don’t you write down “working–teaching new em- ployee.” Now, I also want you to record your mood on a 0- to 10-point scale, so let’s see if we can get some anchors here. What would be 0 mood for you? We can track this in whatever way will be most useful for you, so we could consider that 0 might be feeling really good, with no depression or feeling down at all. If so, we would then consider 10 to be when you
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FIGURE 9.3. Sample completed Activity Record (hourly) (assigned on Monday and reviewed on Thursday).
Instructions: Record your activity for each hour of the day, and record a mood rating associated with each activity. Use the scale below with the anchors that you and your therapist develop to guide your mood rating. Aim to make entries on your Activity Record at least every 3–4 hours each day.
Monday Tuesday Wednesday Thursday Friday Saturday Sunday
5–6
6–7 Awake thinking in bed (9)
7–8
8–9 At work (7)
9–10 Getting ready for work (8)
10–11 At work (7)
11–12
12–1
1–2
2–3
3–4 Working/ teaching employee (5)
Home (7)
4–5
5–6
6–7 Therapy (5) Making Dinner (6)
7–8 TV (9) TV (9)
8–9
9–10
10–11
11–12
12–1
1–2
2–3
3–4
4–5
Mood Ratings: 0: Description, with examples of associated activities: writing; playing with my kids
5: Description, with examples of associated activities: doing a work task that is only
moderately interesting but I’m focused and concentrating
10: Description, with examples of associated activities: thinking about how I’ve screwed
everything up
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feel your absolute worst, the worst you could possibly feel. It might be helpful to think of some activities that are a 5 or in between, when you’re not feeling your best but you’re not feeling particularly bad ei- ther. Which activities might be associated with each?
The therapist and Mark then worked together to identify activities that were associated with the low, middle, and high ends of the scale. Some clients pre- fer to use the low end of the scale to indicate feeling negative mood, whereas others (like Mark) prefer to anchor the low end as indicating feeling positive mood (“ really good” for Mark). Allowing such flexibility can be helpful as long as therapist and client are clear about the anchors that will be used when the client completes the monitoring at home. It should also be noted that therapists may ask clients to rate other dimensions, such as the degree to which activities were associated with mastery and pleasure (Beck et al., 1979) or a sense of being nourished or depleted (Segal et al., 2002). These may be rated instead of or in addition to mood. Often, we begin by asking clients to record mood ratings given that this is an easier starting place for many clients, be- cause it requires less discrimination of subjective experi- ence; moreover, the mood rating provides essential in- formation about potential antidepressant activities. For some clients, it is helpful to build on this by teaching them how to distinguish between mastery and pleasure, and the ways in which both can be helpful in regulating mood. In the case of rating mood or mastery–pleasure, it is important to review carefully the method and scale we want clients to use. For other clients, the dimensions of nourishing and depleting are helpful to identify ac- tivities that are antidepressant.
THERAPIST: Given this scale, what was your mood rat- ing for the 2 hours of “working” today?
MARK: Probably a 5. THERAPIST: That’s exactly it. Now, sometimes what
happens is that people don’t fill it out because they think, “I wasn’t doing anything.” It’s important to realize that even if you are not doing an activity, we want to know that, too.
MARK: What do you mean? THERAPIST: Well, when people think “activities,”
they often think of things like “going to the store,” “watching a movie,” “picking up my child from school.” But we are conceptualizing activity more
broadly. It might be driving by Diana’s house or hav- ing a significant phone conversation with someone, or even lying in bed, spending time thinking about Diana.
MARK: That would be true on a lot of days. THERAPIST: Yes, and you can write that down. Those
are some of the most important things. In some ways, the more detail, the better. We want to start noticing subtle changes. We want to build on those times that you feel just a little better, and we want to figure out what the problem is when you feel worse.
MARK: I think I got it. THERAPIST: Great! People usually come away from
this thinking that it sounds really simplistic. And it does. It sounds simple, but in practice it is not that simple. It can be difficult to do in the beginning, to really look at all your activities and figure out how your mood is related to them. It takes skill and hard work on both our parts. Is there anything that we can think of now that might get in the way of your doing this monitoring this week?
The therapist ended the session by discussing with Mark potential barriers to doing the assignment, en- couraging him to make contact by phone if any ques- tions arise, and offering encouragement about the like- lihood that she could be helpful to him.
Session 3
As noted earlier, one of the necessary competencies of a BA therapist is the ability to review an Activity Re- cord and glean information that will help to custom- ize activation and engagement strategies. Session 3 focused heavily on reviewing Mark’s Activity Record (see Figure 9.3) and using the information collected as a springboard for more detailed assessment of key prob- lem behaviors. Again, the therapist’s focus in these early sessions is on increasing activation in areas that will im- prove Mark’s mood; this work will set the foundation for later work on avoidance modification and problem solving.
THERAPIST: Shall we go over your Activity Record? MARK: OK. (Hands the therapist the record.) THERAPIST: Why don’t you walk me through it? What
did you learn? (Hands the record back to Mark.) MARK: I’m not sure if this is what you had in mind.
Behavioral Activation for Depression 363
I started the next day after our last session. I went to work that day, but I was feeling so lousy that I left early and came home. I was just kind of fiddling around the house until dinner. I felt really down all day up to that point; I rated my mood as a 7. I did make dinner, which was a little better for me. I used to love to cook for Diana and myself, and we would make these big feasts sometimes with the girls. Since the divorce, though, sometimes I just grab a bag of chips or something like that, or on a good night I might order a pizza. When I was cooking, I felt a little better then, about a 5.
THERAPIST: This is terrific. You did a really great job with this. You completed the record exactly as we talked about—writing down your activities and also your mood rating—and all of this information is ex- tremely useful. I want to ask you some more ques- tions about specific parts of the day in a minute, but right now let me just get an overall sense of things.
Notice how the therapist is careful to reinforce the client’s efforts early in the review process. Clients are often uncertain about how to complete the record, and it is not uncommon for them to return with partially or improperly completed records. In such cases, therapists must balance the need to provide corrective feedback and to reinforce the client’s efforts. Frequent client er- rors include writing down activities very globally (e.g., “at work” for 6 hours), failing to record mood ratings, or failing to record anything because he/she did “noth- ing.” In such cases, the therapist should address these problems in a straightforward and matter-of-fact man- ner.
THERAPIST: What happened after you made dinner? MARK: Well, after dinner, I started watching TV, and
everything kind of tanked from there. I sat and watched TV until 2:00 in the morning. I guess it helped in that it kept my mind off of worries about work and just feeling lousy about Diana, but I was really depressed the whole time. In fact, I rated my mood as a 9.
THERAPIST: That is really important information. I see that you were also up the next night watching TV until 1:00 A.M. Is this true of a lot of nights for you, or are these two more like exceptions?
MARK: I wish they were exceptions, but no, it’s been more the rule. And then what happens is that I just
can’t get up in the morning. Well, I guess I do wake up, but I just lie there in bed. I’ve been getting to work pretty late, and some days I just call in sick.
THERAPIST: So we’ll use this log to pick up themes of specific activities that can help you feel good and those that may be contributing to your depression, like we talked about last time, the “up” and “down” activities. It seems like there are a few that might be important. I’m thinking that the watching TV and going to bed late is one big one, and the other two are cooking and how you are doing at work.
MARK: I think the TV is a really big one.
Notice here that the therapist identified a few broad areas that appear to be related to the maintenance of the client’s depression. The BA therapist is also alert to disruptions in the client’s normal routines; in Mark’s case, both eating and sleeping routines appear to have been significantly altered. The therapist then works collaboratively with Mark to target a specific area for further assessment and problem solving (i.e., nighttime TV watching). At this point, the therapist begins the more explicit process of functional analysis.
THERAPIST: OK, why don’t we start there? Let’s get clear first about what the problem is because it doesn’t sound like it’s watching TV in general.
MARK: That’s true. Normally, I would watch some TV, like I might watch for an hour. But, actually, come to think of it, I was more involved in my writing then, too. So, normally, I might watch TV until about 9:00 P.M. and then turn off the TV and write for another hour. Or, if I had the girls, we might watch a show together and then turn off the TV and read or play a game, or just hang out together, or maybe I’d be on a phone call or something.
THERAPIST: So, this is different for you. The problem, then, is that you don’t turn off the TV at 9:00 P.M. and instead watch it for an additional 4–5 hours.
MARK: Yes, that’s the problem. THERAPIST: Are you doing this every night of the week
or just on work nights? MARK: I hate to admit it, but it’s pretty much all nights,
not always so late, but pretty much always later than is good for me.
To this point, the therapist has successfully defined the problem in specific and behavioral terms. With a
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clear and mutual understanding of the problem, thera- pist and client can begin to consider the contingencies that may be maintaining the problem and what may be amenable to change.
THERAPIST: We should probably look at what gets in the way of turning the TV off, since it does not seem to have a great effect on your mood. If you were to turn off the TV at 9:00 P.M. now, what do you think would happen?
MARK: I thought about turning it off last night, but I just didn’t want to think about all of this stuff.
THERAPIST: By “all this stuff,” do you mean the divorce and the pressures at work?
MARK: Yes, both of them. THERAPIST: So, that is what you are actively avoiding.
And the TV helps you to distract? MARK: Yes, I just don’t have the mental awareness now
to start writing. I can’t focus on it, and I’m just not interested.
THERAPIST: I think you have the right idea in terms of distraction, but the problem is that you are distract- ing yourself with something that doesn’t give you much pleasure and not much accomplishment.
MARK: And meanwhile the house is a mess. I haven’t paid my bills in months, and . . .
THERAPIST: Yes, that makes sense. That’s the second downward spiral we talked about. What do you think about working together on the problem of watching TV? Then, we can tackle some of those other things you are raising. The TV problem might be simple to solve, but my guess is that there is more to understand about it.
Notice how easily the client can become over- whelmed and hopeless in response to the myriad prob- lems in his life. The therapist is alert to this possibility during sessions and is careful to refer back to the BA model as a way to understand the client’s experience and to refocus the client on the problem at hand. In addition, the therapist also takes a keen interest in the “minutiae” of the client’s day-to-day behavior, particu- larly if such behavior is related to mood. This detailed level of interest is critical. Its intent is twofold: (1) Such discussions guide the choice of activation targets and specific assignments; (2) it is the intent that such dis- cussions will teach Mark to take a similar interest and
begin to notice patterns that are more and less helpful in working his way out of depression.
THERAPIST: Let’s understand better what happens with the TV. Does it come into your mind, the thought that you might be better off if you turned off the TV?
MARK: Typically, I think, “I should go to bed.” But I know that if I go to bed, I’ll just lie there awake any- way, thinking about what Diana is doing, thinking about how much I am going to hate being at work the next day. So, then I think I might as well watch TV.
THERAPIST: Is that what happens in bed? You lie there and ruminate about Diana or things you have done or haven’t done at work?
MARK: Pretty much exactly.
In this transcript, the therapist has effectively iden- tified a number of key relationships. Nighttime TV watching is associated with (1) deterioration of mood; (2) poor performance at work; and (3) a process of nega- tive reinforcement in which negative affect (specifical- ly, grief and anxiety) potentially is reduced when the client is watching TV. The therapist has done so in a collaborative and nonjudgmental manner, and the cli- ent is on board. At this point, the therapist explicitly examines her hypothesis with Mark about the relation- ship between TV and mood. On the basis of this un- derstanding, they can then consider possible activation strategies.
THERAPIST: I’m wondering if part of what is happen- ing is that watching TV is helpful in the short run because it takes your mind away from these topics that are connected to a lot of potential sadness and also anxiety about the future.
MARK: Yeah, that’s true. THERAPIST: But the tough part is that while it works
in the short run, it’s that same downward spiral or vicious cycle in the long run, because watching TV gives you almost no pleasure and it keeps you from doing activities that you previously got a lot out of, and it sets you up for having problems at work.
MARK: Yes, exactly. It’s crazy, I know, but it’s such an easy way out when I’m just beaten by the day.
THERAPIST: Absolutely! So we have to take that into account when we think about making any changes
Behavioral Activation for Depression 365
here. I’m thinking that you could try going to bed in spite of that, and we could work on the ruminating. Or, if you are going to be up, you could do things that are better than the TV. Which do you lean to- ward?
The therapist attends to the function (distraction) of the problem behavior (TV watching), while engaging in problem solving in a very collaborative manner.
MARK: Probably finding other things, better than the TV. I used to go to a book group one night a week. It was made up of other writers and I liked a few of the people a lot, so when I was doing that, I was also doing reading in the evenings, too.
THERAPIST: OK, does reading seem more of a way you could start getting back into some of your writing, versus jumping in with writing itself?
MARK: Yes, there is no way I could write now. I would just be staring at a blank page, feeling like crap.
THERAPIST: OK, that makes sense. So what about starting with this? One option is that you could have a limit for yourself of 9:00 P.M. for TV and we could work on identifying a book that you could read in- stead.
MARK: It’s a good idea. It’s more a question of my doing it.
It is very important that the therapist not gloss over comments such as Mark’s final statement. When clients express doubt about how or whether they will imple- ment an activation strategy, it is essential to attend to this in detail. Additionally, it is helpful for the therapist to be attentive to statements such as “I’ll just have to make myself do it,” which generally indicate that thera- pist and client have not sufficiently identified the con- tingencies that control the behavior. In our experience, use of sheer willpower is unlikely to meet with great success, and suggestions of such signal that further as- sessment is required, as the therapist illustrates.
THERAPIST: So we need to be sure we are getting at the real problem, instead of just saying, “Oh, you are going to do this,” and leaving it at that. What kind of reader are you? Are you someone who can get really involved in a book?
MARK: I do get really involved. In fact, I’ll think about the book a lot during the day, if I’m already into it.
THERAPIST: But getting yourself to do it is hard. MARK: Yes, it’s getting started on things. THERAPIST: That is great to know. So, we have to
somehow get you involved in the book so that when 9:00 P.M. rolls around, you are already involved, so it will be easier to turn off the TV.
MARK: That would make it easier. THERAPIST: What if you were to buy a book on the way
back from our session and begin reading it in the café of the bookstore.
MARK: Oh, yeah, that is right on the way back. I can do that.
THERAPIST: Mark, I think the trick with all of this is to figure out what is going to help you move toward the things that will be beneficial for your mood. And this is what is really hard—getting yourself to go back to the things that you used to enjoy, when you have no interest in them right now. When you feel good, you take it for granted that it’s easy to do things like reading, spending time with friends or your girls, and even writing. When you don’t feel good, you really notice it. The problem is that you’re in this vicious cycle again. The longer you do not do things, the more badly you feel and the less you want to do. The trick for us is to figure out ways to help you start to do some of the things that will give you pleasure again.
The therapist acknowledges to the client that the new behavior will be hard to initiate because of mood, and that it is necessary to do so anyway. Many times, clients employ an “inside-out” or mood-dependent approach to their depression; that is, they passively wait for their mood to improve before making behavioral changes. BA therapists teach clients that when they feel down, they cannot afford to wait for a better mood to strike them. The goal is to get active when they feel down (as hard as that is). Increasing activation will eventu- ally improve mood, even if not immediately, and it will interrupt the pattern of secondary problems created by withdrawal and avoidance. Addressing mood-depen- dent behavior (or talking about an outside-in vs. inside- out approach) is a sensitive point in therapy, in which a great deal of empathy for the experience of feeling de- pressed is required. The therapist must skillfully balance encouragement of action with validation of the difficulty of activating when depressed. In addition, strongly en- couraging even the smallest signs of increased activa-
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tion (frequently with the use of significant praise) is es- sential in supporting the process of change.
MARK: Yeah, I know. A lot of the time I might know what I need to do, but I have no idea how to get myself to do it. I’ve just dropped a lot of stuff, like anything social in the evenings. I don’t try to make plans. And, like I said, for almost a year I was going to that writer’s book group every Thursday. But then I said to myself, “I’m not writing. This whole divorce is wiping me out. What is the point of going? I have nothing to add.” But it’s true that when I went, I used to get a lot out of it. I’m just not interested now, though.
THERAPIST: Yes, exactly. That’s where you and I will work together. I want to come back to the social con- nections and the routines around writing, but let’s stick with the reading and nighttime TV for a bit longer first, if that’s OK?
MARK: Yeah, that makes sense. THERAPIST: Let’s think through this book plan again.
Is there anything that might come up between here and the bookstore that would derail that plan?
At this point, the therapist and Mark spend the re- mainder of the session discussing particular books he could purchase that would maximize his engagement, and they discuss potential barriers that might arise to derail him from the intended plan. They also contin- ued to review the Activity Record to identify other key problems, including ruminating at work, withdrawing from social networks, and experiencing disruptions in routines that previously brought him pleasure (e.g., cooking, exercise). In each case, the therapist uses a similar method that she used with the problem of TV watching: defining the problem, identifying the ante- cedent and consequences, and checking out hypotheses about how the activity is related to mood with the cli- ent. The therapist also frequently returns to the overall BA model to help explain links between activities and mood. In each case, they work to learn together what possible targets will be most promising for activation.
Also, the therapist continues to emphasize that sim- ply deciding to “make myself do it” is not likely to be an effective activation strategy for Mark, and that it is essential to tie the activation plan to a clear under- standing of the function of the problem behaviors. The therapist employs a combination of gentle question- ing, consistent validation of the roles of withdrawal
and avoidance through reliance on the BA model, and repeated discussion of potential barriers to activation plans. Importantly, the therapist also highlights for Mark that compliance with the homework assignments may not bring immediate relief.
“What will be really good this week is to see what effect these things have on your mood. Even if they have just a little bit of a positive effect, then we know that we are on the right track. And, Mark, they might not have an immediate positive effect on your mood. It might be that the act of getting yourself to do it is the success itself, and that you need to keep doing it for a while before you start to feel better. But, it’s my guess that some of this stuff will help your mood a little bit, even in the short run.”
The session concluded with the therapist and Mark reviewing the homework assignments, which included purchasing a new book, starting to read it in the café, and turning off the TV every night at 9:00 P.M. and reading. In addition, they agreed that Mark would re- turn a telephone call of an old friend, Mary, who lived in his neighborhood and had been trying to contact him recently.
Session 4
Mark arrived for Session 4 with little improvement in the severity of his depression. He reported that he had increased his social contact but was not feeling any bet- ter. Mark also had delayed the task of purchasing the new book and continued to watch TV late at night. The therapist addressed both of these problems in a direct, matter-of-fact way, with curiosity and interest.
MARK: It was a really bad weekend. I did call Mary and ended up going to this kind of cocktail party at the community pool that she had organized. I was kind of shocked that I went, but I thought being outside would do me good. I was thinking about what we were talking about, and I thought about how much I used to love swimming. I was actually a lifeguard during summers in college. But I think I felt worse after I went. I suppose there were mo- ments that were fun, but I was so frustrated by it all. I just spent the rest of the weekend holed up in my apartment.
THERAPIST: Would that be good to put on the agenda?
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Doing things that you used to enjoy and not enjoy- ing them?
MARK: Sure. THERAPIST: And I want to make sure we check in about
how it went with the book versus the TV, too. Which do you want to talk about first—calling Mary and the party or the TV?
MARK: I guess we can do the TV first. I just bought the book today. On Friday, I was at that party, so I didn’t get home and in bed until midnight.
THERAPIST: Did you watch TV then? MARK: No, I do think I was more tired from being
outside all night, so I just fell asleep when I got back. THERAPIST: And what about Saturday and last night? MARK: It was kind of par for the course. I stayed up
late both nights.
Given the importance of attending consistently and regularly to the completion of homework, here the ther- apist assesses what interfered with Mark’s full comple- tion of the previous assignment.
THERAPIST: I’m glad you bought the book. That’s ter- rific! I’m curious, too, though, about what got in the way of getting it sooner. Am I recalling correctly that you were going to buy it on the way back from the session last week?
MARK: Yeah, I was, but when I left, someone called me from work about needing to meet, so I didn’t have as much time as I thought. But I thought I could do it after work, and then in the evening, I thought, “I’ll get it on the weekend because I’ll have more time.” I don’t know.
THERAPIST: If you go back to your leaving the session last time, when you got the phone call from work, was there anything else that derailed the plan?
MARK: No, that was really it. I was still pretty optimis- tic about getting the book. It was just that I didn’t have as much time as I thought I would, and I had to get to work.
THERAPIST: OK, that is good to know. So your plan was to get the book on the weekend, and you just bought it today. On the weekend, did you think about getting it, or did it just come up again today?
MARK: I did, but I felt so bad after the party I just couldn’t get myself to do it.
THERAPIST: It sounds like you were really down. Do you remember that diagram we used in our first ses- sion to understand the big picture of depression? I think it fits here, too.
MARK: How so? THERAPIST: So, if we think about the party as what
happened, then you felt really down and discour- aged, right? (Pulls out the model and writes in this situation.)
MARK: Definitely. THERAPIST: And you pulled away by staying at home
over the weekend and not buying the book. My guess is that this fueled feeling more discouraged. Is that right?
MARK: Totally. I thought, good heavens, I can’t even do a simple thing like buy a damn book.
THERAPIST: That’s it, so there is that downward spiral getting set into motion.
MARK: It’s it exactly. I wanted to do less and less and I felt worse and worse.
THERAPIST: It’s great that you can see how these are all connected. I’m curious how it was that you got yourself to get the book today. Are you feeling better, or is it something else?
MARK: I’m not feeling quite as bad, and given that I was already out, it was easier to go get the book. Plus I knew that we were going to meet and you were probably going to ask me about it.
THERAPIST: That is so great to know! So one thing we know is that I have got to keep following up about these things because it helps you do them.
MARK: (laughing a little) True, not that I enjoyed imag- ining being called to task on it, but it did help, I guess.
THERAPIST: And getting yourself out of the house to buy a book this weekend was a lot harder than get- ting yourself out this morning, since you were al- ready leaving to go to work. Being out already made it easier to accomplish your task.
MARK: Right. That sort of thing seems to happen a lot lately.
THERAPIST: So one solution would be to not wait for the weekend when you’ve got a specific task to do, because that seems to be a harder time for you to ac- complish things. The other thing would be for us to set up a system of phone check-ins when you are feel-
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ing particularly down, since it seems to help to know that we will be following up on these tasks when we meet. The other issue, though, is to figure out what brought you down so much this weekend, and what to do about that.
MARK: I think that is the biggest thing. THERAPIST: Shall we talk a bit about the party and the
weekend in order to figure out what is going to help most? How does that sound? And we’ll make sure to come back to the TV and reading plan.
MARK: OK. I would like not to feel as lousy as I was feeling.
THERAPIST: Why don’t we take a look at your Activity Record? (Reviews the record.) It looks like your mood ratings were moderate on Thursday and Friday after we met. Then, Friday, at the party and for the rest of the weekend, they were high—7’s, 8’s, and 9’s, too.
MARK: I’m not sure this is for me, honestly. I think I gave it a fair shot, calling Mary, going to the party. I didn’t want to do either, but I did. And I felt worse afterwards.
When clients report that they are increasing activa- tion and their mood is not improving, it is important to assess a number of possible explanations. First, thera- pists may consider whether the activation assignments were too ambitious and did not incorporate successful grading. In such cases, it is important for therapists to acknowledge responsibility for this and recommend an assignment based on smaller components of the task. Second, therapists want to consider whether the func- tional analysis was accurate. Is it possible that they are activating the client in a domain that is unlikely to yield improvements in mood? Third, therapists want to con- sider whether ruminative thinking is interfering with activation. In such cases, clients “physically” engage in the activation assignments, whereas “mentally” they re- main disengaged from their context and are less likely to have an opportunity to experience reward. Fourth, it is possible that although activation may not immedi- ately improve mood, it may still be “on the right track,” because clients are taking active steps toward solving problems and addressing important life goals.
In Mark’s case, the therapist decided initially to pursue the possibility that rumination was interfering with activation, based on Mark’s comments in earlier sessions about frequently ruminating about Diana and their divorce.
THERAPIST: I guess one thing we could explore to- gether is what was on your mind during the party. When you were standing by the pool talking to other people, or even swimming in the water, what was on your mind?
MARK: You know, when I was diving into the water, I do remember that those were the pleasurable mo- ments of the party. The sound of the water splashing, the coolness, the silence under the water, that was all great. That is what I used to love about swim- ming, too. But the other part—I think I was men- tally checking out. I was with a lot of people I really like. Mary is great, and her whole family was back visiting from the East Coast. I haven’t seen them in years, and I really enjoy all of them. They are great people. But it didn’t really matter. I just wasn’t there.
THERAPIST: Were you thinking about Diana or your- self in relation to her?
MARK: Yeah, that was mainly it. THERAPIST: Were the other folks there conversing with
you? MARK: Yes, and I was talking with them. I mean, I
could hear the words coming out of my mouth, but I was just not there.
THERAPIST: So you have one rating on this record for the party, a 7. But, if we were to break these different pieces apart—the swimming, when you were fully engaged with the activity, and the talking, when your mind was elsewhere—what would you rate each?
MARK: The swimming . . . it was good. I guess that would be a 3, if 0 is feeling good; I mean it didn’t take it all away. But the talking . . . that was terrible, a 9.
The therapist has successfully identified the problem that was interfering with the potential benefits of acti- vation. She continues to assess the nature and scope of the problem.
THERAPIST: I’m trying to figure out if when you are actively engaged in an activity that kind of requires some attention to it, are those the times that are more enjoyable?
MARK: Yeah, that’s true. THERAPIST: Is this a problem that also interferes with
your mood and accomplishment of tasks at work? MARK: Yes, exactly. I go into my office and it’s like
Behavioral Activation for Depression 369
where does the time go? Hours go by and I haven’t done a damn thing. I’m just wandering over and over things that happened with Diana, what I said, what I could have said. It’s awful.
THERAPIST: OK, so we know this is an important prob- lem to address. It’s interfering with your enjoyment of times that have the potential to improve your mood, and it’s interfering with managing your job well. Can we spend a little more time on what hap- pened at the party?
MARK: OK. THERAPIST: How would you normally be when talk-
ing with Mary’s family, if you were not thinking about all these things? What would I see differently in those times than what I might have observed on Friday?
MARK: I’d be talking to everyone. I wouldn’t be feeling so bad.
THERAPIST: Yes, that is exactly true. What I’m really curious about is, when you are not feeling so bad, what would you be doing differently? Would you be asking them more questions? Making more eye con- tact? Responding differently?
MARK: Yeah, all of those things. I’d be more active in the conversation.
THERAPIST: So you would be more engaged. MARK: Yes, more engaged. Less of that heavy feeling;
you know, that “this really sucks” feeling.
In the preceding portion of the session, the therapist has begun to define behaviorally what Mark does in in- terpersonal interactions when he is not depressed. Care- fully specifying these behaviors is an important step in developing some possible plans for targeted change in how Mark approaches similar situations.
THERAPIST: Do you think that if you could practice talking, when you weren’t feeling down, more like you normally would with these people that you might feel better?
MARK: I don’t know. THERAPIST: I think the key is to notice what you do in
response to the ruminating and to see whether that is helping or not helping your mood, and then for us to begin to explore what you may need to do differently. It seems that at the party, what you were doing when your mood was better, was to be more engaged.
MARK: It’s true. But, when I’m like this, I don’t have much to say.
THERAPIST: Yes, when you are depressed, you are more quiet and withdrawn.
MARK: Yes, because it’s painful. I see Mary’s parents and I think, “They’ve been married for 30 years. I could have had that with Diana.” Then, I start thinking that she is with someone else. It just goes downhill from there.
THERAPIST: You are absolutely right. There is a lot of pain there. And what’s happened is that in response to that pain, you have narrowed activity in your life. So you not only feel the pain of being reminded of that loss, but also there is not a lot else going on in your life. And even when you are doing things, you are not as engaged, because you are feeling so much pain. I think we need to get you back to doing the things you did before you had the breakup, and be- fore the two of you got together. We need to get you back to your baseline, and once we do that, we can figure out how to get you feeling even better than that.
MARK: It sounds good. THERAPIST: I know you are thinking this is like pie in
the sky, but we can figure out how to do this. The key is to figure out some concrete and manageable steps to help you engage more when you are doing some of these activities, like going to the party. You are right. It’s worlds harder to do when you are not feeling well, but these behaviors are partly why you enjoyed those occasions more in the past. We know that you en- joyed Mary and her family in the past, and we know that you got a lot of pleasure from swimming when your mind was fully present with the activity. So the trick is not only to call your friends, like you did so wonderfully with Mary, but also to go to the gather- ing, and to get yourself really to interact instead of just being there at the party. For times when you find yourself withdrawing into your thoughts, we need to develop specific strategies to help you do less of that. Can you think of anything that would help you do that?
MARK: I don’t know. I just don’t seem to have much to say these days.
THERAPIST: I know it’s hard. There are a variety of things you could try, such as asking more questions, and then closely attending to the response. Or you could focus on something more specific, such as
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voice or facial expression, to keep your mind from wandering. Sometimes it works just to notice that you’ve drifted and to take a deep breath to refocus on your goal in that moment.
MARK: I suppose I could try it. My mind just seems to keep wandering.
THERAPIST: I know. So your job here would be to prac- tice being more vigilant as to when that happens, because it will happen. The more you notice you’re drifting, the more you can practice refocusing your- self back on your friend. Does your mind wander in here?
MARK: I guess a little. THERAPIST: Why don’t we try it in here? Let’s pick
something to focus on, and then you can practice here.
MARK: OK. What do I do? THERAPIST: I’m going to time us for the next 5 minutes
and, as we talk, I want you to practice fully engag- ing in our discussion. Your mind is going to wander, particularly if we are talking about something that reminds you of Diana, I would guess. So let’s pick something you can focus on to bring your atten- tion back to our conversation. How about the sound of my voice, like changes in tone, how I articulate words, the pace of my speech?
MARK: I can try. THERAPIST: Great. So, let’s talk about some options for
social connections that you could make this week- end.
The therapist and Mark continued this discussion for the next few minutes, at which time, the therapist interrupted their conversation to ask Mark for feedback about his experience.
THERAPIST: What did you notice? MARK: I don’t know, maybe you are talking kind of
softly. THERAPIST: How engaged were you with our discus-
sion? Why don’t you give me a rating, with 0 being not engaged at all and 10 being totally engaged?
MARK: I guess maybe 7. It wasn’t that hard here because I was really focused. I guess I did start to think about Diana a little when we were talking about my calling Mary. I did remind myself to pay attention to your voice, and I guess you just sounded so interested. It
made it harder for me to wander off in my thoughts when you seemed to be paying so much attention to what we were talking about.
THERAPIST: That was my impression, too, that your engagement was generally high, and that you did ap- pear to refocus your attention a couple times. That is terrific!
MARK: Yeah, but it was a little strange. I mean, usually people aren’t that focused when they are just talking about usual stuff.
THERAPIST: That is very true. I might have been pay- ing closer attention to what you were doing and say- ing than other folks are in typical social interactions. And this may feel pretty artificial now in general. My guess, though, is that once you get more engaged in social interactions, it won’t be necessary to concen- trate so hard. It will just come automatically again.
MARK: That makes sense.
In this way, the therapist generates a strategy to block avoidance (rumination) by substituting a new behav- ior in the form of attending to direct and immediate experience. Although, in this case, Mark experimented with directing his attention to interpersonal stimuli, clients may also be directed to experiment with atten- tion to other aspects of sensory stimuli, such as sights, smells, and so forth. The in-session behavioral rehearsal is very important, in that it allows the client to practice and receive direct feedback from the therapist, both of which increase the likelihood of success outside of the session. The therapist then returns to the specific task of reviewing and developing behavioral assignments for the next session.
THERAPIST: Let’s go back to your not getting out all weekend. Do you think going out to buy the book was too hard? Is there something easier you could’ve done to help you get a little more engaged this week- end?
MARK: I’m not sure. How hard is it to go out and buy a book?
THERAPIST: Very hard, when you’re really down. Let’s think about smaller steps. If you can do a smaller step and get a little reinforcement for it, then it be- comes easier to move toward your goal.
Therapist and client continue along these lines with graded task assignment. Given that Mark has previ-
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ously enjoyed socializing, he and the therapist came up with a plan that on the weekend, he would start by returning some phone calls from friends and inviting Mary for lunch. During lunch, he would focus specifi- cally on attending to their conversation. The therapist also raised the possibility of swimming as an exercise activity. Mark reported that he thought his plate was full with the assignments they had already developed, and they decided to table further discussion of swim- ming. The therapist then uses the final moments of the session to review the homework, to encourage progress, to validate the difficulty of change, and to reinforce the basic treatment model.
Session 5
At the outset of the session, Mark reports improvement in his mood, and the therapist includes this as an item on the agenda. Their discussion allows the therapist to emphasize an important point about maintaining new behaviors in consistent and regular routines. In this ses- sion, the therapist continues to emphasize the pattern of social connections and to assess factors that increase Mark’s vulnerability to exacerbated mood when alone.
THERAPIST: Let’s understand in more detail how it is that you are feeling better?
MARK: I think the reading plan is helping. I finished the book.
THERAPIST: Great! So you probably need another book. MARK: (laughing) I guess that’s true. You don’t think
just the one cured the problem? THERAPIST: (laughing) Oh, how I wish that were the
case! Seriously, though, Mark, I think that is such an important question. There is a real temptation when you start feeling a little better to back off from some of the very things that are helping. It makes sense, because making these changes requires so much ef- fort, I know. But maintaining the routines are so im- portant.
MARK: It’s true. I actually think I’ve been doing pretty well with that this week. I’ve been reaching out more to other people.
THERAPIST: This is fantastic. MARK: And Mary called me again. So, I guess I didn’t
do what we talked about in terms of calling her, but I did ask her about lunch when she called. I didn’t really want to, because I was feeling down when
she called. I had just gotten a letter from the lawyer about some new money stuff with Diana. But I did ask Mary, and I took the girls, too. I think they en- joyed it a lot. I did really focus on asking them all a lot of questions during lunch. I think that helped, too.
THERAPIST: Mark, you have definitely had more social contact in the last few days! You are doing a huge part of this treatment, which is acting in accordance with the goals and plans that we are setting here, as opposed to being directed by how you feel in the mo- ment.
MARK: I tried. THERAPIST: You did it! You talked about having lunch
with your coworker. Did you do that? MARK: I did do that. THERAPIST: You did a lot! That’s great. OK, I may be
pushing our luck here, but what do you think about adding swimming to our agenda?
MARK: I knew you were going to ask about that again. THERAPIST: (laughing) You know me too well. What’s
your thought about it? MARK: It’s probably a good idea. There is actually a
swim lesson that the girls like to do on the weekends, and I could take them and do laps at the same time in the other pool.
THERAPIST: Fantastic! Do you have them with you this weekend? Could we schedule that for the weekend?
MARK: Yeah, I think that would help. THERAPIST: Mark, do you think that reconnecting
with people and some of these activities, like reading, are connected with your improved mood?
MARK: Yes, that definitely had a lot to do with it. I am still not sure that we are getting to the real problem with all of this, but you are right that it does help.
THERAPIST: So we should talk about that, too. Before we move to that, is there anything else that you think is contributing to your positive mood, or is it mostly having more social contact, which you find reinforc- ing?
MARK: It’s the social contact and trying to distract my- self with the reading.
THERAPIST: That is so great! Good reminder, too. Let’s talk some about another book and how to keep up that schedule.
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At this point, the therapist and Mark focus on devel- oping a specific plan for selecting and purchasing a new book to continue the reading routine. Next, the thera- pist returns to Mark’s comments about whether the in- terventions are addressing what is most important.
THERAPIST: What you mentioned before about the real problem . . . I’m curious what you meant.
MARK: I guess I’m still thinking about Diana a lot. I think that there is a part of me that has to let go, yet just isn’t letting go. I am thinking, just asking myself, “Is there still a chance for us? What did I do to screw it all up so badly?” And then I start thinking, “Is this all I have now—having lunch with people, read- ing by myself at night?” You know, the kind of stuff we’ve been focusing on . . . I don’t know. Is it really going to fix anything?
THERAPIST: Mark, I know it feels like this stuff isn’t really getting at the real problem in terms of your thinking about Diana, and I agree that is really im- portant to talk about. At the same time, I don’t want us to lose sight of the fact that this other stuff makes a huge difference. It’s important for you to reconnect with ways to buoy up your mood before you start to tackle some of the past problems and those that still come up with Diana. Also, I think we will find that there are some similar patterns, so maybe the ways you have tended to pull away from other people since you’ve been down might have some connections with what happened with Diana.
MARK: That’s true. I guess they are not totally separate. THERAPIST: Are you saying that it’s time now to start
focusing our time more directly on those topics?
MARK: I think so. Maybe I’m more aware of it because I’m feeling a little better. I guess I’m asking more often, “Is this all there is now?” It just seems like a damn lonely life to be leading, if this is it.
The therapist and Mark end the session by reviewing the assignments. In addition, they agree on a plan to re- turn to Mark’s important questions in the next session.
Sessions 6–9
In this next series of sessions, the therapist and Mark return to Mark’s question from Session 5. In repeated sessions, he reports improvements in mood related to making progress on projects at home, exercising, and becoming more socially connected in casual and friend- ship circles. These areas of progress are reflected consis- tently on his Activity Record forms, which now specifi- cally target the areas of social engagement, reading, and swimming (see Figure 9.4). (This version of the Activity Record can be considered when the activation targets are clear and well developed, and the detailed informa- tion gained via hour-by-hour monitoring is not as nec- essary. It can also be used for clients who have difficulty with the more detailed Activity Record.)
Even with clear areas of improved activation and mood, Mark also reports that his mood is vulnerable to his tendency to ruminate frequently about his ex-wife. The therapist and Mark begin to explore the potential function of rumination about his ex-wife. As they did with respect to both TV watching and rumination dur- ing social interactions, they develop some initial hy- potheses about the consequences of Mark’s ruminating about his ex-wife.
FIGURE 9.4. Sample completed Activity Record (daily).
Task Monday Tuesday Wednesday Thursday Friday Saturday Sunday
Reading
Reaching out to other people
Swimming
Mood 5 5 5 6 8 3 3
Behavioral Activation for Depression 373
THERAPIST: Is it possible that ruminating might be a form of avoidance itself? It’s like your mind gets stuck in a broken record format. You keep replaying what you did wrong, what you could have done, and one of the effects is that you are actually avoiding the painful emotions about the loss of the relation- ship, and maybe also avoiding exploring new rela- tionships?
MARK: It feels like I can’t stand the loss of it. That’s what I can’t accept—that it is lost. I keep thinking maybe there is a way to recapture it, even though I know there simply is not. We can’t even communi- cate about the kids’ health care without a lawyer.
THERAPIST: So, in a way, ruminating may be a way to avoid feeling grief and sadness. I wonder if part of this comes from what you learned about how to cope with major loss after your dad left. It seems like no one talked about that and you got pretty caught up in thinking about how you might have been respon- sible. I wonder if it’s hard to know what to do emo- tionally right now.
MARK: It’s certainly true about what happened when I was a kid.
THERAPIST: So one possibility we could experiment with is taking time specifically to experience the sad- ness and loss.
MARK: I don’t know. Thinking about her and what I’ve lost seems overwhelming. I just want to be done with it and move on.
THERAPIST: I know. Exactly! The problem is that rumi- nating seems to have the effect of keeping you from moving on. Instead of moving onto other relation- ships or pursuits in your life, your mind keeps replay- ing what happened and didn’t happen with Diana.
MARK: I just don’t know if I’m ready for other relation- ships.
THERAPIST: So, if you weren’t ruminating as much, do you think you might experience more fear?
MARK: When I think about getting into another rela- tionship. . . . You know, I think that there is actu- ally a person at work who is interested in dating, but that’s been part of the reason that I’ve kind of held back from doing things with her. She’s asked me to lunch a couple of times. I just don’t want to be back in the same place again 2 years from now. I can’t take this whole thing again, and I don’t want to subject my kids to it either.
THERAPIST: So, it may be possible that ruminating has the effect of keeping at bay not only feelings of loss about Diana but also fears about future loss.
The therapist also emphasized the importance of continuing with activation plans developed in earlier sessions to maintain adaptive routines and improve mood. In particular, they highlight the need for consis- tent attention to social contact, exercise, and reading. In addition, the therapist and Mark discuss his return to the writers’ group into more detail, beginning to break down that larger task into manageable pieces. Work on these targets forms the majority of the middle of the course of treatment. As Mark begins to address feelings of loss more directly and continues his work on social connections, exercise, and limiting TV watching, he also begins to express interest in dating again.
Sessions 10–15
In this section of treatment, the therapist and Mark begin to address directly the prospect of his developing new intimate relationships in his life, specifically with a woman at work to whom he is attracted. They explore what is necessary to approach rather than avoid Mark’s fear of starting a new relationship, and the therapist hypothesizes in particular that Mark’s ruminative style may have functioned to avoid learning from patterns in past relationships. The therapist used the TRAP/ TRAC acronym as a simple way to help Mark recognize the conditions under which he was likely to avoid (the TRAP), and to then engage in more adaptive coping behavior to get back on “TRAC.” For example, Mark reported that he would see the woman at work (trig- ger), begin to feel nervous (response), and either not talk with her or restrict his conversation to perfunc- tory work issues (the avoidance pattern). His alternative coping under the same conditions involved asking her if she would like to have coffee. Sessions then focus heavily on examining in detail what Mark might learn from his former marriage that would be instructive in future relationships. The following dialogue provides an example of the types of foci that these sessions tar- get.
MARK: One of the things that happened a lot with Diana is I never felt like I was really present with her or the girls. It was like they were in this little world together and I was always on the outside somehow. I often thought that I should put myself more in the
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center, like say more of what I thought, but I just didn’t. I never did.
THERAPIST: Did that cause conflict with her? MARK: Yes, absolutely. It was one of things that she said
when she ended things. Being on the outside is a big thing for me.
THERAPIST: What does being on the outside involve specifically? How would I know if you were doing that?
MARK: It’s just not being willing to speak up about things. She always said it was like I wasn’t really in or out on anything, just kind of on the fence the whole time.
THERAPIST: Can you think of a specific example when that was an issue?
MARK: Well, my mother and brothers never really liked Diana very much, but I didn’t do much to stand up for her with them. I just kind of let things unfold. . . .
THERAPIST: So, that might have been a TRAP with her? Was it a trigger that you thought she wanted something from you in terms of your commitment?
MARK: Yes, it was, because I ended up feeling really overwhelmed by that.
THERAPIST: And the avoidance pattern was withdraw- ing.
MARK: I did. I just backed off, and she had to handle the whole scene with my family.
THERAPIST: So with your coworker, if you were to take a stand with her now, what would that look like? What would alternative coping be?
MARK: I have no idea. THERAPIST: Do you think there is a similar trigger? MARK: Maybe, because I think she is wondering what’s
up with me? Like am I interested or not? THERAPIST: Have you been clear with her about being
interested in dating her? MARK: Not really. We talk often at work, but I can’t say
that I’ve really said much about it. THERAPIST: Would you like to ask her out? MARK: Yes, I guess I would. THERAPIST: Why don’t we think of some specific
things you could say as alternatives to withdrawing and practice with some of them?
In these sessions, the therapist and Mark define, in very specific and concrete terms, the types of behaviors associated with decreased satisfaction and quality in his former marriage. For instance, the therapist’s following question to Mark is a central question asked repeatedly over the course of BA: “What does being on the out- side involve specifically? What does it look like? How would I know if you were doing that?” The therapist emphasizes identifying clear, specific, and observ- able behaviors when analyzing behaviors and defining goals. Then, the therapist and Mark work to identify specific strategies that he can use to practice alternative behaviors in pursuing a future relationship. They con- tinue to use the TRAP/TRAC framework to examine situations that arise and Mark’s response, and to guide him toward a more engaged approach to intimate in- terpersonal relationships. As Mark begins dating, they have ample opportunity to revise and refine strategies through activation assignments that target being direct and present in intimate interactions.
Sessions 16–19
By Session 16, the therapist and Mark agree that the bulk of the work of understanding and problem-solving Mark’s depression in terms of his unique life context and avoidant response patterns that maintain his de- pression has been completed. Mark has successfully activated in terms of his secondary problem behaviors (e.g., increased reading, exercise, social contacts, and projects around the house; decreased TV watching), and he has taken steps toward solving the problems of grief and fear of intimacy via initiating a new relation- ship.
Thus, the final sessions of treatment focused on re- viewing and consolidating primary themes and meth- ods used in therapy. Specifically, the therapist and Mark identified the importance of continuing to prac- tice his new skills of blocking rumination by attend- ing to immediate goals and to his direct and immediate experience, and being more direct and expressive with his new partner. In addition, the therapist carefully reviewed with Mark the ways he had learned to use the BA fundamentals himself. Together they reviewed ways that Mark would know when he was starting to feel depressed or to engage in avoidance response pat- terns. They also reviewed specific steps he could take to begin self-monitoring his mood and activities, and to problem-solve alternative coping behaviors. They also specifically identified a number of alternative behaviors
Behavioral Activation for Depression 375
that were uniquely helpful in breaking the vicious cycle of depression, avoidance, and withdrawal; these anti- depressant behaviors included, for example, exercise, calling a friend, and reading. Mark reported that he felt well equipped with these tools and the opportunities he had had to practice them in therapy. He also reported feeling encouraged about the positive changes he had already made in his life. He ended treatment express- ing optimism about his future and warmly thanked the therapist for all of their work together. Over time, Mark continued to maintain the gains he made in treatment. He established a new relationship with a woman, and they became engaged over the course of the follow- ing year. He continued to practice many of the skills he had learned in therapy in the context of this new relationship, with his children, and with his coworkers and friends.
Case Summary
The course of treatment with Mark provides an example of many of the core principles and strategies of BA. The treatment followed from careful and ongoing function- al analysis of key problems that Mark presented, which in turn allowed the therapist to develop the organizing case conceptualization. This work was completed in collaboration with Mark during sessions and was also a focus of the ongoing clinical consultation team meet- ings, of which Mark’s therapist was a member. During treatment, the therapist used a range of specific strat- egies, including goal setting, self-monitoring, graded task assignment, problem solving, behavioral rehearsal, and attention to experience. She also addressed a num- ber of important treatment targets frequently observed in BA, including interpersonal avoidance, rumination, and routine disruption.
Overall, the therapist worked as a coach throughout therapy, helping Mark to problem-solve specific steps to overcome patterns of avoidance and to engage in ac- tivities. She also taught Mark to identify links between activity and mood, so that they could learn together where to focus time and attention. She used the EN- LIVEN strategies within each session. She maintained the structure of each session and the overall course of treatment, with a sustained focus on learning together and taking action. She maintained a matter-of-fact, nonjudgmental, problem-solving approach to the chal- lenge of treating depression and the difficulties that arose during the course of Mark’s therapy, responding with warmth, encouragement, and understanding. She
relied consistently on the BA model, acknowledging the difficulty of change when depressed and the im- portance of action, especially when mood is low. She re- turned regularly and persistently to an activation focus on the selected targets of change and worked as a team with Mark to support him in learning how to build a life that was rich and rewarding.
CONCLUSION
This chapter has provided the conceptual basics and the how-to specifics that are required to use BA with depressed clients. Evolving from the seminal founda- tion established by the work of Ferster, Lewinsohn, and Beck, BA highlights the power of direct and sustained attention to behavior change. BA aims to help clients become active and engaged in their lives in ways that reduce current depression and help to prevent future episodes. BA therapists help depressed clients to in- crease activities that bring greater reward and to solve important problems. Both outcome research and other converging lines of empirical inquiry suggest that BA holds promise as an efficacious treatment for depression (Dimidjian et al., 2011). Future research will examine in greater detail the process of change in BA and the ease with which BA can be transported to a wide range of clinical practice settings.
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This chapter presents one of the more remarkable developments in all of psychotherapy. Few thera- pists are willing to undertake the overwhelmingly difficult and wrenching task of treating individu- als with “borderline” characteristics, particularly those at the severe end of the spectrum, yet these people are among the neediest encountered in any therapeutic setting. These patients also impose an enormous burden on the health care system. Over the past several decades, Linehan and her col- leagues have developed a demonstrably effective treatment for individuals with borderline personal- ity disorder (BPD) that constitutes one of the most substantial contributions to the armamentarium of the psychotherapist in recent times. What is even more interesting is that this approach blends emo- tion regulation, interpersonal systems, and more traditional cognitive-behavioral approaches into a coherent whole. To this mix Linehan adds her personal experience with Eastern philosophies and religions, yet the authors remain true to the empirical foundations of their approach. In this compre- hensive revision, the authors provide the latest updates and also describe the extension of dialectical behavior therapy (DBT) in recent years to other conditions characterized to some extent by emo- tion dysregulation, underscoring the transdiagnostic nature of this intervention. The fascinating case study presented in this chapter illustrates Linehan’s therapeutic expertise and strategic timing in a way that will be invaluable to all therapists who deal with personality disorders. The surprising and tragic outcome highlights the enormous burden of clinical responsibility inherent in any treatment setting, as well as the practical issues that arise when treatment ultimately fails. —D. H. B.
C linicians generally agree that clients with a diag- nosis of borderline personality disorder (BPD) are
challenging and difficult to treat. As a result, BPD has become a stigmatized disorder that incites negative atti- tudes, trepidation, and concern with regard to providing treatment (Aviram, Brodsky, & Stanley, 2006; Bourke & Grenyer, 2013; Lam, Poplavskaya, Salkovskis, Hogg, & Panting, 2016; Lequesne & Hersh, 2004; Paris, 2005). BPD is prevalent in 1–3% of the general popu- lation in the United States (Lenzenweger, Lane, Lor-
anger, & Kessler, 2007; Tomko, Trull, Wood, & Sher, 2014), with a lifetime prevalence of up to 5.9% (Grant et al., 2008), and can be found across the globe, with little variations in presentation and frequency (Neacsiu, Eberle, Shian-Ling, Fang, & Rosenthal, 2017). While the incidence in the general population may seem low, approximately 9.3% of those who seek outpatient psy- chiatric care (Zimmerman, Rothschild, & Chelminski, 2005), and 20% of those receiving inpatient psychiatric care meet criteria for BPD (Swartz, Blazer, George, &
C H A P T E R 10
borderline Personality Disorder
Andrada D. Neacsiu Noga Zerubavel K. Maria Nylocks Marsha M. Linehan
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Winfield, 1990; Torgersen, Kringlen, & Cramer, 2001), and this patient group consumes a disproportionate amount of resources (Ansell, Sanislow, McGlashan, & Grilo, 2007; Bagge, Stepp, & Trull, 2005; Bender et al., 2001; Bode, Vogel, Walker, & Kroger, 2017; Tomko et al., 2014).
Perhaps of greatest concern is the generally high incidence of suicidal behavior in this population. Ap- proximately 79% of adult clients who meet criteria for BPD have a history of suicide attempts, with 60% of clients reporting two or more attempts, and 32% re- porting five or more attempts (Goodman et al., 2017). Suicide threats and crises are frequent, even among those who never engage in any suicidal or nonsuicidal self-injurious behavior (NSSI; James & Taylor, 2008; Wedig, Frankenburg, Bradford Reich, Fitzmaurice, & Zanarini, 2013). However, there is evidence to suggest that suicide threats might predict suicide attempts, and the authors of this research consider both behaviors to be dangerous (Wedig et al., 2013). Suicidal ideation is also frequent and contributes to the onset and main- tenance of daily negative mood (Nisenbaum, Links, Eynan, & Heisel, 2010). Although much of this be- havior is without lethal consequence, follow-up studies of adults with BPD have found suicide rates of about 7–8%, and the percentage who eventually commit sui- cide is estimated at 3–10% (for a review, see Linehan, Rizvi, Shaw-Welch, & Page, 2000). Among all adults who have committed suicide, from 7 to 38% meet criteria for BPD, with the higher incidence occurring primarily among young adults with the disorder (e.g., Brent et al., 1994; Isometsa et al., 1994). In adolescents, 76% of clients who meet criteria for BPD have a history of suicide attempts, with 51.9% of adolescents reporting two or more attempts, and 15.4% reporting five or more attempts (a significant difference from the percentage of adults who have attempted five or more times; Good- man et al., 2017). Because of these high-risk behaviors, one of the main approaches to addressing suicidality in BPD is to send clients in crisis to inpatient services. Nevertheless, emerging data highlight that hospitaliza- tion during treatment increases the likelihood of at- tempts after treatment, even when researchers control for severity and history of suicidal behavior (Coyle, Shaver, & Linehan, 2018).
Advancements in neuroscience and psychophysiol- ogy demonstrate that self-harm has a differential effect in those who meet criteria for BPD when compared to healthy controls. Specifically, following distress induc- tion, cutting led to a decrease in distress in adults with
BPD, and to an increase in distress in healthy controls (Reitz et al., 2015). Adults with BPD have also been found to self-report negative reinforcement as a main reason for engaging in self-harm behaviors, and NSSI has been shown to most often be preceded by negative emotional experiences that were improved following self-harm behavior (Kleindienst et al., 2008). Further- more, there is evidence to suggest that adults with BPD have less integration of areas within the default mode network (DMN), an area of the brain that has been as- sociated with self-referential and pain processing, such that adults with higher BPD severity might appraise pain as less self-relevant and aversive, as compared to healthy controls (Kluetsch et al., 2012). Also, adoles- cents (mean age 16.4 years) with BPD showed higher pain threshold (lower pain sensitivity) as compared to healthy controls (age matched) in thermal stimuli as- sessed in both hands (Ludäscher et al., 2015).
BPD, as defined in the fifth edition of the Structured Clinical Interview for DSM Disorders (SCID-5; First, Williams, Karg, & Spitzer, 2016), is a disorder that re- flects a pervasive pattern of instability and dysregulation across all domains of functioning. In the 10th revision of the International Classification of Diseases (ICD-10), BPD is defined as a disorder characterized by an endur- ing pattern of unstable self-image and mood, together with volatile interpersonal relationships, self-damaging impulsivity, recurrent suicidal threats or gestures and/ or self-mutilating behavior (World Health Organiza- tion [WHO], 2018). The “gold standard” for the as- sessment of BPD is the Structured Clinical Interview for DSM-5 Personality Disorders (SCID-5-PD; First, Wil- liams, Benjamin, & Spitzer, 2015) and for ICD BPD, the International Personality Disorder Examination (IPDE; Loranger, 1995). In addition to diagnostic in- terviews, researchers and clinicians have found utility in using self-reports such as the Zanarini’s Rating Scale for BPD (ZAN-BPD; Zanarini, 2003) or the Borderline Symptom List (BSL; Bohus et al., 2001, 2007) to get a quick idea of the potential presence and severity of BPD psychopathology.
Adults and adolescents with BPD generally have a highly complex diagnostic profile and are difficult to treat (American Psychiatric Association, 2000; Grant et al., 2008; Miller, Muehlenkamp, & Jacobson, 2008; Winograd, Cohen, & Chen, 2008). In particular, dif- ficulties with anger and problematic interpersonal pat- terns may lead to frequent disruptions in the therapeu- tic relationship (Bourke & Grenyer, 2013; Koerner, Dimeff, & Rizvi, 2021), frequent dropout, and in-
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creased anxiety for providers (Bourke & Grenyer, 2013). Furthermore, over 80% of those who meet criteria for BPD also meet criteria for one or more comorbid condi- tions, with a mean of 3.2 comorbid conditions (Len- zenweger et al., 2007). Specifically, results from the National Comorbidity Survey Replication (NCS-R) show that 60.5% of adults with BPD also meet criteria for an anxiety disorder, 34.3% meet criteria for a mood disorder, 38% meet criteria for intermittent explosive disorder, and 38.2% meet criteria for a substance use disorder (Lenzenweger et al., 2007).
One of these comorbidities that has received special attention in the past two decades is the overlap between BPD and posttraumatic stress disorder (PTSD). In epi- demiological research, 30% of adults with BPD also meet criteria for PTSD (Pagura et al., 2010), whereas in community samples, about 50% of adults with BPD have comorbid PTSD (Harned, Rizvi, & Line- han, 2010). Comorbid BPD–PTSD results in greater functional impairment (Barnicot & Priebe, 2013; Boritz, Barnhart, & McMain, 2016; Harned et al., 2010), poorer quality of life, more comorbid mental health conditions (Pagura et al., 2010), nearly double the risk of suicide attempts (Wedig et al., 2013), greater emotional dysregulation (Jowett, Karatzias, & Albert, 2020), and more than double the frequency of NSSI (Harned et al., 2010; Rüsch et al., 2007) when com- pared to BPD or PTSD alone.
The well-established comorbidity between BPD and PTSD has led some theorists to conceptualize BPD as a trauma-related disorder referred to as complex PTSD (Briere & Spinazzola, 2005; Herman, 1992), which oc- curs as a result of prolonged and repeated experiences of victimization, and includes both standard PTSD symp- toms and problems in emotion regulation, self-concept, and relational capacities. Treatment guidelines have been developed for this population and require a stage- based model in which first stabilization and safety are secured (often via emotion regulation skills training), then trauma processing occurs, and finally reappraisal of traumatic memories into more adaptive views of self, other, and the world (Cloitre et al., 2012; Courtois & Ford, 2009). The current American diagnostic system has rejected the complex PTSD diagnosis and estab- lished BPD and PTSD as distinct, often co-occurring disorders (DSM-5; American Psychiatric Association, 2013), while the WHO international system has estab- lished complex PTSD as a diagnosis in the ICD-10 as of 2018. There has been great controversy over complex PTSD; central concerns contributing to rejection of
complex PTSD include theoretical elements and em- pirical findings, as well as whether a stage-based model is necessary or may potentially both delay symptom re- lief from trauma processing and reinforce the idea that the client is unable to handle trauma processing (Resick et al., 2012). In regard to BPD, complex PTSD does not account for those individuals who meet criteria for BPD but have not experienced traumatic events. On the other side of the controversy, there are theoretical elements and empirical findings that support complex PTSD as distinct from BPD and PTSD (Cloitre, Gar- vert, Brewin, Bryant, & Maercker, 2013; Cloitre, Gar- vert, Weiss, Carlson, & Bryant, 2014), and proponents suggest that the stage-based model facilitates optimiz- ing of patient outcomes and quality of care (Cloitre, 2015; International Society for Traumatic Stress Stud- ies [ISTSS], 2018). As DBT is a principle-based treat- ment grounded in behaviorism, in DBT the diagnos- tic label is less of a driver in clinical decision-making than functional understanding of behaviors. Therefore, given that for many trauma survivors meeting criteria for BPD, life-threatening behaviors (i.e., suicidal be- haviors and NSSI) function to facilitate coping with overwhelming trauma memories and trauma-related emotions, a stage-based model is required in keeping with treatment guidelines for posttraumatic stress re- sponses (Forbes, Bisson, Monson, & Berliner, 2020). As such, the DBT approach is consistent with treatment for complex PTSD, while it does not require endorse- ment of this formulation. Furthermore, the flexibility of the DBT prolonged exposure (PE) protocol, which we discuss later, allows for a safely implemented trauma protocol applied as rapidly as possible for the particular individual.
Linehan (1993), followed by additional theorists, proposed BPD to be a disorder of pervasive emotion dysregulation (see also Conklin & Westen, 2005; Lives- ley, Jang, & Vernon, 1998). Indeed, most BPD criterion behaviors can be defined either as a direct consequence of emotion dysregulation or as responses that function to modulate the aversive emotions (Ebner-Priemer et al., 2015; Linehan, 2015; McMain, Korman, & Dimeff, 2001).
More recent research indicates that problems with emotion dysregulation are common in many other men- tal health disorders (Kring & Sloan, 2010). Adults di- agnosed with a variety of other mental health disorders appear to have emotion dysregulation patterns that are similar to those seen in BPD (Neacsiu, Bohus, & Line- han, 2014). Increased sensitivity and reactivity, when
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compared to controls, has been connected to general- ized anxiety disorder (GAD; Mennin, Heimberg, Turk, & Fresco, 2005), substance dependence (Thorberg & Lyvers, 2006), and social anxiety disorder (SAD) and specific phobias (Etkin & Wager, 2007). Furthermore, the transaction between vulnerability and an insuffi- cient coaching environment is similar to the etiologi- cal theories presented in panic disorder (Barlow, Allen, & Choate, 2004), GAD (Mennin, 2004), and some specific phobias (Cisler, Olatunji, Feldner, & Forsyth, 2010). Thus, pervasive emotion dysregulation is likely relevant to many other clinical populations beyond BPD.
In particular, individuals who have experienced trau- ma, and especially chronic and/or prolonged trauma, are at a greater risk of developing pervasive emotion dysregulation and BPD. There is strong evidence to suggest that traumatic experiences may be a risk factor associated with the development of BPD, particularly if viewed within the contextual complexity of a trans- actional model rather than as direct etiology (Sabo, 1997). Historically, treatments for BPD and PTSD have involved separate protocols and long waiting periods to establish completion of the traditional first stage of treatment for trauma survivors, the stabiliza- tion phase, due to suicidal and NSSI behaviors. Best- practice guidelines for treatment of PTSD indicate that acutely suicidal individuals require stabilization prior to engaging in trauma-focused treatment (Forbes et al., 2020). Individuals with BPD and PTSD who do not engage in suicidal and NSSI behaviors have been included in standard treatment studies of exposure- based and cognitively based approaches to treatment of PTSD and have demonstrated comparable reductions in PTSD severity to adults with only BPD (Clarke, Rizvi, & Resick, 2008; Feeny, Zoellner, & Foa, 2002). Nonetheless, at the end of standard PTSD treatment, despite improvement in PTSD, adults meeting criteria for comorbid BPD and PTSD are less likely to achieve good end-state functioning (i.e., significant reduction in PTSD severity and scores in normal range on anxiety and depression) than for those without BPD (Feeny et al., 2002). Furthermore, exclusion based on suicidal be- havior is problematic given how common this behavior is among adults and adolescents with PTSD, leading to a call for further development of PTSD protocols to in- clude contingencies to address suicidal behavior (Brad- ley, Greene, Russ, Dutra, & Westen, 2005). Harned, Korslund, Foa, and Linehan (2012; Harned, Korslund, & Linehan, 2014) have demonstrated support for an
adaptation of PE (Foa, Hembree, & Rothbaum, 2007) in a DBT PE protocol that is integrated into DBT and includes procedures for addressing suicidal and NSSI behaviors.
This chapter focuses primarily on describing DBT as a treatment of BPD (Linehan, 1993, 2015) and of perva- sive emotion dysregulation. Before describing DBT, we first summarize other treatments for BPD and provide information on their theoretical rationales and support- ing data (when such data are available). We then present the empirical support for DBT as a treatment for BPD and for emotion dysregulation. This is followed by a more in-depth description of DBT—its philosophical roots, underlying theory, and treatment protocols. In addition, because of the large BPD–PTSD comorbid- ity, we discuss the manner in which DBT integrates trauma-informed conceptualizations and treatments when clinically indicated, along with empirical support for specialized protocol integration in the treatment of comorbid BPD and PTSD.
OVERVIEW OF OTHER TREATMENT APPROACHES
Various approaches have been applied to the treatment of BPD. Although it is not our purpose to present a scholarly review of all the many treatments for BPD, we believe it helpful to summarize briefly the status of other treatments before presenting DBT in detail (for reviews, see Choi-Kain, Finch, Masland, Jankins, & Unruh, 2017; Cristea et al., 2017).
Psychodynamic
Psychodynamic approaches currently receiving the most attention include those of Kernberg (1984; Kern- berg, Selzer, Koenigsberg, Carr, & Appelbaum, 1989), Adler and Buie (1979; Adler, 1981, 1993; Buie & Adler, 1982), and Bateman and Fonagy (2004). Among these, Kernberg’s (1984) theoretical contributions are clearly prominent. His expressive psychotherapy, transference- focused psychotherapy (TFP), for clients with “bor- derline personality organization” (BPO) or BPD aims to expose and resolve intrapsychic conflict (Clarkin, Levy, Lenzenweger, & Kernberg, 2007; Mann, 2016). The data supporting the use of TFP are not extensive. In support of this treatment model for BPD are find- ings reported by Clarkin and colleagues (2007) from a multisite randomized controlled trial (RCT) suggesting that TFP (as well as DBT and another psychodynamic
Borderline Personality Disorder 385
psychotherapy treatment included as a control condi- tion) demonstrated improvement in depression, anxi- ety, global functioning, and interpersonal adjustment. In this study, TFP was also associated with significant reductions in suicidality (small effect sizes) and only the psychodynamic treatments, as compared to DBT, resulted in significant reductions in anger (medium effect sizes). According to the Clarkin and colleagues, irritability, physical and verbal assault, and impulsivity only changed in TFP. These results represent within- condition changes, as there were no differences between conditions. TFP was also shown to be superior to con- trol conditions in a secondary analysis including several measures of psychodynamic constructs, such as meta- cognitive and social-cognitive capacities, and reflective functioning (Levy & Scala, 2012). These results must be interpreted with caution. While positive changes were evident in all conditions, the mechanism of change proposed for TFP was not supported, and the compari- son condition was questionable given that it is unclear whether the DBT therapists were adherent to the model. An independent RCT compared TFP with treatment by behavioral and nonbehavioral community experts in a sample of adult women with a diagnosis of BPD (Doer- ing et al., 2010) and found that after 1 year of treatment, TFP was superior in reducing dropout, borderline psy- chopathology, and poor global functioning. This study has been criticized for including all participants in the analyses (regardless of whether they attended any ther- apy session) and for choosing post hoc a statistical test that did not accurately reflect the findings on suicidal behavior (Kleindienst, Krumm, & Bohus, 2011).
Mentalization-based therapy (MBT), developed by Bateman and Fonagy (2004), is an intensive therapy grounded in attachment theory (i.e., BPD is viewed as an attachment disorder), with a focus on relationship patterns and nonconscious factors inhibiting change. MBT has been successfully offered as an 18-month partial hospitalization followed by 18-month biweekly therapy (Bateman & Fonagy, 1999) or as an 18-month outpatient individual and group intervention (Bateman & Fonagy, 2009), and evidence in support of this treat- ment model for BPD comes from two RCTs. The first RCT compared 18 months of treatment as usual (TAU) with MBT for 18 months in a partial hospitalization setting, followed by 18 months of outpatient MBT (Bateman & Fonagy, 1999). Clients were randomly as- signed to either standard psychiatric care without indi- vidual psychotherapy (control condition) or to partial hospitalization, a treatment program. At the end of the
18-month partial hospitalization treatment, those re- ceiving MBT showed significant reductions in suicidal behavior (suicide attempts and self-mutilation), inpa- tient hospitalization stays, measures of psychopathol- ogy (including depression and anxiety), and improved social functioning relative to the control group. These gains were maintained and increased during an 18- month follow-up period that comprised twice-weekly group therapy (Bateman & Fonagy, 2001). Gains were maintained at a 5-year follow-up, although participants in MBT continued to have impairments in general so- cial function (Bateman & Fonagy, 2008). The second RCT (Bateman & Fonagy, 2009) compared 18 months of outpatient MBT with a structured clinical manage- ment (SCM) control condition in a sample of adults with a diagnosis of BPD and a recent history of suicidal behavior. It was, however, unclear from the study de- scription whether participants in both conditions were offered a similar amount of time in therapy. Analyses were conducted at each assessment time point (at 6 and 12 months), and not longitudinally, which makes results difficult to interpret. Nevertheless, substantial improvements in both conditions were reported, with MBT being superior to SCM in reducing suicide at- tempts in the last 6 months, self-injury episodes in the last 12 months, and hospitalization throughout the treatment year. SCM was superior to MBT in reducing self-harm episodes in the first 6 months of treatment. MBT was also found to significantly increase general assessment of functioning (GAF ratings), reduce de- pression, and improve social adjustment, as compared to SCM (Bateman & Fonagy, 2009).
Psychopharmacological
Reviews of the literature regarding drug treatments for BPD highlight a dilemma for the prescribing pharma- cotherapist: BPD involves dysregulation in too many domains for a single drug to serve as a panacea (Dimeff, McDavid, & Linehan, 1999; Lieb, Zanarini, Linehan, & Bohus, 2004; Nose, Cipriani, Biancosino, Grassi, & Barbui, 2006). In general, results indicate that several agents may be useful for improving global functioning, cognitive–perceptual symptoms (e.g., suspiciousness, ideas of reference, transitory hallucinations), emotion dysregulation, or impulsive–behavioral dyscontrol (for reviews, see Hancock-Johnson, Griffiths, & Picchioni, 2017; Lieb et al., 2004; Nose et al., 2006).
Lieb, Völlm, Rücker, Timmer, and Stoffers (2010) conducted a meta-analysis of 27 RCTs and organized
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the evidence based on class of medications. They found that for first-generation antipsychotics, evidence sup- ports the effectiveness of haloperidol in the reduction of anger and flupentixol in the reduction of suicidal be- havior. Thiothixene was found not to be effective. For second-generation antipsychotics, evidence supports aripiprazole’s effectiveness in reducing pathological symptoms of BPD, as well as comorbid psychopathol- ogy. Evidence of the positive effect of olanzapine is ac- cumulating with regard to reducing affective instabil- ity, anger, and psychotic symptoms, although findings for its effect on suicidal behavior are mixed (Lieb et al., 2010). In addition to superiority to placebo, olanzap- ine has been shown to decrease impulsive aggression and chronic dysphoria more effectively than fluoxetine (Zanarini, Frankenburg, & Parachini, 2004). In an open-label RCT conducted in adults with a diagnosis of BPD, olanzapine (5–10 mg/day) was compared with asenapine (5–10 mg/day), and both drugs were found to reduce psychiatric symptoms such as self-harm and impulsiveness. Olanzapine was found to be signifi- cantly more effective in reducing dissociation/paranoid ideation, as compared to asenapine, and asenapine was found significantly more effective in reducing af- fective instability, as compared to olanzapine (Bozza- tello, Rocca, Uscinska, & Bellino, 2017). Olanzapine is consistently found to have a weight gain side effect. Ziprasidone has not been found not to be effective in the treatment of BPD (Lieb et al., 2010).
With regard to mood stabilizers and antidepressants, valproate semisodium was found to have a significant effect in reducing interpersonal problems and depres- sion in clients with BPD, including those with aggres- sive and impulsive behavior (Stein, Simeon, Frenkel, Islam, & Hollander, 1995). Topiramate was found to have a significant side effect of weight loss. Antidepres- sants evidenced limited effectiveness in the treatment of BPD problems. Finally, omega-3 fatty acids were found to reduce suicidality and depression above and beyond placebo (Lieb et al., 2010). A blinded, randomized trial comparing lamotrigine to placebo over a 12-month period found no clinical effectiveness of lamotrigine (Crawford et al., 2015, 2018). The authors of this re- search do not recommend lamotrigine as a treatment for BPD.
In summary, some drug treatments may be effective in treating aspects of the BPD psychopathology. Nev- ertheless, caution is in order when considering pharma- cotherapy for BPD (Starcevic & Janca, 2018). Clients with BPD are notoriously noncompliant with treatment
regimens, may abuse the prescribed drugs or overdose, and may experience unintended effects of the drugs. With these caveats in mind, carefully monitored phar- macotherapy may be a useful and important adjunct to psychotherapy in the treatment of BPD.
Cognitive‑Behavioral
The cognitive approach views the problems of the client with BPD as residing within both the content and the process of the individual’s thoughts. Beck’s approach to treating BPD (Beck & Freeman, 1990) specifically fo- cuses on decreasing negative and polarized beliefs that result in unstable affect and destructive behaviors. In an open clinical trial of cognitive therapy for clients with BPD, decreases in problems associated with BPD, in- cluding depression, hopelessness, and suicide ideation, were found at the end of treatment and during follow- up (Brown, Newman, Charlesworth, Crits-Christoph, & Beck, 2004).
An RCT compared 1 year of cognitive therapy (CT) and Rogerian supportive therapy (RST) pro- vided to adults with a diagnosis of BPD. Participants were offered one session weekly in each condition for 6 months, followed by 12 sessions aimed at maintaining gains over the subsequent 6 months. Cottraux and col- leagues (2009) found that CT was superior to RST in retaining clients in therapy. No additional differences between conditions were found, although CT led to faster reductions in hopelessness and impulsivity than did RST. Follow-up analyses, nevertheless, showed a significant difference between conditions, with partici- pants who underwent CT demonstrating higher clini- cal global improvement than participants treated with RST. Given the small sample size and the large number of dropouts from this study, the effectiveness of CT is still unclear (Cottraux et al., 2009).
The cognitive-behavioral therapies of Young, Klos- ko, and Weishaar (2003; Kellogg & Young, 2006), Pretzer (1990), Blum, Pfohl, St. John, Monahan, and Black (2002), and Schmidt and Davidson (as cited in Weinberg, Gunderson, Hennen, & Cutter, 2006) at- tempt to address some of the difficulties experienced in applying traditional cognitive approaches to the treat- ment of BPD. Pretzer’s approach emphasizes modifying standard CT to address difficulties often encountered in treating clients with BPD, such as establishing a collaborative relationship between therapist and cli- ent, maintaining a directed treatment, and improving homework compliance. Blum and colleagues (2002)
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developed a twice-weekly outpatient group treatment that uses a psychoeducational approach to teaching cognitive-behavioral skills (e.g., distancing, goal set- ting, and problem solving) to clients with BPD and to their support systems (e.g., family, friends, other care providers). The treatment is offered in a group setting and has been tested under the acronym STEPPS (sys- tems training for emotional predictability and problem solving). The treatment focuses on destigmatization of BPD, emotional control, and behavioral control. Bos, van Wel, Appelo, and Verbraak (2011) conducted the most recent RCT on STEPPS. In their study, par- ticipants loosely diagnosed with BPD received either STEPPS and individual therapy or TAU for 18 weeks. STEPPS was found to be more effective in reducing general and BPD-specific psychopathology and im- proving quality of life, as compared to TAU (at the end of treatment, as well as after 6 months following treat- ment). These findings, coupled with prior studies com- paring STEPPS and TAU with rigorously selected BPD samples (Blum et al., 2008; Bos, van Wel, Appelo, & Verbraak, 2010) support the effectiveness and efficacy of this intervention. Young’s schema-focused therapy (SFT; Young et al., 2003; also see Young, Ward-Ciesiel- ski, Rygh, Weinberger, & Beck, Chapter 7, this volume) postulates that stable patterns of thinking (“early mal- adaptive schemas”) can develop during childhood and result in maladaptive behavior that reinforces the sche- mas. SFT includes a variety of interventions aimed at challenging and changing these early schemas through the identification of a set of dysfunctional schema modes that control the individual’s thoughts, emotions, and behaviors (i.e., detached protector, punitive par- ent, abandoned/abused child, angry/impulsive child). Giesen-Bloo and colleagues (2006) completed the first RCT of TFP and SFT. TFP was compared to SFT in a study in which 86 participants received 3 years of twice-weekly individual sessions of either SFT or TFP. Both treatments were found to reduce BPD symptoms; however, SFT was found superior in overall improve- ments and saw a lower attrition rate. A follow-up sec- ondary analysis study also demonstrated that SFT’s cost to implement was 20% lower than the cost needed to implement TFP (van Asselt et al., 2008). Other studies have also found SFT to be effective in reducing BPD symptoms. Indeed, Farrell, Shaw, and Webber (2009) tested the effectiveness of SFT in an 8-month group format (augmenting TAU). When compared to TAU alone, TAU+SFT resulted in significantly higher remis- sion from BPD. Additionally, Nadort and colleagues
(2009) tested a disseminated version of SFT in regu- lar health care centers with or without afterhours crisis support by phone. Data from 62 participants suggested that the added phone availability did not result in ad- ditional improvement, and that across conditions, SFT was successful, leading to 42% recovery from BPD after 1.5 years of treatment.
Last, Weinberg and colleagues (2006) completed an RCT of manual-assisted cognitive treatment (MACT) and TAU. MACT is a brief cognitive-behavioral treat- ment that incorporates strategies from DBT, CT, and bibliotherapy. The treatment targets NSSI behaviors in participants diagnosed with BPD. MACT was provided as an adjunctive treatment to TAU for study partici- pants, 30 women diagnosed with BPD, with a history of NSSI behaviors and at least one in the last month; however, participants with elevated suicide risk and im- mediate suicidal intent were excluded. Participants were randomly assigned to MACT plus TAU or to TAU- alone conditions. Upon completion of the 6-week treat- ment and at the 6-month follow-up, participants who received MACT had significantly fewer and less severe NSSI behaviors than those in the TAU-alone condition. These results should be interpreted with caution due to the small sample size and the use of self-report measures only in assessment of NSSI behaviors.
EVIDENCE FOR DBT AS AN EFFECTIVE BPD TREATMENT
DBT evolved from standard cognitive-behavioral ther- apy as a treatment for BPD, particularly for recurrently suicidal, severely dysfunctional adults. The theoretical orientation to treatment is a blend of three theoretical positions: behavioral science, dialectical philosophy, and Zen practice. Behavioral science, the principles of behavior change, is countered by acceptance of the cli- ent (with techniques drawn both from Zen and from Western contemplative practice); these poles are bal- anced within the dialectical framework. Although dialectics was first adopted as a description of this em- phasis on balance, dialectics soon took on the status of guiding principles that have advanced the therapy in di- rections not originally anticipated. DBT is based within a consistent behaviorist theoretical position. However, the actual procedures and strategies overlap consider- ably with those of various alternative therapy orienta- tions, including psychodynamic, client-centered, stra- tegic, and cognitive therapies.
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Efficacy
Although several treatments (described earlier) have demonstrated efficacy in the treatment of people di- agnosed with BPD, DBT has the most empirical sup- port at present and is generally considered the frontline treatment for the disorder. DBT as a treatment for BPD has been evaluated in a number of controlled trials. Four of the RCTs specifically recruited clients with sui- cidal behaviors (Linehan et al., 1999, 2006; Linehan, Armstrong, Suárez, Allmon, & Heard, 1991; McMain et al., 2009).
Two RCTs included DBT in both conditions, with the addition of medication in one condition (Line- han, McDavid, Brown, Sayrs, & Gallop, 2008; Soler et al., 2005). RCTs have also been conducted to test effectiveness of DBT for adolescents (McCauley et al., 2018; Mehlum et al., 2014). The results in general have shown DBT to be highly effective. In adults diagnosed with BPD who are at high risk for suicide, 1 year of DBT yielded significantly greater reductions in anger outbursts, suicidal behavior, and hospitalization com- pared to TAU (Linehan et al., 1991l Linehan, Tutek, Heard, & Armstrong, 1994; Linehan, Heard, & Arm- strong, 1993), client-centered therapy (CCT, Turner, 2000), and community treatment by nonbehavioral experts (CTBE; Linehan et al., 2006) but not to a dy- namic emotion-focused treatment plus protocol-based pharmacotherapy program (McMain et al., 2009). One study showed that participants treated with DBT were half as likely to engage in suicidal behaviors compared to participants in the CTBE condition, further indi- cating that DBT is an effective treatment for reducing suicidal behavior. During the 1 year of treatment, de- pression, hopelessness, and suicidal ideation decreased in both DBT and control treatments (Linehan et al., 1991, 2006; McMain et al., 2009). Furthermore, there was similar remission from major depressive disorder (MDD) and anxiety disorders in the DBT and in the control condition (Harned et al., 2008), although re- mission from substance dependence was significantly higher in DBT. Treatment superiority was maintained when participants in the DBT condition were com- pared to only those control subjects who received stable individual psychotherapy during the treatment year, and even after researchers controlled for number of hours of psychotherapy and telephone contacts (Line- han & Heard, 1993; Linehan et al., 1999). Superior- ity was also maintained when comparing DBT with a treatment that had equal prestige and was administered
by expert therapist with allegiance to the treatment model (CTBE; Bedics, Atkins, Comotois, & Linehan, 2012; Linehan et al., 2006). These studies suggest that the efficacy of DBT is due to specific treatment factors and not general factors or the expertise of the treating psychotherapists. In RCTs that compared medication (olanzapine) in addition to DBT versus DBT plus pla- cebo, individuals in the medication condition showed a faster reduction in irritability and physical aggression, but the placebo condition showed a greater reduction of NSSI. Both conditions showed reductions in de- pression, irritability, aggression, and NSSI (Linehan et al., 2008). Furthermore, Soler and colleagues (2005) showed that DBT skills training plus olanzapine was more effective than DBT skills training plus placebo in reducing depression, anxiety, and impulsive/aggressive behavior.
Additionally, Linehan et al. (2015) published a dis- mantling study with the aim of testing the multiple components during 1 year of DBT (individual therapy, skills training, telephone coaching, and therapist con- sultation team) in a sample of 99 women with a diag- nosis of BPD with a least two suicide attempts or NSSI acts in the last 5 years. When comparing standard DBT (including all components) to DBT-I (individual ther- apy only) and DBT-S (group skills training only) the authors found greater reductions in NSSI and depres- sion in study conditions that included skills training (standard DBT and DBT-S), and the standard DBT skills group component was found superior in reducing patient dropout, use of crisis services, and psychiatric hospitalizations.
In BPD samples selected regardless of suicide risk, findings are mixed with regard to suicidal behavior; nevertheless, DBT outperforms control conditions in improving indices of emotion regulation. Specifically, in a sample of women veterans, standard DBT for 6 months was found to reduce depression, hopelessness, and anger expression (Koons et al., 2001, 2006). In a sample of adult women, standard DBT was found to reduce self-damaging impulsive acts, compared to TAU (Van den Bosch, Verhuel, Schippers, & van den Brink, 2002; Verheaul et al., 2003). DBT is also effective for adults diagnosed with BPD and a comorbid drug de- pendence disorder (Linehan et al., 1999, 2002).
Evidence also suggests that DBT adaptations are suc- cessful in treating people diagnosed with BPD. Soler and colleagues (2009) found a 13-week DBT skills- only intervention to be more successful in reducing prob- lematic emotions than a psychodynamically informed
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standard group therapy (SGT) for participants meeting diagnostic criteria for BPD. Another study revealed that standard DBT, provided to adults with BPD for 1 year, adapted to include medication management, improved global functioning and social adjustment, as well as reduced suicidality, depression and anxiety (Clarkin et al., 2007). DBT that was adapted to reduce therapy time and incorporate psychodynamic techniques was also found to be more effective, as compared to TAU, in improving mental health functioning and decreasing suicidal behavior in adults with BPD (Turner, 2000). Additionally, Wolf and colleagues (2011) found greater improvement in skills acquisition and knowledge when adding a CD-ROM-based self-help program for adults with BPD as an adjunct to DBT skills training, com- pared to DBT skills training alone. In adults with BPD, Waltz and colleagues (2009) showed that viewing a DBT skills video on “opposite action” versus an infor- mational video (as the control) was effective in reducing emotional intensity and increasing skill use. Indeed, at follow-up, 80% of participants had used the skill (op- posite action) at least once.
Bohus and colleagues (2004) compared a 12-week inpatient DBT adaptation with TAU for females di- agnosed with BPD who reported a history of suicidal behavior and found DBT to be superior in reducing symptoms of depression and anxiety. Moreover, in a self-harming subsample, significantly more patients in DBT than in TAU abstained from NSSI at posttreat- ment (62 vs. 31%). Roepke and colleagues (2011) also found that a 12-week inpatient course of DBT resulted in significant improvement in depression and self- esteem when compared to TAU for women diagnosed with BPD. In a different sample of adult women with a history of NSSI (at least three episodes in the last year), standard DBT for 6 months was effective in reducing disability (days spent in bed) and improving quality of life, as compared to TAU (wait list). In this study, number of NSSI episodes and number of hospitaliza- tions were reduced in both conditions (Carter, Willcox, Lewin, Conrad, & Bendit, 2010).
Beyond BPD, studies have demonstrated the effec- tiveness of DBT in other clinical populations. Lynch, Morse, Mendelson, and Robins (2003) compared stan- dard DBT in combination with medication to medi- cation alone in older depressed adults and found that DBT achieved quicker remission from MDD. Also in older depressed adults, DBT skills training plus 30-minute phone coaching per week (for 7 months), in combination with medication, was found more effec-
tive than medication alone in achieving remission from major depression (Lynch et al., 2007). Standard DBT (1 year) has been found to reduce dysfunctional eating behaviors and attitudes, severity and use of substances, and improve ability to cope and regulate negative emo- tions in adult women with an eating disorder and sub- stance abuse or dependence (Courbasson, Nishikawa, & Dixon, 2012). In adolescent females with anorexia or bulimia nervosa, an adapted version of DBT (25 weeks) was compared to CBT, as well as to a wait-list condition, and found effective in reducing eating dis- order symptoms (62.5% remitted in DBT group and 57.9% remitted in CBT group, whereas 0% remitted in the wait-list group) and the DBT intervention pro- duced small positive effect sizes in emotion regulation (Salbach-Andrae et al., 2009). DBT skills training has also been adapted for adults with binge-eating disorder and compared to an active comparison group therapy (manual-based supportive group therapy designed to control for nonspecific therapeutic factors), with both treatment conditions offering 20 weekly sessions and asking patients to monitor binges and self-esteem, as well as complete a Weekly Diary Card (Safer & Joyce, 2011; Safer, Robinson, & Jo, 2010). These studies showed that DBT skills training produced similar post- treatment bingeing abstinence and a moderate effect size favoring DBT in self-reports on restraining and eat- ing concerns. Evershed and colleagues (2003) adapted DBT for a residential forensic sample of males receiving inpatient treatment in a high-security hospital. This study showed that DBT (provided for 18 months) was more effective, compared to TAU, in reducing serious- ness of violent incidents and self-reported hostility and anger. Another study adapted DBT to treat PTSD in an inpatient setting (Bohus et al., 2013; see details of treatment modification in Bohus et al., 2019). This treatment approach was tested in adult women referred for childhood sexual abuse; the study revealed that the adapted version of DBT (provided for 3 months) was superior to TAU (wait list) in remission of PTSD (large effect sizes). Last, standard DBT for 1 year has also been found effective in reducing aggression and anger expression in adults with a cluster B personality disor- der (Feigenbaum et al., 2012).
Two RCTs have been conducted to test effectiveness of DBT in adolescents with high risk for suicidal and self-harm behaviors (McCauley et al., 2018; Mehlum et al., 2014). Broadly, these RCTs show that compared to both supportive group therapy (McCauley et al., 2018) and enhanced usual care (Mehlum et al., 2014), DBT
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is superior in reducing self-harm, suicidal ideation, suicide attempts, and depression. Secondary analyses have also shown long-term (3-year follow-up) effec- tiveness of DBT for adolescents in reducing self-harm (Mehlum et al., 2019). Also in adolescents, a residen- tial DBT program was found to significantly decrease behavioral problems, as compared to TAU (Trupin, Stewart, Beach, & Boesky, 2002). Moreover, residential DBT that was adapted due to lack of resources was ad- ministered with adolescents at KidsPeace and was more effective than the control condition (standard therapeu- tic milieu) in reducing overall psychopathology. Both treatment conditions in this study were found to sig- nificantly reduce depression, and the control condition was more effective than DBT in reducing psychomotor excitation (Wasser, Tyler, McIlhaney, Taplin, & Hen- derson, 2008). DBT has also been found to be an effec- tive treatment for suicidal adolescents (Barnoski, 2002; Katz, Cox, Gunasekara, & Miller, 2004; McDonell et al., 2010; Rathus & Miller, 2002). For example, Mc- Donell and colleagues (2010) found significantly fewer NSSI episodes during 1 year of DBT treatment in a residential setting, as compared to residential TAU, and Rathus and Miller (2002) showed that an adapted DBT treatment protocol (lasting for 12 weeks, with twice- weekly sessions) was more effective in reducing psychi- atric hospitalizations than TAU in adolescents with a suicide attempt in the last 16 weeks. DBT has also been found effective in decreasing NSSI, use of psychotropic medication, and suicidality, and increasing quality of life in suicidal college students, as compared to supervi- sion by experts in psychodynamic treatments (Pistorel- lo, Fruzzetti, MacLane, Gallop, & Iverson, 2012). In addition, residential DBT (17 weeks) versus no treat- ment was found to improve control in interpersonal re- lationships, social networks, intentionality, and global functioning, in a sample of patients at a young adult services residential program (Rakfeldt, 2005).
EVIDENCE FOR DBT AS AN EFFECTIVE TREATMENT FOR EMOTION DYSREGULATION
As noted earlier, many mental disorders, including BPD, can be conceptualized as disorders of emotion regulation with deficits in both emotion up-regulation and down-regulation (Neacsiu et al., 2014). Once one realizes that emotions include both actions and ac- tion tendencies, one can see the link between emotion dysregulation and many disorders defined as behavior
dyscontrol (e.g., substance dependence). In addition, problems with recognizing emotions, describing and la- beling emotions, knowing what to do when an emotion is on the scene, and emotional avoidance are common in many mental health disorders. An important theo- retical premise in DBT is that people who exhibit emo- tion dysregulation lack the skills needed for successful regulation. DBT includes a set of skills aimed at im- proving emotion regulation in BPD in particular, and in people who report emotion dysregulation in general. DBT is formulated to provide skills training integrated into a comprehensive behavioral psychotherapy aimed at reducing suffering and building resilience.
An increasing number of RCTs suggest that DBT skills training alone is a promising intervention for a variety of populations. Specifically, DBT skills train- ing has been adapted and shown effective for treat- ment-resistant depression (Feldman, Harley, Kerrigan, Jacobo, & Fava, 2009; Harley, Sprich, Safren, Jacobo, & Fava, 2008), bipolar disorder (van Dijk, Jeffrey, & Katz, 2013), binge-eating disorder (Safer et al., 2010; Safer & Joyce, 2011; Telch, Agras, & Linehan, 2001), bulimia nervosa binge–purge behaviors (Hill, Craig- head, & Safer, 2011; Safer, Telch, & Agras, 2001), and attention-deficit/hyperactivity disorder (ADHD) in a Swedish population (Hirvikoski et al., 2011). DBT skills training has also been modified as a group thera- py component for incarcerated women with a history of interpersonal violence (Bradley & Follingstad, 2003), as a 16-week treatment for adults with high emotion dysregulation (Neacsiu, Eberle, Kramer, Weismann, & Linehan, 2014), and as treatment for adult males at risk for interpersonal violence perpetration (Cavanaugh, Solomon, & Gelles, 2011). In several of these varied populations, DBT skills training resulted in significant- ly greater reductions in clinical targets, as compared to the control condition. Indeed, DBT skills training was found to decrease symptoms (significantly more than the control) of depression, emotion dysregulation, and trauma symptoms (Bradley & Follingstad, 2003; Feld- man et al., 2009; Harley et al., 2008; Hill et al., 2011); improve anger management skills, adaptive coping, and empathy; decrease risk for interpersonal violence (Cava- naugh et al., 2011); improve emotion regulation, affect control, anxiety severity; and increase skill use (Neacsiu et al., 2014). The majority of these studies offered only the skills training component of DBT. Thus, although skills training was originally developed to be part of a comprehensive intervention, the number of studies sug- gests that DBT skills training by itself can be a success-
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ful intervention for a variety of populations with emo- tion regulation difficulties. Furthermore, DBT skills use (the product of skills training) has been shown to be an active mechanism of change for emotion regula- tion outcomes in treatment for BPD (Neacsiu, Rizvi, & Linehan, 2010).
DBT TREATMENT OVERVIEW
Philosophical Basis: Dialectics
The term dialectics as applied to behavior therapy re- fers both to a fundamental nature of reality and to a method of persuasive dialogue and relationship (see Wells, 1972, cited in Kegan, 1982, for documentation of a shift toward dialectical approaches across all the sciences during the last 150 years; more recently, Peng & Nisbett, 1999, discussed both Western and Eastern dialectical thought). As a worldview or philosophical position, dialectics guides the clinician in developing theoretical hypotheses relevant to the client’s problems and to the treatment. Alternatively, as dialogue and re- lationship, dialectics refers to the treatment approach or strategies used by the therapist to effect change. Thus, central to DBT are a number of therapeutic dialectical strategies.
Dialectics as a Worldview
DBT is based on a dialectical worldview that empha- sizes wholeness, interrelatedness, and process (change) as fundamental characteristics of reality. The first char- acteristic, the principle of interrelatedness and whole- ness, provides a perspective of viewing the system as a whole, and how people relate to the system, rather than seeing people as if they exist in isolation. Similar to con- textual and systems theories, a dialectical view argues that analysis of parts of any system is of limited value unless the analysis clearly relates the part to the whole. The second characteristic is the principle of polarity. Although dialectics focuses on the whole, it also em- phasizes the complexity of any whole. Thus, dialectics asserts that reality is nonreducible; that is, within each single thing or system, no matter how small, there is polarity. For example, physicists are unable to reduce even the smallest of molecules to one thing. Where there is matter, there is antimatter; even every atom is made up of both protons and electrons: A polar oppo- site is always present. The opposing forces are referred to as the thesis and antithesis, present in all existence.
Dialectics suggests that the thesis and antithesis move toward a synthesis, and inherent in the synthesis will be a new set of opposing forces. It is from these op- posing forces that the third characteristic is developed. This characteristic of the dialectical perspective refers to the principle of continuous change. Change is pro- duced through the constant synthesis of the thesis and the antithesis, and because new opposing forces are present within the synthesis, change is ongoing. These dialectical principles are inherent in every aspect of DBT and allow for continuous movement throughout the therapy process. A very important dialectical idea is that all propositions contain within them their own oppositions. Or, as Goldberg (1980, pp. 295–296) put it, “I assume that truth is paradoxical, that each article of wisdom contains within it its own contradictions, that truths stand side by side. Contradictory truths do not necessarily cancel each other out or dominate each other, but stand side by side, inviting participation and experimentation.” One way that client and therapist ad- dress this is by repeatedly asking: “What is being left out?” This simple question can assist in finding a syn- thesis and letting go of an absolute truth (i.e., dogma), a nondialectical stance.
Dialectics as Persuasion
From the point of view of dialogue and relationship, dialectics refers to change by persuasion and by mak- ing use of the oppositions inherent in the therapeutic relationship rather than by formal impersonal logic. Through the therapeutic opposition of contradictory positions, both client and therapist can arrive at new meanings within old meanings, moving closer to the essence of the subject under consideration. The spirit of a dialectical point of view is never to accept a propo- sition as a final truth or an undisputable fact. Thus, the question addressed by both client and therapist is “What is being left out of our understanding?” Hold- ing a dialectical stance invites curiosity and idiographic data collection, and scaffolds cognitive flexibility for DBT therapists and clients. Dialectics as persuasion is represented in the specific dialectical strategies we de- scribe later in this chapter. As readers will see when we discuss the consultation strategies, dialectical dialogue is also very important in therapist consultation meet- ings. Perhaps more than any other factor, attention to dialectics can reduce the chances of what psychody- namic therapists have labeled “staff splitting,” that is, the frequent phenomenon of therapists’ disagreeing or
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arguing (sometimes vehemently) about how to treat and interact with an individual client who has BPD. This “splitting” among staff members is often due to one or more factions within the staff deciding that they (and sometimes they alone) know the truth about a particu- lar client or clinical problem.
Dialectical Case Conceptualization
Dialectical assumptions influence case conceptual- ization in DBT in a number of ways. First, dialectics suggests that a psychological disorder is best conceptu- alized as a systemic dysfunction characterized by (1) de- fining the disorder with respect to normal functioning, (2) assuming continuity between health and the dis- order, and (3) assuming that the disorder results from multiple rather than single causes (Hollandsworth, 1990). Similarly, Linehan’s biosocial theory of BPD assumes that BPD represents a breakdown in normal functioning, and that this disorder is best conceptual- ized as a systemic dysfunction of the emotion regula- tion system. The theory proposes that the pathogenesis of BPD results from numerous factors: Some are ge- netic–biological predispositions that create individual differences in susceptibility to emotion dysregulation, known as “emotion vulnerability”; others result from the individual’s interaction with the environment, re- ferred to as the “invalidating environment.” Assuming a systemic view compels the theorist to integrate work from a variety of fields and disciplines.
A second dialectical assumption that underlies the biosocial theory is that the relationship between the individual and the environment is a transaction be- tween the person and the environment. Within social learning theory, this is the principle of “reciprocal de- terminism.” Besides focusing on reciprocal influence, a transactional view also highlights the constant state of flux and change of the individual–environment system. Therefore, BPD can occur in multiple environments and families, including chaotic, “perfect,” and even or- dinary families.
Both transactional and interactive models, such as the diathesis–stress model of psychopathology, call at- tention to the role of dysfunctional environments in bringing about disorder in the vulnerable individual. A transactional model, however, highlights a number of points that are easy to overlook in an interactive diathesis–stress model. For example, a person (Person A) may act in a manner stressful to an individual (Per- son B) only because of the stress Person B is putting
on Person A. Take the child who, due to an accident, requires most of the parents’ free time just to meet sur- vival needs. Or consider the client who, due to the need for constant suicide precautions, uses up much of the inpatient nursing resources. Both of these environments are stretched in their ability to respond well to further stress. Both may invalidate or temporarily blame the victim if any further demand on the system is made. Although the system (e.g., the family or the therapeu- tic milieu) may have been predisposed to respond dys- functionally in any case, such responses may have been avoided in the absence of exposure to the stress of that particular individual. A transactional, or dialectical, ac- count of psychopathology may allow greater compas- sion, because it is incompatible with the assignment of blame, by highlighting the reality of the situation rather than judgments about each person. This is particular- ly relevant with a label as stigmatized among mental health professionals as “borderline” (for examples of the misuse of the diagnosis, see Reiser & Levenson, 1984).
A final assumption in DBT regards the definition of behavior and the implications of defining behavior broadly. Linehan’s theory, and behaviorists in general, take behavior to mean anything an organism does in- volving action and responding to stimulation (Merri- am-Webster’s New Universal Unabridged Dictionary, 1983, p. 100). Conventionally, behaviorists categorize behavior as motor, cognitive/verbal, and physiologi- cal, all of which may be either public (i.e., overt) or private (i.e., covert). There are several points to make here. First, dividing behavior into these three catego- ries is arbitrary and is done for conceptual clarity rather than in response to evidence that these response modes actually are functionally separate systems. This point is especially relevant to understanding emotion regula- tion given that basic research on emotions demonstrates that these response systems are sometimes overlapping, somewhat independent, but definitely not wholly inde- pendent, thus remaining consistent with the dialecti- cal worldview. A related point here is that in contrast to biological and cognitive theories of BPD, biosocial theory suggests that there is no a priori reason for fa- voring explanations emphasizing one mode of behav- ior as intrinsically more important or compelling than others. Rather, from a biosocial perspective, the crucial questions are under what conditions a given behavior– behavior relationship or response system–response system relationship holds, and under what conditions these relationships enter causal pathways for the etiol- ogy and maintenance of BPD.
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BIOSOCIAL THEORY
Emotion Dysregulation
Linehan’s biosocial theory suggests that BPD is pri- marily a dysfunction of the emotion regulation system. Behavioral patterns in BPD are functionally related to or are unavoidable consequences of this fundamental dysregulation across several, perhaps all, emotions, including both positive and negative emotions. From Linehan’s point of view, this dysfunction of the emo- tion regulation system is the core pathology; thus, it is neither simply symptomatic nor definitional. Emo- tion dysregulation is a product of the combination of emotional vulnerability and difficulties in modulating emotional reactions. Emotional vulnerability is concep- tualized as high sensitivity to emotional stimuli, intense emotional responses, and a slow return to emotional baseline. Deficits in emotion modulation may be due to difficulties in (1) inhibiting mood-dependent be- haviors; (2) organizing behavior in the service of goals, independently of current mood; (3) increasing or de- creasing physiological arousal as needed; (4) distract- ing attention from emotionally evocative stimuli; and/ or (5) experiencing emotion without either immediately withdrawing or producing an extreme secondary nega- tive emotion (see Crowell, Beauchaine, & Linehan, 2009, for further discussion).
Conceptually, the deficit in the emotion regulation system leads to not only immense emotional suffering but also multiple behavioral problems in people diag- nosed with BPD. When clinicians’ ratings of charac- teristics associated with psychopathology are examined, tendencies toward being chronically anxious and un- happy, depressed, or despondent are the most highly de- scriptive of the BPD (Bradley, Zittel, & Westen, 2005). Dysfunction leads the individual to attempt to escape aversive emotions, often leading to further suffer- ing. For example, a female client experiencing intense anger after a fight with her partner may, in an effort to escape the anger, engage in cutting behaviors. She begins to feel relief from her anger for a short period of time. However, once her anger begins to subside, shame in response to the cutting behavior begins to increase and the cycle of emotion escape behavior continues. Although the mechanisms of the initial dysregulation remain unclear, it is likely that biological factors play a primary role. Siever and Davis (1991) hypothesized that deficits in emotion regulation for clients with BPD are related to both instability and hyperresponsiveness of catecholamine function. The etiology of this dysregu-
lation may range from genetic influences to prenatal factors, to traumatic childhood events affecting devel- opment of the brain and nervous system. Furthermore, adoption studies of monozygotic (MZ) twins (Davison & Neale, 1994) suggest a genetic vulnerability. How- ever, researchers do not claim that genetic or biologi- cal factors account for all pathology. If pathology were solely determined by genetics, then 100% of the MZ twins would presumably share the same pathology. Because this does not occur, we can explain the dif- ferences through the transactions between biology, as described earlier, and the environment.
Invalidating Environments
Most people with an initial temperamental vulnerabili- ty to emotion dysregulation do not develop BPD. Thus, the theory suggests further that particular developmen- tal environments are necessary. The crucial develop- mental circumstance in Linehan’s theory is the trans- action between emotion vulnerability and the presence of the invalidating environment (Linehan, 1987, 1993), which is defined by its tendency to negate, punish, and/ or respond erratically and inappropriately to private experiences, independent of the validity of the actual behavior. Private experiences, and especially emotional experiences and interpretations of events, are not taken as valid responses to events by others; are punished, trivialized, dismissed, or disregarded; and/or are at- tributed to socially unacceptable characteristics, such as overreactivity, inability to see things realistically, lack of motivation, motivation to harm or manipulate, lack of discipline, or failure to adopt a positive (or, conversely, discriminating) attitude. The invalidating environment can be any part of an individual’s social environment, including immediate or extended family, school, work, or community. Within each of these environments are even more specific idiosyncrasies that may impact the environment, such as birth order, years between sib- lings, teachers and peers, and/or coworkers. It is im- portant to note that because two children grew up in the same home does not mean that they were raised in identical environments. Furthermore, people are often not aware of their invalidating behaviors and are not acting with a malicious intent.
There are three primary characteristics of the invali- dating environment. First, the environment indiscrimi- nately rejects communication of private experiences and self-generated behaviors. For example, a person may be told, “You are so angry, but you won’t admit it”
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or “You can’t be hungry, you just ate.” Second, the in- validating environment may punish emotional displays and intermittently reinforce emotional escalation. For example, a woman breaks up with her partner and is feeling depressed. Her friends and family begin telling her, “Get over it. He wasn’t worth it,” and “Don’t feel sad.” Over the course of the next week, she becomes more depressed and is beginning to withdraw from daily activities. Again, her environment responds in an invalidating manner. Finally after another 3 days of high emotional arousal, she makes a suicide attempt. At that moment, the environment jumps in and provides support by taking care of her. Unfortunately, this type of pattern often results in inadvertent reinforcement of extreme dysfunctional behavior. Finally, the invalidat- ing environment may oversimplify the ease of problem solving and meeting goals for an individual.
The high incidence of childhood sexual abuse report- ed by adults diagnosed with BPD (e.g., Herman, 1986; Herman, Perry, & van der Kolk, 1989) suggests that sex- ual abuse may be a prototypical invalidating experience for children. The relationship of early sexual abuse to BPD, however, is quite controversial and open to many interpretations. On the one hand, Silk, Lee, Hill, and Lohr (1995) reported that the number of criterion BPD behaviors met was correlated with severity of childhood sexual abuse in a group of clients with BPD. On the other hand, a review by Fossati, Madeddu, and Maffei (1999) suggested that sexual abuse is not a major risk factor for BPD. More broadly, families in which abuse occurs often include elements of unpredictable, erratic behavior that can elicit fear, guilt, shame, sadness, and/ or disgust for children who are being victimized.
The overall results of this transactional pattern be- tween the emotionally vulnerable individual and the invalidating environment are the emotional dysregu- lation and behavioral patterns exhibited by the adult with BPD. Such an individual has never learned how to label and regulate emotional arousal, how to tolerate emotional distress, or when to trust his/her own emo- tional responses as reflections of valid interpretations of events, resulting in self-invalidation (Linehan, 1993). In more optimal environments, public validation of one’s private, internal experiences results in the development of a stable identity. In the family of a person with BPD, however, private experiences may be responded to er- ratically and with insensitivity. Thus, the individual learns to mistrust his/her internal states, and instead scans the environment for cues about how to act, think, or feel. This general reliance on others results in the
individual’s failure to develop a coherent sense of self. Emotional dysfunction also interferes with the develop- ment and maintenance of stable interpersonal relation- ships, which depend on both a stable sense of self and a capacity to self-regulate emotions. The invalidating environment’s tendency to trivialize or ignore the ex- pression of negative emotion also shapes an expressive style later seen in the adult with BPD—a style that vacillates from inhibition and suppression of emotional experience to extreme behavioral displays. Behaviors such as overdosing, cutting, and burning have impor- tant affect-regulating properties and are additionally quite effective in eliciting helping behaviors from an environment that otherwise ignores efforts to amelio- rate intense emotional pain. From this perspective, the dysfunctional behaviors characteristic of BPD may be viewed as maladaptive solutions to overwhelming, in- tensely painful negative affect.
DIALECTICAL DILEMMAS
Linehan (1993) describes dialectical dilemmas as be- havioral patterns of the client that often interfere with therapy. These behavioral patterns, also referred to as “secondary targets” in treatment (compared to other targets we describe later), represent six behaviors that are dichotomized into a set of three dimensions of be- havior defined by their opposite poles (see Figure 10.1). At one end of each dimension is the behavior that theo- retically is most directly influenced biologically via def- icits in emotion regulation. At the other end is behavior that has been socially reinforced in the invalidating en- vironment. These secondary targets are characteristics of people diagnosed with BPD that often interfere with change, thus interfering with therapy.
Emotion Vulnerability–Self‑Invalidation
One dialectical dilemma is represented by biologically influenced emotional vulnerability on the one hand (e.g., the sense of being out of control or falling into the abyss) and by socially influenced self-invalidation on the other (e.g., hate and contempt directed toward the self, dismissal of one’s accomplishments). Along this dimension of behavior, clients with BPD often vacillate between acute awareness of their own intense, unbear- able, and uncontrollable emotional suffering on the one hand, and dismissal, judgment, and invalidation of their own suffering and helplessness on the other.
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Emotion vulnerability here refers to the client’s acute experience and communication of emotional vulner- ability and excruciating emotional pain. Vulnerability here means the acute experience of vulnerability rather than the sensitivity to emotional cues that defines the term when discussing the emotion dysregulation dif- ficulties of the person diagnosed with BPD. Three reac- tions to emotional vulnerability are common in BPD: (1) freezing or dissociating in the face of intense emo- tion; (2) rage, often directed at society in general or at people who are experienced as invalidating; and (3) intense despair. Suicide here can function to commu- nicate to others the depth of one’s suffering (“I’ll show you”) and/or as an escape from an unendurable life.
On the other side of this polarity is self-invalidation. What is invalidated, in essence, is one’s own emotional experiencing and dysregulated responses. The most typical pattern here is a reaction to emotional pain with intense self-blame and self-hate. These people identify themselves as perpetrators, which results in intense lev- els of shame and contempt toward the self (“There is nothing wrong with me, I’m just a bad person”). Mood- dependent perfectionism is also common. Here, the individual belittles, ignores, or discounts the difficulty of his/her own life or may overestimate the ease of solv- ing current problems. Unfortunately, this may initiate a cycle that may eventually end in death. Extreme per- fectionism often ultimately leads to failure, especially in people who overestimate their abilities; the failure then results in self-hatred, which cues suicidal behaviors in
these people. Finally, self-invalidation can also be ex- pressed through willful suppression, meaning that the individual actively denies the experience of all emotion. Often clients who come into our offices simply state, “I don’t do emotions.” As with emotion vulnerability, self- invalidation needs to be attended to actively and direct- ly, due to the lethal consequences of these behaviors.
Active Passivity–Apparent Competence
A second dimension of behavior is a tendency toward active passivity versus the socially mediated behavior of apparent competence. Either pole of this dimension can lead to anger, guilt, or shame on the part of the client, and a tendency for the therapist to either under- or over- estimate the client’s capabilities.
Active passivity may be defined as passivity in solving one’s own problems, while actively engaging others to solve one’s problems. It can also be described as passiv- ity that appears to be an active process of shutting down in the face of seeing problems coming in the future. In a sense, people diagnosed with BPD do not appear to have the ability to regulate themselves internally, par- ticularly when the regulation required is non-mood- dependent behaviors. People diagnosed with BPD ap- pear to be “relational selves” rather than “autonomous selves”; that is, they are more highly regulated by their environment than by internal dialogues, choices, and decisions. Their best form of self-regulation is to regu- late their environment, such that it then provides the regulation they need. The problem here is that man- aging one’s environment and getting the support one needs requires a good deal of emotional consistency and regulation, characteristics that ordinarily are difficult for people diagnosed with BPD. Lorna Benjamin has described this characteristic as “My misery is your com- mand” (1996, p. 192).
On the opposite side of the polarity is apparent com- petence, which refers to the tendency of other people to overestimate the capabilities of the individual with BPD. Thus, this characteristic is defined by the behavior of the observer rather than the behavior of the individual with BPD. This failure to perceive their difficulties and “disability” accurately has serious effects on people di- agnosed with BPD. Not only do they not get the help they need, but also their emotional pain and difficulties may easily be invalidated, leading to a further sense of being misunderstood. A number of behavioral patterns can precipitate this overestimation of the competence of the individual with BPD. Often, as a result of a sig-
FIGURE 10.1. Dialectical dilemmas in DBT.
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nificant discrepancy between the individual’s verbal and nonverbal presentations, the individual with BPD believes that he/she has sufficiently communicated his/ her level of distress, when, in fact, the observer inter- prets the individual as effectively managing a difficult situation. An example would be a woman speaking nonchalantly and without emotion about urges toward suicide after a fight with her husband. People diagnosed with BPD also frequently have difficulty generalizing behaviors across situations, especially in relationships. For example, the person may be able to cope well in the presence of one person, such as a therapist, but be unable to cope when he/she is alone or with someone other than the therapist. The therapist, understandably, may then fail to predict the dysregulation that occurs as the client walks away from the therapy session. Ad- ditionally, there may be a difficulty in generalizing cop- ing behaviors across different moods. In one mood, a problem is solvable; in another, it is not. This may not be so difficult to figure out if mood changes are readily apparent to the observer, but often they are not. Thus, accurate estimates of the person’s competence actually require the observer, such as the therapist, constantly to anticipate mood changes that might occur to be able to predict what a client might or might not do. It is this characteristic, more than any other, that leads so often to a client walking out of a session, with the therapist believing that all is well, only to end up in the emer- gency department with a suicide attempt 2 hours later. At times, client failures are nothing more than failures of the therapist (and often the client, also) to predict future behavior accurately.
Unrelenting Crisis–Inhibited Grieving
The third dimension of behavior is the tendency of the client with BPD to experience life as a series of unre- lenting crises as opposed to the behavior of “inhibited grieving” (i.e., an inability to experience emotions as- sociated with significant trauma or loss). The client ex- periences each of these extremes in a way that facilitates movement to the other extreme; for example, attempt- ing to inhibit emotional experiences related to current crises may result in problem behaviors that add to ex- isting crises. As with all of these dialectical dilemmas, the solution is for therapist and client to work toward a more balanced position that represents a synthesis of the opposing poles.
People diagnosed with BPD who experience unre- lenting crises have lives that are often characterized as
chaotic and in crisis. Crisis is defined as the occurrence of problems that are extreme, with significant pressure to resolve them quickly. The consequence of the unre- lenting crisis is that the individual with BPD, as well as the person’s environmental resources, such as family, friends, coworkers, and even the therapist, slowly wear down. There are three typical scenarios that result in a pattern of unrelenting crisis. First, people with extreme impulsivity and emotion dysregulation engage in be- haviors that result in crisis situations. Poor judgment is a key element to assess when analyzing the impulsive behaviors of people diagnosed with BPD. Second, situ- ations that do not start out as crises can quickly become critical due to the lack of resources available to many people with a BPD diagnosis. This may be due to so- cioeconomic status, or to lack of family or peer support. Finally, unrelenting crises can be due simply to fate or bad luck at a given moment, a phenomenon that is out of the person’s control. For example, an unexpected di- saster in a client’s apartment due to a neighbor running water in the sink for an extended period of time might occur. The floors in the client’s apartment are damaged by the water, and he/she does not have the financial re- sources to pay for renter’s insurance or to replace the carpet in the apartment. His/her apartment is now un- inhabitable, but he/she does not have any place else to stay. This problem is out of the person’s control, but it is still that person’s responsibility to solve.
At the other extreme, and often precipitated by a cri- sis, is the phenomenon of “inhibited grieving.” In this context, grief refers to the process of grieving, which includes experiencing multiple painful emotions as- sociated with loss, particularly traumatic loss, not just the one emotion of deep sadness or grief. People with a BPD diagnosis may not be able to experience or process the grief related to loss of the life they had expected for themselves, and ordinarily they do not believe they will recover from the grief if they actually try to experi- ence or to cope with it on their own. As one client said to us, “I don’t do sadness.” Another said, “I feel sad, I die.” People diagnosed with BPD may not recognize their own emotional avoidance and shutdown. Thus, it is crucial for the therapist to attend to emotional avoidance, particularly of sadness and grief, and to as- sist clients through the grief process. Areas that must be confronted, grieved, and finally accepted include an in- surmountably painful childhood, a biological makeup that makes life harder rather than easier, inability to “fit in” in many environments, absence of loving people in the current environment, or loss of hope for a particular
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future for which one had ardently hoped. What must be confronted by the therapist is that egregious losses can be real and clients might be right: They really can- not get out of the abyss if they fall into it. Regardless of the situation to be grieved, avoidance of these situations may lead to increased shame. The shame is a result of believing that one is unloved, being alone, or fearing that one will not be able to cope in the face of emotional situations. Many of our clients believe that if they begin to address any of these areas, they will not be able to function in their lives, and often this is true. They do not have the skills or resources to assist them with the process of experiencing emotions. We often tell clients that managing grief or processing emotions requires going to the cemetery to pay tribute to what is lost, but building a house at the cemetery and living there is not a good idea. It is a place to visit, experience the sadness of the loss, and then leave. The use of this metaphor has helped many of our clients to experience emotion without falling into the abyss.
STAGES OF THERAPY AND TREATMENT GOALS
In theory, treatment of all clients with BPD can be orga- nized and determined based on their levels of disorder, and is conceptualized as occurring in stages. Level of disorder is defined by the current severity, pervasiveness, complexity, disability, and imminent threat presented by the client. Clients can enter into five stages of treat- ment based on their current level of disorder. First, all clients begin with a pretreatment stage that prepares the client for therapy and elicits a commitment to work to- ward the various treatment goals. Orientation to specif- ic goals and treatment strategies, and the commitment to work toward goals that is elicited during this stage, are likely to be fundamental to scaffolding all stages of treatment and leveraged in times of increased hopeless- ness, discouragement, ambivalence, or willfulness.
In Stage 1 of therapy, the primary focus is on stabiliz- ing the client and achieving behavioral control. Out-of- control behaviors constitute those that are disordered due to the severity of the disorder (e.g., as seen in an actively psychotic client) or severity combined with the complexity of multiple diagnoses (e.g., as seen in a sui- cidal client who has BPD with comorbid panic disorder and depression). Generally, the criteria for putting a cli- ent in Stage 1 are based on level of current function- ing, together with the inability of the client to work on any other goals before behavior and functioning come
under better control. As Mintz (1968) suggested in discussing treatment of the suicidal client, all forms of psychotherapy are ineffective with a dead client. In the subsequent stages (2–4), the treatment goals are to re- place “quiet desperation” with nontraumatic emotional experiencing (Stage 2); to achieve “ordinary” happiness and unhappiness, and to reduce ongoing disorders and problems in living (Stage 3); and to resolve a sense of incompleteness and to achieve freedom (Stage 4). In summary, the orientation of the treatment is first to get action under control, then to help the client to feel bet- ter, to resolve problems in living and residual disorder, and to find freedom (and, for some, a sense of tran- scendence). Most research to date has focused on the severely or multiply disordered clients who enter treat- ment at Stage 1. The construct of stages aids in treat- ment planning and conceptualization with the client, and in identifying the appropriate level of care needed.
Pretreatment: Orientation and Commitment
Specific tasks of orientation are twofold. First, client and therapist must arrive at a mutually informed deci- sion to work together. Typically, the first one to four sessions are presented to the client as opportunities for client and therapist to explore this possibility. Diag- nostic interviewing, history taking, and formal behav- ioral analyses of high-priority, targeted behaviors can be woven into initial therapy sessions or be conducted separately. Second, client and therapist must negotiate a common set of expectancies to guide the initial steps of therapy. Client and therapist discuss, outline, and agree specifically on what they can expect from each other. When necessary, the therapist attempts to modify the client’s dysfunctional beliefs regarding the process of therapy. Issues addressed include the rate and magni- tude of change that can reasonably be expected, the goals of treatment and general treatment procedures, and various myths the client may have about the process of therapy in general. The dialectical/biosocial view of BPD is also presented. Orientation covers several ad- ditional points. First, DBT is presented as a supportive therapy requiring a strong collaborative relationship between client and therapist. DBT is not a suicide pre- vention program, but a life enhancement program in which client and therapist function as a team to cre- ate a life worth living. Second, DBT is described as a cognitive-behavioral therapy with a primary emphasis on analyzing problematic behaviors and replacing them with skillful behaviors, and on changing ineffective
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beliefs and rigid thinking patterns. Third, the client is told that DBT is a skills-oriented therapy, with special emphasis on behavioral skills training. The commit- ment and orientation strategies, balanced by validation strategies described later, are the most important strate- gies during this phase of treatment. The therapist places a strong effort into getting the client to commit to not engaging in suicidal or NSSI behaviors for some speci- fied period of time before allowing the client to leave the session; it can be for 1 year, 6 months, until the next session, or until tomorrow.
Stage 1: Attaining Basic Capacities
The primary focus of the first stage of therapy is attain- ing behavioral control in order to build a life pattern that is reasonably functional and stable. Furthermore, DBT does not promote itself as a suicide prevention program; instead, it focuses on “building a life worth living.” Therefore, the primary treatment goal in DBT and in Stage 1 specifically is to assist clients in build- ing a life they will experience as worth living. DBT attains this goal by focusing the treatment on specific behavioral targets agreed upon by both therapist and client. Specific targets in order of importance are to re- duce life-threatening behaviors (e.g., suicide attempts, suicide ideation, NSSI behaviors, homicidal threats and behaviors), therapy-interfering behaviors (e.g., late to session, missing sessions, not following treatment plan, hostile attacks on the therapist), and quality-of- life–interfering behaviors (e.g., substance abuse, eating disorder, homelessness, mental health disorders), and to increase behavioral skills. These targets are approached hierarchically and recursively as higher-priority behav- iors reappear in each session. However, this does not mean that these behaviors must be addressed in this specific order during a session; it means that, based on the hierarchy, all relevant behavior must be addressed at some point within the session. For example, if a client is 30 minutes late to session (therapy-interfering behavior) and has attempted suicide within the last week (life- threatening behavior), the therapist may choose to ad- dress the therapy-interfering behavior first, then move on to address the life-threatening behaviors.
With severely dysfunctional and suicidal clients, sig- nificant progress on Stage 1 targets may take up to 1 year or more. In addition to these therapy targets, the goal of increasing dialectical behaviors is universal to all modes of treatment. Dialectical thinking encour- ages clients to see reality as complex and multifaceted,
to hold contradictory thoughts simultaneously and learn to integrate them, and to be comfortable with in- consistency and contradictions. For people with a BPD diagnosis, who are extreme and dichotomous in their thinking and behavior, this is a formidable task indeed. A dialectical emphasis applies equally to a client’s pat- terns of behavior, because the client is encouraged to integrate and balance emotional and overt behavioral responses. In particular, dialectical tensions arise in the areas of skills enhancement versus self-acceptance, problem solving versus problem acceptance, and affect regulation versus affect tolerance. Behavioral extremes, whether emotional, cognitive, or overt responses, are constantly confronted while more balanced responses are taught.
Life‑Threatening Behaviors
Keeping a client alive must, of course, be the first prior- ity in any psychotherapy. Thus, reducing suicide crisis behaviors (any behaviors that place the client at high and imminent risk for suicide or threaten to do so, in- cluding credible suicide threats, planning, preparations, obtaining lethal means, and high suicide intent) is the highest priority in DBT. The target and its priority are made explicit in DBT during orientation and through- out treatment, simply because suicidal behavior and the risk of suicide are of paramount concern for clients with BPD. Similarly, any acute, intentional NSSI behaviors share the top priority. The priority here is due to the risk of suicidal and NSSI behavior as the single best predic- tor of subsequent suicide. Similarly, DBT also targets suicide ideation and client expectations about the value and long-term consequences of suicidal behavior, al- though these behaviors may not necessarily be targeted directly.
Therapy‑Interfering Behaviors
Keeping clients and therapists working together col- laboratively is the second explicitly targeted priority in DBT. The chronic nature of most problems among clients with BPD, including their high tendency to end therapy prematurely and the likelihood of therapist burnout and iatrogenic behaviors when treating BPD, requires such explicit attention. Both client and thera- pist behaviors that threaten the relationship or thera- peutic progress are addressed directly, immediately, consistently, and constantly—and most importantly, before rather than after either the therapist or the client
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no longer wants to continue. Interfering behaviors of the client, including those that actually interfere with receiving the therapy (e.g., lateness to sessions, missed sessions, lack of transportation to sessions, dissociating in sessions) or with other clients benefiting from ther- apy (in group or milieu settings; e.g., selling drugs to other clients in the program), and those that burn out or cross the personal limits of the therapist (e.g., repeated crisis calls at 3:00 A.M., repeated verbal attacks on the therapist) are treated within therapy sessions. Behaviors of the therapist include any that are iatrogenic (e.g., inadvertently reinforcing dysfunctional behaviors), as well as any that cause the client unnecessary distress or make progress difficult (e.g., therapist arriving late to sessions, missing sessions, not returning phone calls within a reasonable time frame). These behaviors are dealt with in therapy sessions, if brought up by either the client or the therapist, and are also discussed during the consultation/supervision meeting.
Quality‑of‑Life‑Interfering Behaviors
The third target of Stage 1 addresses all other behav- iors that interfere with the client having a reasonable quality of life. Typical behaviors in this category in- clude serious substance abuse, severe major depressive episodes, severe eating disorders, high-risk and out-of- control sexual behaviors, extreme financial difficul- ties (uncontrollable spending or gambling, inability to handle finances), criminal behaviors that are likely to lead to incarceration, employment- or school-related dysfunctional behaviors (a pattern of quitting jobs or school prematurely, getting fired or failing in school, not engaging in any productive activities), housing-re- lated dysfunctional behaviors (living with abusive peo- ple, not finding stable housing), mental health-related patterns (going in and out of hospitals, failure to take or abuse of necessary medications), and health-related problems (failure to treat serious medical disorders). The goal here is for the client to achieve a stable lifestyle that meets reasonable standards for safety and adequate functioning.
When necessary, DBT incorporates evidence-based behavioral interventions to address specific quality-of- life–interfering behaviors. Because DBT is a principle- based treatment, it allows seamless integration of other evidence-based protocols as long as they are compatible with the basic assumptions and philosophy of DBT. For example, we have recently added to DBT a pro- longed exposure protocol to treat PTSD among highly
suicidal clients with BPD (Harned et al., 2012). Fol- lowing Harned and colleagues’ guidelines for client readiness and implementation of the protocol within standard DBT, a pilot study was conducted with 13 women diagnosed with comorbid BPD and PTSD, and at high risk for suicide. Outcomes showed 70% with reliable improvement in PTSD symptoms and a 60% remission rate, results similar to PE findings in the standard PTSD literature. An RCT conducted with 26 women with comorbid BPD and PTSD demonstrated that this protocol led to greater and more stable re- ductions in PTSD symptoms, and among DBT treat- ment completers, PTSD remission rate was doubled for those whose treatment included the DBT PE protocol (Harned et al., 2014). Individuals completing the DBT PE protocol were 2.4 times less likely to make suicide attempts and 1.5 times less likely to engage in NSSI than those in standard DBT. This study also reliably demonstrated that trauma-focused exposure proce- dures in DBT PE did not exacerbate suicide and NSSI urges and behaviors, and indicated that, in fact, DBT PE may reduce these behaviors. To the extent that some individuals reported infrequent intensification of urges for suicide or NSSI following sessions, the degree was consistent with reports following standard DBT ses- sions.
Behavioral Skills
The fourth target of Stage 1 is for the client to achieve a reasonable capacity for acquiring and applying skill- ful behaviors in the areas of distress tolerance, emo- tion regulation, interpersonal effectiveness, self-man- agement, and the capacity to respond with awareness without being judgmental (“mindfulness” skills). In our outpatient programs, the primary responsibility for skills training lies with the weekly DBT skills group. The individual therapist monitors the acquisition and use of skills over time, and aids the client in applying skills to specific problem situations in his/her own life. Additionally, it is the role of the individual therapist, not the skills group leader, to provide skills coaching to the client as needed when problems arise.
Stage 2: Quiet Desperation
Stage 1 of DBT takes a direct approach to managing dysfunctional behavioral and regulating emotional pat- terns. Although the connection between current behav- ior and previous traumatic events (including those from
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childhood) may be explored and noted, the focus of the treatment is distinctly on analyzing the relationship among current thoughts, feelings, and behaviors, and on accepting and changing current patterns. The aim of Stage 2 DBT is to reduce quiet desperation, which can be defined as extreme emotional pain in the presence of control of action (Linehan et al., 1999). A wide range of emotional experiencing difficulties (e.g., avoidance of emotions and emotion-related cues) are targeted in this stage, with the goal of increasing the capacity for nor- mative emotional experiencing (i.e., the ability to ex- perience a full range of emotions without either severe emotional escalation or behavioral dyscontrol). Stage 2 addresses four goals: remembering and accepting the facts of earlier distressing and/or traumatic events; re- ducing stigmatization and self-blame often associated with traumatic social invalidation; reducing oscillating denial and intrusive response syndromes; and resolving dialectical tensions regarding placement of blame for past difficulties. Historically in DBT, trauma- focused treatment (e.g., PE, cognitive processing therapy [CPT]) in Stage 2 often occurred after skills training was completed; however, as discussed earlier, these treatments are currently integrated alongside skills ac- quisition of standard DBT using Harned’s DBT+PE protocol (Harned et al., 2012, 2014).
Stage 3: Resolving Problems in Living and Increasing Respect for Self
In the third stage, DBT targets the client’s unacceptable unhappiness and problems in living. At this stage, the client with BPD has either done the work necessary to resolve problems in the prior two stages or was never se- verely disordered enough to need it. Although problems at this stage may still be serious, the individual is func- tional in major domains of living. The goal here is for the client to achieve a level of ordinary happiness and unhappiness, as well as independent self-respect. To this end, the client is helped to value, believe in, trust, and validate him/herself. The targets here are the abilities to evaluate one’s own behavior nondefensively, to trust one’s own responses, and to hold on to self-evaluations, independent of the opinions of others. Ultimately, the therapist must pull back and persistently reinforce the client’s independent attempts at self-validation, self- care, and problem solving. Although the goal is not for clients to become independent of all people, it is impor- tant that they achieve sufficient self-reliance to relate to and depend on others without self-invalidating.
Stage 4: Attaining the Capacity for Freedom and Sustained Contentment
The final stage of treatment in DBT targets the resolu- tion of a sense of incompleteness and the development of a capacity for sustained contentment. The focus on freedom encompasses the goal of freedom from the need to have one’s wishes fulfilled, or one’s current life or behavioral and emotional responses changed. Here, the goals are expanded awareness, spiritual fulfillment, and the movement into experiencing flow. For clients at Stage 4, insight-oriented psychotherapy, spiritual direc- tion or practices, or other organized experiential treat- ments and/or life experiences may be of most benefit.
STRUCTURING TREATMENT: FUNCTIONS AND MODES
Functions of Treatment
Standard DBT is structured around five essential func- tions: (1) to enhance behavioral capabilities by expand- ing the individual’s repertoire of skillful behavioral pat- terns; (2) to improve the client’s motivation to change by reducing reinforcement for dysfunctional behaviors and high-probability responses (cognitions, emotions, actions) that interfere with effective behaviors; (3) to ensure that new behaviors generalize from the thera- peutic to the natural environment; (4) to enhance the motivation and capabilities of the therapist, so that ef- fective treatment is rendered; and (5) to structure the environment so that effective behaviors, rather than dysfunctional behaviors, are reinforced.
Modes of Treatment: Who Does What and When
Responsibility for performing functions and meeting target goals of treatment in standard DBT is spread across the various modes of treatment, with focus and attention varying according to the mode of therapy. The individual therapist (who is always the primary therapist in DBT) attends to the order of targets and is also, with the client, responsible for organizing the treatment so that all goals are met. In skills training, a different set of goals is targeted; during phone calls, yet another hierarchy of targets takes precedence. In the consultation/supervision mode, therapists’ behav- iors are the targets. Therapists engaging in more than one mode of therapy (e.g., individual, group, and tele-
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phone coaching) must stay cognizant of the functions and order of targets specific to each mode, and switch smoothly from one hierarchy to another as the modes of treatment change.
Individual Therapy
DBT assumes that effective treatment must attend both to client capabilities and behavioral skills deficits, and to motivational and behavioral performance issues that interfere with use of skillful responses (function 2). Al- though there are many ways to effect these principles, in DBT, the individual therapist is responsible for the assessment and problem solving of skill deficits and mo- tivational problems, and for organizing other modes to address problems in each area.
Individual outpatient therapy sessions are scheduled on a once-a-week basis for 50–90 minutes, although twice-weekly sessions may be held as needed during crisis periods, at the beginning of therapy, or in order to effectively conduct necessary treatment components such as those in the DBT PE protocol. The priorities of specific targets within individual therapy are the same as the overall priorities of DBT discussed earlier. Therapeutic focus within individual therapy sessions is determined by the highest-priority treatment target relevant at the moment. This ordering does not change over the course of therapy; however, the relevance of a target does change. Relevance is determined by either the client’s most recent, day-to-day behavior (since the last session) or by current behavior during the therapy session. If satisfactory progress on one target goal has been achieved or the behavior has never been a prob- lem, or if the behavior is currently not evident, then the therapist shifts attention to another treatment target ac- cording to the hierarchy. The consequence of this prior- ity allocation is that when high-risk suicidal behaviors or intentional self-injury, therapy-interfering behaviors, or serious quality-of-life-interfering behaviors occur, at least part of the session agenda is devoted to each of these topics. If these behaviors are not occurring at the moment, then the topics to be discussed during Stages 1, 3, and 4 are set by the client. The therapeutic focus (within any topic area discussed) depends on the stage of treatment, the skills targeted for improvement, and any secondary targets. During Stage 1, for example, any problem or topic area can be conceptualized in terms of interpersonal issues and skills needed, opportunities for emotion regulation, and/or a necessity for distress toler- ance. During Stage 3, regardless of the topic, the thera-
pist focuses on helping the client decrease problems in living and achieve independent self-respect, self-valida- tion, and self-acceptance both within the session and in everyday life. (These are, of course, targets all through the treatment, but the therapist pulls back further dur- ing Stage 3 and does less work for the client than during the two preceding stages.) During Stage 2, the major focus is on reducing pervasive “quiet desperation,” as well as changing the extreme emotions and psychologi- cal meanings associated with traumatizing cues.
For highly dysfunctional clients, it is likely that early treatment will necessarily focus on the upper part of the hierarchy. For example, if suicidal or NSSI behavior has occurred during the previous week, attention to it takes precedence over attention to therapy-interfering behav- ior. In turn, focusing on therapy-interfering behaviors takes precedence over working on quality-of-life-inter- fering behaviors. Although it is often possible to work on more than one target (including those generated by the client) in a given session, higher-priority targets al- ways take precedence, but all relevant targets must be addressed adequately during the session. Again, targets do not need to be addressed in sequential order; they just have to be addressed during the session. Determin- ing the relevance of targeted behaviors is assisted by the use of diary cards, filled out by the client during at least the first two stages of therapy and brought to weekly sessions. Failure to complete or to bring in a card is considered a therapy-interfering behavior and should be openly addressed as such, beginning with initial discus- sions in the orientation and commitment stage. Weekly Diary Cards record daily instances of suicidal and NSSI behavior, urges to self-harm or to engage in suicide be- haviors (on a 0- to 5-point scale), “misery” and other emotions, use of substances (licit and illicit), and use of behavioral skills. Other targeted behaviors (bulimic ep- isodes, daily productive activities, flashbacks, etc.) may also be recorded on the blank area of the card. The ther- apist doing DBT must develop the pattern of routinely reviewing the card at the beginning of each session and using it to inform agenda setting. The card acts as a road map for each session; therefore, a session cannot begin until a Weekly Diary card has been completed. If the card indicates that a life-threatening behavior has occurred, it is noted and discussed. If high suicide or self-harm urges are recorded, or there is a significant in- crease (e.g., an increase of 3 points or higher on the 0- to 5-point scale for urges) over the course of the week, they are assessed to determine whether the client is at risk for suicide. If a pattern of substance abuse or dependence
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appears, it is treated as a quality-of-life-interfering be- havior.
Work on targeted behaviors involves a coordinated array of treatment strategies, described later in this chapter. Essentially, each session is a balance among structured, as well as unstructured, problem solving (including simple interpretive activities by the therapist) and unstructured validation. The amount of the thera- pist’s time allocated to each—problem solving and vali- dating—depends on (1) the urgency of the behaviors needing change or problems to be solved, and (2) the urgency of the client’s needs for validation, understand- ing, and acceptance without any intimation of change being needed. However, there should be an overall bal- ance in the session between change (problem solving) and acceptance (validation) strategies. Unbalanced at- tention to either side may result in a nondialectical ses- sion, in addition to impeding client progress.
Skills Training
The necessity of crisis intervention and attention to other primary targets makes skills acquisition within individual psychotherapy very difficult. Thus, a sepa- rate component of treatment directly targets the acqui- sition of behavioral skills (function 1). In DBT this usu- ally takes the form of separate, weekly, 2- to 2½-hour group skills training sessions that clients must attend, ordinarily for a minimum of 6 months and preferably for a year. Skills training can also be done individually, although it is often more difficult to stay focused on teaching new skills in individual than in group therapy. After a client has gone through all skills modules twice (i.e., for 1 year), remaining in skills training is a matter of personal preference and need. Some DBT programs have developed graduate groups for clients who have ac- quired the skills but still need weekly consultation in applying the skills effectively to everyday difficulties. It is important to note that there is no research to date on the effectiveness of graduate groups. In adolescent programs, family members are usually invited. Some programs include a separate friends and families skills training group as well.
Each group typically has a leader and a coleader. Whereas the primary role of the leader is to teach the skills, the coleader focuses on managing group process by keeping members both focused and attending to the material being taught, as well as processing the infor- mation (e.g., ensuring that everyone is on the correct page, noticing when the leader’s invalidation has led
to a member shutting down, waking someone up, sit- ting next to a member who is crying during group). We have found that it is difficult to keep the group focused and the leader on schedule for teaching the skills if the leader attempts to manage both roles on his/her own. Oftentimes, the coleader role is more difficult to learn.
Skills training in DBT follows a psychoeducational format. In contrast to individual therapy, in which the agenda is determined primarily by the problem to be solved, the skills training agenda is set by the skill to be taught. As mentioned earlier, skills training also uses a hierarchy of treatment targets to keep the group focused: (1) therapy-destroying behaviors (e.g., using drugs on premises, which could lead to the clinic being shut down; property damage; threatening imminent suicide or homicidal behavior to a fellow group member or therapist); (2) increasing skills acquisition and strength- ening; and (3) decreasing therapy-interfering behaviors (e.g., refusing to talk in a group setting, restless pacing in the middle of sessions, attacking the therapist and/ or the therapy). However, therapy-interfering behaviors are not given the attention in skills training that they are given in the individual psychotherapy mode. If such behaviors were a primary focus, there would never be time for teaching behavioral skills. Generally, therapy- interfering behaviors are put on an extinction schedule, while a client is “dragged” through skills training and simultaneously soothed. In standard (i.e., full model) DBT, all skills training clients are required to be in con- current individual psychotherapy. Throughout group or individual skills training, each client is urged to ad- dress other problematic behaviors with his/her primary therapist; if a serious risk of suicide develops, the skills training therapist refers the problem to the primary therapist.
Although all of the strategies described below are used in both individual psychotherapy and skills train- ing, the mix is decidedly different. Skills acquisition, strengthening, and generalization strategies are the predominant change strategies in skills training. In ad- dition, skills training is highly structured, much more so than the individual psychotherapy component. Half of each skills training session is devoted to reviewing homework practice of the skills currently being taught, and the other half is devoted to presenting and practic- ing new skills. Except when interpersonal process issues seriously threaten progress, the agenda and topics for discussion in skills training are usually predetermined.
Four skills modules are taught on a rotating basis over the course of 6 months. In standard DBT, mindfulness
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skills are taught for 2 consecutive weeks at the begin- ning of each of the subsequent modules. New members join a group during either the 2 weeks of mindfulness or the first 2 weeks of the subsequent module.
Mindfulness skills are viewed as central in DBT; thus, they are labeled the “core” skills. These skills rep- resent a behavioral translation of meditation (including Zen and contemplative prayer) practice and include observing, describing, spontaneous participating, being nonjudgmental, focusing awareness, and focusing on effectiveness. Unlike standard behavioral and cognitive therapies, which ordinarily focus on changing distress- ing emotions and events, a major emphasis of DBT is on learning to manage pain skillfully. Mindfulness skills reflect the ability to experience and to observe one’s thoughts, emotions, and behaviors without evaluation, and without attempting to change or control them. Distress tolerance skills comprise two types of skills. First, crisis survival skills are used to regulate behavior, in order to manage painful situations without making them worse (e.g., without engaging in life-threatening behavior) until the problem can be solved. Second, “ac- cepting reality” skills are used to tolerate the pain of problems that cannot be solved in either the short-term future or that may have occurred in the past and, there- fore, cannot be changed ever.
Emotion regulation skills target the reduction of emotional distress and include affect identification and labeling, mindfulness of current emotions (i.e., experiencing nonjudgmentally), identifying obstacles to changing emotions, increasing resilience, and act- ing opposite to the emotion. Interpersonal effectiveness skills teach effective methods for deciding on objectives within conflict situations (either asking for something or saying “no” to a request) and strategies that maxi- mize the chances of obtaining those objectives without harming the relationship or sacrificing self-respect.
It is important to highlight here one skill that is es- sential in the DBT emotion regulation module: the skill of opposite action. This emotion regulation skill encourages clients to act opposite to their emotional urge, in order to reduce their emotional arousal. The theoretical premise behind opposite action is that act- ing in accordance with the action urge associated with an emotion increases the likelihood that that emotion will fire again (Linehan, Bohus, & Lynch, 2007). Cli- ents are taught that reversing expressive (e.g., facial ex- pression, posture, voice tone) and action components of emotion responses is common to many treatments that address emotional disorders and, in essence, can be one
of the main mechanisms of change in effective psycho- therapy. For example, effective treatments for anxiety are based on principles of exposure and response pre- vention that encourage active replacement of an emo- tion-consistent behavior with an emotion-inconsistent behavior (e.g., Foa & Kozak, 1986). The skill of op- posite action expands this principle to be applicable all emotions, not just to fear. It also provides specific guidelines for how exactly to implement opposite ac- tions for each problematic emotion. Therefore, if an emotion is not justified in the situation or is not effec- tive, opposite action involves (1) exposure to the stimuli or cues evoking the emotion, (2) blocking of the be- havior prompted by the emotion’s action urge, and (3) acting in a way that is opposite or inconsistent with the emotional response (Linehan, 2015). For example, the action urge of fear is to avoid; therefore, the oppo- site action is to fully approach the situation. For anger, the action urge is to attack physically or emotionally, clench fists, and judge the situation. The opposite ac- tion to anger therefore involves gently removing oneself from the situation, unclenching the fists, and opening the palms of hands, relaxing the shoulders, making empathic statements, and actively working to generate empathy for the person or situation with whom one is angry (Linehan, 2015).
The skill of opposite action is very similar to the recommendation to change action tendencies in order to change anxiety, which was proposed by Barlow in 1988. According to Barlow and colleagues (2004; also see Payne, Ellard, Farchione, & Barlow, Chapter 6, this volume), negative emotionality is a latent factor under- lying depression and anxiety disorders; therefore, they proposed a unified treatment protocol for mood and anxiety disorders. Barlow and colleagues’ unified proto- col suggests that difficulties with negative emotions can be treated through altering antecedent cognitive reap- praisals (i.e., the probability of an event to happen and the likelihood of a catastrophic outcome), preventing emotional avoidance, and facilitating action tendencies that are not associated with the emotion. For this last strategy, they highlight that a crucial step is to prevent action tendencies associated with the emotion and to facilitate different action tendencies, encouraging ap- proach when emotions says avoidance. The examples given are similar to opposite action (e.g., asking an in- dividual diagnosed with GAD to engage in nonperfect behavior; encouraging someone with an anger problem to act detached and passive; asking someone diagnosed with depression to act active and not withdraw).
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Self-management skills are taught in conjunction with the other behavioral skills; however, there is not a specific module allocated to these skills, because behav- ioral principles are inherent in all of DBT. Self-manage- ment skills include knowledge of the fundamental prin- ciples of learning and behavior change, and the ability to set realistic goals, to conduct one’s own behavioral analysis, and to implement contingency management plans.
Telephone Consultation
Telephone calls between sessions (or other extrath- erapeutic contact when DBT is conducted in other settings; e.g., as-needed skills coaching on inpatient units) are an integral part of DBT. Telephone consulta- tion calls also follow a target hierarchy: (1) to provide emergency crisis intervention and simultaneously break the link between suicidal behaviors and therapist at- tention; (2) to provide coaching in skills and promote skills generalization; and (3) to provide a timely context for repairing the therapeutic relationship. With respect to calls for skills coaching, the focus of a phone call varies depending on the complexity and severity of the problem to be solved and the amount of time the thera- pist is willing to spend on the phone. It is important to note that these calls are not considered therapy sessions and should not be used as such. With easy or already clear situations, in which it is reasonably easy to deter- mine what the client can or should do in the situation, the focus is on helping the client use behavioral skills (rather than dysfunctional behaviors) to address the problem. Alternatively, with complex problems, or with problems too severe for the client to resolve soon, the focus is on ameliorating and tolerating distress, and in- hibiting dysfunctional problem-solving behaviors until the next therapy session. In the latter case, resolving the crisis is not the target of telephone coaching calls.
With the exception of taking necessary steps to pro- tect the client’s life when he/she has threatened suicide, all calls for help are handled as much alike as possible. This is done to break the contingency between suicidal and NSSI behaviors, and increased phone contact. To do this, the therapist can do one of two things: refuse to accept any calls (including suicide crisis calls), or insist that the client who calls during suicidal crises also call during other crises and problem situations. As Linehan (2015) notes, experts on suicidal behaviors uniformly say that therapist availability is necessary with suicidal clients. Thus, DBT chooses the latter course and en-
courages (and at times insists) on calls during nonsui- cidal crisis periods. In DBT, calling the therapist too infrequently, as well as too frequently, is considered therapy-interfering behavior. Through orientation to coaching calls during pretreatment the client learns what to expect during the calls. For example, a thera- pist may communicate to the client in session what he/ she will ask during the call: “What’s the problem? What skills have you used? Where is your skills book? Go get it, and let’s figure out what other skills you can use to get through this situation.” It is important to highlight that clients and therapists can easily fall into the trap of considering the act of calling for phone consultation a skill. Although asking for help may be a current target of treatment, it is not considered a skill to be used when the client is in distress. A therapist wants to reinforce the client for effectively reaching out; however, he/she does not want to reinforce the client who does not try using actual skills to manage the problem at hand prior to calling him/her.
Additionally, the therapist is balancing the change- focused strategies with validation throughout the call. It is important that the therapist be aware of contingency management principles that may be occurring during the phone calls to avoid inadvertently reinforcing crisis behaviors and to increase contact between sessions.
A skills trainer uses phone calls only to keep a cli- ent in therapy (including, of course, when necessary, to keep the client alive). All other problems, including suicidal crises, are turned over to the primary therapist as soon as possible. We have learned that this can be one of the most difficult distinctions for group leaders to uphold. Clients may call for a variety of reasons, and it is the role of the group leader consistently to refer the client back to the individual therapist.
The final priority for phone calls to individual thera- pists is relationship repair. Clients with BPD often experience delayed emotional reactions to interactions that have occurred during therapy sessions. From a DBT perspective, it is not reasonable to require clients to wait up to a whole week before dealing with these emotions, and it is appropriate for a client to call for a brief “heart-to-heart” talk. In these situations, the role of the therapist is to soothe and to reassure. In-depth analyses should wait until the next session.
Consultation Team
DBT assumes that effective treatment of BPD must pay as much attention to the therapist’s behavior and ex-
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perience in therapy as it does to the client’s. Treating clients with BPD is enormously stressful, and staying within the DBT therapeutic framework can be tremen- dously difficult (function 4). Thus, an integral part of the therapy is the treatment of the therapist. Every therapist is required to be on a consultation team either with one other person or with a group. DBT consulta- tion meetings are held weekly and attended by thera- pists currently providing DBT to clients. At times, the clinical setting may require that the team be part of an administrative meeting due to time and space re- straints. When this occurs, it is important to set a spe- cific agenda and time limitations on each part of the meeting (administration, DBT) to ensure that therapist consultation issues are addressed. The roles of consul- tation are to hold the therapist within the therapeutic framework and to address problems that arise in the course of treatment delivery. Thus, the fundamental target is increasing adherence to DBT principles for each member of the consultation group. The DBT con- sultation team is viewed as an integral component of DBT; that is, it is considered peer group therapy for the therapists, in which each member is simultaneously a therapist to other members and a client. The focus is on applying DBT strategies to increase DBT-adherent behaviors and decrease non-DBT behaviors.
There are three primary functions of consultation to the therapist in DBT. First, a consultation team helps to keep each individual therapist in the therapeutic relationship. The role here is to cheerlead and to sup- port the therapist. Second, the supervisor or consulta- tion team balances the therapist in his/her interactions with the client. In providing balance, consultants may move close to the therapist, helping him/her maintain a strong position. Or consultants may move back from the therapist, requiring the therapist to move closer to the client to maintain balance. Third, within program- matic applications of DBT, the team provides the con- text for the treatment.
JOINING THE CONSULTATION TEAM
Each team comprises therapists who are currently treat- ing a DBT client or are available to take on a DBT cli- ent. The consultation team is a community of therapists treating a community of clients. Prior to joining the team, it is important that the therapist be completely aware of his/her commitment. As with clients during the pretreatment phase of DBT, therapists must make a commitment to the team (see Table 10.1). The team
TABLE 10.1. DBT Consultation Team Commitment Session
1. To keep the agreements of the team, especially remaining compassionate, mindful, and dialectical.
2. To be available to see a client in whatever role one has joined the team for (e.g., individual therapist, group skills trainer, clinical supervisor, pharmacotherapist).
3. To function as a therapist in the group (to the group) and not just be a silent observer or a person that only speaks about his or her own problems.
4. To treat team meetings in the same way one treats any other group therapy session (i.e., attending the weekly meetings [not double scheduling other events or clients], on time, until the end, with pagers, PDAs, and phones out of sight and off or, if necessarily on, on silent).
5. To come to team meetings adequately prepared. 6. To be willing to give clinical advice to people who have
more experience (especially when it’s hard to imagine yourself as being able to offer anything useful).
7. To have the humility to admit your mistakes/difficulties and the willingness to have the group help you solve them.
8. To be nonjudgmental and compassionate of your fellow clinicians and clients. To ring the bell of nonjudgmentalness to remind yourself to not be judgmental or unmindful, but not to ring it as a proxy for criticizing someone. The bell is a reminder, not a censor.
9. To properly assess the problem before giving solutions (do unto others as you wish they would more often do unto you).
10. To call out “Elephant in the room” when others are ignoring or not seeing the elephant.
11. To be willing to go through a chain analysis even though you were only 31 seconds late and you would have been there on time if it were not for that traffic light that always takes all day to change.
12. To participate in team by sharing the roles of Leader, Observer, Note Taker or other tasks critical to team functioning.
13. If you feel that the consult team is not being useful or don’t like the way it is being run, then say something about it rather than silently stewing in frustration.
14. To repair with the team in some way when team meetings are missed, because the team is only as strong as the weakest link. Therefore, the absence of any team member is felt.
15. To carry on even when feeling burnt out, frustrated, tired, overworked, underappreciated, hopeless, ineffective (easier committed to than done, of course).
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member conducting the commitment session will use the same strategies and techniques used in a first ses- sion with a DBT client (e.g., devil’s advocate, pros and cons, troubleshooting). New therapists must commit to doing the behaviors listed in Table 10.1), to working actively toward increasing their own effectiveness and adherence when applying DBT principles and to being responsible for treatment and outcomes of all clients treated by the team. For example, members of the team are agreeing that if a client being treated by any member of the team commits suicide, then all members will say “Yes” when asked if they have ever had a client commit suicide.
CONSULTATION MEETING FORMAT
There are multiple ways to run a DBT team meeting. The following is the way we conduct our meetings at the University of Washington and at Duke Univer- sity Medical Center (although it is important to note that even this format may change as needs of members change). Each of our DBT teams has an identified team leader. This person is typically the most experienced DBT therapist on the team, and his/her role is to articu- late the DBT principles when necessary for overseeing the fidelity of the treatment provided. Additionally, our teams include an observer who rings a bell whenever team members make judgmental comments (in content or tone) about themselves, each other, or a client; stay polarized without seeking synthesis; fall out of mind- fulness by doing two things at once; or jump in to solve a problem before assessing the problem. The point of these observations is not to lay blame but to focus the team’s awareness on the behavior and move past it.
Our teams begin with a mindfulness practice. There are several functions of mindfulness on a team. First, it helps members transition into the team by participating fully and focusing on only one thing in the moment, using a DBT mindset. Second, it can provide an op- portunity for team members to enhance their skills in leading and providing feedback about the practice with other team members. Consultation team agreements (see Table 10.2) have been developed to facilitate a DBT frame and help to create a supportive environment for managing client–therapist and therapist–therapist dif- ficulties. Therefore, a team may elect to read one or all of the team agreements during the team meeting. Most importantly, an agenda is set by the team following the DBT hierarchy of targets, with a specific focus on the needs of the therapist rather than the problems of the
clients. Our agenda uses the following format; however, the following items can be prioritized differently based on the needs of an individual team: (1) the therapists’ need for consultation around clients’ suicidal crises or other life-threatening behaviors; (2) therapy-interfering behaviors (including client absences and dropouts, as well as therapist therapy-interfering behaviors); (3) ther- apist team-interfering behaviors and burnout; (4) severe or escalating deterioration in quality-of-life behaviors; (5) reportage of good news and therapists’ effective behaviors; (6) a summary of the work of the previous
TABLE 10.2. DBT Consultation Team Agreements
1. Dialectical agreement: We agree to accept a dialectical philosophy: There is no absolute truth. When caught between two conflicting opinions, we agree to look for the truth in both positions and to search for a synthesis by asking questions such as “What is being left out?”
2. Consultation to the client agreement: We agree that the primary goal of this group is to improve our own skills as DBT therapists, and not serve as a go-between for clients to each other. We agree to not treat clients or each other as fragile. We agree to treat other group members with the belief that others can speak on their own behalf.
3. Consistency agreement: Because change is a natural life occurrence, we agree to accept diversity and change as they naturally come about. This means that we do not have to agree with each others’ positions about how to respond to specific clients, nor do we have to tailor our own behavior to be consistent with everyone else’s.
4. Observing limits agreement: We agree to observe our own limits. As therapists and group members, we agree to not judge or criticize other members for having different limits from our own (e.g., too broad, too narrow, “just right”).
5. Phenomenological empathy agreement: All things being equal, we agree to search for nonpejorative or phenomenologically empathic interpretations of our clients’, our own, and other members’ behavior. We agree to assume that we and our clients are trying our best and want to improve. We agree to strive to see the world through our clients’ eyes and through one another’s eyes. We agree to practice a nonjudgmental stance with our clients and with one another.
6. Fallibility agreement: We agree ahead of time that we are each fallible and make mistakes. We agree that we have probably either done whatever problematic things we’re being accused of, or some part of it, so that we can let go of assuming a defensive stance to prove our virtue or competence. Because we are fallible, it is agreed that we will inevitably violate all of these agreements, and when this is done, we will rely on each other to point out the polarity and move to a synthesis.
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skills group and graduate group by group leaders; and (7) discussion of administrative issues (requests to miss team or be out of town, new client contacts, changes in skills trainers or group time, format of consultation group, etc.). This agenda spans the 1-hour consultation meeting. Although the agenda may look impossibly long, therapists ordinarily manage the time by being explicit about their need for help and consultation from the team. Our teams typically span 2 hours and dur- ing the second hour, we focus on didactics and educa- tional goals of the various team members, for example, we might watch session video provided by a therapist on the team or discuss relevant educational topics such as provider wellness, phone coaching, or novel DBT- focused research.
Ancillary Care
When problems in the client’s environment interfere with functioning or progress, the therapist moves to the case management strategies. There are three case man- agement strategies: the consultant-to-the-client strat- egy, environmental intervention, and the consultation/ supervision team meeting (described earlier). Because DBT is grounded in dialectics and avoids becoming rigid, a therapist intervenes in the client’s environment only under very specific conditions: (1) The client is unable to act on his/her own behalf and outcome is ex- tremely important; (2) a key person in the environment will only speak with someone who is in high power (e.g., the therapist instead of the client); (3) when the client’s or others’ lives are in imminent danger; (4) when it is the humane thing to do and will cause no harm; and (5) when the client is a minor.
CONSULTATION-TO-THE-CLIENT STRATEGY
The consultation-to-the-client strategy was developed with three objectives in mind. First, clients must learn how to manage their own lives and care for themselves by interacting effectively with other people in the en- vironment, including health care professionals. The consultation-to-the-client strategy emphasizes clients’ capacities and targets their ability to take care of them- selves. Second, this strategy was designed to decrease instances of “splitting” between DBT therapists and other people interacting with clients, which occurs when different providers in a client’s network hold dif- fering opinions on how to treat the client. A fundamen- tal tenet of this strategy is that therapists do not tell
others, including other health care professionals, how to treat the client. The therapist may suggest but may not demand. What this means in practice is that the therapist is not attached to others treating a client in a specific way. By remaining in the role of a consultant to the client, the therapist stays out of such arguments. Fi- nally, the consultation-to-the-client strategy promotes respect for clients by imparting the message that they are credible and capable of performing interventions on their own behalf.
As mentioned previously, it is the responsibility of the individual DBT therapist to coordinate and orga- nize care with ancillary treatment providers (function 5; e.g., case managers, pharmacotherapists). The con- sultation-to-the-client strategy balances the consulta- tion-to-the-therapist strategy described earlier, primar- ily by providing direct consultation to the client in how to interact with other providers rather than consulting with people in the client’s environment on how to in- teract with the client. Except for special circumstances listed earlier, DBT therapists do not discuss clients with ancillary providers, or other providers in the client’s environment, without the client present. The therapist works with the client to problem-solve difficulties he/ she has with his/her network, leaving the client to act as the intermediary between the therapist and other pro- fessionals.
ENVIRONMENTAL INTERVENTION
The bias in DBT is toward teaching the client how to interact effectively with his/her environment. Thus, the consultation-to-the-client strategy is the dominant case management strategy and is used whenever pos- sible. There are times, however, when intervention by the therapist is needed. In general, the environmental intervention strategy is used over the consultation-to- the-client strategy when substantial harm may befall the client if the therapist does not intervene. The gen- eral rule for environmental intervention is that when clients lack abilities that they need to learn or that are impossible to obtain, or are not reasonable or necessary, the therapist may intervene.
Client Variables
DBT was developed to treat multidiagnostic, difficult- to-treat clients. Therefore, there are a number of req- uisite client characteristics for Stage 1 DBT. Of these, voluntary participation and a commitment to a speci-
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fied time period (e.g., 16 weeks, 6 months to 1 year) are critical. The effective application of DBT requires a strong interpersonal relationship between therapist and client. The therapist must first work to become a major reinforcer in the life of the client, then use the relationship to promote change in the client. Continu- ing the relationship can only be used as a positive con- tingency when a client wants to be in treatment; thus, contingency management is seriously compromised with involuntary clients. Court-ordered treatment is acceptable, if clients agree to remain in therapy even if the order is rescinded. A client characteristic neces- sary for group therapy is the ability to control overtly aggressive behavior toward others. In addition, patient problem behaviors must be managed to the degree that they are not disruptive to the learning of other group members. If the client is unable to participate in group therapy for skills training, skills training needs to take an alternative form; in such circumstances, often, indi- vidual skills training is used as an alternative. DBT was developed and has been most extensively evaluated with perhaps the most severely disturbed portion of the pop- ulation with BPD; all clients accepted into treatment had histories of multiple suicidal and NSSI behaviors. However, the treatment has been designed flexibly and is also effective with less severely disturbed clients.
Therapist Variables
In comparison to other aspects of therapy, the therapist characteristics that facilitate DBT have received little attention. However, evidence supports the assumption that effective therapy for clients with BPD requires the proficient balancing of acceptance and change strate- gies (Shearin & Linehan, 1992). This research also re- vealed that therapists’ nonpejorative perceptions of cli- ents were associated with less suicidal behavior.
Linehan (2015) describes requisite therapist charac- teristics in terms of three bipolar dimensions that must be balanced in the conduct of therapy. The first dimen- sion represents the balance of an orientation of accep- tance with an orientation of change. The therapist must be able to inhibit judgmental attitudes (often under very trying circumstances) and to practice acceptance of the client, of oneself, and of the therapeutic process exactly as these are in the current moment. Neverthe- less, the therapist remains cognizant that therapy im- plies necessity to change, and he/she assumes respon- sibility for directing the therapeutic influence. Second, the therapist must balance unwavering centeredness
with compassionate flexibility. Unwavering centeredness is the quality of believing in oneself, the therapy, and the client. Compassionate flexibility is the ability to take in relevant information about the client and to modify one’s position accordingly by letting go of a previously held position. In balancing these two dimensions, the therapist must be able to observe his/her own limits without becoming overly rigid. Finally, the DBT thera- pist must be able to balance a high degree of nurturing with benevolent demanding. Nurturing refers to teach- ing, coaching, resourcing, assisting, and strengthening the client, whereas benevolent demanding requires the therapist to recognize existing capabilities, to reinforce adaptive behavior, and to refuse to “do” for the client when the client can “do” for him/herself. Above all, the ability to demand requires willingness to believe in the client’s ability to change.
TREATMENT STRATEGIES
Treatment strategies in DBT refer to the role and focus of the therapist, as well as a coordinated set of proce- dures that function to achieve specific treatment goals. Although DBT strategies usually comprise a number of steps, use of a strategy does not necessarily require the application of every step. It is considerably more im- portant that the therapist apply the intent of the strat- egy than that he/she should inflexibly lead the client through a series of prescribed maneuvers.
DBT employs five sets of treatment strategies to achieve the previously described behavioral targets: (1) dialectical strategies, (2) core strategies, (3) stylis- tic strategies, (4) case management strategies (discussed earlier), and (5) integrated strategies. DBT strategies are described in detail in Linehan’s 1993 text. Within an individual session and with a given client, certain strat- egies may be used more than others, and all strategies may not be necessary or appropriate. An abbreviated discussion of the first three types of DBT treatment strategies follows.
Dialectical Strategies
Dialectical strategies permeate the entire therapy, and their use provides the rationale for adding the term dia- lectical to the title of the therapy. There are three types of dialectical strategies: those having to do with how the therapist structures interactions; those pertaining to how the therapist defines and teaches skillful behaviors;
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and certain specific strategies used during the conduct of treatment.
Dialectics of the Relationship: Balancing Treatment Strategies
Dialectical strategies in the most general sense of the term have to do with how the therapist balances the dialectical tensions within the therapy relationship. As noted earlier, the fundamental dialectic within any psychotherapy, including that with a client who has BPD, is that between acceptance of what is and efforts to change what is. A dialectical therapeutic position is one of constant attention to combining acceptance and change, flexibility and stability, nurturing and challenging, and focusing on capabilities and also on limitations and deficits. The goals are to bring out the opposites, both in therapy and in the client’s life, and to provide conditions for syntheses. The presumption is that change may be facilitated by emphasizing ac- ceptance, and acceptance, by emphasizing change. The emphasis on opposites sometimes takes place over time (i.e., over the whole of an interaction) rather than simul- taneously or in each part of an interaction. Although many, if not all, psychotherapies, including cognitive and behavioral treatments, attend to these issues of bal- ance, placing the concept of balance at the center of the treatment ensures that the therapist remains attentive to its importance.
Three primary characteristics are needed to main- tain a dialectical stance in the therapeutic relationship: movement, speed, and flow. Movement refers to acting with certainty, strength, and total commitment on the part of the therapist. If the therapist only moves half- heartedly, the client will only move halfheartedly. Speed is of the essence and entails keeping the therapy mov- ing, so that it does not become rigid or stuck. Finally, flow refers to being mindful of the moment-to-moment unfolding of a session and responding smoothly, and with apparent effortlessness.
Teaching Dialectical Behavior Patterns
Dialectical thinking is emphasized throughout the en- tire treatment. Not only does the therapist maintain a dialectical stance in his/her treatment of the client but he/she also focuses on teaching and modeling dialecti- cal thinking to the client. The therapist helps the cli- ent move from an “either–or” position to a “both–and” position, without invalidating the first idea or its po-
larity when asserting the second. Behavioral extremes and rigidity—whether cognitive, emotional, or overtly behavioral—are signals that synthesis has not been achieved; thus, they can be considered nondialectical. Instead, a “middle path” similar to that advocated in Buddhism is advocated and modeled. The important thing in following the path to Enlightenment is to avoid being caught and entangled in any extreme and always follow the Middle Way (Kyokai, 1966). This emphasis on balance is similar to the approach advocated in re- lapse prevention models (e.g., Marlatt & Gordon, 1985) for treating addictive behaviors.
Specific Dialectical Strategies
There are eight specific dialectical treatment strategies: (1) entering and using paradox, (2) using metaphor, (3) playing the devil’s advocate, (4) extending, (5) activat- ing the client’s “wise mind,” (6) making lemonade out of lemons (turning negatives into positives), (7) allow- ing natural change (and inconsistencies even within the therapeutic milieu), and (8) assessing dialectically by al- ways asking the question “What is being left out here?” Due to space limitations, a selection of these strategies is included in the following sections. For a complete re- view, the interested reader is referred to the DBT treat- ment manual (Linehan, 1993).
ENTERING THE PARADOX
Entering the paradox is a powerful technique, because it contains the element of surprise. The therapist pres- ents the paradox without explaining it and highlights the paradoxical contradictions within the behavior, the therapeutic process, and reality in general. The essence of the strategy is the therapist’s refusal to step in with rational explanation; the client’s attempts at logic are met with silence, a question, or a story designed to shed a small amount of light on the puzzle to be solved. The client is pushed to achieve understanding, to move to- ward synthesis of the polarities, and to resolve the di- lemma him/herself. Linehan (2015) has highlighted a number of typical paradoxes and their corresponding dialectical tensions encountered over the course of ther- apy. Clients are free to choose their own behavior but cannot stay in therapy if they do not work at changing their behavior. They are taught to achieve greater inde- pendence by becoming more skilled at asking for help from others. Clients have a right to kill themselves, but if they ever convince the therapist that suicide is immi-
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nent, they may be locked up. Clients are not responsible for being the way they are, but they are responsible for what they become. In highlighting these paradoxical realities, both client and therapist struggle with con- fronting and letting go of rigid patterns of thought, emotion, and behavior, so that more spontaneous and flexible patterns may emerge.
USING METAPHOR: PARABLE, MYTH, ANALOGY, AND STORYTELLING
The use of metaphor, stories, parables, and myth is extremely important in DBT and provides alternative means of teaching dialectical thinking. Stories are usu- ally more interesting, easier to remember, and they en- courage the search for other meanings of events under scrutiny. Additionally, metaphors allow clients to dis- tance themselves from the problem. In general, the idea of metaphor is to take something the client does under- stand and use it as an analogy for something the cli- ent does not understand. Furthermore, metaphors and stories can be developed collaboratively over the course of treatment. When used in the context of a mindful- ness practice, such a parable is referred to as a koan fol- lowing the Zen tradition. When therapist and client relate to a metaphor, it can be a powerful tool to use throughout the treatment, reminding the client what he/she is working on. For example, changing behavior by learning new skills can be compared to building a new hiking trail in the woods. At first, the current trail is defined and easy to navigate; however, it always leads to a dead end (old dysfunctional behavior). To build a new trail (skillful behaviors), the hiker must repeat- edly go through a new, undefined area until it becomes worn in. This takes time, and the hiker moves slowly and deliberately, clearing away the brush. Additionally, while the new path is developing, the old path is slowly becoming grown over. The therapist can return to this story each time the client begins to struggle between trying new skills and returning to old dysfunctional behavior.
PLAYING DEVIL’S ADVOCATE
The devil’s advocate technique is quite similar to the argumentative approach used in rational–emotive and cognitive restructuring therapies. With this strategy, the therapist presents a propositional statement that is an extreme version of one of the client’s own dysfunctional beliefs, then plays the role of devil’s advocate to counter
the client’s attempts to disprove the extreme statement or rule. For example, a client may state, “Because I’m overweight, I’d be better off dead.” The therapist argues in favor of the dysfunctional belief, perhaps by suggest- ing that because this is true for the client, it must be true for others as well; hence, all overweight people would be better off dead. The therapist may continue along these lines: “And since the definition of what con- stitutes being overweight varies so much among people, there must be an awful lot of people who would be con- sidered overweight by someone. That must mean they’d all be better off dead!” Or “Gosh, I’m about 5 pounds overweight. I guess that means I’d be better off dead, too.” Any reservations the client proposes can be coun- tered by further exaggeration, until the self-defeating nature of the belief becomes apparent. The devil’s advo- cate technique is often used in the first several sessions to elicit a strong commitment from the client and in commitment sessions with new therapists joining the DBT team. The therapist argues to the client that since the therapy will be painful and difficult, it is not clear how making such a commitment (and therefore being accepted into treatment) could possibly be a good idea. This usually has the effect of moving the client to take the opposite position in favor of therapeutic change. To employ this technique successfully, it is important that the therapist’s argument seem reasonable enough to in- vite counterargument, and that the delivery be credible, made in a naive but offbeat manner.
EXTENDING
The term extending has been borrowed from aikido, a Japanese form of self-defense. In that context, extend- ing occurs when the student of aikido waits for a chal- lenger’s movements to reach their natural completion, then extends a movement’s endpoint slightly further than what would naturally occur, leaving the challenger vulnerable and off balance. In DBT, extending occurs when the therapist takes the severity or gravity of what the client is communicating more seriously than the cli- ent intends. This strategy is the emotional equivalent of the devil’s advocate strategy. It is particularly effective when the client is threatening dire consequences of an event or problem to induce change in the environment. Take the interaction with the following client, who threatens suicide if an extra appointment time for the next day is not scheduled. The following interchange occurred after attempts to find a mutually acceptable time failed.
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CLIENT: I’ve got to see you tomorrow, or I’m sure I will end up killing myself. I just can’t keep it together by myself any longer.
THERAPIST: Hmm, I didn’t realize you were so upset! We’ve got to do something immediately if you are so distressed that you might kill yourself. What about hospitalization? Maybe that is needed.
CLIENT: I’m not going to the hospital! Why won’t you just give me an appointment?
THERAPIST: How can we discuss such a mundane topic as session scheduling when your life is in danger? How are you planning to kill yourself?
CLIENT: You know how. Why can’t you cancel some- one or move an appointment around? You could put an appointment with one of your students off until another time. I can’t stand it anymore!
THERAPIST: I’m really concerned about you. Do you think I should call an ambulance?
The aspect of the communication that the therapist takes seriously (suicide as a possible consequence of not getting an appointment) is not the aspect (needing an extra appointment the next day) that the client wants taken seriously. The therapist takes the consequences seriously and extends the seriousness even further. The client wants the problem taken seriously, and indeed is extending the seriousness of the problem.
MAKING LEMONADE OUT OF LEMONS
Making lemonade out of lemons is similar to the no- tion in psychodynamic therapy of utilizing a client’s resistances; therapeutic problems are seen as opportu- nities for the therapist to help the client. The strategy involves taking something that is apparently problem- atic and turning it into an asset. Problems become op- portunities to practice skills; suffering allows others to express empathy; weaknesses become one’s strengths. To be effective, this strategy requires a strong thera- peutic relationship; the client must believe that the therapist has a deep compassion for his/her suffering. The danger in using this strategy is that it is easily con- fused with the invalidating refrain repeatedly heard by clients with BPD. The therapist should avoid the ten- dency to oversimplify a client’s problems, and refrain from implying that the lemons in the client’s life are really lemonade. While recognizing that the cloud is indeed black, the therapist assists the client in finding
the positive characteristics of a situation—thus, the sil- ver lining.
Core Strategies
Validation
Validation and problem-solving strategies, together with dialectical strategies, make up the core of DBT and form the heart of the treatment. Validation strate- gies are the most obvious acceptance strategies, whereas problem-solving strategies are the most obvious change strategies. Both strategies are used in every interac- tion with the client, although the relative frequency of each depends on the particular client, the current situ- ation, and the vulnerabilities of that client. However, throughout an entire session, there should be an over- all balance between the acceptance and change strate- gies. We discuss validation strategies in this section and problem-solving strategies in the next.
Clients with BPD present themselves clinically as people in extreme emotional pain. They plead, and at times demand, that their therapists do something to change this state of affairs. It is very tempting to focus the energy of therapy on changing the client by modi- fying irrational thoughts, assumptions, or schemas; cri- tiquing interpersonal behaviors or motives contributing to interpersonal problems; giving medication to change abnormal biology; and reducing emotional overreactivi- ty and intensity; and so on. In many respects, this focus recapitulates the invalidating environment by con- firming the client’s worst fears: The client is the prob- lem and indeed cannot trust his/her own reactions to events. Mistrust and invalidation of how one responds to events, however, are extremely aversive and can elicit intense fear, anger, and shame, or a combination of all three. Thus, the entire focus of change-based therapy can be aversive, because the focus by necessity contrib- utes to and elicits self-invalidation. However, an entire focus of acceptance-based therapy can also be invalidat- ing when it appears to the client that the therapist does not take his/her problems seriously. Therefore, once again, a dialectical stance focuses on a balance between the two poles.
Validation (according to the Oxford English Dic- tionary; Simpson & Weiner, 1989) refers to identifying the validity of an object or making something valid. It also encompasses activities such as corroborating, substantiating, verifying, and authenticating. The act of validating includes providing support from an au-
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thoritative source about the truth or validity of some- thing (Merriam-Webster, 2006). Communicating that something is valid implies that objective evidence and reputable authority support or justify the response given (Simpson & Weiner, 1989). These are precisely the meanings associated with the term when used in the context of psychotherapy in DBT.
The essence of validation is this: Therapists com- municate to clients that their responses make sense and are understandable within their current life context or situation. Therapists actively accept clients and com- municate this acceptance to clients. Clients’ responses are taken seriously and are not discounted or trivialized. Validation strategies require the therapists to search for, recognize, and reflect to the clients and/or the group as a whole the validity inherent in their responses to events. With unruly children, parents have to “catch them while they’re good” in order to reinforce their be- havior; similarly, therapists have to uncover the validity within the clients’ responses, sometimes amplify this validity, and then reinforce it. (Linehan, 2015, pp. 88)
Two things are important to note here. First, valida- tion means the acknowledgment of that which is valid. It does not mean “making” valid. Nor does it mean validating that which is invalid. The therapist observes, experiences, and affirms, but he/she does not create validity. Second, valid and scientific are not synonyms. Science may be one way to determine what is valid, logi- cal, sound in principle, and/or generally accepted as au- thority or normative knowledge. However, an authentic experience or apprehension of private events (at least, when similar to the same experiences of others or when in accord with other, more observable events) is also a basis for claiming validity. Validation can be consid- ered at any one of six levels. Each level is correspond- ingly more complete than the previous one, and each depends on the previous levels. They are definitional of DBT and are required in every interaction with the client. These levels are described most fully in Linehan (1997), and the following definitions are taken from her discussion.
LISTENING AND OBSERVING (V1)
Level 1 validation requires listening to and observing what the client is saying, feeling, and doing, as well as a corresponding active effort to understand what is being said and observed. The essence of this step is that the therapist is staying awake and interested in the client, paying attention to what the client says and does in the
current moment. The therapist notices the nuances of response in the interaction. Validation at Level 1 com- municates that the client per se, as well as the client’s presence, words, and responses in the session, have “such force as to compel serious attention and [usu- ally] acceptance” (see earlier definitions of validation; pp. 360–361).
ACCURATE REFLECTION (V2)
The second level of validation is the accurate reflection back to the client of his/her own feelings, thoughts, assumptions, and behaviors. The therapist conveys an understanding of the client by hearing what the client has said and seeing what the client does, and how he/she responds. Validation at Level 2 sanctions, empowers, or authenticates that the individual is who he/she actually is (p. 362).
ARTICULATING THE UNVERBALIZED (V3)
In Level 3 of validation, the therapist communicates understanding of aspects of the client’s experience and response to events that have not been communicated directly by the client. The therapist “mind-reads” the reason for the client’s behavior and figures out how the client feels and what he/she is wishing for, thinking, or doing just by knowing what has happened to the client. The therapist can make the link between precipitating event and behavior without being given any informa- tion about the behavior itself. The therapist can also articulate emotions and meanings the client has not ex- pressed (p. 364).
VALIDATING IN TERMS OF PAST LEARNING OR BIOLOGICAL DYSFUNCTION (V4)
At Level 4, behavior is validated in terms of its causes. Validation here is based on the notion that all behavior is caused by events occurring in time; thus, in prin- ciple, it is understandable. The therapist justifies the client’s behavior by showing that it is caused by past events. Even though information may not be available to determine all the relevant causes, the client’s feelings, thoughts, and actions make perfect sense in the context of the client’s current experience, physiology, and life to date. At a minimum, what “is” can always be justified in terms of sufficient causes; that is, what is “should be,” in that whatever was necessary for it to occur had to have happened (p. 367).
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VALIDATION IN TERMS OF PRESENT CONTEXT OR NORMATIVE FUNCTIONING (V5)
At Level 5, the therapist communicates that behavior is justifiable, reasonable, well grounded, meaningful, and/or efficacious in terms of current events, normative biological functioning, and/or the client’s ultimate life goals. The therapist looks for and reflects the wisdom or validity of the client’s response and communicates that the response is understandable. The therapist finds the relevant facts in the current environment that sup- port the client’s behavior. The therapist is not blinded by the dysfunctionality of some of the client’s response patterns to those aspects of a response pattern that may be either reasonable or appropriate to the context. Thus, the therapist searches the client’s responses for their in- herent reasonableness (as well as commenting on the inherent dysfunctionality of much of the response, if necessary) (pp. 370–371).
RADICAL GENUINENESS (V6)
In Level 6, the task is to recognize the client as he/ she is, seeing and responding to his/her strengths and capacities, while keeping a firm empathic understand- ing of his/her actual difficulties and incapacities. The therapist believes in the client and his/her capacity to change and move toward ultimate life goals, just as the therapist may believe in a friend or family member. The client is responded to as a person of equal status, due equal respect. Validation at the highest level is the vali- dation of the individual as “is.” The therapist sees more than the role, more than a “client” or “disorder.” Level 6 validation is the opposite of treating the client in a con- descending manner or as overly fragile. It is respond- ing to the individual as being capable of effective and reasonable behavior rather than assuming that he/she is an invalid. Whereas Levels 1–5 represent sequential steps in validation of a kind, Level 6 represents change in both level and kind (p. 377).
Cheerleading strategies constitute another form of validation and are the principal strategies for combating the active passivity and tendencies toward hopelessness in clients with BPD. In cheerleading, therapists com- municate the belief that clients are doing their best and validate clients’ ability to eventually overcome their dif- ficulties (a type of validation that, if not handled care- fully, can simultaneously invalidate clients’ perceptions of their helplessness). In addition, therapists express a belief in the therapy relationship, offer reassurance, and
highlight any evidence of improvement. Within DBT, cheerleading is used in every therapeutic interaction. Although active cheerleading should be reduced as cli- ents learn to trust and to validate themselves, cheerlead- ing strategies always remain an essential ingredient of a strong therapeutic alliance.
Finally, functional validation, another form of valida- tion used regularly in DBT, is a form of nonverbal or be- havioral validation that at times may be more effective than verbal validation. For example, a therapist drops a 50-pound block on the client’s foot. It would be consid- ered invalidating for the therapist simply to respond ver- bally, saying, “Wow, I can see that really hurts! You must be in a lot of pain.” Functional validation would entail the therapist removing the block from the client’s foot.
Problem Solving
We have previously discussed how clients with BPD typically experience therapies with a primary focus on change as invalidating. However, therapies that focus exclusively on validation can prove equally problematic. Exhortations to accept one’s current situation offer little solace to an individual who experiences life as painfully unendurable. Within DBT, problem-solving strate- gies are the core change strategies, designed to foster an active problem-solving style. For clients with BPD, however, the application of these strategies is fraught with difficulties. The therapist must keep in mind that in clients with BPD, the process will be more difficult than that with many other client populations. In work with clients who have BPD, the need for sympathetic understanding and interventions aimed at enhancing current positive mood can be extremely important. The validation strategies just described, as well as the irreverent communication strategy described later, can be tremendously useful here. Within DBT, problem solving is a two-stage process that concentrates first on understanding and accepting a selected problem, then generating alternative solutions. The first stage involves (1) behavioral analysis, (2) insight into recurrent behav- ioral context patterns, and (3) giving the client didac- tic information about principles of behaviors, norms, and so on. The second stage specifically targets change through (4) analysis of possible solutions to problems, (5) orienting the client to therapeutic procedures likely to bring about desired changes, and (6) strategies de- signed to elicit and strengthen commitment to these procedures. The following sections describe in more detail some of these procedures.
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Behavioral Analysis
Behavioral analysis is one of the most important strate- gies in DBT. It is also the most difficult. The purpose of a behavioral analysis is first to select a problem, then to determine empirically what is causing it, what is pre- venting its resolution, and what aids are available for solving it. Behavioral analysis addresses four primary questions:
1. Are ineffective behaviors being reinforced, are ef- fective behaviors followed by aversive outcomes, or are rewarding outcomes delayed?
2. Does the client have the requisite behavioral skills to regulate his/her emotions, respond skillfully to conflict, and manage his/her own behavior?
3. Are there patterns of avoidance, or are effective behaviors inhibited by unwarranted fears or guilt?
4. Is the client unaware of the contingencies operat- ing in his/her environment, or are effective behav- iors inhibited by faulty beliefs or assumptions?
Answers to these questions guide the therapist in the selection of appropriate treatment procedures, such as contingency management, behavioral skills training, exposure, or cognitive modification. Thus, the value of an analysis lies in helping the therapist assess and understand a problem fully enough to guide effective therapeutic response. The first step in conducting a be- havioral analysis is to help the client identify the prob- lem to be analyzed and describe it in behavioral terms. Identifying the problem can be the most difficult task for the therapist, and if not done accurately and spe- cifically, can lead therapist and client astray. Problem definition usually evolves from a discussion of the pre- vious week’s events, often in the context of reviewing diary cards. The assumption of facts not in evidence is perhaps the most common mistake at this point. An identified problem is further assessed with a chain analysis—an exhaustive, blow-by-blow description of the chain of events leading up to and following the be- havior. In a chain analysis, the therapist constructs a general road map of how the client arrives at dysfunc- tional responses, including where the road actually starts (highlights vulnerability factors and prompting events), and notes possible alternative adaptive path- ways or junctions along the way. Additional goals are to identify events that automatically elicit maladaptive behavior, behavioral deficits that are instrumental in maintaining problematic responses, and environmen-
tal and behavioral events that may be interfering with more appropriate behaviors. The overall goal is to deter- mine the function of the behavior (i.e., the problem the behavior was instrumental in solving).
Chain analysis always begins with a specific environ- mental event. Pinpointing such an event may be dif- ficult, because clients are frequently unable to identify anything in the environment that set off the problem- atic response. Nevertheless, it is important to obtain a description of the events co-occurring with the onset of the problem. The therapist then attempts to identify both environmental and behavioral events for each sub- sequent link in the chain. Here, the therapist must play the part of a very keen observer, thinking in terms of very small chunks of behavior, and repeatedly identify- ing what the client was thinking, feeling, and doing, and what was occurring in the environment from mo- ment to moment. The therapist asks the client, “What happened next?” or “How did you get from there to there?” Although, from the client’s point of view, such links may be self-evident, the therapist must be care- ful not to make assumptions. For example, a client who had attempted suicide once stated that she decided to kill herself because her life was too painful for her to live any longer. From the client’s point of view, this was an adequate explanation for her suicide attempt. For the therapist, however, taking one’s life because life is too painful was only one solution. One could decide life is too painful, then decide to change one’s life. Or one could believe that death might be even more painful and decide to tolerate life despite its pain. In this instance, careful questioning revealed that the cli- ent actually assumed she would be happier dead than alive. Challenging this assumption, then, became a key to ending her persistent suicide attempts. It is equally important to pinpoint exactly what consequences are maintaining the problematic response. Similarly, the therapist should also search for consequences that serve to weaken the problem behavior. As with antecedent events, the therapist probes for both environmental and behavioral consequences, obtaining detailed de- scriptions of the client’s emotions, somatic sensations, actions, thoughts, and assumptions. A rudimentary knowledge of the rules of learning and principles of re- inforcement is crucial.
The final step in behavioral analysis is to construct and test hypotheses about events that are relevant to generating and maintaining the problem behavior. The biosocial theory of BPD suggests several factors of primary importance. For example, DBT focuses most
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closely on intense or aversive emotional states; the ame- lioration of negative affect is always suspected as being among the primary motivational variables for dysfunc- tional behavior in BPD. The theory also suggests that typical behavioral patterns, such as deficits in dialec- tical thinking or behavioral skills, are likely to be in- strumental in producing and maintaining problematic responses.
Solution Analysis
Once the problem has been identified and analyzed, problem solving proceeds with an active attempt at finding and identifying alternative solutions. DBT pos- its that there are five responses to any one problem: (1) Solve the problem; (2) change the emotional reaction to the problem; (3) tolerate the problem; (4) stay miser- able, or (5) make things worse. These five options are presented as needed prior to problem solving to ensure that therapist and client are consistently working to- ward the same goal.
At times, solutions are discussed throughout the be- havioral analysis, and pointing to these alternative so- lutions may be all that is required, rather than waiting until the behavioral analysis is completed. The therapist may ask, “What do you think you could have done dif- ferently here?” Throughout this process, the therapist is actively modeling effective problem solving and solu- tion generation, with a heavier emphasis on modeling and guiding the client early on in treatment. At other times, a more complete solution analysis is necessary. Here the task is to “brainstorm” or generate as many al- ternative solutions as possible. Solutions should then be evaluated in terms of the various outcomes expected. The final step in solution analysis is to choose a solu- tion that will somehow be effective. Throughout the evaluation, the therapist guides the client in choosing a particular behavioral solution. Here, it is preferable that the therapist pay particular attention to long-term over short-term gain, and that chosen solutions render maximum benefit to the client rather than benefit to others.
Problem‑Solving Procedures
DBT employs four problem-solving procedures taken directly from the cognitive and behavioral treatment literature. These four—skills training, contingency procedures, exposure, and cognitive modification—are viewed as primary vehicles of change throughout DBT,
since they influence the direction that client changes take from session to session. Although they are dis- cussed as distinct procedures by Linehan (2015), it is not clear that they can in fact be differentiated in every case in clinical practice. The same therapeutic sequence may be effective because it teaches the client new skills (skills training), provides a consequence that influences the probability of preceding client behaviors occurring again (contingency procedures), provides nonreinforced exposure to cues associated previously but not currently with threat (exposure procedures), or changes the cli- ent’s dysfunctional assumptions or schematic process- ing of events (cognitive modification). In contrast to many cognitive and behavioral treatment programs in the literature, these procedures (with some exceptions noted below) are employed in an unstructured manner, interwoven throughout all therapeutic dialogue. Thus, the therapist must be well aware of the principles gov- erning the effectiveness of each procedure in order to use it strategically. The exceptions are in skills training, where skills training procedures predominate.
Skills Training
An emphasis on skills building is pervasive throughout DBT. In both individual and group therapy, the thera- pist insists at every opportunity that the client actively engage in the acquisition and practice of behavioral skills. The term skills is used synonymously with ability and includes, in its broadest sense, cognitive, emotional, and overt behavioral skills, as well as their integration, which is necessary for effective performance. Skills training is called for when a solution requires skills not currently in the individual’s behavioral repertoire, or when the individual has the component behaviors but cannot integrate and use them effectively. Skills train- ing in DBT incorporates three types of procedures: (1) skills acquisition (modeling, instructing, advising); (2) skills strengthening (encouraging in vivo and within- session practice, role playing, feedback); and (3) skills generalization (phone calls to work on applying skills; taping therapy sessions to listen to between sessions; homework assignments).
Contingency Procedures
Every response within an interpersonal interaction is potentially a reinforcement, a punishment, or a with- holding or removal of reinforcement. Contingency management requires therapists to organize their be-
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havior strategically, so client behaviors that represent progress are reinforced, while unskillful or maladaptive behaviors are extinguished or punished. Natural conse- quences are preferred over arbitrary consequences. An important contingency in DBT is the therapist’s inter- personal behavior with the client, which is contingent on alliance.
Effective contingency management requires that the therapist orient the client to the principles of learn- ing. The therapist must attend to the client’s behaviors and use the principles of shaping to reinforce those behaviors that represent progress toward DBT targets. Equally important is that the therapist take care not to reinforce behaviors targeted for extinction. In theory, this may seem obvious, but in practice, it can be quite difficult. The problematic behaviors of clients with BPD are often quite effective in obtaining reinforcing outcomes or in stopping painful events. Indeed, the very behaviors targeted for extinction have typically been intermittently reinforced by mental health pro- fessionals, family members, and friends. Contingency management at times requires the use of aversive con- sequences, similar to “setting limits” in other treatment modalities. Three guidelines are important when using aversive consequences. First, punishment should “fit the crime,” and a client should have some way of termi- nating its application. For example, in DBT, a detailed behavioral analysis follows a suicidal or NSSI act; such an analysis is an aversive procedure for most clients. Once it has been completed, however, a client’s ability to pursue other topics is restored. Second, it is crucial that therapists use punishment with great care, in low doses, and very briefly, and that a positive interpersonal atmosphere be restored following any client improve- ment. Third, punishment should be just strong enough to work. Although the ultimate punishment is termina- tion of therapy, a preferable fallback strategy is putting clients on “vacations from therapy.” This approach is considered when all other contingencies have failed, or when a situation is so serious that a therapist’s thera- peutic or personal limits have been crossed. When uti- lizing this strategy, the therapist provides contingency clarification by clearly identifying what behaviors must be changed and explains that once the conditions have been met, the client can return. The therapist main- tains intermittent contact by phone or letter, and pro- vides a referral or backup while the client is on vacation. (In colloquial terms, the therapist kicks the client out, clarifies conditions for return, and then pines for the client’s return.)
Observing limits constitutes a special case of contin- gency management involving the application of prob- lem-solving strategies to client behaviors that threaten or cross a therapist’s personal limits. Such behaviors interfere with the therapist’s ability or willingness to conduct the therapy. Therapists must take responsibil- ity for monitoring their own personal limits and for clearly communicating them to clients. Therapists who do not do this eventually burn out, terminate therapy, or otherwise harm their clients. DBT favors natural over arbitrary limits. Thus, limits vary among thera- pists, over time, and over circumstances. Limits should also be presented as being for the good of the therapist, not for the good of the client. What the client argues is in his/her best interests may not ultimately be good for the therapists.
Cognitive Modification
The fundamental message given to clients in DBT is that cognitive distortions are just as likely to be caused by emotional arousal as to be the cause of the arousal in the first place. The overall message is that, for the most part, the source of a client’s distress is extremely stress- ful life events rather than a distortion of benign events. Cognitive restructuring procedures, such as those ad- vocated by Beck, Brown, Berchick, Stewart, and Steer (1990) and Ellis (1973), are used and taught in DBT, al- though they do not hold a dominant place. In contrast, contingency clarification strategies described earlier are used relentlessly, highlighting contingent relationships operating in the here and now.
Exposure
All of the change procedures in DBT can be reconcep- tualized as exposure strategies. The principles of ex- posure used in DBT have been developed for anxiety disorders (see Foa & Kozak, 1986) and expanded in DBT to address all problematic emotions. These strate- gies work by reconditioning dysfunctional associations that develop between stimuli (e.g., an aversive stimulus, hospitalization, may become associated with a positive stimulus, being nurtured; a client may later work to be hospitalized) or between a response and a stimulus (e.g., an adaptive response, expression of emotions, is met with an aversive consequence, rejection by a loved one; a client may work to suppress emotions). As noted earlier, the DBT therapist conducts a chain analysis of the eliciting cue, the problem behavior (including emo-
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tions), and the consequences of the behavior. Working within a behavior therapy framework, the therapist operates according to three guidelines for exposure in DBT: (1) Exposure to the cue that precedes the problem behavior must be nonreinforced (e.g., if a client is fear- ful that discussing suicidal behavior will lead to his/her being rejected, the therapist must not reinforce the cli- ent’s shame by ostracizing him/her); (2) dysfunctional responses are blocked in the order of the primary and secondary targets of treatment (e.g., suicidal or NSSI behavior related to shame is blocked by getting the cli- ent’s cooperation in throwing away hoarded medica- tions); and (3) actions opposite to the dysfunctional behavior are reinforced (e.g., the therapist reinforces the client for talking about painful, shame-related suicidal behavior).
Formal and informal exposure procedures involve first orienting the client to the techniques and to the fact that exposure to cues is often experienced as pain- ful or frightening. Thus, the therapist does not remove the cue to emotional arousal, and at the same time he/ she blocks both the action tendencies (including escape responses) and the expressive tendencies associated with the problem emotion. Rationale is reviewed extensively, such that clients themselves can explain the rationale for exposure procedures. In addition, a crucial step of exposure procedures is teaching the client some means of titrating or ending exposure when emotions become unendurable. Therapist and client collaborate in devel- oping positive, adaptive ways for the client to end expo- sure voluntarily, preferably after some reduction in the problem emotion has occurred.
Stylistic Strategies
DBT balances two quite different styles of communica- tion that refer to how the therapist executes other treat- ment strategies. The first, reciprocal communication, is similar to the communication style advocated in CCT. The second, irreverent communication, is quite similar to the style advocated by Whitaker (1975) in his writ- ings on strategic therapy. Reciprocal communication strategies are designed to reduce a perceived power dif- ferential by making the therapist more vulnerable to the client. In addition, they serve as a model for appropriate but equal interactions within an important interper- sonal relationship. Irreverent communication is usu- ally riskier than reciprocity. However, it can facilitate problem solving or produce a breakthrough after long periods when progress has seemed thwarted. To be used
effectively, irreverent communication must balance re- ciprocal communication, and the two must be woven into a single stylistic fabric. Without such balancing, neither strategy represents DBT.
Reciprocal Communication
Responsiveness, self-disclosure, warm engagement, and genuineness are the basic guidelines of reciprocal communication. Responsiveness requires attending to the client in a mindful (attentive) manner and taking the client’s agenda and wishes seriously. However, this does not mean that the therapist gives priority to the client’s agenda over the treatment hierarchy. It refers to the therapist validating the importance of the client’s agenda openly. It is a friendly, affectionate style reflect- ing warmth and engagement in the therapeutic inter- action. Self-involving self-disclosure is the therapist’s immediate, personal reactions to the client and his/her behavior. This strategy is used frequently throughout DBT. For example, a therapist whose client complained about his coolness said, “When you demand warmth from me, it pushes me away and makes it harder to be warm.” Similarly, when a client repeatedly failed to fill out diary cards but nevertheless pleaded with her thera- pist to help her, the therapist responded, “You keep ask- ing me for help, but you won’t do the things I believe are necessary to help you. I feel frustrated, because I want to help you, but I feel that you won’t let me.” Such statements serve both to validate and to challenge. They constitute both an instance of contingency manage- ment because therapist statements about the client are typically experienced as either reinforcing or punishing, and an instance of contingency clarification because the client’s attention is directed to the consequences of his/her interpersonal behavior.
Self-disclosure of professional or personal informa- tion is used to validate and model coping and norma- tive responses. The key point here is that a therapist should only use personal examples in which he/she has successfully mastered the problem at hand. This may seem like an obvious point, but it is very easy to fall into this pit by trying actively to validate the client’s di- lemma. For example, when working with a client whose goal is to wake up early each morning to exercise, but who is having difficulty getting out of bed, the therapist may attempt to validate the behavior as normative by stating, “Yeah, I struggle with getting up every morn- ing, too, even though I tell myself every night that I am going to exercise in the morning.” However, this
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self-disclosure is only useful to the client if the therapist continues by stating what skillful behavior he/she uses to get up each morning and exercise successfully.
Irreverent Communication
Irreverent communication is used to push the client “off balance,” get his/her attention, present an alterna- tive viewpoint, or shift affective response. It is a highly useful strategy when the client is immovable, or when therapist and client are “stuck.” It has an “offbeat” fla- vor and uses logic to weave a web the client cannot es- cape. Although it is responsive to the client, irreverent communication is almost never the response the client expects. For irreverence to be effective it must be both genuine (vs. sarcastic or judgmental) and come from a place of compassion and warmth toward the client. Otherwise, the client may become even more rigid. When using irreverence, the therapist highlights some unintended aspect of the client’s communication or “re- frames” it in an unorthodox manner. For example, if the client says, “I am going to kill myself,” the therapist might say, “I thought you agreed not to drop out of ther- apy.” Irreverent communication has a matter-of-fact, al- most deadpan style that is in sharp contrast to the warm responsiveness of reciprocal communication. Humor, a certain naiveté, and guilelessness are also characteristic of the style. A confrontational tone is also irreverent, communicating “bullshit” to responses other than the targeted adaptive response. For example, the therapist might say, “Are you out of your mind?” or “You weren’t for a minute actually believing I would think that was a good idea, were you?” The irreverent therapist also calls the client’s bluff. For the client who says, “I’m quitting therapy,” the therapist might respond, “Would you like a referral?” The trick here is to time the bluff carefully, with the simultaneous provision of a safety net; it is im- portant to leave the client a way out.
CASE STUDY
Background
At the initial meeting, “Cindy,” a 30-year-old married woman with no children, was living in a middle-class suburban area with her husband. She has a college ed- ucation and successfully completed almost 2 years of medical school. Cindy was referred to one of us (M. M. L.) by her psychiatrist of 1½ years, who was no longer willing to provide more than pharmacotherapy follow-
ing a recent hospitalization for a near-lethal suicide at- tempt. In the 2 years prior to referral, Cindy had been hospitalized at least 10 times (once for 6 months) for psychiatric treatment of suicidal ideation; had engaged in numerous instances of both NSSI behavior and sui- cide attempts, including at least 10 instances of drink- ing Clorox bleach, multiple deep cuts, and burns; and had had three medically severe or nearly lethal suicide attempts, including cutting an artery in her neck. At the time of referral, Cindy met DSM-III-R (American Psychiatric Association, 1987) and Gunderson’s (1984) criteria for BPD. She was also taking a variety of psy- chotropic drugs. Until age 27, Cindy was able to func- tion well in work and school settings, and the marriage was reasonably satisfactory to both partners, although her husband complained about Cindy’s excessive anger. When Cindy was in the second year of medical school, a classmate she knew only slightly committed suicide. Cindy stated that when she heard about the suicide, she immediately decided to kill herself also but had very little insight into what about the situation actually elic- ited her inclination to kill herself. Within weeks she left medical school and became severely depressed and ac- tively suicidal. Although Cindy self-presented as a per- son with few psychological problems before the class- mate’s suicide, further questioning revealed a history of severe anorexia nervosa, bulimia nervosa, and alcohol and prescription medication abuse, originating at the age of 14 years. Indeed, she had met her husband at an Alcoholics Anonymous (AA) meeting while attend- ing college. Nevertheless, until the student’s suicide in medical school, Cindy had been successful at maintain- ing an overall appearance of relative competence.
Treatment
At the initial meeting, Cindy was accompanied by her husband, who stated that he and Cindy’s family consid- ered his wife too lethally suicidal to be out of a hospital setting. Consequently, he and Cindy’s family were seri- ously contemplating the viability of finding long-term outpatient care. However, Cindy stated a strong prefer- ence for inpatient treatment, although no therapist in the local area other than M. M. L. appeared willing to take her into outpatient treatment. The therapist agreed to accept Cindy into therapy, contingent on the client’s stated commitment to work toward behavioral change and to stay in treatment for at least 1 year. (It was later pointed out repeatedly that this also meant the client had agreed not to commit suicide.) Thus, the thera-
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pist began the crucial first step of establishing a strong therapeutic alliance by agreeing to accept the client de- spite the fact that no one else was willing to do so. She pointed out, however, that acceptance into therapy did not come without a cost. In this manner, the therapist communicated acceptance of the client exactly as she was in the current moment, while concomitantly mak- ing clear that Cindy’s commitment toward change was the foundation of the therapeutic alliance. At the fourth therapy session, Cindy reported that she felt she could no longer keep herself alive. When reminded of her pre- vious commitment to stay alive for 1 year of therapy, Cindy replied that things had changed and she could not help herself. Subsequent to this session, almost every individual session for the next 6 months revolved around the topic of whether (and how) to stay alive versus committing suicide. Cindy began coming to ses- sions wearing mirrored sunglasses and would slump in her chair or ask to sit on the floor. Questions from the therapist were often met with a minimal comment or long silences. In response to the therapist’s attempts to discuss prior self-injurious behavior, Cindy would be- come angry and withdraw (slowing down the pace of therapy considerably). The client also presented with marked dissociative reactions, which would often occur during therapy sessions. During these reactions, Cindy would appear unable to concentrate or hear much of what was being said. When queried by the therapist, Cindy would describe her experience as feeling “spacey” and distant. The client stated that she felt she could no longer engage in many activities, such as driving, work- ing, or attending school. Overall, the client viewed her- self as incompetent in all areas.
The use of Weekly Diary Cards, which Cindy filled out weekly (or at the beginning of the session, if she forgot), assisted the therapist in carefully monitoring Cindy’s daily experiences of suicidal ideation, misery, and urges to harm herself, as well as actual suicide at- tempts and NSSI behaviors. Using behavioral analyses, identification of the sequence of events leading up to and following Cindy’s suicidal behavior soon became an important focus of therapy. At every point, the therapist conceptualized self-injurious behavior as to be expected given the strength of the urge (but considered it ultimately beatable), and pointed out repeatedly that if the client committed suicide, therapy would be over, so they had better work really hard now, while Cindy was alive.
Over the course of several months, the behavioral analyses began to identify a frequently recurring be-
havioral pattern that preceded suicidal behaviors. For Cindy, the chain of events would often begin with an interpersonal encounter (almost always with her hus- band), which culminated in her feeling threatened, crit- icized, or unloved. These feelings were often followed by urges either to self-mutilate or to kill herself, depend- ing somewhat on the covarying levels of hopelessness, anger, and sadness. Decisions to self-mutilate and/ or to attempt suicide were often accompanied by the thought, “I’ll show you.” At other times, hopelessness and a desire to end the pain permanently seemed pre- dominant. Both are examples of emotional vulnerabil- ity. Following the conscious decision to self-mutilate or to attempt suicide, Cindy would then immediately dis- sociate and at some later point cut or burn herself, usu- ally while in a state of “automatic pilot.” Consequently, Cindy often had difficulty remembering specifics of the actual acts. At one point, Cindy burned her leg so badly (and then injected it with dirt to convince the doctor that he should give her more attention) that recon- structive surgery was required. Behavioral analyses also revealed that dissociation during sessions usually fol- lowed Cindy’s perception of the therapist’s disapproval or invalidation, especially when the therapist appeared to suggest that change was possible. The therapist tar- geted in-session dissociation by immediately addressing it as it occurred.
Several months into therapy, an apparently long- standing pattern of suicidal behaviors leading to in- patient admission was apparent. Cindy would report intense suicidal ideation, express doubts that she could resist the urge to kill herself, and request admission to her preferred hospital; or, without warning, she would cut or burn herself severely and require hospitalization for medical treatment. Attempts to induce Cindy to stay out of the hospital or to leave the hospital before she was ready typically resulted in an escalation of suicidality, followed by her pharmacotherapist’s (a psychiatrist) in- sistence on her admission or the hospital’s agreement to extend her stay. Observation of this behavioral pattern led the therapist to hypothesize that the hospitalization itself was reinforcing suicidal behavior; consequently, she attempted to change the contingencies for suicidal behaviors. Using didactic and contingency clarifica- tion strategies, the therapist attempted to help Cindy understand how hospitalization might be strengthen- ing the very behavior they were working to eliminate. This issue became a focal point of disagreement within the therapy, with Cindy viewing the therapist’s posi- tion as unsympathetic and lacking understanding of
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her phenomenal experience. In Cindy’s opinion, the intensity of her emotional pain rendered the probability of suicide so high that hospitalization was necessary to guarantee her safety. She would buttress her position by citing frequently her difficulties with dissociative reactions, which she reported as extremely aversive and which, in her opinion, made her unable to func- tion much of the time. From the therapist’s perspective, the deleterious long-term risk of suicide created by re- peated hospitalization in response to suicidal behavior was greater than the short-term risk of suicide if hos- pitalization stays were reduced. These differences in opinion led to frequent disagreements within sessions. It gradually became clear that Cindy viewed any expla- nations of her behavior as influenced by reinforcement as a direct attack; she implied that if hospitalization was reinforcing her suicidal behavior, then the thera- pist must believe that the purpose of her suicidality was for admission into the hospital. This was obviously not the case (at least some of the time), but all attempts to explain reinforcement theory in any other terms failed. The therapist compensated somewhat for insisting on the possibility that she (the therapist) was correct by doing three things. First, she repeatedly validated the client’s experience of almost unendurable pain. Second, she made certain to address the client’s dissociative be- havior repeatedly, explaining it as an automatic reaction to intensely painful affect (or the threat of it). Third, she frequently addressed the quality of the relationship between Cindy and herself to strengthen the relation- ship and maintain Cindy in therapy, even though to do so was a source of even more emotional pain. By the fifth month, the therapist became concerned that the current treatment regimen was going to have the unin- tended consequence of killing the client (via suicide). At this point, the therapist’s limits for effective treatment were crossed; therefore, she decided to employ the con- sultation-to-the-client strategy to address Cindy’s hos- pitalizations. The first-choice strategy would have been to get Cindy to negotiate a new treatment plan with her preferred hospital and admitting psychiatrist. Cindy re- fused to go along, however, because she disagreed with the wisdom of changing her current unlimited access to the inpatient unit. The therapist was able to get Cindy to agree to a consultation meeting with all of her treat- ment providers, and, with some tenacity, the therapist actually got Cindy to make all the calls to set up the meeting (including inviting her insurance monitor, who was coordinating payment for treatment).
At the case conference, the therapist presented her hypothesis that contingent hospitalization was reinforc-
ing Cindy’s suicidal behavior. She also assisted Cindy in making the case that she (the therapist) was wrong. Using reciprocal communication and contingency management, the therapist stated that she simply could not conduct a therapy she thought might kill the client (and she had to go along with what she thought was best even if she were wrong, stating that “to do other- wise would be unethical”), and she requested that a new system of contingencies be agreed upon to disrupt the functional relationship between Cindy’s suicidal behav- ior and hospitalization. Therefore, a plan was developed wherein the client was not required to be suicidal to gain hospital admittance. Under this new set of contingen- cies, Cindy could elect, at will, to enter the hospital for a stay of up to 3 days, at the end of which time she would always be discharged. If she convinced people that she was too suicidal for discharge, she would be transferred to her least-preferred hospital for safety. Suicidal and NSSI behaviors would no longer be grounds for admis- sion except to a medical unit, when required. Although there was some disagreement as to the functional rela- tionship between suicidal behavior and hospitalization, this system was agreed upon. Following this meeting, Cindy’s husband announced that he was no longer able to live with or tolerate his wife’s suicidal behavior, and that the constant threat of finding her dead had led to his decision to file for divorce. The focus of therapy then shifted to helping Cindy grieve over this event and find a suitable living arrangement. Cindy alternated be- tween fury that her husband would desert her in her hour of need (or “illness,” as she put it) and despair that she could ever cope alone. She decided that “getting her feelings out” was the only useful therapy. This led to many tearful sessions, with the therapist simultaneously validating the pain; focusing on Cindy’s experiencing the affect in the moment, without escalating or block- ing it; and cheerleading Cindy’s ability to manage with- out going back into the hospital. Due to Cindy’s high level of dysfunctionality, she and her therapist decided that she would enter a residential treatment facility for a 3-month period. The facility had a coping skills orien- tation and provided group but not individual therapy. Cindy saw her therapist once a week and talked to her several times a week during this period. With some coaching, Cindy looked for and found a roommate to live with and returned to her own home at the end of 3 months (the ninth month of therapy). Over the course of treatment, the therapist used a number of strategies to treat Cindy’s suicidal, NSSI, and therapy-interfer- ing behaviors. In-depth behavioral chain and solution analysis helped the therapist (and sometimes the client)
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gain insight into the factors influencing current suicid- al behavior. For Cindy, as for most clients, performing these analyses was quite difficult, because the process usually generated intense feelings of shame, guilt, or anger. Thus, behavioral analysis also functioned as an exposure strategy, encouraging the client to observe and experience painful affect. It additionally served as a cognitive strategy in helping to change Cindy’s expec- tancies concerning the advantages and disadvantages of suicidal behavior, especially as the therapist repeatedly made statements such as “How do you think you would feel if I got angry at you and then threatened suicide if you didn’t change?” Finally, behavioral analysis served as contingency management, in that the client’s ability to pursue topics of interest in therapy sessions was made contingent on the successful completion of chain and solution analysis.
Cindy presented early in therapy with exceedingly strong perceptions as to her needs and desires, and with a concomitant willingness to engage in extremely lethal suicidal behavior. As previously mentioned, several of these acts were serious attempts to end her life, whereas others functioned as attempts to gain attention and care from significant others. This client also presented with an extreme sensitivity to any attempts at obvious change procedures, which she typically interpreted as communicating a message about her incompetence and unworthiness. Although Cindy initially commit- ted herself to attending weekly group skills training for the first year of therapy, her attendance at group meet- ings was quite erratic, and she generally tended either to miss entire sessions (but never more than three in a row) or to leave during the break. Cindy answered the therapist’s attempts to address this issue by stating that she could not drive at night due to night blindness. Although considered a therapy-interfering behavior and frequently addressed over the course of therapy, missing skills training was not a major focus of treatment due to the continuing presence of higher-priority suicidal behavior. The therapist’s efforts to engage the client in active skills acquisition during individual therapy ses- sions were also somewhat limited and always preceded by obtaining Cindy’s verbal commitment to problem solving. The stylistic strategy of irreverent communica- tion was of value to the therapeutic process. The thera- pist’s irreverence often served to “shake up” the client, resulting in a loosening of dichotomous thinking and maladaptive cognitions. The result of this was Cindy’s increased willingness to explore new and adaptive be- havioral solutions. Finally, relationship strategies were heavily employed as tools to strengthen the therapeutic
alliance and to keep it noncontingent on suicidal and/or dissociative behaviors. Included here were between-ses- sion therapist-initiated telephone calls to check in, the therapist routinely giving out phone numbers when she was traveling, and sending the client postcards when she was out of town.
By the 12th month of therapy, Cindy’s suicidal and self-injurious behavior, as well as urges to engage in such behavior, receded. In addition, her hospital stays were reduced markedly, with none occurring after the eighth month. While living at home with a roommate, Cindy was readmitted to medical school. Part of the reason for returning to school was to turn her life around, so that she could try to regain her husband’s love and atten- tion, or at least his friendship. As the therapy continued to focus on changing the contingencies of suicidal be- havior, reducing both emotional pain and inhibition, and tolerating distress, a further focus on maintaining sobriety and reasonable food intake was added. During the first months of living in her home without her hus- band, Cindy had several alcoholic binges, and her food intake dropped precipitously. These behaviors became immediate targets. The therapist’s strong attention to these behaviors also communicated to Cindy that the therapist would take her problems seriously even if she were not suicidal. Therapy focused as well on expand- ing her social network. As with suicidal behaviors, at- tention to these targets served as a pathway to treat- ing associated problems. As crisis situations decreased in frequency, greater attention was paid to analyzing family patterns, including experiences of neglect and invalidation, that might have led to Cindy’s problems in later life. Cindy did not report a history of sexual or physical abuse. Thus, the explicit goal of Stage 2 was to understand Cindy’s history and its relationship to her current problems.
In other cases, especially when there has been sexual and/or physical abuse in childhood, movement to Stage 2 before Stage 1 targets have been mastered is likely to result in retrogression to previously problematic be- haviors. For example, “Terry,” another client treated by the same therapist (M. M. L.), had been quite seriously abused physically by her mother throughout childhood and sexually abused by her father, beginning at age 5. The sexual advances were nonviolent at first but be- came physically abusive when Terry was approximately age 12. Prior to this therapy, Terry had not disclosed the incidents of abuse to anyone.
After successful negotiation of Stage 1 targets, the therapist proceeded to expose Terry to trauma-related cues by simply having her begin to disclose details of
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the abuse. These exposure sessions were intertwined with work on current problems in Terry’s life. Follow- ing one exposure session focused on the sexual abuse, Terry reverted to some of her previously problematic behaviors, evidenced by withdrawal and silence in ses- sions, suicidal ideation, and medication noncompli- ance. The appearance of such behavior marked the necessity of stopping Stage 2 discussions of previous sexual abuse to address Stage 1 targets recursively. Three sessions were devoted to a behavioral analysis of Terry’s current suicidal, therapy-interfering, and quality-of-life-interfering behaviors; these were eventu- ally linked both to fears about how the therapist would view her childhood emotional responses to her father, and to holiday visits with her father that precipitated conflicts over how Terry should be feeling about him in the present. This two-steps-forward, one-step-back approach is common to therapy for clients with BPD, and in particular may mark the transition between Stage 1 and Stage 2.
As previously mentioned, Stage 3 targets the client’s self-respect, regardless of the opinions of others. “Betty,” who was also in treatment with the same therapist (M. M. L.), had successfully negotiated Stages 1 and 2, and had become a highly competent nurse with training and supervisory responsibilities. Therapy with Betty was then focused on maintaining her self-esteem in the face of very powerful significant others (e.g., her super- visor) who constantly invalidated her. Components of the treatment included the therapist noting and high- lighting Betty’s tendency to modify her self-opinion in accordance with that of others, persistent attempts to extract from Betty self-validation and self-soothing, and imagery exercises wherein Betty imagined and ver- balized herself standing up to powerful others. Much of the therapy focus was on Betty’s interpersonal behavior within the therapy session, with attention to relating this behavior to her interactions with other important people. Thus, treatment at that point was very similar to the functional analytic psychotherapy regimen de- veloped by Kohlenberg and Tsai (1991). Overall, this third stage of therapy involved the movement to a more egalitarian relationship between client and therapist, in which emphasis was placed on the client standing up for her own opinions and defending her own actions. This approach required that the therapist both rein- force the client’s assertions, and step back and refrain from validating and nurturing the client in the manner characteristic of Stages 1 and 2. In addition, therapy sessions were reduced to every other week, and issues
surrounding eventual termination were periodically discussed.
Stage 4 of DBT targets the sense of incompleteness that can preclude the experience of joy and freedom. “Sally” started Stage 1 treatment with the same thera- pist (M. M. L.) 15 years ago. Stage 1 lasted 2 years; this was followed by a break of 1 year, after which treatment resumed for several years of bimonthly sessions leading to monthly sessions, and currently comprising four or five sessions a year. Sally has been married for 30 years to an irregularly employed husband who, though de- voted and loyal, is quite invalidating of her. Although apparently brilliant, he is usually dismissed from jobs for his interpersonal insensitivity. She has been em- ployed full-time at the same place for years, working with children. The son Sally felt closest to died in a plane accident 2 years ago; her mother died last year, and her father is very ill. Despite having a stable mar- riage, working in a stable and quite fulfilling job, hav- ing raised two well-adjusted sons, and still being ath- letic, life feels meaningless to Sally. In the past she was very active in spiritual activities; following meditation retreats or extended periods of daily meditation, she would report contentment and some sense of joy. Since her son died, Sally has let go of most of her spiritual activities. Following a 2-year focus on grieving, she is now ready for Stage 4. Treatment planning is focused on actively practicing and keeping track of progress in radical acceptance (or “letting go of ego,” in Zen termi- nology), either alone or with group support.
TRANSCRIPTS
The following (composite) transcripts represent actual examples of the process of therapy occurring over sev- eral sessions with different clients. These particular dia- logues between therapist and client have been chosen to provide the reader with comprehensive examples of the application of a wide range of DBT treatment strat- egies. The session targets in the following transcript were orienting and commitment. The strategies used were validation, problem solving (insight, orienting, and commitment), dialectical (devil’s advocate), and integrated (relationship enhancement).
Obtaining the commitment of clients with BPD is a crucial first step in beginning therapy. As illustrated in the following transcript, the dialectical technique of devil’s advocate can be highly effective when used as a commitment strategy. In this first therapy session, the
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therapist’s ultimate goal was to obtain the client’s com- mitment to therapy, as well as a commitment to elimi- nate suicidal behavior. She began by orienting the client to the purpose of this initial session.
THERAPIST: So are you a little nervous about me? CLIENT: Yeah, I guess I am. THERAPIST: Well, that’s understandable. For the next
50 minutes or so, we have this opportunity to get to know each other and see if we want to work together. So what I’d like to do is talk a little bit about the program and how you got here. So, tell me, what do you want out of therapy with me, and what are you doing here?
CLIENT: I want to get better. THERAPIST: Well, what’s wrong with you? CLIENT: I’m a mess. (Laughs.) THERAPIST: How so? CLIENT: Umm, I don’t know. I just can’t even cope
with everyday life right now. And I can’t even . . . I’m just a mess. I don’t know how to deal with anything.
THERAPIST: So what does that mean exactly? CLIENT: Umm, well, everything I try these days just
seems overwhelming. I couldn’t keep up on my job, and now I’m on medical leave. Plus everyone’s sick of me being in the hospital so much. And I think my psychiatrist wants to send me away because of all my self-harming.
THERAPIST: How often do you self-harm? CLIENT: Maybe once or twice a month. I use my lighter
or cigarettes, sometimes a razor blade. THERAPIST: Do you have scars all over? CLIENT: (Nods yes.) THERAPIST: Your psychiatrist tells me you’ve also
drunk Clorox. Why didn’t you mention that? CLIENT: I guess it didn’t enter my mind. THERAPIST: Do things just not enter your mind very
often? CLIENT: I don’t really know. Maybe. THERAPIST: So maybe with you I’m going to have to be
a very good guesser. CLIENT: Hmm. THERAPIST: Unfortunately, though, I’m not the great-
est guesser. So we’ll have to teach you how to have
things come to mind. So what is it exactly that you want out of therapy with me? To quit harming your- self, quit trying to kill yourself, or both?
CLIENT: Both. I’m sick of it. THERAPIST: And is there anything else you want help
with? CLIENT: Um, well, I don’t know how to handle money,
and I don’t know how to handle relationships. I don’t have friends; they don’t connect with me very often. I’m a former alcoholic and a recovering anorexic/bu- limic. I still have a tendency toward that.
THERAPIST: Do you think maybe some of what is going on with you is that you’ve replaced your alcoholic and anorexic behaviors with self-harm behaviors?
CLIENT: I don’t know. I haven’t thought about it that way. I just feel that I don’t know how to handle myself, and—you know, and I guess work through stuff, and that is obviously getting to me, because if it wasn’t, I wouldn’t be trying to kill myself.
THERAPIST: So, from your perspective, one problem is that you don’t know how to do things. A lot of things.
CLIENT: Yeah, and a lot of it is, I do know how, but for some reason I don’t do it anyway.
THERAPIST: Um hmm. CLIENT: You know, I mean, I know I need to save
money, and I know that I need to budget myself, and I do every single month, but every single month I get in debt. But, um, you know, it’s really hard for me. You know, it’s like sometimes I know it, or I know I shouldn’t eat something and I do it anyway.
THERAPIST: So it sounds like part of the problem is you actually know how to do things; you just don’t know how to get yourself to do the things you know how to do.
CLIENT: Exactly. THERAPIST: Does it seem like maybe your emotions are
in control—that you are a person who does things when you’re in the mood?
CLIENT: Yes. Everything’s done by the mood. THERAPIST: So you’re a moody person. CLIENT: Yes. I won’t clean the house for 2 months, and
then I’ll get in the mood to clean. Then I’ll clean it immaculately and keep it that way for 3 weeks—I mean, just immaculate—and then when I’m in the mood, I go back to being a mess again.
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THERAPIST: So one of the tasks for you and me would be to figure out a way to get your behavior and what you do less hooked up with how you feel?
CLIENT: Right.
The therapist used insight to highlight for the client the observed interrelationship between the client’s emo- tions and her behavior. She then began the process of shaping a commitment through the dialectical strategy of devil’s advocate.
THERAPIST: That, of course, is going to be hell to do, don’t you think? Why would you want to do that? It sounds so painful.
CLIENT: Well, I want to do it because it’s so inconsis- tent. It’s worse, you know, because when I’m . . . I know that, like with budgeting money or whatever, I know I need to do it, and then when I don’t do it, it makes me even more upset.
THERAPIST: Why would you ever want to do some- thing you’re not in the mood for?
CLIENT: Because I’ve got to. Because I can’t survive that way if I don’t.
THERAPIST: Sounds like a pretty easy life to me. CLIENT: Yeah, but I can’t afford to live if I just spend
my money on fun and stupid, frivolous things that I . . .
THERAPIST: Well, I guess maybe you should have some limits and not be too off the wall, but in general, I mean, why clean the house if you’re not in the mood?
CLIENT: Because it pisses me off when it’s a mess. And I can’t find things, like I’ve lost bills before and then I end up not paying them. And now I’ve got collection agencies on my back. I can’t deal with all this, and I end up self-harming and going into the hospital. And then I just want to end it all. But it still doesn’t seem to matter, because if I’m not in the mood to clean it, I won’t.
THERAPIST: So the fact that it makes horrible things happen in your life so far hasn’t been enough of a motivation to get you to do things against your mood, right?
CLIENT: Well, obviously not (laughs) because it’s not happening.
THERAPIST: Doesn’t that tell you, though? This is going to be a big problem, don’t you think? This isn’t going to be something simple. It’s not like you’re
going to walk in here and I’m going to say, “OK, magic wand,” and then all of a sudden you’re going to want to do things that you’re not in the mood for.
CLIENT: Yeah. THERAPIST: Yeah, so it seems to me that if you’re not in
the mood for things, if you’re kind of mood-depen- dent, that’s a very tough thing to crack. As a matter of fact, I think it’s one of the hardest problems there is to deal with.
CLIENT: Yeah, great. THERAPIST: I think we could deal with it, but I think
it’s going to be hell. The real question is whether you’re willing to go through hell to get where you want to get or not. Now I figure that’s the question.
CLIENT: Well, if it’s going to make me happier, yeah. THERAPIST: Are you sure? CLIENT: Yeah, I’ve been going through this since I was
11 years old. I’m sick of this shit. I mean, excuse my language, but I really am, and I’m backed up against the wall. Either I need to do this or I need to die. Those are my two choices.
THERAPIST: Well, why not die? CLIENT: Well, if it comes down to it, I will. THERAPIST: Um hmm, but why not now? CLIENT: Because, this is my last hope. Because if I’ve
got one last hope left, why not take it? THERAPIST: So, in other words, all things being equal,
you’d rather live than die, if you can pull this off. CLIENT: If I can pull it off, yeah. THERAPIST: OK, that’s good; that’s going to be your
strength. We’re going to play to that. You’re going to have to remember that when it gets tough. But now I want to tell you about this program and how I feel about you harming yourself, and then we’ll see if you still want to do this.
As illustrated by the foregoing segment, the thera- pist’s relentless use of the devil’s advocate strategy suc- cessfully “got a foot in the door” and achieved an ini- tial client commitment. The therapist then “upped the ante” with a brief explanation of the program and its goals.
THERAPIST: Now, the most important thing to under- stand is that we are not a suicide prevention program; that’s not our job. But we are a life enhancement pro-
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gram. The way we look at it, living a miserable life is no achievement. If we decide to work together, I’m going to help you try to improve your life, so that it’s so good that you don’t want to die or hurt yourself. You should also know that I look at suicidal behav- ior, including drinking Clorox, as problem-solving behavior. I think of alcoholism the same way. The only difference is that cutting, burning, unfortu- nately—it works. If it didn’t work, nobody would do it more than once. But it only works in the short term, not the long term. So, to quit cutting, trying to hurt yourself, is going to be exactly like quitting alcohol. Do you think this is going to be hard?
CLIENT: Stopping drinking wasn’t all that hard. THERAPIST: Well, in my experience, giving up self-harm
behavior is usually very hard. It will require both of us working, but you will have to work harder. And like I told you when we talked briefly, if you commit to this, it’s for 1 year—individual therapy with me once a week, and group skills training once a week. So the question is, are you willing to commit for 1 year?
CLIENT: I said I’m sick of this stuff. That’s why I’m here.
THERAPIST: So you’ve agreed to not drop out of therapy for a year, right?
CLIENT: Right. THERAPIST: And do you realize that if you don’t drop
out for a year, that really does, if you think about it, rule out suicide for a year?
CLIENT: Logically, yeah. THERAPIST: So we need to be absolutely clear about
this, because this therapy won’t work if you knock yourself off. The most fundamental mood-related goal we have to work on is that, no matter what your mood is, you won’t kill yourself or try to.
CLIENT: All right. THERAPIST: So that’s what I see as the number one pri-
ority—not our only one but number one—that we will work on that. And getting you to agree—mean- ingfully, of course—and actually follow through on staying alive and not harming yourself and not at- tempting suicide, no matter what your mood is. Now the question is whether you agree to that.
CLIENT: Yes, I agree to that.
The therapist, having successfully obtained the cli- ent’s commitment to work on suicidal behavior again
employed the strategy of devil’s advocate to reinforce the strength of the commitment.
THERAPIST: Why would you agree to that? CLIENT: I don’t know. (Laughs.) THERAPIST: I mean, wouldn’t you rather be in a ther-
apy where, if you wanted to kill yourself, you could? CLIENT: I don’t know. I mean, I never really thought
about it that way. THERAPIST: Hmm. CLIENT: I don’t want to . . . I want to be able to get to
the point where I could feel like I’m not being forced into living.
THERAPIST: So are you agreeing with me because you’re feeling forced into agreeing?
CLIENT: You keep asking me all these questions. THERAPIST: What do you think? CLIENT: I don’t know what I think right now, honestly.
A necessary and important skill for the DBT therapist is the ability to sense when a client has been pushed to his/her limits, as well as the concomitant skill of being willing and able to step back and at least temporarily refrain from further pressuring the client. In these in- stances, continued pressure from the therapist is likely to boomerang and have the opposite effect of what the therapist intends. Here, the therapist noticed the client’s confusion and sensed that further pushing was likely to result in the client’s reducing the strength of her com- mitment. Consequently, the therapist stepped back and moved in with validation.
THERAPIST: So you’re feeling pushed up against the wall a little bit, by me?
CLIENT: No, not really. (Starts to cry.) THERAPIST: What just happened just now? CLIENT: (pauses) I don’t know. I mean, I don’t think
I really want to kill myself. I think I just feel like I have to. I don’t think it’s really even a mood thing. I just think it’s when I feel like there’s no other choice. I just say, “Well, you know there’s no other choice, so do it.” You know. And so right now, I don’t see any ray of hope. I’m going to therapy, which I guess is good. I mean, I know it’s good, but I don’t see any- thing any better than it was the day I tried to kill myself.
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THERAPIST: Well, that’s probably true. Maybe it isn’t any better. I mean, trying to kill yourself doesn’t usu- ally solve problems. Although it actually did do one thing for you.
CLIENT: It got me in therapy. THERAPIST: Yeah. So my asking you all these questions
makes you start to cry. You look like you must be feeling pretty bad.
CLIENT: Just overwhelmed, I guess the word is. THERAPIST: That’s part of the reason we’re having this
conversation, to try to structure our relationship so that it’s very clear for both of us. And that way, at least, we’ll cut down on how much you get over- whelmed by not knowing what’s going on with me. OK?
CLIENT: Um hmm. THERAPIST: And so I just want to be clear on what our
number one goal is, and how hard this is, because if you want to back out, now’s the time. Because I’m going to take you seriously if you say, “Yes, I want to do it.”
CLIENT: I don’t want to back out. THERAPIST: OK. Good. Now I just want to say that
this seems like a good idea right now. You’re in kind of an energized mood today, getting started on a new program. But in 5 hours, it might not seem like such a good idea. It’s kind of like it’s easy to commit to a diet after a big meal, but it’s much harder when you’re hungry. But we’re going to work on how to make it keep sounding like a good idea. It’ll be hell, but I have confidence. I think we can be successful working together.
Note how the therapist ended the session by prepar- ing the client for the difficulties she was likely to experi- ence in keeping her commitment and working in ther- apy. Cheerleading and relationship enhancement laid the foundation for a strong therapeutic alliance. The following session occurred approximately 4 months into therapy. The session target was suicidal behavior. The therapist used validation, problem solving (contingency clarification, didactic information, behavioral analysis, and solution analysis), stylistic (irreverent communica- tion), dialectical (metaphor, making lemonade out of lemons), and skills training (distress tolerance) strate- gies.
The therapist reviewed the client’s Weekly Diary Card and noted a recent, intentional self-injury, in
which the client opened up a previously self-inflicted wound following her physician’s refusal to provide pain medication. The therapist began by proceeding with a behavioral analysis.
THERAPIST: OK. Now you were in here last week tell- ing me you were never going to hurt yourself again because this was so ridiculous, you couldn’t stand it, you couldn’t hurt yourself any more. So let’s figure out how that broke down on Sunday, so we can learn something from it. OK. So when did you start hav- ing urges to hurt yourself?
CLIENT: My foot began to hurt on Wednesday. I start- ed to have a lot of pain.
THERAPIST: It hadn’t hurt before that? CLIENT: No. THERAPIST: So the nerves were dead before that or
something, huh? So you started having a lot of pain. Now when did you start having the pain, and when did the urge to harm yourself come?
CLIENT: At the same time. THERAPIST: They just come at the identical moment? CLIENT: Just about.
The specification of an initial prompting environ- mental event is always the first step in conducting a behavioral chain analysis. Here, the therapist began by directly inquiring when the urges toward suicide and NSSI began. Note also the therapist’s use of irreverent communication early in the session.
THERAPIST: So how is it that feeling pain sets off an urge to self-harm? Do you know how that goes? How you get from one to the other?
CLIENT: I don’t know. Maybe it wasn’t until Thursday, but I asked my nurse. I go, “Look, I’m in a lot of pain, you know. I’m throwing up my food because the pain is so bad.” And the nurse tried. She called the doctor and told him I was in a lot of pain, and asked if he’d give me some painkillers. But no! So I kept asking, and the answer kept being no, and I got madder and madder and madder. So I felt like I had to show somebody that it hurt, because they didn’t believe me.
THERAPIST: So, let’s figure this out. So is it that you’re assuming that if someone believed it hurt as bad as you said it does, they would actually give you the painkillers?
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CLIENT: Yes. THERAPIST: OK. That’s where the faulty thinking is.
That’s the problem. You see, it’s entirely possible that people know how bad the pain is but still aren’t giv- ing you medication.
CLIENT: I believe firmly, and I even wrote it in my journal, that if I’d gotten pain medication when I really needed it, I wouldn’t have even thought of self- harming.
The therapist proceeded by obtaining a description of the events co-occurring with the onset of the prob- lem. It was not completely clear what about not get- ting pain medication set off self-harm. In the follow- ing segment, the therapist used the dialectical strategy of metaphor to analyze what factors might have been important. Notice that the example is presented as an experiment in which different scenarios are given and responses are elicited.
THERAPIST: Now let me ask you something—you’ve got to imagine this, OK? Let’s imagine that you and I are on a raft together out in the middle of the ocean. Our boat has sunk and we’re on the raft. And when the boat sank, your leg got cut really badly. And to- gether we’ve wrapped it up as well as we can. But we don’t have any pain medicine. And we’re on this raft together and your leg really hurts, and you ask me for pain medicine, and I say no. Do you think you would then have an urge to hurt yourself and make it worse?
CLIENT: No, it would be a different situation. THERAPIST: OK, but if I did have the pain medication
and I said no because we had to save it, what do you think?
CLIENT: If that were logical to me, I’d go along with it and wouldn’t want to hurt myself.
THERAPIST: What if I said no because I didn’t want you to be a drug addict?
CLIENT: I’d want to hurt myself. THERAPIST: OK. So we’ve got this clear. The pain is not
what’s setting off the desire to self-harm. It’s someone not giving you something to help, when you feel they could if they wanted to.
CLIENT: Yes.
The therapist used contingency clarification to point out the effects of others’ responses on the client’s own
behavior. In the following segment, the therapist again employed contingency clarification in a continued ef- fort to highlight for the client the communication func- tion of NSSI.
THERAPIST: So, in other words, hurting yourself is communication behavior, OK? So what we have to do is figure out a way for the communication behav- ior to quit working.
CLIENT: Why? THERAPIST: Because you’re not going to stop doing it
until it quits working. It’s like trying to talk to some- one; if there’s no one in the room, you eventually quit trying to talk to them. It’s like when a phone goes dead, you quit talking.
CLIENT: I tried three nights in a row in a perfectly as- sertive way and just clearly stated I was in a lot of pain.
THERAPIST: You know, I think I’ll switch chairs with you. You’re not hearing what I’m saying.
CLIENT: And they kept saying, “No,” and then some little light came on in my head.
THERAPIST: I’m considering switching chairs with you. CLIENT: And it was like, “Here, now, can you tell that
it hurts a lot?” THERAPIST: I’m thinking of switching chairs with you. CLIENT: Why? THERAPIST: Because if you were sitting over here, I
think you would see that no matter how bad the pain is, hurting yourself to get pain medication is not a reasonable response. The hospital staff may not have been reasonable either. It may be that they should have given you pain medicine. But we don’t have to say they were wrong in order to say that hurting yourself was not the appropriate response.
CLIENT: No, I don’t think it was the appropriate re- sponse.
THERAPIST: Good. So what we’ve got to do is figure out a way to get it so that the response doesn’t come in, even if you don’t get pain medicine. So far, it has worked very effectively as communication. And the only way to stop it is to get it to not work anymore. Of course, it would be good to get other things to work. What you’re arguing is “Well, OK, if I’m not going to get it this way, then I should get it another way.”
CLIENT: I tried this time!
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THERAPIST: Yes, I know you did, I know you did. CLIENT: A lady down the hallway from me was getting
treatment for her diabetes, and it got real bad, and they gave her pain medication.
THERAPIST: Now we’re not on the same wavelength in this conversation.
CLIENT: Yes, we are. What wavelength are you on? THERAPIST: I’m on the wavelength that it may have
been reasonable for you to get pain medicine, and I certainly understand your wanting it. But I’m also saying that no matter what’s going on, hurting your- self is something we don’t want to happen. You’re functioning like if I agreed with you that you should get pain medication, I would think this was OK.
CLIENT: Hmm? THERAPIST: You’re talking about whether they should
have given you pain medication or not. I’m not talk- ing about that. Even if they should have, we’ve got to figure out how you could have gotten through with- out hurting yourself.
As illustrated by the foregoing exchange, a client with BPD often wants to remain focused on the crisis at hand. This poses a formidable challenge for the thera- pist, who must necessarily engage in a back-and-forth dance between validating the client’s pain and push- ing for behavioral change. This segment also illustrates how validation does not necessarily imply agreement. Although the therapist validated the client’s percep- tion that the nurse’s refusal to provide pain medication may have been unreasonable, she remained steadfast in maintaining the inappropriateness of the client’s re- sponse.
CLIENT: I tried some of those distress tolerance things and they didn’t work.
THERAPIST: OK. Don’t worry, we’ll figure out a way. I want to know everything you tried. But first I want to be sure I have the picture clear. Did the urges start building after Wednesday and get worse over time?
CLIENT: Yeah. They started growing with the pain. THERAPIST: With the pain. OK. But also they started
growing with their continued refusal to give you pain medicine. So you were thinking that if you hurt yourself, they would somehow give you pain medi- cine?
CLIENT: Yeah. ‘Cause if they wouldn’t listen to me, then I could show them.
THERAPIST: OK, so you were thinking, “If they won’t listen to me, I’ll show them.” And when did that idea first hit? Was that on Wednesday?
CLIENT: Yeah. THERAPIST: OK. Well, we’ve got to figure out a way for
you to tolerate bad things without harming yourself. So let’s figure out all the things you tried, and then we have to figure out some other things, because those didn’t work. So what was the first thing you tried?
At this juncture, the behavioral analysis remained incomplete, and it would normally have been prema- ture to move to the stage of solution analysis. However, in the therapist’s judgment, it was more critical at this point to reinforce the client’s attempts at distress toler- ance by responding to the client’s communication that she had attempted behavioral skills.
CLIENT: I thought that if I just continued to be asser- tive about it that the appropriate measures would be taken.
THERAPIST: OK, but that didn’t work. So why didn’t you harm yourself right then?
CLIENT: I didn’t want to. THERAPIST: Why didn’t you want to? CLIENT: I didn’t want to make it worse. THERAPIST: So you were thinking about pros and
cons—that if I make it worse, I’ll feel worse? CLIENT: Yeah.
One aspect of DBT skills training stresses the use- fulness of evaluating the pros and cons of tolerating distress as a crisis survival strategy. Here, the therapist employed the dialectical strategy of turning lemons into lemonade by highlighting for the client how she did, in fact, use behavioral skills. Note in the following response how the therapist immediately reinforced the client’s efforts with praise.
THERAPIST: That’s good thinking. That’s when you’re thinking about the advantages and disadvantages of doing it. OK, so at that point the advantages of mak- ing it worse were outweighed by the disadvantages. OK. So you keep up the good fight here. Now what else did you try?
CLIENT: I tried talking about it with other clients. THERAPIST: And what did they have to say?
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CLIENT: They said I should get pain medication. THERAPIST: Right. But did they say you should cut
yourself or hurt yourself if you didn’t get it? CLIENT: No. And I tried to get my mind off my pain by
playing music and using mindfulness. I tried to read and do crossword puzzles.
THERAPIST: Um hmm. Did you ever try radical accep- tance?
CLIENT: What’s that? THERAPIST: It’s where you sort of let go and accept the
fact that you’re not going to get the pain medication. And you just give yourself up to that situation. You just accept that it ain’t going to happen, that you’re going to have to cope in some other way.
CLIENT: Which I did yesterday. I needed a little Ativan to get me there, but I got there.
THERAPIST: Yesterday? CLIENT: Yeah. I took a nap. When I woke up, I basical-
ly said, “Hey, they’re not going to change, so you’ve just got to deal with this the best that you can.”
THERAPIST: And did that acceptance help some? CLIENT: I’m still quite angry about what I believe is
discrimination against borderline personalities. I’m still very angry about that.
THERAPIST: OK. That’s fine. Did it help, though, to accept?
CLIENT: Um hmm. THERAPIST: That’s good. That’s great. That’s a great
skill, a great thing to practice. When push comes to shove, when you’re really at the limit, when it’s the worst it can be, radical acceptance is the skill to practice.
CLIENT: That’s AA.
During a solution analysis, it is often necessary that the therapist facilitate the process by helping the cli- ent “brainstorm,” or by making direct suggestions for handling future crises. Here, the therapist suggested a solution that is also taught in the DBT skills training module on distress tolerance. The notion of radical ac- ceptance stresses the idea that acceptance of one’s pain is a necessary prerequisite for ending emotional suffer- ing.
THERAPIST: OK. Now let’s go back to how you gave in to the urge. Because you really managed to battle all the way till then, right? OK. Usually, with you, we
can assume that something else happened. So let’s figure out Sunday and see if there wasn’t an interper- sonal situation that day that made you feel criticized, unloved, or unacceptable.
CLIENT: Well, on Saturday I was so pissed off and I went to an AA meeting. And it got on my brain how alcohol would steal away my pain. I went looking all around the neighborhood for an open store. I was going to go get drunk. That’s how much my pain was influencing me. But I couldn’t find a store that was open, so I went back to the hospital.
THERAPIST: So you got the idea of getting alcohol to cure it, and you couldn’t find any, so you went back to the hospital. You were in a lot of pain, and then what happened?
CLIENT: I told the nurse, “I’ve been sober almost 10 years and this is the first urge I’ve had to drink; that’s how bad my pain is.” And that wasn’t listened to.
THERAPIST: So you figured that should have done it? CLIENT: Yeah. THERAPIST: Yeah. ‘Cause that’s a high-level communi-
cation, that’s like a suicide threat. Very good, though. I want you to know, that’s better than a suicide threat because that means you had reduced the severity of your threats.
The response above was very irreverent, in that most clients would not expect their therapists to view making a threat as a sign of therapeutic progress. The therapeu- tic utility of irreverence often lies in its “shock” value, which may temporarily loosen a client’s maladaptive beliefs and assumptions, and open the client up to the possibility of other response solutions.
CLIENT: And I just told her how I was feeling about it, and I thought that would do it. And the doctor still wouldn’t budge.
THERAPIST: So what did she do? Did she say she would call?
CLIENT: She called. THERAPIST: OK. And then what happened? CLIENT: She came back. She was really sweet, and she
just said, “I’m really sorry, but the doctor said no.” THERAPIST: Then did you feel anger? CLIENT: I don’t know if I was really angry, but I was
hurt.
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THERAPIST: Oh, really? Oh, that’s pretty interesting. OK. So you were hurt . . .
CLIENT: Because I ended up hugging my teddy bear and just crying for a while.
THERAPIST: Before or after you decided to hurt your- self?
CLIENT: Before. THERAPIST: OK. So you didn’t decide right away to
hurt yourself. You were thinking about it. But when did you decide to do it?
CLIENT: Later on Saturday. THERAPIST: When? CLIENT: After I got sick of crying. THERAPIST: So you laid in bed and cried, feeling un-
cared about and hurt, abandoned probably, and un- lovable, like you weren’t worth helping?
CLIENT: Yes. THERAPIST: That’s a really adaptive response. That’s
what I’m going to try to teach you. Except that you’ve already done it without my teaching it to you. So how did you get from crying, feeling unloved and not cared about, and you cry and sob—how did you get from there to deciding to hurt yourself, instead of like going to sleep?
CLIENT: Because then I got angry. And I said, “Fuck this shit, I’ll show him.”
THERAPIST: Now did you quit crying before you got angry, or did getting angry make you stop crying?
CLIENT: I think getting angry made me stop crying. THERAPIST: So you kind of got more energized. So you
must have been ruminating while you were lying there, thinking. What were you thinking about?
CLIENT: For a long time I was just wanting somebody to come care about me.
THERAPIST: Um hmm. Perfectly reasonable feelings. Makes complete sense. Now maybe there you could have done something different. What would have happened if you had asked the nurse to come in and talk to you, hold your hand?
An overall goal of behavioral analysis is the construc- tion of a general road map of how the client arrives at dysfunctional responses, with notation of possible al- ternative pathways. Here, the therapist was searching for junctures in the map where possible alternative re- sponses were available to the client.
CLIENT: They don’t have time to do that. THERAPIST: They don’t? Do you think that would have
helped? CLIENT: I don’t know. She couldn’t help me. THERAPIST: She could have made you feel cared about.
That would have been a caring thing to do. CLIENT: Yeah, but I don’t think it would have helped. THERAPIST: What would have helped? CLIENT: Getting pain medication. THERAPIST: I thought you’d say that. You have a one-
track mind. Now listen, we’ve got to figure out some- thing else to help you, because it can’t be that noth- ing else can help. That can’t be the way the world works for you. There’s got to be more than one way to get everywhere, because we all run into boulders on the path. Life is like walking on a path, you know, and we all run into boulders. It’s got to be that there are other paths to places. And for you, it really isn’t the pain in your ankle that’s the problem; it’s the feel- ing of not being cared about. And probably a feeling that has something to do with anger, or a feeling that other people don’t respect you—a feeling of being invalidated.
CLIENT: Yes. THERAPIST: So I think it’s not actually the pain in your
ankle that’s the problem. Because if you were out on that raft with me, you would have been able to han- dle the pain if I hadn’t had any medicine, right? So it’s really not the pain; it’s the sense of being invali- dated and the sense of not being cared about. That’s my guess. Do you think that’s correct?
CLIENT: Yes. THERAPIST: See, the question is, is there any other way
for you to feel validated and cared about, other than them giving it to you?
CLIENT: No. THERAPIST: Now is this a definite, like “I’m not going
to let there be any other way,” or is it more open, like “I can’t think of another way, but I’m open to the possibility?”
CLIENT: I don’t think there’s another way. THERAPIST: Does that mean you’re not even open to
learning another way? CLIENT: Like what? THERAPIST: I don’t know. We have to figure it out. See,
what I think is happening is that when you’re in a
Borderline Personality Disorder 431
lot of pain and you feel either not cared about or not taken seriously, invalidated, that’s what sets you up to hurt yourself, and also to want to die. The prob- lem that we have to solve is how to be in a situation that you feel is unjust without having to harm your- self to solve it. Are you open to that?
CLIENT: Yeah.
As illustrated here, behavioral analysis is often an excruciating and laborious process for client and thera- pist alike. The therapist often feels demoralized and is tempted to abandon the effort, which may be likened to trying to find a pair of footprints hidden beneath lay- ers of fallen leaves; the footprints are there, but it may take much raking and gathering of leaves before they are uncovered. With repeated analyses, however, the client learns that the therapist will not “back down.” Such persistence on the part of the therapist eventually extinguishes a client’s refusal to attempt new and adap- tive problem-solving behaviors. As clients increasingly acquire new behavioral skills, more adaptive attempts at problem resolution eventually become discernible.
In the following session (approximately 10 months into therapy), the client arrived wearing mirrored sun- glasses (again) and was angry because collection agen- cies were persistent in pressuring her for payment on de- linquent accounts. In addition, her therapist had been out of town for a week. The session targets were emotion regulation and interpersonal effectiveness. Dialectical (metaphor), validation (cheerleading), problem solving (contingency clarification, contingency management), stylistic (reciprocal communication, irreverent commu- nication), and integrated (relationship enhancement) strategies were used. In this first segment, the therapist used cheerleading, contingency clarification, and the contingency management strategy of shaping to get the client to remove her sunglasses and work on expressing her anger.
THERAPIST: It’s not a catastrophe that the collector did this to you, and it’s not a catastrophe to be mad at the collector. It’s made your life a lot harder, but you can handle this. You can cope with this. This is not more than you can cope with. You’re a really strong woman; you’ve got it inside you. But you’ve got to do it. You’ve got to use it. I’m willing to help you, but I can’t do it alone. You have to work with me.
CLIENT: How? THERAPIST: Well, by taking off your sunglasses, for
starters.
The therapist began the exchange by attempting to normalize the issue (“It’s not a catastrophe”), validating the client (“It’s made your life a lot harder”), and cheer- leading (“You can handle this. You can cope. . . . You’re a really strong woman”). The therapist then moved to contingency clarification by pointing out that provi- sion of the therapist’s assistance was contingent on the client’s willingness to work. She immediately followed this by requesting a response well within the client’s be- havioral repertoire.
CLIENT: I knew you’d say that. THERAPIST: And I knew you knew I’d say that. CLIENT: Sunglasses are your biggest bitch, I think. THERAPIST: Well, how would you like to look at your-
self talking to someone else? (long pause) They make it difficult for me. And I figure they make it harder for you. I think you do better when you’re not wear- ing those sunglasses. It’s like a step; you always do better when you go forward. And when you do, you feel better. I’ve noticed that. (long pause) So that’s what you should do; you should take off your sun- glasses, and then we should problem-solve on how to cope when you can’t get angry. There’s nothing freakish about that. Something has happened in your life that has made it so that you’re afraid to be angry, and we just have to deal with that, you and me. It’s just a problem to be solved. It’s not a catastrophe; it’s not the worst thing anyone ever did. It’s just a prob- lem that you have, and that’s what you and I do. We solve problems; we’re a problem-solving team. (pause)
CLIENT: (Removes sunglasses.) All right. THERAPIST: Thank you. That’s a big step, I know, for
you.
The therapist’s use of reciprocal communication informed the client of her feelings regarding the sun- glasses. Note the matter-of-fact attitude taken by the therapist and her continued attempt to normalize the issue (i.e., “There’s nothing freakish about that. . . . It’s not the worst thing anyone ever did”). Also note the framing of the issue as a problem to be solved, as well as the therapist’s use of the relationship strategy to en- hance the therapeutic alliance. The therapist also made a point of validating the client by letting her know that she realized this was difficult.
THERAPIST: Now, c’mon, I want you to find it inside yourself. I know you’ve got it; I know you can do it. You can’t give up. You can’t let your feet slip. Keep
432 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
going. Just express directly to me how you feel. That you’re angry at yourself, that you’re angry at the col- lection agency, and that you’re damn angry with me. (long pause)
CLIENT: (barely audible) I’m angry at you, at myself, and the collection agency.
The therapist continued to rely on cheerleading and praise as she continued the shaping process in an at- tempt to get the client to express her anger directly.
THERAPIST: Good, did that kill you? (long pause) That’s great. Is that hard? (long pause) It was, wasn’t it? Now say it with a little vigor. Can’t you say it with a little energy?
CLIENT: (Shakes her head no.) THERAPIST: Yes, you can. I know you’ve got it in you.
I have a good feel for what your strengths are. I don’t know how I’ve got this good feel, but I do. And I know you can do it and you need to do it, and you need to say it with some energy. Express how angry you are. You don’t have to yell and scream or throw things. Just say it aloud—“I’m angry!” (long pause) You can scream, of course, if you want; you can say, “I’m angry!”
CLIENT: That’s it. That’s all I can do. THERAPIST: Listen, you have to take the risk. You’re not
going to get past this or through this. You have to take the risk. You are like a person mountain climbing and we’ve come to this crevasse and it’s very deep, but we can’t go back, because there’s an avalanche, and the only way to go forward is for you to jump over this crevasse. You’ve got to do it. Tell me how mad you are, in a way that I can understand how you really feel.
CLIENT: (long pause) I can’t do any of it. THERAPIST: That is bullshit. CLIENT: You want me to get angry at you, don’t you? THERAPIST: I don’t care who you get angry at. I think
you already are angry. I just want you to express it. I’m not going to ask you to do anything more today, by the way. I figure the only thing today you have to do is say, “I’m angry,” in a voice that sounds angry, and I figure you’re capable of that. And I might be angry if you don’t do it. I don’t think I will be, but I might. That’s OK. I can be angry, you can be angry, we can be angry sometimes, and it isn’t going to kill either one of us.
Cheerleading and metaphor were unsuccessful in moving the client to express her anger more forcefully. Consequently, the therapist switched to irreverent com- munication in an attempt to get the client to “jump track.” Also note how the therapist communicated to the client the potential negative consequences of her continued refusal to express her anger (i.e., “I might be angry . . . ”). In this manner, the therapist used the re- lationship as a contingency in order to promote change in the client.
THERAPIST: OK, so how angry are you? On a scale of 1 to 100, how angry would you say you are? At 100, you’re ready to kill. You’re so enraged, you’d go to war if you could.
CLIENT: (barely audible) Maybe 100. THERAPIST: Really? CLIENT: They know my situation. THERAPIST: Um hmm. CLIENT: They’re persistent. THERAPIST: Um hmm. (pause) Who’s the safest to be
angry at? Yourself, me, or the collection agency? CLIENT: Collection agency. THERAPIST: OK, then, tell me how angry you are. You
don’t have to make it sound like 100. Try to make it sound like 50.
CLIENT: They really pissed me off! (said in a loud, angry voice)
THERAPIST: Well, damn right. They piss me off, too.
As illustrated by the foregoing exchange, a primary difficulty in working with clients who have BPD is their not uncommon tendency to refuse to engage in behav- ioral work. Thus, it is absolutely necessary that the ther- apist maintain persistence and not give up in the face of a client’s “I can’t” statements. In situations like these, the use of irreverent communication often succeeds in pro- ducing a breakthrough and gaining client compliance.
POSTVENTION BY LINEHAN
After completing the writing of Cindy’s case history for publication in this Handbook, 14 months into therapy, Cindy died of a prescription drug overdose plus alco- hol. I (M. M. L.) considered dropping the case history and replacing it with a more successful case. However,
Borderline Personality Disorder 433
in Cindy’s honor, and because I think much can be learned from both failed and successful therapy, I de- cided to leave the case in. The immediate precipitant for Cindy’s overdose was a call to her estranged hus- band, during which she discovered that another woman was living with him. As Cindy told me during a phone call the next morning, her unverbalized hope that they might someday get back together, or at least be close friends, had been shattered. She phoned again that eve- ning in tears, stating that she had just drunk half a fifth of liquor. Such drinking incidents had occurred several times before, and the phone call was spent “remoral- izing” Cindy, offering hope, problem-solving how she could indeed live without her husband, and using crisis intervention techniques to get her through the evening, until her appointment the following day. Cindy’s room- mate was home and agreed to talk with her, watch a TV movie together, and go to bed (plans on which the roommate did follow through). Cindy stated that al- though she felt suicidal, she would stop drinking and would not do anything self-destructive before her ap- pointment. She was instructed to call me back later that evening if she wanted to talk again. The next day, when Cindy did not arrive for her appointment, I called her home, just as her roommate discovered Cindy dead, still in bed from the night before. At this point, I was faced with a number of tasks. I called to inform other therapists who had been treating the client, and spoke with a legal consultant to review the limits of confiden- tiality when a client has died. Once the family (Cindy’s parents and estranged husband) were alerted, I called each to offer my condolences. The next day, as the se- nior therapist and supervisor on the treatment team, I called a meeting of the treatment team to discuss and process the suicide. It was especially important to no- tify the individual therapists of the remaining members of Cindy’s skills training group. Group members were notified of the suicide by their individual psychothera- pists. Within minutes of the beginning of the next group session, however, two members became seriously suicidal, and one of them had to be briefly hospitalized. (By the third week following the suicide, however, both had regained their forward momentum.) A third group member took this occasion to quit DBT and switch to another therapy, saying that this proved the treatment did not work. In the days and weeks following the sui- cide, I attended the funeral and met with Cindy’s room- mate and with her parents.
What can we learn from this suicide? First, it is im- portant to note that even when a treatment protocol is
followed almost to the letter, it may not save a client. Even an effective treatment can fail in the end. In this case, DBT failed. This does not mean that the progress made was unimportant or not real. Had this “slippery spot over the abyss” been negotiated safely, perhaps the client would have been able to develop, finally, a life of quality. Risk is not eliminated, however, just because an individual makes substantial progress. In this case, I did not believe during the last phone call that the client was at higher than ordinary risk for imminent suicide. In contrast to many previous phone calls and therapy sessions in which the client had cried that she might not be able to hold on, during the last call the client made plans for the evening, agreed to stop drinking and not to do anything suicidal or self-destructive, and seemed to me (and to the roommate) to be in better spirits fol- lowing the phone call. Her roommate was home and available. Thus, I did not take extraordinary measures that evening to prevent suicide. Indeed, the problem behavior focused on during the call was the drinking. I brought up the topic of suicide while conducting a risk assessment.
Second, could I have known? Only (perhaps) if I had paid more attention to the precipitant and less to the affect expressed at the end of the phone call. In re- viewing notes about the client, I saw that each previous nonlethal self-injury was a result of intense anger at her husband. Each previous near-lethal attempt was a result of the client’s belief that the relationship with her hus- band had irrevocably ended. Although the client could tolerate losing her husband, she could not tolerate losing all hope for a reconciliation at some point, even many years hence. Had I linked these two ideas (complete loss of hope and suicide attempt), I might have been able to work out a better plan for a reemergence of the crisis later in the evening. I definitely would have handled the situation differently. “Oh, that woman’s obviously a floozy, we will figure out a way to get him back! I’m sure of it,” I would have said. The value of both con- ducting thorough behavioral assessments and organiz- ing them into a coherent pattern is highlighted in this case. In this sense, I provided DBT almost to the letter but not all the way.
Third, when all is said and done, an individual with BPD must ultimately be able and willing to tolerate the almost unimaginable pain of his/her life until the therapy has a chance to make a permanent difference. Ultimately, the therapist cannot save the client; only the client can do that. Even if mistakes are made, the client must nonetheless persevere. In this case, the DBT pro-
434 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
tocol of “no lethal drugs for lethal people” was violated, even though the client had a past history of near-lethal overdoses. Why was the protocol not enforced? There were two primary reasons. First, the client came into therapy with a strong belief that the medication regi- men she was on was essential to her survival. Any at- tempt on my part to manage her medications would have been met by very strong resistance. Although the drugs were dispensed in small doses, the only safe alter- native would have been to have the person living with her (her husband at first, then her roommate) manage her medications, which the client also resisted. In ad- dition, some professionals disagree with the “no lethal drugs” protocol of DBT, because they believe that psy- chotropic medications are a treatment of choice for sui- cidal clients. In the face of professional and client resis- tance I relented. The second reason was that behavioral analyses indicated that her preferred lethal behavior was cutting; thus, I allowed myself a false sense of safety in thinking that her use of drugs to commit suicide was not likely.
Fourth, a group member’s suicide is extraordinarily stressful for clients with BPD who are in group thera- py. Although it is easy to believe that alliances are not strong in a psychoeducational behavioral skills group, this has universally not been our experience. The sui- cide of one member is a catastrophic event and can lead to contagious suicide and NSSI behavior, and therapy dropouts. Thus, extreme care is needed in the conduct of group meetings for some time following a suicide. Similar care is needed with the treatment team, where the thread of hope that maintains therapists in the face of a daunting task is also strained. It is important that the personal reactions of therapists, as well as a period of mourning and grieving, be shared and accepted. Fears of legal responsibility, never far from the surface, must be confronted directly; legal counsel should be sought as necessary; and, in time, a careful review of the case and the therapy must be conducted, if only to improve treatment in the future.
ACKNOWLEDGMENTS
The writing of this chapter was supported by National In- stitute of Mental Health Grant No. MH34486 to Marsha M. Linehan. Parts of this chapter are drawn from Linehan (2015), Linehan and Koerner (1992), Koerner and Linehan (1992), and Linehan (1997). The quotations from Linehan (1997) in the section on validation are reprinted with the per- mission of the American Psychological Association. Finally,
this chapter is a revision of the same chapter in the previous edition of this book, with contributions made by previous authors Bryan M. Cochran, Constance A. Kehrer, and Liz Dexter Mazza.
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Self-injurious thoughts and behaviors (SITBs), including those that are suicidal and nonsuicidal in nature, are major public health problems in need of immediate attention. In the United States, suicide is one of the 10 leading causes of death across most age groups, and rates of death by suicide have been climbing since 2010 (National Center for Health Statistics, 2018; Centers for Disease Control and Prevention, 2020). SITBs also are highly comorbid with anxiety, depressive, and related emo- tional disorders, which can pose challenges for effective and efficient treatment of those disorders. Existing evidence-based psychological treatments showing some efficacy for suicidal thoughts and behaviors, with dialectical behavior therapy the best known and best validated among them (see Neacsiu, Zerubavel, Nylocks, & Linehan, Chapter 10, this volume), nevertheless largely target single disorders or symptom sets. This chapter, which is new to this edition, details the theoretical and empirical foundations of a transdiagnostic treatment framework, along with case illustrations for a broader range of self-injurious behavior not specific to any one disorder and sometimes occurring in the absence of any formal diagnosis. Only recently have clinical investigators begun to focus exclu- sively on SITBs, and the authors of this chapter are widely recognized as leaders in the world on this topic. Thus, clinicians should benefit from incorporating this information into their practice. —D. H. B.
self-injurious thoughts and behaviors (SITBs) can be enacted with either intent to die (i.e., suicidal
thoughts and behaviors) or no intent to die (i.e., nonsui- cidal self-injury [NSSI]; Nock, 2010). Suicidal thoughts and behaviors include suicidal ideation (thoughts of killing oneself), suicide plan (considering a specific method through which an individual intends to kill him/herself), suicide attempt (engaging in potentially self-injurious behavior with at least some intent to die), and suicide death (Nock, 2010). Nonsuicidal self-inju-
rious thoughts and behaviors primarily consist both of thoughts of engaging in NSSI (deliberate, self-inflicted destruction of one’s own bodily tissue without sui- cidal intent and for purposes not socially or culturally sanctioned; International Society for the Study of Self- Injury, 2018; Nock & Favazza, 2009), and NSSI itself (Nock, 2010). Though historically, these distinct forms of SITBs were often lumped together under umbrella terms such as parasuicide or deliberate self-harm, the sci- entific and clinical value of distinguishing carefully and
C H A P T E R 11
Addressing self-injurious Thoughts and behaviors within the Context of Transdiagnostic Treatment for emotional Disorders
Kate H. Bentley Joseph S. Maimone Matthew K. Nock
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consistently between these behaviors has been increas- ingly recognized (e.g., Hooley, Fox, & Boccagno, 2020; Nock, 2010).
This shift toward more precise definitions of SITBs is also reflected in recent classification of these behav- iors. In prior iterations of the Diagnostic and Statistical Manual of Mental Disorders (e.g., DSM-IV-TR; Ameri- can Psychiatric Association, 2000), SITBs appeared only as symptoms of other disorders (e.g., suicidal ide- ation in major depressive disorder [MDD], NSSI in borderline personality disorder [BPD]). More recently, in acknowledgment that SITBs do not occur just in the context of these diagnoses (an issue we discuss further below), two new diagnoses were included as “conditions for further study” in DSM-5 (American Psychiatric As- sociation, 2013): suicidal behavior disorder and NSSI disorder. Whether either or both of these diagnoses will be formally adopted in future DSM versions remains to be seen, though regardless, the ongoing research aimed to evaluate their validity, reliability, and clinical utility has the potential to contribute to improved understand- ing of SITB phenomenology (e.g., Buelens et al., 2020; Hooley et al., 2020; Oquendo & Baca-Garcia, 2014).
Regarding suicidal SITBs, suicide accounts for more deaths per year than war, homicide, accidents, or AIDS worldwide (World Health Organization, 2012). In the United States, suicide is the 10th leading cause of death across for most age groups (Centers for Disease Control and Prevention [CDC], 2020) and for those ages 10–34 years, it is the second leading cause of death (CDC, 2020). In 2018, over 48,000 suicide deaths occurred in the United States, which works out to about 129 suicide deaths per day. After 13 years of consecutive increases, the suicide rate in the United States declined (by 2.1%) from 2018 to 2019 (Centers for Disease Control and Prevention, 2021a). However, most states did not ex- perience significant decreases and it is unclear whether this trend will continue in future years (Centers for Disease Control and Prevention, 2021b). In addition to these sobering statistics about completed suicide, ap- proximately 1.4 million adults make a suicide attempt and about 3.3 million make a suicide plan each year in the United States (CDC, 2020; Substance Abuse and Mental Health Services Administration, 2019). For every completed suicide, it has been estimated that approximately 185 people experience serious suicidal thoughts (Crosby, Han, Ortega, Parks, & Gfroerer, 2011; Substance Abuse and Mental Health Services Ad- ministration, 2019). Nonfatal suicidal thoughts and be- haviors are not only predictive of future suicide deaths (e.g., Ribeiro et al., 2016), but also associated with sig-
nificant psychological suffering for affected individuals and their families and communities alike.
NSSI—common forms of which include self- cutting, burning, or hitting—is also alarmingly common, espe- cially among adolescents and young adults. It is estimat- ed that about 17–18% of young adults have engaged in NSSI at least once. Across age groups, current estimates of NSSI prevalence range from 5.5 to 17.2% (Swannell, Martin, Page, Hasking, & St John, 2014). Though age of onset and course can differ drastically, most often rates of NSSI increase through early to midadolescence before declining later in adolescence (Plener, Schum- acher, Munz, & Groschwitz, 2015). NSSI can also be persistent, lasting at least several years prior to remis- sion (Plener et al., 2015). NSSI is among the strongest known predictors of suicidal behavior (e.g., Ribeiro et al., 2016) and has been associated with worsened de- pression and anxiety, as well as consequences such as physical injury, medical complications, and lower over- all functioning (e.g., Briere & Gil, 1998; Nock et al., 2006; Turner, Austin, & Chapman, 2014).
In summary, SITBs are extremely prevalent, and in some cases, rates of these behaviors are rising. SITBs are also associated with significant economic costs (an es- timated almost $70 billion per year in lifetime medical and work loss costs in the United States; CDC, 2020). Despite this, these problems receive disproportionately low federal funding in comparison to other common medical and psychiatric illnesses (e.g., Fortgang & Nock, 2020). The clear and urgent need for improved strategies to reduce SITBs on a large scale will include both developing new strategies to treat individuals who experience (or are at risk for developing) these problems and improving access to existing evidence-based inter- ventions (Kazdin & Rabbit, 2013) for SITBs.
OVERVIEW OF EXISTING EVIDENCE‑BASED TREATMENTS
A number of evidence-based psychological treatments for SITBs have been developed to date. Here we provide a nonexhaustive overview of the more comprehensively studied multisession protocols. We focus on treatments designed to target SITBs directly rather than those primarily addressing symptoms associated with SITBs (e.g., depression) (Meerwijk et al., 2016).
Often considered the “gold-standard” treatment for SITBs, dialectical behavior therapy (DBT; Linehan, 1993) is a multimodal, cognitive-behavioral treatment designed to target BPD and self-injurious behavior
Self‑Injurious Thoughts and Behaviors 445
(see Neacsiu et al., Chapter 10, this volume). Based in a dialectical philosophy (i.e., balance of acceptance and change), and as described in Chapter 10, the core process of DBT consists of reducing ineffective action tendencies linked with dysregulated emotions, such as NSSI. The first phase of DBT focuses on reducing SITBs by providing patients with new coping skills, addressing barriers to motivation, and promoting skills generalization. This goal is obtained through skills training groups, individual therapy sessions, and as- needed phone consultation (as well as therapist consul- tations/team meeting; Neacsiu et al., Chapter 10, this volume).
With regard to research support, the results of sev- eral studies suggest that DBT reduces the occurrence of SITBs relative to other treatments (e.g., DeCou, Comtois, & Landes, 2019; Kliem, Kröger, & Kosfelder, 2010), with some noteworthy caveats. For one, earlier research on DBT often combined suicidal and NSSI together as “parasuicide,” which renders it difficult to isolate treatment effects specific to different types of SITBs. Some randomized controlled trials (RCTs) have shown differing effects for suicide-related behavior ver- sus NSSI; for example, Linehan and colleagues (2006) found that although DBT resulted in greater reductions in suicide attempts in adult patients with BPD, it was no more efficacious than community treatment by experts in reducing NSSI. A recent meta-analysis of 18 con- trolled trials indicated that DBT reduces self-injurious behavior, but not necessarily suicidal ideation (DeCou & Lynch, 2019). Overall, however, DBT (or its vari- ants; e.g., Asarnow, Hughes, Babeva, & Sugar, 2017) remains the most well-established psychotherapy for SITBs in adults and adolescents currently available (e.g., Ougrin, Tranah, Stahl, Moran, & Asarnow, 2015). Bar- riers to accessing DBT include its duration (typically 1 year), multimodal and intensive structure, and relatively time-intensive and costly therapist training (Comtois & Linehan, 2006; Rizvi, Steffel, & Carson-Wong, 2013; Zanarini, 2009), all understandable considering that DBT targets the totality of severe BPD symptomatology and does not focus exclusively on SITBs.
Other cognitive-behavioral (or cognitive; e.g., Rush & Beck, 1978) treatments have also been developed specifically to address suicidal thoughts and behaviors for both adults and adolescents (e.g., Ougrin et al., 2015; see Young, Ward-Ciesielski, Rygh, Weinberger, & Beck, Chapter 7, this volume). Among the more well-studied are cognitive therapy (CT) or cognitive- behavioral therapy (CBT) for suicide prevention (often referred to as CT-SP or CBT-SP), a manualized treat-
ment that focuses on building cognitive, behavioral, and interpersonal skills aimed to enable patients to refrain from suicidal behavior (Stanley et al., 2009; Wenzel & Jager-Hyman, 2012). In a seminal early study, Brown and colleagues (2005) showed that suicide-focused CT, when delivered in an outpatient setting to adults who recently attempted suicide (N = 120), resulted in a lower suicide reattempt rate (but not suicidal ideation) than usual care over the 18-month assessment period. More recently, brief suicide-focused CBT has also demon- strated positive effects on suicide attempts in military samples (Bryan, Peterson, & Rudd, 2018; Rudd et al., 2015). Overall, systematic reviews and meta-analyses generally suggest that when compared with treatment as usual, CBT protocols (including related strategies such as problem solving; e.g., Hatcher, Sharon, Parag, & Collins, 2011) generally reduce suicide attempts and to a more moderate degree, suicidal ideation (D’Anci, Uhl, Giradi, & Martin, 2019; Leavey & Hawkins, 2017; Hawton et al., 2016; Tarrier, Taylor, & Gooding, 2008). Though other non-CBT approaches such as psy- chodynamic therapy (e.g., Levy, Yeomans, & Diamond, 2007) and mentalization-based treatment (MBT; Bate- man & Fonagy, 1999) have been examined for suicidal thoughts and behaviors, the vast majority of evidence- based treatments for SITBs involve CBT components (Meerwijk et al., 2016).
The Collaborative Assessment and Management of Suicidality (CAMS; Jobes, 2006, 2012) was developed to provide a comprehensive treatment framework for working with suicidal individuals. It is not necessar- ily a specific therapeutic protocol; rather, CAMS fo- cuses on collaborative assessment and treatment plan- ning between clinicians and suicidal patients, as well as outcome tracking over time. Importantly, CAMS encourages clinicians to bring in other clinically in- dicated treatment strategies, such as DBT and CBT components. Overall, CAMS has generated promising empirical support across a variety of treatment settings (for reviews, see Hanratty, Kilicaslan, Wilding, & Cas- tle, 2019; Jobes, 2012); two recent RCTs showed that CAMS outperformed alternative treatments in terms of reducing suicidal ideation (but not suicidal behavior or suicide-related hospital visits) in outpatient soldiers and college students (Jobes et al., 2017; Pistorello et al., 2020).
Regarding NSSI, several CBT protocols designed and tested specifically for NSSI have generally shown promising effects (Labelle, Pouliot, & Janelle, 2015). Emotion regulation group therapy (ERGT; Gratz & Gunderson, 2006) is an adjunctive, group-based pro-
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tocol that provides adaptive emotion regulation strate- gies and reduces emotional avoidance to self-injuring individuals. The effects of ERGT on NSSI have been evaluated in a number of trials (several randomized) for individuals with BPD, and generally indicate that this intervention is associated with reductions in NSSI (Gratz & Gunderson, 2006; Gratz & Tull, 2011; Gratz, Tull, & Levy, 2014; Sahlin et al., 2017). The Treatment for Self-Injurious Behaviors (T-SIB), developed as a brief intervention to target NSSI in young adults both with and without BPD, delivers cognitive, behavioral, distress tolerance, and social skills based on antecedents and consequences of NSSI identified through function- al assessment. In pilot studies to date, T-SIB has shown feasibility, acceptability, and preliminary efficacy in terms of decreased NSSI frequency (Andover, Schat- ten, Morris, & Miller, 2015; Andover, Schatten, Mor- ris, Holman, & Miller, 2017). Manual-assisted CBT (MACT, designed to target both suicidal and nonsui- cidal forms of self-injury), delivered as an adjunct to usual care, has also been shown to be more effective at reducing NSSI than usual care alone (Weinberg, Gunderson, Hennen, & Cutter, 2006).
In summary, a number of promising psychologi- cal interventions exist for SITBs. However, the lack of methodological rigor of many trials, and in many cases mixed findings, limit the strength of conclusions we can currently make regarding efficacy (e.g., Brown & Jager-Hyman, 2014). Indeed, a meta-analysis of all RCTs of interventions for SITBs to date (>300 unique RCTs) shows that, overall, effects of existing treatments on SITBs are small, have not improved over time, and do not vary by intervention type (Fox et al., 2020). As mentioned earlier, some existing treatments have only shown efficacy for suicidal ideation or behavior (Brown & Jager-Hyman, 2014); ideally, interventions would be equally effective for different SITB types. Finally, the fact that SITBs remain quite prevalent may reflect dif- ficulties with treatment access and frontline clinicians not using existing evidence-based treatments for SITBs and commonly co-occurring conditions.
SITBs AND THE EMOTIONAL DISORDERS
Individuals who experience SITBs are much more likely than not to meet criteria for at least one psychiatric con- dition. Regarding suicidal thoughts and behaviors, it has been estimated that 90% of people who die by sui- cide have a mental disorder (Arsenault-Lapiere, Kim, & Turecki, 2004; Bertolote & Fleischmann, 2002). Prior
studies have also shown that between one-half and two- thirds of people who have seriously considered suicide meet criteria for a mental disorder (Nock, Hwang, et al., 2009; Nock, Hwang, Sampson, & Kessler, 2010), and these proportions are even higher (approximately 80%; e.g., Nock et al., 2010) among individuals who report a suicide plan or attempt.
The emotional disorders (an umbrella term encom- passing anxiety, depressive, and related disorders to which we return later in this chapter; Bullis, Boettcher, Sauer-Zavala, Farchione, & Barlow, 2019) are particu- larly common among people experiencing SITBs. For one, depression has long been considered among the most important diagnoses in determining suicide risk. Several leading theories of suicide refer to psychologi- cal symptoms of depression as necessary components in the development and maintenance of suicidal thoughts and behaviors (e.g., Beck, Kovacs, & Weissman, 1975; Joiner, 2005). Indeed, psychological autopsy studies have implicated depression as the most common psychi- atric disorder among suicide decedents (Conwell et al., 1996; Harwood, Hawton, Hope, & Jacoby, 2001), and depressive disorders have been linked to suicidal behav- ior in numerous epidemiological or treatment-seeking samples (e.g., Nock, Hwang, et al., 2009; Nordentoft, Mortensen, & Pedersen, 2011; Zimmerman et al., 2014).
Studies have also generally shown that anxiety and related disorders are risk factors for suicidal thoughts and behaviors (e.g., Bentley, Casiello-Robbins, Vittorio, Sauer-Zavala, & Barlow, 2015; Kanwar et al., 2013; Nock, Hwang et al., 2009; Nock et al., 2010). Of the anxiety disorders and related disorders, posttraumatic stress disorder (PTSD) has been associated with espe- cially elevated rates of these behaviors (e.g., Bentley et al., 2016; Gradus et al., 2010; Panagioti, Gooding, & Tarrier, 2009). In addition to anxiety disorders, acute anxiety symptoms such as agitation have been theo- retically (and to an increasing degree, empirically) im- plicated as clinically significant proximal risk factors for and potential facilitators of suicidal behavior (e.g., Busch, Fawcett, & Jacobs, 2003; Fawcett et al., 1990; Ribeiro et al., 2014; Rogers, Ringer, & Joiner, 2016). Individuals with BPD, also recently conceptualized as an emotional disorder (Bullis et al., 2019; Sauer-Zavala & Barlow, 2014), often present with SITBs, with some studies estimating that at least three-fourths of patients with BPD attempt suicide and up to 10% ultimately die by suicide (e.g., Black, Blum, Pfohl, & Hale, 2004; Rodante et al., 2019; Soloff, Lynch, Kelly, Malone, & Mann, 2000; Zanarini, Frankenburg, Hennen, Reich, & Silk, 2005).
Self‑Injurious Thoughts and Behaviors 447
In terms of NSSI, studies have indicated that the vast majority (80–85%) of people who engage in NSSI meet criteria for at least one mental disorder (Kiekens et al., 2018; Nock et al., 2006). Research has consis- tently shown that NSSI commonly co-occurs with the emotional disorders (Bentley et al., 2015; Jacobson, Muehlenkamp, Miller, & Turner, 2008; Klonsky, Olt- manns, & Turnheimer, 2003). For example, Nock and colleagues (2006) found that about 50% of adolescents engaging in NSSI meet criteria for generalized anxiety disorder (GAD), MDD, or PTSD. Individuals who engage in NSSI also evidence higher levels of anxiety and depression than those who do not (e.g., Andover, Pepper, Ryabchenko, Orrico, & Gibb, 2005; Brunner et al., 2013).
It is important to note that relatively small absolute proportions of individuals who meet criteria for an emotional disorder engage in self-injurious behavior: Estimates for completed suicide among individuals with depression, for example, are between 5 and 8% (Nordentoft et al., 2011). Thus, our team and others have argued that the clinical utility of relatively stable risk factors such as psychiatric (and specifically, emo- tional) disorders as prospective risk factors for SITBs is limited (e.g., Bentley et al., 2016; Franklin et al., 2017). Most relevant to this chapter, however, treatment-seek- ing individuals who report SITBs often meet criteria for an emotional disorder or at least exhibit clinically significant anxiety or depressive symptoms, suggest- ing that there may be clinical utility in a treatment ap- proach that targets both areas of concern.
CONCEPTUALIZING SITBs WITHIN A FUNCTIONAL MODEL OF EMOTIONAL DISORDERS
To make the case for a treatment approach that si- multaneously targets SITBs and emotional disorders, one must consider the functional similarities between SITBs and emotional disorders. In this section, we briefly describe key underlying mechanisms that have been proposed as contributing to the emergence and maintenance of emotional disorders, then argue that these transdiagnostic mechanisms may also apply to SITBs.
Functional Model of Emotional Disorders
Barlow, Sauer-Zavala, Carl, Bullis, and Ellard (2014) have proposed the following definition for emotional disorders: The disorder is characterized by (1) experi-
ence of frequent and intense negative emotions; (2) aversive reactivity to the experience of emotions (driven by a diminished sense of control and negative appraisal of the emotion); and (3) efforts to dampen, escape, or avoid negative emotion, either preemptively or in reac- tion to onset of the emotion. Regarding criterion 1, in- dividuals with emotional disorders are predisposed to experience negative emotions frequently and intensely (Bullis et al., 2019), a temperamental style that has been referred to variously as neuroticism, trait anxiety, or negative affect. Evidence to support this criterion comes from seminal classification studies showing that these higher-order temperamental constructs account for substantial variability in the development and tem- poral covariance of anxiety and depression (e.g., Brown, 2007; Brown & Barlow, 2009), as well as the affective neuroscience literature (see Bullis et al., 2019).
In terms of criterion 2, it is well-established that in- dividuals with anxiety and depressive disorders display more aversive reactivity (e.g., negative valuation or ap- praisals) to and are less likely to accept the experience of negative emotions than those without these condi- tions (e.g., Campbell-Sills, Barlow, Brown, & Hof- mann, 2006; McLaughlin, Mennin, & Farach, 2007; Tull & Roemer, 2007). Such aversive reactivity, natu- rally, leads individuals to being less willing to tolerate the experience of negative emotion (Barlow, Ellard, Sauer-Zavala, Bullis, & Carl, 2014). Recent treatment outcome research also suggests that reactivity to nega- tive emotions may play a more critical role in anxiety and depression symptom reduction than frequency of experiencing negative emotion (criterion 1) (e.g., Hayes, Orsillo, & Roemer, 2010; Sauer-Zavala et al., 2012). Fi- nally, aversive reactivity to (and the unwillingness to ex- perience) negative emotions results in individuals with these disorders engaging in efforts to avoid or dampen the experience of emotion (criterion 3). Behavioral (e.g., avoiding distressing situations, withdrawal) and cogni- tive forms of avoidance (e.g., thought suppression, ru- mination) that may relieve negative affect in the short term but paradoxically increase the intensity and fre- quency of negative emotion in the long term have long been documented in anxiety and depression (see Bullis et al., 2019).
In summary, a strong literature supports emotional disorders as being maintained by the following func- tional mechanism: disturbances in the appraisal of un- wanted, frequent and intense negative emotions leading to the use of maladaptive avoidance strategies. These tendencies serve to maintain the experience of frequent/ intense negative emotion through a “boomerang” effect
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and by preventing individuals from having opportu- nities to learn about their ability to cope with and re- cover from such emotions (Bullis et al., 2019), as well as strengthening the perceived intolerability of negative emotions. This functional model is consistent with in- creasing interest in identifying underlying mechanisms that drive a range of psychopathology (e.g., Research Domain Criteria [RDoC]; Insel et al., 2010), as well as dimensional approaches to the classification of mental health conditions with shared etiologies and mainte- nance factors (e.g., the Hierarchical Taxonomy of Psy- chopathology [HiTop]; Kotov et al., 2017).
SITBs within This Functional Model
Collectively, evidence from a variety of sources—clini- cal observation, leading theories, and growing empiri- cal findings—suggest that SITBs may also share the aforementioned functional mechanisms. Regarding criterion 1, there is a multitude of theoretical and em- pirical support for frequent and intense negative affect playing an important role in the emergence and main- tenance of SITBs. Leading theories of suicide posit that negative emotion (or constructs closely related to nega- tive affect)—for example, psychological pain (Shneid- man, 1993), emotion dysregulation (Linehan, 1993), hopelessness (Abramson et al., 2000; Beck, 1967), and perceived burdensomeness (Joiner, 2005)—contribute substantially to suicidal SITBs. In one such theory, sui- cide is specifically conceptualized as a form of escape from aversive negative affect states (e.g., Baumeister, 1990; Maltsberger, 2004). Negative affect intensity has been associated with suicidal ideation over long (e.g., Lynch, Cheavens, Morse, & Rosenthal, 2004) and short (e.g., Armey, Brick, Schatten, Nugent, & Miller, 2020; Ben-Zeev, Young, & Depp, 2012) time intervals. Neuroticism has been shown to prospectively predict suicidal ideation (e.g., Handley et al., 2012; Rappaport, Flint, & Kendler, 2017), suicide attempts (e.g., Orme et al., 2020; Wedig et al., 2012), and deaths (e.g., Pe- ters, John, Bowen, Baetz, & Balbuena, 2018; Tanji et al., 2014). Indeed, in our team’s meta-analysis of the past 50 years of research on risk factors for suicide, we observed that internalizing psychopathology (a broad category that included negative emotion and neuroti- cism, as well as anxiety and depression) is significantly prospectively associated with suicidal thoughts and be- haviors—although the magnitude of this relationship, like that for other known risk factors, is weak (Franklin et al., 2017). Similar meta-analytic findings show that
negative emotion-related constructs (e.g., hopelessness, affect dysregulation, internalizing symptoms), predict NSSI (Fox et al., 2015). Unsurprisingly, many studies have also demonstrated that neuroticism distinguishes self-injuring from non-self-injuring individuals and that people who engage in NSSI have heightened lev- els of anxiety and other negative emotions compared to those who do not (for a review, see Bentley et al., 2015).
In a related vein, a strong literature supports the role of emotion reactivity (defined as experiencing emotions in response to a wide range of stimuli, strongly or in- tensely, and for a prolonged period of time; Nock et al., 2008) in SITBs specifically. Nock, Wedig, Holmberg, and Hooley (2008) found that emotion reactivity is both elevated in individuals with SITBs and mediates the association between psychopathology (e.g., emo- tional disorders) and suicidal and nonsuicidal SITBs. A number of other studies have similarly indicated that emotion reactivity is associated with suicidal ideation (e.g., DeCou & Lynch, 2019; Liu, You, Ying, Li, & Shi, 2020; Polanco-Roman, Moore, Tsypes, Jacobson, & Miranda, 2018), suicidal behavior (e.g., Shapero et al., 2019), and NSSI (e.g., Smith, Hayes, Styer, & Wash- burn, 2017). Theoretical models also implicate emotion reactivity as conferring risk for NSSI (e.g., Nock et al., 2010).
Regarding criterion 2, there is evidence to suggest that individuals who engage in SITBs display aversive reactivity to (and are less accepting of) emotional expe- rience. Studies have shown that experiential avoidance and related coping strategies (e.g., suppression of un- wanted thoughts) are associated with the presence and frequency of suicidal and nonsuicidal SITBs (Brausch & Woods, 2019; Chapman, Specht, & Cellucci, 2005; Ellis & Rufino, 2016; Najmi, Wegner, & Nock, 2007; Pettit et al., 2009; Wolff et al., 2019). A recent system- atic review of the literature on experiential avoidance and NSSI (17 studies) indicated that experiential avoid- ance is common among self-injuring individuals (Brere- ton & McGlinchey, 2019).
Last, and most crucially from a treatment perspec- tive, suicidal and nonsuicidal SITBs have widely been conceptualized as efforts to avoid or escape aversive internal states (criterion 3). Indeed, by far the most frequently endorsed reason for engaging in suicidal behavior and NSSI is to reduce or relieve unwanted thoughts or feelings (e.g., Brereton & McGlinchey, 2019; Boergers, Spirito, & Donaldson, 1998; Hawton, Cole, O’Grady, & Osborn, 1982; Nock & Prinstein, 2004, 2005; Nock, Pristein, & Sterba, 2009). Fanta-
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sizing about suicide, making a suicide plan, and even engaging in nonfatal suicidal behavior may also serve the function of temporarily relieving extremely intense negative emotional states, though these behaviors do not provide sustained relief and are likely to worsen negative affect (and suicidal ideation) over time (e.g., Crowell, Derbidge, & Beauchaine, 2014; Pettit et al., 2009). Multiple prominent theories of NSSI also high- light the role of decreased aversive cognitions or feel- ing states in maintaining NSSI (e.g., Nock & Prinstein, 2004, 2005; Chapman, Gratz, & Brown, 2006; Klon- sky, 2007). Such theories are complemented by a grow- ing body of empirical literature (using both retrospec- tive self-report and increasingly, more ecologically valid and higher-resolution methods such as ecological mo- mentary assessment [EMA]) showing that negative af- fect tends to precede episodes of both suicidal ideation (e.g., Ben-Zeev et al., 2012; Mou et al., 2018) and NSSI (e.g., Hamza & Willoughby, 2015; Muehlenkamp et al., 2009). There is growing support from EMA stud- ies demonstrating that SITBs serve an affect regulation function (e.g., Armey, Crowther, & Miller, 2011; Klei- man et al., 2018; Muehlenkamp et al., 2009).
Although more research that sets out explicitly to test whether SITBs are maintained via the same functional, mechanistic process as emotional disorders would be beneficial, multiple converging lines of research suggest that SITBs may share underlying fundamental prop- erties with emotional disorders. It follows that trans- diagnostic treatments designed to directly target this underlying mechanism of emotional disorders may also be applicable for SITBs, especially for suicidal or self- injuring individuals with co-occurring emotional dis- orders or symptoms.
ADDRESSING SITBs WITHIN TRANSDIAGNOSTIC TREATMENT FOR EMOTIONAL DISORDERS
Having established this preliminary evidence for shared functional properties between SITBs and emotional disorders, we now introduce one such transdiagnostic treatment: the Unified Protocol for Transdiagnostic Treatment of Emotional Disorders (UP; Barlow et al., 2011b, 2018a; see Payne, Ellard, Farchione, & Barlow, Chapter 6, this volume). We first outline mechanisms of the UP, then demonstrate the strong support for its application to anxiety disorders, along with promising preliminary results for its application to individuals with emotional disorders and comorbid SITBs.
Rationale
The UP is a cognitive-behavioral intervention designed to address the full range of emotional disorders or prob- lems characterized by the aforementioned functional process (frequent and intense negative affect, aversive reactivity, and efforts to avoid/relieve aversive emo- tional states). In brief, the UP consists of eight treat- ment modules that address (1) goal setting and fostering motivation for treatment; (2) psychoeducation on the functional nature of emotions; (3) promoting mindful emotion awareness; (4) fostering cognitive flexibility; (5) changing maladaptive, emotion-driven behaviors; (6) interoceptive exposure; (7) emotion exposure; and (8) relapse prevention (Payne, Ellard, Farchione, Fairholme, & Barlow, 2014). These modules focus on increasing individuals’ willingness to approach and ex- perience a wide range of emotional experiences with- out avoidance, thus reducing reliance on maladaptive avoidant coping strategies that serve to increase the fre- quency and intensity of negative affect in the long term. The UP’s putative mechanism of action is extinguish- ing distress in response to the experience of emotion, which ultimately leads to reductions in severity and in- terference of emotional disorder symptoms (and other functionally similar problems).
The UP was developed largely in response to issues with dissemination of evidence-based psychological treatments (McHugh & Barlow, 2010; McHugh, Mur- ray, & Barlow, 2009). Over the past several decades, many manualized CBT protocols have been developed to target individual anxiety and depressive, trauma- related, and obsessive–compulsive disorders. The goal of such manualized treatments was to facilitate deliv- ering evidence-based therapeutic strategies on a large scale; however, the proliferation of such manuals—the American Psychological Association (2019) lists over 50 distinct protocols with at least modest research sup- port—means that frontline clinicians are unable to re- ceive training, which is often time- intensive and costly, in multiple different approaches. Given the high rates of comorbidity among emotional disorders (and clinically significant symptoms), it can also be difficult for pro- viders to choose which “single-disorder protocol” to use for the many patients who present more than one prob- lem warranting treatment. Thus, the UP has the po- tential to facilitate more efficient treatment for patients with a wide range of potentially complex “real-world” presentations. Given the clear need to improve access to evidence-based treatment strategies for suicidal and
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self-injuring individuals, the UP may be a promising treatment framework to consider for patients who pres- ent with SITBs and co-occurring emotional disorders (or subclinical symptoms).
Research Support
To date, the UP has amassed considerable empiri- cal support for treating emotional disorders. A recent meta-analysis of 15 controlled and uncontrolled stud- ies of the UP (N = 1,244) found large effect sizes for reducing anxiety and depressive symptoms, as well as specific disorders: GAD, panic disorder, social anxiety disorder, obsessive–compulsive disorder, and BPD (Sa- kiris & Berle, 2019). The UP also had moderate effect sizes for increased use of adaptive (and decreased use of maladaptive) emotion regulation strategies. These find- ings are complemented by a recent systematic review of 77 studies summarizing that the UP has been ap- plied to a wide range of problems and adapted (primar- ily in terms of individual vs. group format and session duration/frequency, and less commonly, modifications to the therapeutic content) to meet the needs of many diverse settings (Cassiello-Robbins, Southward, Tir- pak, & Sauer-Zavala, 2020). Overall, the most rigor- ous, large-scale clinical trials of the UP have focused on treating prototypical emotional disorders: anxiety disorders, and to a lesser extent, unipolar depression. The largest RCT of the UP in the United States to date (N = 223) compared the UP to four “gold-standard” single-diagnosis CBT protocols for anxiety disorders and OCD (Barlow et al., 2017), and observed statis- tically equivalent improvements in diagnostic severity and anxiety and depressive symptoms across the treat- ment conditions.
There is also promising preliminary evidence to sup- port using the UP to treat SITBs. Regarding suicidal thoughts and behaviors, Bentley, Sauer-Zavala, and colleagues (2017) conducted a small proof-of-concept study evaluating the acceptability and feasibility of delivering a condensed five-session version of the UP to suicidal individuals on an acute crisis stabilization unit (N = 12). The sessions focused on psychoeducation about emotions, mindful emotion awareness, cognitive flexibility, changing emotion-driven behaviors, and emotion exposure. Results indicated good acceptability and feasibility of the adjunctive UP, as well as excel- lent skills acquisition. Though the UP was associated with reductions in anxiety, depression, and suicidal ide- ation from baseline to posttreatment, no strong conclu-
sions could be made regarding efficacy given the small sample size and poor retention after discharge. Based in part on these promising pilot data, the UP was recently implemented clinically (in group-based, rolling admis- sion format) on a psychiatric inpatient unit for adults with suicidal thoughts and behaviors and emotional (primarily depressive) disorders (Bentley, Sauer-Zavala, Stevens, & Washburn, 2020). High acceptability was observed for the UP groups, whereas clinician fidel- ity to the protocol was variable. Routinely collected clinical intake and outcome data from before and after implementation (N = 194) indicated that reductions in depression, suicidal ideation, anxiety, and emotion regulation over the course of inpatient hospitalization were similar before and after UP implementation.
Regarding applications of the UP for NSSI, one sin- gle-case experimental design study examined the effects of two UP modules (Mindful Emotion Awareness and Cognitive Flexibility) on NSSI urges and acts among 10 self-injuring individuals meeting criteria for NSSI disorder (American Psychiatric Association, 2013) and other emotional disorders (Bentley, Nock, Sauer-Zava- la, Gorman, & Barlow, 2017). EMA data indicated that eight of 10 participants demonstrated clinically mean- ingful reductions in NSSI with either one or both UP modules, and group-based analyses indicated signifi- cant reductions in NSSI urges and acts (as well as anxi- ety, depression, and emotion regulation skills) after the interventions were introduced. A previous case study (e.g., Bentley, 2017) of the UP for NSSI also reported positive outcomes for NSSI, as well as levels of depres- sive and anxiety symptoms.
Overall, despite the promising initial findings, only a handful of small-scale studies have been conducted to date that evaluate the UP (or its core components) for treating SITBs; thus, further larger-scale, controlled research in this area is needed. In the remainder of this chapter, we turn to clinical applications of the UP for SITBs and co-occurring emotional disorders within the outpatient treatment setting, including key consider- ations for determining suicidal or self-injuring patients’ appropriateness for this time-limited protocol.
Treatment Variables
The UP has great promise as a broadly effectively treat- ment, yet, as with any therapy, there is need to be dis- cerning in its use, especially for SITBs. Attention must be paid to the variables that impact treatment efficacy, including the setting and format of treatment, as well
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as the comfort of the therapist with cognitive therapies and of the patient directly addressing SITBs. This sec- tion expands on these variables in order to guide opti- mal treatment selection.
Treatment Setting
As we detailed earlier, the vast majority of studies evalu- ating the UP have been conducted in traditional outpa- tient psychiatry or psychology clinic settings. Increas- ingly, this intervention has also been adapted for use in more intensive treatment settings that serve individuals at higher (current) suicide risk, such as (as described earlier) an acute crisis stabilization unit (Bentley, Sauer- Zavala, et al., 2017) and a psychiatric inpatient unit (Bentley et al., 2020). Work is ongoing by members of our team to evaluate a modified, three-session interven- tion that delivers core UP skills for suicidal adults on a hospital-based psychiatric inpatient unit (National Clinical Trial No. NCT03950765 on ClinicalTrials.gov [https://clinicaltrials.gov/ct2/show/NCT03950765]; Evan Kleiman, Principal Investigator). The UP has also been implemented for non-outpatient settings that serve other populations with higher levels of clinical sever- ity, including a residential treatment program for eating disorders (Thompson-Brenner, Boswell, Espel-Huynh, Brooks, & Lowe, 2019) and a community-based health care organization for homeless individuals (Sauer-Zava- la, Ametaj, et al., 2019).
Though applications of the UP in non-outpatient settings are growing, here we focus on using the UP to address SITBs in a traditional outpatient psychothera- py clinic for two reasons: (1) This setting is well suited to delivering the UP in the individual, weekly-session format that provides the richest case illustration details (as opposed to abbreviated or group formats typically needed for shorter-term inpatient treatment), and (2) treating suicidal or self-injuring individuals in outpa- tient settings necessitates thoughtful and ongoing risk assessment and determination of patients’ appropriate- ness for outpatient care, which we describe below. It is our goal, however, that these case illustrations will pro- vide a foundational understanding of how the UP or its components may be used to address SITBs across a variety of treatment settings.
Treatment Format
Here, we focus on delivering the UP in its original and most widely utilized format of delivery: 16–20 weekly,
individual, in-person, 45- to 60-minute, sequential (Modules 1 through 8) sessions. The UP has increas- ingly been adapted to other formats, as noted earlier, and initial studies have examined delivering selected UP modules in isolation (e.g., Bentley, Nock, et al., 2017) or “in alternative orders” based on individual patient characteristics (e.g., Sauer-Zavala et al., 2017; Sauer- Zavala, Cassiello-Robbins, et al., 2019). Initial efforts have also translated the UP into Internet-based, self-guided formats (see Cassiello-Robbins et al., 2020 for a review) and (as noted earlier) are currently under- way to use UP components in a smartphone-based, just- in-time intervention for recently discharged suicidal in- patients (National Clinical Trial No. NCT03950765). Here we focus on a traditional delivery format, however, because this maximizes the richness of case illustration, though the same therapeutic principles and techniques would apply across other formats.
Therapist Characteristics
There are two primary therapist characteristics to con- sider when determining whether the UP is an appro- priate framework to use when treating outpatients with SITBs and emotional disorders. First, therapists with a cognitive-behavioral orientation are likely to find the protocol most consistent with their current therapeu- tic approach. As the UP was developed to facilitate training in evidence-based psychological treatment, a strong foundation in or considerable experience de- livering CBT is not a prerequisite; however, cognitive- behavioral therapists will likely find that using the UP feels “natural” and complements well the strategies they already use. Indeed, the UP was not intended to be a “brand new” treatment approach, but rather a distilla- tion of key CBT principles across single-diagnosis pro- tocols in a package that is easily applied to a broad range of commonly presenting problems. This said, we have also observed anecdotally that psychodynamic thera- pists who receive UP training have found the protocol more consistent with their typical approach to therapy than expected given the treatment’s emphasis on the function and experience of emotion. So, although expe- rienced CBT therapists may be most immediately com- fortable with the UP, more novice CBT providers and even therapists of other theoretical orientations might ultimately find the UP to be a good fit.
Second, therapists who consider using the UP with suicidal or self-injuring patients must be comfortable assessing and managing suicide risk. As mentioned ear-
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lier, treating individuals with SITBs in an outpatient context necessitates continuous monitoring of and at- tention to changes in risk levels, which may warrant consultations or referrals to other additional providers if not already a part of the patient’s treatment team, escalations to a higher level of care (e.g., partial hospi- talization, inpatient treatment), or modifications to the treatment plan (e.g., increased between-session moni- toring). For example, therapists using the UP as their general framework may need to pivot during the course of treatment to prioritize safety planning (Stanley & Brown, 2008, 2012) or choose to incorporate non-UP skills (e.g., DBT distress tolerance skills such as distrac- tion, tip the temperature, or paced breathing) that may offer more immediate relief from intense self-injurious urges but are not directly in line with underlying UP principles of approaching and experiencing negative affect. The UP was designed to be flexible, so incor- porating other strategies and techniques aimed to en- sure patient safety can be incorporated on an as-needed basis, though therapists must be comfortable determin- ing when this is warranted and ideally foster an explicit understanding with the patient of when and why to use them. More novice therapists or trainees would benefit from supervision by providers with experience man- aging suicide risk, and as is the case for managing all suicidal or actively self-injuring individuals, having a team-based approach to treatment may be optimal.
Patient Characteristics
There are also two main patient characteristics to con- sider when determining whether an individual present- ing with SITBs is a good fit for the UP. First, patients usually present with at least one emotional disorder (or clinically significant symptoms) that they hope to address. The UP may be particularly well-suited to in- dividuals with multiple comorbidities, as distinct con- stellations of symptoms may all be addressed within the same framework. In our experience, suicidal or self-injuring individuals are often more distressed by and motivated to work on their anxiety or depression, for example, than SITBs. Importantly, the functional model discussed earlier (intense and frequent negative affect, aversive reactivity, efforts to avoid/relieve nega- tive affect) will be relevant to the patient’s experience (and maintenance) of SITBs. Through functional analysis and assessment (as detailed below), it will be determined that the primary function that the patient’s SITBs serves is to reduce or relieve intense negative af-
fect. In the case of NSSI enacted primarily for interper- sonal reasons (e.g., to communicate or seek help/atten- tion), for example, other therapeutic strategies directly targeting this interpersonal function (e.g., DBT inter- personal skills) may be more directly relevant; however, and as noted earlier, the UP’s flexibility allows for other content such as interpersonal skills training to be in- corporated.
The other key patient characteristic to consider when deciding whether to use the UP to treat patients with SITBs and emotional disorders is SITB acuteness. When using the UP in an outpatient setting, at least as a stand-alone intervention, it is imperative that the patient is appropriate for outpatient level of care and does not require more immediate, intensive treatment or stabilization in the form of emergency evaluation or inpatient hospitalization (e.g., in the case of imminent suicide risk or medically severe NSSI). A thorough as- sessment of the individual’s remote and recent history of SITBs, as well as associated clinical risk factors (e.g., substance use, social isolation, recent relationship or fi- nancial stressors, treatment history), is critical in mak- ing this determination. A comprehensive review of sui- cide risk assessment is beyond the scope of this chapter; however, the following tools have been recommended for gathering information about SITBs to inform clini- cal decision making: the Linehan Risk Assessment and Management Protocol (LRAMP; Linehan, 2009; Linehan, Comtois, & Ward-Ciesielski, 2012), which includes recommended actions and dispositions accord- ing to level of SITB risk, the Columbia Suicide Severity Rating Scale (C-SSRS; Posner et al., 2011), and the Self- Injurious Thoughts and Behaviors Interview (SITBI; Nock et al., 2007). Therapists may also choose to ad- minister a brief structured assessment of SITBs (e.g., the self-report version of the SITBI or Patient Health Questionnaire–9 [PHQ-9; Kroenke, Spitzer, & Wil- liams, 2001], which includes an item about suicidal or self-injurious thoughts) at each session to monitor risk in an ongoing way.
If a suicidal or self-injuring patient is determined to be appropriate for outpatient care based on his/ her SITB severity (perhaps with other treatment team members in place) or other reasons (e.g., potential iatro- genic effects of an inpatient stay), when would a thera- pist choose the UP instead of a suicide- or NSSI-specific protocol (e.g., suicide-focused CT, ERGT) or DBT? Myriad factors could contribute to this decision. For one, perhaps the outpatient therapist does not special- ize in treating suicidal or self-injuring individuals, and
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thus may have not received training in these other more specialized interventions; however, he/she may encoun- ter patients with suicidal ideation or self-injurious urges in the context of other disorders—depression, anxiety, PTSD, and so forth—in his/her practice. This harkens back to the UP’s strengths in terms of dissemination and therapist training, as providers may receive train- ing in one approach they can use across a wide range of patients, with and without SITBs.
A therapist may also choose the UP when a patient does not immediately identify suicidal thoughts and behaviors or NSSI as a primary concern, perhaps due to a perception that other symptoms/disorders (e.g., social anxiety, depression, PTSD) are more distressing and interfering, the stigma associated with SITBs (e.g., Reynders, Kerkhof, Molenberghs, & Van Audenhove, 2015; Downs & Eisenberg, 2012), or low motivation to reduce SITBs (e.g., viewing NSSI as an effective or adaptive coping strategy; Brausch & Muehlenkamp, 2018). In these cases, proceeding within a transdiagnos- tic, emotion-focused framework may foster more buy- in from the patient than a SITB-focused protocol. It is also possible that SITBs may emerge during the course of treatment for anxiety or depression (e.g., in the con- text of worsening mood symptoms), and the therapist may want to apply existing concepts and strategies to these new (or returning) problems. Finally, a therapist may choose the UP over DBT specifically when either the duration (1 year) or multiple formats (group, con- sultation, phone coaching) of DBT—at least as DBT is traditionally delivered—are unfeasible, and a briefer protocol is needed.
ASSESSMENT
During the initial evaluation, conducting a thorough assessment of SITBs is recommended to determine both the patient’s appropriateness for outpatient level of care (as detailed earlier) and whether SITBs fit within the functional framework outlined earlier. The SITBI (long-form, available for download on the Nock Lab Tasks and Measures webpage [https://nocklab.fas.har- vard.edu/tasks]; Nock, Holmberg, Photos, & Michel, 2007) is a structured tool that achieves both aims via detailed questions about the recency, frequency, and se- verity of SITBs, as well as SITB functions (e.g., “On a scale of 0 to 4, how much did you think of killing your- self as a way to get rid of bad feelings?”). Experienced providers may choose to forego a structured or semi-
structured tool and instead use clinical interviewing to probe about the patient’s past and current SITBs, as well as to potentially conduct a brief behavioral analy- sis of current engagement in SITBs. For example, the therapist may begin to inquire about the patient’s un- derstanding of typical external (e.g., social situations, work/financial stressors) and internal triggers (e.g., low mood, high anxiety) and effects of thinking about suicide or engaging in NSSI (e.g., relieve distress, feel better)—a functional analysis that is elaborated upon as part of UP Module 2, detailed below. As the focus of this chapter is on treating SITBs and co-occurring emotional disorders, there are a variety of semistruc- tured interviews well suited to capturing detailed in- formation about anxiety and related disorders, such as the Anxiety Disorders Interview Schedule for DSM-5 (ADIS-5; Brown & Barlow, 2014) or the Structured Clinical Interview for DSM-5 Disorders—Clinician Version (SCID-5-CV; First, Williams, Karg, & Spitzer, 2016). These (and other) measures help provide a com- prehensive picture of the diagnoses or symptoms that co-occur and may either interact with or contribute to SITBs.
In terms of ongoing assessments during treatment, as noted earlier, providers may choose to include a brief, weekly symptom-based measure that assesses SITBs to determine at the start of the session whether there have been recent changes in SITB frequency or severity, such as the self-report SITBI or PHQ-9. When treating individuals with recent or current SITBs in an outpa- tient setting, however, it is generally recommended that one also verbally assess for changes in suicidal thoughts and behaviors (e.g., “Have you had any thoughts of not wanting to be alive this week? Or taking your own life?”) and NSSI (e.g., “Have you had any urges to hurt your- self this week? Done anything to hurt yourself?”) and not rely exclusively on structured self-report measures, as the information gleaned from each mode of assess- ment does not always align (Kaplan et al., 1994; Mill- ner, Lee, & Nock, 2015; Brown, Currier, Jager-Hyman, & Stanley, 2015). The UP includes two brief, five-item measures of anxiety and depression severity and inter- ference (the Overall Anxiety Severity and Impairment Scale [OASIS; Norman, Cissell, Means-Christensen, & Stein, 2006] and the Overall Depression Severity and Impairment Scale [ODSIS; Bentley, Gallagher, Carl, & Barlow, 2014]) that patients are asked to complete weekly and track their scores over time using a Progress Record (all included in the patient workbook; Barlow et al., 2011a, 2018b). This facilitates ongoing therapist-
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patient discussion about contributors and potential bar- riers to progress, thus informing treatment planning. The second edition of the UP (Barlow et al., 2018a; also see Payne et al., Chapter 6, this volume) includes an equivalent third measure for severity and interference due to “other emotions,” which patients can choose to track another emotion (e.g., anger) or behavioral prob- lem. This measure could be easily adapted and used to track suicidal ideation or behavior, or NSSI urges or acts over UP treatment.
TREATMENT COMPONENTS
Next, we provide a module-by-module description of how the UP can be used to treat patients with emo- tional disorders and SITBs. Throughout this discus- sion, we offer a number of example transcripts taken from multiple suicidal or self-injuring patients we have treated with the UP, followed by a brief case study sum- marizing the initial presentation, course of treatment, and outcomes of one patient who underwent the full UP in individual format.
Rationale/Preparation
Providing a rationale for the transdiagnostic UP ap- proach to the patient is an important first step before launching into the treatment modules/skills. At this point, the therapist has used information from the in- take (often, a diagnostic evaluation) to first inform his/ her case formulation of the patient, attending to not only diagnoses but also how the patient’s symptoms and behaviors may fit into the aforementioned functional framework of (1) frequent and intense negative emotion, (2) negative reactions to the experience of emotion, and (3) maladaptive, avoidant responses. Thus, the therapist already has strong reason to believe that the UP may be an appropriate approach. In an initial session, the thera- pist will then offer a brief rationale for transdiagnostic, emotion-focused treatment and collaboratively explore with patient the ways they may or may not identify with the three key features of emotional disorders.
The therapist may begin by stating that the UP was developed to be helpful for a wide range of people who are struggling with intense or overwhelming emotions that may be interfering in their lives. The therapist can share that although the ways in which emotions interfere differ from one person to another, the so-called “emo- tional disorders” tend to share three common features,
starting with the tendency to feel emotions strongly/ often. The therapist can point out emotions the pa- tient has already mentioned struggling with during the evaluation. It can be noted that though some people are “hardwired” this way, the other two features are what really determines whether emotions are distressing and interfering. When discussing the second feature (nega- tive reactions to emotions), the therapist may provide examples of the tendency to view emotions negatively, such as “I shouldn’t be feeling this way,” “Getting upset means I’m weak,” “Everyone will see I’m anxious,” or “If I let myself feel sad, I’ll fall into a hole I can’t get out of” (Barlow et al., 2018b), and ask the patient whether any of these examples sound familiar to him/her. The therapist may choose to explore with the patient how early life experiences (e.g., modeling, family relation- ships) may have contributed to developing such views of negative emotion. The therapist then introduces the third feature (efforts to avoid or escape emotion), high- lighting that it makes good sense that people who view emotions negatively do things to try to avoid them, and may also begin to explore the corresponding negative reinforcement cycle of short-term effects (e.g., relief) and long-term consequences of avoidance (e.g., feeling more stuck in negative emotion, day-to-day activities and relationships becoming limited). Here, the thera- pist can elicit examples from the patient of ways (cogni- tive or behavioral) in which he/she might be avoiding or attempting to control his/her emotions.
The patient may or may not spontaneously identify SITBs as forms of emotion avoidance at this point. The therapist should use clinical judgment to determine whether to pose the possibility that thinking about suicide or engaging in NSSI may fit into this frame- work. For some (e.g., those who do not identify SITBs as problematic or significant issues for them), it may make sense to wait until the patient has built more of an understanding of the problematic nature of avoid- ance (e.g., during UP Modules 2 or 5) to broach this topic. Especially if the patient is presenting with mul- tiple emotional disorder comorbidities, the therapist may also mention during a preparatory session that de- velopment of the UP was based on observations of how common it is for different emotional disorders or symp- toms to “hang together,” and therefore simultaneously address a wide range of problems that a given individual may be experiencing.
The therapist then makes sure to introduce the pri- mary aim of the UP: to build more helpful, adaptive ways of responding to emotion that ultimately will
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make emotions feel more manageable. The therapist can prepare the patient for what is to come by provid- ing a brief overview of the UP’s core skills for manag- ing emotions. During an initial preparatory session (or sessions), the therapist also orients the patient to key aspects of time-limited CBT (not specific to the UP): the importance of symptom tracking over time (which may typically include setting expectations about non- linear change) and between-session practice/homework assignments. Generally, patients are encouraged—if feasible for them—to purchase the UP workbook (Bar- low et al., 2011a, 2018b) for outside-of-session readings and homework assignments, as well as a resource for the future if/when refreshers on content may be needed. Of note, in our prior work using the UP in non-outpatient settings or modified formats, we have often provided patients with modified versions of the workbook in word document format (e.g., Bentley, 2017; Bentley, Boettcher, et al., 2017).
Module 1 (Setting Goals and Increasing Motivation)
After the introductory session(s), the UP begins with a motivation enhancement module. This module is not considered a “core” module, as it does not provide a skill that directly targets the treatment’s overarch- ing mechanism (extinguishing distress in response to negative emotion) but helps set the stage for modules to come. The overall aims of this module—based in mo- tivational interviewing (Arkowitz, Miller, & Rollnick, 2017)—are to increase self-efficacy and to enhance and foster motivation for treatment. This module is used for all patients given that even for the most motivated individuals, it is common for motivation to fluctuate throughout treatment, and fostering motivation both initially and continuously throughout care as needed helps bolster chances of successfully making changes.
In an initial goal-setting exercise, the therapist works with the patient to identify the key problems that over- whelming emotions may be causing in his/her life, fol- lowed by measurable and concrete short- or long-term goals (ideally that are fully in the patient’s control; e.g., “asking someone out on a date” rather than “starting in a romantic relationship”) and corresponding steps or objectives. When working with individuals who en- gage in SITBs, patients may or may not include NSSI or suicidal ideation or behavior as a primary problem area or goal. As long as the therapist guides the patient toward goals that are concrete and manageable, includ- ing SITBs during the goal-setting exercise is not neces-
sarily critical. As mentioned earlier, in our experience, patients may present to therapy expressing a stronger desire to work on their anxiety or depression than on SITBs, so letting the patient lead with the goals he/she finds most meaningful and of highest priority is consis- tent with a motivational interviewing framework.
In the second activity, a decisional balance exercise, patients are asked to identify the pros/benefits and cons/costs of making changes (or engaging in treat- ment) and staying the same. Through this exercise, the therapist will first identify with the patient that am- bivalence about making changes (including with regard to SITBs, as we discuss in more detail below) is natu- ral. Then the therapist may encourage the patient that becoming aware of any ambivalence he/she may have (e.g., comfort/familiarity of staying the same, increased hopelessness if treatment doesn’t “work”) can help them to plan together how to handle fluctuations in motiva- tion that arise later on. As applied to SITBs specifically, the decisional balance exercise may be extended in a few ways. In our previous work using the UP in inpatient contexts for acutely suicidal individuals (e.g., Bentley, Sauer-Zavala, et al., 2017), we have focused part of this discussion specifically on the pros/benefits and cons/ costs of staying alive. For the individual who has re- cently made a suicide attempt or seriously considered suicide, the therapist may choose to guide the patient toward identifying reasons for living (e.g., watching a child graduate, more time with loved ones, responsi- bilities, potential for circumstances to improve) as such pros/benefits. When discussing costs/cons, consistent with the UP emphasis on approaching and experienc- ing negative emotions, the therapist can validate (if the patient identifies it) or offer as a possibility that choos- ing to stay alive may involve feeling, at times, painful negative emotions.
When treating suicidal or self-injuring patients who may not have as seriously considered suicide (so a discussion of “staying alive” may not be as relevant or indicated), the therapist may choose to address the benefits and costs of making changes with regard to suicidal thinking or NSSI. Importantly, this may help elicit from the patient the important factors serving to reinforce/maintain SITBs (e.g., short-term benefits of relief or distraction from painful emotional experienc- es; “It’s the only thing that works”), doubts about their ability to change, or other sources of ambivalence (e.g., shame about NSSI potentially making it challenging to address in therapy). To wrap up this exercise, the thera- pist can ask their patient to reflect on the pros and cons
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of changing (or potentially, staying alive) and consider which side feels more significant or weighty. If the pa- tient states that at the time the cons/costs of change (or staying alive or reducing SITBs) seem more substantial, the therapist can validate his/her experience and may instill hope and gently encourage the patient to remain open to the possibility that he/she may begin to experi- ence more benefits to change (or staying alive) over the coming weeks/months.
Module 2 (Adaptive Nature of Emotion)
UP Module 2 (the first core module), which usually spans two sessions, focuses on psychoeducation about the adaptive nature of emotions. The aim of this module is to begin to build understanding of emotions as they occur, in particular, the interactions among thoughts, physical sensations, and behaviors. This typically be- gins with the therapist using Socratic questioning to explore with the patient how all emotions, even those that may feel most uncomfortable or undesirable, serve an important purpose. The overall aim of this discus- sion is for patients to begin to view their emotions as adaptive or functional, albeit painful at times, and thus not always warranting efforts to avoid or escape them. The therapist asks the patient to consider the function that specific emotions serve: for example, fear (escape or fight), sadness (slow down, withdraw, process a loss, seek help), anxiety (focus, vigilance), anger (stand your ground, speak up for yourself or someone close to you), guilt (make amends), and joy (continue what you are doing). When working with individuals with SITBs, the therapist addresses how the specific negative emo- tions that tend to contribute to thoughts of suicide or NSSI may be communicating important information to them. For example, when working with a suicidal in- dividual, thoughts of ending one’s life might be framed as one response to overwhelming sadness or loneliness, which could be indicating the need to seek out more positive relationships. It can also be noted that, cer- tainly, emotions can surge to such an intense or over- whelming level that they become interfering and are no longer helpful to us, but that some level of each of these emotions is adaptive, and we would not want to eliminate them. The transcript below is from a session with a patient who recently experienced severe suicidal thoughts, during which the function of intense nega- tive emotions, which lead to suicidal thinking, is dis- cussed:
THERAPIST: It sounds like for you, sadness is an emo- tion that reminds you of things that are important to you . . .
PATIENT: . . . it slows me down. It makes me think about a lot of stuff. I’m sad about a lot of things that I’m going through right now. I’m not depressed about it, it’s just like, I’m sad. Because it’s like, you can do better, you know.
THERAPIST: Yeah. Imagine that everything this past week happened, but you weren’t sad about it. What might be bad about that?
PATIENT: That would mean something is really wrong, if you weren’t sad about it. . . . I’m sad because of the pain I caused [significant other], I wasn’t at my niece’s soccer game—she scored a goal, and said that she wished I was there. I’m sad about stuff like that.
THERAPIST: Yeah. So, there are two ways to deal with sadness when it comes up. The first way is to say, this is uncomfortable, let me push it away—let me go use or do something so I don’t feel it. Another way we could use sadness is to say, maybe I did some things that I could do differently next time. The sadness is there to tell us, that didn’t work out so well last time, so maybe let’s make some different choices. Gotta make sure I’m at that soccer game, because I’m going to feel sad afterwards if I don’t go. If you’re thinking about ending your life and the things that happened this past week and you don’t feel sad about it . . .
PATIENT: . . . something is wrong. . . . It’s like what you said about coping skills, you learn to really deal with your emotions. But again, a lot of people don’t have the chance to deal with their emotions. . . . When you stop and think about a lot of things, there are ways to get your emotions to work for you in good ways.
THERAPIST: Yeah, that’s what the emotions are there to tell you . . .
PATIENT: Emotions are like blinkers on your car. THERAPIST: Exactly! That’s such a good example—
they’re guiding you in the way to move forward. PATIENT: Right. THERAPIST: Let’s talk about how this could apply to
thoughts of suicide. If fear protects you from getting hurt, and sadness tells you to slow down, think about the choices you’ve made, and maybe do something different, and anger tells you to talk to somebody
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and tell them stop doing that, what do thoughts of suicide do for you?
PATIENT: Hmm . . . Thoughts of suicide really let you know that you’ve got some bottled-up feelings that you need to vent. I feel like every emotion that you go through, suicidal or depression, whatever—it’s like the trash can in your house. Once it gets filled, you need to take it out. On trash day, if you don’t pick it up, it’s going to sit in the back and have an odor, and cause trouble. That’s the way life, emo- tions, and suicidal thoughts are. You gotta talk about it. It’s crazy that you just asked me that question be- cause I’ve been sitting here thinking, I want to kill myself. That’s crazy. Wanting to take your own life. That’s sad. But when you’re caught up in your emo- tions, it gets overwhelming, you can’t help it.
THERAPIST: That’s such a good point. It’s like, when you experience a lot of emotions, and you have a lot of problems you don’t deal with them, and it just piles up like a big trash can, thoughts of suicide are a last resort.
PATIENT: Right, and then thoughts of suicide are like, one way to not have that worry any more. I won’t be here to worry about that trash.
Patients are then taught what the UP (like many CBT protocols) consider a foundational skill: breaking down emotional experience into its three components parts (cognitions [what you are thinking or telling your- self ], physical sensations [what you are feeling in your body], and behaviors [what you are doing or want to do/urges]). The therapist can emphasize that breaking down emotion into these components can make over- whelming emotional experiences—which are common for patients presenting with SITBs—feel more man- ageable and identify points for intervention with later skills. After introducing the three-component model of emotion, the therapist typically asks the patient to walk them through a recent intense emotional experi- ence (potentially a recent episode in which the patient was feeling suicidal or had urges to engage in NSSI) in order to illustrate the interactive relationships among these three components. For example, the therapist may ask the patient to explore how certain thoughts (e.g., “I’ve screwed everything in my life up”) might lead to emotional reactions (e.g., hopelessness, self-hate), which in turn may contribute to behaviors and behavioral urges (e.g., urges to end one’s life, drinking or drug use,
cutting). The therapist also encourages the patient to consider the antecedents leading up to the emotional experience, both distal (e.g., not sleeping well for several days in a row) and proximal (e.g., family conflict), as well as the short- and long-term consequences of his/ her responses (e.g., NSSI providing relief from intense negative emotions in the short-term, subsequent shame about the behavior and embarrassment about resultant scars).
Module 3 (Mindful Emotion Awareness)
The aim of UP Module 3 (typically two or three ses- sions) is to build from the foundational skill of breaking down emotions by helping patients foster more mindful (i.e., nonjudgmental and present-focused) awareness of emotional experiences through a combination of mind- fulness and mood induction exercises. With increased nonjudgmental awareness of emotional experiences as they unfold in the present moment, individuals can become better able to approach and engage more adap- tively with their ongoing emotional experiences instead of getting “carried away by” or reacting negatively to them, over time reducing the need to use SITBs as strat- egies to relieve distressing emotions.
First, the therapist introduces the notion that re- sponding judgmentally to negative emotions tends to intensify (or bring about new) negative emotions. When working with suicidal or self-injuring patients, the ther- apist may explore the possibility that judgments about experiencing negative emotions (e.g., “I shouldn’t be feeling this way”) may contribute to urges to self-injure for relief from the emotion they find distressing or for self-punishment (or engage in other problematic avoid- ance behaviors that serve to increase the magnitude of negative emotions over the long-term). The therapist also discusses the value—in many situations—of at- tending to the present moment (i.e., remaining present- focused) instead of focusing on the past or the future. For suicidal or self-injuring individuals, learning first to notice when they may be ruminating about past events or worrying about future consequences, and then work- ing toward shifting their attention toward the demands of the present moment, can be extremely beneficial.
After this initial discussion, the therapist guides the patient in a brief meditation exercise aimed to promote nonjudgmental awareness of one’s present experience— specifically, cognitions, physical sensations, urges, and emotions—using a script in the UP workbook. The
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script introduces the concept that one’s breath can al- ways be returned to when one might find oneself being carried away by a thought or feeling: a concept that we elaborate upon later in this module. When process- ing this exercise, the therapist can validate that many people find this extremely challenging especially when starting out, gently point out any judgmental reactions (e.g., “I am so bad at this”), and praise nonjudgmental or present-focused reactions. After the patient has prac- ticed this mindful meditation exercise on his/her own for homework, the therapist moves to the next step of building the mindful emotion awareness “muscle”: a mindful mood induction. The therapist provides the rationale for practicing mindfulness in the context of an emotion—it is harder to remain nonjudgmental and present-focused when experiencing a moderate or strong emotion—and plays a song (or songs) during session that the patient has brought in or one the therapist se- lects that is likely to elicit some level of emotion. Again, the therapist processes the patient’s experience attempt- ing to remain present-focused and nonjudgmental while listening to the song(s) with the patient afterwards and asks him/her to continue practicing on his/her own.
The last part of UP Module 3 is dedicated to trans- lating more formal mindful emotion awareness prac- tice into an “anchoring in the present” skill to be used during emotional situations as they naturally occur. This skill involves pairing a cue (typically, a single deep breath, though patients can feel free to choose other cues that will always be with them and unobtrusive; e.g., pushing their feet against the floor) with a shift in attention to objectively serving one’s ongoing emotion- al experience using a “three-point check” of thoughts, physical sensations, and behaviors/urges. Patients learn (and during the session, practice) the three steps of an- choring in the present: (1) using their cue, (2) doing a three-point check (“what am I thinking, feeling in my body, and doing or want to do”), and (3) assessing whether their responses are in line with the demands of the present moment (or based on past events or predic- tions about the future). If the latter (based on past or future), patients are encouraged to bring their responses (e.g., thoughts, behaviors, attention) in line with what’s happening in the here and now. With continued use of this skill, patients often describe becoming better able to “step back” and take an objective stance toward their emotional experiences—including during situations that tend to elicit urges to self-injure (e.g., interpersonal conflict, work/school stress)—as they arise.
When working with suicidal or self-injuring individ- uals, it can be especially useful to think through when use of anchoring in the present may be most appropri- ate. It is unlikely, for example, that practicing mindful emotion awareness as a stand-alone emotion regulation strategy will be helpful when experiencing extremely strong, overwhelming urges to engage in NSSI or sui- cidal behavior. Below is such an excerpt from a session with a self-injuring patient (adapted from Bentley et al., 2018):
PATIENT: (after describing a conflict with her roommate) I was just starting to feel really frustrated because I felt like there was no way to make it go away.
THERAPIST: Make what go away? PATIENT: Well, I guess, thinking about how I can’t do
anything right. And how I felt—I was so sad and just, like, hopeless. Totally hopeless.
THERAPIST: OK. Are those thoughts and feelings what led to you wanting to cut?
PATIENT: Yeah, completely. I just couldn’t handle feel- ing that way anymore . . . and I tried, you know, to anchor in the present. Like we’ve been working on. But it felt, like way too hard.
THERAPIST: Can you tell me more about what felt too hard about it?
PATIENT: Well, it was almost like, I felt so bad in that moment, I just focused on how bad everything was . . . like focusing on my thoughts, feelings, and behaviors almost made everything feel more intense.
THERAPIST: I think I understand. It sounds like by this point, your emotions had built up to a really high level. That same level we’ve talked about, when it feels like you can’t tolerate your feelings, and self- harming is the only thing that you feel like will make it better.
PATIENT: Exactly. THERAPIST: That makes sense. Once you’ve gotten
to that “breaking point,” anchoring in the present doesn’t really work (and here, even made your emo- tions feel even more intense). Thinking about the whole night, though, are there times when it might have been more helpful?
PATIENT: I guess, like, earlier on. When everything was actually happening with my roommate, I could’ve probably tried to focus on what I was feeling and
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what was going on in front of me . . . instead of, like, trying to pretend I was OK but really being so upset. (Therapist nods.) And also, probably in the couple hours after we talked. I mean, I didn’t cut right when she left. I got really worked up after she left, crying and alone, you know, back in my room.
THERAPIST: OK, got it. So maybe, in future situations, trying to practice mindful awareness of your emo- tions earlier on, like when you first start to feel more emotional and your feelings aren’t super intense yet, is when it’s going to be most helpful for you.
PATIENT: Yeah. As, like, more of a way to keep me from getting to that breaking point.
Along these lines, for patients with SITBs, it may be useful to frame mindful emotion awareness (and, spe- cifically, anchoring in the present) as a strategy for ob- serving and accepting (instead of suppressing or push- ing away) emotions as they occur on an ongoing basis. By generally approaching negative emotions in this way, patients may notice that this helps prevent negative emotions from escalating to a point where intense sui- cidal thoughts or NSSI urges arise. Finally, self-injuring individuals also often report pushing away (or rarely experiencing) positive emotions; it is not uncommon for patients to also describe engaging in NSSI, for ex- ample, to “feel something” (i.e., for automatic positive reinforcement; Nock & Prinstein, 2004, 2005). Thus, mindful emotion awareness may also be encouraged as a strategy to tune into more positive thoughts or feel- ings that arise in situations comprising pleasurable ac- tivities or interactions.
After working through Modules 2 and 3, ideally, pa- tients will have developed more objective awareness of their emotional experiences and practice shifting their attention toward the present moment during real-world emotion-provoking situations. These are, of course, challenging skills to master, particularly for self-injur- ing individuals who tend to feel their emotions very strongly and become overwhelmed by them. Thus, the therapist should continue to frame these skills as new “muscles” that require ongoing practice and strength- ening.
Module 4 (Cognitive Flexibility)
UP Module 4 (generally two sessions) hones in on one key component of the three-component model of emo-
tion: cognitions. Of all the UP modules, Module 4 looks perhaps most similar to how other CBT protocols deliver cognitive restructuring; however, there are sev- eral key nuances. For one, the UP emphasizes flexibility rather than changing cognitions (as we elaborate below). Consistent with the principles of mindful emotion awareness, automatic interpretations are not referred to as maladaptive or unhelpful negative thoughts; rather, patients are encouraged to notice automatic thoughts nonjudgmentally and to consider them as one of many possible interpretations or reactions to a situation. Along these lines, patients are encouraged to notice any discrepancies between their initial interpretation(s) of a situation and what is actually happening in the present, as oftentimes, automatic interpretations include a focus on what has happened in the past or worry about what might happen in the future—rather than attending to what the situation in front of them calls for. Finally, cognitive flexibility is viewed as only one part of more adaptive emotional processing and responding more broadly in the UP.
This module begins with the therapist providing psychoeducation on the interactive relationship be- tween thoughts (or interpretations) and emotions. This can be illustrated through an example scenario of the patient seeing someone he/she knows across the street, and upon waving, the person does not acknowledge him/her back. The therapist can ask the patient for his/her initial interpretations (typically, “They ignored me,” “They don’t want to talk to me,” etc.) and the subsequent effects on his/her emotions and behaviors/ urges (e.g., ruminate, text the person for reassurance) followed by eliciting (or offering) a potential alterna- tive interpretation (e.g., “They didn’t see me”) and the corresponding downstream effects. Such an example can also be used to illustrate the impact of emotions on interpretations—for instance, “If you had just gotten some bad news and were feeling really down, how would you be most likely to interpret this situ- ation?” and then “What if you had just gotten some really great news and were feeling excited, might you be more likely to interpret the situation differently?” Next, the therapist briefly introduces the concept of automatic interpretations, potentially pointing out that our minds tend to work like filters, which in many sit- uations is adaptive, because it allows us to process and respond to situations quickly. Over time, however, we can develop “habits” of how we tend to interpret situa- tions and place a great deal of trust in these initial, au-
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tomatic interpretations, which can come at the expense of thinking flexibly based on ever-changing situational demands. An in-session exercise (the “ambiguous pic- ture”; Barlow et al., 2011a, 2018b) can be conducted to highlight that (1) there are often at least several differ- ent interpretations for the same situation and (2) once an automatic interpretation has been formed, it can be challenging to take a different perspective, especially if there are already moderate or strong emotions pres- ent. In the following exchange (adapted from Bentley, Sauer-Zavala, Cassiello-Robbins, & Vento, 2018), the therapist works with a suicidal patient to identify au- tomatic interpretations that recently contributed to in- tense suicidal thoughts:
THERAPIST: I’d like you to think of a situation, recent- ly, when you felt a strong emotion—particularly sad or anxious?
PATIENT: The day before I came [to the hospital]. I was living aimlessly. I wasn’t doing what I know I should be doing . . . beating myself up.
THERAPIST: So the situation was a few days before you came to the hospital. Do you remember where you were? Let’s try to get down some more details.
PATIENT: I was walking around the city, crying. Just depressed. Like, thinking about walking in front of the bus. Jumping on the train tracks. It’s so sad, be- cause somebody always says something to me to try to cheer me up. . . . I’m sitting here, beat down emo- tionally. I want to pick up the phone to call some- body, but who do I call? . . . I have a lot of sh** that’s on my mind. Honestly, I’ve never spoke to anyone about it. . . . It’s really tough.
THERAPIST: That is really tough. So, you’ve said that a few days before coming to the hospital, you were walking around the city, feeling extremely depressed. What were some of the negative thoughts that were going through your mind?
PATIENT: I just wanted to end my life. THERAPIST: Why? PATIENT: Just because, it’s like my computer is out of
order. It’s like I’ve been hacked. I can’t tune myself out.
THERAPIST: You were thinking, “I just want to end my life because . . . ”?
PATIENT: Because I can’t focus or tune back in. . . . I just can’t. It’s hard—I feel like I haven’t put myself in
the right situations or with the right people. I haven’t gotten the help that I really need.
THERAPIST: So, “I just want to end my life because I can’t focus or tune back in” and “I haven’t put myself in good situations”?
PATIENT: Exactly. I haven’t put myself in the best of situations.
THERAPIST: And when you were thinking “I haven’t put myself in good situations,” were you also think- ing anything else?
PATIENT: Yeah . . . my biggest fear is ending up in the street homeless. It’s just so lonely.
THERAPIST: Is that something you were afraid was going to happen last week?
PATIENT: Yeah. THERAPIST: So was another thought “I’m going to end
up homeless”? PATIENT: Yeah—I feel like I am. THERAPIST: Good—these are all perfect examples of
automatic thoughts for us to talk about some more.
The therapist then introduces the idea that for in- dividuals who are more vulnerable to experiencing frequent and intense levels of anxiety, sadness, and other negative emotions, over time certain “thinking traps” (i.e., habitual patterns of automatic interpreta- tions) may develop. These thinking traps include over- estimating the likelihood that a negative outcome will occur (i.e., jumping to conclusions) and catastrophiz- ing (assuming that if a negative outcome occurs, it will be catastrophic and they will be unable to cope; i.e., thinking the worst). Patients are encouraged to chan- nel their mindful emotion awareness skill to, as a first step, notice when they are falling into one (or both) of these thinking traps. In our experience, patients with SITBs tend to quickly identify examples of interpreting ambiguous or trivial interpersonal situations negatively (e.g., “My friends don’t want me around” [jumping to conclusions], “Everyone here treats me badly” [jumping to conclusions], “I can’t handle this anymore” [catastro- phizing]), which can in turn lead to maladaptive be- havioral responses (e.g., withdrawing, fantasizing about suicide). The therapist can also choose to connect these “surface-level” automatic interpretations with more pervasive, negative core beliefs the patient may hold.
The next step, once a thinking trap is identified, is to work toward generating alternative interpretations.
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Here, the UP’s emphasis on flexibility comes into play: Patients are encouraged to generate alternative perspec- tives to their initial interpretation, even if they seem much less believable, not to try to replace the automatic interpretation with a more “positive” thought. The therapist can praise more balanced interpretations that take into account the demands of the situation (i.e., are present-focused), and encourage patients to con- sider their initial interpretation as just one of several (or many) possible interpretations. A list of “challenging questions” is provided to help generate such alternative perspectives. Consistent with the UP emphasis on ap- proaching and accepting emotions, UP therapists may consider specifically applying the cognitive flexibility skill to thoughts about emotions. For example, thera- pists may work with their patients to challenge judg- mental thoughts such as “I shouldn’t feel anxious” or “It is weak to feel this way” and entertain alternatives (e.g., “It would be weird if I didn’t feel a little anxiety about this,” “Emotions are hardwired into me, and ev- eryone”). When working with suicidal or self-injuring patients, the therapist can also aim to apply this cog- nitive flexibility skill to automatic cognitions specifi- cally about SITBs (“Cutting is the only way I can make myself feel better”), as illustrated in the vignette below (adapted from Bentley et al., 2018):
THERAPIST: What was going on that led to you want- ing to cut that night?
PATIENT: Well, I had to finish a paper, so was in the library till midnight. . . . It was awful. I was already really depressed, which was making it really hard to focus, but I had to get it done.
THERAPIST: It sounds like this was a stressful night. PATIENT: Yeah. It was really nice, though, because one
of my friends, who was working there too, stayed. She was going to go home, but then was like, “I’m going to stay with you for a while.” She could tell that something wasn’t right. But I was thinking, “Well, I sort of wish you would just go away, because it would be so much easier to just cut, and then not feel sad.”
THERAPIST: Right. PATIENT: But I knew that was unreasonable, so I said
she could stay. Then, there was one point when my roommate texted me about forgetting to call him back. . . . I just lost it. I started bawling.
THERAPIST: Then what happened?
PATIENT: Well, she just looked at me and asked, “Are you OK?” and I was immediately like, “I’ll be fine!” but I didn’t think I would [be fine]. Then, a few min- utes later, I actually was OK. I felt better. I think that was like, a different kind of release . . .
THERAPIST: Crying was a different kind of release than cutting?
PATIENT: Yeah, exactly. When I cry, especially in front of other people, I feel so vulnerable. With my friend, I was surprised at how OK I was with it. I think that was good to learn—that I’m OK with crying and being vulnerable around her.
THERAPIST: Right. It’s so interesting that you said crying was a different kind of release—letting your emotions out in front of her. It sounds like before she ended up staying, and you were thinking about cut- ting, you noticed the automatic thought, “It would be so much easier if she left, and I could just cut, and feel less sad.”
PATIENT: Yeah—that was when I was like, “Cutting is the only good way to cope right now.”
THERAPIST: But then, she stayed . . . PATIENT: She stayed, and I felt so much better after-
wards. I still felt sad, really tired, and frustrated that I had stuff to finish, but better. . . . I feel like I don’t appreciate the little interactions, like this one, that I have with my really close friends. That was really powerful.
THERAPIST: Very powerful. How could you use that powerful experience to help you think more flexibly during other times when you feel like cutting is the only good option to feel better?
PATIENT: Well, I think part of it with cutting is that I have to be in the right place, physically—so usually in my room, by myself. In the same way, to be vul- nerable like I was then, I have to physically be in the same place with someone I trust. [pause] I think that as purposefully as I would seek out a place to cut, I need to seek out a place to just cry or do something else.
THERAPIST: And it sounds like this time, you got a good, helpful release from that. So, would you say that there are other ways to get that same release, even if they take purposeful action?
PATIENT: Completely. Even in those moments, to ask myself, “Really? Is cutting the only thing that will help me?” I know the answer is no.
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Module 5 (Countering Emotional Behaviors)
In UP Module 5, which typically spans two sessions, the focus moves from cognitions to another key com- ponent of emotional experience: behaviors (and urges). The aim in this module is to identify and counter two types of problematic or maladaptive “emotional behav- iors,” which refers to any cognitive or behavioral strat- egy enacted in response to an uncomfortable emotion (or the anticipation of such an emotion). The therapist begins by defining emotional behaviors and may also give examples of specific types of emotional behaviors: emotion-driven behaviors, overt behavioral avoidance, subtle behavioral avoidance, cognitive avoidance (e.g., rumination, worry), and safety signals. The therapist emphasizes the paradoxical effects of seeking to avoid emotions, which by this point during UP treatment should not come as a surprise, and may choose to highlight this with a brief in-session thought suppres- sion exercise (e.g., Barlow et al., 2018a). Then, thera- pist and patient collaboratively identify the patient’s key emotional behaviors. It may be useful to organize these by emotion—for example, “What are your go-to emotional behaviors when anxious? What about angry? Sad?” The therapist may also discuss the notion that in some cases, determining whether an emotional be- havior is problematic or adaptive may not be obvious (e.g., canceling social plans when tired). This tends to hinge on the function of the behavior: Does canceling plans, for example, serve to avoid anxiety or “give in” to depression, or a skillful action to refuel? The exact same behavior can be maladaptive or adaptive, depending on the context and individual.
This module is, of course, highly relevant to self- injuring or suicidal individuals, as SITBs can be explic- itly framed as emotion-driven behavioral responses that may provide short-term relief, but over time, paradoxi- cally, increase the frequency and intensity of the emo- tions that the individual is trying to escape or reduce in the first place. By this point during UP treatment, patients will have developed a stronger understanding of how their behaviors interact with cognitions and physical sensations during emotional experiences and are generally already conceptualizing NSSI or suicidal behavior as having short-term positive yet long-term negative effects, so this is usually not a big leap to make. For patients whose suicidal ideation also fits within this functional framework (e.g., fantasizing about suicide providing immediate relief or comfort but keeping them “stuck” in cycles of avoidance over the long term),
suicidal thinking can also be explicitly framed as cogni- tive avoidance (a type of emotional behavior).
After collaboratively exploring the patient’s emo- tional behaviors, the therapist offers a rationale for acting alternatively to emotion-driven urges. “Alterna- tive actions” typically bring individuals into contact with their emotions rather than avoiding them, and though they may increase or intensify emotion in the short term, they serve to reduce the distressing nature of (or interference due to) emotion over the long term. The therapist then works with the patient to generate examples of personally relevant, and ideally accessible and realistic, alternative actions to the key emotional behaviors. Alternative actions may involve acting op- posite (Barlow, 1988; Linehan, 1993; see Neacsiu et al., Chapter 10, this volume) to the patient’s emotion- driven urges but also can include almost any action that is alternative to what the patient would normally do. When identifying alternative actions for SITBs, some viable alternatives (e.g., distraction, self-soothing) may not immediately bring the patient into closer contact with the uncomfortable emotion. For self-injurious or suicidal individuals, prioritizing safety is undoubtably the priority, so if the patient is able to identify a non- self-injurious alternative action to SITBs that over the short term will help him/her stay safe and over the long term has the potential to increase his/her ability to cope with and tolerate intense emotions, that is still consis- tent with the UP framework. Last, patients are encour- aged to replace emotional behaviors with an alternative behavior, rather than to simply “not do” the emotional behavior.
When working with suicidal individuals, the thera- pist may focus on the behavioral responses that serve to avoid or escape patients’ painful emotions during past suicidal episodes. For example, one patient identified using substances, withdrawing from others, “bottling [her] emotions up,” and lashing out as relevant emo- tional behaviors. Developing a plan to end her life was explicitly framed as an emotion-driven response that might provide some temporary relief from her emo- tional pain, but not an effective long-term solution for managing strong emotions. When considering the short- and long-term consequences of these responses, this patient explained that although acting on her sui- cidal urges would “end all emotions” and offer relief in the moment, it would be “harmful . . . and cause so many problems” (e.g., missing out on time with her family) over the long term. When generating specific alternative actions to counter her emotional behaviors,
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this patient identified calling someone who does not use substances, going on a run, watching Netflix, being present with her breath, and caring for a pet as alterna- tive actions when she feels suicidal. She also noted the potential utility of consulting this list if and when she experiences suicidal thoughts in the future and added “looking at her safety plan” (developed early on in treat- ment with the therapist) as another alternative action.
After generating personally relevant alternative ac- tions (e.g., reaching out to a loved one for distraction or support, vigorous exercise, self-soothing activities), pa- tients begin setting small, realistic goals toward imple- menting these new, more adaptive behavioral responses. It can, of course, be very challenging for individuals who have come to rely on SITBs to change ingrained patterns of emotional responding. Patients are encour- aged to utilize the skills they have learned thus far— breaking down an emotion, anchoring in the present, and cognitive flexibility—in conjunction with alterna- tive action, and are reminded that practicing alterna- tive actions will be addressed further later in treatment (within the final core UP module of emotion exposure).
Module 6 (Interoceptive Exposure)
After targeting cognitions in Module 4 and behaviors in Module 5, Module 6 (typically two sessions) address- es the remaining component of the three-component model of emotion: physical sensations. The aim of this module is to improve awareness and tolerance of un- comfortable physical sensations associated with emo- tion through repeatedly confronting physical sensations via interoceptive exposure exercises. By noticing the physical sensations that arise during an emotional expe- rience nonjudgmentally and without aversive responses (e.g., “I must do something to make this feeling go away,” “Others are going to notice”), patients are better able to “ride out” and manage emotional experiences adaptively (without avoidance), ultimately resulting in reductions in the frequency and intensity of nega- tive emotion. Historically, interoceptive exposure was originated as a treatment component for panic disorder (see Craske, Wolitzky-Taylor, & Barlow, Chapter 1, this volume); however, given increasing research to show its relevance for a wide range of emotional disorders (e.g., Boswell et al., 2013; Boswell, Anderson, & Anderson, 2015), the UP utilizes interoceptive exposure for all pa- tients, regardless of the primary diagnosis.
The therapist starts by highlighting a few key points that support a rationale for interoceptive exposure. For
one, it is the interpretation of physical sensations that tend to play the biggest role in physical sensations con- tributing to the intensity of an emotional experience. This is often illustrated by the “playground metaphor”: Patients are asked to first describe the physical sensa- tions that occur for a child when playing on a play- ground, which are typically experienced as “fun” or en- joyable. Then, the therapist makes the point that when these exact same physical sensations (e.g., heart beat- ing rapidly, sweating, face flushing, dizziness, stomach dropping) occur for an adult vulnerable to, say, anxi- ety or depression, they can quickly become threaten- ing and a sign that the individual cannot cope with the situation. The therapist then explains that the goal of interoceptive exposure is to give the patient the oppor- tunity to begin challenging the interpretations he/she may hold about physical sensations, with the goal of learning that uncomfortable physical sensations do not last forever, do not always escalate (e.g., lead to a panic attack), and that other people usually do not notice that the individual is experiencing them.
The therapist begins by leading the patient in a se- ries of interoceptive exposure exercises that are likely to elicit physical sensations commonly associated with anxiety (e.g., breathing through a thin straw, hyper- ventilating, spinning while standing); the therapist first demonstrates the exercise, then has the patient try it with him/her. Beforehand, it is important to assess for any medical conditions (e.g., asthma, vertigo, car- diovascular disease) that may be exacerbated by certain procedures. During these initial practices, the patient is encouraged to focus entirely on experiencing the physi- cal sensations, and not attempt to begin to challenge the negative interpretations that may arise; the therapist will also want to look out for any subtle signs of avoid- ance or escape (e.g., distraction, ending early). After each exercise, the therapist asks the patient rate his/her distress and the “similarity” of the physical sensations elicited to those typically experienced during intense emotional experiences. The goal is to identify the ex- ercises that are at least moderately distressing and most similar to the patient’s experience of emotion in “real life.” The therapist also suggests exercises that are likely to elicit physical sensations the patient has previously identified (e.g., while breaking down emotions) as com- mon. For example, a patient may try wearing a heavy backpack around while going about daily tasks to elicit the heaviness or sensation of being “weighted down” often associated with depression, sitting next to a space heater in a heavy coat or repeatedly tensing muscles to
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elicit the flushed/hot sensations that often arise with anger, or drinking carbonated beverages quickly (possi- bly combined with constricting clothing or doing brief vigorous physical activity) to elicit the stomach distress often associated with guilt or anxiety. After modeling the exercises together in session, the therapist asks the patient to practice moderately distressing, highly simi- lar interoceptive exercises on his/her own (until their distress ratings are low) for homework.
Therapists working with self-injuring individuals aim to identify and have the patient practice specific exercises that elicit physical sensations that typically occur during suicidal or self-injurious episodes, or at least those sensations that are typically experienced during emotions that tend to precede suicidal or self- injurious urges. Research has shown that patients with SITBs report higher levels of distressing bodily symp- toms (e.g., headaches, stomachaches; Hielscher, Whit- ford, Scott, & Zopf, 2019) and interoceptive avoidance (e.g., Schmidt, Woolaway-Bickel, & Bates, 2001) than those without, which suggests that promoting mindful awareness and tolerance of bodily sensations may be useful for this population. In our experience, by this point in treatment, therapist and patient generally are able to identify together at least a handful of uncom- fortable physical sensations that are often present while (or immediately prior to) experiencing SITBs—for ex- ample, restlessness or jitteriness, muscle tension, lump in throat, shakiness, or feeling weighted down.
For example, when treating a patient who engaged in NSSI to control or reduce intense anxiety triggered by distressing interpersonal situations or school and work demands, breathing through a thin straw was highly ef- fective in bringing about uncomfortable physical sensa- tions associated with intense anxiety (e.g., shortness of breath, dizziness) that resulted in self-injurious behavior (Bentley, 2017). This patient also practiced lying down on her couch with heavy books on her chest for ex- tended periods of time and wearing weights around her wrists and ankles while doing her work, which elicited the “weighted down” sensation she often noticed when depressed. Given that this patient also presented with subclinical symptoms of an eating disorder (a common comorbidity with NSSI) (e.g., Claes & Muehlenkamp, 2014; Wang, Pisetsky, Skutch, Fruzzetti, & Haynos, 2018), she found that wearing a belt cinched tightly around her waist to induce distressing physiological sensations of “fullness” and constriction was also a rel- evant interoceptive exposure exercise. With continued practice of these exercises, this patient observed that the
elicited sensations tend to be temporary and may not al- ways warrant an immediate reactive/avoidant response.
Module 7 (Emotion Exposure)
The final core UP module consists of emotion exposure exercises, and usually is delivered over approximately three to eight sessions. This module focuses on iden- tifying and practicing activities/tasks that are designed to bring on moderate to strong levels of emotion. Emo- tion exposure exercises are utilized in the UP for several reasons. For one, patients put their (often negative or catastrophic) predictions about what may happen in an emotion-provoking situation to the test. Exposure exercises also help patients learn that strong emotions tend to be temporary, and that they can cope with and tolerate uncomfortable emotions without engaging in avoidant emotional behaviors. Importantly, emotion exposure can also be framed as giving patients the op- portunity to put the skills they have learned thus far into practice when they are most needed: during emo- tional experiences. Through such “learning by doing,” patients have the opportunity for skills rehearsal and consolidation in the context of emotion. The therapist may choose to share the metaphor of learning to ride a bike: You can read about and be instructed on each part of riding a bike (e.g., grab the handlebars, swing one leg over the bike, put one foot on a pedal, then the other), but until you put it all together on the bike itself, you will not be able to master this skill.
After providing the rationale for emotion exposure, therapists work with their patients to develop an ex- posure hierarchy (organized by ratings of anticipated distress and level of avoidance), typically starting by asking the patient to brainstorm situations or activities that cause distress or that they avoid. Given the trans- diagnostic nature of the UP, any situation or activity that elicits moderate to strong emotion (including posi- tive emotions, if the patient finds the experience of joy, excitement, and so forth, distressing) can go on the hi- erarchy. For depression, emotion exposures may include activities designed to provoke sadness and the desire to engage in avoidant emotional behaviors (including tak- ing risks that may lead to failure or disappointment), during which the patient practices adaptive alternative actions (reminiscent of classic “behavioral experiments” in CT for depression; see Young et al., Chapter 7, this volume); exposures for depressed patients may also focus on engaging in previously enjoyable activities that elicit distress because the activity may not provoke as
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much joy as it did when the person was not depressed (Bentley, Conklin, Boswell, Shapero, & Olesnycky, 2019). The hierarchy may also include imaginal expo- sures, which typically involve creating, audio recording, and listening to a script detailing a feared “worst-case scenario” occurring, which may be especially useful for individuals with GAD, depression, or OCD. Emotion exposures may also be combined with interoceptive ex- ercises to intensify emotion; for example, a patient may hyperventilate before a difficult conversation with a loved one.
After creating the hierarchy, typically, the therapist conducts an initial exposure exercise with the patient in session, beginning with a task that seems more manageable. Therapist and patient can use an expo- sure practice form (Barlow et al., 2018b) to prepare for the exercise by recording anticipated distress, au- tomatic thoughts/predictions (and potential alternative thoughts), and anticipated emotional behaviors (and potential alternative actions). After completing the ex- ercise, patient and therapist process the task by record- ing the patient’s distress ratings; the thoughts, physical sensations, and behaviors/urges they noticed during the exercise; how they were able to implement their anchoring, cognitive flexibility, and alternative action skills; and key take-aways (perhaps involving themes of negative predictions not occurring or the ability to tol- erate/cope with uncomfortable feelings without avoid- ance). Patients are asked to continue practicing emo- tion exposure exercises on their own, using this same framework for homework and likely in subsequent ses- sions with the therapist.
There are several key considerations when imple- menting emotion exposure exercises with individuals who experience SITBs. Exposure tasks are not designed specifically to provoke suicidal or self-injurious urges, nor is it a goal of these activities for patients to habituate to or become more comfortable with thoughts of sui- cide. Given that exposures are designed to bring about moderate to strong emotions, however, it is possible (and for many patients, likely) that suicidal thoughts or NSSI urges may arise during exposures that involve more intense emotions. The therapist emphasizes to the patient that should such self-injurious urges arise during an exposure task, this is an opportunity to practice responding differently and more adaptively to such urges—either by noticing and “sitting with” the thoughts nonjudgmentally or by implementing an adaptive alternative action. We emphasize again that a goal of these exercises is to foster confidence in pa-
tients’ ability to access and apply treatment strategies and cope adaptively without avoidant responses in “real-world,” emotion-provoking situations when skills are most needed. With more acute suicidal or self-in- juring patients, of course, the therapist must use clini- cal judgment to help determine what specific tasks the patient is ready to take on without compromising his/ her safety. In-session exposures may involve more dis- tressing tasks than those the patient is encouraged to try on his/her own outside of session, and the therapist may also consider building in time for processing in- session exposures to allow the emotion(s) to decrease to more manageable levels before the patient leaves. The therapist can also encourage the patient to engage in relevant alternative actions or self-soothing exercises after an exposure task if self-injurious urges continue to persist—for example, physical exercise, going for a walk with a friend, or taking a bath—and reminding the patient to use his/her safety plan as needed.
Imaginal exposure tasks may also be particularly well-suited for suicidal individuals. Consider the ex- ample of a patient who recently learned about his part- ner’s infidelity, which contributed to intense suicidal ideation (Bentley, Sauer-Zavala, et al., 2017). During an in-session imaginal emotion task, he might first be asked to recall and describe in vivid detail the anger and sadness (e.g., specific thoughts, physical sensations, behaviors and urges). While experiencing at least mild to moderately intense emotion, this patient may be en- couraged by the therapist to use his anchoring in the present skill to notice a suicidal thought in a nonjudg- mental way or cognitive flexibility to consider alterna- tive interpretations (e.g., “I would rather know than continue to be in the dark,” “I’ve gotten through worse than this before”), or imagine himself acting alterna- tively to his emotion-driven urges (e.g., engage in NSSI, overdose to end his life) by reaching out to a supportive friend or family member, or implement other strate- gies (e.g., distress tolerance, intense physical exertion) to ensure that he stays safe. Another patient may first do a role play with her therapist of a stressful interac- tion with an authority figure or family member that resulted in a NSSI episode. This exercise may serve as a stepping-stone to an in vivo conversation with the same person, in which the patient practices implementing more helpful responses. Through graduated emotion exposure tasks, during which adaptive skills for coping with strong emotions are utilized, it is expected that the degree to which patients can tolerate negative emotions without resorting to SITBs will improve.
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Below is an excerpt from a transcript in which a pa- tient with NSSI (and multiple anxiety disorders, as well as a trauma history) and the therapist process an ex- posure that involved her sharing with people she does not know well (e.g., why she came to therapy, prog- ress in treatment) sensitive personal experiences that she expects will bring about intense levels of anxiety, guilt, and shame. The interaction below involves pro- cessing the end of the task, during which confederates expressed their admiration for her courage and perse- verance, which brought about uncomfortable positive emotions for this patient (adapted from Bentley, 2017):
THERAPIST: How was that, at the end, for you? PATIENT: Uncomfortable! I’m not used to compli-
ments, and wasn’t expecting that. THERAPIST: Can you tell me more about how you felt? PATIENT: Well, it was intense because, you know, I had
just finished all the other stuff. . . . I guess it made me feel even more guilty, because, like, I don’t think I deserve that.
THERAPIST: Deserve what? To be complimented? PATIENT: Yeah, that. And also, it’s hard to explain. . . .
I started to feel, almost like, proud of myself. But feeling good about myself, you know, it used to make me uncomfortable.
THERAPIST: Used to? PATIENT: I mean, it still does. But part of me also feels
like, bad stuff has happened to me, and I’m working hard to get past that. . . . It’s good to hear people acknowledge that.
Module 8 (Relapse Prevention)
In the final UP module (relapse prevention), which is typically delivered over one to two sessions, the patient’s progress and key treatment material are reviewed, and therapist and patient create a plan for future skills prac- tice. Patients are first asked to reflect on changes they have experienced in terms of anxiety and depressive symptoms (and potentially other target symptoms or behaviors they have been tracking; e.g., suicidal ide- ation, NSSI) using their Progress Record, as well as the goals they set at the beginning of treatment. The therapist encourages the patient to view ending weekly therapy as starting the next “phase” of treatment, and that as long as they continue to work on practicing and implementing the skills learned thus far, they are likely
to continue experiencing gains and making progress toward their goals. Along these lines, the goal-setting exercise can be revisited to set longer-term goals and specific steps for the next six months, year, and so on.
The therapist also reviews with the patient each of the key UP skills learned—breaking down an emotion, anchoring in the present, cognitive flexibility, and coun- tering emotional behaviors—and what progress has been made with implementing these, as well as reduc- tions he/she has noticed in the distress about physical sensations (Module 6) and avoidance of intense emo- tions (Module 7). The patient will also develop plans for how to continue practicing the skills learned; this may involve some combination of weekly self-check- ins (e.g., the patient is becoming his/her own therapist) at the same time as he/she used to meet for therapy, specific plans for how often and when to practice each skill (or continue conducting exposure exercises), and other strategies for keeping the skills fresh in his/her mind (e.g., having a list of challenging questions from Module 4 saved on his/her phone, a recurring reminder to practice mindful meditation once a day, rereading parts of the workbook at regular intervals). Finally, the therapist works with the patient to identify and trouble- shoot common potential triggers (e.g., big life changes, interpersonal conflicts), as well as encourage both ex- pectations that symptoms will fluctuate naturally and a nonjudgmental stance toward such changes. With sui- cidal or self-injuring patients, therapist and patient may identify specific “warning signs” (e.g., more intense sui- cidal thoughts, resurgence of NSSI) that would indicate the need for booster sessions or reinitiating weekly (or more intensive) treatment.
CASE STUDY
Here, we provide a summary of the initial presentation, course of treatment, and outcomes for “Alex,” a 27-year old, single, heterosexual male who received the full UP across a total of 19 sessions. Alex presented seeking help for “anxiety,” noting that he had gone to a handful of therapists over the past 5 or so years but stopped going after a few sessions each time due to “not feeling a con- nection.” He was referred by his primary care physician, who had prescribed Alex an antidepressant for the past 6 months. About a year before, Alex had been laid off from his entry-level job in marketing and as such was temporarily living at home with his parents while look- ing for another job. He reported a history of verbal and
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emotional abuse by his older brother, with whom nei- ther Alex nor his parents had had any contact for about 2 years. He was financially dependent on his parents, who were paying off his college loans.
During his intake, the SITBI and SCID-5 were used to assess SITBs and psychiatric diagnoses, respec- tively. Alex endorsed currently experiencing suicidal ideation, noting that his suicidal thoughts “come and go” throughout the week, typically following a diur- nal pattern of passive suicidal ideation (wishing that he could go to sleep and never wake up or that he had “never existed”) first thing in the morning and later in the evenings. He described his suicidal thinking as “oc- casionally” (once or twice a week) escalating to more active forms of ideation, including “fantasizing” about potential methods such as driving his car into the me- dian on a highway. He denied any intent to act on these thoughts. He had experienced similar patterns of sui- cidal ideation during previous depressive episodes (see below), but denied ever making a concrete suicide plan, engaging in preparatory actions, or making a suicide at- tempt. He did describe often thinking that people in his life would be “better off without him,” but his parents were also one of his primary reasons for living, as he knew that killing himself would devastate them. No- tably, Alex was not particularly forthcoming about his suicidal ideation at the outset of treatment; therefore, obtaining this information required gentle, but persis- tent questioning by his therapist and revisiting the topic over the first three to four sessions as the therapeutic alliance solidified. He also reported infrequent engage- ment in NSSI (fewer than 10 times total in his life, most of which were during high school, and twice in the past year [severely scratching his arms]). These more recent NSSI episodes occurred in the context of acute episodes of anxiety and agitation brought on by intense frus- tration with himself, typically about not meeting his career-related goals.
Alex was also assigned a principal (most severe and interfering) diagnosis of MDD, recurrent, moderate. His current symptoms included low mood, anhedonia, sleep disturbance (hypersomnia), impaired concentra- tion, excessive guilt and feelings of worthlessness, irri- tability, and suicidal ideation (as described earlier). He had experienced at least two prior depressive episodes in his life, most recently about 2 years earlier, following a heated argument with a close friend that led to this friend “cutting him out of his life.” He also met crite- ria for a diagnosis of social anxiety disorder, describing significant fear and avoidance of many social situations
(including speaking with unfamiliar people, pursuing romantic relationships, and applying for jobs), report- ing fear that he would “be judged” or people would talk badly about him behind his back. Last, Alex also met criteria for alcohol use disorder, mild. He reported typi- cally drinking most nights per week, about 3 to 4 beers at a time, with occasional episodes of heavier drinking (hard alcohol) when out with friends. Alex reported that he continued to drink despite knowing it likely contrib- uted to his depression (though it provided short-term relief and distraction from symptoms of depression and anxiety, as well as suicidal ideation, in the evenings), that he regularly had times when he ended up drink- ing more or longer than he intended, and the next-day effects of drinking (e.g., fatigue, feeling “cloudy”) got in the way of taking steps toward his career goals. See Table 11.1 for Alex’s scores on self-report questionnaires at the initial session (and over time).
Regarding the case formulation, Alex’s constellation of diagnostic symptoms (MDD, social anxiety) and maladaptive behaviors (SITBs, alcohol use) shared sig- nificant functional overlap, and as such fit well within the UP framework. First, a tendency to experience fre- quent and intense negative emotions resonated with Alex, as he explained that he perceived himself to have always “felt things” more intensely than other people, for which his brother teased him harshly as a child. Along these lines, Alex stated that although his parents were supportive and loving, neither had a mental health history or had ever received psychotherapy, which, cou- pled with his brother’s bullying when he showed any signs of emotional vulnerability, led him to develop an ingrained aversive reactivity to the experience of emo- tion. For example, Alex voiced his desire to “not feel anything” and described becoming frustrated with and beating himself up for experiencing anxiety, especially in social situations. He learned to value “sucking it up” and engage in a variety of behavioral strategies to avoid or quell the experience of emotion in the short-term, including withdrawing from friends, to spend a lot of time playing video games, to procrastinate working on his resume or take other steps to find a new position (e.g., looking online for job openings, submitting ap- plications), drinking, and during more acute anxiety, infrequently engaging in NSSI. For Alex, fantasizing about suicide sometimes offered relief, but when his suicidal thoughts increased in intensity, he found it dis- tressing (and thus engaged in other avoidant strategies, namely, drinking, to relieve them). Alex also reported that he had been avoiding activities he previously en-
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joyed, such as hanging out with close friends and box- ing/working out at his local gym. He felt extremely guilty about avoiding these activities but found it dif- ficult to motivate himself to reengage in them. Such avoidant coping strategies were serving to exacerbate and maintain Alex’s low self-esteem and negative core beliefs (e.g., of worthlessness and incompetence), as he had few opportunities to disprove these negative think- ing patterns. Notably, Alex also had secondary, judg- mental reactions about his engagement in SITBs: On multiple occasions, he described his thinking about ending his life and engaging in NSSI as “pathetic” and shameful, thus evidencing secondary judgmental reac- tions to SITBs that fueled his negative core beliefs.
The UP was selected for multiple reasons. First, the treatment framework could directly address the core transdiagnostic factors that underlie the range of Alex’s emotional disorder symptom sets, thus simultaneously addressing his depression and anxiety rather than tar- geting one symptom cluster before turning to another. Alex’s problematic risky behaviors—thinking about suicide as a way out, NSSI, and alcohol use—could all be conceptualized as emotion avoidance strategies (in the case of alcohol, “self-medication”; Bolton, Rob- inson, & Sareen, 2009), and thus targeted within UP Modules 5 and 7 (Countering Emotional Behaviors and Emotion Exposure). Importantly, Alex was seeking treatment for anxiety, and was hesitant to disclose and discuss openly his current experience of SITBs (under- standably, given his shame about these sensitive behav- iors). Thus, the therapist anticipated that the UP might offer a framework in which SITBs could ultimately be
targeted, but that would foster buy-in from Alex early on given the UP’s emphasis on delivering strategies for a broad range of emotional experiences, especially as Alex had dropped out of prior therapy before after only a few initial sessions.
In the paragraphs that follow, we highlight key com- ponents of how the UP was implemented for Alex and specific challenges that arose. Although he was skep- tical that therapy would help, from the outset, Alex agreed that the transdiagnostic, emotion-focused UP framework resonated with his experience of anxiety and depression and goals for treatment. In Module 1 (Mo- tivation), during the decisional balance exercise, Alex initially had difficulty identifying any pros of staying the same (and cons of change), which is not uncom- mon during this module. With his therapist’s guidance, Alex acknowledged that “effort” and pushing himself out of his comfort zone, potentially leading to increased distress over the short term, were significant sources of ambivalence for him. Along these lines, when engaging in goal setting, Alex was open to consider changes to his typical patterns of alcohol use when out with friends (i.e., limiting heavy drinking episodes), though was less eager to consider cutting back on his regular drinking as key to making meaningful change in his anxiety/de- pression.
Module 2 included an explicit focus on SITBs, as Alex began tracking his emotional experiences as they unfolded, and on several occasions recorded “think- ing about suicide” or “wanting to hurt myself” in the behaviors/urges component of the three-component model. As a result of this monitoring, he noticed that
TABLE 11.1. Self‑Report Questionnaire Data and Ranges for Alex
Session 1 Session 4 Session 8 Session 13 Session 18
PHQ-9 18 (severe) 16 (moderate) 10 (moderate) 5 (mild) 4 (minimal)
PHQ-9, item 9 2 (more than half the days)
2 (more than half the days)
1 (several days) 0 (not at all) 0 (not at all)
GAD-7 11 (moderate) 10 (moderate) 6 (mild) 4 (minimal) 2 (minimal)
OASIS 12 (clinical) 11 (clinical) 10 (clinical) 7 (subclinical) 6 (subclinical)
ODSIS 13 (clinical) 11 (clinical) 8 (clinical) 5 (subclinical) 5 (subclinical)
Note. PHQ-9, Patient Health Questionnaire (Kroenke et al., 2001; item 9 assesses frequency of suicidal or self-injurious thoughts in the past 2 weeks); GAD-7, Generalized Anxiety Disorder Questionnaire (Spitzer et al., 2006); OASIS, Overall Anxiety Severity and Impairment Scale (Norman et al., 2006); ODSIS, Overall Depression Severity and Impairment Scale (Bentley et al., 2014).
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his suicidal ideation was more likely to arise during acute moments of low mood and depression, whereas urges to engage in NSSI only occurred in the context of higher-arousal states such as anger and extreme anxi- ety. Though Alex evidenced a strong understanding of the interaction among his thoughts, physical sensa- tions, and behaviors/urges (and corresponding short- and long-term consequences) in Module 2, Module 3 (Mindful Emotion Awareness) proved more challeng- ing for Alex, as he found “sitting with [his] emotions” during mindfulness exercises aversive, and remaining nonjudgmental of both his own emotions, as well as the exercises (e.g., “This stuff won’t help me”), challeng- ing. As a result, his compliance with daily mindfulness exercises was fairly poor, though he gained more trac- tion practicing the anchoring in the present skill during real-world moments of distress.
Compared to Module 3, Alex found the cognitive flexibility strategies introduced in Module 4 (Cogni- tive Flexibility) more immediately helpful. He readily applied the UP’s questions for generating alternative interpretations to recurrent themes of jumping to con- clusions (e.g., “They will reject me”) and catastroph- izing (e.g., “I’ll never function on my own”) in his life, which generally helped with regulating his experiences of anxiety (more so than in acute moments of depres- sion, for which he found behavioral strategies [intro- duced in Module 5] more accessible and, over time, effective). Of note, Alex found that practicing cogni- tive flexibility specifically for negative thought patterns related to suicide (e.g., “Ending my life would mean no longer feeling this way, and also never seeing my family or friends again,” “There are other ways to feel better”) tended to reduce the duration and intensity of episodes of suicidal thinking. In Module 5 (Countering Emo- tional Behaviors), Alex identified alternative actions for his key emotion-driven behaviors (including NSSI) corresponding to anger (e.g., going outside [even if in his parent’s yard], exercise), anxiety (e.g., taking a cold shower, calling or texting a friend), and low mood (e.g., getting out of bed, following through on social plans). He began to set small goals for implementing these al- ternative actions, and, as is typical for most patients, had more success acting alternatively to some emotion- driven behavioral urges than others. For example, Alex was able to prevent NSSI urges from escalating to more intense levels with adaptive alternative actions, whereas he had more variable success limiting his drinking in social contexts.
Module 6 (Interoceptive Exposure) involved symp- tom induction exercises targeting physical sensations associated with both anxiety (e.g., shortness of breath, muscle tension) and depression (e.g., feeling weighted down/heavy) for Alex. Though Alex engaged with such exercises during session with the therapist, as is not uncommon for CBT patients, he did not consistently follow through on outside-of-session interoceptive ex- posure practice and as a result reaped little benefit from this module. Per his therapist’s guidance, however, a few in-session exposures during Module 7 combined symptom induction exercises with emotion exposure tasks (e.g., hyperventilating before opening and editing his resumé on a laptop) so as to increase the intensity of the overall exposure exercise. Key emotion exposure ex- ercises for Alex spanned the range of his diagnostic and symptom domains, including MDD (e.g., taking risks that may lead to failure or disappointment [submitting a job application], doing previously enjoyable activities such as boxing), social anxiety (e.g., initiating contact with friends he had been avoiding, talking to a roman- tic interest while sober), and alcohol use (e.g., exercising in the evening instead of drinking). A number of these exposure exercises offered the opportunity for Alex to practice utilizing the UP skills (e.g., anchoring in the present, cognitive flexibility, countering emotion-driv- en urges) when experiencing suicidal or self-injurious urges. For example, while ruminating about a social interaction (initiated as an exposure) that Alex believed had not gone smoothly, he noticed passive suicidal thoughts (e.g., wishing he could “escape it all” by going to sleep and never waking up) arising. In response, he was increasingly able to anchor in the present using his breath, coupled with thinking flexibly (e.g., “I may feel like this now, but it will pass”). Overall, Alex reported finding emotion exposures such as this helpful in that he was able to witness and learn that intense negative emotions do not last forever and build confidence in his ability to experience and tolerate aversive emotions without avoidance.
Module 8 (Relapse Prevention) focused on reviewing Alex’s progress and the skills learned, as well as planning for future practice and identification of “warning signs” (e.g., intense suicidal thoughts, NSSI, increases in sub- stance use) that would warrant booster sessions or addi- tional treatment. He reported confidence in his ability to continue applying UP skills in the pursuit of his lon- ger-term goals, namely, living independently again and finding a steady romantic partner. As shown in Table
470 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
11.1, Alex experienced steady decreases in depression, suicidal ideation, and anxiety, with questionnaire scores all falling in the minimal or subclinical range by the end of treatment. Notably, Alex had received a job offer mid- way through treatment, which was observed to also have a significant positive effect on his symptoms. Though neither a structured self-report measures of NSSI nor alcohol were used, per Alex’s verbal report during ses- sions, he noticed significant reductions in frequency and intensity of NSSI urges and did not engage in NSSI during the course of treatment. Alex made less progress on his alcohol use, and despite having significant reduc- tions in depression and anxiety, there was concern about a future relapse of depression in the context of continued alcohol use. Alex was not interested in referrals to sub- stance use-focused treatment at the time.
TYPICAL PROBLEMS AND SUCCESSES/FAILURES
Typical Problems
One common problem that can arise when using the UP for patients with emotional disorders and SITBs is lack of engagement in and compliance with treat- ment procedures, in particular between-session prac- tice, which is critical to skills acquisition and treatment gains. For individuals with SITBs, many factors may serve as barriers to consistent engagement and compli- ance, including severe depressive symptoms (e.g., lack of motivation, hopelessness), stressful life events or in- terpersonal problems, views that they “already know” the skills (as they may have been exposed to CBT or DBT concepts previously), skepticism that the skills will help them during intense emotional experiences, or anxiety about deliberately bringing on emotion in exposure-based tasks. The Decisional Balance Exercise (Module 2) can be conducted again at any point in treatment to identify and to troubleshoot such barriers to engagement and compliance. Having a family mem- ber or friend provide encouragement and regular ac- countability to attend sessions and complete homework may be beneficial. The therapist encourages the patient to be mindful of changes in his/her level of motivation, to use planned methods for overcoming obstacles, and to have open conversations with the therapist if he/she notices him/herself struggling to practice skills outside of sessions.
Additionally, the UP is intended to be a flexible pro- tocol, such that, especially when working with more complex or severe patients, it can be complemented by
bringing in other evidence-based strategies. Thus, the therapist can consider weaving in other “off-protocol” content as indicated; for example, problem-solving techniques may be used to address key problems or situ- ations that may be interfering with the patient’s ability to effectively engage in treatment. Regarding patients’ observations that the skills are redundant relative to what they already know, the therapist can validate that although some skills presented in the UP may not be new, the way that the skills are brought together and implemented during real-world practice may lead to different results than what they have noticed previous- ly. Finally, though the guidelines offered here include the typical number of sessions dedicated to each UP module, to address these barriers, the therapist can be flexible in how much time is spent on each module; for example, the exposure-based modules may be delivered over more sessions to provide ample opportunities for successful practice of less emotion-provoking activities before the more challenging tasks.
Another typical problem that may become appar- ent when treating suicidal or self-injuring individuals is the need for more therapeutic content or interven- tions between sessions. As previously indicated, hav- ing a treatment team in place may be necessary for this population, and regular, ongoing risk assessment at in-person sessions is critical to determining whether outpatient therapy remains the appropriate level of care. Given its flexible structure, the UP can also be deliv- ered in more intensive formats—two or more sessions per week, for example. Though the UP does not in- clude out-of-session phone coaching as a key treatment component (unlike DBT), it is not at all inconsistent with the framework for the therapist to offer such in- the-moment coaching on applying the skills. Last, the therapist may consider leveraging recent advances in mobile technologies (e.g., CBT-based smartphone apps) to facilitate outside-of-session skills practice, including reminders for skills practice. Indeed, work is ongoing by our team to develop a smartphone-based just-in- time adaptive intervention (JITAI; Nahum-Shani et al., 2018) that delivers UP-based skills interventions to recently discharged suicidal inpatients when they are needed (National Clinical Trial No NCT03950765; Evan Kleiman, Principal Investigator). Though there are not yet specific UP apps for download, given initial promising work (largely in terms of acceptability) of translating the UP to online formats (e.g., Rondung et al., 2018; Wurm et al., 2017), there is reason to believe that recent advancements in nearly ubiquitous technol-
Self‑Injurious Thoughts and Behaviors 471
ogies (e.g., Internet, smartphones) may be well-suited to bolstering weekly in-person sessions with additional intervention content between sessions.
Factors Associated with Success–Failure
There are a number of clinical predictors of success when using the UP for patients with emotional disor- ders and SITBs. For one, and along the lines of the pre- vious discussion, patients who are motivated to engage in therapy and evidence high compliance with outside- of-session practices are likely to reap the most benefits from this skills-based intervention. Additionally, given the UP’s emphasis on understanding and attending to the experience of emotion, individuals who are more open to discussing (and potentially changing aspects of how they may respond to) internal states may find they are best able to “hit the ground running” with this pro- tocol. Patients who, even after multiple rapport-build- ing sessions, remain closed off to the possibility of tak- ing a curious stance toward their emotional experiences with their therapist may be less ideally suited to the UP (than, for example, more “concrete” protocols such as behavioral activation or problem solving). Another fac- tor associated with UP treatment failure may be a lack of social support or an unwillingness to share aspects of treatment with important people in their lives, given that having family members or friends support the in- dividual with their outside-of-session practice (e.g., re- minders, accountability) or challenging exposure-based exercises can be useful. When treating suicidal or self- injuring individuals, of course, it can also be impor- tant to have the patient’s permission to involve a family member or friend should a crisis emerge. Finally, and as noted earlier, patients who present with multiple emo- tional disorder comorbidities or symptoms—as well as SITBs—may be most likely to find the UP’s transdiag- nostic approach, which permits simultaneously address- ing multiple sets of symptoms or problem behaviors, most appealing, and thus most likely to engage with and experience benefits from the treatment.
CONCLUSION
SITBs are prevalent and clinically serious phenomena for which effective, efficient, and scalable treatment ap- proaches are urgently needed. There are high rates of co-occurrence between SITBs and emotional disorders, as well as striking functional overlap between SITBs
and the maladaptive, avoidant processes that character- ize emotional disorders. In brief, both suicidal thoughts and behaviors and NSSI often serve to provide short- term relief from intense emotional experiences, but over the long term, are likely to maintain or increase nega- tive emotion. The UP is a transdiagnostic, mechanism- based psychological treatment designed to address the underlying processes that cut across the range of emo- tional disorders and, potentially, SITBs. Thus, given the potential advantages of the transdiagnostic UP for dissemination and training, this may be a valuable and applicable therapeutic framework to consider for indi- viduals with emotional disorders and SITBs.
This chapter has provided practice-based guidance on how to simultaneously address SITBs and emotional disorder comorbidities during outpatient treatment with the UP. Though there are promising initial pilot data from small-scale or single-case experimental de- sign studies to date, larger-scale, controlled evaluations of the efficacy and effectiveness for this population are still needed. It may also be fruitful to consider match- ing patients to individual UP module(s) or the optimal ordering of modules most likely to produce the stron- gest and most rapid treatment response, in line with a personalized medicine approach. Given that not all sui- cidal or self-injuring individuals are appropriate for out- patient treatment with the UP, this time-limited inter- vention may be well suited to a potential stepped-care model to care for SITBs, in which individuals with less acute suicidal thoughts and behaviors or NSSI would receive the UP as a first-line intervention, and more chronic or severe self-injuring individuals would be pri- oritized to receive more time-intensive and costly care. The UP may also hold promise in adjunctive (or group- based) format to routine care for patients with SITBs in hospital or community settings. In conclusion, though more research is needed, it is our hope that this chapter has encouraged clinicians who encounter patients with emotional disorders and SITBs in their practice (wheth- er from the initial presentation or see such urges or be- haviors emerge during the course of emotion-focused treatment) to consider how SITBs may be addressed within the transdiagnostic UP framework.
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Wurm, M., Klein Strandberg, E., Lorenz, C., Tillfors, M., Buhrman, M., Holländare, F., et al. (2017). Internet de- livered transdiagnostic treatment with telephone support for pain patients with emotional comorbidity: A replicated single case study. Internet Interventions, 10, 54–64.
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Our goal in this book is to present creative and important psychological treatments with empirical support. This chapter on bipolar disorder by David J. Miklowitz, thoroughly updated for this edition, presents his innovative approach called family-focused treatment (FFT), a treatment with substantial existing evidence for efficacy. Based on years of systematic research on psychological factors con- tributing to the onset and maintenance of bipolar disorder, this sophisticated family therapy approach targets the most important psychosocial factors linked to the disorder and associated with poor out- come (e.g., appropriate psychoeducation, communication enhancement training, and problem-solv- ing skills training). This chapter, and especially the very useful case study, also illustrates an essential link between psychological and pharmacological approaches in the successful treatment of this very severe form of psychopathology. —D. H. B.
b ipolar disorder is one of the oldest and most reli- ably recognized psychiatric disorders. Our think-
ing about this disorder has evolved over the last 100 years, but the original descriptions (Kraepelin, 1921) of “manic–depressive insanity” greatly resemble our current conceptualizations. This chapter begins with a review of basic information about the disorder, its diag- nosis, its longitudinal course, and drug treatment. This information about the illness is interesting in its own right, but it also provides the rationale for using psycho- social treatment as an adjunct to pharmacotherapy. The majority of the chapter describes a focused, time-limit- ed, outpatient psychosocial treatment—family-focused treatment (FFT)—that comprises three interrelated modules: psychoeducation, communication enhance- ment training (CET), and problem-solving skills train- ing (Miklowitz, 2010). It is designed for adult or ado- lescent patients who have had a recent episode of mania or depression.
DIAGNOSIS
DSM‑5 Criteria
The core characteristic of bipolar disorder is extreme affective dysregulation, or mood states that swing from extremely low (depression) to extremely high (mania). Patients in a manic episode have euphoric, elevated mood or irritable mood and behavioral activation, usually indicated by an increase in energy and activ- ity, talking very fast, and sleeping very little or not at all. They may engage in risky sex, drive recklessly, or impulsively spend excessive amounts of money. Mania also affects thinking, as evidenced by “grandiose” or psychotic ideas (e.g., beliefs about one’s special powers, superior intelligence, or artistic ability), extreme dis- tractibility, and the tendency to jump from one idea to another when speaking. The reaction of listeners is one of confusion, disbelief, and often, intimidation. Manic symptoms typically go on for one or more weeks. For
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bipolar Disorder
David J. Miklowitz
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the diagnosis of bipolar I, most diagnostic systems also require that the person show disrupted functioning (e.g., marital problems, arrests, loss of job) or require emergency treatments such as hospitalization. In this chapter, the term bipolar disorder refers either to bipolar I or bipolar II disorder (see below) as defined in the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5; American Psychiatric Asso- ciation, 2013).
A patient in a hypomanic episode shows many of the same symptoms, but the duration is typically shorter (i.e., 4 days or more). Additionally, hypomanic symp- toms do not bring about severe impairment in social or occupational functioning and are not associated with the need for hospitalization or with psychosis. However, the symptoms must reflect a real change in a person’s ordinary behavior—one that is observable by others. The distinction between mania and hypomania, which is really one of degree rather than type of illness, is dif- ficult for clinicians to make reliably. Often the degree to which the behavioral activation affects a patient’s functioning is underestimated by the patient, who can see nothing but good in his/her behavior. A theme of this chapter is the value of including significant others (i.e., parents, spouses/partners, and siblings) in patients’ assessment and treatment.
In previous editions of the DSM, patients could be diagnosed with bipolar I disorder on the basis of a sin- gle “mixed” episode, in which the criteria for a major depressive episode and a manic episode are met near- ly every day for 1 or more weeks. This definition has caused considerable confusion among clinicians, who may ignore the requirement that episodes of both poles be syndromal and use the mixed designation to describe patients with a variety of co-occurring subsyndromal depressive and hypomanic or manic symptoms (Frank, 2011). One large-scale population study found that “mixed hypomania” is particularly common among women with bipolar I or II disorder (Suppes et al., 2005). These considerations have relevance for progno- sis as well as diagnosis. Patients with major depressive disorder (MDD) who have two or more co-occurring manic symptoms have more similarity to patients with bipolar depression than to patients with MDD without manic symptoms on variables such as age at onset, fam- ily history of bipolar disorder, functional impairment, suicide attempts, and risk of long-term conversion to bipolar I disorder (e.g., Sato, Bottlender, Schröter, & Möller, 2003; Fiedorowicz et al., 2011).
In DSM-5, the mixed-episode criteria are a much broader course specifier for manic, depressive, or hypo- manic episodes. The specifier with mixed features is ap- plied when three or more subthreshold symptoms from the opposite pole occur during a mood episode. There are unanswered questions about the treatment implica- tions of this definition, such as whether depression with subthreshold mixed symptoms should be treated with mood stabilizers in conjunction with antidepressants (First, 2010).
DSM-5 proceeds with the diagnosis of bipolar dis- order somewhat differently than earlier DSM systems. First, the diagnostician determines whether the patient satisfies the cross-sectional criteria for a manic episode. If he/she does meet these criteria, the diagnosis of bipo- lar I disorder is applied. If the patient currently meets DSM-5 criteria for a major depressive episode, he/she is diagnosed as having bipolar disorder only if there is a past history of one or more manic, mixed, or hypomanic episodes; otherwise, the diagnosis is likely to be MDD or another mood disorder, such as persistent depressive disorder. If the patient is in remission, there must be evi- dence of prior manic or mixed episodes. One implication of this rather complicated set of diagnostic rules is that a single manic (and in DSM-IV [American Psychiatric As- sociation, 1994], a single mixed) episode, even in the ab- sence of documentable depression, is enough to warrant the bipolar I diagnosis. The key word here is document- able, because patients often underreport their depression histories and reveal them only upon careful questioning.
How Has the Diagnosis of Bipolar Disorder Changed?
Every version of the DSM has brought changes in the way we think about bipolar disorder, and modifications are likely to continue as new editions are published. One consistent area of controversy has been the pro- posal to use separate criteria for child- and adolescent- onset bipolar illness. Manic and hypomanic episodes in children appear to be shorter than those in adults, with more polarity switches and longer subthreshold mixed states (Birmaher et al., 2009). Previously, DSM- IV used the same criteria to diagnose mania in adults and children, despite the clear developmental differ- ences in presentation (Leibenluft, Charney, Towbin, Bhangoo, & Pine, 2003). However, DSM-5 includes a new category, disruptive mood dysregulation disorder, to characterize children with frequent and explosive tem- per outbursts and persistent irritability. Although this
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category may reduce false-positive diagnoses of bipolar disorder in children (Leibenluft, 2011), there are many questions about its predictive validity and utility for treatment recommendations (e.g., Axelson, Birmaher, Findling, et al., 2011). The high rates of comorbidity between disruptive mood dysregulation disorder and oppositional defiant disorder, conduct disorder, and attention-deficit/hyperactivity disorder (ADHD) also raise questions about its distinctiveness as a diagnostic entity (e.g., Bruno et al., 2019).
DSM-5 distinguishes between bipolar I and bipolar II disorders. In the former, patients have fully syndro- mal manic episodes, but in bipolar II, patients must have had at least one major depressive episode and one hypomanic episode. DSM-5 also includes a course de- scriptor, “rapid cycling,” which appears to characterize between 12 and 24% of patients in specialty outpatient clinics (Bauer, Beaulieu, Dunner, Lafer, & Kupka, 2008). Rapid cycling is applied when patients have had four or more discrete major depressive, manic, or hypomanic episodes in a single year. The confusion in applying this course descriptor lies in the fact that it is difficult to tell when one episode has ended and an- other begins: If a patient quickly switches from mania to depression in a 48-hour period (what some refer to as “ultrarapid cycling”), is this truly a new episode or just a different presentation of the same episode (perhaps with mixed features)? Additionally, rapid cycling appears to be a transient state of the disorder and not a lifelong phenomenon (Bauer et al., 2008).
DSM-5 deals with the thorny problem of patients with depression who develop manic or hypomanic epi- sodes that are brought on by antidepressants or other activating drugs. Because of the effects of antidepres- sants on the serotonin, norepinephrine, and dopamine systems, there is the potential for these drugs to induce activation, particularly in a patient who is already bio- logically vulnerable to mood swings and is not taking a mood stabilizing agent (e.g., lithium). If a patient has never had a manic episode but then develops a brief period of hypomanic or manic activation while taking an antidepressant, substance-induced mood disorder is suspected. However, when a patient develops a fully syndromal hypomanic or manic episode while taking an antidepressant, and these symptoms persist beyond what one would expect from the physical effects of an antidepressant, the diagnosis of bipolar disorder is given. Similar diagnostic considerations apply to patients who abuse drugs (e.g., cocaine, amphetamine) that are psy- chotomimetics and can induce manic-like states.
Epidemiology and Differential Diagnosis
Across studies, cultures, and age groups, bipolar I and bipolar II disorders affect at least 2% of the population. The National Comorbidity Survey Replication (NCS- R), an epidemiological study of 9,282 U.S. adults using a lay-administrator structured diagnostic interview, re- ported lifetime prevalence rates of 1.0% for bipolar I disorder, 1.1% for bipolar II disorder, and 2.4% for sub- threshold bipolar illness (unspecified bipolar disorder, previously called bipolar disorder not otherwise speci- fied or cyclothymic disorder) (Merikangas et al., 2007). In the international World Health Organization World Mental Health Survey Initiative, a study of 61,392 adults in 11 countries using a single diagnostic instru- ment, lower lifetime prevalence rates were reported: 0.6% for bipolar I disorder, 0.4% for bipolar II disorder, and 1.4% for subthreshold bipolar disorder (Merikan- gas et al., 2011). In a community sample of adolescents (ages 13–18), 2.5% met lifetime DSM-IV criteria for bipolar I or II disorder, with the prevalence increasing in older adolescents (Merikangas et al., 2012).
The most striking prevalence estimates come from a meta-analysis of 19 studies involving 56,103 youth (ages 7–21) from studies across the world (Van Meter, Moreira, & Youngstrom, 2019). In this analysis, the overall prevalence rate of pediatric bipolar spectrum disorders, including bipolar I and II disorders and subthreshold bipolar disorder, was 3.9%. The pooled estimate for bipolar I was only 0.6%, suggesting that the majority of affected youth have subthreshold forms. Contrary to popular opinion, pediatric bipolar disorder was not more likely to be diagnosed in the United States than in other countries, nor was the prevalence increas- ing over time. There was considerable heterogeneity across studies, however, suggesting the need for agreed- upon and validated diagnostic criteria (Van Meter et al., 2019).
The distinction between bipolar disorder and per- sonality disorders—especially borderline personality disorder—is especially challenging given the presence of affective instability in both categories. In some cases, residual affective symptoms (e.g., irritability, sudden changes in mood) are mistaken for personality pathol- ogy. When patients with bipolar disorder are assessed during a period of clinical remission, approximately 29% meet diagnostic criteria for a personality disorder, and about 13% have borderline personality disorder (George, Miklowitz, Richards, Simoneau, & Taylor, 2003).
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The boundaries between bipolar and unipolar illness are surprisingly difficult to draw. Depressions in bipolar and unipolar disorders may look quite similar, but, on average, bipolar depression has a younger age of onset and more short-term mood variability, and is more dif- ficult to treat than MDD (Cuellar, Johnson, & Win- ters, 2005). In the National Epidemiologic Survey on Alcohol and Related Conditions (N = 13,048), patients with bipolar depression endorsed suicidal ideation and psychomotor disturbance more often than did patients with unipolar depression, and patients with unipolar depression were somewhat more likely to endorse fa- tigue (Weinstock, Strong, Uebelacker, & Miller, 2009). Otherwise, the differences between bipolar and unipo- lar depression are not large. A past history of mania or hypomania (or a family history of mania in a depressed patient who has not had a manic episode) provides more information for the differential diagnosis.
The distinction between bipolar disorder and schizo- phrenia is often a source of disagreement among clini- cians. When a patient who has schizophrenia presents with a psychotic episode, he/she can appear acutely ac- tivated, grandiose in thinking and actions, and elated or depressed. Likewise, a floridly manic patient can be- lieve that people are putting thoughts in his/her head or broadcasting his/her thoughts on the Internet. In conditions once thought to be etiologically distinct, more and more studies are finding a significant degree of genetic overlap between bipolar disorder and schizo- phrenia or other psychotic conditions (Bellivier et al., 2013). A recent genomewide association study found significant overlap in gene variants among patients with schizophrenia and patients with bipolar disorder who had mood-incongruent psychotic features (e.g., delusions or hallucinations that have no clear content related to sadness or elation) (Goes et al., 2012).
DSM-5 makes a distinction between schizoaffec- tive disorder and major mood disorders with psychotic features. In schizoaffective disorder, delusions and hal- lucinations have been present for at least 2 weeks, in the absence of prominent affective symptoms. In major mood disorders, psychotic symptoms occur only during periods of significant mood disturbance. A 20-year fol- low-up of patients with schizophrenia, schizoaffective disorders, and major affective disorders (both bipolar and unipolar) found that frequent or chronic hallucina- tions were a feature of 54% of patients with schizophre- nia but only 20% of patients with schizoaffective dis- orders and 8% of patients with bipolar I disorders (all of whom entered the study with psychotic symptoms).
Moreover, persistent hallucinations were a strong pre- dictor of lack of recovery and poorer work functioning, core features that are more frequent in schizophrenia than in bipolar disorder (Goghari, Harrow, Grossman, & Rosen, 2013).
DSM-5 also describes a subsyndromal or subaffec- tive condition: cyclothymic disorder. Patients with cy- clothymic disorder alternate between periods of hypo- manic symptoms and brief periods of depression that fall short of the criteria for major depressive illness. As soon as the person develops a full manic, mixed, or depressive episode, the diagnosis of bipolar I or II dis- order is given. Again, these distinctions really concern the degree and duration of symptoms rather than their form. In my experience, clinicians are prone to “push” patients with cyclothymia into the bipolar II category, especially if they feel that the patients are not reliable in their historical reporting. Sometimes it is better to observe the mood lability of a patient over time than at- tempt to distinguish cyclothymic disorder and bipolar disorder cross-sectionally.
Comorbidity
Bipolar disorder virtually always co-occurs with other conditions, some of which become the focus of imme- diate treatment. The disorders with which bipolar dis- order is comorbid have the common underpinning of affective dysregulation. When 1-year prevalence rates were considered in the NCS-R adult survey, the highest correlations were observed between mania/hypomania and anxiety disorders (62.9%), followed by behavior disorders (ADHD and oppositional defiant disorder; 44.8%) and substance use disorders (36.8%) (Merikan- gas et al., 2007).
The comorbidity of bipolar disorder and ADHD in children is between 60 and 90%, even when overlap- ping symptoms (e.g., irritability, poor concentration, distractibility, motor hyperactivity, and rapid speech) are not considered (Kim & Miklowitz, 2002). The symptoms that best distinguish bipolar disorder from ADHD are elated mood, grandiosity, flight of ideas or racing thoughts, decreased need for sleep, hypersexual- ity, and psychotic symptoms (Geller et al., 2002).
Risk for substance use disorders is five times greater in adolescents with bipolar disorder than in healthy ad- olescents (Wilens et al., 2004). Comorbidity with anxi- ety disorders in children is approximately 44% (Masi et al., 2012; Sala et al., 2010). Interestingly, about 40% of offspring of parents with bipolar disorder have anxi-
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ety disorders (Axelson et al., 2015), suggesting that sig- nificant anxiety may be a prodromal feature of bipolar disorder in young patients (Duffy, Goodday, Keown- Stoneman, & Grof, 2018; Hafeman et al., 2016; Faedda et al., 2019).
Comorbid disorders are associated with a worse course of illness in both adults and children, underlin- ing the importance of recognizing them at the outset of treatment. However, many clinicians “double-count” overlapping symptoms, such that, for example, a child with irritability and motor hyperactivity is classified as having symptoms of two disorders. Overlapping symp- toms that occur only during manic or depressive epi- sodes—for example, motor hyperactivity—should not be used to indicate a comorbid disorder. Conversely, overlapping symptoms that persist even when the pa- tient is in remission from bipolar disorder is stronger ev- idence for a comorbid disorder (Goldstein et al., 2017).
DRUG TREATMENT AND COURSE
Standard Pharmacotherapy
The course of bipolar illness (its pattern of relapsing and remitting over time) is best considered with refer- ence to the drug treatments that help stabilize patients and allow most to function in the community. In the prepharmacological era (i.e., prior to 1960), patients were hospitalized for years at a time (Cutler & Post, 1982). Nowadays, the availability of mood stabilizers such as lithium carbonate, anticonvulsants (e.g., val- proate [Depakote], lamotrigine [Lamictal], carbam- azepine [Tegretol], and other agents), and atypical or “second-generation” antipsychotics (e.g., olanzapine [Zyprexa], quetiapine [Seroquel], risperidone [Risp- erdal], ziprasidone [Geodon], aripiprazole [Abilify], asenapine [Saphris, Sycrest], lurasidone [Latuda], and cariprazine [Vraylar]) has done much to ameliorate the course of bipolar illness (Goldstein et al., 2017; Yatham et al., 2018). Some of these drugs not only control the acute episodes of the illness but also have “prophylactic value,” which means that they help prevent future epi- sodes or minimize the duration or severity of episodes that do occur.
Most psychiatrists describe three phases of drug treatment: an “acute phase,” in which the goal is to con- trol the most severe symptoms of the manic, mixed, or depressive disorder; a “stabilization phase,” in which the goal is to help the patient recover fully from the acute phase, which often means treating residual symptoms
(e.g., mild depression) or levels of social–occupational impairment; and a “maintenance phase,” in which the goal is to prevent recurrences and continue to treat re- sidual symptoms. The drugs recommended for bipolar disorder vary according to the phase of treatment. Dur- ing the acute and stabilization phases, an antipsychotic medication may accompany a mood stabilizer. An anti- depressant may be recommended after a manic episode has stabilized if a patient has ongoing, residual depres- sion symptoms. These phases of treatment are also rel- evant to the psychosocial–psychotherapeutic treatment of bipolar disorder, which I discuss later.
Symptomatic Outcome
If drug treatment is so effective, then why do we need psychosocial treatment? The problem that consistent- ly arises in the drug treatment of bipolar disorder is “breakthrough episodes.” With lithium or anticonvul- sant treatment, the rate of relapse averages between 37 and 49% over 1 year and about 60% in 2 years (Gig- nac, McGirr, Lam, & Yatham, 2015). In 1,469 adults with bipolar I and II disorders, 49% had recurrences over 1 year; twice as many of these recurrences were of depressive (rather than manic or hypomanic) episodes. In a 12.8-year follow-up of 146 adult patients with bi- polar I disorder, patients had syndromal or subsyndro- mal depressive symptoms for about 32% of the weeks of their lives, manic or hypomanic symptoms for 9%, and mixed or cycling symptoms states for 6%; patients were in remission only about half of the time (Judd et al., 2002).
Of patients who have a manic or mixed episode, only 35% fully recover in 1 year, and only 25% regain their prior level of social and occupational functioning (Gignac et al., 2015). Rates of recovery and recurrence in adolescents are similar to those of adults (DelBello, Hanseman, Adler, Fleck, & Strakowski, 2007). Predic- tors of poor outcome included lower socioeconomic status, nonadherence with medication regimens, and longer duration of illness.
Social–Occupational Functioning
Patients with bipolar disorder experience significant impairment in work, social, and family functioning, and their chances of early illness recurrence increase dramatically when they have subsyndromal depressive symptoms (Gitlin & Miklowitz, 2017). Additionally, patients with persisting depressive symptoms often have
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cognitive impairment, which strongly affects their so- cial and occupational functioning (Altshuler, Bearden, Green, van Gorp, & Mintz, 2008). A study of 253 bi- polar I and II patients revealed that only about 33% of the patients worked full time, and only 9% worked part time outside of the home; 57% of patients reported being unable to work or able to work only in protected settings (Suppes et al., 2001). Poor social and occupa- tional functioning predicts a shorter time to the next mood disorder relapse (e.g., Weinstock & Miller, 2008).
Medication Nonadherence
Nonadherence is one of the major reasons that patients with bipolar disorder have so many breakthrough epi- sodes. In one review, Colom, Vieta, Tacchi, Sanchez- Moreno, and Scott (2005) estimated that at least 60% of patients with bipolar disorder discontinue their med- ications at some point in their lives. Rates of adherence with anticonvulsants and second-generation antipsy- chotics appear to be higher than with lithium (Perlis et al., 2010). Nonadherence has considerable implications for the course of the disorder: When patients stop their medications suddenly, they are at much higher risk for relapse or suicide (Baldessarini, Tondo, & Hennen, 2003).
The reasons that patients stop taking mood stabiliz- ers are varied, and include side effects, lack of insight into the illness, younger age, lower socioeconomic sta- tus, lack of information about medications, missing high periods or negative feelings about having one’s moods controlled, recent hospitalizations, and low family support (Colom, Vieta, Tacchi, et al., 2005). Notably, negative patient attitudes about taking mood- stabilizing medications are most highly correlated with family attitudes, the working alliance between physi- cian and patient, levels of social support, and the pa- tient’s knowledge of bipolar disorder (Chakrabarti, 2019). Some of these issues are amenable to modifi- cation through adjusting dosages or substituting one agent for another. Other problems related to nonadher- ence can be addressed in adjunctive psychotherapy.
Why Psychotherapy?
What is the role of psychosocial treatment in a disorder with such a heavy biological and genetic basis? There is little doubt that medication is the first-line treatment for bipolar disorder. The evidence that lithium, the an- ticonvulsants, and the second-generation antipsychot-
ics reduce relapse rates and improve functioning is sub- stantial. But can we do better? An optimal and perhaps overly optimistic view of the outcome of patients with bipolar disorder would include symptom stability for extended periods, minimal disruptions in social func- tioning after episodes, and having satisfying work and family lives. Indeed, these outcomes are highly valued by patients, who often devise their own self-manage- ment strategies to cope with the illness (Murray et al., 2011).
The roles of adjunctive psychotherapy can include teaching skills for symptom management; helping pa- tients navigate the social, familial and occupational environments; and encouraging adherence to drug regimens. Implicit in these objectives is that the physi- ology and psychology of bipolar disorder are not fully separable. We have long known that changes in neural function (as revealed in positron emission tomogra- phy [PET] or functional magnetic resonance imagery [fMRI] scans) can occur among patients who respond to psychotherapy (e.g., Kumari et al., 2011). For bipo- lar disorder, psychotherapy and medication can work synergistically in hastening mood stabilization and pre- venting recurrences.
The strongest argument for including psychotherapy in an outpatient treatment program is to help patients cope with stress triggers. As noted in the next section, certain forms of life events and family conflicts are risk factors in the course of bipolar disorder. Psychotherapy can target these factors and teach patients adaptive cop- ing mechanisms, which can then be brought to bear during periods of wellness to help stave off the likeli- hood of a recurrence.
A VULNERABILITY–STRESS MODEL OF RECURRENCES
Implicit in the notion that psychotherapy would be helpful to a patient with bipolar disorder is the notion that stress plays a role in eliciting symptoms of mood disorder. What is the evidence for this view? What are the targets for psychosocial intervention?
Life Events and Social Rhythms
Life events are consistently associated with relapses of bipolar depression, and in some studies, of mania as well (Aldinger & Schulze, 2017). Two major path- ways have been proposed for the association of life
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events and mood relapses. The first of these, the social rhythm stability hypothesis (Ehlers, Kupfer, Frank, & Monk, 1993), posits that major life events disrupt daily rhythms (i.e., when one wakes, eats, exercises, social- izes, works, and sleeps) in mood disorders. Life events can act as zeitstorers, which disrupt established social and circadian rhythms (e.g., the production of neuroen- docrines as a function of the time of day). For example, a previously unemployed patient who gets a job with constantly shifting work hours is forced to adopt a new pattern of daily routines, which may include changes in sleep–wake habits. Major events can also result in the loss of social zeitgebers—people or events that help maintain the stability of rhythms. For example, a spouse or partner helps to maintain a person on predictable sleep schedules. A divorce or separation, in addition to being a significant emotional event, results in the loss of this human timekeeper.
Patients with bipolar disorder are exquisitely sensi- tive to even minor changes in sleep–wake habits. Manic episodes are often precipitated by life events that change sleep–wake habits (e.g., changing time zones due to air travel; Levenson, Wallace, Anderson, Kupfer, & Frank, 2015; Malkoff-Schwartz and colleagues, 1998, 2000). The association between depressive episodes and rhythm-disruptive life events is less certain. One of the clinical implications of these findings is that if pa- tients can be taught to regularize their social rhythms, especially when facing life events that normally would disrupt those rhythms, the outcome of bipolar disor- der should be improved. Variability in the sleep–wake cycle is a key target for interpersonal and social rhythm therapy (IPSRT; Frank, 2005), as discussed below.
Goal Dysregulation and Mania
Across more than 12 studies, people with a history of mania and students who are vulnerable to mania have described themselves as more likely to react with strong emotions to reward (Johnson, Edge, Holmes, & Carver, 2012). Self-reported reward sensitivity has been found to predict a more severe course of mania among those with bipolar I disorder (Meyer, Johnson, & Winters, 2001; Salavert et al., 2007), and of conversion from bipolar spectrum disorder to bipolar I or II disorder in high-risk college students (Alloy et al., 2012). A related construct, heightened ambition, is associated with a more severe course of mania among patients with bipolar I disorder (Johnson et al., 2012). Impulsive responding, in which
people pursue rewards during positive affective states without awareness of potential negative consequences, becomes elevated during the escalation to mania (John- son, Carver, Mulé, & Joormann, 2013; Swann, Dough- erty, Pazzaglia, Pham, & Moeller, 2004).
Johnson and colleagues (2000) hypothesize that ex- cess reward sensitivity may heighten reactivity to suc- cesses, such that manic symptoms are more likely after life events involving goal attainment (e.g., getting a pro- motion). Goal attainment may increase confidence and impulsive responding, which then fuels increased goal engagement and accelerates the development of manic symptoms (Johnson et al., 2013). In two longitudinal studies of patients with bipolar I disorder, goal-attain- ment life events predicted increases in manic symptoms but not depressive symptoms (Johnson et al., 2000, 2008).
Family Stress
Family conflicts are also a breeding ground for recur- rences of bipolar disorder. One method of measuring family stress is to evaluate a family’s level of “expressed emotion” (EE). In this procedure, a researcher admin- isters the Camberwell Family Interview (Vaughn & Leff, 1976) to a family member (parent, spouse/partner, or sibling) for approximately 1 hour to assess the rela- tive’s reactions to the patient’s psychiatric disorder, with particular emphasis on a recent illness episode. Later, a trained judge evaluates tapes of these interviews on three primary dimensions: critical comments (e.g., “When I talk to him, I get upset that he just shuts down. It’s like there’s no one there!”); hostility, or personal, general- ized criticism of the patient (e.g., “I like nothing about him”); and emotional overinvolvement, or the tendency to be overconcerned, overprotective, or to use inordi- nately self-sacrificing behaviors in the patient’s care (e.g., “I don’t invite people to the house, because Allen [son] doesn’t like it”). Family members who score high on one or more of these dimensions are called “high- EE”; those who do not are called “low-EE.”
EE is a well-established predictor of the course of schizophrenia: Patients who are discharged from hospi- tal to the care of high-EE families are two to three times more likely to relapse in the next 9 months than those discharged to low-EE, less critical or overinvolved fami- lies (Hooley, 2007). Several studies have documented a similar link between high-EE attitudes in family mem- bers and relapse among patients with bipolar disorder
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(e.g., Miklowitz, Goldstein, Nuechterlein, Snyder, & Mintz, 1988; Miklowitz, Biuckians, & Richards, 2006; Yan, Hammen, Cohen, Daley, & Henry, 2004).
On first examination, one might conclude that pa- tients with bipolar disorder are sensitive to stress in the family milieu, and that levels of EE elicit an underly- ing biological vulnerability. But the relationship is far from simple. First, it appears that the high-EE rela- tives of patients with bipolar illness, unipolar illness, or schizophrenia are more likely than low-EE relatives to interpret the patients’ negative problem behaviors as controllable by the patients (e.g., Hooley & Licht, 1997; Wendel, Miklowitz, Richards, & George, 2000; Domínguez-Martínez, Medina-Pradas, Kwapil, & Barrantes-Vidal, 2017). Second, relatives and patients coping with bipolar disorder are often locked into ver- bally aggressive, negative cycles of face-to-face interac- tion. Simoneau, Miklowitz, and Saleem (1998) found that high-EE relatives of patients with bipolar disorder were more negative than low-EE relatives during face- to-face problem-solving interactions. The relatives and patients in high-EE families were also more likely to engage in counterproductive “attack–counterattack” cycles. Often the patients were provocateurs in these interchanges; they were not the “victims” of verbally aggressive or punitive relatives (Miklowitz, Wendel, & Simoneau, 1998).
Clearly, a psychosocial treatment program should consider aspects of the family’s affective environment— such as high-EE attitudes in relatives or the negative interchanges that characterize relative–patient com- munication—to be targets for intervention. But does one attempt to change these attitudes and interaction patterns directly, or instead make an “end run” around them? Family members coping with a spouse/partner, offspring, or sibling who has bipolar disorder are un- derstandably quite angry, and it makes little sense to tell them they should not be. Others feel that their overprotective behavior is more than warranted by the situation.
In developing FFT, my associates and I concluded that at least one component of dealing with these at- titudes and transaction patterns is psychoeducation, which involves the provision of information to patients and family members about the disorder and its manifes- tations. As discussed earlier, relatives (parents, spouses, or siblings) need to realize that at least some proportion of the patient’s aversive behaviors (e.g., irritability, ag- gression, inability to work, or low productivity) can be
attributed to a biologically driven illness state. This may seem obvious to us as clinicians, but to family members who deal with the patient on a day-to-day basis, it is easy to attribute aversive behaviors to personality fac- tors or laziness, or to believe that “he/she is doing this to hurt me.” In parallel, patients need to become more cognizant of the way they provoke anger and resent- ment in family members.
Negative face-to-face interactions cannot be eradi- cated, but they can be made more productive through the techniques of communication and problem-solving skills training. Thus, families or couples can be taught to stick with one problem topic rather than trying to solve many at a time, or to use listening skills to avoid counterproductive attack–counterattack cycles. Later in this chapter, I explain these methods with reference to a difficult treatment case.
PSYCHOSOCIAL TREATMENT STUDIES
This section describes several randomized controlled trials (RCTs) of individual and family/marital inter- ventions. More thorough reviews of the studies in this area are available (Geddes & Miklowitz, 2013; Salcedo et al., 2016), as is a network meta-analysis (Miklowitz, Efthimiou, et al., 2021).
Individual Therapy
Two models of individual therapy deserve empha- sis here. Cognitive-behavioral therapy (CBT) models focus on risk factors for relapse, including medication nonadherence, excessive risk taking (or reward overesti- mation) prior to mania, and behavioral inactivity dur- ing depression. Lam, Hayward, Watkins, Wright, and Sham (2005; Lam et al., 2003) examined a 6-month, 12- to 18-session CBT model with drug treatment ver- sus drug treatment alone (N = 103). Patients had been in remission for at least 6 months but had had at least three episodes in the past 5 years. At a 1-year follow-up, 44% of patients in CBT had relapsed compared with 75% of the patients who received drug treatment alone. Twelve to 30 months after treatment, CBT did not pre- vent relapse relative to drug treatment alone, but it did continue to show a positive influence on mood and days spent in episodes.
A multicenter effectiveness trial of CBT in the Unit- ed Kingdom (N = 253) indicated that not all subpopu-
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lations of patients with bipolar disorder are equally like- ly to benefit from CBT (Scott et al., 2006). The study compared 22 sessions of CBT plus pharmacotherapy to treatment as usual (TAU) plus pharmacotherapy. The patients had been in a variety of symptomatic states before study entry. No effects were found for CBT on time to recurrence. A post hoc analysis revealed that patients with less than 12 prior episodes had fewer re- currences in CBT than in TAU, whereas the reverse was true in patients with 12 or more episodes. The au- thors concluded that CBT is most applicable to patients in the early stages of their disorder or in those whose course is less recurrent.
Ellen Frank and colleagues (2005) investigated the efficacy of IPSRT—a treatment that includes the core elements of Klerman, Weissman, Rounsaville, and Chevron’s (1984) model of interpersonal psychothera- py for depression and a bipolar-specific component in which patients self-regulate their daily routines and sleep–wake cycles. Patients with a recent mood episode were randomly assigned to either 45-minute IPSRT sessions and mood-stabilizing medications or an active clinical management intervention, also with medica- tions. Randomization was done twice: first during an acute phase of treatment, with sessions held weekly, and again at the beginning of a maintenance phase, with sessions held biweekly or monthly for up to 2 years. Pa- tients who received IPSRT in the acute phase had longer intervals prior to recurrences in the maintenance phase than patients who received clinical management in the acute phase. IPSRT was more effective in delaying re- currences in the maintenance phase among patients who succeeded in stabilizing their daily routines and sleep–wake cycles during the acute phase (Frank et al., 2005). IPSRT also had a positive impact on vocational functioning (Frank et al., 2008). Thus, consistency of routines may protect against a worsening course of the disorder and enhance functioning.
Group Psychoeducation
The effects of group psychoeducation have been docu- mented in several large-scale RCTs, including one at a Veterans Administration outpatient clinic (Bauer et al., 2006) and another at a health maintenance organiza- tion (Simon, Ludman, Bauer, Unutzer, & Operskalski, 2006). In both studies, psychoeducation groups were embedded in larger systems of care, including patient monitoring by a nurse care manager and monitoring of the physician’s adherence to pharmacotherapy guide-
lines. These systematic care models were shown to be highly effective in improving illness course and func- tioning compared to usual care for bipolar patients in these settings.
An RCT focused on the combination of pharmaco- therapy and group psychoeducation was undertaken at the University of Barcelona (Colom et al., 2003; Colom, Vieta, Sanchez-Moreno, et al., 2005). A total of 120 re- mitted patients with bipolar disorder who were receiv- ing pharmacological treatment were allocated to (1) 21 sessions of structured group psychoeducation or (2) 21 sessions of an unstructured support group, both ad- ministered by psychologists. Over 2 years, individuals who received group psychoeducation were significantly more likely than those allocated to the unstructured group to show lower relapse and hospitalization rates and higher, more stable plasma lithium levels (Colom et al., 2003; Colom, Vieta, Sanchez-Moreno, et al., 2005). Moreover, a 5.5-year follow-up of this sample revealed that the gains associated with group psychoeducation were sustained and resulted in much lower treatment and illness-related costs (Colom et al., 2009).
In another large-scale trial by the Barcelona group, 293 adults with remitted bipolar I and II were randomly assigned to functional remediation (FR), which com- prised 21 weekly individual and group sessions provid- ing psychoeducation, interpersonal skills, and cognitive skills training (attention, memory, executive function- ing), or to structured group psychoeducation or TAU. Patients with bipolar disorder who received FR showed greater improvements in social and occupational func- tioning than those in TAU, but there were no differ- ences between FR and structured psychoeducation groups (Torrent et al., 2013). At a 1-year follow-up, however, functional improvements persisted only for the FR group (Bonnín et al., 2016). In summary, group psychoeducation appears to be an effective adjunct to pharmacotherapy for adult patients with bipolar disor- der who begin while in remission.
Family Therapy
There are now several studies of family interventions as adjuncts to medication for patients with bipolar dis- order. Here, I focus on trials published after 2000; the reader is referred to more comprehensive reviews (Mik- lowitz & Chung, 2016; Salcedo et al., 2016) for cover- age of earlier family and marital studies.
Four randomized trials have been completed on FFT in adult bipolar samples. Two of these were conducted
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with adults recruited from hospital settings following an acute episode, one at the University of California, Los Angeles (UCLA; Rea et al., 2003) and one at the University of Colorado (Miklowitz, George, Richards, Simoneau, & Suddath, 2003). One trial was conducted in the context of the Systematic Treatment Enhance- ment Program for Bipolar Disorder (STEP-BD; Mik- lowitz et al., 2007a, 2007b), which examined three intensive psychotherapies (FFT, IPSRT or CBT) in comparison with a control condition for patients with bipolar depression. A fourth trial compared FFT for parents of adult patients with bipolar disorder (without patients present) to a standardized health care interven- tion for parents (Perlick et al., 2018). These studies are examined in detail below.
The UCLA and Colorado Studies
These studies each examined a 9-month, 21-session FFT intervention that comprised psychoeducation, CET, and problem-solving training. Participants were patients and their parents or spouses. Patients were re- cruited during an index episode of bipolar disorder and maintained on mood-stabilizing medications, with or without antipsychotic or antidepressive agents. How- ever, the studies differed in an important respect: At Colorado, the comparison “crisis management” group received two sessions of family education and indi- vidual crisis sessions, as needed, over 9 months. In the UCLA study, patients in the comparison group received an individual case management and problem-solving intervention that was of similar intensity (21 sessions) to the FFT intervention.
Despite these design differences, the results that emerged from the Colorado and UCLA studies were quite similar. In the Colorado study (Miklowitz et al., 2003), FFT and medication led to lower frequencies of relapses and longer delays prior to relapses over a 2-year period than did crisis management and medica- tion. FFT was also associated with more reductions in depression and mania symptoms. In the UCLA study (Rea et al., 2003), FFT was associated with delays in time to relapse and hospitalization over 2 years. Rates of rehospitalization in the 1- to 2-year period follow- ing the 9-month treatment were 12% in the FFT group and 60% in the individual therapy group; for relapse, the rates were 28% and 60%, respectively. Results of both trials found that the majority of the effects of FFT were in the posttreatment period, with symptoms wors- ening in the comparison groups after 9 months to 1
year. Thus, patients and family members may need to “absorb” the treatment and incorporate the education and skills training into their day-to-day lives before it has ameliorative effects on the illness.
This latter point was clarified further by Simoneau, Miklowitz, Richards, Saleem, and George (1999), who examined family interaction transcripts obtained in the Colorado study before and after FFT or crisis manage- ment treatment. Families (patients with their parents or spouses) participated in interactional assessments that comprised 10-minute problem-solving discussions that were transcribed and coded for negative and positive interactional behaviors. Forty-four families returned at 1 year for the same assessment, after the FFT or crisis management protocol had been completed. Interest- ingly, at the posttreatment (1 year) interactional assess- ments, patients in FFT and those in crisis management could not be distinguished on the basis of frequency of negative interactional behaviors (e.g., criticisms). But there were clear differences at posttreatment in positive interactional behaviors, particularly in the nonverbal sphere. After FFT, patients and relatives were more likely to smile at each other, nod when others were speaking, and lean toward each other when speaking. Moreover, the degree to which patients improved in their nonverbal interactional behavior over the course of psychosocial treatment was correlated with their de- gree of symptom improvement over the year of treat- ment. FFT studies using multiple, time-lagged assess- ments of family interaction and patients’ symptoms would help to disentangle the directional relationship between improvements in family communication and improvements in patients’ outcomes.
FFT for Relatives of Adults with Bipolar Disorder
As many as 90% of caregivers for people with bipolar disorder report moderate to high levels of “burden” from their roles, resulting in sleep disturbance, chron- ic medical conditions, and depression (Perlick et al., 2016). Thus, caregivers are often in need of supportive and psychoeducational interventions as well. In a small RCT, parents and other caregivers of 46 patients with bipolar disorder were randomly assigned to 8–12 ses- sions of standard health education or 12–15 sessions of a caregiver-only version of FFT. Patients received phar- macotherapy during the same interval but did not at- tend the treatments sessions. Over a 6-month period, depressive symptoms decreased in caregivers and pa- tients. Additionally, treatment-associated reductions in
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depressive symptoms among patients with bipolar dis- order were mediated by reductions in depressive symp- toms among caregivers (Perlick et al., 2018).
In another Barcelona trial, caregivers given group psychoeducation while their patient–relative was re- ceiving pharmacotherapy and support in an outpa- tient service reported increased knowledge of how to manage bipolar disorder, decreased burden, and fewer attributions of blame toward the patients com- pared to untreated caregivers whose bipolar relative were treated with pharmacotherapy and support only. Interestingly, the patients whose caregivers received group psychoeducation had lower rates of recurrence and longer well intervals over 18 months compared to patients whose caregivers received no treatment (Rein- ares et al., 2008). Hence, patients and their caregivers both benefit from the increased understanding of and ability to cope with bipolar disorder obtained from psychoeducation.
The STEP‑BD Study
STEP-BD examined the effectiveness of treatment with mood stabilizers in combination with three different types of psychosocial treatment in 15 participating sites in the United States (Miklowitz et al., 2007b). Patients with bipolar disorder in a depressive episode (N = 293) were randomly assigned to mood-stabilizing medica- tions—with or without antidepressants—and 30 ses- sions of FFT, IPSRT, CBT, or collaborative care (CC), a three-session psychoeducational treatment. Patients assigned to any intensive psychotherapy had higher re- covery rates over 1 year and were more likely to remain stable than patients in CC. In FFT, 77% of the patients recovered by 1 year; in interpersonal therapy, 65%; and in CBT, 60%. In the CC condition, 52% recovered. Furthermore, patients in the intensive therapies had greater gains in psychosocial functioning than those in the control condition (Miklowitz et al., 2007a). The differences between the intensive modalities did not reach statistical significance.
STEP-BD, one of the largest randomized treatment studies for bipolar disorder, suggests that psychother- apy is an essential component of the effort to stabilize patients with bipolar disorder in a depressive episode. When clinicians are treating bipolar, depressed patients with mood stabilizers or atypical antipsychotics, adding an intensive therapy may be associated with more rapid recovery than adding an antidepressant (Miklowitz et al., 2007b). The common ingredients of intensive treat-
ments—such as teaching strategies to manage mood, identifying and intervening early with prodromal symptoms, enhancing patients’ compliance with medi- cations, and working toward resolution of key inter- personal or family problems—may contribute to more rapid recoveries. FFT proved to be a particularly potent treatment in this study, although its limitations also be- came apparent: Only 54% of the patients assessed for the study had families who were accessible and willing to participate in treatment.
Family Psychoeducation and Skills Training in Early‑Onset Bipolar Disorder
More recent applications of family psychoeducation have focused on patients with juvenile-onset bipolar disorder, who most frequently live with their families of origin. FFT for adolescents with bipolar disorder (FFT-A; Miklowitz et al., 2004) uses the same 21-ses- sion structure, adapted to the developmental needs of this age group (e.g., the occurrence of more frequent and briefer episodes, typically with a mixed presenta- tion). A 2-year RCT of 58 adolescent patients with bipolar disorder revealed that compared to patients who received three sessions of family psychoeducation (enhanced care [EC]) and pharmacotherapy, patients in FFT-A and pharmacotherapy recovered more rap- idly from their baseline depressive symptoms, spent less time depressed at follow-up, and had greater improve- ments in depressive symptoms over a 2-year follow-up (Miklowitz et al., 2008). Degree of improvement was greatest in adolescents from high-EE families who re- ceived FFT-A; the effects of FFT-A in adolescents from low-EE families were not as robust (Miklowitz et al., 2009).
A replication and extension of this study in three sites and a larger sample (N = 145) was less conclusive. In this study, all patients received guideline-adherent pharmacotherapy from expert study-affiliated psychia- trists rather than from community practitioners. Fol- lowing an acute mood episode, adolescents in FFT-A and EC had equivalent rates of recovery and recurrence as those who received three sessions of EC (Miklowitz et al., 2014). Secondary analyses revealed that patients in FFT-A showed greater improvements in manic and hypomanic symptoms in the second year of the study, whereas those in EC tended to worsen during the sec- ond year. Additionally, patients in FFT-A showed great- er improvements in quality of life over 2 years than did those in EC (O’Donnell et al., 2017).
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FFT was extended to children and adolescents at high risk for developing bipolar disorder. High-risk youth are defined as those with (1) a first- or second-degree rela- tive (usually a parent or grandparent) with bipolar I or II disorder and (2) significant mood dysregulation and impairment in the form of a major depressive episode or a diagnosis of bipolar disorder not otherwise specified. Children with bipolar disorder not otherwise specified have brief (1–3 day) periods of mania or hypomania that are impairing and represent a change from base- line. Follow-ups of children with mood instability, sub- threshold mania/hypomania, depression, and a positive family history of mania have found that more than half convert to bipolar I or II disorder within 8 years (Axelson, Birmaher, Strober, et al., 2011; Birmaher et al., 2018).
In a 1-year RCT, 40 high-risk children (ages 9–17) with MDD or bipolar disorder not otherwise specified were randomly assigned to a high-risk version of FFT (FFT-HR) or to a one- to two-session education control (Miklowitz et al., 2013). The FFT-HR was given in 12 sessions over 4 months. The participants in FFT-HR had more rapid recovery from their initial mood symp- toms, more weeks in remission, and more improvement in hypomania symptoms over 1 year than did partici- pants in the education control. As was found in the ado- lescent sample, the magnitude of the treatment effect was greater among high-risk children in high-EE (vs. low-EE) families.
A second trial examined 127 high-risk children with MDD or bipolar disorder not otherwise specified, who were randomly allocated to FFT-HR (12 sessions in 4 months) or a more intensive EC comparison, compris- ing six sessions of individual and family psychoeduca- tion in 4 months. Over a 1- to 4-year follow-up (av- erage 2 years), youth in FFT-HR had longer intervals of wellness prior to prospectively observed depressive episodes than those in EC. The treatment did not af- fect the onset of manic or hypomanic episodes (Mik- lowitz, Efthimiou, et al., 2021; Miklowitz, Schneck, et al., 2020).
Other models of family intervention for pediatric bipolar disorder have also shown efficacy. In a large (N = 165) wait-list trial, Fristad Verducci, Walters, and Young (2009) found that children with mood disor- ders who were assigned to multifamily groups showed greater mood improvement over 6 study months than children on a wait list. Children on the wait list who participated in multifamily groups 1 year later showed the same amount of improvement between 12 and 18
months as those who had received the groups imme- diately after study entry. A family-focused CBT devel- oped for school-age children (ages 7–14) with bipolar disorder incorporates individual and family sessions of psychoeducation, cognitive restructuring, and affect regulation interventions (West et al., 2014). In an RCT involving 69 youth with bipolar spectrum disorders, youth who received this 18-session treatment showed greater improvements in parent-reported mania and depression scores, and higher global functioning at 6-month follow-up than youth who received individual supportive therapy (West et al., 2014).
Summary
The addition of psychosocial treatment—family, group, or individual—to pharmacotherapy leads to more posi- tive outcomes of bipolar disorder than can be achieved with pharmacotherapy alone. In drawing conclusions, we must keep in mind the different clinical conditions of patients at the outset of treatment. For example, most of the studies of CBT and group psychoeducation fo- cused on patients in remission, whereas those of family intervention and IPSRT focused on patients who were still symptomatic following an acute episode.
The remainder of this chapter is devoted to the spe- cifics of delivering FFT to adult and adolescent pa- tients. For whom is it intended? How does it proceed? How are families educated about bipolar disorder, and how do they learn new styles of communicating or solv- ing problems? In reviewing these methods, the reader may wish to reflect on the various targets of family intervention (i.e., family attitudes or expectations, in- terpersonal conflict, medication nonadherence) and the various domains of outcome that are presumed to be influenced by family interventions via their impact on these targets.
CONTEXT OF FFT
Treatment Objectives and Structure
FFT has six objectives, all of which concern coping with an episode of bipolar disorder. These are summa- rized in Table 12.1. Some of these pertain to dealing with the current episode; others focus more on antici- pating episodes in the future, and the stress triggers for these episodes. A strong case is made for the protective effects of medications and a stable, nonstressful family environment.
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For patients with fully syndromal bipolar I or II, FFT is usually given in 21 outpatient sessions lasting 1 hour each. Sessions are given weekly for 3 months, biweekly for 3 months, and monthly for 3 months. Although the 21-session version is described here, a 12-session version is used for high-risk populations. These youth are usually less in need of the intensive psychoeduca- tion concerning management of mania and depression symptoms given when patients have syndromal bipolar disorder.
The session plan (Table 12.2) is a guide for clinicians rather than a requirement, because some families re- quire less intensive contact at the beginning, others re- quire more intensive contact later, and still others sim- ply do not need this much treatment. The treatment is designed to parallel stages of recovery from a mood epi- sode. During the stabilization phase, about seven ses- sions are devoted to psychoeducation, in which patients and their relatives become acquainted with the nature, course, and treatment of bipolar disorder. At this stage, patients are often still symptomatic and usually func- tionally impaired compared to their pre-illness state. Psychoeducation is an attempt to hasten clinical stabili- zation by reducing family tensions, encouraging medi- cation adherence, and teaching illness management skills. This is done through helping a patient and his/ her family members make sense of the different events that precipitated the acute episode, come to a common understanding of the causes and the treatment of the illness, develop plans for how the family members will
act if there are signs of a developing recurrence, and modulate expectations for the patient’s and the family’s functioning in the recovery period.
When the family commences communication train- ing (seven to 10 sessions), the patient is usually able to tolerate exercises oriented toward resolving family con- flict and promoting behavior change. For example, he/ she can practice listening while another family member speaks, and family members can do the same for him/
TABLE 12.1. The Six Objectives of Family‑Focused Treatment
Assist the patient and relatives in the following:
• Integrating the experiences associated with recent episodes of bipolar disorder
• Identifying prodromal signs of recurrences and developing familywide prevention plans
• Accepting the need for mood-stabilizing medications for symptom stabilization
• Distinguishing between the patient’s personality or developmentally normative behaviors and bipolar symptoms
• Recognizing and learning to cope with stressors that trigger recurrences of mania or depression
• Reestablishing functional family relationships after a mood episode
TABLE 12.2. Structure and Topical Outline of FFT
1. Psychoeducation (7 sessions) The symptoms and course of bipolar disorder • The signs and symptoms of (hypo)mania and depression • The development of the most recent mood episode • The role of life stress in most recent episode • The course of the disorder over time
The etiology of bipolar disorder • The vulnerability–stress model
| The role of environment | Genetic and biological predispositions
• Risk and protective factors in the course of the disorder
Interventions and self-management • Keeping a mood chart • Types of medications • Types of psychosocial treatments • How the family can help • Self-management of the disorder • The relapse prevention drill
2. Communication enhancement training (7–10 sessions) • Expressing positive feelings • Active listening • Making positive requests for change • Communication clarity • Expressing negative feelings
3. Problem-solving skills training (4–5 sessions) • Define problems • Generate solutions • Evaluate advantages–disadvantages • Choose one or a combination of solutions • Develop an implementation plan • Review the problem’s status
4. Termination
Note. Session numbers are meant as guidelines only. The clinician may decide to elongate certain modules and shorten others, skip cer- tain skills, or add illness management strategies from other protocols (e.g., mindfulness meditation or relaxation exercises) as relevant to the patient’s and family’s needs.
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her. These exercises can be difficult when a patient’s emotions are still dysregulated, but the structure intro- duced by communication training can help the patient modulate how he/she expresses emotions.
During the final phase, problem-solving train- ing (four to five sessions), the original mood episode is largely remitted and the patient has moved into the maintenance phase of drug treatment. At this stage, and sometimes even earlier, patient and family members are motivated to identify and address quality-of-life issues that have been disrupted by the illness (e.g., how a mar- ried/cohabiting patient can find work; how parents can help a young adult offspring move out of the home and gradually become more independent). The last few ses- sions of FFT, held monthly, help to consolidate gains made during the 9-month treatment.
Setting
FFT has been done in a variety of outpatient settings, including the Child and Adolescent Mood Disorders Program (CHAMP) at the UCLA School of Medicine; the Didi Hirsch Community Mental Health Services in Los Angeles, California; the Colorado Family Project clinic in Boulder, Colorado; the Pediatric Bipolar Dis- orders program at Stanford University; the University of Cincinnati School of Medicine; and the Child and Adolescent Bipolar Services Program at the University of Pittsburgh School of Medicine. FFT has also been evaluated internationally, with clinical trials in Turkey (Ozerdem, Oguz, Miklowitz, & Cimilli, 2009) and the United Kingdom (Sharma et al., 2015).
Client Variables
FFT is conducted with patients with bipolar I, bipolar II, or bipolar disorder not otherwise specified who live with (or in close proximity to) their parents, siblings, or spouses/partners. Patients can be of any age. Pa- tients who have received FFT have come from all racial and ethnic groups and sexual orientations. When the patient is a child or adolescent and the parents are di- vorced, we often conduct some of the sessions with the patient and one parent and other sessions with the pa- tient and the other parent. Ideally, some of the sessions involve both parents, so that there can be agreement on common strategies for managing the disorder.
Patients with bipolar disorder usually present for FFT with mania, depression, mixed episodes, or rapid
cycling. Although there is no contraindication for offer- ing FFT to patients who have been symptomatically re- covered for lengthy periods, in our experience, they and their family members are less motivated for treatment than those who have recently dealt with a mood epi- sode. The polarity of the presenting episode, however, is a moving target—it may change before the patient is seen next. Patients who are manic or hypomanic, par- ticularly those who are elated and grandiose, are often in denial about whether they are ill, and may believe that the disorder and its treatment are simply ways for others to control them. Depressed patients may have difficulty assimilating the educational content of ses- sions or following through on homework assignments. Any of these presentations may require emergency in- terventions such as changes in medications or hospital- ization during treatment.
Patients with comorbid alcohol or other substance use disorders pose special problems. These patients are usually resistant to psychosocial treatment and medi- cation. They are also difficult to diagnose; the effects of drugs or alcohol can mimic the cycling of a mood disorder. Generally, patients with active substance use disorders are more successfully treated if they are “dry” before FFT commences. It may be necessary to supple- ment FFT with chemical dependency programs (e.g., dual-diagnosis Alcoholics Anonymous groups). None- theless, a protocol for treating adolescents with bipo- lar disorder and substance abuse has been developed (Goldstein et al., 2014; Miklowitz, 2012).
Concurrent Drug Treatment
When the patient has syndromal bipolar disorder, we usually require that he or she be seen simultaneously by a psychiatrist, who monitors patients’ medications. Typically, a regimen includes a primary mood stabi- lizer, usually lithium carbonate, divalproex sodium (Depakote), or lamotrigine (Lamictal). Lithium has been convincingly demonstrated to reduce suicide risk in bipolar and unipolar depression (Cipriani, Hawton, Stockton, & Geddes, 2013). More and more, patients are treated with second-generation antipsychotics as ei- ther primary mood stabilizing agents or adjuncts to tra- ditional mood stabilizers. There is strong evidence that these agents are highly effective in controlling mania (Cipriani et al., 2011), and some (notably, quetiapine) are effective for bipolar depression (Avery & Drayton, 2016). Antidepressants (e.g., paroxetine [Paxil], venla-
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faxine [Effexor], bupropion [Wellbutrin]) are still rec- ommended as adjuncts to mood stabilizers or atypical antipsychotics if the patient’s depression does not remit. There has been considerable debate about whether an- tidepressants precipitate mania (mood switching) in patients with bipolar disorder, but the bulk of the evi- dence is that antidepressants do not cause higher rates of mood switching if they are given alongside a mood stabilizer or second-generation antipsychotic (Yatham et al., 2018; Goodwin et al., 2016).
A core principle of FFT and most forms of psycho- social intervention for bipolar disorder is that the thera- pist must have regular contact with the patient’s psy- chiatrist. This contact is established early in treatment. A close affiliation between the psychosocial and phar- macological treatment team enhances the likelihood of the patient’s remaining compliant with his/her medica- tions; it also decreases the likelihood of “splitting,” or the tendency for a patient (or even family members) to have a “good doctor” and a “bad doctor.” For example, patients frequently complain about their physicians and say to their FFT clinicians, “I wish you could just moni- tor my medications.” An FFT clinician who has a regu- lar dialogue with a patient’s physician can avoid the trap that is being set by encouraging the patient to bring up these problems with the physician directly (Gitlin & Miklowitz, 2016).
Some patients who refuse all medications assume that coming to therapy will be a substitute for drug treat- ment. These patients often have had bad experiences with pharmacotherapy and psychiatrists, and may also believe that they are not ill, or that the illness they do have can be treated using “alternative medicines.” We have generally taken a hard line with these patients and do not accept them into FFT unless they commit to standard pharmacotherapy (usually lithium, anticon- vulsants, and/or atypical antipsychotics). Patients with bipolar disorder who are unmedicated are highly likely to have relapses, and it is not in their best interests for the clinician to imply that their illness can be managed with psychotherapy alone.
Therapist Variables
In our UCLA and Colorado studies, therapists’ ages have ranged from 23 to 70 years, with from 1 to 40 years of clinical experience. The majority have been graduate students in clinical psychology or psychology interns, psychiatry fellows, or postdoctoral psychology fellows. Few have had extensive background in family therapy
before learning FFT. The 15-site STEP-BD program involved psychiatrists, clinical psychologists, and social workers who varied considerably in treatment experi- ence. In other words, there is no requirement that an FFT therapist have a certain degree or amount of clini- cal training at the outset.
Although there have been no studies of therapist variables as predictors of the outcome of FFT, our clini- cal experience has been that two variables influence the uptake of this intervention. The first is the ability to think of a family or couple as a system in which mem- bers are interdependent and mutually influence other members’ behaviors. Therapists who have trouble with FFT often have difficulty making the transition to this systemic way of thinking. They tend, for example, to conduct family sessions as if they were individual ses- sions, with one patient and several observers. Some of these same problems arise in learning other forms of family therapy.
The second positive predictor is the willingness to think biopsychosocially—that is, to see psychiatric dis- orders as biologically based illnesses that require medi- cations, even if the patient’s symptoms are partially evoked by concurrent stressors. Thus, a therapist often must argue for the patient’s medical adherence even when psychosocial issues are more interesting and seem more pressing.
We have found that the following training protocol works well for learning FFT. First, therapists attend an FFT workshop conducted over 1–2 days. Then, they begin attending group supervision sessions in which trained FFT therapists discuss their cases, and in which they are able to observe sessions (or listen to tapes). They read the published treatment manual (Miklowitz, 2010) and, when relevant, the adapted manuals for adolescents with bipolar disorder and children at risk for bipolar dis- order. Then they serve as cotherapists to trained FFT therapists. After treating two cases with close supervi- sion, they are usually ready to see families or couples independently, or even take on trainees themselves.
The cotherapy model has several advantages for training. It has a long history in the family therapy liter- ature (see, e.g., Napier & Whitaker, 1988). Cotherapists have a way of keeping their fellow therapists on track. If one person appears to be feeling ganged up on by the clinician and other family members, the other therapist can bridge the gap by allying him/herself with this fam- ily member. In-session dialogue between the clinicians can also provide effective modeling of communication skills for members of a family or couple.
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PRETREATMENT ASSESSMENTS
Diagnostic Evaluation
Bipolar disorder is becoming an increasingly common diagnosis in inpatient and outpatient community set- tings. Although this is a positive development given its underidentification in the past, there is also an el- ement of sloppiness in modern diagnostic evaluations. Nowhere is this more obvious than in the diagnosis of children and adolescents, who are being called “bipo- lar” with little supporting evidence (e.g., Carlson et al., 2009). The inadequacy of community diagnostic evalu- ations derives in part from inadequate insurance reim- bursement for the evaluation phases of patients’ treat- ment. Some of the patients referred to us have been more aptly diagnosed as having cyclothymic disorder, border- line personality disorder, ADHD, or even MDD. Many children and adolescents are referred with “rage attacks” that someone has equated with bipolar disorder.
Upon seeing a new patient, clinicians often find it useful to determine the reliability of the diagnosis with a formal assessment, using all or part of a structured diagnostic interview. Within our research protocols, we have used the Structured Clinical Interview for DSM-5 (SCID-5; First, Williams, Benjamin, & Spitzer, 2015) as the diagnostic assessment device. When the patient is under age 18, we use the Schedule for Affective Dis- orders and Schizophrenia for School-Age Children— Present and Lifetime Version (KSADS-PL), with the accompanying KSADS Depression and Mania Rating Scales (Axelson et al., 2003; Chambers et al., 1985; Kaufman et al., 1997). The K-SADS-PL requires sepa- rate interviews with the child and at least one parent, followed by consensus ratings of each symptom item. Some of the factors that can affect the reliability of the data obtained from the SCID or K-SADS-PL include whether the patient is acutely ill or stable; acutely ill patients are less reliable in their symptom reports. Typi- cally, patients in a manic state minimize their symp- toms, whereas depressed patients may do the reverse. Patients with bipolar disorder also have trouble with retrospective reporting: “I’ve had over 1,000 episodes” and “I’ve been constantly manic–depressed since I was an infant” are common responses to diagnostic inter- views.
Whether one uses the structured or an open-ended clinical interview, it is often difficult to determine whether a patient’s mood dysregulations and associated changes in activity are at the subsyndromal or syndro- mal levels. Some patients report brief periods of hypo-
mania or irritability that alternate with more severe de- pressions. These brief, activated periods do not always reach the DSM duration threshold for hypomania (4 days or more), especially among children and teens. In these cases, the diagnosis of bipolar disorder otherwise specified (formerly not otherwise specified) is often ap- propriate.
Hagop Akiskal (1996) has encouraged clinicians to consider a broader bipolar spectrum that includes core temperamental disturbances, including hyperthymia (exuberance, overoptimism, grandiosity, stimulus seek- ing, physical intrusiveness with others) or “sub-bipolar dysthymia.” In FFT, the broadening of the bipolar spec- trum to include these patients introduces a quandary: Does the clinician proceed with such patients in the same way as with patients with bipolar I or bipolar II disorder? How does the clinician educate the patient and family about the factors that bring about manic or depressive episodes if discrete episodes cannot be iden- tified? If a patient has never had a full manic episode, should the therapist proceed under the assumption that the patient eventually will develop mania spontane- ously? Do the same self-management techniques (e.g., using problem solving to minimize family conflict) apply?
In our outpatient Childhood and Adolescent Mood Disorders Clinic at UCLA, we have adapted FFT for youth who are not on the bipolar spectrum, such as those with depression with anxiety, ADHD, disruptive mood dysregulation disorder, or oppositional defiant disorder. The communication enhancement and prob- lem-solving modules can be given to families of these youth in the same manner as I have described; the psy- choeducation module, however, has to be altered to fit these diagnoses. For example, in disruptive mood dys- regulation disorder, the focus may be on strategies the family can use to prevent or respond to “meltdowns” (periods of intense anger that have a build-up phase); or in depression with ADHD, on identifying and coping with stressors that are relevant to the individual’s worst periods of functioning. Psychoeducational interven- tions almost certainly have a role to play in the stabili- zation of patients with these disorders.
Mood Chart
Clarity on the diagnosis, as well as the patient’s progress in treatment, is aided by asking the patient to keep a Daily Mood Chart. One such instrument, the Social Rhythm Metric (Monk, Kupfer, Frank, & Ritenour,
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1991), asks the patient to document daily mood on a –5 (Depressed) to +5 (Euphoric or activated) scale, along with social routines that may influence these moods (e.g., sleep–wake times, times when the patient social- izes, the intensity of this social stimulation, the patient’s exercise habits, and other factors).
Data from mood and activity charts, many of which are available online (e.g., https://moodapps.wordpress. com/tag/mood-reporter) help the clinician and patient to evaluate collaboratively the type of cycling the patient experiences and the degree to which social stressors contribute to mood fluctuations. Figure 12.1 is an ex- ample of a handwritten mood chart; note the cycling of the disorder in relation to specific social stressors and sleep patterns reported by the patient. In this example, a stressor (a pet’s illness) is associated with sleep disrup- tion and the appearance of mixed mood symptoms at the subsyndromal level.
Family Assessments
FFT begins with a thorough assessment of family at- titudes and behaviors to identify the targets of interven- tion. The research studies at UCLA have begun with the Camberwell Family Interview, the instrument for rating EE (discussed earlier). This interview, usually done when the patient is acutely symptomatic, focuses on the prior 3-month period, which usually includes the prodromal phases of symptom buildup. The inter-
view yields answers to the following questions: What is the current level of tension in the household and in the relative–patient relationship? Which of the patient’s behaviors are eliciting stimuli for family arguments or hostility? Do family members understand that the pa- tient has bipolar disorder, or are they likely to attribute the patient’s negative behaviors to internal or control- lable factors?
A problem with the EE/Camberwell Family Inter- view method is its lack of exportability to community care settings. Interviews with two parents can total 3 hours, and the coding of interview tapes for EE can add an additional 6 person-hours per family. If a clinician’s purpose is treatment planning rather than research, he/ she may be able to substitute a self-report measure such as the Perceived Criticism Scale (Masland & Hooley, 2017). This measure simply asks the patient to rate, on a 1- to 10-point scale, the degree to which close rela- tives express critical comments toward him/her, and the degree to which he/she expresses critical comments toward relatives. We evaluated the predictive validity of this scale in a sample of 360 bipolar adults followed over 1 year (Miklowitz, Wisniewski, Miyahara, Otto, & Sachs, 2005). The degree to which patients reported being upset or distressed by criticism from relatives was a strong predictor of their levels of depression over a 1-year prospective period. Interestingly, the amount of criticism they perceived from relatives was not prognos- tically significant.
FIGURE 12.1. Example of a self-rated mood chart.
5
4
3
2
1
0
–1
–2
–3
–4
–5 1/27 1/28 1/29 1/30 1/31 2/1 2/2 2/3 2/4 2/5 2/6 2/7 2/8 2/9 2/10 2/11 2/12
High
Low
Normal mood
Hours of sleep 7 6 8 6 6 6 7 10 3 5 6 5 6 4 5 6
went to co ncert,
stayed out ti
l
3 am
argu ment
with Dad rejec
ting
even t with
boyf rien
d
cat got sick went to hospital
cat out of hospital
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In our research protocols, we typically bring the fam- ily in for an interactional assessment before treatment is initiated. First, each member of the family, includ- ing the patient, identifies one or several family problem topics. Then, the family members discuss one or more of these topics while the clinician observes through a one-way mirror. Transcripts of these 10-minute prob- lem-solving discussions can then be coded using manu- als such as the O’Brien system for coding family inter- actions (O’Brien, Miklowitz, & Cannon, 2014), which capture constructive and conflictual verbal and nonver- bal statements or behaviors as exhibited by both parents and offspring (or two members of a couple).
The clinician can also rely on simple observations of the family’s communication and problem-solving be- havior to inform the skills training modules of FFT. To quote Yogi Berra, “You can observe a lot by just watching.” First, many family members or patients are unable to focus on a single problem and instead “cross- complain” or accuse other family members to counter- act the accusations directed at them. Some engage in attack–counterattack cycles. For any particular family, the clinician must first identify the form these inter- changes take, which dyadic or triadic relationships they involve, the content areas that trigger the interchanges (e.g., medication-taking habits, independence, interper- sonal boundaries), and whether members of the fam- ily are able to stop these cycles before they deteriorate. Who criticizes whom, and how often? How does the target person respond? Does the original problem ever get solved? How clear (or disorganized) is the speech of patients or relatives? A key difference between low-EE and high-EE families is whether one more family mem- bers is able to arrest negative interchanges before they spiral out of control.
PROCESS OF TREATMENT
Psychoeducation
Table 12.2 summarizes the topical domains that are covered in FFT. The initiation of the psychoeducation module of FFT requires three conditions. First, the pa- tient should be seeing a psychiatrist and have begun a medication regimen, unless his or her illness is not se- vere enough to warrant medications (e.g., a child with subthreshold bipolar disorder). Second, a diagnostic as- sessment must have been completed, and the clinician should have enough information to be able to plan the psychoeducation module. Third, the patient must be
able to tolerate family sessions, and at least one family member in the role of caregiver should be able to attend. There is no requirement that the patient be in remission or recovery. FFT sessions can be conducted “live” in the clinic or remotely by telehealth, which is often more convenient for the family.
In the seven or more weekly sessions that comprise the psychoeducation module, participants (patients and their relatives) become acquainted with the symptoms of bipolar disorder; the way episodes develop; the roles of genetics, biology, and stress; pharmacological treat- ments; and the role of stress management strategies.
The Initial Sessions: Providing a Rationale
As in most other forms of therapy, the clinicians begin by explaining the rationale for FFT. Many participants ask why family or couple sessions should accompany medication for a patient adjusting to a recent episode of bipolar disorder. Particularly helpful in orienting participants is the “reentry model” (Miklowitz, 2010, p. 104):
An episode of mood disorder . . . can be quite traumatic to all members of the family. . . . In bipolar disorder, when the person gets over the worst of the episode and begins to recover, there is a “getting reacquainted” pe- riod in which everyone has to get to know everyone else again, and when everyone tries to make sense of what happened. This is a tough time for any family, and part of our purpose here is to make this “reacquaintance period” less disturbing to all of you. We’d like during this year to get you, as a family, back to where you were before became ill. We want to give you some tools to deal with this recovery period.
There are two purposes for this introduction. First, it communicates to family members that their emotional reactions to the patient’s illness—even if quite nega- tive—are normal and expectable. Second, it implies that the therapy will include exploration and clarifica- tion of participants’ emotional reactions to information about the disorder. This feature of the therapy can be made even more explicit:
If feelings come up for you when we’re discussing this material, please bring them up. We want to know how this material applies to you and your own experiences. You may or may not agree with some of the material we present here. . . . The purpose of focusing on this material is to put your experiences into a context that will make sense. (p. 110)
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Next, the treatment is previewed:
We’re going to work with you on two different levels. One is on encouraging ’s ongoing work with his psychiatrist so that he can get himself stabilized on medications. The second is on how you as a fam- ily can minimize stress. . . . We think there are several ways to do this, including acquainting you with the facts about bipolar disorder, and working with you on improv- ing your communication and problem solving with each other. These strategies should increase ’s chances of making a good recovery and help you as a family cope with the disorder. How does this sound to you? (p. 107)
The Symptoms of Bipolar Disorder
FFT proceeds with a series of handouts that are used as stimuli for generating family or couple discussions. These contain descriptions of the symptoms of manic, hypomanic, or depressive episodes, with illustrations. The purpose of these handouts is not for the partici- pants to memorize the diagnostic criteria. Rather, they provide a starting point for destigmatizing the illness and breaking family taboos against talking about it.
We often begin by designating the patient—whether he/she is a child, adolescent or adult—as the “expert” in bipolar disorder: “You’re the one who’s actually gone through it and I expect that we (the clinicians), and your family will learn a lot from your descriptions of how it feels.” The patient is asked to look at the lists and describe to family members what it feels like to be eu- phoric, irritable, unable to sleep, or activated by racing thoughts or grandiose plans. Family members describe the behaviors they observed when the patient cycled into his/her most recent episode of mania or hypoma- nia. A similar dialogue is undertaken for depression symptoms. Consider the following dialogue among a patient, mother, father, and therapist.
PATIENT: Well, the thing is, there’s the manic and then there’s the hypomanic. When I’m manic, I really should be hospitalized. I control the weather, I can read people’s minds, I’m famous. When I’m hypo- manic, well, I just can get into that from having too much stress, too much caffeine, and being all revved up . . .
MOTHER: I can tell when she’s high, because I start getting real mad at her. She provokes me.
FATHER: And she gets this look in her eyes. And she says we’re not listening to her . . .
PATIENT: But you’re not! That’s when you’re most likely to tune me out.
THERAPIST: Let’s hold on that for now, about listen- ing. It’s very important, and certainly something we’ll want to focus on later, but what else do you notice when you get manic or hypomanic [redirects the focus]?
PATIENT: I get sort of, well, reactive. . . . I experience everything so intensely, but see, they know this as who I am.
Note the themes that arise in this discussion of symptoms, and how these relate to the six objectives of FFT outlined in Table 12.1. The patient’s vulnerabil- ity to recurrences is made explicit by the identification of prodromal signs of her episodes. The patient points to the role of disturbed family communication. She al- ludes to questions about whether some of her symptoms are really just personality traits (i.e., intensity and reac- tivity). There is a beginning discussion of stress factors that may play a role in triggering her episodes.
The Vulnerability–Stress Model
Early in psychoeducation, the family clinician makes a strong argument for the conjoint influences of stress, biological imbalances of the brain, and genetic vulner- ability in the course of bipolar illness. A handout illus- trating these vulnerability–stress interactions is provid- ed, and various risk and protective factors are reviewed. For example, the patient and family members are warned of the impact of poor sleep hygiene (i.e., keep- ing irregular hours, having unpredictable bedtimes), alcohol and drug use, stressful family interchanges, and provocative, overstimulating interpersonal interactions. They are encouraged to make use of available protec- tive factors (e.g., social supports), and help the patient maintain adherence to his/her pharmacotherapy regi- men. The purposes of the patient’s various medications are given. In outlining protective factors, a special em- phasis is placed on keeping the family environment low in conflict and on maintaining reasonable performance expectations of the patient during the recovery period. In the following vignette, the clinician reminds the pa- tient and his mother that depression is not the same as lack of effort, and that a period of recovery prior to
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regaining one’s previous occupational status is to be ex- pected.
THERAPIST: (to Gary, the patient) I think you can’t ex- pect too much just yet. You’re still recovering from your episode. It may take some time to get back on track.
MOTHER: How long? He’s been like this now for a while.
THERAPIST: I’m sure that’s frustrating, but you have to think of this as a convalescent period. When some- one has a bad flu, he may need an extra day or two in bed to recover completely. For bipolar disorder, this period of time can average 3 to 6 months. But, Gary, with your medication treatments and our fam- ily sessions, and the fact that you’ve maintained good friendships, I have every expectation that you’ll re- cover and be able to get back to work.
The clinician here offers hope but does not paint a rosy picture of the future. Often the family has been through these episodes before, and a clinician who of- fers an excessively optimistic view of the future will be dismissed as unrealistic.
Describing the biology and genetics of the disorder is critical to justifying the role of medications. How- ever, it is not necessary for the clinician to go into detail about how cells communicate with each other. Instead, the clinician begins by asking the participants to review their family pedigree and discuss any other persons in the family who may have had episodes of depression or mania. The clinician explains that the vulnerability to bipolar disorder may take many forms, including major depression without mania, alcoholism, suicide, and dys- thymia. Next, the clinician explains the notions behind neural dysregulation in bipolar disorder:
“We know that people with bipolar disorder have trouble regulating their emotional states, sleep, and arousal, all of which are regulated by the limbic sys- tem, an important circuit in your brain. In mania, we think that the limbic system becomes overactive, and the frontal cortex—the ‘executive’ in your brain— stops being able to do its job. It’s almost like having your foot on the gas pedal when the brakes are not working. When a person gets depressed, the system shuts down, and the circuits become underactive. These changes in brain activity can’t be controlled
through your conscious efforts, but the medications you take can go a long way toward balancing the ac- tivity in your nervous system.”
When family members begin to attribute the pa- tient’s aversive behaviors to willfulness (the “fundamen- tal attributional error”), the clinician can remind them of the neurological underpinnings of the disorder. But the family and patient should also be discouraged from overemphasizing the biological nature of the disorder, to the point of neglecting stress factors such as long- standing family conflicts. The patient is not taken off of the hook: He/she is encouraged to self-monitor when getting into arguments with family members, and to determine whether his/her reactions to these conflicts reflect an unresolved symptom state or a reemergence of conflicts that would have been troublesome even before he/she became ill.
Clarifying the stress triggers for the most recent epi- sode is aided by a handout describing life changes that may have occurred when the episode was developing. Some of these changes are quite severe and negative (e.g., death of a parent); others are mild but may have provoked changes in sleep–wake cycles (e.g., taking a vacation). The clinician engages the family or couple in a discussion about what stressors may have provoked the patient’s current episode, with the caveat that the trig- gers for mania and depression may be quite different. It is not critical that the participants agree on a singular cause for the most recent episode, but they may benefit from the awareness that mood episodes are affected by environmental as well as neurobiological factors.
The Relapse Drill
Toward the end of psychoeducation, the family mem- bers and patient are given their first exposure to problem solving. The task is to review the patient’s past prodro- mal signs of developing episodes and to go through the steps that are necessary to prevent a full relapse. Partici- pants are asked to generate alternative courses of action should the patient begin to relapse into mania or depres- sion, which can include calling the patient’s psychiatrist or taking the patient to the emergency room, introduc- ing behavioral activation exercises for depression, trying to discourage the patient from going out late at night, or, depending on their past experiences, removing access to credit cards or car keys. Each family member is asked to perform a function in the relapse prevention plan. For
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example, in some families it may make sense for a parent to undertake contact with the physician. In others, the patient may want the first opportunity to do so. The family or couple is encouraged to leave phone numbers of emergency contact people, including the family clini- cians, in an easily accessible place.
Dealing with Resistance to the Illness Concept
Patients with bipolar disorder often have strong reac- tions to the psychoeducational materials, as do their family members. These materials require that the par- ticipants recognize bipolar disorder as an illness that will eventually recur. Younger patients are particularly likely to reject the notion of a recurrent illness, particu- larly if they are still hypomanic; they may feel powerful and in control, and the idea of having an illness feels like shackles. Moreover, they are particularly attuned to the stigma associated with psychiatric diagnoses, and fear that their behavior will now be labeled as that of a crazy person. Resistance can also originate with family members. Relatives of depressed patients are apt to see the disorder as willfully caused and not the product of biochemical imbalances. Resistance from one or more members is often associated with intense family con- flicts.
Accepting a psychiatric disorder is a painful process for patients and relatives, particularly when the patient is a late teen or young adult being diagnosed for the first time. Often the psychoeducational materials raise questions such as “Why me? Why now? What kind of life will I have? Will people treat me like I’m mentally ill from now on? Will I ever get back to normal?” Rela- tives ask themselves similar painful questions such as “Will I always have to take care of him/her? Are my dreams and hopes for him/her gone?” Spouses/partners may ask, “Should I leave him/her?” When asking them- selves these questions, some patients respond by “un- deridentifying,” or denying the reality of the disorder, or by acknowledging the illness superficially but living their lives as if it were not real. Family members may also be in denial about the significance of the patient’s behavior—“He’s just a teenager” is a common refrain.
Others “overidentify” and unnecessarily limit them- selves. For example, one 35-year-old woman avoided ro- mantic relationships because “no one will ever be able to get close to me because of my mood swings.” Likewise, family members can deny the realities of the disorder or, in contrast, overmonitor the patient’s health status and try to limit his/her behavior unnecessarily. Family
conflict reaches a maximum when there is a mismatch between coping styles, such as when patients underi- dentify and relatives overidentify, or the reverse.
FFT clinicians proceed with a sensitivity to the pain- ful emotional issues underlying these reactions to the illness. One method for dealing with these reactions is to predict that denial will occur, and to reframe it as a sign of health. For example, consider a young man with hypomania who has accepted taking medications but denies being ill, and whose parents overcontrol and overmonitor his behavior. To this young man, the clini- cian might say:
“Although I appreciate that you’re taking medication and going along with the treatment plan, I’m going to guess that you’re not always going to want to do this. You probably have some questions about whether this diagnosis is right for you or whether you’ll have more symptoms—am I right? I can understand why you’d have these questions. Coming to terms with having bipolar disorder—or really any illness—is a very painful process that can be hard to accept. This is a normal and a healthy struggle. So, as we’re going through our material, you may find yourself reacting to it and feeling that it can’t be relevant to you. But I’d like for you to agree that if you have these reac- tions, you’ll bring them up so we can discuss them.”
Note that this intervention has a paradoxical flavor, but the clinician stops short of actually encouraging the patient to remain resistant or to increase his level of disagreement with the diagnosis. Instead, the clini- cian reframes the young man’s denial as healthy and ex- pectable, and connects it with an underlying emotional struggle.
A second way to intervene is through “spreading the affliction.” Being labeled as mentally ill can put a person in a one-down position vis-à-vis other family members, including siblings with whom he/she may already feel competitive. A possible side effect of psychoeducation is the exaggeration of these structural family problems. The clinician can avoid this trap by encouraging other members of the family to discuss their own experiences with depression, anxiety, or other problems. This pro- cess can help normalize mood problems and take the patient off the hot seat.
The following vignette involves Josh, a 25-year- old with a recent manic episode. He reacted strongly, because he thought everyone was telling him he was “whacked out.” According to Josh, all he had done was
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“party too much.” During one of the psychoeducation sessions, his father admitted to having had a depressive episode in college.
THERAPIST: Josh, you seem like you’re reacting to something I just said about bipolar disorder. Were you offended?
JOSH: I dunno. It wasn’t anything you said; just I get tired of being the only one in the family who has problems.
THERAPIST: Is that really true? Has anyone else in the family ever had any problems with depression? Or what I’ve called mania?
FATHER: (pause) I did, and I’ve told Josh about this. Remember what I told you about college?
JOSH: (sullen) I don’t know. Why don’t you clue us in? FATHER: I had that long period when I couldn’t sleep
and eat, and I couldn’t study. I dropped out for a semester.
The session then focused on the father and his own history of depression. He revealed a history of psycho- sis involving delusional thinking. Although the patient was sullen at first, he became more cooperative in the discussions that followed, and more willing to talk about how the illness label made him feel stigmatized.
A third method of dealing with resistance to the di- agnosis involves making analogies to medical disorders. The illness feels less stigmatizing to patients and fam- ily members if they can see it within the continuum of other kinds of chronic physical illness. Diabetes and hypertension are often good comparisons, particularly because the influence of stress can also be brought to bear:
“Bipolar disorder involves biological imbalances much like hypertension does, and it’s affected by stress in much the same way. Most people have changes in blood pressure when something stressful happens, but not everyone is vulnerable to heart disease. Peo- ple with hypertension have a vulnerability to extreme shifts in their blood pressure. In the same way, most people have mood changes when something impor- tant happens, but people with bipolar disorder oper- ate at greater extremes.”
In making these analogies, the clinician validates the patient’s feelings about social stigma:
“Although there are some similarities with illnesses like hypertension, bipolar disorder can be tougher to live with because other people tend to be afraid of it or don’t know what it means. Some people will think you’re dangerous. Others will laugh it off and say, ‘Isn’t everyone bipolar?’ You have to take the time to educate other people—particularly those people who are most important to you—and explain it in a way that they won’t react to it.”
Communication Enhancement Training
The second module of FFT, CET, lasts for about seven to 10 sessions (the first five of which are weekly fol- lowed by every 2 weeks). CET is guided by two assump- tions. First, aversive family communication is a com- mon sequel to an episode of a psychiatric illness and reflects distress within the family or couple in members’ attempts to deal with the disorder. Second, the frequen- cy of aversive communication can be reduced through skills training.
CET uses a role-playing format to teach patients and their relatives five communication skills: express- ing positive feelings, active listening, making positive requests for changes in others’ behaviors, communica- tion clarity, and giving negative feedback. These skills are central to the behavioral family management ap- proach to schizophrenia of Falloon, Boyd, and McGill (1984). The degree to which each of these skills domi- nates the role-play exercises varies according to the fam- ily assessments conducted earlier. Treatment of a fam- ily with much heated conflict and high-EE attitudes might focus on adaptive ways participants could ask for changes in each other’s behaviors. Treatment of an emotionally disengaged couple might focus on positive feedback and listening skills to coax the partners into experimenting with a more interdependent relationship.
The module begins with an explication of the CET method for the family:
“A person can be at risk for another relapse of bipolar dis- order if the home environment is tense. . . . Good com- munication and problem solving can be among those ‘protective factors’ against stress that we talked about before. For a family member, learning effective com- munication skills can be a way of decreasing tension and improving family relationships. . . . We want to help you communicate in the most clear and the least stressful way possible. . . . We’ll be asking you to turn your chairs to each other and practice new ways of talking among your- selves.” (Miklowitz, 2010, p. 208)
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Note that CET is linked with two of the six objec- tives of the larger treatment program: helping partici- pants to cope with stress triggers and restoring func- tional family relationships after an illness episode. The first two skills, positive feedback and active listening, generally foster a feeling of collaboration between mem- bers of the couple or family. In contrast, making posi- tive requests for change and giving negative feedback are more conflict-oriented and are only introduced once participants are used to the role-playing and behavioral rehearsal format. Communication clarity is often used with parents who tend to lecture their offspring instead of giving concrete instructions or expressing succinct opinions.
For each skill, the clinician gives participants a handout that lists the skill’s components (e.g., for ac- tive listening: make good eye contact, nod your head, ask clarifying questions, paraphrase/check out what you heard). Then the clinician models the skill for the fam- ily. For example, the clinician might compliment one member of the family for his/her cooperativeness with the treatment, or model effective listening while an- other family member talks about a problem. After the skill is introduced and modeled, participants are asked to turn their chairs toward one another and practice the skill with each other, with coaching and shaping by the clinician. Typically, the therapist asks one of the family members to be the speaker and the other the listener, and coaches the pair on using the skill (e.g., “Make a positive request of your mom. Mom, all you need to do is listen—you don’t need to say yes or no”). Once a participant has practiced the skill, the feedback of other family members (especially the person he/she was talk- ing to) is actively solicited. The speaker or listener is then asked to try the skill again, until he/she has ap- proximated its use. A homework assignment, in which participants keep a written log of their efforts in using the skills between sessions, facilitates generalization of the learning process to the home and work settings.
The skills can be harder than they look. Consider “Jessie,” a 38-year-old woman with bipolar disorder, who had had several episodes of psychotic mania and also a developmental disability. She worked part-time as a gift wrapper in a department store. Jessie was trying to move into her own apartment and required help find- ing a moving van. She was instructed to make a positive request of her father, with whom she and her sister lived.
THERAPIST: Maybe that’s a good topic to ask your dad about. Can you look at this “Positive Requests”
handout and use these steps to ask your dad to help you move?
FATHER: It won’t help. There won’t be anything to move, because she still hasn’t packed a single box! (Laughs.)
JESSIE: Well, get me the damn boxes and I’ll do it. THERAPIST: (derailing this interchange) Do you think
you could ask your dad for something specific, like helping you find a moving company?
JESSIE: (Looks at father, smirking.) Dad, will you help me find a moving company? (Giggles.)
FATHER: (more serious) You’re not . . . you’re not looking at this. (Indicates handout.) You’re supposed to say, “I’d appreciate it if you would . . . ”
JESSIE: (Shrugs.) All right, I’d appreciate it if you would! Get me a phone number. Please.
THERAPIST: (after a pause) Well, you got part of it that time, Jessie. Dad, what did you like about what she just said to you?
FATHER: (sarcastically) Gee, all the sincerity. JESSIE: (Laughs nervously.) THERAPIST: Well, if you didn’t care for it, can you say
how she might say it to you? FATHER: How about something like “I’d appreciate it
if you’d get me those phone numbers of the moving companies. It’d make it a lot easier for me to plan my move.”
THERAPIST: Nice job, Dad. Jessie, what did your dad do that you liked or didn’t like?
JESSIE: He followed the sheet. He did all the things you said.
THERAPIST: True, but you don’t have to say it exactly the way he did. You can put your own spin on it. Do you feel you could try doing it one more time?
JESSIE: (Gasps, giggles.) THERAPIST: I know it’s hard being in the hot seat. But
you’re doing fine. Keep trying. JESSIE: Dad, could you get me those phone numbers of
the movers? I’d appreciate it. That way I could be . . . I wouldn’t have to worry about the move, and, well, just thank you for your help.
THERAPIST: That was very good, Jessie. Dad, how did you like it that time?
FATHER: (a little tentative) That was better. It made a lot more sense.
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These kinds of skills are most difficult to learn if the patient is highly symptomatic and/or cognitively impaired, or if the level of conflict in the family is so severe that productive conversations cannot ensue. This patient was moderately hypomanic and also had limited intellectual resources. Clearly, the skills training taxed her and made her nervous. However, with patience and practice, Jessie was able to adopt some of the skills, and her relationship with her father gradually improved. Her father, who was often quite critical, became more and more convinced that her limited functioning was a result of her illness rather than lack of effort, as he had believed previously.
The FFT manual (Miklowitz, 2010) describes “short- fuse” families. These families begin with apparently in- nocuous discussions that quickly escalate into angry, back-and-forth volleys of criticism or hostility. We have been surprised that relatives who, on the surface, appear benign and supportive of the patient during the Cam- berwell Family (EE) Interview become quite aggres- sive and confrontational when facing the patient in a one-to-one interaction. Not surprisingly, the likelihood that this will occur is greatly augmented if the patient is hypomanic and irritable. Short-fuse families typically have difficulty with communication training, because the participants’ emotions quickly get out of hand (see the case study presented later). But much can be ac- complished by adapting the skills training to the family members’ natural styles. For example, the therapist can encourage the participants to use active listening skills during their arguments. After a negative, back-and- forth interchange involving a couple, a clinician said:
“I think this is an important discussion. You’re a cou- ple that really likes to get things out in the open. But I’m afraid that you’re missing out on each other’s viewpoints. So let’s see if we can make it more pro- ductive. I want you each to paraphrase each other’s statements before making your next argument, like we did in the active listening exercises. Also, why don’t you turn your chairs to each other so that you can more easily keep eye contact?”
Note again the use of reframing. It is better to cast a couple’s or family’s ongoing dynamics (unless clearly abusive or threatening) as an adaptive way of coping that needs modification than to label these dynamics as “dysfunctional.”
A short-fuse family may also be able to make good use of positive requests for change or negative feedback
exercises, in which the partners make constructive sug- gestions about specific aspects of each other’s behavior (e.g., “I don’t like it when you talk down to me about my health habits”) and offer suggestions as to ways these behaviors could be improved (e.g., “Could you be more aware of your tone of voice?”). These exercises often set the stage for problem solving, the final mod- ule of FFT.
Problem‑Solving Skills Training
Problems in adjusting to the aftermath of a manic or de- pressive episode can be summarized in four categories: medication nonadherence, difficulty resuming prior work and social roles, repairing the financial and so- cial damage done during manic episodes, and relation- ship/living situation conflicts. In FFT, the purposes of problem solving are to open a dialogue among family members about conflicts that haven’t been resolved, to allow them a context to share their emotional reactions regarding these problems, and to help them develop a framework for defining, generating, evaluating, and implementing effective solutions to these conflicts. This module occupies the final four to five biweekly or monthly sessions of FFT. Problem solving is positioned last in FFT, because the patient is usually in remission by this point and is more able, both cognitively and emotionally, to experiment with new ways of behaving. Furthermore, if the psychoeducation and CET have gone well, family members are more ready to see their own role in generating or maintaining family conflicts and are more open to hearing each other’s viewpoints.
In problem solving, families are taught to break down broad problems into smaller units that are more amenable to solution. Family members are given a problem-solving worksheet in which they are asked to take the following steps: Define the problem (with each participant’s input), “brainstorm” all possible solutions without evaluating them, consider each solution indi- vidually and weigh its advantages and disadvantages, choose a best solution or combination of solutions, and plan and implement the chosen solutions. Once they have had a successful experience in solving a relatively minor problem, participants are given a homework task in which they record their attempts to solve a new, larg- er problem. Assignments are often modest at first, such as assigning the task of defining one or more problems to work on in the upcoming session.
The rationale for problem solving is presented as fol- lows:
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“Up until now, we’ve been talking mainly about how you communicate with each other. Now we’d like to deal with some of the concrete problems of living you’ve all been alluding to. But rather than our just giving you suggestions about what to do about these—which prob- ably wouldn’t work that well anyway—we’d like to teach you a way of solving problems cooperatively, as a family.” (Miklowitz, 2010, p. 259)
This rationale is then followed by a review of the steps for solving problems and familiarizing the family or couple with the problem-solving worksheet. The cli- nician also reviews some of the problems the members raised during earlier phases of treatment.
The key to successful family problem solving is to define each problem as having two sides: It is a disagree- ment between two or more people about expectations, attitudes or behaviors. “Jack won’t do his homework” is not a great definition; “Mom resents that she has to tell Jack to do his homework, but Jack resents being told to do things he had planned to do anyway” gets closer to a bidirectional problem definition. Additionally, the more specific the definition, the better. Is it all home- work, at all times? Or is it only math homework on the weekends? Is it any kind of reminder from Mom, or only reminders that are delivered in a negative tone of voice?
For example, Karla, age 35, who had bipolar II dis- order, moved in with her new boyfriend (Taki) shortly after her divorce. When they met, she was depressed and in poor shape financially; she described her tendency to “go on spending sprees to improve my self-esteem.” Karla became hypomanic shortly after meeting Taki, who was quite well off. Perhaps due to an eagerness to make the relationship work, he gave Karla access to one of his credit cards. During their first months of living together, his bills increased considerably. Karla’s own employment was inconsistent. She had had trouble for years keeping to a budget and maintaining a checking account. They began to fight heavily about this prob- lem. Karla argued that money was his way of control- ling women, and Taki argued that she was taking ad- vantage of him and being inconsiderate. Although they had discussed breaking up, neither wanted to do so.
Following a brief period of psychoeducation, the clinician focused on communication enhancement exercises. He encouraged the couple to expand on the broader issues before zeroing in on the more specific problem of spending. Karla voiced her opinion about what she felt was the “meat of the problem” (her per-
ception that he controlled women) while Taki listened. Then Taki described his take on the underlying issues, while Karla listened and paraphrased. The structure imposed by problem solving eventually helped them define the issue more specifically: Karla spent more on clothing and “comfort items” than either of them thought she should, but it was unrealistic for her to try to support herself given her ongoing symptomatic state. Taki wanted to support her, but he also wanted there to be externally imposed limits so that he was not always accused of being controlling.
Various options were then considered: Taki doing most of the buying, Karla having her own account with an upper limit negotiated each month, and the two of them simply separating their finances. These and other options were evaluated as to their advantages and dis- advantages. Finally, they agreed on a somewhat com- plicated but clever solution: Taki obtained three bank debit cards with preassigned spending limits, each asso- ciated with a joint bank account. Each card was labeled with an expense item (e.g., “doctor bills”) and had a spending limit written on it. They were to meet weekly to determine whether the system was working and their conflicts over finances were diminishing. Both were to practice active listening skills when they began to dis- agree.
In this example, the problem was to some degree generated by the patient’s hypomanic symptoms. There were also important relationship dynamics: Karla tend- ed to become overly dependent on men, then devalue them, and Taki tended to rescue women, then become angry about being in the rescuer role. The clinician decided to let them first “ventilate” about these larger relationship themes. Encouraging emotional expression about loaded issues, although sometimes risky, often reduces a family’s or couple’s resistance to dealing with these issues at a more concrete level.
Resistance to Problem Solving
From the outset, FFT clinicians must monitor patients’ and relatives’ reactions to the communication and problem-solving methods. Reactions can vary from “This is just what we need” to “Gee, how superficial.” Patients with bipolar disorder and their family mem- bers seem to crave spontaneity and enjoy fast-paced, unpredictable interchanges. They get bored easily. The skills-training exercises impose structure and encour- age goal directedness but can also generate resistance. Resistance can take the form of changing the subject,
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“cross-complaining,” or being unwilling to cooperate with the homework tasks.
When addressing resistances, a clinician reiterates the rationale for the communication or problem-solv- ing task (e.g., “Sometimes you have to gain confidence from solving minor problems before you move on to bigger ones”). But often he/she must determine whether it is really the skills-training method that family mem- bers object to or whether there are certain costs or pain- ful consequences associated with communicating better or solving problems. For example, one father feared that actively listening to his 30-year-old daughter’s emotion- al distress would make her more dependent on him. A mother avoided setting up agreements with her 22-year- old son about age-appropriate tasks (e.g., doing his own laundry), because she feared he would be unable to fol- low through and would then feel worse about himself.
Family members who fear the consequences of solv- ing a problem often approach solutions, then quickly abandon the process, arguing that “this problem is not really the issue.” The therapist has a number of options available. One is to take responsibility for the unsolved problem. For example, he/she can say, “Perhaps it was wrong of me to encourage you to solve this problem. Maybe you have other things you want to deal with first. Would you like to table it for now?” Alternatively, the clinician may proceed more paradoxically, framing the family’s difficulty as being due to “healthy avoidance”:
“Solving a problem as a family involves thinking about costs and benefits. There are certainly some benefits to solving this problem, but there may be some hidden costs as well. I think if the costs of solv- ing this problem outweigh the benefits, it’s certainly understandable that you’d want to avoid putting a solution in place. Is that what’s happening here? Are there any costs to solving this problem?”
Both of these interventions give the family mem- bers permission to leave the problem untouched. Later, when the pressure is off, they may be able to return to the problem and have more success the second time around.
Terminating FFT
FFT is terminated after 9 months (or, in the case of youth with high-risk syndromes, after 4 months). As termination approaches, a therapist reviews with family members the six goals for treatment (discussed earlier)
and the degree to which each was or was not realized. The status of the patient’s mood disorder is evaluated, compared to that at the beginning of treatment. In some cases, maintenance or “tune-up” FFT sessions are recommended.
Referrals for subsequent treatment for both the pa- tient and family members are discussed. For example, some patients follow up FFT with individual therapy or mutual support groups involving other persons with bipolar disorder. Family members may choose to attend support groups of the Depressive and Bipolar Support Alliance (www.dbsalliance.org) or the National Alliance on Mental Illness (www.nami.org). In our experience, it is unusual for families to request additional family or couple therapy after a full course of FFT, but referrals are made when requested.
The clinicians reiterate the importance of continued medication adherence and incorporation of communi- cation and problem-solving skills into the family’s day- to-day life. Finally, a review of the relapse drill (see the earlier “Psychoeducation” section) is conducted: The patient’s prodromal signs are reviewed, and steps the patient and family can take to avert a relapse are reiter- ated.
CASE STUDY
Debra, a 36-year-old woman, lived with her husband, Barry, age 46, and their 8-year-old daughter, Jill. She had completed 2 years of college and worked part time as a sales clerk in a luggage shop. She had been married previously. Debra was referred for FFT by a university clinic, where she had been diagnosed with bipolar II disorder. The initial SCID diagnostic interview con- firmed this diagnosis, along with generalized anxiety disorder. Her depression was marked by loss of inter- ests and “being bummed” for several weeks at a time. She also complained of loss of appetite, waking several times each night, fatigue, guilt, and loss of concentra- tion. She denied having active suicidal thoughts but re- marked that she tended to be preoccupied with morbid topics. She recounted that her current depression was “a really big one” that had lasted most of a year, but that she had also had “tons of small ones.” She dated the first onset of her depression to approximately 12 years earlier, following her divorce from her first husband.
Debra admitted to having had at least two prior hy- pomanic episodes, one in the previous month, includ- ing about 5 days of elevated and irritable mood. She
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explained, “My confidence level was up.” She reported to racing thoughts, increased activity and talkativeness, and becoming involved in many different projects. She had trouble dating the onset and offset of these periods, noting, “I’ve been this way all my life.” She did admit that Barry had commented on these mood phases. Debra complained, “He now tells me I’m getting manic every time we get in an argument. . . . It’s his newest weapon against me.” She denied having delusions or hallucinations.
Debra had been treated previously with sertraline (Zoloft) and bupropion (Wellbutrin). Her psychiatrist had recently started her on valproate (Depakote) at 1,500 mg/day, a medication that she said had made a difference in stabilizing her mood.
Barry, an attorney, presented as a no-nonsense type of man. He responded to the clinicians in a brusque and businesslike manner, and insisted that he had no problems of his own to discuss “except those that relate to Debra’s care.” He denied any psychiatric history. He preferred to talk about FFT as an educational course and became defensive if his wife referred to it as thera- py. The FFT clinicians, a male–female cotherapy team, did not dissuade him from labeling the treatment this way, believing that they would need to work on build- ing rapport with him before addressing his defensive style.
Family Assessment
Based on the Camberwell Family Interview, Barry met the criteria for a high level of EE. He voiced nine criti- cisms of Debra during his 1-hour interview. He com- plained at length about Debra’s memory, work habits, and disorganization (e.g., “She never remembers about parent–teacher meetings. . . . She forgets to turn in her time sheet at work—it drives me crazy”). Barry ex- pressed that he loved Debra but found her very frustrat- ing. He was convinced that she had ADHD as well as bipolar disorder.
Debra and Barry arrived well-dressed and smiling for the family interactional assessment. The clinicians interviewed them individually, and arrived at an impor- tant problem topic for them to discuss: Barry’s claim that Debra lied to him. Her response was to apologize for her past misdeeds and to argue, “I’m not lying or withholding. . . . Those are usually things I’ve forgot- ten or just don’t think are important.” Upon discuss- ing this issue, the couple’s dynamics became apparent, with Barry speaking in an accusatory, lawyerly, scold-
ing mode, summarizing the facts that were not in her favor. Debra repeatedly apologized and tried to justify her behavior. As Barry became more accusatory, Debra looked more and more withdrawn.
BARRY: Lying is a way of life for you. You twist the truth and say you don’t remember things.
DEBRA: But I really don’t. I’ve been trying to tell you everything. Sometimes I just forget. (Starts rocking her chair.)
BARRY: (holding Debra’s chair still) Why do you think it’s OK to lie to me?
DEBRA: I don’t. I’m being up front with you. Maybe you want to believe there’s more, but there’s not.
BARRY: I think you’ll always do this. It’s your thing. How would you like it if I lied to you? How would it make you feel? Would you want to stay married to me?
DEBRA: (sullen) No, probably not. But I’m trying to be open with my feelings, kinda with you as a practice case. (Smiles awkwardly.)
BARRY: You’re doing that little smile again. The one you do when you’re trying to get away with something.
DEBRA: (defensive) Oh, give me a break. BARRY: Is it because we’re talking so directly? I don’t
know if it’s your personality or if it’s the bipolar stuff acting up, but you have no tolerance for anything these days, especially people.
The therapists who viewed this assessment were struck by Barry’s harsh and critical tone, paired with Debra’s tendency to take a one-down position. They also learned that Barry doled out Debra’s medications and made her doctor appointments for her, and usu- ally attended them with her. An initial appointment for FFT was set with these two clinical psychologists, one of whom was a trainee.
Psychoeducation (Sessions 1–7)
During the initial session, the clinicians (Therapist 1 and Therapist 2 in the dialogues below) described the FFT program to the couple, with particular emphasis on the psychoeducational component. They previewed the communication enhancement and problem-solving modules. The couple listened politely but expressed skepticism.
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BARRY: We’ve been in and out of therapy for years. I haven’t been impressed.
THERAPIST 1: When you say “We,” do you mean you as a couple?
BARRY: As a couple, and she’s had her own therapy. DEBRA: I thought Dr. Walker was good. BARRY: Yeah, but you hadn’t had the bipolar diagnosis
yet. She was just treating you for depression. And she got you into that whole “You were probably abused as a child and forgot about it” thing.
THERAPIST 1: What was your couple therapy like? BARRY: A lot of digging into our childhoods and get-
ting in touch with our feelings. THERAPIST 1: Debra? DEBRA: It wasn’t that bad. I thought it was pretty use-
ful. THERAPIST 1: Well, it sounds like you’ve got different
opinions on how those sessions went. Let me tell you how this will be different. Our treatment is going to be focused mainly on the present, and we’ll be work- ing on how you as a couple are coping with Debra’s bipolar disorder. Barry, you’re going to be affected by the cycling of Debra’s moods, and Debra, you’re going to be affected by the way Barry responds to your symptoms. I’m not saying your past will be ir- relevant, but it’s just not our focus.
BARRY: I need help dealing with all of this. The more information I get, the better.
THERAPIST 1: I’m sure that’s true. But we won’t just throw a lot of information at you—we want to in- dividualize it to your situation. I think you’ll have a much easier time if you come to an understanding of the disorder as a couple and learn to communicate about it.
In this dialogue, the therapist made a distinction be- tween FFT and more generic forms of couple therapy. At this point, the clinicians already suspected that there would be resistance from Barry, especially regarding tasks in which he was asked to look at his own behavior and its contribution to Debra’s moods.
The psychoeducation itself began in the second ses- sion and continued through the seventh. The first task was to encourage the couple to come to a shared defini- tion of bipolar disorder. During the assessments, both used the term cycling, but without apparent agreement on what it meant.
THERAPIST 1: I want to be sure we’re all on the same page when we talk about the term bipolar. Debra, you did a great job just now of explaining what de- pression feels like. Let’s talk about the other side now. (Passes around a handout listing the symptoms of mania/hypomania.) Debra, which of these do you remember having the last time you got hypomanic?
DEBRA: (surveying the handout) Well, all of these except increased sexual thoughts.
BARRY: (answering for her) Pretty much all of these. I guess you could say she has overconfidence—she thinks one day she’ll be wealthy. (Laughs.)
THERAPIST 2: When was the last time you think she was like that?
BARRY: Last time I was working on a case—she always gets like that when I’m working on a case.
DEBRA: I agree, but I think it’s because I have a lot more to do when he’s working all the time. . . . He thinks it’s some “abandonment” thing, but I think he forgets the realities I face when he’s gone. (Looks at list.) I get more energy, I feel uncomfortable in my own body, I jump outta my skin . . . probably a good day to go shopping! (Giggles.) I probably get crankier. I don’t have much tolerance for people in general.
BARRY: Especially me. (Smiles.)
This was the first time that Debra had defended her- self, by commenting on how relationship problems fed into her mood swings. Interestingly, her assertive stance cut through some of her husband’s negativity.
The therapists soon realized that Barry and Debra lacked a consensus about what really constituted a mood episode. This is a critical point in FFT: The members of a couple or family need to come to a shared perception of when the patient is getting ill, so that they can institute procedures to keep his/her episodes from spiraling (e.g., scheduling immediate sessions with the physician, reducing the patient’s workload, learning to deescalate negative verbal exchanges). But it was not yet clear that Debra had discrete episodes.
THERAPIST 2: Do you think you have what we’re call- ing “episodes”? Like a couple of days of being wired?
DEBRA: There can be, like, maybe 5 days during a week when I can do a lot of stuff, my memory gets better, and then on the weekend it’s just not gonna work. I can . . .
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BARRY: (Interrupts.) It’s that household project thing. She starts redoing Jill’s room over and over. She’ll sponge-paint it purple and then wipe it out that same evening, put in new closets.
DEBRA: I can filter all my energy into housework in- stead of killing somebody. (They both chuckle.)
THERAPIST 1: Maybe I’m a little slow today, but I’m trying to figure out whether you both agree on when these high and low periods are. Debra, have you ever kept a mood chart?
The therapist then produced a written assignment in which Debra and Barry were asked to track indepen- dently, on a daily basis, the ups and downs of Debra’s mood states, so that agreements and disagreements about what constituted the symptoms of the disorder (as opposed to personality traits) could be tracked.
The dynamics of this couple became more evident in Sessions 3–5. Debra was inconsistent about keep- ing her mood chart, and Barry felt that his consci- entiousness in charting her mood was not being re- warded. “She won’t take responsibility for her illness,” he argued. Nonetheless, Debra had good recall of her mood swings, even though she had not written them down. The therapists offered the couple much praise for their somewhat halfhearted attempt to complete this assignment (shaping). Interestingly, Barry noted small changes in mood that he called her “manic-ness,” which Debra countered were just her reactions to ev- eryday annoyances.
BARRY: You were manic as hell on Saturday morning. THERAPIST 2: What do you mean, Barry? BARRY: I went to tell her that Jill needed to get to soc-
cer, and she practically bit my head off! DEBRA: Because you had told me eight times already.
I wasn’t manic, I was just getting annoyed. Even Jill said something about you overdoing it.
This became a theme throughout the treatment: Barry tended to overlabel Debra’s mood swings, to the extent that he often called her “manic” when the real issue appeared to be her transient irritability. He also called her “depressed” when Debra felt that she was just “relaxing, feeling bored . . . trying to unwind and keep to myself for a while.” The therapists were careful not to attribute blame or to take sides with either of them. Therapist 1 said,
“I think this is a very hard distinction to make. I wish I could give you a simple rule for determining when Debra is in and out of an episode. But as you’ve seen, it’s not always so clear. I usually suggest that people go back to the symptom list and ask, ‘Is there more than one of these symptoms? Does irritability go with more sleep disturbance? Racing thoughts?’ Just being annoyed is not enough to be called ‘manic,’ unless it’s ongoing, it cuts across different situations, it goes along with some of these other symptoms and causes you problems in getting through your day.”
The therapists explained that mood episodes are due to “vulnerability—your individual biology and genet- ics—with the stress you encounter.” They supplement- ed this discussion with a handout on risk factors (e.g., substance abuse, sleep irregularity, unpredictable daily routines, family conflict) and protective factors (e.g., regular medications, good family communication). Debra described her mother’s long-term, recurrent de- pression and her father’s alcohol abuse: “My mom was probably bipolar, but we just didn’t call it that back then.”
The clinicians encouraged a discussion of Debra’s prior depressive episodes. Barry became very vocal when discussing her risk factors: He believed that crowded places (e.g., shopping malls) made her hypomanic, and that alcohol, even in small amounts, contributed to her sleep disturbance and her hypomanias.
Next, the clinicians helped Barry and Debra devise a relapse prevention plan:
THERAPIST 1: The people who do best with this illness are those who can rely on their spouses and other close family members at times of crisis. It’s a fine line you have to walk between being able to turn to your spouse and say, “I think I’m getting sick again,” and take some of their advice without giving up con- trol altogether. Debra, when your moods are going up and down, you are going to want more control. Barry, maybe you feel like you’re walking a fine line as well: You want to say, “Yes, you are getting sick, and I’d like to help you,” without rubbing it in, to be able to give suggestions without taking over.
BARRY: That’s one thing we have in common. We’re both control freaks.
THERAPIST 1: Well, maybe the fact that you both like to be in control of your fate was part of what attract- ed the two of you in the first place [reframing]. But
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like many things that attract people initially, some- thing like not wanting to give up control can become a problem later.
The partners came to some agreement about what the prodromal signs of Debra’s hypomania looked like (e.g., increased interest in household projects, getting up extraordinarily early, irritability that occurred in multiple situations) and some of her risk factors (e.g., alcohol). They conjointly developed a relapse preven- tion plan that involved keeping emergency phone num- bers handy, avoiding alcohol, and avoiding high-stress interpersonal situations (e.g., conflicts between Debra and her mother, or extended discussions of household finances). Barry and Debra also discussed how they could communicate if her symptoms started to esca- late. Barry admitted that he “had to learn not to lash out” at such times, and not to “just blurt out every- thing I think.” Interestingly, both showed resistance to the suggestion that Debra maintain regular sleep–wake cycles, even on weekends, when she had her worst mood swings. Barry scoffed, “Maybe we should just join the Army,” and both emphasized that they were not about to give up their love of late-night partying.
The psychoeducation module ended with a discus- sion of the effects of the illness label on Debra’s sense of self. She had been alluding throughout the first six sessions to her discomfort with the diagnosis of bipolar II disorder.
THERAPIST 1: Sometimes when we go through our symptom lists and talk about the causes of bipolar disorder, people can feel labeled or picked apart. Debra, have you ever felt that way in here?
DEBRA: When I first came in here, I felt picked on. I felt like it was “blame Debbie time,” and now there was this real biological reason to pin all our problems on.
THERAPIST 1: I hope you don’t think we’re saying that all of your problems as a couple stem from your bi- polar disorder.
DEBRA: No, I think you guys have been fair about that. But sometimes I think Barry is just objecting to me as a person.
THERAPIST 1: Do you think the line between your per- sonality and your disorder gets blurred?
DEBRA: Yes, and to me they’re very different.
THERAPIST 1: I’m glad you’re bringing this up. I think that’s very important, to be very clear on when we’re just talking about you, your styles of relating to peo- ple. . . . Not everything you do has to be reduced to this illness.
BARRY: And I probably do bring it up [the illness] too much.
DEBRA: (becoming activated) Yes, and you bring it up in front of other people. . . . That can be a real problem for me. We used to have such great conversations! I get tired of talking with you about my disorder all the time. That’s all you seem to wanna talk about.
BARRY: (startled) Why haven’t you told me this? DEBRA: I probably do need to tell you. . . . I just want
more of a happy medium, between talking about it and not.
BARRY: So what do you want? DEBRA: (becoming tearful) I’m not sure. THERAPIST 1: (after a pause) I think it’s understandable
that you wouldn’t know. . . . You’re not always sure how much help you need from Barry. Maybe you’re trying to find a good balance. That may take some time. I hope you don’t feel that all we’re interested in is your disorder, and not in you as a person [examines reactions to psychoeducational material].
DEBRA: I usually don’t feel that way, except when I try to do the damn mood chart (chuckles) [acknowl- edges emotional pain associated with this assignment]. I just want to have conversations with Barry like I have with my girlfriends. I’d like to talk about things other than my illness and my doctors.
Communication Enhancement Training (Sessions 8–14)
During Session 8, the therapists introduced CET to the couple. Barry and Debra both described a “de- mand–withdrawal” pattern in their communication. Barry would become intrusive in trying to understand Debra’s mood state, and Debra would withdraw and be- come uncooperative. Debra admitted that she had a dif- ficult time acknowledging being depressed and talking about it, because “you just didn’t do that in my family.” She grew up in a Southern family, where “you didn’t air your dirty laundry.” In contrast, Barry hailed from Los Angeles, where “you might spill your guts to whoever was stuck in traffic next to you.”
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The therapists began by exploring the demand–with- drawal pattern:
THERAPIST 1: This is one of the dynamics we’ve seen in couples dealing with bipolar disorder. People with the disorder can get irritable with their spouses, and then their spouses react because they feel under at- tack, and when they react, the arguments can re- ally spiral. The person with the disorder feels there’s something he/she is legitimately angry about, but their spouse sees the anger as evidence of the illness.
BARRY: Well, my problem is that Debra’s not aware of her symptoms.
DEBRA: I’m aware of them, but I wanna be left alone about them. You finish my sentences.
BARRY: And then you walk out of the room. You don’t want to have anything to do with normal communi- cation. It’s just like it was with your parents . . .
DEBRA: When I’m in that state [depression], the last thing I want is a serious conversation or to have someone question what I want to do or why.
THERAPIST 2: Let’s talk about what happens between the two of you [draws couple back to relationship focus]. When you try to talk about something, what happens? One of you just won’t talk? You do talk, but it doesn’t go well?
BARRY: She procrastinates, she won’t deal with things; then I yell; then she won’t be around me and she withdraws; and then I start thinking about how long I can live like this.
THERAPIST 2: Debra, how would you describe it? DEBRA: Barry gets frustrated when I don’t give him the
answers he’s looking for, and then I feel bad that I frustrated him, and he feels bad that he got upset at me, and then I feel bad that I made him feel bad about upsetting me.
THERAPIST 2: Is that something you’d like to work on more—your communication as a couple?
BARRY: Yes. There’s been no communication because of the bipolar disorder. I don’t know if we’d have these problems if she weren’t bipolar. She gets depressed, her thoughts don’t get communicated, she never even tries . . . and that reminds me of what I was gonna ask you: Do you think she might have ADD [attention deficit disorder], as well as being bipolar?
DEBRA: Oh, no, here we go . . .
THERAPIST 1: Barry, no one can tell for sure, but re- gardless of what the cause is, it sounds like you’re ready for us to start focusing more on your relation- ship [redirects discussion but doesn’t directly challenge Barry’s definition of the problem]. At least part of what you’re describing sounds like the habits you have communicating with each other as a couple. We’ll be teaching you some fairly straightforward skills for talking to each other, like how to praise each other for things done well, how to listen, and how to ask for changes in each other’s behavior. This will help you during these cycles, whether they be real mood cycles or just rocky periods in your rela- tionship [provides rationale for upcoming communica- tion module].
DEBRA: Yeah, I need to learn how to argue. He’s a law- yer; he’s a much better arguer than me.
BARRY: (still angry) But you see, no one ever said a damn thing in your family; no one was ever really there. So, of course, you’re going to react to me because I’m passionate, and then when I get really pissed off, you finally take stock and listen. It’s the only way I can get through to you.
THERAPIST 1: I think there’s a lot for us to work with here. Debra, I’d like to take you off the “bipolar hook” for a while, and let’s just talk about how you both act and react with each other. We don’t have to work only on your communication about bipolar disorder.
BARRY: But that’s all about doing it in here. . . . How are you gonna know how we communicate at home?
THERAPIST 1: We’re gonna bug your house. (laughter) We’ll do some exercises in here that involve role play- ing new ways of talking and listening, but you’ll have to practice these new ways between sessions at home. I personally think this will benefit you a great deal, if you have the time to do it [expresses optimism].
The therapists were gaining a better understand- ing of this couple’s communication patterns. The de- mand–withdrawal interaction derived in part from their different family histories, but it was equally true that Barry was rewarded for being critical; it got re- sults, even if these results were accompanied by Debra’s resentment. They disagreed on the extent to which these communication patterns were driven by her bi- polar disorder. Barry assumed that most or all of their
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couple problems could be attributed to the disorder, but Debra saw this assumption as just an attempt to blame her for everything. The therapists’ take was that the marital dynamics were independent of Debra’s mood swings but became magnified by her hypomanic and depressive episodes. During hypomanic episodes, she was more touchy and reactive and Barry became more critical; when depressed she was more likely to withdraw, and he was more likely to accuse her of not trying hard enough.
In Session 9, Therapist 2 introduced the Express- ing Positive Feelings handout, in which each partner is directed to praise the other for some specific behavior and to tell the partner how this behavior makes him/ her feel. Placing this skill at the beginning of commu- nication training increases the likelihood that family members collaborate when dealing with more difficult issues. The therapists first modeled the skill. One of them praised Barry, saying, “I appreciate you taking the long drive up here [to the clinic] and making an adjustment to your schedule to make this possible. . . . It makes me feel like you value what we do here.” Barry expressed appreciation for the compliment. The thera- pist then asked Barry and Debra to turn their chairs toward each other and select a behavior to praise in each other. Interestingly, neither had trouble selecting a topic. The problem was staying with positive emotions and not letting negative ones leak in.
BARRY: I appreciated your taking Jill to soccer on Wednesday. It made me feel like you . . . like you knew I was overwhelmed that day, and that, you know, I’m usually the one doing all the parenting while you . . .
THERAPIST 2: (interrupting) Barry, I’d like to stop you before we get into that. Debra, can you tell me what you liked so far about how Barry said that? Did he follow the instructions on this sheet?
DEBRA: Well, like you said, he was starting to get into it, but I liked the first part. I’m glad he feels that way.
BARRY: Do you feel I give you enough positive feed- back?
DEBRA: (pause) You have your days. THERAPIST 2: Barry, I thought you did that pretty well.
Could you try it without the tail at the end? BARRY: (Chuckles.) There you go, stealing my thunder.
OK, um, Deb, thanks again for taking Jill to soccer.
It made me feel like you . . . like my schedule is im- portant to you, and that you’re thinking of me.
THERAPIST 2: Good. Debra, what’d you think? DEBRA: Much better. BARRY: Sometimes I think I was put on this earth to
learn tact.
Sessions 10 and 11 of CET focused on active listen- ing skills. One member of the couple listened while the other spoke, first about issues outside of the marriage (e.g., work relationships) and then about couple-relat- ed matters. Both Barry and Debra required coaching. Specifically, Debra tended to “space out” when Barry spoke and required prompting to stay with the issues. She acknowledged that she sometimes felt she was being tested by Barry when he talked to her, to determine whether she could come up with thoughtful, intuitive replies. Her “checking out” was a way of coping with the performance anxiety that she experienced when lis- tening to him.
Not surprisingly, Barry’s difficulty with listening centered on withholding his natural tendency to give advice. When Debra began to talk, he would listen re- flectively for a minute or two, but then would begin to ask questions, such as “Well, when are you gonna call that person?” or “Last time we talked, you said you were going to finish that resumé. Why haven’t you?” Repeated practice within sessions—supplemented by homework assignments to practice these skills—led Barry to become more aware of what he was doing. During a particularly poignant moment, he admitted, “I don’t like the way I react to her. . . . I don’t like the person I’m becoming.”
As FFT passed the 3-month point and the frequency changed to biweekly, the clinicians introduced po- tentially more heated forms of communication, such as the partners making requests for changes in each other’s behaviors and expressing negative feelings (Ses- sions 12–14). At this point, Debra was not as depressed as she had been during the assessment phase, although Barry continued to complain about her low function- ing. He argued that she had “become unable to tell me what she’s accomplished during the day” and that she tried to make it appear that she had accomplished things that she had not. He labeled this as her “lack of follow-through” problem. In contrast, Debra became increasingly assertive about his “micromanagement” of her behavior.
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THERAPIST 1: Let’s talk next about how you ask for changes in each other’s behavior. What’s an appro- priate way to ask someone to do things differently? (Gives Barry and Debra the Making a Positive Request handout.) There are three steps to this: look at the person, say what you would like him or her to do, and how it would make you feel. Debra, a minute ago you were talking about how Barry microman- ages you. Can you turn this into a positive—ask him what you would like him to do differently? How can he ask you to follow through without nagging you?
DEBRA: (looking at handout) Uh, Barry, it would really make me happy if you . . . in situations where there’s a dilemma, if you’d give me a little more freedom.
BARRY: For example? Do you mean you want us to do things at your pace?
THERAPIST 1: Barry, let it come from her. DEBRA: Um, like, if there’s some shopping to do, it
would help me out if I could just say, “Yes, this is on my list and I’ll do it . . . if you could wait for me to get it done in my own time.” That would help ease the tension.
THERAPIST 2: Barry, how did you feel about how Debra asked you? Did she follow this sheet?
BARRY: I think she asked me just fine, but my question is, will she then do the shopping?
DEBRA: I think it would really help me if we had some plan—like agreeing that if I do this part of the shop- ping, you’ll do that part. Maybe that would stop me from saying, “I’ll show him. He’s not gonna run my life; I’m not gonna do it his way.”
THERAPIST 1: Sure. When a person feels one-down they often react by refusing to go along with the plan, even though going along with it might be of help to them personally. Debra, do you get into that sometimes?
The therapists were encouraging assertiveness in Debra, and at the same time gently confronting what Barry had earlier called her “passive–aggressiveness.” Next, they asked Barry to make a positive request of Debra.
THERAPIST 2: Barry, can you think of something you could ask Debra to do, to change her behavior?
BARRY: (looking at therapists) Where do I start? OK, Deb, it’s very important to me . . .
THERAPIST 2: Can you tell this to her? BARRY: (Turns toward Debra.) OK, it’s very important
to me that you not just walk away when we have dis- cussions. That you don’t just withdraw. Especially when we talk about Jill and our differences about her. That really irritates me.
The therapists again observed Debra withdraw in re- action to Barry’s critical comment. They commented on her reactions.
THERAPIST 1: Debra, what’s happening now? You seem like you’re checking out.
DEBRA: (Snaps back, smiles.) Yeah, I guess I am. What were we talking about?
BARRY: You see, I think that’s part of her attention defi- cit disorder. Do you think she needs Ritalin?
THERAPIST 1: Barry, in this case, I don’t think so. I think that what happened, Debra, if I can speak for you for a moment, is that you withdrew because you felt you were under attack.
DEBRA: That’s probably true. He got into his “You do this, you do that.”
BARRY: ( frustrated) Well, you just asked me to change something! Am I supposed to do all the work here?
THERAPIST 1: Barry, I’m going to encourage you to try again. Only this time, I’d like you to be more aware of how you phrase things. Notice you said what you didn’t want her to do—withdraw when you were talking to her. That’s quite important. But what would you like her to do instead?
BARRY: I want her to engage with me! To talk it out! THERAPIST 1: Can you try again, only this time tell her
what you want her to do? BARRY: (Sighs.) Deb, when we talk, I’d really like . . . I’d
really appreciate it if you’d hang in there and finish talking to me, especially about Jill. That would make me feel, I don’t know, like we’re partners.
THERAPIST 2: Barry, that was much better, and I’ll bet it was easier to hear. Debra?
DEBRA: Yeah, I liked it . . . that’s easier. We need to do more of this.
Much emphasis was placed throughout CET on be- tween-session homework assignments. Debra and Barry
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were encouraged to hold weekly meetings and to record their efforts to use the skills. It was difficult for them to avoid slipping into old patterns, but both reported a reduction in tension when they remembered to use the skills. The clinicians moved on to the problem-solving module.
Problem Solving and Termination (Sessions 15–21)
FFT sessions were held less frequently (biweekly) in the fourth, fifth, and sixth months. In Session 15, after explaining the rationale for problem solving, the thera- pists asked Debra and Barry to identify several specific problems for discussion, then reviewed the problem- solving steps with them.
The first issue they chose seemed superficial at first. They had two cats, one of which belonged to Debra (and had come with her from a previous marriage) and the other of which Barry had bought. They disagreed on how much the cats should be fed: Debra “wanted mine to be fat” and fed it frequently, whereas Barry wanted his to be thin. As a result, Barry’s cat was wak- ing them up in the middle of the night, needing to be fed. The resulting changes in Debra’s sleep–wake cycles had resulted in her becoming irritable, restless, and possibly hypomanic. Despite a conscientious literature search, the therapists were unable to find any research on the influence of cat diets on the cycling of bipolar disorder.
The couple threw out several alternatives, some of which were not meant seriously: teaching the cats to feed themselves, keeping Debra’s cat in the garage, giv- ing away Barry’s cat, and feeding both cats before the couple went to bed. They eventually settled on the last of these. The problem itself generated humor and play- fulness between them, and they derived some satisfac- tion from being able to deal with it collaboratively.
A second and potentially more serious source of conflict concerned their night life. Both liked going to parties, but Barry liked to stay longer than Debra, who thought that parties contributed to her mood cycling. She tended to become overstimulated by the interac- tions with many people and would quickly become fa- tigued. They considered several alternatives: going to the parties in separate cars, Barry agreeing to leave ear- lier, Debra going to the car and sleeping when she felt tired, and Debra taking an Uber home. They eventu- ally decided to discuss and agree on a departure time before going to a party.
Debra and Barry were able to apply the problem- solving method successfully to other issues, such as pay- ing the bills and helping Jill get to her afterschool activi- ties. They continued to have trouble breaking problems down into smaller chunks, and tended to “cross-com- plain” or bring up larger problems in the middle of try- ing to solve smaller ones. Barry often complained, “We aren’t dealing with the source of these problems, which is her bipolar disorder. We wouldn’t have these prob- lems if she weren’t bipolar.” Again, the therapists did not challenge his definition of the problem but contin- ued to offer the message that regardless of the causes of the problems, the couple still needed to work collabora- tively to generate acceptable compromises.
The last three sessions were held monthly. During this interval, Debra’s depression had largely remitted, and she obtained a job working in sales at a department store. The therapists began the termination phase of treatment, which focused on reviewing what the couple had taken away from the psychoeducation, CET, and problem-solving skills modules. Both reported that their relationship had improved, and that they “occa- sionally” used the communication skills at home. The therapists commented on how far they had come and encouraged them to pick a time each week to meet and rehearse one or more of the skills.
Barry was not entirely convinced of Debra’s clinical improvement, however. In one of the final sessions, he returned to the issue of Debra’s symptoms and her “un- willingness” to follow through on tasks such as cook- ing, depositing her paycheck, cleaning Jill’s clothes, and doing other tasks they had agreed she would perform. The following interchange ensued:
BARRY: (Laughs nervously.) I had this dream the other night that I was getting married, and I knew that I was marrying Debra, but I couldn’t see her face, and I wasn’t sure it was really her. And I wasn’t sure if I should be there.
THERAPIST 1: And you were standing in front of every- one wearing your pajamas as well.
BARRY: (Laughs.) Yeah, and I was about to take the exam that I hadn’t studied for. But really, sometimes I feel like she’s not the same person, especially when she doesn’t want to follow through on things we’ve talked about.
THERAPIST 1: Let me give you some perspective on this. I think a dilemma many spouses face is “Should
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I stick it out with my husband or my wife, or should I leave and take care of me?” There are certainly people who do that, who leave, and there are many others who hang out and wait for things to get better, which in fact they often do.
BARRY: And I think things have gotten better. DEBRA: I think so. I don’t know why you’re being so
negative. BARRY: Well, if you . . . THERAPIST 1: (Interrupts.) Let me finish this thought.
Barry, I think it’s critical for you to make a distinc- tion in your own mind between what Debra can and can’t control. That’s sometimes vague between the two of you. When you say she doesn’t want to follow through, that certainly sounds like an intentional be- havior—something she’s doing to hurt you or annoy you. Debra, do the problems with following through ever feel like they’re about problems with your con- centration? Your attention or your memory?
DEBRA: (nodding emphatically) Absolutely! If you could get him to realize that, we’d be a lot farther along.
BARRY: That memory stuff—is that her bipolar disor- der or her attention deficit disorder?
THERAPIST 1: I’m not sure that’s really the question. That’s just a diagnostic distinction, and I’m not sure my answering one way or the other will help you. Maybe what you’re really wondering is whether these problems are controllable by her or not.
BARRY: (Pauses.) Yeah, probably. THERAPIST 1: If I were in your position, the things
that would really anger me would be those things I thought she was doing intentionally.
BARRY: Yeah, and I don’t always think about that. THERAPIST 1: Debra, am I being accurate here—that
sometimes Barry gets upset about things that are re- ally hard for you to control?
DEBRA: Totally. Like if I had a broken leg or some- thing, he probably wouldn’t complain if I held him up.
In this segment, the therapist was addressing di- rectly what he felt was a major source of Barry’s criti- cal attitudes toward Debra: the belief that many of her negative behaviors were controllable and intentional. In some instances, Barry may have been right about Deb- ra’s motivations. But questioning the controllability of
her symptoms forced him to consider a different set of causal explanations for her behavior. The distinction between controllable and uncontrollable behavior is a key point in the psychoeducational treatment of fami- lies of patients with bipolar disorder.
Barry and Debra’s Progress
After completing FFT, Debra continued to have mild periods of depression despite her adherence to medica- tion. Her depressions were unpleasant but not so severe that she was unable to keep her job or attend to her par- enting duties. Her brief hypomanic periods sometimes caused arguments between herself and Barry but were not otherwise debilitating. They were communicating better, and both agreed that Barry was more patient and less critical.
When reviewing the changes in her clinical state, Debra recalled the line from a now famous movie: “What if this is as good as it gets?” Although she was more functional, she expressed chagrin that she could not have the life she had wanted—a successful career, a more intimate relationship with her husband, more friendships, an easier relationship with her daughter, and more financial success. The reality of her disorder and its psychosocial effects were difficult for her to ac- cept. However, she felt that FFT had been helpful for her moods, especially the communication and problem- solving training. She acknowledged that her medica- tions had also improved her mood and energy level, and she had no inclination to discontinue them. Barry found the psychoeducation module to be the most use- ful, and agreed that their relationship had improved but attributed the improvement mostly to her clinical state: “When she’s feeling better we get along better, and that’s really all there is.”
The therapists offered Debra a referral for individual therapy, but she decided to forgo further psychosocial treatment for the time being. Barry was given the name of a local Depression and Bipolar Support Alliance (DBSA) group for spouses of persons with mood dis- orders.
CONCLUSIONS
Family psychoeducational treatment is a useful adjunct to pharmacotherapy in the aftermath of an episode of bipolar disorder. However, not all patients with bipolar disorder have families, and individual or group treat-
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ment approaches are important alternatives to consider. The finding that mood-stabilizing and antipsychotic medications are more powerful in alleviating manic than depressive symptoms, whereas the reverse may be true for psychotherapy, is an argument for combining medical and psychosocial interventions in the outpa- tient maintenance of the disorder.
There is limited research on which families are the best candidates for FFT. In several of our trials, patients in high-EE families have shown greater reductions in mood severity scores over 1–2 years than those in low- EE families. But reductions in relapses have been ob- served in patients from both high- and low-EE families treated with FFT. Our clinical observations also sug- gest that there are subgroups of patients who do not respond well to FFT. Specifically, patients who are un- usually resistant to accepting the diagnosis often resent the educational focus of FFT. These patients usually see their troubles as having external origins (i.e., being mis- treated by others) and resist interventions that require them to take more responsibility for their behavior. They may also reject pharmacotherapy. Sadly, we have seen many patients go through several hospitalizations before the reality of their disorder sets in.
A different kind of resistance originates from viewing the disorder as biologically based. Some patients prefer to limit their mental health contacts to a psychiatrist for medication and regard psychotherapy as irrelevant. We see nothing wrong with this position; a subset of patients does function well on medication only. Future research needs to determine whether this self-selected group is different from patients who request psycho- therapy, in terms of symptomatic, course-of-illness, stress, or genetic variables. Equally importantly, some patients with bipolar II depression may recover just as quickly with psychotherapy alone as with medications (Swartz, Frank, & Cheng, 2012).
Family members are sometimes a major source of re- sistance. Their reasons can include a desire to distance themselves from the patient (whom they may have tried to help for years without reward), time or distance constraints, or the discomfort of talking about fam- ily or couple issues in front of a stranger. More subtle is the fear of being blamed for the disorder (Hatfield, Spaniol, & Zipple, 1987). The family therapy move- ment has come a long way, but it still has its roots in a culture that faulted parents for causing mental illness. The theoretical model underlying FFT does not in any way link poor parenting to the onset of bipolar disor- der. Nonetheless, a clinician often needs to make clear
early in treatment that he/she does not adhere to this antiquated position.
FUTURE DIRECTIONS
Future studies need to focus on implementation of psychotherapy with patients in “real-world” (typically, community mental health) settings, by the clinicians who work in these settings and the time constraints within which they work. As explained earlier, FFT was found to be effective in stabilizing depression and maintaining wellness in the large-scale STEP-BD study of community effectiveness, which included therapists working in 15 clinic sites (Miklowitz et al., 2007a, 2007b). It remains to be seen whether FFT, along with CBT, IPSRT, and group psychoeducation approaches, will be taken up by practicing clinicians.
A related problem is determining the proper structure of FFT. In many community settings, insurance com- panies only pay for six to eight sessions. FFT is rather time-intensive (12–21 sessions over 4–9 months), and research is needed to determine which of its components predict the greatest proportion of variance in patient and family functioning and quality of life. Some families may benefit from just the psychoeducation module or just the communication module. Perhaps these modules could be streamlined without a significant loss in treat- ment effect size. Ideally, decisions to modify treatments such as FFT will be based on clinical outcomes research rather than solely on cost containment.
FFT and other psychotherapy treatments are now being tested in randomized trials with child and ado- lescent patients with bipolar disorder and genetically vulnerable children who are showing early prodromal signs. The fact that bipolar disorder even exists in school-age or early adolescent youth has only recently been recognized, and factors that predict the onset of the full disorder—such as the presence of mood insta- bility and a family history of mania—are being identi- fied (Hafeman et al., 2016; Birmaher et al., 2018; Faed- da et al., 2019). Our research indicates that giving FFT in the early, prodromal stages of the disorder increases time in remission and delays future mood episodes; we have not, however, been able to show that the disorder can be prevented (Miklowitz et al., 2013; Miklowitz, Schneck, et al., 2020). Nonetheless, the negative symp- tomatic and psychosocial consequences of bipolar dis- order may be mitigated through early detection and carefully planned preventive interventions.
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ACKNOWLEDGMENTS
The research reported in this chapter was supported by Na- tional Institute of Mental Health Grant Nos. MH43931, MH55101, MH42556, MH62555, MH073871, MH077856, MH093676, MH093666, MH097007, MH117200, and MH123575; Distinguished Investigator Awards from the National Association for Research on Schizophrenia and De- pression and the Brain and Behavior Research Foundation; the American Foundation for Suicide Prevention and AIM for Mental Health; and the Attias, Danny Alberts, Deutsch, Kayne, Max Gray, and Robert Sutherland family foundations.
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Among the most remarkable advances in the last two decades is the direct treatment of “positive” symptoms of schizophrenia with psychological treatments. Many of these advances originally ema- nated from the United Kingdom, where a group of senior investigators working in the context of the National Health Service (NHS) developed and evaluated these approaches. Nick Tarrier was at the forefront of this group during this period. In the context of case management and antipsychotic medication, this very creative mix of treatment components has been proven effective for people who do not fully respond to medication, as well as those in an acute stage of the disorder. Evidence is now sufficient that government-sponsored treatment guidelines in both the United Kingdom and the United States have incorporated these approaches into comprehensive treatment recommendations. More recently, clear evidence has emerged supporting the use of these procedures for preventing the onset of the disorder for those at risk. The thrusts and parries of these techniques are illustrated in the case of “Jim,” who had developed an intricate web of delusions reminiscent of Russell Crowe’s char- acter in A Beautiful Mind, concerning complex schemes by others, including friends and family, to take advantage of him and steal his money and his girlfriend. The therapist’s skill in carrying out these approaches is never better illustrated than in this chapter. These empirically supported psychological treatments represent the front line of our therapeutic work with people who are severely distressed by psychotic experiences. —D. H. B.
schizophrenia is a serious mental health problem that is characterized by positive symptoms of hal-
lucinations, delusions, and disorders of thought. Typi- cally, hallucinations are auditory, in the form of hearing voices that often talk about the person and in the third person, although hallucinations can occur in other senses. Delusions are strongly held beliefs that are cul- turally unacceptable or that other people do not share and often involve a misinterpretation of perception or experience. The content of delusions may include a va- riety of themes, including alien control; persecution; reference; and somatic, religious, or grandiose ideas. Disorders of thought are inferred from disruption and disorganization in language. Hallucinations and delu-
sions, and sometimes thought disorders, are referred to as “positive symptoms” and reflect an excess or distor- tion of normal functioning. “Negative symptoms” are also frequently present and reflect a decrease in or loss of normal function, including restrictions in the ex- pression of emotions, in the fluency and productivity of thought and language, and in the initiation of behavior. The consequences of these symptoms can be disrup- tions in personal, social, occupational, and vocational functioning. Comorbid disorders, especially depression and anxiety, are frequently present and further impair functioning. Suicide risk is high. Aspects of description, diagnosis, and classification of schizophrenia and other psychotic disorders have stimulated much debate and
C H A P T E R 13
schizophrenia and other Psychotic Disorders
Nicholas Tarrier Katherine Berry
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controversy over the decades, and details can be found in most psychiatry and abnormal psychology text- books. They do not concern us here except to say that there can be considerable variation in clinical presenta- tion between people and in the same person over time. Furthermore, cognitive-behavioral therapy for psycho- sis (CBTp) in recent years has mainly focused on the reduction of positive symptoms and associated distress, and that is our major concern in most of this chapter. The standard treatments for schizophrenia remain an- tipsychotic medication and some type of case manage- ment, and CBTp described in this chapter is assumed to be in addition to this. Indeed, recent revisions to the National Institute for Health and Care Excellence (NICE; 2014) guidelines in the United Kingdom, and the Schizophrenia Patient Outcomes Research Team (Dixon et al., 2010) in the United States, have suggest- ed that CBTp be offered alongside medication for all those with schizophrenia. The authors of the recently updated American Psychiatric Association Practice Guideline for the Treatment of Patients with Schizo- phrenia (American Psychiatric Association, 2021), also voted unanimously in favor of recommending CBTp.
DEVELOPMENT OF COGNITIVE‑BEHAVIORAL THERAPY FOR SCHIZOPHRENIA
Cognitive-behavioral therapy (CBT) for schizophrenia, although following a common theme and set of prin- ciples, has developed in a number of centers, mostly in the United Kingdom, and has been informed by a number of theoretical and conceptual perspectives. A dramatic expansion in the use of CBT in the 1980s and 1990s in the treatment of anxiety and affective disorders influenced clinical psychologists in the field of schizophrenia, who were trying to understand and treat schizophrenia from a psychological perspective. This was especially true in the United Kingdom, where clinical psychologists treated a range of mental health problems in adults and were able to transfer their treat- ment methods across diagnostic groups. The structure and function of a system of universal health care in the United Kingdom, the National Health Service (NHS), facilitated such skills transfer and multidisciplinary work. Furthermore, funding of the professional train- ing of health professionals, especially clinical psycholo- gists, has aided awareness and dissemination of CBT in general and for people experiencing psychosis in par- ticular. However, dissemination of treatments into the
health service and the universal availability of CBTp has been slow and not without its problems (Berry & Haddock, 2008; Brooker & Brabban, 2006; Ince, Had- dock & Tai, 2016; Tarrier, Barrowclough, Haddock, & McGovern, 1999).
RESEARCH EVIDENCE
Clinical, ethical, and economic considerations have encouraged clinical practitioners to be guided by an evidence base produced from evaluations of treatments. The evidence develops from uncontrolled studies and small-scale projects to controlled studies, then to large randomized controlled trials (RCTs) of efficacy and ef- fectiveness. In spite of criticisms of the appropriateness of RCTs in mental health (Richardson, Baker, Burns, Lilford, & Muijen, 2000; Slade & Priebe, 2001), they remain the “gold standard” by which all treatments are judged (Doll, 1998; Pocock, 1996; Salkovskis, 2002; Tarrier & Wykes, 2004). Once a database of controlled trials has been established, then meta-analysis can pro- vide a measure of the average level of therapeutic ef- fect for that treatment. For schizophrenia, a number of published meta-analyses indicate that CBTp is effective in treating symptoms in schizophrenia and related psy- choses (e.g., Burns, Erickso, & Brenner, 2014; Gould, Mueser, Bolton, Mays, & Goff, 2001; Pilling et al., 2002; Rector & Beck, 2001; Tarrier & Wykes, 2004; van der Gaag, Valmaggia, & Smit, 2014; Zimmermann, Favrod, Trieu, & Pomini, 2005; Sarin, Wallin, & Wid- erlöv, 2011; Turner, van der Gaag, Karyotaki, & Cuij- pers et al., 2014), although there have been conflicting findings (e.g., Lynch, Laws, & McKenna, 2010; Jones, Hacker, Cormac, Meaden, & Irving, 2012; Jauhar et al., 2014; Laws, Darlington, Kondel, McKenna, & Jau- har, 2018). Discrepancies in the results of meta-analyses reflect debates about which data should be included in effect size calculations—for example, whether trials with different intervention targets are included, wheth- er both group and one-to-one format intervention are included, whether the quality of the trial is taken into consideration, and whether CBTp is compared to other therapies or treatment as usual (Thomas, 2015).
In terms of effect sizes, an earlier seminal review and meta-analysis by Wykes, Everitt, Steele, and Tarrier (2008) indicated that effect sizes were 0.476 for CBTp on positive symptoms from 30 trials, 0.474 for negative symptoms from 14 trials, 0.477 for social functioning from 11 studies, and 0.424 for depression from 11 stud-
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ies. The authors noted that more rigorously designed studies tended to have lower effect sizes, which means that weaker studies may overestimate effects. In a more recent meta-analysis including 52 studies, Jauhar et al. (2014) reported a pooled effect size of –0.33 favoring CBTp from 34 studies reporting on overall symptoms and a pooled effect size of –0.25 favoring CBTp from 33 studies of positive symptoms. However, as in the ear- lier review, results were moderated by the rigor of the study design.
Symptom Management in Schizophrenia
In spite of maintenance medication, a considerable per- centage of patients with schizophrenia continue to have persistent hallucinations and delusions that do not re- spond further to medication. The majority of the CBTp studies have been carried out with people who have ex- perienced symptoms over a number of years and have not fully responded to medical treatments. A review and meta-analysis of medication-resistant psychosis in- cluding 12 RCTs (16 studies) indicated that beneficial effects of CBT at posttreatment for positive symptoms (Hedges’s g = 0.47) and for general symptoms (Hedges’s g = 0.52). Effects were maintained at follow-up for both positive and general symptoms (Hedges’s g = 0.41 and 0.40, respectively). Another strategy has been to adopt a less generic approach and instead use CBTp to target a more defined participant group or specific symptoms. Examples of more targeted approaches include CBT to reduce harmful compliance with command hallucina- tions (Birchwood et al., 2014); CBT to treat delusional beliefs by addressing worry, insomnia, and reasoning biases, which are hypothesized to maintain the per- sistence of delusions and related distress (Freeman, 2011); and a recovery-focused CBT package to improve functioning and negative symptoms in people with schizophrenia who had neurocognitive impairments (Grant, Huh, Perivoliotis, Stolar, & Beck, 2012). In a recent article, Lincoln and Peters (2019) systematically reviewed and discussed CBT symptom-specific ap- proaches to delusions and hallucinations. The authors identified 12 RCTS evaluating symptom-specific ap- proaches (four focused on delusions and eight focused on hallucinations). All trials reported effect sizes above 0.4 compared to treatment as usual on at least one pri- mary outcome at posttherapy, and some effects were substantially larger. Effects were maintained for five of the seven studies that had significant primary outcomes and reported follow-up comparison data, although
most of the follow-up periods were brief. The authors concluded that although targeted studies are still in their infancy, as nine of the trials were pilot trials, the results were promising, with higher effects compared to the small-to-moderate range found for generic CBTp.
Symptom Recovery in Acute Schizophrenia
A handful of studies has investigated the use of CBTp in the treatment of patients hospitalized for an acute psychotic episode. Because the participants may well be suspicious, agitated, and unstable, the therapy is often implemented as a “therapy envelope,” which comprises a range of durations of therapy that can be delivered in a flexible manner. The Study of Cognitive Reality Align- ment Therapy in Early Schizophrenia (SoCRATES; Lewis et al., 2002), which is by far the largest and meth- odologically most rigorous study, recruited 309 patients with early-onset schizophrenia and produced an effect size of 0.12. In an 18-month follow-up of this trial, both CBTp and supportive counseling continued to confer clinical benefit over treatment as usual (TAU) alone, although there was a trend toward significance for audi- tory hallucinations to respond better to CBTp (Tarrier, Lewis, et al., 2004).
There have been two recent reviews of inpatient psy- chological therapy for inpatients. A systematic scoping review by Jacobsen and colleagues found 65 studies over- all evaluating psychological therapies delivered during acute inpatient admissions including 35 studies of CBT (Jacobsen, Hodkinson, Peters, & Chadwick, 2018). A full range of study designs were included in the review, from single-case studies to large-scale RCTs, but RCTS were more likely to describe CBT rather than non-CBT interventions. The review was a scoping review, so the authors made no formal attempt to synthesize efficacy data and draw any firm conclusions in terms of what psychological interventions are most efficacious within acute inpatient settings. However, on the basis of re- ported outcomes in the studies, they did conclude that there appears to be some promising evidence for the role of CBT-based approaches in reducing psychotic symp- toms and reducing risk of relapse over the short term. In another recent review, Paterson and colleagues (2018) conducted a meta-analysis of psychological therapies for patients in acute mental health settings evaluated using both randomized and nonrandomized trials. The au- thors did not place a restriction on diagnosis or type of therapy, but they looked at the effects of interventions on psychotic symptoms and compared efficacy of CBT
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versus other types of therapy. The authors reported 11 trials of CBT and concluded that there was an overall moderate effect size for symptom improvement in the studies included in the meta-analysis (kappa = 8, stan- dardized mean difference [SMD] = –0.45, 95% con- fidence interval [CI] = –0.85 to –0.07). However, the quality of the evidence was deemed to be low, reflecting issues of small sample sizes, unblinded outcome assess- ment, and nonrandomized designs, also highlighted in the Jacobsen et al. (2018) review.
Relapse Prevention
A number of studies have investigated relapse preven- tion, or the ability of CBTp to prevent or delay future acute episodes. Relapse is an important outcome be- cause of the disruption, distress, and economic costs that symptom exacerbation brings. Studies of CBTp interventions in which relapse prevention was just one of a series of components achieved little success, with four studies showing a mean reduction in relapse of only 1.4% compared to control treatments, whereas studies in which CBTp focused on and was dedicated to relapse prevention resulted in some success, with two studies showing a mean relapse reduction of 21% (Tar- rier & Wykes, 2004). However, Gumley and colleagues (2003) found that CBT focused on relapse prevention greatly reduced hospital admission and relapse rates in people with schizophrenia, as well as significantly im- proving symptoms, global psychopathology, and social functioning. This study emphasized the importance of early relapse indicators, which can trigger negative beliefs about relapse and hospitalization. A study of re- lapse prevention therapy (combing individual and fam- ily CBT) in patients with early psychosis (Gleeson et al., 2009) found that the intervention was effective in re- ducing relapse rates over 7 months of follow-up, but this did not generalize to other outcomes, with no improve- ment in medication adherence, psychosocial function- ing, or quality of life. The authors suggest that focusing on relapse prevention alone is not enough to influence other outcomes, and further consideration of other rel- evant targets for early CBT interventions is important.
A large, multicenter, methodologically robust RCT investigated the effectiveness of CBTp and family inter- vention specifically designed for relapse prevention and symptom reduction in people with psychosis who had recently relapsed (Garety et al., 2008). Both interven- tions had no effects on remission or relapse at 12- or 24- month follow-up, although CBTp reduced depression
and symptoms, and improved social functioning, and family work improved the distress associated with delu- sions. However, in a later study by the same research group, Dunn et al. (2012) used novel statistical meth- odology to reexamine the data. CBTp was found to be effective at increasing months in remission and reduc- ing symptoms, but only when therapy was completed in full and included a range of cognitive and behavioral strategies targeting relapse prevention and symptoms.
Early Intervention
In addition to the effect on individuals with more es- tablished psychoses, there has been growing interest in diverting the course in schizophrenia at an early stage. Morrison and colleagues (2004) reported a study using CBT techniques in this early group to attempt to avert or postpone the first acute episode of the disorder by intervening during a prodromal period. Their tech- nique focused not on frank positive symptoms but on problem-solving difficulties. The results of this first RCT appeared promising. CBTp proved more benefi- cial than TAU in preventing progression into psychosis and the prescription of antipsychotic medication, and reducing symptoms. However, findings from subse- quent studies suggest a more mixed evidence base for early intervention. For example, in a more recent, much larger multisite RCT by Morrison and colleagues that compared cognitive therapy offered to young people at risk for serious mental illness and TAU, earlier find- ings were not replicated. There were no differences between the groups in terms of transition to psychosis over 12–24 months, although the authors discussed the possibility that their study lacked the power to detect a difference due to unexpectedly low conversion rates in the control group, and they questioned the at-risk men- tal state of their sample, as well as the impact of their active monitoring control condition (Morrison, French, Stewart, et al., 2012). Therapy did confer clinically meaningful benefits with regard to symptom frequency and intensity.
In a meta-analysis of CBT for psychosis prevention, Hutton and Taylor (2014) examined evidence for the effectiveness of CBT-informed treatment for preventing psychosis in people who are not taking antipsychotic medication, when compared to usual or nonspecific control treatment. The authors reported findings from seven studies and concluded that the relative risk (RR) of developing psychosis was reduced by more than 50% for those receiving CBT at every time point, including
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6 months, 12 months, and 18–24 months. CBT was also associated with reduced subthreshold symptoms at 12 months, but not at 6 or 18–24 months. However, the authors report no significant effects on functioning, symptom-related distress, or quality of life.
A more recent review and meta-analysis of psycholog- ical interventions for adults with psychotic experiences, but not psychotic disorders, included eight reports from seven studies of CBT, four of which compared CBT (with or without TAU) with TAU only. CBT was supe- rior to TAU in reducing distress (pooled SMD = –0.24 favoring CBT; 95% CI = –0.37 to –0.10). No other sta- tistically significant differences were found for positive psychotic symptoms, depression, anxiety, functioning, or quality of life (Soneson et al., 2020).
Morrison, Hutton, and colleagues (2012) have also been leaders in the development of cognitive therapy for those within early interventions services who discontin- ued antipsychotic medication. All participants received therapy, which was associated with reductions in posi- tive and negative symptoms and functioning at the end of treatment and follow-up, and increases in self-rated recovery at follow-up.
A recent meta-analysis of RCTs of early intervention services (EIS), which include access to CBT, family interventions, and medication as a package of care for those with early psychosis (3–5 years after illness onset), confirmed the positive effects of intervening in this cru- cial period (Correll et al., 2018). Across 10 RCTs, EIS was associated with better outcomes than TAU at the end of treatment for all 13 meta-analyzable outcomes. These outcomes included the following: treatment discontinuation, psychiatric hospitalization, involve- ment in school or work, total symptom severity, posi- tive symptom severity, and negative symptom severity. Superiority of EIS regarding all outcomes was evident at 6, 9–12, and 18–24 months of treatment (except for general symptom severity and depressive symptom se- verity at 18–24 months). In a similar earlier review, Bird and colleagues (2010) found that CBTp alone reduced symptom severity at 2-year follow-up, while family therapy improved relapse rates and hospital admissions at the end of treatment. Therefore, a holistic treatment plan provided by EIS appears advantageous during the initial stages of illness.
Summary of Evidence
The evidence for CBTp reducing positive symptoms in people with long-standing, partially remitted symp-
toms is good. Evidence that CBTp speeds recovery in acutely ill patients to the level of achieving a significant clinical benefit is more equivocal. Reductions in relapse rates are achieved when the intervention focuses on and is dedicated to relapse reduction, but they are disap- pointing for standard CBTp. There is positive evidence that CBTp and family intervention can benefit patients in EIS who are in the early stages of illness. Offering CBT in the prodromal phase appears to provide some additional benefit in terms of preventing full psychosis in vulnerable individuals and levels of distress can be improved.
THEORETICAL ADVANCES
There has been considerable debate about the theo- retical understanding of schizophrenia, with biological explanations being dominant. However, psychological and social factors have consistently been shown to be influential, certainly, in affecting the course of schizo- phrenia, and have been incorporated into stress–vul- nerability models that have emphasized the importance of these psychosocial factors in both precipitating and maintaining psychotic episodes (Nuechterlein, 1987). For example, it is now widely acknowledged that child- hood adversity can play a significant role in the etiol- ogy of the positive symptoms of psychosis. In a seminal review and meta-analysis, Varese and colleagues (2012) concluded that childhood trauma increased the risk of psychosis, with an odds ratio of 2.78. While evidence for this relationship has largely relied on cross-sectional data and relatively small participant samples, a growing number of investigations has replicated these findings in both longitudinal cohort studies (e.g., Cutjar et al., 2010) and large-scale epidemiological studies demon- strating clear dose–response relationships (i.e., the more traumas experienced in childhood, the stronger the risk of developing psychosis later in life; e.g., Shevlin, Do- rahy, & Adamson, 2007; Croft et al., 2019).
Cognitive models have been developed in tandem with advances in CBT (e.g., Garety, Kuipers, Fowler, Freeman, & Bebbington, 2001; Kuipers et al., 2006). It is expected that as these cognitive models develop and are subjected to empirical tests, further refine- ments of CBTp treatment will develop. For example, despite the high incidence of trauma in people present- ing with symptoms and relatively high levels symptoms of posttraumatic stress disorder in people experiencing psychosis (Grubaugh Zinzow, Paul, Egede, & Frueh,
Schizophrenia and Other Psychotic Disorders 527
2011), CBTp does not typically focus directly on trau- ma sequelae (Keen, Hunter, & Peters, 2017). Attempts to integrate theories of trauma and posttrauma sequelae into cognitive models of psychosis have been pivotal in driving the development of trauma-focused CBT for psychosis (TF-CBTp; e.g., Keen et al., 2017; Steel et al., 2017).
BASIC CLINICAL PRINCIPLES
A number of common clinical strategies underlie all variants of CBTp for schizophrenia: engagement and establishment of a therapeutic relationship; assessment based on an individualized case formulation that iden- tifies psychotic experience (symptoms) and establishes associations between the person’s cognition, behavior, and affect within the environmental context in re- sponse to this experience; and an intervention strategy based on this formulation that uses cognitive and be- havioral methods to reduce psychotic symptoms and associated emotional distress. People are taught to be aware of their symptoms and to learn methods to man- age them (e.g., learning to control auditory hallucina- tions by switching their attention away from them, or by thinking about alternative explanations for their experiences).
People can acquire coping strategies that are bro- ken down into elements, learned individually, then aggregated into an overall strategy. To ensure that these coping strategies can be implemented outside of therapy, people overlearn them during the therapy ses- sion. Learning such control techniques allows people to challenge beliefs they may have had about voices, such as “The voices are uncontrollable,” “The voices are all powerful,” and “I must obey the voices.” Thus, by learning to control basic psychological processes such as attention, through attention switching and distrac- tion, people also learn to challenge their beliefs about their experiences and symptoms. Behavioral experi- ments and reality tests may also be used to disprove de- lusional and inappropriate beliefs. Particular attention is paid to identifying avoidance and safety behaviors that reinforce inappropriate beliefs. Changing these be- haviors is a powerful method of changing beliefs and delusions. People may be assisted in their attempts at behavior change by means of self-instruction and cop- ing strategies that decrease arousal (e.g., breathing ex- ercises; quick relaxation; guided imagery; and encour- aging positive task-oriented internal dialogue). In some
cases, people are convinced and unshakable in the belief that their delusions are true, and they do not wish to examine the veracity of this experience. In these cases, the clinician must negotiate treatment goals aimed at reducing distress rather than the symptoms themselves. A failure to do this will probably result in the person disengaging and refusing treatment.
It is frequently the case that the person’s delusional beliefs persist in spite of evidence to contradict them, including evidence that occurs naturally and that is manufactured by the therapist through behavioral ex- periments and reality testing. To weaken these delu- sional explanations, the therapist should use all avail- able opportunities, through guided discovery and Socratic questioning, to reappraise the evidence for the person’s explanation of events, thus weakening the delusions. Pointing out the contradictory evidence in a quizzical and puzzled manner, often known as the “Columbo technique,” is advised, so the person has to account for contradictions and review his/her explana- tion in light of this new and contradictory evidence. When delusions are strongly held, this can be a slow process, but the weakening of delusional beliefs can occur, or, as happens in some cases, the delusional inter- pretations remain or return, but their importance and distressing nature are greatly reduced. For example, an older adult female patient treated by one of the authors (N. T.) experienced auditory hallucinations that were of a blasphemous and obscene nature. She believed that her brain acted as a transmitter and broadcast her thoughts, so that other people in the vicinity could hear her blasphemous and obscene thoughts. Her main so- cial contact was with her local church and associated social club. One Sunday, during the church service, she heard the voices and became convinced that her own thoughts about the voices were broadcast aloud to the congregation. She was mortified and so ashamed that she left the church and was unable to return or to have any contact with her friends. She was convinced that she had become ostracized by the church congregation. On being asked about the evidence for this, she replied that she had since met other members of the church congregation in town and they had totally ignored her, which had further reinforced her sense of exclu- sion, shame, and self-disgust. On further questioning, she revealed that she had been walking on the pave- ment and had seen her friends drive by some distance away. There was a high probability that they had not seen her. Thus, her evidence for being ostracized was challenged. She and her therapist agreed on a treatment
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goal that would test her interpretation of the situation. If the fear that the church congregation would shun her if she returned was real, then she should expect a nega- tive reaction when she returned to church. If the fear was unfounded, there would be no negative reaction; in fact, the others should be pleased to see her return. She experienced considerable anxiety at the thought of re- turning to church but managed the return using meth- ods she had learned to cope with both the experience of auditory hallucinations and anxiety. To her surprise, far from being shunned or ostracized, she was greeted with warmth and concern. This experience consider- ably weakened her beliefs that others could hear her thoughts, and her delusions were rated as minimal. On being asked about the events some months later at fol- low-up, she said that she believed others could hear her thoughts, but because it did not appear to bother them, she was no longer concerned about it either! In this case, her delusional explanation of past events had returned but no longer caused her any distress or disrupted her social functioning.
Emphasis has also been placed on improving the in- dividual’s self-esteem and feelings of self-worth due to strong evidence that people diagnosed with schizophre- nia are more likely to have low self-esteem compared to the general population (Berry & Bucci, 2014). This addition to the treatment has been found to be effec- tive and well received by those engaged in therapy (Hall & Tarrier, 2003). In this chapter, we have placed these methods after the treatment of symptoms, indicating a progression from symptom reduction to improved self- esteem. However, there is no reason why improvements in self-esteem cannot be initiated at the beginning of treatment and, in some cases, this may be desirable.
The future may hold exciting new opportunities to use new technology such as smartphones to implement real-time assessment and interventions, and to indi- vidualize treatment protocols. For example, Actissist, is a digital health intervention developed in the United Kingdom and grounded in the cognitive model of psy- chosis (Bucci et al., 2018). Actissist targets five domains associated with early psychosis relapse: auditory verbal hallucinations; paranoia; perceived criticism; social- ization; and cannabis use. The system that is accessed through a smartphone identifies and challenges un- helpful appraisals of psychosis-related experiences and provides alternative, more helpful coping strategies in the real-time context of one’s daily life. A recent feasi- bility and acceptability study of Actissist compared to
a symptom monitoring only system showed promising results in terms of acceptability to people experiencing psychosis and treatment effects for negative symptoms, general psychotic symptoms, and mood. A larger RCT of the intervention is underway and will be completed later this year.
BACKGROUND AND ASSOCIATED FACTORS
Phases of Schizophrenia and Relationship to Aims of Treatment
Schizophrenia, a complex disorder that may well be lifelong, passes through a number of phases. For ex- ample, the prodromal phase that occurs before a full- blown psychotic episode is characterized by nonspecific symptoms and symptoms of anxiety, depression, irrita- bility, insomnia, and quasi-psychotic experience (e.g., magical thinking, feelings of paranoia). The prodro- mal phase develops into a psychotic episode, during which the most florid psychotic symptoms are present and seriously interfere with functioning. A psychotic episode usually requires acute management, frequently including hospitalization. Recovery from an acute epi- sode of psychosis is followed by a period of remission or partial remission with maintenance doses of anti- psychotic medication. It is not uncommon for residual symptoms to remain during the recovery and remission phase, and in some cases, there is little recovery at all. Treatment aims and strategies for CBTp vary depend- ing on the phase of the disorder. For example, during the prodromal phase, the aim is to prevent transition into a full psychotic episode; during an acute episode, the aim is to speed recovery; during partial remission, the aim is to reduce residual symptoms and to prevent further relapse; and in full remission, the aim is to keep the person well. The specifics of CBTp may vary de- pending on these aims and the phase in which they are applied. For example, during an acute admission for a psychotic episode, the person is often disturbed, dis- tressed, and agitated. Thus, therapy sessions are often brief and frequent, whereas for people living within the community, therapy sessions follow the normal out- patient format. In all cases, therapy is tailored to the needs of the person. In all but the most exceptional cases, CBTp is used in addition to appropriate antipsy- chotic medication. The various phases of schizophre- nia and appropriate treatment strategies are outlined in Table 13.1.
Schizophrenia and Other Psychotic Disorders 529
Associated Features and Complicating Factors
It is important that the clinician attend to associated features and complicating factors, as well as the symp- toms of the disorder. These vary from the effects of symptoms on basic psychological processes (e.g., atten- tion) to clinical issues (e.g., suicide risk) to social issues (e.g., social deprivation and poor employment opportu- nities). These associated features are outlined in Table 13.2.
The crucial point is that the clinician be aware that these problems can arise. Some of them can be dealt with by keeping the message simple and brief, but with plenty of repetition (i.e., use of overlearning in teach- ing coping strategies). Writing down simple points for the person as a memory aid can also be helpful, as can creating a small “workbook,” so that the person has a continuous record of these points. This is usually more effective than providing handouts, which are rarely read and frequently are lost. It is important to balance the nature and duration of sessions against the person’s level of tolerance. Initially, it might be best to keep ses- sions brief or allow the person to leave when he/she has had enough. The one-to-one nature of therapy is highly stressful, so initial sessions may serve merely to provide habituation to the social stress of being with the cli- nician. Teaching the person simple strategies to deal
with tension and anxiety (e.g., brief relaxation) may be helpful in habituating to the therapy situation and may also provide a concrete task on which to focus atten- tion. Simple attention-focusing tasks, such as focusing on some item in the room for a short period, may be helpful in reducing the effect of irrelevant stimuli on the person’s conscious awareness. It is also important to recognize that the verbal and nonverbal cues the thera- pist might expect to indicate severe distress, depression, or suicidality may not be expressed by someone with schizophrenia. Affect may be flat or inappropriate, which may result in the therapist missing important signs of risk. This can be avoided, in part, by knowing
TABLE 13.1. Treatment Aims and Methods in Different Phases of Schizophrenia
Phase Aim Treatment method
Prodrome Prevention of translation into full psychosis
CBT for early signs and prevention of symptom escalation
Acute episode Speed recovery CBT and coping training
Partially remitted residual symptoms
Symptom reduction
CBT, coping training, self-esteem enhancement
Remission Relapse prevention
CBT for staying well and family intervention
Relapse prodrome Abort relapse Early signs identification and relapse prevention
TABLE 12.2. Associated Features of Schizophrenia: Features That Need to Be Assessed and Considered as Potential Difficulties in the Psychological Treatment of Schizophrenia
Psychological • Disrupted or slowed thought processes • Difficulty discriminating signal from noise • Restricted attention • Hypersensitivity to social interactions • Difficulty in processing social signals • Flat and restricted affect • Elevated arousal and dysfunctional arousal regulation • Hypersensitivity to stress and life events • High risk of depression and hopelessness • Effects of trauma • Stigmatization • Low self-esteem and self-worth • High risk of substance and alcohol abuse • High risk of suicide and self-harm • Interference of normal adolescent and early adult
development due to onset of illness
Psychosocial • Hypersensitivity to family and interpersonal environment
(including that created by professional staff ) • Risk of perpetrating or being the victim of violence
Social • Conditions of social deprivation • Poor housing • Downward social drift • Unemployment and difficulty in competing in the job
market • Restricted social network • Psychiatric career interfering with utilization of other social
resources
530 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
the person and how he/she reacts, by never making as- sumptions about mental state, and by having the person agree from the outset that he/she will inform the thera- pist of important changes in his/her life or mood.
Unfortunately, some issues, such as social condi- tions, are often beyond the therapist’s power to change but may well have an impact on the treatment process. However, there is nothing wrong in assuming an advo- cacy role or in helping people to empower themselves by aiding their attempts to improve their own circum- stances. Finally, it is important that therapists adopt a noncritical approach and learn to accommodate their own frustrations if therapy is progressing more slowly than they had hoped. Aspects of schizophrenia can make interaction with some people difficult, and the therapist needs to be aware of this and develop a tol- erant approach. The lack of a positive relationship be- tween case managers and patients has been shown to be associated with poorer prognosis (Berry, Barrowclough, & Haddock, 2011).
THE CONTEXT OF THERAPY
It is highly probable that by the time a referral is made for CBT, the person will be under the care of a multidis- ciplinary mental health team and be receiving antipsy- chotic medication and some type of case management. People who develop psychosis are usually diagnosed by a general practitioner or primary care team, or in an accident and emergency department, and referred on to mental health services. Mental health services are organized in different ways in different countries, de- pending on health care philosophies and structures, but what is delivered in terms of therapy content may be independent of how that service is organized. Thus, the therapeutic procedures described in this chapter can be utilized in different types of service structure and orga- nization. We have provided CBTp to people on closed and open wards, in hospital and health center outpa- tient facilities, in community facilities, and in people’s own homes. It is probable that the more flexible the system, the more likely the person will be engaged and attend. To this end, we often deliver treatment in the person’s home, which is a common procedure in the United Kingdom.
Evidence from research trials indicates that cognitive- behavioral treatments are delivered over about 20 treat- ment sessions. These can be intensive, over 3 months, or
less intensive, over 9 months or longer. Clinical impres- sions indicate that some people benefit from continued, although less intensive treatment, whereas others ben- efit from booster sessions. The clinician should always be led by the clinical need of the person and take a col- laborative approach rather than adhering to a rigid “one size fits all” protocol. It should be remembered that CBT does not “cure” schizophrenia, but it does help the person cope with distressing symptoms.
The presence of possible associated factors, as out- lined earlier, signifies that people may present with a number of difficulties, as well as psychotic symptoms. The clinician needs to be aware that this may be the case and be prepared to address or treat these present- ing problems before moving on to treat the psychotic symptoms. It may be necessary to tackle problems such as high levels of anxiety, depression, hopelessness, and suicidal behavior and risk, because they are not only clinical priorities but also there may be important inter- actions between these issues and the psychosis.
The treatment described here is for individual CBTp. It is possible to deliver treatment in a group format. Groups are well received by some people and are ad- vantageous, in that participants can learn from each other. The results suggest clinical benefits in terms of enhanced self-esteem, but reductions in symptoms are modest compared to those in individual treatments (e.g., Barrowclough et al., 2006), and any improve- ments appear to get lost at follow-up (Lecomte, Leclerc, & Wykes, 2012).
Other psychosocial treatments may also be available, such as family interventions. There is a considerable lit- erature on family interventions, which have been shown to reduce relapse rates in at-risk individuals, for those in the early stages, and in later psychosis (Bird et al., 2010;
Pharoah, Mari, Rathbone, & Wong, 2010; Onwu- mere, Bebbington, & Kuipers, 2011; Onwumere & Kuipers, 2011). Details of family intervention are be- yond the scope of this chapter (for the clinical applica- tion of family interventions, see Barrowclough & Tar- rier, 1992; Kuipers, Onwumere, & Bebbington, 2010; Mueser & Glynn, 1995; see also Miklowitz, Chapter 12, this volume). We have combined individual CBT and family intervention with some success and suggest that therapists consider whether this strategy would be clinically beneficial. Others have offered family therapy to those with co-occurring schizophrenia spectrum diagnoses and substance misuse, with some benefits in symptoms and functioning for both people with
Schizophrenia and Other Psychotic Disorders 531
schizophrenia and their relatives (Mueser et al., 2013). Concomitant family intervention may reduce stressful home environments and help to sustain improvement. Many people with psychosis live alone or are estranged from their relatives, so family intervention may not be an option.
Patient Variables
People with schizophrenia represent a heterogeneous group, around 30% of whom may be resistant to medi- cation treatment (Lally, Gaughran, Timms, & Curran, 2016) and 5–10% show no benefit from antipsychotic medication (Pantelis & Barns, 1996). Although there is confusion among the terms treatment-resistant, in- complete recovery, and treatment intolerance, it is clear that conventional treatment with antipsychotic medi- cation is ineffective for a significant number of people, in spite of well-publicized advances in antipsychotic medication. It is important, therefore, in tailoring and refining treatments, to understand what factors predict a good response to psychological treatment and per- haps the converse—which people do not derive benefit. Unfortunately, little is known in any great detail about which people will or will not benefit from cognitive- behavioral treatments (Tarrier & Wykes, 2004). Factors that have been associated with poor outcome include negative symptoms of affective flattening and alogia (cognitive impoverishment) (Tarrier, 1996). Factors as- sociated with better outcome include a shorter duration of illness, a younger age (Morrison, Turkington, et al., 2012), greater pretherapy coping ability (Premkumar et al., 2011) and better clinical and cognitive insight (Emmerson, Granholm, Link, McQuaid, & Jeste, 2009; Perivoliotis et al., 2010), less severe symptoms at pretreatment (Tarrier, Yusupoff, Kinney, et al., 1998), higher baseline functioning and educational achieve- ment (Allott et al., 2011), and receptiveness to hypo- thetical contradiction (Brabban, Tai, & Turkington, 2009; Garety et al., 1997). These results suggest that those people who are younger with less severe illness, fewer severe cognitive deficits, and better functioning may respond better, but no hard-and-fast rules are cur- rently supported by evidence. Treatment dropout is a further issue of importance.
A recent study of predictors of disengagement from CBTp in an NHS setting in the United Kingdom in- volving 103 referrals and a disengagement rate of al- most 50% found that disengagement was associated
with younger age; overactive, aggressive, disruptive, or agitated behavior; problem drinking or drug taking; depressed mood; and problems with occupation and ac- tivities (Richardson et al., 2019). There was no impact of gender or ethnicity, and no impact of clinical vari- ables such as risk history and comorbid diagnosis. The authors conclude that it may not be psychosis symp- toms themselves that disrupt engagement, but associ- ated behavioral and emotional factors. They suggest a more proactive approach to these factors, particularly in younger people prior to or early on in therapy to increase engagement in CBTp. Another study investi- gating disengagement from early intervention for psy- chosis services revealed that fewer negative symptoms, cannabis or other drug use, and factors such as not hav- ing a family member involved with treatment predicted disengagement (Stowkowy, Addington, Liu, Hollowell, & Addington, 2012). An earlier study carried out by one of the authors (N. T.) suggested that positive symp- toms and depression are also important in determining disengagement. Those who dropped out of therapy ex- perienced both hallucinations and delusions, were para- noid, although not necessarily suspicious of the treat- ing clinician, and depressed and moderately hopeless. The majority reported that they did not see the point of psychological treatment or that that they thought they would not personally benefit from treatment (Tarrier, Yusupoff, McCarthy, Kinney, & Wittkowski, 1998).
Therapist Variables
Therapist variables encompass a number of factors, in- cluding training, experience, competency, supervision, and personal style. There is a tendency for health care planners to expect, mainly on economic grounds, that these complex therapies will be delivered by minimally qualified clinicians. This may well be a mistake (Tarrier et al., 1999). Psychological treatment of someone with psychosis is complex, and besides having the skills and experience to treat the psychotic symptoms themselves, as outlined in this chapter, the clinician may well need to be able to treat a range of comorbid disorders, includ- ing anxiety, posttraumatic stress, depression, and addic- tive disorders. It seems reasonable that to treat success- fully someone with a severe mental health problem and very possibly a range of comorbid disorders, the clini- cian should be experienced and sufficiently well trained in CBT to be able to react to various clinical demands and levels of complexity. A recent study showed better
532 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
outcomes from CBTp to be associated with therapists who spend the majority of their clinical time deliver- ing this specific intervention, and who receive frequent supervision (Steel, Tarrier, Stahl, & Wykes, 2012). In our opinion, the treatment of schizophrenia and related psychoses does not lend itself well to merely following a highly prescriptive manual. As indicated in the previous section on associated features and complicating factors, the clinician needs to be competent in recognizing and prioritizing a range of presenting problems for treat- ment. Similarly, the clinician needs to have personal qualities that engage the person, who may well be high- ly distressed and distrusting of the therapy, and to tailor the treatment to that individual. Previous research sug- gests that the absence of a positive relationship is associ- ated with a poorer outcome (Berry et al., 2011). There is good evidence of an association between the quality of therapeutic alliance and outcomes in psychological therapy for schizophrenia including CBTp (Shattock, Berry, Degnan, & Edge, 2018; Browne, Nagendra, Penn, Berry, & Kurtz, 2019). Therefore, the clinician needs the experience and patience to develop that rela- tionship and maintain engagement. A study that used the Delphi method to examine what experts in the field viewed as important ingredients in CBTp found that el- ements such as a detailed assessment, use of a cognitive model and formulation, and implementation of change strategies were agreed to be essential, as well as thera- pist attitudes (e.g., normalizing rationale for symptoms) (Morrison & Barratt, 2010).
CBT PROCEDURE: THE MANCHESTER MODEL
The Coping–Recovery Clinical Model
The model developed and described by Tarrier bears many similarities to other models and has benefited from contact and discussion with other clinical re- searchers in the field. The basic tenet is the recovery model, in which patients are coping with potentially persistent symptoms that may well change many aspects of their lives, affect their hopes and aspirations, and be associated with comorbid disorders such as depression and anxiety disorders. The therapist aids the patient in facilitating, as much as possible, the process of recovery. The coping model strongly resembles and uses many methods of other CBT approaches but emphasizes cop- ing with symptoms rather than curing them, and inter- venes to modify cognitive processes (e.g., attention), as well as cognitive content and behavior.
The clinical model that guides treatment is pre- sented in Figure 13.1. It assumes that the experience of psychotic symptoms, hallucinations, and delusions is a dynamic interaction between internal and external factors. Internal factors may be either biological or psy- chological and can be inherited or acquired. For exam- ple, genetic factors may influence both the biochemical functioning of the brain and cognitive capacity. Alter- natively, biological and psychological dysfunction may be acquired, for example, in deficits in cognitive flex- ibility and in the development of maladaptive attitudes. Such internal factors increase individuals’ vulnerability to psychosis, and their risk is further increased through exposure to environmental stress, such as certain in- terpersonal or excessively demanding environments. The interaction between internal and external factors is important both in the origins of schizophrenia and in maintaining symptoms. A dysfunction in the process- ing of information, such as source monitoring in hal- lucinations (i.e., a belief about where the voice is com- ing from) and probabilistic reasoning in delusions, in combination with dysfunctions in the arousal system and its regulation, result in disturbances of perception and thought that are characteristic of psychosis. The individual is reactive to these experiences, and there is a process of primary and secondary appraisal in which the individual attempts to interpret these experiences and give them meaning, then react to their conse- quences. Often people’s appraisal of experience results in feelings of threat to their physical integrity or social standing and concomitant emotional reactions, and avoidant and safety behavior. The immediate reaction to the psychotic experience is multidimensional, in- cluding emotional, behavioral, and cognitive elements. Secondary effects, such as depressed mood, anxiety in social situations, and the effect of trauma, may further compound the situation.
The important aspect of the model is that appraisal (including beliefs about experience) and reaction to the psychotic experience feed back through a number of possible routes and increase probability of the main- tenance or recurrence of the psychotic experience. For example, the emotional reaction to hearing threatening voices or experiencing strong feelings of paranoia may well be anxiety or anger. Both these emotions include elevated levels of autonomic arousal that act either di- rectly, through sustained increased levels of arousal, or indirectly, through further disrupting information pro- cessing, to increase the likelihood of psychotic symp- toms. Similarly, behavioral responses to psychotic symp-
Schizophrenia and Other Psychotic Disorders 533
toms may increase exposure to environmental stress or increase risk of trauma (e.g., becoming involved in vio- lence or indulging in dangerous behavior) that main- tains or aggravates psychotic symptoms. For example, paranoid thoughts may result in interpersonal conflict or, alternatively, social avoidance and withdrawal. Both situations are likely to increase the probability of symp- toms occurring. Interpersonal conflict is likely to be interpreted as evidence for persecution, whereas with- drawal and isolation probably result in confirmatory
rumination and resentment, with a lack of opportunity to disconfirm these paranoid beliefs. The appraisal of the content of voices or delusional thoughts as valid and true may result in behavior consistent with these beliefs and a confirmatory bias to collecting and evaluating evidence on which to base future judgments of reality.
Psychotic experiences can lead to unhelpful beliefs that are then acted on in a way that leads to their con- firmation or a failure to disconfirm. This can be termed the experience–belief–action–confirmation (EBAC) cycle.
FIGURE 13.1. A clinical model of the origins and maintenance of psychotic symptoms.
534 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
It is suggested that such cycles maintain psychotic expe- rience through reinforcement of maladaptive beliefs and behavior. The generic model indicated in Figure 13.1 provides an overarching picture of how the patient’s problems arise and are maintained. Embedded within this model are the microelements of specific, time- linked events such as the EBAC cycle (see Figure 13.2).
Assessment
The clinician needs to be able to assess and develop a formulation of the determinants of the person’s psychot- ic symptoms. Clinicians may find the use of standard- ized assessment instruments helpful (there are many of these, and they assess a range of functions; see Kleiger & Khadivi, 2015, for a detailed description and review of assessments). We recommend the Psychotic Symptom Rating Scales (PSYRATS; Haddock, McCarron, Tarri- er, & Faragher, 1999) as an effective method of assessing the multidimensional nature of positive psychotic symp- toms. The clinician needs to understand the individual variation in psychotic symptoms. This can be achieved by the use of a semistructured interview (the Antecedent and Coping Interview [ACI]; for more details, see Tar- rier, 2002, 2006) that covers the nature and variation of positive psychotic symptoms experienced by the person, including beliefs about psychotic symptoms, emotional reactions that accompany each symptom, antecedent stimuli and context in which each symptom occurs, consequences resulting from the symptoms and how the
person’s behavior and beliefs are affected, and methods the patient uses to cope and manage his/her experiences. This allows the clinician to build up a comprehensive picture of how the person experiences the psychosis on a daily basis and how his/her affect, behavior, and beliefs are changed. The clinician should be careful to identify avoidance and safety behaviors that occur because of psychotic symptoms, and examples in which the person fails to disconfirm irrational or delusional beliefs. The clinician should use the clinical models shown in Fig- ures 13.1 and 13.2 as a guide.
Intervention
Coping Strategies
When the clinician has constructed a comprehensive picture of the person’s psychotic experience, the ratio- nale for CBTp can be presented. There may well be people who are completely convinced of the truth of their delusional thoughts and will not accept any alter- native view, in which case coping with distress should be advanced as a suitable goal.
The characteristics of CBTp and coping training fol- low:
• They are based on an individualized assessment or formulation.
• They emphasize a normal and general process of dealing with adversity.
• They emphasize that this is part of the recovery process.
• They are carried out systematically through over- learning, simulation, and role play.
• They are additive in that different strategies can be added together in a sequence that progresses to in vivo implementation.
• They are based on providing a new response set that will be a method of coping with an ongoing problem rather than being curative.
• Cognitive coping skills are learned through a pro- cess of external verbalization that is slowly dimin- ished until the required procedure is internalized as thought under internal control.
• They enhance executive function. • The learning of cognitive and behavioral coping
skills develops through a process of graded practice or rehearsal.
• They provide opportunities for reappraisal and re- attributions.
FIGURE 13.2. The experience–belief–action–confirma- tion (EBAC) cycle.
Schizophrenia and Other Psychotic Disorders 535
These coping methods include the following changes in cognitive processes, cognitive content, and behavior.
ATTENTION SWITCHING
A process whereby people actively change the focus of their attention from one subject or experience to an- other, attention switching, involves inhibiting an ongo- ing response and initiating an alternative. People are trained within the session to switch attention on cue through rehearsal to external stimuli (e.g., an aspect of their environment, such as describing a picture or being aware of background traffic noise) or to internal stimuli, often to a set of positive images. For example, one person who was asked to choose a positive scene to which to attend chose a restaurant in Blackpool, where he had had an enjoyable meal. He was trained to be able to elicit a visual image of the restaurant by describ- ing the scene, furniture, decorations, and such in great detail. He was then asked to remember the experience of the meal in all his senses: the visual memory of the food; its smell and taste; the feel of holding the knife and fork in his hands; the experience of eating; and so on. He continually rehearsed the memory of the meal in the restaurant until he was able to elicit it at will. He then rehearsed switching his attention away from delu- sional thoughts to images of the meal. He was taught to use the onset of a delusion as a cue for attention switch- ing (see “Awareness Training” below).
ATTENTION NARROWING
In attention narrowing, a process whereby people re- strict the range and content of their attention, many people talk about “blanking” their mind or focusing their attention as a method of coping. Evidence suggests that one problem faced by people with schizophrenia is a difficulty in filtering information input and there- fore distinguishing signal from noise. Training people to focus their attention and improve attentional control may assist them in overcoming this difficulty by nar- rowing and regulating their attention.
MODIFIED SELF-STATEMENTS AND INTERNAL DIALOGUE
It has been known for some years that it is possible to incorporate self-statements into interventions. The use of self-statements and internal dialogue may take on a number of functions in emotion control, such as teach-
ing people to overcome negative emotions associated with their voices, cueing goal-directed behavior, and cueing and directing reality testing. In each case, the person is taught statements that direct the appropriate response, such as “I don’t need to be afraid,” “I need to keep going and get on the bus,” or “Why do I think that man is looking at me when I’ve never seen him before?” Within the session, the person is first asked to repeat the set of statements or questions out loud when given the appropriate cue. The verbalized statements are then gradually reduced in loudness until they are internal- ized. The person then practices these in simulated situ- ations within the session. Learning such questioning statements is a useful stage in generating and evaluating alternative explanations for experience.
REATTRIBUTION
People are asked to generate an alternative explanation for an experience, then practice reattribution statements when that experience occurs. Initially, when we started coping training, we used reattributions that were illness related, such as “It’s not a real voice, it’s my illness.” We have since abandoned this as unhelpful. We now try to use other, alternative explanations: “It may seem like a real voice, but it’s just my own thoughts” and “It may seem as though people are looking at me, but they have to look somewhere.” If people do make changes that increase their control over their symptoms or circum- stances, or challenge the omnipotence or infallibility of their voices, then these changes can be evidence for a re- attribution concerning the nature of their symptoms or their ability to exert control—for example, “How can the voice be all powerful if it talks rubbish?” or “I don’t have to believe it if it isn’t true.”
AWARENESS TRAINING
People are taught to be aware of and monitor their posi- tive symptoms, especially their onset. People not only become aware of their experiences but they also try to accept these experiences but not react to them. For example, people are aware of their voices but do not react to them or become captured by their content. One function of awareness training is to make people aware of the form and characteristics of their thoughts and perceptions rather than the content—for example, to monitor the physical onset of a voice, then use atten- tion switching to reduce the emotional impact of the content. The aim is twofold: to assist people in becom-
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ing mentally disengaged from their symptoms, especially the content, and to use symptoms as a cue to alternative action.
DEAROUSING TECHNIQUES
Because high levels of arousal frequently occur as both antecedents and responses to psychotic experience, teaching people to cope with these is important. These coping strategies may be simple passive behaviors to avoid agitation, such as sitting quietly instead of pacing up and down, or they may be more active methods of arousal control, such as breathing exercises or quick re- laxation. We have not favored lengthy relaxation train- ing, such as traditional progressive relaxation exercises, because these are time-consuming and off the point. What is functional here is a quick, usable skill.
INCREASED ACTIVITY LEVELS
Many people with schizophrenia are vulnerable to de- lusional thought or hallucinations during periods of inactivity. Inactivity can be a common problem associ- ated with the negative symptoms of schizophrenia or fears of leaving the house due to distressing delusions or voices. Many people report that finding something to do is helpful. Thus, simple activity scheduling can be a powerful coping strategy, especially if implemented at the onset of the symptom, thus creating a dual task competing for attentional resources. Besides increasing purposeful activity, this also reduces exposure to condi- tions under which symptoms are aggravated.
SOCIAL ENGAGEMENT AND DISENGAGEMENT
Although many people with schizophrenia find social interactions difficult, surprisingly, many also find so- cial engagement a useful method of coping. Possibly this may occur because social interaction serves as a dual task and source of distraction, and because it may help people modify maladaptive thinking. It is benefi- cial to be able to titrate the amount of social stimulation involved in any interaction with the person’s individual tolerance level, and to teach the person that levels of social disengagement may be used to help develop toler- ance of social stimulation. Social withdrawal and avoid- ance are common responses to experiencing overstimu- lation as a result of social interaction. However, people can learn less drastic methods of disengagement, such
as leaving the room for a short period and then return- ing, temporarily moving away from the social group, and practicing functional disengagement by not convers- ing for short periods or lowering their gaze. By using these methods, people can control and tolerate social stimulation. People may also initiate social interaction more confidently as a method to reduce the impact of their symptoms, if they feel they have some control over the intensity of those interactions. Simple training in specific skills for interaction and role plays can facilitate this.
BELIEF MODIFICATION
People can learn to examine their beliefs and to chal- lenge them if they are unhelpful by examining the evi- dence and generating alternative explanations. Many people do this to some extent already, but the level of arousal experienced, or the level of isolation and avoid- ance, can make these attempts unsuccessful. These methods are very similar to those used in traditional cognitive therapy except that the person may need more prompting, and the goal is to incorporate the skills of belief modification into a self-regulatory process. Peo- ple can be encouraged to question their beliefs as they occur: “What would be the purpose of someone spying on me; how much effort and cost would it take; how would this be resourced and organized; and for what gain?” Similarly, people can be encouraged to look for inconsistencies and use these to challenge their beliefs. For example, the patient who was involved in a fight 15 years earlier, and still avoids young men because he fears that the same group is out to get revenge, may be asked to reflect on the fact that because the members of the gang are now in their middle to late 30s, he has been vigilant for the wrong age group. This can be used to challenge his fear that he needs to be vigilant to stay safe. In effect, his safety behaviors have not protected him from the source of danger. People can also learn to examine evidence to challenge their beliefs about the voices they hear. When people perceive their voices as omnipotent and truthful, clinicians can investigate to see whether the voices have been wrong or incorrect. For example, the patient whose voices told him he was going to be murdered because he was a spy, concluded that the voices must be true and that he must deserve this fate. However, the voices also told him that he was soon to be married, and because he could find no sup- porting evidence for this, he decided it was untrue.
Schizophrenia and Other Psychotic Disorders 537
However, he had never thought to challenge the voices’ veracity concerning the threat of murder. Realizing that he was unlikely to be married in the near future, as the voices had asserted, helped him to challenge the idea that he was to be murdered by doubting the truthful- ness of the voices and to look for further supporting, objective evidence of the spy ring, which was not forth- coming.
REALITY TESTING AND BEHAVIORAL EXPERIMENTS
Probably the strongest way to test beliefs is to test them out in reality by some type of action; behavior change is probably the best way to produce cognitive change. People sometimes do this naturally, although a tenden- cy toward biased interpretation and hypothesis protec- tion may lead them to erroneous conclusions. People can learn to identify specific beliefs and to generate competing predictions that can be tested. The failure to do this in real life usually leads to patterns of avoid- ance, which can be reversed to challenge the beliefs that they underpin.
Enhancing Coping Strategies
Coping methods develop over time and vary in their complexity, from simple and direct attempts to control cognitive processes, such as attention, to more complex, self-directed methods that modify cognitive content and inference. Frequently, combinations of different coping strategies are built up; for example, the use of attention switching and dearousing techniques helps to dull the strength of a delusion, so that reality test- ing can be implemented. Without these initial coping methods, the person would not be able to undergo re- ality testing. Furthermore, the initial coping strategies can be used to challenge the strength of the delusion of the omnipotence of the voices and provide an increase in self-efficacy. The therapist may ask questions, such as “You’ve used these attention-switching methods to cope effectively with your voices. What does that tell you about them being in total control and you being helpless?” The person may well make statements that indicate the voices have been demonstrated to be fal- lible and he/she has some control over the situation, which can then be used as self-statements or a modified internal dialogue to further enhance self-efficacy and coping.
Modification of Behavior or Cognition
Changes in behavior and cognition complement each other, and one is not necessarily better than the other. Changes in behavior should always be used to exam- ine and potentially challenge unhelpful thoughts and beliefs or as learning experiences. Similarly, changes in cognition should be used as opportunities to change behavior and to establish new behaviors. The therapist should always look for opportunities to prompt people to reappraise their beliefs. This can be carried out as part of formal behavioral experiments, naturally occur- ring changes, and frequent reflections on what has been achieved in treatment. In assessment and during for- mulation, the therapist should always be alert to avoid- ance or safety behaviors, or when people do not behave in a way that could disconfirm their fears, delusions, or unhelpful cognitions. These can be used very early on in treatment as behavioral experiments to test out beliefs or to provide opportunities for quick improve- ments to challenge despondent or hopelessness beliefs such as “Nothing is worth it if I cannot change” or “I have no control over my life or circumstances.” The belief of “no control” is often present and can be re- futed by many small behavioral changes that may be repeated and referred to frequently. Finally, it is often helpful at the beginning of treatment to obtain some behavior changes, although often small, and increase activity that may have a number of associated benefits and provide the opportunity for reappraisal.
Modification of Cognitive Content or Cognitive Process
Therapists frequently face the choice of whether to try to modify the content of hallucinations or delusions, or the attentional processes that these phenomena have captured. Traditionally, in cognitive therapy, the con- tent of cognition is the main focus. In the coping model intervention, this is broadened to modification of cog- nitive processes, because modifying cognitive processes provides greater flexibility, and because deficits of the regulation of attention and executive function are often present in people experiencing psychosis. In practice, these tactics can work together. Initial modification of attentional processes through attention switching, for example, can decrease the emotional impact of the ex- perience. A similar effect can be produced by attending to the physical characteristics of a hallucination rather
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than what the voice is actually saying. This can provide not only an opening to challenge the truth of the con- tent of the voice or delusional thought but also a sense of control over these experiences. Take, for example, a young man who is experiencing voices that accuse him of having committed a murder and also say he is Rus- sian. Initially, he can be taught to turn his attention away from the voices in a systematic way to reduce their emotional impact. This technique can be used to weak- en the emotional strength of the experience, to elicit a sense of control, and to challenge the belief that the voices are all-powerful. With increased self-efficacy and a greater sense of power, the patient can later challenge the content of the voices that accuse him of murder by investigating the objective evidence that a murder has been committed. Furthermore, the untruthfulness of the voices in saying he is Russian can be used to chal- lenge the veracity of the murder accusation; if the voices had been wrong about one issue, then they could be wrong about the other. Modification of cognitive pro- cess and content provides the therapist with two basic routes to intervention and the flexibility to move from one tactic to the other.
CASE STUDY
The following case example gives some indication of how CBTp works.
History
“Jim,” a 28-year-old man, first starting experiencing psychosis when he was 22. During his first episode, Jim became increasingly paranoid and accused people, including his friends, of stealing his money. He said that he could feel people taking money and his wallet from his pockets when he was socializing in his local pub and also when he was traveling by bus. The feeling that “something was wrong” had been with him for a few months, and Jim then began to hear voices warning him that people were against him and scheming to “do me down.” These voices talked to Jim, warning him against “the schemes” and telling him who was involved and to be on his guard. These voices were especially insistent that those closest to Jim were the people most against him and the “worst schemers.” The voices also told Jim that his girlfriend was unfaithful, and he ex- perienced “visions,” sent by the voices, of his girlfriend
having sex with other men. He did not actually believe that his girlfriend was unfaithful, but he became very angry that the voices should make these accusations. On some occasions, Jim did lose control and confronted some male friends about having affairs with his girl- friend. Usually, he accepted their denials.
Jim also heard voices talking about him. These dif- ferent voices were usually “scheming” and making insulting and accusatory comments. Sometimes these voices would laugh at Jim because his girlfriend was cheating on him, and make remarks about his sexual inadequacy, to which they attributed her infidelity.
Jim’s friends and family noticed that he began to withdraw and became increasingly disheveled. He was often found muttering to himself or making sarcastic comments to family members about how they were “growing rich on my hard work.” The voices also told him to “look for signs that the scheming is coming to a head.” Jim began to write down an account of everyday events, such as the time certain buses arrived near his house and the type of advertisements on their sides. His parents, who would find these writings left around the house with various passages heavily underlined, were increasingly worried about Jim and also concerned that he was drinking considerable amounts of alcohol. Jim’s friends began to avoid him, and he was increasingly iso- lated. He broke up with his girlfriend, who could no longer deal with his accusations of infidelity.
The situation deteriorated very rapidly during the summer months, and Jim was hospitalized one evening and detained under the Mental Health Act. He had gone out early to his local pub. A number of his friends were there, but he kept away from them, drinking alone in a corner. Suddenly Jim got out of his seat and began shouting at his friends, accusing them of stealing his money, undermining his confidence, and spreading rumors about him. He took some loose change from his pockets and threw it at his friends. They tried to ignore him, but Jim became increasingly agitated and aggressive, and finally physically attacked one of them. A number of people became involved, and the situa- tion became more chaotic as a fight broke out. The po- lice were called and Jim was arrested. He had suffered minor physical injuries, so he was taken to the accident and emergency department of the local hospital and from there was admitted to the mental health ward. Jim spent about 5 weeks in the hospital, during which time he was treated with antipsychotic medication. His health care plan included counseling, and his family
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members received psychoeducation, in that they were given information about psychosis and general advice on how to support him at home. Jim’s symptoms remit- ted during his hospital stay, and he was discharged, with frequent outpatient appointments with his psychiatrist and home treatment with the assertive outreach team.
Over the intervening years, Jim had five more re- lapses, during which a similar pattern would follow. He would become paranoid, hear voices and become isolated, and have increasing difficulty in caring for himself. Each relapse was followed by a short period of hospitalization with increased medication. However, residual symptoms became common following an epi- sode, and in spite of increased medication and changes to atypical antipsychotics, Jim continued to experience auditory hallucinations, paranoid delusions, and delu- sions of reference. He often avoided going out or con- tacting people because of his paranoia. He was able to initiate and maintain a relationship, although the voices continued to send him “visions” and to question his girlfriend’s faithfulness.
Jim was referred for CBT to treat his persistent posi- tive psychotic symptoms as part of a multidisciplinary approach to his care and to promote recovery.
Current Situation
Jim now lives in his own apartment. He has good re- lations with his parents, who live quite close by and whom he sees every few weeks. He is unemployed and receives disability benefits. Jim attends a day center for people with mental health problems 2 or 3 days a week. He had attended a local college to study computers but recently discontinued schooling because he found the social contact too stressful. Jim has a steady girlfriend, Sue, whom he sees regularly. He has lost contact with the friends he had before he became ill, and although he occasionally sees them, he avoids them and places he thinks they might go. He receives antipsychotic medi- cation, attends monthly outpatient appointments with a psychiatrist, and is visited at home once a week by a community psychiatric nurse who provides counseling and support, and monitors his mental state.
Mental State at Referral
Jim experienced auditory hallucinations in the form of a variety of voices talking to and about him. He described these as “helpful” voices and “evil” voices. The “help-
ful” voices warned him of the “schemes” of others and told him about dangerous situations and times when he was under threat. They warned him to avoid “dodgy people” who might attack or assault him. Jim thought their warnings were very helpful and was convinced that acting on these warnings kept him from harm. The “evil” voices generally spoke about him, saying that he was “stupid, useless, and no good,” “not up to it sexu- ally,” and other personally defamatory statements.
There were voices that told Jim that his girlfriend Sue was unfaithful and cheating on him. He was un- sure whether these voices were “helpful” or “evil.” These voices also sent Jim pictures of Sue being unfaithful and simultaneously told him that he was stupid and useless to put up with it. He described these pictures as “visions” that he found extremely distressing. Although Jim said he did not believe that Sue was unfaithful, the voices became increasingly more intense and compelling, and he was unable to resist shouting back at them. Sue was able to reassure Jim that his fears were groundless.
Engagement
Initially, Jim was resistant to contact with the clini- cian (in this case, Jim had been referred to a clinical psychologist for CBT). At the time of referral, he was quite paranoid, and when he was visited at his home for the first appointment, having failed to attend his clinic appointment, Jim refused to open the door. (It is common practice for mental health professionals in the United Kingdom to do home visits.) A short con- versation through the letter box ensued, ending with the clinician’s statement that he would return at a more convenient time. Two further visits resulted in Jim re- fusing to open the door. The strategy here was just to make contact to reassure Jim that his views were per- fectly valid and that another visit would be made at a later date to see how he felt about things then. In situ- ations in which the initial engagement is problematic, the best strategy is to “roll with resistance” and try to defuse the situation and reduce any agitation, maintain contact, and return at another time.
On the next occasion, Jim was more relaxed and al- lowed the clinician into his flat. Given Jim’s paranoia, it was important for the clinician just to establish a posi- tive interaction and relationship at this point, and not to introduce the topic of symptoms or psychological treatment until Jim was completely comfortable with him. So, in Jim’s case, the first couple of sessions were
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kept brief and covered his general well-being and topics of interest for him. The clinician’s primary focus was to keep Jim engaged and to develop the beginnings of a therapeutic relationship. It is not always the case that assessment and treatment cannot be embarked upon more quickly, but maintaining engagement is essential.
The fourth session was longer and the clinician in- troduced the possibility of psychological treatment. This necessitated a discussion of Jim’s symptoms, along the following lines:
“I understand you have been hearing voices when no one is there. What do you make of this? Have you any idea what these voices are? Are the voices a dif- ficulty for you? Would you want to try and do some- thing about these voices?”
These questions not only raise the topic of the psy- chotic experience and the suggestion of treatment but also attempt to obtain an idea of the person’s beliefs about the voices and whether they are perceived as real or not.
Similarly, the clinician can ask questions about the paranoid delusions:
“It is true that you are having difficulties with peo- ple?”
“Are you feeling that some people are against you? What do you make of these thoughts and feelings? Why do you think it is happening?”
“Are they a difficulty for you?” “Would you want to try and do something about these thoughts and worries?”
Again, the clinician attempts to assess quickly how strongly Jim holds these delusions and whether he would consider treatment.
Jim was not enthusiastic about treatment. He thought that his fears, as well as the voices, were real, and that psychological treatment was not appropriate in his case. This reaction is often encountered in people with re- sidual and persistent psychotic symptoms. A number of important points should be considered:
• What needs to be done to maintain engagement? • How can a clinically relevant problem be identified
and mutually agreed upon? • How can treatment be framed so that the person
sees it as achieving a positive and desired benefit?
First, it is important to validate the experience, but it is not necessary to agree on the cause. For example, in this case, it was important to agree that Jim did hear voices and believe that some people were against him. This can be done without agreeing that the voices come from a real entity or that people are actually against him. This helps to separate Jim’s belief about what is happen- ing to him from the experience; that is, that Jim has the belief is not the same as that belief being true. Similarly, that Jim hears voices is not the same as believing these voices exist as an independent and real entity. It may not necessarily be possible to agree on these points at this time, but the clinician can return to these issues. At the moment, engagement is more important.
Next, it is often helpful to investigate the conse- quences of the experience. Some of the voices cause dis- tress, and Jim’s paranoid ideas cause him to be fearful. Thus, distress and fear are more likely to be problems that Jim will be willing to address. This can be intro- duced as follows:
“You have told me that the voices sometimes make you feel very upset. Perhaps that upset is something I can help you with and that you would like to work on?
“The thoughts that some people out there are against you and want to harm you make you very frightened. Perhaps that fear is something we can work on together, so you feel less afraid? Maybe if you were less afraid you could cope better with deal- ing with people. Would that be helpful to you?”
So in cases when people hold delusional beliefs with very high levels of conviction and do not accept that they are experiencing a psychotic episode, trying to per- suade them to eliminate their symptoms and the experi- ences they believe to be real can be counterproductive and jeopardize engagement. However, trying to reduce distress may be a viable alternative for a collaborative goal. There is also an assumption from the model that reducing emotional reactions to symptoms may well weaken the symptoms themselves.
However, Jim remained unenthusiastic about this treatment goal as well. His view was that being fearful about people was a reasonable reaction given that there were people who would harm him, and this emotion kept him on his “edge,” so that he was more vigilant for threat and danger. His belief was that such vigilance actually kept him safe from harm, so there was little motivation to change and put himself in harm’s way.
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To protect engagement, it is important not to dis- pute or argue with the person, and most definitely not at this early stage, when the person is not convinced that there is any benefit to be gained from treatment. The next strategy the clinician used to engage Jim was to ask about his goals in life.
CLINICIAN: Jim, what sort of goals do you have? Is there anything you would like to achieve person- ally? Is there anything you would like to do that you haven’t been able to do, for whatever reason?
JIM: Yes, lots of things. I’d like to get a job that’s well paid. I’d like to go back to college. That would help me get a good job.
CLINICIAN: Going to college would help you get a good job. That is a very good idea. Would you like to go back to college?
JIM: I would, but when I went before, I had problems. CLINICIAN: What sort of problems were they? JIM: Well, I got scared of the people there. I thought
some of them were scary, dodgy, money grubbers. The voices told me not to go. I have to do what the voices tell me.
CLINICIAN: So one of your important goals is to get to college so as to help you get a good job, but being scared of the people there and the voices is stopping you from going to college and achieving your goals. Is that about it?
JIM: Yes, I suppose you are right.
In this way, Jim has realizes that his important goals are being impeded by his psychosis, and he and the clinician are able to agree on a problem that needs to be addressed. Thus, Jim can see a benefit to receiving treatment.
As well as maintaining engagement, the clinician has learned quite a lot about Jim and his problems. The voices warn Jim about certain situations, and he listens to them and takes avoidant action; thus, he has developed a number of safety behaviors that protect him from perceived harm. Opportunities to test out or refute these threat cognitions by dropping safety be- havior are not taken up. However, there are situations that lend themselves to reality testing. Jim experiences command hallucinations (voices that give him a direct order) to which he responds. The likelihood that Jim thinks the voices are powerful, and that he has little or no control over them, provides future opportunity to
refute these attributions. Jim experiences some feelings of dissonance in that he is now aware that his valued goals are impeded.
Case Formulation
Treatment naturally follows from an accurate assess- ment of the person’s problems, and it is important to establish details of the antecedents and consequences of psychotic symptoms (see Tarrier & Calam, 2002, for a discussion of case formulation in general). In this case, Jim has many psychotic symptoms, and it is probably best to deal with them in stages.
Paranoid Delusions
Jim has paranoid delusions that occur in a number of situations. When alone in his flat, Jim worries that his old friends and family have stolen all his money and are scheming against him. This is reinforced by the voices telling Jim he needs to be on his guard. Jim also be- comes very paranoid when he goes out. For example, in the street, he scans the crowds for signs of his old friends, so that he can make good his escape if he sees them or “scary people” who might assault him. He is also paranoid at the day center, just as he was at col- lege. The voices tell him the situation is dangerous, that there are dangerous people about, and that he must take care. Jim knows the voices will warn him of danger, so he listens out for them and is attentive to them when they occur. At the day center, Jim becomes more agi- tated the longer he is there, and he usually goes home after a short time. In doing so, he feels reassured that the voices have helped him and kept him from harm. Jim also wonders why the voices help him and con- cludes that it must be because he is special in some way. This puzzles him, because the “evil” voices are unpleas- ant and nasty to him. Jim concludes that because he is special, he is being tested by the “evil” voices to see whether he is worthy of their help. Only special people would be helped and be tested. In thinking this way, Jim has resolved the dissonance posed by experiencing both “helpful” and “evil” voices.
The clinician and Jim decide jointly to focus on the difficult situation at the day center:
CLINICIAN: OK, Jim, I’d like you to talk me through what happens at the day center. The reason I ask this is because you remember that attending college was an important goal you wanted to achieve but couldn’t
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because you felt suspicious of people there. Well, the situation at the day center is a lot like that at college, so we might learn how you can cope with return- ing to college if we examine the day center situation. Does that sound OK to you?
JIM: OK. Well one of the things that happens is that I know the voices know I’m vulnerable because they can tell when I’m like that, which is when they attack me, but they also want to help me, so they warn me about the scary people there.
CLINICIAN: How do the voices know you are vulner- able?
JIM: They can tell, because they know how I feel. CLINICIAN: How do you feel when you are vulnerable? JIM: All shaky and on edge. CLINICIAN: Is that like a feeling of being anxious or
stressed? JIM: Yes, a bit like that.
It appears that Jim becomes anxious in anticipation of going to the day center. There may be a range of reasons for this, such as anticipatory and situational anxiety, social anxiety, fear of being attacked, or general elevated levels of arousal. One hypothesis is that Jim picks up on this feeling of anxiety and misattributes it to being “vulnerable” to the voices. This is because his increased anxiety is associated with an increased prob- ability of experiencing auditory hallucinations, but Jim attributes meaning to this association. Voices are im- bued with attributes of power and intent.
CLINICIAN: OK, Jim, so you’re feeling anxious and vulnerable. What happens next?
JIM: Well usually the voices will start. They can say a lot of things, but they will warn me about danger. I know that the voices will attack me, but I want to keep safe, and they will warn me so I listen out for them.
Here, Jim is indicating that not only do the voices occur in this situation but also his attention is focused on listening out for them, which may indicate that the threshold for detecting them is being lowered. This suggests that a redirection of attention may be a help- ful method of coping with this situation. The clinician does not suggest this method at this stage, but he may call upon it later.
CLINICIAN: When they warn you, how does it happen? JIM: The voices will see someone that is dangerous and
they will say, “See him? He’s going to get you, he’ll attack you. You better get out of here.” When they say that, I can see this guy looks vicious and he’s going to have a go at me, so I get out of there as fast as I can.
CLINICIAN: Then what happens? JIM: I get out of there, and I feel real relieved that I’ve
escaped. I feel real lucky that I’ve got the voices to keep me safe. Otherwise, I’d be in for it, I’d be in ter- rible trouble. The more I think about it, the luckier and more special I feel. They keep me safe.
It appears that Jim attributes both personal meaning to his voices and power to keep him safe. In fact, he has developed a type of safety behavior that reduces his anxiety and helps him escape a feared consequence. His avoidant behavior also reinforces his feeling of being special.
This establishes a useful behavior cycle that the clini- cian may utilize to help Jim abandon his safety behav- iors and to disprove his catastrophic predictions that he will be attacked. First, it is helpful to establish a little more detail.
CLINICIAN: You said that the voices warn you about danger at the day center most of the time. Does this always happen?
JIM: No, not every time. I always listen out very care- fully for the voices, but sometimes they aren’t there.
CLINICIAN: So when the voices aren’t there, what hap- pens?
JIM: Sometimes I still feel vulnerable, but I just get on with it.
CLINICIAN: Do you mean you don’t leave, you stay there?
JIM: Yes, sometimes I get bored and go home, but usu- ally I stay and have a chat and a cup of tea.
CLINICIAN: Tell me, Jim, is it pretty much the same people there whether you hear the voices or not?
JIM: Yes, that’s it, pretty much the same people all the time.
CLINICIAN: So sometimes the voices tell you someone is dangerous, and you get out pretty quick and feel relieved you weren’t attacked, and at other times the voices aren’t there, but you stay with the same people,
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those that you thought were dangerous before, and nothing happens. Doesn’t that mean that at times they are dangerous and other times they’re not dan- gerous? Isn’t that strange?
JIM: Yes, I suppose it is. I’d not thought about that be- fore.
Here, the clinician is looking for inconsistencies in situations that can be used to refute Jim’s beliefs. The clinician highlights the inconsistency in the logical presence of threat and feeds it back to Jim, asking him what he makes of it. The clinician pursues the point about the inconsistency of the occurrence of the voices.
CLINICIAN: Sometimes the voices aren’t there. Why is that?
JIM: I don’t know that, either. Maybe they have to look after someone else on that day. Yes, that must be it. There must be other special people that they have to look after, and they are helping them. Just goes to show how important the voices are if they have lots of special people to look after. Means I’m really special, too, one of the real special people.
At this point, Jim appears to be confabulating and absorbing this new information into his delusional thought network. New information is processed in a way that protects rather than challenges the delusional system. This is useful, because an alternative explana- tion—that the voices occur when Jim attends to them and feels stressed and are less likely to occur if he is more relaxed and engaged—can be advanced and test- ed as an alternative belief.
The clinician now needs to motivate Jim to test out some of his beliefs. He compares the day center situa- tion with college and the achievement of an important goal to motivate Jim to attempt to cope better at the day center. Furthermore, it is established that generally Jim enjoys going, although ambivalence is maintained by his fear of attack. Being taught how to manage his fear and be more relaxed in the situation is also a motivat- ing factor.
Jim needs to have a plausible set of alternative expla- nations of what is going on, so that he may process any new information differently and not reinforce his delu- sions. In the past, Jim has been told that he is paranoid because he has a mental illness involving an imbalance of biochemicals in his brain. This is not a particularly attractive explanation to Jim. It does not reflect his
actual experience, and it is stigmatizing. Jim needs to be presented with an alternative model of his experi- ences that allows him to collaborate in his psychological treatment.
The clinician might suggest that paranoia is a result of misunderstanding or misinterpreting situations, and that if Jim feels stressed and anxious, as he does at the day center, then he may misattribute this physical state to a “vulnerability.” He is more likely to experience the voices when he is anxious, but this does not mean that the voices know he is vulnerable. The clinician might also suggest that Jim ignore the voices when they tell him he is about to be attacked and just get on with what he is doing at the day center. Because the same people are there, and they do not attack him when the voices are absent, it is unlikely that he will be attacked when the voices are present. Thus, a behavior experiment can be established to test out whether the voices keep Jim safe. This may help challenge Jim’s belief that the voices are both truthful and helpful, and that they are power- ful and all knowing.
When Jim did enter these situations, he was acutely aware that his voices might occur, so that he developed an internal focus to monitor for feeling “vulnerable” and an external attention scan for hearing the voices. The former meant that he was more likely to amplify any internal sensations. The latter meant that he was more likely to verbalize what the voices usually said to him as a match and also, paradoxically, to focus his at- tention internally. This process of internal focus and at- tention scanning was more likely to trigger the voices. Intervention here involved persuading Jim to use other attentional strategies when he entered these situations. These strategies were rehearsed in the sessions and prompted with appropriate internal dialogue.
Jim also made a number of attributions about the voices. He believed that the voices warned him of threat because he “might be special”; he thought they might be able to do this through telepathy, and that he had little control over this process. Jim was troubled because the voices were often unpleasant, and he could not un- derstand why they would be so if they were helping him to avoid danger. But Jim concluded that because he was special, he needed to “be tested” by the voices, which in turn confirmed his belief that he was special. Of course, much of this explanation had been built up on the in- correct premise that the voices were actually warning him of a real danger, which could be challenged. An alternative explanation of his experience could be based on a normalization of this experience. Everyone has
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self-referent or bizarre thoughts at times, and in Jim’s case, these are perceived as external voices rather than being identified as part of the self and merely thoughts. Jim found this explanation plausible, although he was not entirely accepting of it. This is not unusual; how- ever, it did seed doubt in his mind and could be referred to constantly, further weakening his delusional expla- nations.
Two difficulties arose with Jim. He did not have an alternative explanation for the voices other than they represented some, albeit vague and poorly defined, powerful entities or beings (delusional), or that they were the manifestation of a biochemical imbalance in his brain (disease). The clinician suggested to Jim that his voices might be his own thoughts or a leakage from memory into consciousness that was not identified as being part of his self. This was why the voices often reflected Jim’s fears or concerns, or aspects of his past.
The voices warned Jim when he was in danger. He believed that the voices helped and protected him in these situations. For example, on one occasion, when Jim was walking down a road, the voices told him that a man coming from the other direction was going to attack him. Jim crossed the road to avoid the man and believed that in doing so he had avoided being attacked. He also noticed that the man looked “suspicious,” which further confirmed his belief that the voices had saved him from danger. Here is an example of an EBAC cycle to which we referred earlier in the chapter.
Experience—Voices tell him of a suspicious person approaching.
Belief—He is in imminent danger. Action—He crosses the road. Confirmation—He has avoided being attacked.
This can be used as another therapeutic example:
CLINICIAN: You’ve told me that when the man ap- proached you in the street, he was looking at you and the voices told you that you were in danger. What happened next?
JIM: Well, I knew he would go for me, so I crossed the street and got away.
CLINICIAN: When you crossed the street, did the man look at you or follow you, or say anything?
JIM: No, I don’t think so.
CLINICIAN: Isn’t that strange, if he was out to attack you?
JIM: Yes, I suppose so. I’d not thought about that be- fore, I was so glad to get away.
CLINICIAN: Tell me, Jim, when you walk down the street, where do you look?
JIM: Well, where I’m going, of course. That’s a silly question!
CLINICIAN: Well, it may seem so, but think where was the man going when you thought he was looking at you to attack you.
JIM: Well, he was walking toward me, and he was look- ing in that direction.
The clinician continues his questioning, so that Jim keeps returning to the conclusion that the man hap- pened to be looking at him because Jim was in his line of vision, nothing more. There was no evidence of an intent to attack, and once Jim was out of his line of vision, the man paid no further attention to him. Ex- periments can be constructed to emphasize this point further. Sometimes Jim may be drawing attention to himself by his own actions, which make people look at him (the self-fulfilling prophecy). Again, this can be drawn out by a similar line of questioning and tested. A similar approach can be taken with other examples of Jim’s paranoid behavior, and his behavior with friends and family. The clinician always comes back to these past examples of successful belief and behavior change, and asks Jim how he feels about them and whether he can identify any common factors between these past successes and current problems.
“Visions” Sent by the Voices
Jim was very upset with the “visions” he experienced of his girlfriend having sex with other people. He thought these visions were sent by the voices, also by a process of telepathy. Jim did not believe his girlfriend was unfaith- ful, but he became very upset and angry when the voic- es told him this. He tried to push the images out of his mind, but when this strategy failed, he became further convinced that the images were sent via telepathy. The more angry and upset Jim became, the more difficult he found it to resist the belief and to view the experi- ence of the visions as collateral evidence. An alternative explanation was that the visions were mental images
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that had become very vivid and occurred in response to his catastrophic thoughts about his girlfriend’s infi- delity and persisted because Jim attempted to suppress them. The voices were his own thoughts, which again posed questions about his girlfriend’s fidelity, because his constant ruminations on the topic had made Jim feel insecure about his relationship. This alternative explanation, in conjunction with a review of the objec- tive evidence regarding the security of his relationship, significantly weakened Jim’s delusional beliefs about infidelity, telepathy, and the reality of the voices. The clinician introduced thought suppression exercises to demonstrate the rebound effect of Jim pushing the im- ages out of his mind. Exposure to the “visions” was also useful in this case (although it might not be in all cases), demonstrating that images held in attention fade with time, along with the distress they cause, which was fur- ther evidence of an internal phenomenon and not exter- nal telepathy. Jim was also taught to identify the onset of the voices and to switch his attention to alternative stimuli as a way to reduce their impact and to demon- strate that these experiences were more likely generated internally rather than coming from an external entity. The clinician compared these experiences with anxiety disorders in which catastrophic beliefs and images serve to fuel irrational and threatening beliefs, pointing out that vivid imagery of “what might happen” or an imag- ined “catastrophe” would produce a sudden cascade of intense emotions. These experiences could then be re- labeled as unpleasant but highly improbable situations rather than reality.
Any slight reduction in the strength of a delusional belief was also used to challenge Jim’s general beliefs about control, threat, and veracity.
LOW SELF‑ESTEEM: A COMMON PROBLEM
People with schizophrenia frequently have a poor per- ception of themselves and low self-esteem. These global concepts can be hypothesized to be manifest in terms of a negative self-schema. This is postulated as being a consequence of severe mental health problems and all that goes with this. This can involve suffering the stigma of a mental health problems and even harass- ment and exclusion, the effects of social rejection and negative interpersonal environments, and the projected sense of being valueless and devalued. People with de- pression and suicidal ideation may feel increased feel-
ings of low self-worth because of their depressed mood. Furthermore, an attribution process can make them think that if they feel they want to kill themselves, then they must be worthless and deserve to die.
The factors that potentially impact on and maintain negative self-schemas are represented in Figure 13.3. As can be seen, the factors that influence and maintain negative self-schema are strong, multiple, and relent- less. The consequence of having a severe mental health problem is the formation of such negative self-schemas, which then serve to bias the way information is assimi- lated, so that these negative schemas are maintained and strengthened rather than being challenged and modified.
Feelings of low self-worth can both inhibit the ef- fective use of coping strategies and increase the risk of depression and self-harm.
Improving Self‑Esteem
The aim of this set of techniques is to generate posi- tive attributes, challenge negative self-schemas, improve global self-esteem, and elicit positive emotional reac- tions. This method can be carried out in two stages. The first stage elicits positive cognitions about the self, and the second elicits a positive emotional response. Al- ternatively, the two stages can be combined, so that the processes of cognitive and emotional responding occur together. The procedure for the two-stage process is de- scribed for convenience as follows.
Stage 1: Cognitive Responding
• Ask the person to produce up to 10 positive qualities about him/herself (the number can be varied dependent on the person’s capabilities; it is important that the person not fail in generating the required num- ber).
• Once the person has produced a list of these quali- ties, ask him/her to rate each on how much he/she really believes it to be true on a 0- to 100-point scale (where 0 = Not at all and 100 = Completely).
• Ask the person to produce specific examples of evidence of each quality; prompt specifically for actions that have occurred recently and can be time linked, such as “last week”; also use your knowledge of the pa- tient to elicit examples. Prompt and list as many ex- amples as possible.
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• Ask the person to rehearse the list of examples for each quality, which may be done through verbal description and mental imagery of the event, then to rerate his/her belief that he/she possesses this quality. (Usually, the belief rating changes to show an increase; it should be emphasized to the person that his/her belief can change depending on the evidence on which he/she focuses attention.)
• The person is given a homework exercise to moni- tor his/her behavior over the next week and to record specific evidence to support the contention that he/she has these qualities. The aim is to produce generaliza- tion and experiential learning of a number of positive attributes.
• At the next session, provide feedback on examples and prompt further examples. Again, ask the person to rerate his/her belief that he or she actually has these qualities, and further point out any changes in these beliefs.
• Ask the person to reflect on the effect that elicit- ing and focusing on specific behaviors and evidence
has on beliefs and qualities about him/herself and how this could affect the general opinion of him/herself. Reinforce all positive attributes and the process where- by the person comes to a more positive view of him/ herself.
• Continue to repeat this procedure. Continually emphasize that the person’s beliefs about him/herself vary depending on what is the focus of attention, and that self-esteem can be greatly affected by belief and is thus amenable to change.
The case of “Dave” illustrates implementation of this procedure. Dave had very successfully learned to cope with his symptoms, which had been markedly re- duced, and he had significantly improved his level of functioning. Dave produced a number of attributes that he thought he might have: “helpful,” which he gave a belief rating of 60 out of 100; “friendly,” which he rated 50; and “a good father,” which he rated as 30. He was then asked to suggest concrete and specific evidence to support all of these. For “helpful,” he cited having lent money to a friend some months before, opening a door
FIGURE 13.3. Maintenances of negative schemas.
Schizophrenia and Other Psychotic Disorders 547
to someone the previous week, and helping his father in the garden that week. He rerated this belief as 90.
For “friendly,” Dave cited that he had had many friends of 10–20 years’ standing; his friends contacted him regularly and enjoyed his company; he could talk comfortably to people in pubs or on buses. He got on well with the friends of his parents. Dave thought he got on well with the therapist and enjoyed speaking to him, and that he could talk to different types of people from different backgrounds without difficulty or re- serve. He rerated this belief as 100.
For being a “good father,” Dave said that he enjoyed taking his son and daughter out every week (he was di- vorced from their mother, who had custody). He was upset when he did not see them. He liked to buy them presents. He was happy for them to decide on activi- ties rather than doing things purely for convenience, and this in itself gave him pleasure. Dave rerated this belief as 60. However, at this point he introduced some negative evaluations. He felt that he could not be a good father, because he did not live with his children. He did not get on with their mother. He said that it was always easier for absent fathers who saw their children for short periods of time and tended to spoil them. This was not responsible parenting in his view. At this point, it was helpful for the clinician to go through the model of how negative views such as this are maintained (see Figure 13.3), to discuss these thoughts as being negative schema–congruent, and to indicate that the statements were “overgeneralizations,” a process by which negatives are maximized and positives minimized. Furthermore, although these thoughts and beliefs had a depressing effect on his mood and maintained Dave’s negative be- liefs about himself, they did not accurately reflect cir- cumstances. To challenge Dave’s views of himself as a bad father, various exercises where undertaken: He was asked to define a “bad father” in explicit terms, then objectively compare his behavior to this definition. He was asked to compare his behavior with that of others in similar circumstances. Last, he was asked to give a realistic and objective appraisal of his performance and circumstances. While carrying out these exercises, the clinician emphasized the potential for negatively biased self-appraisals, along with strategies for coping with this in the future.
Stage 2: Affective Responding
Dave was also asked to explain why these qualities were important and the potential benefits of possessing
them. The clinician used guided discovery and imagery during this process to ensure that the qualities selected were meaningful and important to Dave. He was then asked to generate practical examples of each quality. Particular emphasis was placed on describing specific behaviors associated with the quality and the context in which they were carried out. Attention was directed to Dave’s emotional experiences when displaying that quality, thus generating the positive affect associated with that experience. Dave was asked to imagine the positive emotional reaction that another person would experience in interaction with him as he displayed a positive quality, and to vividly imagine the other per- son’s experience and describe how he/she would feel and attempt to mimic this experience. Dave was then asked to describe how he himself felt when he had evoked the positive emotion in the other person.
For example, in displaying generosity by helping out a friend, Dave was asked to imagine through guided imagery how that friend felt when assisted by Dave. He was asked to intensify and sustain this positive emo- tion. Then, through a similar process, Dave was asked to imagine and describe how he himself felt when he realized how positive his friend had felt in being helped out. Again, Dave was asked to intensify and sustain this emotion. A similar process should be carried out for all positive characteristics and scenarios.
RELAPSE PREVENTION
Relapses rarely occur without any forewarning. They are usually preceded by a period of prodromal symp- toms that can last for days, or more usually weeks, and in some cases, months; the average prodrome is, how- ever, about 4 weeks (Birchwood, Macmillan, & Smith, 1994). Common prodromal signs and symptoms in- clude nonpsychotic symptoms (e.g., mild depression or dysphoria, anxiety, insomnia, irritability, mood fluctuations and interpersonal sensitivity) and low- level psychotic symptoms (e.g., suspiciousness, magical thinking, ideas of reference, feelings that “something is strange or wrong” and that the individual does not “fit in” with others around him/her). During the pro- dromal phase, people display behavior change, such as becoming more withdrawn, avoiding social contact, abandoning hobbies or interests, appearing more pre- occupied, and being unable to continue with work or other routine or demanding activities. As the prodrome progresses, these signs and symptoms intensify, and
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people may exhibit behavior that is out of character, such as being unable to care for themselves, becoming socially or sexually inappropriate, making accusations against others, muttering to themselves, and discon- necting the television or telephone.
People may be asked to recall prodromal signs and symptoms that preceded previous episodes and relaps- es, which can be based on the onset of the episode or admission to the hospital, then identify when changes were first noticed, what changes occurred, and how they progressed and in what sequence. Each sign or symptom may be written on a card, and the person may be asked to arrange them in temporal order of occur- rence. In this way, the person’s relapse signature, that is, the individual set of signs and symptoms that charac- terized the person’s prodrome and its time course lead- ing to relapse, can be identified. Family members or professional mental health staff, if available, can help identify prodromal changes and their sequence. Clini- cians may find the use of standardized assessments of prodromal symptoms helpful, such as the Early Signs Scale (Birchwood et al., 1989). Such instruments can also help the clinician cue or inquire about possible prodromal symptoms not spontaneously recalled by the person. The person needs to be able to discriminate between an actual relapse prodrome and normal mood fluctuations that do not signal a relapse. This is done through a process of discrimination training, whereby the person monitors mood and experiences over a num- ber of weeks, with a goal of learning to distinguish a real prodrome from the “false alarm” of a normal fluc- tuation in affect.
The next stage is to formulate a “game plan” to deal with a prodrome should one occur. Coping strategies can be formulated and rehearsed, the help of others can be elicited, and the assistance of mental health services can be requested, which may include an increase or change in medication. With an understanding of the time course of people’s prodromes, the clinician can identify different actions for different phases of the prodrome and the “window of opportunity” to inter- vene. An important part of the treatment approach is to plan for the future, especially for potentially stressful events that may occur and how to be aware of emerging symptoms and relapse. People can be monitored by re- turning to the clinician postcards that indicate they are well or that a prodrome may have started. Technology such as smartphones and e-mail provide new, innova- tive platforms and methods for clinicians to monitor patients and maintain contact, to identify early signs
of relapse, and to intervene at the optimal time. For example, smartphone-based personalized technology has been used successfully to enable real-time symp- tom self-monitoring, and detection by the clinical team of early signs of relapse in people with severe mental health problems (Lewis et al., 2020).
CLINICAL PROBLEMS AND DIFFICULTIES
Thought Disorder
Thought disorder, typically characterized by disrup- tion to language, makes it difficult to comprehend the meaning that the person is imparting. However, with experience and patience, it is often possible to follow some internal logic in the patient’s speech. This can be accomplished by asking the person to explain the meaning, or by reflecting back one’s own understand- ing, which is then rephrased in more coherent lan- guage. Progressing through these organized steps in a calm manner can help prevent the person from feeling overloaded with the emotional content of the discus- sion, which can occur, especially when the material being discussed is emotionally salient.
Persistent Psychotic Symptoms
Regrettably, there are cases in which the therapist’s best efforts and optimum medication produce little im- provement in the person’s symptoms. A number of op- tions are available in such cases. First, it is necessary to ensure that appropriate support services are in place, so that the person’s quality of life is maximized. Second, there should be regular reviews of treatment, especially of medication and of environmental circumstances, so that excessive stresses are avoided. Last, it is always worth continuing with a few simple and direct cogni- tive-behavioral strategies because, over a long period of time, these may begin to have an effect.
Risk of Suicide and Self‑Harm
The risk of suicide in people with schizophrenia is sig- nificant. Risk factors include being young and male, having long-standing symptoms with numerous exacer- bations, high levels of symptomatology and functional impairment, feelings of hopelessness in association with depression, fear of further mental deterioration, and excessive dependence on treatment or loss of faith in treatment. In one study, two paths to suicide risk, both
Schizophrenia and Other Psychotic Disorders 549
of which were mediated by hopelessness, were also iden- tified: (1) increased social isolation, to which longer ill- ness duration, more positive symptoms, older age, and being unemployed contributed, and (2) more negative views of the self, higher frequency of criticism from relatives, and more negative symptoms, to which being male, unmarried, and unemployed significantly con- tributed (Tarrier, Barrowclough, Andrews, & Gregg, 2004). Another cohort study and systematic review has confirmed and extended previous findings. Being young and male, with a history of violent offending, were identified as predictors of suicide, although this latter finding was restricted specifically to those with lower IQ (Webb, Långström, Runeson, Lichtenstein, & Fazel, 2011). A systematic review of 51 studies addition- ally identified important illness-related predictors such as depressive symptoms, hallucinations and delusions, and comorbid physical illness and substance misuse (Hor & Taylor, 2010).
It is important for therapists to be aware that sui- cide attempts are a very real possibility while treating someone with schizophrenia. Unfortunately, people with schizophrenia often commit suicide impulsively and use lethal methods, such as jumping from heights, immolation, or firearms. The presence of suicidal ide- ation needs to be assessed, and the person needs to be asked whether he/she has made any specific plans or taken any actions, and whether the normal barriers to self-harm and suicide have broken down. It is necessary to be aware of factors that can elevate risk, including erosion of self-esteem; increased sense of hopelessness and despair, especially related to the person’s percep- tion of their symptoms and recovery; disruptive fam- ily or social relationships; and any changes in social circumstances or loss of supportive relationships (e.g., changes in mental health staff, staff holidays, or leave). Furthermore, the occurrence of major life events, loss, or shameful experiences can lead to despondency.
Some factors that can increase risk for suicide are quite unique to the experience of psychosis, such as the experience of command hallucinations telling patients to self-harm. Other examples are more idiosyncratic. One of us (N. T.) had a patient who experienced strange physical sensations that he interpreted as the Queen of England entering his body. As a loyal subject, he thought he should vacate his body to give her sole pos- session, and he attempted to kill himself by slashing his wrists. This was not the result of a will to die, but was more driven by some sense of social protocol toward royalty. Fortunately, the attempt was unsuccessful.
Many clinicians hypothesize that psychotic symp- toms have a protective aspect in masking the harsh re- alities of the burden of a serious mental health problem. Improvement in awareness of reality and symptomatol- ogy can bring with it an increased exposure to this bur- den, thus increasing the probability of potential escape through suicide. The clinician needs to be aware of all these factors, to know the people he/she is working with well, and to monitor changes in their circumstances or mood that may be problematic. It is important to be aware of predictable changes and plan for them, to es- tablish good communication with other mental health workers, and to address depressed mood and hopeless- ness in an open manner. Assessing acute suicide risk is further complicated by flat or incongruous affect, so that the cues a clinician would look for in a person with depression may not be exhibited by a person with schizophrenia. When risk is high, emergency mental health services should be called.
Dual Diagnosis: Comorbidity of Alcohol and Substance Use
Comorbid substance use disorders are an escalating problem in people with schizophrenia. So-called “dual- diagnosis” patients tend to do worse than people with schizophrenia alone on a range of outcomes. They tend to be more persistently symptomatic; to have more fre- quent and earlier relapse and readmission; to be more likely to present to the emergency services; and to have higher levels of aggression and violence, and greater risk of suicide and self-harm.
Motivational interviewing has been used effectively to enhance motivation to change substance use behav- ior in people with schizophrenia (Barrowclough et al., 2001; Haddock et al., 2003). Motivational interviewing has been termed a “style” rather than a specific interven- tion, and can be incorporated into a CBT approach to increase the person’s motivation to change substance or alcohol use behavior and concurrently address the psy- chosis. It is postulated that an important interaction be- tween alcohol or substance use and psychotic symptoms requires this dual-treatment approach. Many people do not consider their alcohol or substance use a problem and perceive the positive benefits, such as self-medica- tion, peer identification, or enjoyment, as outweighing any negative consequences. The aim during the initial sessions is to elicit change or motivational statements from the person. The therapist uses the motivational interviewing skills of reflective listening, acceptance,
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and selective reinforcement to elicit such statements. Once the person identifies substance or alcohol use as a problem and expresses a desire to change, therapy can then progress to practical ways to achieve this goal. The largest RCT to date compared a combined condition of TAU, motivational interviewing, and CBT with TAU alone in those with psychosis and co-occurring sub- stance use. Results showed treatment to be beneficial in improving motivation to change substance use, and sig- nificantly reduced the amount of substance consumed per day, with this latter finding being maintained at 24-month follow-up. However, there were no effects on clinical outcomes such as relapse rates, symptoms, and functioning (Barrowclough et al., 2010).
CONCLUSION
CBTp does have significant benefits for people with schizophrenia and psychosis. It should be carried out as part of a comprehensive care plan. It is unlikely to “cure” people, but it may assist them in coping with and recovering from distressing experiences. Intervention is based on a detailed assessment and formulation. It does require considerable skill, experience, and knowledge of CBT and psychosis, and it does not lend itself easily to a simple protocol format. Further research on theoreti- cal aspects of understanding psychosis from a psycho- logical perspective is important to inform and further develop CBT procedures. Required is research into dis- semination and how new psychological treatments pen- etrate into mental health services and become accessible to patients.
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Clinicians working with individuals with alcohol use problems, as well as clinicians in training, have found this chapter to be an extraordinarily useful resource in guiding their treatment approaches. In this thoroughly updated and edited revision, the authors begin by describing how recent societal trends and legislative initiatives have increased the need for highly trained clinicians to treat addiction. After briefly reviewing the available empirical evidence on treatment approaches that range from Al- coholics Anonymous to brief interventions, to intensive inpatient treatment, the authors describe the myriad factors that every clinician must consider in choosing and carrying out appropriate interven- tions for individuals with drinking problems. Using a variety of illuminating case vignettes, Barbara S. McCrady and Elizabeth E. Epstein illustrate important therapeutic strategies, including methods for motivating these clients to begin treatment. In a manner that emphasizes the humanity of the couple and makes the partners come to life, the extended case study in this chapter illustrates the all-too- frequent tragic consequences of excessive drinking. In the context of this case description, the au- thors describe in great detail what clinicians will not find in books that simply lay out various treatment procedures—that is, the thrusts and parries of superb and experienced clinicians in overcoming the roadblocks that inevitably emerge during treatment. —D. H. B.
A lcohol use disorder (AUD) ranges in severity and context from the heavy drinking college student
who misses classes to the person with severe and chronic AUD experiencing accumulated life-threaten- ing medical and social consequences of drinking. Al- though the prevalence of AUD is higher in males than in females and in younger than in older adults, alcohol- related problems affect individuals from any sociode- mographic, racial/ethnic, or occupational background, and the prevalence is converging across genders (Grant et al., 2017). In mental health and medical settings, at least 25% of clients are likely to have an AUD as part of their presenting problems (e.g., Zimmerman, Lub- man, & Cox, 2012), so clinicians in medical and men- tal health professions need to be competent to identify,
assess, and plan an effective course of treatment for these clients.
The need for clinicians who are competent in treat- ing AUD and other substance use disorders (SUDs) will increase because of two Federal laws passed in recent years. The Patient Protection and Affordable Care Act, passed in 2010 in the United States, mandates alcohol and drug screening and brief intervention in primary care settings as a covered benefit, and the Wellstone– Domenici Mental Health Parity and Addiction Equity Act of 2008 mandates comparable health care coverage for treatment for physical health, mental health, and addictions problems. As a result of these laws, more in- dividuals with AUD and other SUDs are being identi- fied and referred to treatment.
C H A P T E R 14
Alcohol Use Disorders
Barbara S. McCrady Elizabeth E. Epstein
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Contemporary treatment of AUD and SUD is shift- ing due to advances in our understanding of the bio- logical and neuroscientific underpinnings of addiction, as well as increasingly wide dissemination of evidence- based motivational enhancement, cognitive-behavioral, and pharmacological treatments. A new perspective to enhance motivation to change substance use behavior has blossomed, along with consideration of a wider range of acceptable treatment goals. In addition, more nuanced understanding of the reciprocal relationship between AUD and other SUDs and co-occurring men- tal health disorders such as depression, anxiety, bipo- lar disorder, psychosis, and attention deficit disorder demands overall greater sophistication in treatment approaches and clinician training. These new treat- ment options are gradually claiming their rightful place alongside traditional recovery perspectives that have dominated addiction treatment for decades (Roman, 2013); it is an exciting time to treat AUD and other SUDs.
In this chapter we describe the diagnostic, biological, and social context of drinking and drinking problems, provide an integrative model for conceptualizing and treating alcohol use problems, and present both a series of case vignettes and an extended case study to illustrate the clinical model. Useful and effective tools are pro- vided for clinicians to work with persons with drinking problems. Persons with drinking problems are treatable; they are both challenging and rewarding to treat, and when they change successfully, it is gratifying to have the opportunity to participate in helping people make major and satisfying changes in their lives.
DIAGNOSIS AND DEFINITIONS OF ALCOHOL PROBLEMS
Diagnosis
In the diagnosis of alcohol problems, the fifth edition of the Diagnostic and Statistical Manual of Mental Dis- orders (American Psychiatric Association, 2013) treats AUD as a single disorder, ranging along a spectrum of severity. Previous editions of the DSM discriminated between alcohol abuse and dependence; this distinc- tion no longer applies. To be diagnosed with an AUD, an individual must meet at least two of 11 criteria, and the AUD is classified as mild (two to three symptoms), moderate (four to five symptoms), or severe (six to 11 symptoms). For DSM-5, the 11 DSM-IV diagnostic cri- teria for alcohol abuse and dependence were updated by
eliminating “repeated alcohol-related legal consequenc- es,” and adding “craving.” Thus, DSM-5 diagnostic cri- teria focus on impairments in occupational and social role functioning; physical consequences such as with- drawal and tolerance; and disturbed patterns of alcohol consumption. An AUD may be classified as being in partial remission or in full remission; remission may be early (at least 3 months) or sustained (1 year or more).
Contemporary Neuroscience Conceptualization of AUD
The National Institute on Alcohol Abuse and Alcohol- ism (NIAAA) defines AUD as a medical condition, a “chronic relapsing brain disease characterized by an impaired ability to stop or control alcohol use despite adverse social, occupational, or health consequences. AUD can range from mild to severe, and recovery is possible regardless of severity” (NIAAA, 2017, pp. 16– 17). The brain disease presents in a cycle of three stages (Volkow & Koob, 2019):
1. “Binge/intoxication” is loss-of-control drinking, involving structures in the basal ganglia, con- sidered the “reward center” of the brain. Alcohol triggers repeatedly activate the reward center, leading to increased salience of alcohol cues and habit formation by repeated associations of alco- hol cues with reinforcing effects of drinking, via changes in the striatum.
2. “Withdrawal/negative affect” occurs when re- peated periods between drinking episodes create both a reward deficit and enhanced stress reaction in the amygdala.
3. “Preoccupation/anticipation” arises from irregu- larities in the prefrontal cortex, resulting in defi- cits in cognitive control over alcohol-seeking be- havior (Koob, 2013).
AUD, in contemporary cognitive neuroscience, is considered to be a brain disease with deficits in two neurocognitive systems: (1) cognitive control, which leads to an inability to control behavior toward alco- hol, and (2) reward circuitry sensitization, which leads to an increase in the saliency of alcohol cues (Field & Cox, 2008; Goldstein & Volkow, 2011; Koob, 2013; Noël, Bechara, Brevers, Verbanck, & Campanella, 2010). Imaging data suggest a disruption of the neu- ral circuitry for cognitive control, which has been hy- pothesized to be a fundamental agent in substance
Alcohol Use Disorders 557
dependence (Chambers, Garavan, & Bellgrove, 2009; Volkow, Wang, Tomasi, & Baler, 2013). Moreover, ex- cessive drinkers selectively attend to substance-related cues (Cox & Klinger, 2011), and the degree of the atten- tional bias is related to increased saliency and incentive for alcohol cues, the amount of use (Cox, Fadardi, & Pothos, 2006), and subjective craving.
An Alcohol Problems Perspective
In contrast to the formal diagnosis of AUD, behavioral researchers and clinicians have suggested that alcohol problems represent one part of a continuum of alcohol use, ranging from abstinence through nonproblem use to different types and degrees of problem use. DSM-5 is more aligned with this perspective but still considers a cutoff indicative of a disorder. From the continuum per- spective, alcohol problems may be exhibited in a variety of forms—some that are consistent with a formal diag- nosis, and others that are milder or more intermittent. By using an alcohol problems perspective, the clinician can focus more clearly on the pattern of drinking, nega- tive consequences that the client has accumulated, his/ her behavioral excesses and deficits across various areas of life functioning, and his/her particular strengths. A deemphasis on diagnosis forces the clinician to consider clients from a more individual perspective. Therefore, although formal diagnosis is useful for identifying and defining the severity of a client’s problems and is neces- sary for formal record keeping, the approach to clinical assessment emphasized in this chapter attends less to diagnostic issues and more to problem identification.
This chapter views alcohol use problems as a mul- tivariate set, with alcohol consumption as a common defining characteristic. These problems vary in severity from severe AUD to mild and circumscribed problems. For some, alcohol consumption itself is a major present- ing problem; for others, the consequences of alcohol use—such as disruption of a relationship, occupational problems, or health problems—are the major reasons for seeking treatment. In viewing alcohol problems as multivariate, this chapter also assumes the existence of multiple etiologies for these problems, with genetic, psychological, and environmental determinants con- tributing in differing degrees for different clients.
Complicating Problems
Drinking problems are complicated by a variety of con- comitant problems. Of significance is the comorbid-
ity of AUD with other psychiatric diagnoses. A high percentage of those diagnosed with an AUD also ex- perience other DSM-IV Axis I psychological problems (84.2% of women and 75.5% of men), which may be antecedent to, concurrent with, or consequent to their drinking (Khan et al., 2013). The most common dis- orders are other SUDs, mood, and anxiety disorders. Personality disorders also are common.
Alcohol problems also are complicated by problems with cognition, physical health, interpersonal relation- ships, the criminal justice system, the employment set- ting, and the environment. Many people with AUD have subtle cognitive deficits, particularly in the areas of abstract reasoning, memory, cognitive flexibility, problem solving, and difficulties in emotional differ- entiation (see Fama, 2019). Because verbal functioning is usually unimpaired, these cognitive problems are not always immediately apparent. Heavy drinking also causes a variety of medical problems and can affect any organ system in the body. Heavy drinking may cause conditions such as cardiomyopathy, liver diseases, gas- tritis, ulcers, pancreatitis, and peripheral neuropathies. Even when obvious medical conditions are not present, the effects of chronic heavy drinking can be insidious and debilitating. Many people eat poorly when drink- ing heavily, which results in nutritional deficits, poor energy, or vague and diffuse physical discomfort. Mor- tality rates among persons of all ages are elevated with AUD, and are higher among women than among men (Centers for Disease Control and Prevention, 2004).
Interpersonal relationships also may be disrupted. The rates of separation and divorce among individu- als with AUD are about 50% higher than those of the general population (Cranford, 2014); spousal violence is higher among both men and women with AUD (Smith, Homish, Leonard, & Cornelius, 2012); and emotional and behavioral problems are more common among their spouses/partners and children (McCrady & Flanagan, in press). Health care utilization is elevat- ed among the spouses and children of actively drink- ing individuals with AUD (Ray, Mertens, & Weisner, 2009).
Persons presenting for treatment of a drinking prob- lem may be involved with the legal system because of charges related to driving while intoxicated (DWI), other alcohol-related offenses (e.g., assault), involvement with the child welfare system, or drug-related charges. Clients vary in the degree to which they recognize that their drinking is creating problems, and in their degree of motivation to change their drinking patterns.
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In conclusion, the client presenting for treatment may be drinking in a manner that creates concern, be formally diagnosed as having AUD, and have other co- occurring psychological or personality disorders. The person also may have other major problems, such as cognitive impairment, physical health problems, inter- personal or occupational problems, and/or legal prob- lems. Problem recognition and motivation to change may be low. How does the clinician develop a rational approach to conceptualizing and treating this rather complicated clinical picture?
TREATMENT PLANNING MODEL
Our approach to treatment planning is multidimen- sional, and it recognizes that there is more than one ef- fective treatment for alcohol problems. Unlike certain disorders for which one treatment approach has de- monstrable superiority over others, in the alcohol field there are a number of legitimate and empirically sup- ported approaches to treatment (see Blonigen, Finney, Wilbourne, & Moos, 2015; Sancho et al., 2018). These treatments are based in different conceptualizations of the etiology, course, treatment goals, and length of treatment for alcohol problems. Among the behavioral treatments with the best support are brief interven- tions, motivational interviewing, cognitive-behavioral treatment, 12-step facilitation treatment, behavioral couple therapy, cue exposure treatment, mindfulness- based relapse prevention, and the community rein- forcement approach. In addition, several medications have been approved by the U.S. Food and Drug Ad- ministration (FDA) for the treatment of AUD. A num- ber of factors that seem to be common to effective behavioral treatments are summarized in Table 14.1. A key therapist responsibility is to help a client find a treatment approach and treatment setting that is ef- fective for him/her, rather than slavishly adhering to a particular treatment model or setting. A second and equally important therapist responsibility is to enhance the client’s motivation to continue to try, even if the initial treatment setting is not effective. Our approach to treatment planning takes into account eight major considerations: (1) problem severity, (2) concomitant life problems, (3) client expectations, (4) motivation and the therapeutic relationship, (5) variables main- taining the current drinking pattern, (6) social support systems, (7) maintenance of change, and (8) diversity among individuals with AUD.
TABLE 14.1. Principles for Treatment of SUDs
1. Structure and organization of the treatment setting • Clear and well organized • Actively involve the clients in the program • Provide a supportive and emotionally expressive
environment • Emphasize self-direction, work, and social skills
development • Expect clients to take responsibility for their treatment
and follow through
2. Type of provider and what the provider does • Treatment by addictions specialists or mental health
clinicians • Develop an effective therapeutic alliance
| Accurate empathy | Respect for the experience of clients in therapy | Avoidance of confrontational struggles
• Provide goal direction for the clients • Provide a moderate level of structure for the therapy • Handle ambivalence about changing or being in
treatment: | Titrate level of confrontation to the level of clients’
reactance | Avoid arguing with angry clients | Avoid pushing clients hard to accept their diagnosis
or the need to change
3. Level of care, continuity of care, and elements of treatment • Pay attention to retaining clients in treatment • Determine the intensity and length of treatment
partly by considering the severity of the substance use disorder. | For heavy drinkers with low alcohol dependence,
less intense, briefer treatments are appropriate and intensive inpatient therapy yields poorer outcomes.
| Clients with severe alcohol dependence have better outcomes with more intensive initial treatment, and respond most positively to treatment that focuses on 12-step counseling and involvement with 12-step groups.
• Assess and arrange for attention to clients’ other social service and medical care needs
4. Contextual factors • Involve a significant other • Help clients restructure their social environments to
include persons that support change and abstinence. • With clients who have little commitment to remain in
treatment or change their substance use, involve the family or other member of the social support system in the treatment to foster retention in treatment
• In the treatment of adolescents with substance use disorders, use approaches that involve multiple systems, including the family, peers, and others
(continued)
Alcohol Use Disorders 559
Problem Severity
Problem severity is relatively atheoretical and is most important in decision making about the types of treat- ments to be offered, the intensity of the treatment, and the initial treatment setting. Severe AUD can best be conceptualized as a chronic, relapsing disorder (McLel- lan, Lewis, O’Brien, & Kleber, 2000), with relapses oc- curring even after extended periods of abstinence. As with other chronic disorders, such as diabetes, cardio- vascular disease, or rheumatoid arthritis, the clinician necessarily takes a long-term perspective, maximizing periods of positive functioning and minimizing peri- ods of problem use, as well as minimizing the harm as- sociated with use. In contrast, other individuals have alcohol-related problems that may be circumscribed and not progressive (Finney, Moos, & Timko, 2013). Epidemiological data suggest that for the majority of those with alcohol-related problems, the problems will resolve or remit without any need for formal treatment or intervention. The clinician encountering individuals engaging in risky drinking or at the mild end of the AUD severity spectrum might plan a brief, motivation- ally enhancing intervention to complement the natural
change process and inspire these individuals to make changes in their drinking. However, even among indi- viduals with mild severity, presence of risk factors such as other co-occurring disorders, serious medical prob- lems, or a family history of AUD or SUD, may suggest a fuller course of alcohol treatment.
Concomitant Life Problems
Clients with AUD often have problems in multiple areas of life functioning—physical, psychological/psychiat- ric, familial, social/interpersonal, occupational, legal, child care, housing, and transportation. Assessment of multiple areas of life functioning is crucial for the planning and delivery of effective treatment. Research suggests that targeting client problem areas successfully can result in appreciable changes in these problems, even with clients who are severely alcohol dependent and homeless (Rapp, Van Den Noortgate, Broekaert, & Vanderplasschen, 2014). Furthermore, providing treatment directed at multiple problem areas enhances positive alcohol and drug use outcomes as well (Mor- genstern et al., 2006).
Client Expectations
Clinicians should provide clients with accurate expec- tations about the intensity of their treatment and the probable course of their problems. The clinician can inform clients who are risky drinkers or who have mild AUD without complicating conditions that treatment may be relatively short in duration, that they are likely to be successful in stopping or reducing their drink- ing, and that their long-term prognosis is good. Clients who decide to try to reduce their drinking rather than abstain can be told that now or at some point in the future they may decide to stop drinking completely (Witkiewitz et al., 2017).
Clients with moderate or severe AUD can be pro- vided with psychoeducation to help them develop a set of expectations about treatment and the likely course of their problems. Clinicians should be knowledge- able about treatment outcome research. For example, one review of several large treatment outcome studies found that after a round of treatment for alcohol use problems, about 25% of clients maintained sustained abstinence for at least 1 year after treatment, another 10% used alcohol in moderation and without problems, and that, on average, clients reduced the amount they drank by about 87%, and that alcohol-related prob-
TABLE 14.1. (continued)
5. Client characteristics • Greater client readiness to change is associated with
greater treatment success • Greater severity of the substance use disorder is
associated with a poorer response to treatment
6. Specific therapeutic elements • Focus on client motivation • Help clients develop awareness of repetitive patterns of
thinking and behavior that perpetuate their alcohol or drug use
• Attend to the affective experiences of clients • Consider the role of conditioning in the development
and maintenance of substance use disorders. Clinicians should carefully assess for indicators of specific conditioned responses to alcohol or drugs, and develop ways to change these conditioned responses
• Enhance positive outcome expectancies
7. Client–treatment matching • Assess for comorbid disorders and use empirically
supported treatments for additional presenting problems • Use female-specific treatment with women clients
Note. From Haaga, McCrady, and Lebow (2006). Copyright © 2006 Wiley Journals, Inc. Reprinted by permission.
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lems decreased by about 60% (Miller, Walters, & Ben- nett, 2001). If clinicians share information on possible treatment outcomes with their clients, the discussion should be framed in a way that creates a sense of hope and motivates clients to work hard in therapy. Clients who engage fully in treatment, stay for the full course of treatment, and complete assigned homework have the best chance of positive, sustained outcomes. Risk factors, current or ongoing life stressors, AUD sever- ity, and complications of the case, such as comorbid psychiatric problems, must be taken into account when formulating a discussion about prognosis that the clini- cian shares with each client.
The challenge for all clients is to learn skills to man- age their drinking problem and the changes they have made in a way that makes it minimally disruptive to their lives. Chronic illness metaphors may be helpful. For example, like a patient with diabetes, a client with AUD needs to make and maintain significant lifestyle changes to support healthy functioning. Like the pa- tient with diabetes, the client with AUD needs to know warning signs that he/she may be getting into trouble and know what to do. And neither individual can afford to forget or ignore his/her problem. Therapists also can educate their clients about the persistent neurobiologi- cal and neurocognitive changes associated with AUD to help them better understand that the challenges they face have, in part, a biological basis.
Motivation and the Therapeutic Relationship
Clients vary in the degree to which they recognize their drinking as problematic and in their readiness to change. Motivational models suggest that individuals initiate change when the perceived costs of the behav- ior outweigh the perceived benefits, and when they can anticipate some benefits from behavior change. Com- mon reasons to change include concerns about health, financial issues, major life changes, and weighing the pros and cons of continuing to drink versus changing (reviewed in Bishop, 2018). Prochaska and DiClemente (2005) proposed a continuum of stages of readiness for change. The continuum includes the stages of pre- contemplation, in which a person does not recognize a behavior as problematic; contemplation, in which the person considers that a behavior pattern might be problematic; determination or preparation, in which the individual resolves to change; and action, in which a person initiates active behaviors to deal with the prob- lem. Following action is maintenance, if the behavior
change is successful, or relapse, if the person returns to the problem behavior. These “stages” are fluid and may appear to fluctuate, but the Prochaska and DiClemente model provides a useful heuristic for treatment plan- ning, and a meta-analysis found moderate effect sizes for the relationship between stage of change and out- comes of treatment for AUD (Krebs, Norcross, Nich- olson, & Prochaska, 2018). Clients’ apparent stage of change and self-perception of their problems should guide a clinician’s initial approach to treatment and treatment planning.
Contemporary models such as motivational inter- viewing (MI; Miller & Rollnick, 2013) view motiva- tion as a state that can be influenced by therapeutic behaviors and the client’s life experiences. Therapeutic approaches to enhance motivation lead clients to talk more about changing their drinking (“change talk”) and less about continuing to drink (“sustain talk”) and, in turn, increases in change talk and decreases in sustain talk predict better outcomes (Moyers, Martin, Houck, Christopher, & Tonigan, 2009). Motivation- ally enhancing approaches appear to be particularly effective with clients who enter treatment very angry and hostile (Project MATCH Research Group, 1997b). The treatment model described below integrates cog- nitive-behavioral therapy (CBT) with motivational en- hancement therapy (MET) and is in line with the MI spirit. Clinicians use a nonconfrontational style; use simple and complex reflections, reframes, and sum- maries; and highlight and selectively reinforce clients’ change talk and positive behaviors in desired directions of change. Clinicians also highlight, normalize, and explore clients’ ambivalence and motivation to change their drinking behavior, and ask questions in a way that encourages clients’ answers to include reasons for wanting to reduce drinking. The model is essentially a hybrid CBT/MET approach that incorporates high- quality, common therapist factors that overlap substan- tially with MI techniques.
Factors Maintaining the Current Drinking Pattern
Case conceptualization for treatment planning focuses on factors maintaining the problematic drinking pat- tern. Presented here is a cognitive-behavioral approach to case conceptualization (see Epstein & McCrady, 2009). The cognitive-behavioral case formulation as- sumes that drinking can best be treated by examining current factors maintaining drinking rather than his- torical factors. Factors maintaining drinking may be in-
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dividual, or related to environmental circumstances or interpersonal relationships. The model assumes external antecedents to drinking that have a lawful relationship to drinking through repeated pairings with positive or negative reinforcement, or through the anticipation of reinforcement. The model assumes that cognitions and affective states mediate the relationship between external antecedents and drinking behavior, and that expectancies about the reinforcing value of alcohol play an important role in determining subsequent drinking behavior. Finally, the model assumes that drinking is maintained by its consequences, and that the sources of these consequences may be physiological, psychologi- cal, or interpersonal.
To integrate these assumptions about drinking, we use a functional analytic framework, in which the drinking response (R) is elicited by environmental stimuli (S) that occur antecedent to drinking; that the relationship between the stimulus and response is medi- ated by cognitive, affective, and physiological, or organ- ismic (O) factors; and that the response is maintained by positive consequences or the avoidance of negative consequences (C) as a result of drinking. Various in- dividual, familial, and other interpersonal factors are associated with drinking. At the individual level, envi- ronmental antecedents may be associated with specific drinking situations, times of the day, or the mere sight or smell of alcohol. Organismic variables may include craving for alcohol; withdrawal symptoms; negative af- fect such as anger, anxiety, or depression; negative self- evaluations or irrational beliefs; or positive expectan- cies about the effects of alcohol in particular situations. Organismic factors may be influenced by more distal etiological variables that have proximal impact in re- sponse to triggers. For instance, certain individuals are more prone to experience the stress-reducing effects of alcohol than others, an individual difference that is ge- netically mediated. Thus, anticipation of stress reduc- tion might play a more pivotal role in the functional analysis of drinking for some than for others. Or, for some individuals, one drink serves only to ignite the reward centers and create intense craving for more al- cohol, while for other people, one drink satiates the desire for alcohol; this individual difference may also be genetically mediated. Individual reinforcers may in- clude decreased craving or withdrawal symptoms, de- creases in negative affect or increases in positive affect, decreased negative self-evaluations, or decreased focus on problems and concerns. Recent advances in under- standing the neuroscience of AUD as described earlier
are incorporated into our CBT model by providing psy- choeducation about the relative imbalance between the activated brain reward system (salience of AUD triggers and how cravings are linked to brain reward, memory, and compulsion systems) and impaired cognitive con- trol over alcohol-seeking behavior (Koob, 2013). This framework helps clients understand why it is so dif- ficult to stop drinking, why cravings are experienced as so powerful, and why alcohol triggers are linked to compulsive alcohol-seeking behavior. The drinking behavior chain, presented in the context of this neuro- science framework, helps clients gain new perspective, for example, by thinking about cravings as brain events that do not need to be acted upon with alcohol-seeking behavior and to incorporate thoughts to reduce stimu- lus salience into cognitive restructuring exercises.
At the familial level, various antecedents to drinking occur. Alcohol may be a usual part of family celebrations or daily rituals. Family members may attempt to influ- ence the problematic drinking behavior by nagging the person to stop or by attempting to control the drinking through control of the finances or liquor supply. These actions may become antecedents to further drinking. Families in which a member is drinking heavily may de- velop poor communication and problem-solving skills, as well as marital/couple, sexual, financial, and child- rearing problems that then cue further drinking. The person with the drinking problem may have a variety of reactions to these familial antecedents, experiencing negative affect, low self-efficacy for coping with prob- lems, and/or retaliatory thoughts. Family behaviors may serve to reinforce the drinking. The family may shield the person from negative consequences of drink- ing by taking care of the drinker when intoxicated or assuming his/her responsibilities. A number of investi- gators have observed positive changes in marital/couple interactions such as decreases in negative behaviors by the drinker and by the partner when the drinker con- sumed alcohol, suggesting that these positive behaviors may reinforce the drinking (e.g., Testa, Crane, Quigley, Levitt, & Leonard, 2014).
There also are other interpersonal antecedents to drinking that may include social pressures to drink; work-related drinking situations; friendships in which alcohol consumption plays a major role; or interpersonal conflicts with work associates, friends, or acquaintanc- es. The person may react to interpersonal antecedents to drinking with craving, positive expectancies for alco- hol use, social discomfort, or negative self-evaluations for not drinking. Positive interpersonal consequences of
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drinking may include decreased craving or social anxi- ety, an enhanced sense of social connectedness or fun, or increased social comfort or assertiveness.
Social Support
The behaviors of family and other members of the cli- ent’s social network are integral to the case conceptu- alization. The availability of general social support, as well as social support for abstinence or moderate drink- ing, is crucial to successful treatment. Support from the client’s social network for abstinence is associated with better drinking outcomes; support for continued drinking is associated with poorer outcomes (Long- abaugh, Wirtz, Zywiak, & O’Malley, 2010). Clients in a social network that is strongly supportive of drink- ing may need to take deliberate steps to detach from that social network and access new social networks that support abstinence or moderate drinking. Some data suggest that involvement with Alcoholics Anonymous (AA) can serve such a function (Litt, Kadden, Tennen, & Kabela-Cormier, 2016); there are other social groups that support abstinence (e.g., some religious organiza- tions), and partner- or family-involved treatment may help to change the client’s current social network to be more supportive of recovery.
Maintenance of Change
On average, individuals with AUD have a high prob- ability of relapse, an ever-present consideration, both because long-term, ingrained habits are difficult to change, and because of the permanent physiological and metabolic changes stimulated by heavy drinking (Woodward, 2013). Several models have been proposed to conceptualize the maintenance or relapse process, with associated treatments. The most prominent main- tenance models include the relapse prevention (RP) model (Marlatt & Gordon, 1985; Hunter-Reel, Mc- Crady, & Hildebrandt, 2009; Witkiewitz & Marlatt, 2004), and the disease model, best exemplified by the practices common to AA. The RP model, an exten- sion of the functional analytic model described earlier, focuses on the interplay among environment, coping skills, and cognitive and affective responses in main- taining successful change. In the RP model, relapse occurs in response to a high-risk situation for which the client either lacks or does not apply effective cop- ing skills. Low self-efficacy for coping with the situa- tion may contribute to the difficulties. If the client does
not cope effectively, use of alcohol is likely. Marlatt and Gordon (1985) suggested that, following initial drink- ing, a cognitive factor, the abstinence violation effect (AVE), is activated. The AVE represents all-or-nothing thinking; after drinking, the client makes a cognitive shift to viewing him/herself as “drinking”; therefore, he/she continues to drink. RP treatment focuses on several points of intervention common to cognitive- behavioral treatment, such as identification of high-risk situations and acquisition of coping skills, as well as cognitive restructuring to help the client view a drink- ing episode as a “lapse” from which he/she can learn and return to abstinence rather than a “relapse” into previous drinking patterns. RP also focuses on lifestyle changes to decrease the presence of high-risk situations, and encourages development of a balance between plea- sures and desires, and obligations and responsibilities (a “want–should” balance) in the client’s life. In his more recent work, Marlatt and his colleagues (Mar- latt & Donovan, 2005; Witkiewitz & Marlatt, 2004) described relapse as “multidimensional and dynamic” (Marlatt & Donovan, 2005, p. 21), and considered the influence of longer-term risk factors such as family his- tory and social supports, and well as more proximal in- fluences on relapse. They also suggested that there are reciprocal interactions among cognitions, coping skills, affect, and drinking.
The 12-step, AA model perspective views AUD as a chronic, progressive “disease” that can be arrested but not cured, and conceptualizes “disease” differently than the contemporary neuroscience and NIAAA view of AUD described earlier. Treatment based on the 12- step model focuses on the view that regular participa- tion in AA and a lifelong program of AA-based recovery are the only means to achieve and maintain abstinence (see Kelly & Yeterian, 2013). The model presented in this chapter is most closely allied with the RP model, but clinicians should be knowledgeable about the 12- step model underlying AA, since it well-known and widely available. Many clients find the 12-step model and program of recovery helpful and relevant; atten- dance at 12-step meetings and/or following the 12-step model is compatible with engaging in CBT for AUD with an abstinence goal.
Diversity among Individuals with AUD
Individuals with AUD are as diverse as the general population. Each client coming to treatment presents with the intersectionality of many different identities,
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including (1) demographic elements such as age, sex assigned at birth, occupation, income/socioeconomic status, and education; (2) ability/disability; (3) race and ethnicity; (4) gender identity and sexual orienta- tion; (5) geographic elements such as urban versus rural versus reservation residence, and living context (e.g., stable residence vs. homeless); (6) religious affiliation; (7) military/veterans status; and (8) criminal justice in- volvement.
There are extensive literatures on each of these di- mensions of diversity (see, e.g., reviews by Bekman, Wilkins, & Brown, 2013; Castro, Garvey, Kellison, & Marsiglia, 2013; Green, Bux, & Feinstein, 2013; Mc- Crady, Epstein, & Fokas, 2020; Satre, 2013), and an extensive review is beyond the scope of this chapter. However, clinicians should bring certain broad consid- erations of client diversity to their treatment planning. Most important is that clinicians have some level of cul- tural competence, “the capacity of a service provider, a research scientist, or of an organization to work effec- tively with racial/ethnic minority individuals or groups” (Castro et al., 2013, p. 767). Clinicians should be aware that all individuals have multiple identities, that certain identities are more central to each individual than oth- ers, and that the clinician should both recognize and acknowledge clients’ multiple identities without assum- ing a priori what identities are most important to that individual client. They also should have knowledge and awareness of the unique stresses experienced by mi- nority groups, and that views of AUD, access to care, help-seeking, and mental health professionals differ considerably across and within groups. Thus, clinicians should be deliberate in how they approach the devel- opment of a therapeutic alliance and culturally adapt treatment to incorporate the client’s experience, values, and worldview while still working within the frame- work of an empirically supported treatment for AUD.
CLINICAL APPLICATION OF THE THEORETICAL MODEL
Overview
The major elements of the treatment model have di- rect implications for facilitating problem recognition and entry into treatment, and for the planning and delivery of treatment. If an individual has not entered treatment, there are techniques to help that individual recognize his/her drinking as problematic and in need of change. For a client seeking alcohol treatment, the
therapist must make decisions about the most appro- priate setting in which to provide treatment and select the therapeutic modalities most appropriate to him/ her. Therapeutic techniques must be tailored to the cli- ent’s needs related to drinking and other life problems. The therapist also must consider the social context in which drinking occurs, as well as the social context for change. He/she must be cognizant of the subtle and nonspecific aspects of providing treatment to clients with drinking problems and utilize a therapeutic stance that enhances the client’s motivation to continue to en- gage in the change process. The therapist must attend to the client’s own views about treatment and change, and provide the client with accurate long-term expec- tations about drinking outcomes. Core components of the treatment model are listed in Table 14.2.
Case Identification and Entry into Treatment
Before discussing applications of the model to active treatment, it is important to consider how to help cli- ents enter the treatment system.
Case Identification and Screening
Many individuals who drink do not think they have problems related to drinking. They may be unaware of the high-risk nature of their drinking pattern, or un- aware of the negative consequences that are occurring.
TABLE 14.2. Steps in Treatment
1. Case identification and motivation to enter treatment 2. Assessment 3. Selection of treatment setting 4. Selection of treatment modalities including consideration
of medication 5. Enhancing and maintaining motivation to change 6. Selection of drinking goals 7. Initiation of abstinence or changes in drinking 8, Developing a functional analysis 9. Early sobriety or drinking reduction strategies 10. Coping strategies 11. Partner/family involvement 12. Long-term maintenance 13. Managing complicating conditions 14. Self-help groups
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Feeling ashamed or guilty, they may be reluctant to tell others about their problems, or they may perceive health care professionals as uninterested or unconcerned about drinking. Routine queries about drinking and its con- sequences in both medical and mental health care set- tings can obviate some of these difficulties. Given the high prevalence of drinking problems among individu- als seeking health and mental health services, questions about drinking should be part of all clinicians’ intake interviews not only in SUD or mental health specialty care units but also among primary care clinicians and other health care providers. The Affordable Care Act includes a requirement for screening for alcohol prob- lems of all patients who are seen in primary care set- tings. Given the increased integration of psychological services into primary care, mental health professionals may take the lead in introducing appropriate screening tools into these health care settings.
There are many screening interviews and question- naires to identify clients with alcohol problems. At a minimum, all clients should be asked whether they drink, and drinkers should be asked follow-up ques- tions about the quantity and frequency of their drink- ing. NIAAA defines drinking as high-risk if a man drinks more than 14 standard drinks in a week or more than four on any one day, or a woman drinks more than 7 standard drinks in a week or more than three on any one day (NIAAA, n.d.).1 Concern should also be heightened if a client reports heavy drinking twice or more per month. Follow-up questions may be used to inquire about subjective and objective consequences of drinking. The CAGE interview (cut down, annoyed, guilty, eye-opener; Mayfield, McLeod, & Hall, 1974; see Table 14.3) and the Alcohol Use Disorders Identi- fication Test (AUDIT; Saunders, Aasland, Babor, de la Fuente, & Grant, 1993) are two useful screening mea- sures. Two affirmative responses to the CAGE suggest a high probability of an AUD, but even one positive response warrants further clinical inquiry. The AUDIT includes both direct and subtle approaches to alcohol screening; therefore, it may be useful with clients who are reluctant to self-identify drinking problems. The CAGE and AUDIT questions are reproduced in Table 14.3.
Motivating a Drinker to Enter Treatment
The initial challenge for a clinician is to stimulate the client to initiate any change. Methods for motivating clients to enter treatment vary. For example, MI is a
particularly effective approach for individuals who are ambivalent about change. Miller and Rollnick (2013) describe four key processes in MI: (1) engaging the cli- ent by communicating empathy and respect through specific therapeutic techniques such as the use of open- ended questions, reflections, and emphasizing the cli- ent’s strengths; (2) focusing to help the client identify what is most important; (3) evoking statements about a desire to change by asking open-ended questions and at- tending differentially to change talk rather than sustain talk, and (4) planning by supporting the client’s own interest in making changes consistent with his or her values. Clinicians also may engage a client in treatment by first using a family-focused approach. Community reinforcement and family training (CRAFT; Smith & Meyers, 2004) is a treatment for the families of problem drinkers/drug users; CRAFT helps families change the consequences a drinker experiences from drinking, im- prove communication and self-care, and learn addition- al skills aimed at motivating the individual to change. Clinicians also, at times, may use confrontational ap- proaches, such as an intervention (Liepman, 1993). Research suggests that CRAFT is approximately twice as effective as an intervention in helping persons with AUD to engage with treatment (Roozen, de Waart, & van der Kroft, 2010).
Implementation of motivational principles and tech- niques in ongoing clinical practice, however, presents creative challenges to the clinician. Two examples illus- trate the application of different approaches to motivat- ing clients to enter treatment.
“Bill” was a retired chemist with a long history of heavy drinking, multiple phobias, and bipolar disor- der. I (B. S. M.) was initially contacted by his wife, Diana, who told me that her husband had a 20-year drinking history, that his drinking had increased since his retirement, and that she did not know what to do: The children were angry and threatening to break off contact with him; she and Bill were arguing frequently; and she was beginning to feel increasingly anxious and depressed herself. Diana had consulted with a certified addictions counselor, who told her that they should set up an intervention—a meeting in which Diana and the children would confront Bill about his drinking, insist that he get treatment, then take him directly to an inpa- tient treatment facility. When Diana was hesitant, the counselor told her she was codependent and enabling him. She left the counselor’s office discouraged, certain that she did not want to initiate an intervention, but also certain that something should be done. I tried the most
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TABLE 14.3. Questions to Screen for Alcohol Use and Problems
CAGEa
1. Have you ever felt you should cut (C) down on your drinking?
2. Have people annoyed (A) you by commenting on your drinking?
3. Have you ever felt bad or guilty (G) about your drinking? 4. Have you ever had a drink first thing in the morning—eye-
opener (E)?
Alcohol Use Disorders Test (AUDIT)b
These 10 questionsc are about your use of alcohol during the past 12 months.
1. How often do you have a drink containing alcohol? 0) Never [Skip to questions 9–10] 1) Monthly or less 2) 2 to 4 times a month 3) 2 to 3 times a week 4) 4 or more times a week
2. How many drinks containing alcohol do you have on a typical day when you are drinking?
0) 1 or 2 1) 3 or 4 2) 5 or 6 3) 7, 8, or 9 4) 10 or more
3. How often do you have six or more drinks on one occasion?
0) Never 1) Less than monthly 2) Monthly 3) Weekly 4) Daily or almost daily
4. How often during the last year have you found that you were unable to stop drinking once you had started?
0) Never 1) Less than monthly 2) Monthly 3) Weekly 4) Daily or almost daily
5. How often during the last year have you failed to do what was normally expected from you because of drinking?
0) Never 1) Less than monthly 2) Monthly 3) Weekly 4) Daily or almost daily
6. How often during the last year have you needed a first drink in the morning to get yourself going after a heavy drinking session?
0) Never 1) Less than monthly 2) Monthly 3) Weekly 4) Daily or almost daily
7. How often during the last year have you had a feeling of guilt or remorse after drinking?
0) Never 1) Less than monthly 2) Monthly 3) Weekly 4) Daily or almost daily
8. How often during the last year have you been unable to remember what happened the night before because you had been drinking?
0) Never 1) Less than monthly 2) Monthly 3) Weekly 4) Daily or almost daily
9. Have you or someone else been injured as the result of your drinking?
0) No 2) Yes, but not in the last year 4) Yes, during the last year
10. Has a relative, friend, or a doctor or other health worker been concerned about your drinking or suggested you cut down?
0) No 2) Yes, but not in the last year 4) Yes, during the last year
aFrom Mayfield, McLeod, and Hall (1974). bFrom https://apps.who.int/iris/bitstream/handle/10665/67205/who_msd_msb_01.6a-eng.pdf?sequence=1&isallowed=y. Copyright © World Health Association. Complete scoring is available from this source. cThe first three questions can be used as a briefer screener. Scoring information at www.mdcalc.com/audit-c-alcohol-use.
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minimal intervention first. Over the telephone, I sug- gested that Diana speak with Bill one morning (before he had begun drinking) and say, “Bill, I am concerned about your drinking. I have spoken with a psychologist who specializes in alcohol treatment, and she said that she would be happy to see you for an evaluation. At the end of the evaluation, she’ll give us feedback about what we could do.” I told her not to elaborate on this state- ment, but simply to respond to Bill’s questions. If he refused, she was to get back in touch with me.
I next heard from Diana a month later. Bill had refused her request, and she wondered what else she could do. I suggested an individual consultation with me to discuss how to change her own actions to moti- vate Bill toward change. Diana came in, and after some further assessment of both Bill’s drinking history and her current functioning, I suggested three basic behav- ioral strategies, which I drew from the CRAFT model (Smith & Meyers, 2004). First, I instructed Diana to leave Bill to his drinking as much as possible, to let negative consequences occur naturally. Second, I en- couraged her to give him factual feedback about nega- tive behaviors related to his drinking, but only at times when he was sober. The structure of the feedback was as follows: “Bill, I am concerned that X happened last night when you were drinking.” Third, I encouraged her to spend time with him in positive pursuits when he was not drinking. Given that they were going to Florida for the winter, I suggested that just before they returned, she should repeat her request that he come to see me for an evaluation.
I next heard from Diana in the spring, when she called me to make an appointment for the two of them to come in for an evaluation. They both attended. What follows is our initial discussion.2 (In this and other dia- logues in this chapter, B. S. M. is the therapist.)
THERAPIST: I’m so glad to get to meet you. As you know, Diana first spoke with me a few months ago, so I feel as though I know you a bit. I understand that you were initially reluctant to come in, and I’m pleased that you decided to come. How did that come about?
BILL: Well, Diana asked me, and I know she’s been concerned, so I agreed. But I only agreed to come to- day—I’m not making any kind of commitment here.
THERAPIST: I understand that and certainly won’t try to push you to do anything you’re not comfortable
with. What I’d like to do today is to get a better un- derstanding about your drinking and the kinds of problems it might be causing. At the end of our time together, I’ll give you some feedback and we can dis- cuss some options for you, if you decide you want to make any changes. If I ask you anything that you’re not comfortable answering, just let me know. OK?
Bill was visibly uncomfortable, and pushed his chair as far back into the corner of my office as possible. He sat with his body turned away from Diana and often looked up at the ceiling or sighed when she was speak- ing. Despite his visible discomfort, he gave a clear ac- count of his drinking. He had been drinking heavily for the past 25 years, and at one point had been drink- ing a pint of Jack Daniels whiskey each evening. He was diagnosed with colon cancer in his early 60s and treated surgically. Since the surgery, he had been con- cerned about his health and had attempted to reduce his drinking. His current pattern was almost daily drink- ing, in the evenings, ranging from two to four bottles of Grolsch beer to an occasional (approximately twice per month) pint of Jack Daniels. He reported no with- drawal symptoms on days when he did not drink, and no apparent medical sequelae of his drinking. He said that he did not feel that he had control over his drink- ing, and expressed sadness that Diana was so upset. His love for her, apparent in his speech and demeanor, was clearly the primary reason he had come to see me.
Given Bill’s discomfort, I did not try to complete any standardized assessment instruments or even to struc- ture the initial interview as I might have with other cli- ents. Instead, I followed his lead, made frequent com- ments reflecting the emotions he was expressing, and at times asked Diana not to interrupt, so that Bill could express himself. Although not using a formal MI ap- proach, I used some of the MI principles of engaging in this discussion. In the last 15 minutes of the 1-hour interview, we shifted to feedback and discussion:
THERAPIST: I’d like to stop asking you so many ques- tions now, and see if we can talk about possible op- tions. I am glad that you came in and appreciate that this was not easy for you. From what you and Diana have told me, it does seem that it makes sense to be concerned about your drinking. The amount you’re drinking is above the recommended levels for safe and healthy drinking; you are concerned by your own feelings of lack of control; and your drinking
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has been upsetting to your family, which is painful to you. What do you think?
BILL: I guess talking about all of this at once makes it clearer that I’m drinking too much. I don’t want to stop, though—I appreciate good beer, and look for- ward to having a bottle or two in the evening. I just don’t want to overdo it to the point of hurting Diana.
THERAPIST: So you are concerned and think that some kind of change makes sense, but you’re not sure ex- actly what those changes should be?
BILL: Exactly. THERAPIST: I think you have a number of options.
Making some kind of change makes sense given the problems we’ve discussed. Probably your safest choice is to stop drinking—you can’t create future health problems from drinking if you don’t drink, and in some ways it might be easiest given that you’re in a pretty daily routine of drinking now. But because you don’t want to stop, we could also work toward your reducing your drinking to a level that is safer and healthier, and one that Diana and your children are comfortable with. I’d be willing to work with you to try to reach that goal. I don’t think that you need intensive treatment in a hospital program right now, but you would probably benefit from some help to make changes. What do you think?
BILL: I’m surprised that you think I could reduce my drinking. I have to think about this. I’ll have Diana get back to you.
The discussion continued with input from Diana as well, and the session ended with a commitment only to think about our discussion. Several days later, Diana called to indicate that Bill wanted to begin treatment with me, and we scheduled an appointment.
“Dorothy,” a 78-year-old, widowed, retired school- teacher, was hospitalized at a local medical center after a fall in her apartment. Her blood alcohol level (BAL) on admission was 185 mg%, and she had extensive evi- dence of old bruises, as well as a dislocated shoulder and broken wrist from the fall. She was immediately started on medication for alcohol withdrawal, and our addictions consultation team was called in to see her on the second day of her hospitalization. Dorothy’s son, John, was in the room when I came to see her. With his assistance, I was able to obtain a lengthy history of alcohol consumption that dated back to her early 40s.
Although Dorothy had wanted to stop drinking, she had never been successful for more than a few days at a time, and had never received any form of alcohol treat- ment. Since her husband’s death 2 years earlier, she had been consuming a pint bottle of blackberry brandy each day. She had completely withdrawn from her previous social activities with friends, her hygiene had deterio- rated, and she had had multiple accidents in her house. Dorothy provided this information tearfully, express- ing a great sense of shame about her behavior. John de- scribed her home as “a mess” and said that he was angry and disgusted with her. Dorothy’s family history re- vealed many family members with AUD, including her father, two brothers, and a maternal uncle. Despite the medication, she showed visible signs of alcohol with- drawal during the interview. Dorothy was tearful and stated repeatedly that she was a “sinful, bad” person. My interviewing style with her was empathic: I asked her about her concerns, inquired how she felt, and re- flected back her obvious distress with her current situa- tion. I then told her that there were treatments available to help people with problems like hers. Her immediate and strong reaction was to say that she was too bad, and that her drinking was a sin. I thought it would be particularly helpful to provide Dorothy with some in- formation about the biological and genetic bases of ad- diction as a way to begin to decrease her self-blame and guilt.
“Dorothy, it is clear to me that you are very, very upset by your drinking and by all the problems it has caused for you and your family. I understand that you blame yourself and seem to think your drinking shows that you are a bad person. There is another way of thinking about your drinking that I’d like to tell you about. You may or may not agree with me, but I hope you’ll think about what I say. The National Institutes of Health define alcoholism3 as a disease. In your case, I think that is true. You probably have genes that made you very vulnerable to alcohol— your father, your uncle, and your brothers all seem to have the same disease. We know that the vulner- ability to alcoholism can be inherited, and I would guess that you inherited it. Over time, your body has become adapted to your drinking—it is more com- fortable with alcohol than without it. If you try to stop, your body reacts badly. The shaking and nausea that you’re experiencing now are signs that your body has become hooked on alcohol.
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“What does all this mean? It means that your body reacts differently to alcohol than other people’s, and probably has from the beginning of your drink- ing. It is no more your fault that you have a drink- ing problem than it is the fault of a diabetic that her body can’t make insulin. People are not responsible for the diseases they develop. But they are responsible for making the decision to take care of their disease, for getting help, and for following the advice of the people who give them that help. Except for the prob- lems your drinking has caused, you’re healthy, and you obviously have people who care about you. If you can get help, you have a good chance of getting bet- ter.”
Dorothy initially was skeptical of this reframing of her problems. Without my prompting, when her son left the hospital that day, he picked up some brochures about AUD as a disease and brought them back for his mother to read. When I came to see her the next day, she had many questions about this disease notion and about treatment, which I answered as factually as possible, still maintaining an MI stance—not trying to push her into treatment, but reflecting her interest and concern. By my third visit, she agreed to enter a treatment program. She entered a short-term residential rehabilitation program, followed by longer-term outpa- tient group therapy. She began to volunteer at the hos- pital where I first saw her, and she remained sober and an active volunteer for several years, until advancing age required that she retire.
Assessment
Once a client has entered treatment, the therapist should begin with an initial assessment of drinking, other drug use, problems in other areas of life func- tioning, and the client’s social network. Donovan (2013) provides a comprehensive description of as- sessment for SUDs; Haeney, Boness, McDowell, and Sher (2018) provide an evaluation of the psychomet- ric properties of various assessment instruments for AUD. Assessment of motivation, as well as resources that the client brings to the treatment, is important. If the therapist provides cognitive-behavioral treatment, assessment for a functional analysis of drinking is nec- essary. If the client’s spouse/partner or other family members are involved in the treatment, their role in the drinking, as well as overall relationship function- ing, should be assessed.
Drinking Assessment
The clinical interview is the first tool used to assess drinking. In addition to the clinical interview (see Table 14.4), two structured interviews—the Timeline Follow-Back Interview (TLFB; L. C. Sobell & M. B. Sobell, 1995; M. B. Sobell & L. C. Sobell, 2020), de- signed to assess drinking and drug use behavior each day in a set window of time before treatment, and the alcohol and drug sections of the Structured Clinical Interview for DSM-5 (SCID; First, Williams, Karg, & Spitzer, 2016)—provide standardized information about quantity, frequency, pattern of drinking, and other information needed to establish a formal diagno- sis. Alternative structured interviews, such as the Form 90 (Tonigan, Miller, & Brown, 1997), may be used to obtain information about drinking history, patterns, and consequences of use. Self-report measures may be used to assess negative consequences of drinking (the Drinker Inventory of Consequences [DrInC] or the Short Inventory of Problems [SIP]; Miller, Tonigan, & Longabaugh, 1995).
Assessment of Other Problem Areas
The clinician can draw from a wide variety of mea- sures to assess other life problems. Assessment may range from unstructured interviews to simple problem checklists, to standardized questionnaires, to formal interviewing techniques. The Addiction Severity Index (ASI; McLellan et al., 1992) is a widely used measure of client functioning across multiple domains; sub- scales include Medical, Psychological, Family/Social, Legal, Employment, Alcohol, and Drug. The ASI is in the public domain, and the instrument, instructions, and scoring programs can be downloaded from www. phmcresearch.org/products/addiction-severity-index. The ASI can be administered as an interview in about 45 minutes, and computer-assisted interview versions are available. The ASI, however, does not provide diagnos- tic information for any psychological disorders, and the cautious clinician should use formal diagnostic screen- ing questions to assess for the possible presence of other psychological disorders.
Assessment of Motivation
Assessment of motivation should consider (1) reasons why the client is seeking treatment, with careful at- tention to external factors involved with help seeking;
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(2) the client’s treatment goals; (3) the client’s readi- ness to change; and (4) the degree to which the client sees negative consequences of his/her current drinking pattern and envisions positive consequences of change. Clinical interviewing provides information about rea- sons for seeking treatment, and drinking goals may be assessed either by asking the client directly or by using a simple goal choice form (see Figure 14.1). The Readi- ness Rulers (Miller & Rollnick, 2013) are simple 10- point scales on which clients can indicate their readi- ness to change, desire to change, and confidence in being able to change. The University of Rhode Island Change Assessment Scale (a brief version is described in DiClemente, Doyle, & Donovan, 2009) and the Readiness to Change Questionnaire (Freyer-Adams et al., 2009) both measure stage of change. Perception of negative consequences of drinking and positive con- sequences of change also may be assessed through the clinical interview, or by developing a Decisional Bal- ance Sheet (Epstein & McCrady, 2009) with the client (see Figure 14.2).
Assessment of Social Network
Clients’ social networks may be integrally involved with their drinking and with successful change. Self-report questionnaires such as the Perceived Social Support scale (Procidano & Heller, 1983) may be helpful in as- sessing the overall degree to which clients perceive their family and friends as supportive. The Important People Drug and Alcohol Interview (Zywiak, 2009) provides a more nuanced assessment of alcohol and drug use, sup- port for drinking, support for help seeking, and general support in the social network.
Identifying Drinking Antecedents and Use Patterns
Two assessment techniques may be used to identify an- tecedents to drinking. A self-report questionnaire, the Drinking Patterns Questionnaire (DPQ; Menges, Mc- Crady, Epstein, & Beem, 2008), lists potential environ- mental, cognitive, affective, interpersonal, and intrap- ersonal antecedents to drinking or drinking urges. The Inventory of Drinking Situations (Annis, Graham, & Davis, 1987), a shorter measure that assesses situations in which a client drinks heavily, also is available. Cli- ent monitoring cards (Figure 14.3) are used through- out the treatment to record clients’ drinks and drink- ing urges. Discussing events associated with drinking
TABLE 14.4. Topics to Cover in Initial Clinical Interview
1. Initial orientation a. Introductions b. Breathalyzer reading c. Brief questionnaires
2. Initial assessment a. Presenting problems b. Role of drinking/drug use in presenting problems c. Other concerns d. How the drinking has affected the partnera
e. How the drinking has affected the relationshipa
3. Drinking/drug use assessment a. Identified patient
i. Quantity, frequency, pattern of drinking ii. Last drink/drug use
iii. Length of drinking/drug problem iv. Negative consequences of drinking/drug use v. DSM-5 symptoms
vi. Assessment of need for detoxification b. Partnera
i. Quantity, frequency, pattern of drinking ii. Last drink/drug use
iii. Length of drinking/drug problem iv. Negative consequences of drinking/drug use v. DSM-5 symptoms
vi. Assessment of need for detoxification 4. Assessment of other problems
a. Psychotic symptoms b. Depression c. Anxiety d. Cognitive impairment e. Health status
5. Assessment of social network a. Important people in social network b. Drinking/drug use among important people c. Reactions to drinking of important people d. Support for change in drinking
6. Mental status examinaton 7. Assessment of domestic violencea
a. This assessment is done privately with each partner alone
b. Review of Conflict Tactics Scales i. Identification of episodes of physical aggression
ii. Determination of level of harm/injury from aggression
iii. Assessment of individual’s sense of safety in couple therapy
aThese topics apply if an intimate partner is part of the initial interview.
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or drinking urges can help both client and clinician to develop a clearer picture of drinking antecedents and consequences. Client monitoring cards also allow the clinician to track progress in terms of quantity and fre- quency of drinking, as well as frequency and intensity of urges to drink. Clients with a smartphone also can use an app to track their drinking. We have used the AlcoDroid tracker (https://play.google.com/store/apps/deta ils?id=org.M.alcodroid&hl=en) or DrinkControl (https://
drinkcontrolapp.com), but there are many other useful apps available as well.
Partner Assessment
Questionnaires and client monitoring cards can be used to assess how the client’s partner has coped with the drinking. Each day, the partner who is involved with treatment records his/her perceptions of the drinker’s
FIGURE 14.1. Goal choice questionnaire.
We would like to know the one GOAL you have chosen for yourself about drinking at this time. Please read the goals listed below and choose the ONE goal that best represents your goal at this time by checking the box next to the goal and by filling in any blanks as indicated for that goal.
I have decided not to change my pattern of drinking.
I have decided to cut down on my drinking and drink in a more controlled manner—to be in control of how often I drink and how much I drink. I would like to limit myself to no more than drinks (upper limit amount) per (time period).
I have decided to stop drinking completely for a period of time, after which I will make a new decision about whether I will drink again. For me, the period of time I want to stop drinking is for
(time).
I have decided to stop drinking regularly, but would like to have an occasional drink when I really have the urge.
I have decided to quit drinking once and for all, even though I realize I may slip up and drink once in a while.
I have decided to quit drinking once and for all, to be totally abstinent, and to never drink alcohol ever again for the rest of my life.
None of this applies exactly to me. My own goal is
gniknirDgniknirDtoN
Pros
Cons
FIGURE 14.2. Decisional Balance Sheet.
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drinking and drinking urges on a Likert scale (None, Light, Moderate, or Heavy; see Figure 14.4). In addi- tion, the partner may complete the Coping Question- naire (Orford, Templeton, Velleman, & Copello, 2010) to describe the variety of ways the partner has tried to cope with drinking. These include engaged, tolerant– inactive, and withdrawal coping. It also is important to assess other aspects of the couple’s relationship, if both
partners are to be involved in treatment. The Areas of Change Questionnaire (ACQ; Margolin, Talovic, & Weinstein, 1983) and the Dyadic Adjustment Scale (DAS; Spanier, 1976) are excellent self-report measures of relationship problems and satisfaction. The Revised Conflict Tactics Scales (Straus, Hamby, Boney-McCoy, & Sugarman, 1996) provides a succinct measure of rela- tionship conflict, including physical violence.
sgurD/sknirDsegrU
Time Strength (1–7) Trigger? Time Type Amount
% Alcohol Trigger?
Relationship satisfaction: 1 2 3 4 5 6 7
Worst Greatest ever ever
Client Monitoring Card
FIGURE 14.3. Client monitoring card.
FIGURE 14.4. Family monitoring card.
Day Date Drinking Drug use Urge intensity Relationship satisfaction
No L M H No L M H 0 1 2 3 4 5 6 7 0 1 2 3 4 5 6 7
No L M H No L M H 0 1 2 3 4 5 6 7 0 1 2 3 4 5 6 7
No L M H No L M H 0 1 2 3 4 5 6 7 0 1 2 3 4 5 6 7
No L M H No L M H 0 1 2 3 4 5 6 7 0 1 2 3 4 5 6 7
No L M H No L M H 0 1 2 3 4 5 6 7 0 1 2 3 4 5 6 7
No L M H No L M H 0 1 2 3 4 5 6 7 0 1 2 3 4 5 6 7
Note. Use the reverse side of the card to track behaviors you are learning to change.
Family Monitoring Card
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Selection of Treatment Setting and Level of Care
Information from the assessment of drinking, concomi- tant problem areas, and motivation is used to determine the appropriate setting in which to initiate treatment. As with other areas of health and mental health care, the principle of least restrictive level of care should apply to alcohol and drug treatment. Historically, residential rehabilitation of fixed length (usually 28–30 days) was seen as the treatment of choice. However, early studies comparing the effectiveness of different levels of care (e.g., see Fink et al., 1985; Longabaugh et al., 1983; Mc- Crady et al., 1986) revealed that most clients could be treated effectively in an ambulatory treatment setting, and since health care insurers typically require preau- thorization of episodes of care, inpatient treatment is used less frequently for the treatment of AUD. Outpa- tient treatment is the predominant form of treatment, with the ratio of clients seen in outpatient versus inpa- tient treatment at about 10:1 (Roman, 2013).
Sobell and Sobell (2000) proposed a stepped-care model for making decisions about level of care. The stepped-care model proposes brief interventions as the modal initial approach to treatment, with treatment “stepped up” to more intensive or extensive treatment based on the client’s response to the initial treatment. Such models are economically conservative and main- tain the principle of least restrictive level of care. How- ever, some clients with more severe problems might not be served well by very brief treatment (e.g., Rychtarik et al., 2000), and studies using American Society of Ad- diction Medicine (ASAM) criteria suggest that clients have poorer outcomes if they receive less intensive treat- ment than suggested by these criteria (Stallvik, Gast- friend, & Nordahl, 2015).
Decision-making models to determine level of care have been implemented in many states. The ASAM (2015) has proposed a multidimensional decision- making model for selecting initial level of care. ASAM criteria consider need for supervised withdrawal, medi- cal conditions that might require monitoring, comor- bid psychiatric conditions, motivation for change and degree of treatment acceptance or resistance, relapse potential, and nature of the individual’s social environ- ment in recommending an initial level of care. These criteria are mapped onto five major levels of care, in- cluding early intervention, outpatient, intensive outpa- tient/partial hospitalization, residential/inpatient, and medically managed intensive inpatient treatment. Table 14.5 summarizes how the major criteria are applied to
level-of-care determinations. Studies of the ASAM cri- teria suggest a number of barriers to using the criteria in clinical practice. For example, among indigent individ- uals, treatment facilities may be inaccessible because of lack of insurance or money to pay. Also, such individu- als often are placed on wait lists because programs are full. Some programs also may lack adjunctive services needed by a homeless or indigent populations, such as assistance with pragmatic issues (food stamps, housing, unemployment, medical care, mental health care, or family treatment) (Koegl & Rush, 2012). Among other clients seeking alcohol treatment, some may receive treatment that is more intensive than that suggested by the ASAM criteria because their health insurance only covers inpatient treatment, because there may have been pressure from the family for inpatient treatment, or a specific level of care was mandated by an external agency (e.g., an employee assistance program). Clients also may receive treatment that is less intensive than that suggested by ASAM criteria because of their work schedule or reluctance to commit to more (Kosanke, Magura, Staines, Foote, & DeLuca, 2002). Additional considerations in determining initial level of care are discussed below.
Need for Detoxification
If a client is physically dependent on alcohol, then he/ she may experience alcohol withdrawal symptoms when drinking is decreased or stopped. Signs that a client may be physically dependent on alcohol include daily drinking, drinking regularly or intermittently through- out the day, and morning drinking. Awakening during the night with fears, trembling, or nausea, or experi- encing such symptoms upon first awakening, also sug- gests physical dependence. Cessation or a substantial decrease in drinking may result in the appearance of minor withdrawal symptoms, such as tremulousness, nausea, vomiting, difficulty sleeping, irritability, anxi- ety, and elevations in pulse rate, blood pressure, and temperature. Such symptoms usually begin within 5–12 hours. More severe withdrawal symptoms (e.g., seizures, delirium, or hallucinations) may also occur, usually within 24–72 hours of the cessation of drink- ing. If a client has not consumed alcohol for several days prior to initial clinical contact, concerns about alcohol withdrawal are not relevant. If the client has stopped drinking within the last 3 days, the clinician needs to inquire about and observe the client for signs of with- drawal. The Clinical Institute Withdrawal Assessment
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(CIWA; Sullivan, Sykora, Schneiderman, Naranjo, & Sellers, 1989) provides an objective measure of current withdrawal symptoms. If the client currently is drink- ing, the clinician must rely on drinking history, pattern, and the results of previous attempts to stop drinking to determine whether detoxification will be necessary.
If the client needs detoxification, five alternatives are available: inpatient or partial hospital medically assisted detoxification, inpatient nonmedical detoxification, or outpatient medically assisted or nonmedical detoxifi- cation. Inpatient, medically assisted detoxification is essential if the client has a history of disorientation, delirium, hallucinations, or seizures during alcohol withdrawal; is showing current signs of disorientation, delirium, or hallucinations; or has other serious medi- cal problems. If the client does not believe that he/she can stop drinking without being physically removed from alcohol but does not show any major withdrawal signs, is in good health, and does not use other drugs problematically, a nonmedical detoxification may be
appropriate. If the client has some social supports, then detoxification may be initiated on a partial hospital or outpatient basis. The choice between these two latter settings is determined by how much support the person will need during withdrawal and whether a structured program will be needed after detoxification. If the cli- ent needs a fairly structured program, then the partial hospital is the preferred setting for detoxification. If a client refuses detoxification or a higher level of care, or does not require those options, a protocol to reduce al- cohol consumption gradually over several weeks may be appropriate and useful (Holzhauer et al., 2017).
Physical Health
The clinician who is considering the best setting for detoxification should take into account the presence of other medical problems and can use a brief health screener such as the 36-item Short Form Health Sur- vey (SF-36; available at no cost at https://www.rand.org/
TABLE 14.5. ASAM Criteria for Selection of Treatment Settings
Level of care Criteria
Level 0.5. Early intervention • At risk for developing an SUD • Interest in thinking about change and needs some skills
Level 1. Outpatient treatment • No serious risk for major withdrawal or withdrawal seizures • No acute or chronic medical or psychiatric problems that could interfere with treatment • Some openness to change • Some ability to maintain change • Reasonable environmental support for change
Levels 2.1, 2.5. Intensive outpatient treatment (includes intensive outpatient and partial hospitalization)
• No serious risk for major withdrawal or withdrawal seizures • No acute or chronic medical or psychiatric problems that cannot be managed with
supervision and • Some reluctance to change or • Limited ability to maintain change/substantial relapse risk • Limited environmental supports for change
Levels 3.1, 3.3, 3.5, 3.7. Residential/ inpatient treatment (includes low- and high-intensity residential treatment; medically monitored high-intensity inpatient services and/or withdrawal management)
• Some risk for withdrawal • Some level of acute or chronic medical or psychiatric problems that could be managed
with intensive supervision • Ambivalence about change • Limited ability to maintain change without structured support • Limited environmental supports for change or high-risk environment for relapse
Level 4. Medically managed intensive inpatient treatment
• Serious risk for major withdrawal or withdrawal seizures or • Acute or chronic medical or psychiatric problems that could interfere with treatment
and require active monitoring and care
Note. Adapted from www.asamcontinuum.org/knowledgebase/what-are-the-asam-levels-of-care and www.aetna.com/healthcare-professionals/documents- forms/asam-criteria.pdf.
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health-care/surveys_tools/mos/36-item-short-form.html). If significant physical complaints are noted, the client should receive immediate medical attention. Some cli- ents have medical problems that require hospitalization; if so, the hospitalization should initiate the treatment. A cautious approach dictates that every client should have both a thorough physical examination and blood and urine studies at the beginning of treatment.
Treatment History
After physical health issues have been considered, the clinician should examine the client’s previous treatment history. Questions to consider include the following:
1. Has the client attempted outpatient treatment in the past and been able to stop or decrease drink- ing successfully? If so, then another attempt at outpatient treatment may be indicated.
2. Has the client dropped out of outpatient treat- ment in the past? If so, and there is no indication that any variables have changed in the interim, then a more intensive partial hospital or inpatient program should be considered.
3. Has the client dropped out of, or drunk repeat- edly, while in a partial hospital program? If so, then inpatient treatment may be indicated.
4. Did the client relapse immediately after discharge from an inpatient program? If so, then a partial hospital or outpatient setting may be appropriate because relapse may have been associated with problems in generalization from the inpatient to the natural environment. Alternatively, a halfway house or sober living home may be considered to provide a longer-term structured environment.
Social Support Systems
Social support systems are critical variables to consider in determining the appropriate setting for initial treat- ment. If a client has help from another person who is willing to provide support and reinforcement, then the client may be a good candidate for ambulatory treat- ment. If the client is lacking in social support, or is in an environment that supports heavy drinking, then in- patient or partial hospital treatment may be advisable. Alternatively, a halfway house or sober living home may be appropriate for persons who do not have current so- cial supports and have not been successful at developing them in the past, even during periods of abstinence.
Personal Resources
The next area to consider encompasses the client’s per- sonal psychological resources. Has he/she been suc- cessful in other areas of life in setting goals, chang- ing behavior, and completing tasks? If so, outpatient treatment is more feasible. Another aspect of personal resources is cognitive functioning. If the client shows significant cognitive deficits in memory, attention, ab- straction, or problem solving, a higher level of care may be considered.
Other Psychological Problems
As noted earlier in the chapter, persons with drink- ing problems often have other, significant psychologi- cal problems. The clinician must not only assess these problems but also determine level of care based on the appropriate setting for treatment of these other prob- lems. As with any treatment, clients must be assessed for intent to harm themselves or others and, if present, appropriate precautions should be taken.
Attitudes about Treatment
Although difficult areas to assess, the client’s commit- ment to treatment and desire to change are important factors in selecting level of care. The client who is am- bivalent about change may benefit from MI before dis- cussing any other kind of treatment. Clients who are ambivalent about change but willing to come to treat- ment may respond better to a less intensive treatment that places less demands on their time. Alternatively, a more intensive program that provides higher densi- ty reinforcement for attending treatment and making changes could be beneficial.
Practical Concerns
There also are a number of practical concerns that the clinician must consider. Some practical barriers revolve around employment—whether the client can get time off from work, whether the job is in jeopardy, whether the employer is willing to support treatment, or whether missing any more work would result in termination of employment. A second concern is the client’s financial condition. Can the client afford to take time off from work and perhaps experience a reduction in income if sick time is not available? If not, outpatient treatment or a partial hospital program that allows the person to
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work is appropriate. Another financial concern is the client’s ability to pay for treatment.
Other practical concerns revolve around transporta- tion and child care. Can the client get to outpatient ap- pointments? Does he/she have a driver’s license, and if not, is other transportation available? Is child care avail- able if the person has to be hospitalized? If not, a day treatment setting may be preferred. The clinician must consider a range of pragmatic barriers to treatment.
Personal Preferences
Finally, the client’s own preferences about the treatment must be considered carefully. If the client feels strongly about wanting to be in a hospital or residential treat- ment program, the clinician should listen carefully to this request, even if the initial assessment suggests that outpatient treatment may be feasible. Similarly, if the client wants outpatient treatment and refuses a higher level of care, the clinician should attempt it, even if he/ she believes that a more intensive treatment is prefer- able. Of course, insurance coverage may not allow for the level of care the client prefers, but it is important that the clinician pay attention to client preferences.
General Considerations
In general, the selection of the initial treatment setting must be seen as a tentative decision. Often an initial contract may be established that includes the client’s preferred setting, but with specification of the circum- stances that will dictate a different level of care. For ex- ample, if the clinician believes that the client will find it extremely difficult to discontinue or reduce drinking on an outpatient basis, but this is the client’s desire, then an initial contract may involve a plan for reducing or stopping drinking, learning skills to support that plan, and a time limit. If the person is unsuccessful within the specified time frame, then the contract is reviewed and alternative settings are considered. Thus, although the initial setting decision is important, continuing to consider and discuss other treatment settings is an im- portant early step in the treatment process.
Selection of Treatment Modalities
If a client is referred to inpatient, residential, or in- tensive outpatient treatment, a mixture of treatment modalities is included in the treatment. Many of these are based on the “Minnesota model” (Slaymaker &
Sheehan, 2013), an intensive treatment approach that includes group therapy, education, self-help group in- volvement, and some individual counseling. Programs based on the Minnesota model emphasize confronta- tion of denial, acceptance that one is an alcoholic3 who is powerless over alcohol, development of caring and interdependent relationships, and commitment to AA involvement. The Minnesota model and other inpatient or residential programs often incorporate many behav- ioral strategies and techniques, including social skills and relaxation training, meditation, RP techniques, and pharmacotherapy. Clients who complete these pro- grams often are referred to sober houses for extended care after discharge.
For outpatient treatment, five major treatment mo- dalities are available for the provision of alcohol treat- ment: mutual help groups, individual therapy, group therapy, couple therapy, and family therapy. In the ambulatory setting, the clinician has more flexibility in selecting from among these treatment modalities.
Mutual‑Help Groups
Although not formal treatment, mutual-help groups should be considered among the range of modalities available for clients. Among these, AA is the most com- monly utilized mutual-help group. With groups in all 50 states, as well as more than 150 countries through- out the world, AA is widely available. It offers a specific approach to recovery, rooted in the view that AUD is a physical, emotional, and spiritual disease that can be arrested but not cured. Recovery is viewed as a lifelong process that involves working the 12 steps of AA and abstaining from the use of alcohol. The only require- ment for membership in AA is a desire to stop drinking, and members do not have to pay dues or join the orga- nization. Persons who become involved with AA usual- ly attend different meetings; have a relationship with an AA sponsor, who helps them with their recovery; and become involved with other AA-related activities, rang- ing from making the coffee before meetings to going on “commitments,” in which members of one AA group speak at another group. More active involvement is cor- related with more successful change (McCrady, 2020).
Persons most likely to affiliate with AA have a his- tory of using social supports as a way to cope with problems, experience loss of control over their drink- ing, drink more per occasion than persons who do not affiliate, experience more anxiety about their drinking, believe that alcohol enhances their mental functioning,
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and are more religious or spiritual (McCrady, 2020). Outpatient treatment to facilitate involvement with AA (12-step facilitation) has been found to be as effective as other forms of outpatient therapy in controlled trials, and some evidence suggests that clients receiving 12- step facilitation are more likely to maintain total absti- nence from alcohol than clients receiving more behav- iorally oriented treatments (Project MATCH Research Group, 1997a). Twelve-step facilitation treatment ap- pears to be particularly successful for individuals with social systems that support them in drinking heavily (Longabaugh et al., 1998). Studies of mechanisms of change in AA reveal that success is mediated by in- creases in spirituality, social support, and self-efficacy (McCrady, 2020).
There are other mutual-help groups that are either alternatives to AA or complement what AA provides. Self-Management and Recovery Training (SMART Recovery) is based largely on cognitive-behavioral principles and offers several steps to recovery, empha- sizing awareness of irrational beliefs, self-perceptions, and expectancies as core to successful change. SMART Recovery suggests abstinence as a preferred drinking goal but emphasizes personal choice. Secular Organiza- tions for Sobriety/Save Ourselves (SOS) was developed largely in response to the spiritual aspects of AA and does not invoke a Higher Power as a part of the change process. Women for Sobriety, a self-help approach for women, emphasizes women’s issues such as assertive- ness, self-confidence, and autonomy as a part of the change process. All of these alternative approaches are more compatible with behavioral approaches than is AA, but none are as widely available to clients.
Individual versus Group Treatment
Individual therapy is offered primarily on an outpatient basis. Individual treatment is more costly than group therapy, and few data are available to guide the choice of individual versus group therapy. Many clients ex- press a preference for individual treatment, but there is a strong belief in the alcohol field that group therapy is preferable to individual therapy. Group therapy is more economical to provide, and interaction among group members provides opportunities for modeling, feedback, and behavioral rehearsal that are less avail- able in the individual setting. Behavioral models for providing group therapy (e.g., Sobell & Sobell, 2011) are well documented. Clients who are able to function in a group setting and do not require intensive individ-
ual attention because of other psychological problems can be assigned to group therapy. Our own research has found comparable outcomes for women in group versus individual AUD treatment, somewhat lower levels of treatment attendance in groups (Epstein et al., 2018) and greater cost-effectiveness for group treatment for women with AUD (Olmstead et al., 2019).
Couple Therapy
Involving the spouse/partner in AUD treatment in- creases the probability of a positive treatment outcome (McCrady, Epstein, Cook, Jensen, & Hildebrandt, 2009; McCrady, Epstein, Hallgren, Cook, & Jensen, 2016). Despite the empirical evidence, traditional AUD counselors have not utilized couple therapy to any great extent, because they believe that individual change must be addressed before considering relationship change. Models for treatments that integrate individual and relationship treatment are available (McCrady & Epstein, 2009). Couple therapy is most appropriate for clients who have a stable relationship in which the part- ner is willing to be involved in treatment and can func- tion in a supportive manner in the early phases of treat- ment. Couples who have experienced severe domestic violence, or in which one partner’s commitment to the relationship is highly ambivalent, are less appropriate for couple therapy.
Techniques also have been developed to provide treatment to family members of persons with AUD when the drinker will not seek help. CRAFT emphasiz- es personal decision making, communication, and limit setting around drinking, and is effective in motivating individuals to seek treatment or to decrease drinking (Manuel et al., 2012; Miller, Meyers, & Tonigan, 1999; Smith & Meyers, 2004). Al-Anon offers a self-help ap- proach to partners and other family members affected by AUD that may decrease family members’ anxiety and depression, but it has little impact on help seeking (Miller et al., 1999).
Family Therapy
Despite a strong interest in AUD in the family thera- py field, models for working with whole families with an adult family member with an AUD are scarce. For adolescents, several treatments based in family systems theory are efficacious in decreasing teen alcohol or drug use and improving family functioning (reviewed in Mc- Crady & Flanagan, in press). Within the self-help area,
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Alateen is available for teens affected by a family mem- ber’s AUD, and Alatot is available for younger family members.
Psychopharmacology
Since AUD involves ingestion of a substance that has acute and chronic medical implications, it is important for AUD clinicians to work with a provider team ap- proach and to have knowledge of medications available to complement behavioral AUD treatment. Because AUD is currently viewed by the NIAAA (2017) as a medical condition, there is continuing emphasis on development of additional pharmacotherapy options. Medications for AUD fall into three categories: (1) treatment for alcohol withdrawal, (2) aversion thera- py to support abstinence, and (3) treatment to reduce craving and/or block the rewarding effects of alcohol. Medications have long been used to treat or prevent withdrawal from alcohol. To treat alcohol withdrawal, benzodiazepines (Librium, Valium, Serax, Ativan) are most commonly used, with some evidence for useful- ness of anticonvulsants (Tegretol and gabapentin) (Wil- cox & Bogenschutz, 2013). Three medications current- ly are FDA-approved for treatment of AUD. Disulfiram (Antabuse), an aversion therapy agent, blocks the en- zyme aldehyde dehydrogenase in first pass metabolism, which normally blocks breakdown of an alcohol me- tabolite called acetaldehyde. Build-up of acetaldehyde causes facial flushing, headache, hypotension, nausea, and vomiting. Alcohol consumption thus makes a per- son feel sick, and changes the individual’s expectation (and reality) from a rewarding effect of alcohol to an aversive one. Naltrexone comes in daily pill form (Revia) and a long-acting (1 month) injectable form (Vivitrol). Naltrexone blocks the endogenous opioid system and decreases craving for alcohol, as well as the rewarding effects of alcohol. This helps individuals avoid drink- ing entirely or reduce the amount of alcohol consumed if they do drink. Acamprosate (Campral) works by increasing gamma-aminobutyric acid (GABA) and decreasing N-methyl-D-aspartate (NMDA) to reduce craving for alcohol and lessen negative emotional states during withdrawal to decrease use and prevent relapse. Other medicines not yet FDA approved but studied to reduce alcohol cravings include topiramate (Topamax; an antiseizure medication that may work similarly to Campral), baclofen (Lioresal), ondansetron (Zofran), and gabapentin (Neurontin). Medication development for integrated treatment of AUD and commonly occur-
ring psychiatric problems such as depression, anxiety, posttraumatic stress disorder, eating disorders, and bi- polar disorders also is being conducted (see Rosenthal, 2013).
Enhancing and Maintaining Motivation to Change
Once a decision has been made about the level of care and the client has entered treatment, the clinician needs to continue to focus on motivation to be in treatment and to change. Techniques to enhance motivation in- clude feedback, use of MI techniques, mutual goal set- ting and decision making, treatment contracting, and the instillation of hope. Three clinical examples illus- trate some of these techniques.
Bill (described earlier in this chapter) began treat- ment quite tentatively. He was willing to complete a standardized assessment of his drinking, so we com- pleted a 1-month TLFB (Sobell & Sobell, 1995), the DrInC (Miller et al., 1995), and a Decisional Balance Sheet (Marlatt & Gordon, 1985; see Figure 14.2). Based on this information, I (B. S. M.) provided him with a standardized feedback sheet (Figure 14.5) about his drinking. The sheet provided data about how his drink- ing compared to national norms (Chan, Neighbors, Gilson, Larimer, & Marlatt, 2007), as well as infor- mation about his peak BAL, usual BAL, and negative consequences of his drinking. Bill found the feedback interesting and asked questions about alcohol metabo- lism, epidemiological surveys, and alcohol and health effects. Although his wife, Diana, was somewhat impa- tient with this conversation, I thought that Bill’s inter- est in learning more about alcohol and its effects was a positive sign.
We discussed drinking goals and a range of goals, from abstinence to NIAAA drinking guidelines for men of no more than 14 drinks in a week, no more than 4 days of drinking per week, and no more than four drinks per occasion. Bill indicated that he wanted to continue with daily drinking, but with a limit of three drinks per day. Diana was agreeable, saying that if he kept to this limit she would be “thrilled.” Although his selected goal was higher than I would have liked, I agreed in order to engage him further in treatment. I then gave him his first “homework” assignment—to initiate self-monitoring of his drinking (see Figure 14.3). The assignment of homework serves as a useful behav- ioral probe for level of motivation, and I was pleased when Bill returned to the next session with completed client monitoring cards.
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For the Drinker:
• Based on the information I obtained during the assessment, I calculated the number of “standard drinks” you consumed in a typical week, during the last month:
| Total number of standard drinks per week
| Average number of standard drinks per day
• When we look at everyone who drinks in the United States, you have been drinking more than approximately this percent of the population of women/men in the country.
• I also estimated your highest and average blood alcohol level (BAL) in the past month. Your BAL is based on how many standard drinks you consume, the length of time over which you drink that much, whether you are a man or a woman, and how much you weigh. So,
| Your estimated peak BAL in an average week was
| Your estimated average BAL in an average week was
| This is a measure of how intoxicated you typically become. In [YOUR STATE], the legal intoxication limit is [80 mg%] or higher.
• You have experienced many negative consequences from drinking. Here are some of the most important:
For the Partner: • You have been trying many ways to cope with your partner’s drinking. The things you have tried the most
include:
For the Couple: • You have a number of areas of your relationship that you are concerned about. Some are concerns for
both of you:
• Some concerns are mostly concerns for [IDENTIFIED CLIENT NAME]:
• Some concerns are mostly concerns for [PARTNER NAME]:
FIGURE 14.5. Feedback sheet.
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“Suzanne” was a 39-year-old computer programmer whom I treated in outpatient therapy as part of a treat- ment research project. Suzanne drank daily, typically consuming three glasses of wine per day. She had made a number of unsuccessful attempts to stop drinking and felt that she had completely lost control over her drink- ing even though the amount she drank was not remark- ably high. She was concerned about her ability to be alert and available to her children in the evenings when she was drinking, particularly since her husband trav- eled frequently for his business. Suzanne sought treat- ment voluntarily and wanted to abstain from drinking completely. Despite her self-referral to treatment and her self-defined need for abstinence, Suzanne reacted to the same structured feedback quite differently than Bill did. She had provided information for the TLFB and completed the Rutgers Consequences of Use Ques- tionnaire (RCU), but when I gave her feedback that she had been drinking an average of 21.5 drinks per week, she told me that this figure was too high, and that our measure was not very accurate. She also indicated that she was participating in a research study, not in therapy, which was why she thought it important that we have accurate data. I did not argue with her perspec- tive, agreeing that she was in a research study, but that I hoped that the study would helpful to her. She contin- ued with treatment, and several weeks later commented spontaneously, “You know, I know that I’m in treat- ment, and I really need it. I think I was just protecting my ego at the beginning by focusing on the research part so much.”
“Anne,” a 32-year-old, married college graduate working as a cocktail waitress, was the mother of a 20-month-old daughter, Breanne. Her husband, Char- lie, was working full time and enrolled in a doctoral pro- gram in mechanical engineering. She entered treatment as part of our women’s treatment research program. She was a daily drinker, with a varying pattern of consump- tion. During the evenings, when her husband was at school, she drank one or two bottles of wine per night. When he was home, her typical consumption was one glass of wine with dinner. She also drank at the end of her shift at work, consuming four to six beers on those evenings. When I gave her the feedback about her alco- hol consumption, indicating that her level of consump- tion placed her in the 99th percentile of women, her eyes filled with tears and she looked visibly distraught, saying repeatedly, “I knew it was bad, but I never knew it was this bad.” As treatment progressed, Anne made few changes in her drinking. She canceled or changed
appointments, and said on several occasions, “If I didn’t like you, I’d probably just quit the whole thing.” She continued:
ANNE: I really like to drink. When Charlie is at school, I make myself a nice dinner—a lamb chop, a salad— and have an excellent bottle of wine. No one bothers me, and I enjoy myself. But I know I should stop because of Breanne.
THERAPIST: [As part of the treatment protocol, we had completed a decisional matrix, and I suggest that we return to that form.] Anne, let’s look at your deci- sional matrix again. We did this a few weeks ago. When you look at it now, what strikes you?
ANNE: Everything on it is still true. I’m not being a good mother with all this drinking. I’m out of it at night, and I have no energy during the day. I just plop her in front of the television, and she watches Dora the Explorer. I keep thinking about when she gets older, “Do I want her to have a drunken moth- er?”
THERAPIST: It seems as though those feelings are very strong right now, but it’s hard for you to keep them in the front of your mind each day. I wonder if you could review this sheet every day at some point. Would that help?
ANNE: I think so. I can look at it while Breanne is eat- ing her breakfast. My motivation would be sitting right in front of me then. I’ll try that.
Anne began reviewing her decisional matrix every day. The task seemed helpful for about a month, and she began to decrease her drinking, joined a gym, and came to treatment regularly. However, these changes were short-lived, and she fairly quickly reverted to her pattern of erratic treatment attendance and heavy drinking.
Selection of Drinking Goals
The final major area to consider in treatment planning is the selection of drinking goals. Most approaches to AUD treatment view abstinence as the most appro- priate and safest drinking goal, because heavy drink- ing creates neurobiological changes in the brain that make subsequent moderate drinking difficult to main- tain. Some clinicians have examined alternatives to abstinence and have developed a number of strategies to teach clients how to drink moderately. Moderated
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drinking goals are better accepted as a goal for indi- viduals who are hazardous drinkers or have mild AUD, and are contraindicated for clients who have a history of moderate or severe AUD, or for those with mild AUD with concomitant psychological or social risk factors. Moderated drinking goals for persons with AUD con- tinue to be controversial, and the clinician who elects to provide such treatment may be vulnerable to criti- cism from the AUD treatment community (Davis & Rosenberg, 2013). Long-term outcomes of even severe AUD can, however, include reduced drinking (e.g., Ilgen, Wilbourne, Moos, & Moos, 2008), and recent data suggest that continued drinking after AUD treat- ment may still result in improved psychosocial func- tioning in multiple life areas (e.g., Witkiewitz et al., 2017). Data about the success of moderation training are more mixed. Studies of training in moderate drink- ing using a Web-based intervention (Hester, Delaney, Campbell, & Handmaker, 2009) or a women’s therapy group (Walitzer & Connors, 2007) both found posi- tive outcomes for moderation training with mild AUD drinkers, with the results for the women’s group sus- tained over 30 months of follow-up.
Several considerations should guide a clinician’s approach to treatment goals. Abstinence is clearly de- fined, is the least risky course for most drinkers, and is in accord with usual clinical practice in the United States. Also, agreeing readily to a goal of moderate drinking may reinforce a client’s view that alcohol is important and necessary to his/her daily functioning. However, with some clients, the use of a reduced drink- ing goal is appropriate. Moderation may be used as a provisional goal to engage a client in treatment, or it may be used when the client will not agree to abstinence but wants assistance to change (as with Bill). Clients are more likely to select a moderated drinking goal when they have mild to moderate AUD, fewer alcohol-related consequences, are less ready to change, are more eco- nomically advantaged, and have a social network with a higher proportion of daily drinkers (DeMartini et al., 2014). Clinicians should be more cautious about a mod- erated drinking goal for clients with medical or psy- chological problems that would be exacerbated by con- tinued drinking, or who have a family history of AUD or a history of moderate to severe AUD. Even if clini- cian and client select a moderation goal, a period (1–3 months) of initial abstinence is typically recommended to help evaluate the function of alcohol in one’s life, to give the brain a chance to heal and reset the reward cen- ters, and to help allow for a more informed, data-driven
decision about how much to drink moderately and in what pattern after the abstinence period. In selecting a moderation goal, the clinician should be careful to help the client recognize the current and potential negative consequences of excessive drinking, and make an in- formed and thoughtful choice in selecting a treatment goal. The clinician should view any initial drinking goal (abstinence or moderation) as tentative, to be re- evaluated as therapy progresses.
Initiating Abstinence or Reduced Drinking
The clinician has a variety of alternatives to help a client initiate abstinence. As noted earlier, several alternative detoxification strategies are available, including inpa- tient detoxification, ambulatory detoxification, “cold turkey” detoxification (in which the client simply stops drinking abruptly), or a graduated program of reduc- tion of drinking over a period of weeks, until the cli- ent reaches abstinence (Holzhauer et al., 2017). A case example illustrates a protocol of gradual reduction of drinking to achieve abstinence by a collaboratively set quit date (Holzhauer et al., 2017).
“Steve,” a 48-year-old unemployed man with a long history of heroin and cocaine use, and AUD, entered treatment after heroin detoxification but was still drinking an average of eight standard drinks per day (usually a half-pint of hard liquor plus one to two beers). He was healthy and had no history of alcohol with- drawal symptoms. No inpatient detoxification facility was available to him given his economically destitute state. Initial treatment focused on helping him stabilize his living situation and obtain temporary General As- sistance (welfare). Following these social interventions, the therapist (one of our practicum students) began to focus on Steve’s drinking. Steve expressed a strong preference for a program of graduated reduction in drinking. He was evaluated by a physician at the local free clinic and cleared medically. We had him record his drinking for 1 week to establish a clear baseline. We then collaborated with him to set a quit date of 3 weeks forward, and to reduce his drinking accordingly, in a linear fashion—never to drink more on any day than the amount he drank on the previous day during the titration period. We agreed that Bill would limit his drinking to two beers and three standard drinks of hard liquor for 5 days, then reduce to two beers and one standard drink of hard liquor for 5 days, then 7 days of just two beers each day with optional abstinence days interspersed, then 4 days of one beer each with
Alcohol Use Disorders 581
abstinent days mixed in. We discussed specific strate- gies to achieve this goal each week, and Steve continued to monitor his drinking. During the alcohol reduction period, Steve reestablished contact with a former long- term girlfriend who had terminated their relationship when he relapsed to alcohol and heroin use. She had heard that he was off heroin and expressed interest in being involved with him again. Her presence provided a strong incentive for him to follow the alcohol reduction program, because she was unaware that he had been drinking. The program progressed smoothly, and Steve stopped drinking after 3 weeks. If clients have diffi- culty with titrating, which is usually clear after a week or two, it is important to consider a consultation with an addiction physician to try an anticraving medication such as naltrexone to assist the titration, or to consider a different approach to attain abstinence, such as inpa- tient detoxification.
Developing a Functional Analysis
Completing a behavioral assessment of factors associ- ated with a client’s drinking includes both a structured and a qualitative dimension, and incorporates clinical interviewing, questionnaires, and self-monitoring of drinking and drinking urges. Suzanne, briefly described earlier, provides an excellent illustration of the complex- ity and results of the behavioral assessment process.
Suzanne came from a large Jewish family, many members of whom made demands on her. She had three daughters, ages 10, 8, and 4 years old. Her drinking had increased 5 years prior to treatment, after a car accident that took the life of her fraternal twin brother. They had gone out to a Bruce Springsteen concert together, and her brother had had several drinks at the concert. An autopsy after the accident revealed that he had also been using cocaine, but Suzanne had been unaware of his drug use. She blamed herself for allowing him to drive and for not insisting that he stop when he began to drive in a reckless manner. She began to drink im- mediately after the accident and quickly established a pattern of daily consumption of a half-bottle of wine per day.
Although the amount was not that great, she re- ported that the alcohol was very important, because it helped her avoid her overwhelming sadness about her brother’s death, especially at the end of the day. The re- sults of the behavioral assessment revealed a more com- plex pattern of drinking antecedents. On the DPQ, Suzanne rated emotional antecedents as most impor-
tant, endorsing feelings of sadness, hurt, and frustra- tion. She also indicated that certain environments were triggers for drinking, such as specific restaurants, times of the day (evening), and activities (particularly watch- ing television). Other major triggers emerged from Su- zanne’s self-monitoring cards—her interactions with extended family members and with friends, and situ- ations related to her children. Her parents were highly critical of how she was raising her children. Suzanne and her husband, Josh, were attending a conservative temple, kept kosher in their home, did not allow violent video games, and expected each daughter to participate in a fine arts activity (music, dance, or painting). Her parents believed that their grandchildren’s upbringing and Suzanne and Josh’s standards were too strict and conservative, and they were vocal in their criticisms. Other familial stressors included her interactions with a sister, who was getting divorced, and a cousin, who was in economic straits. Each contacted Suzanne on a regular basis, demanding either her attention or her money. Suzanne’s functional analysis is provided in Figure 14.6.
Early Drinking Reduction or Sobriety Strategies
Early sobriety strategies help the client maintain absti- nence from alcohol or a reduction in drinking. Cog- nitive-behavioral techniques vary with the individual but may include stimulus control strategies to avoid or rearrange high-risk situations, development of skills to deal with urges to drink, learning to think differently about drinking and not drinking, identification of be- haviors alternative to drinking in high-risk situations, development of alternative ways to obtain the reinforc- ers previously obtained from alcohol, and learning to refuse drinks.
Stimulus Control
Stimulus control strategies are designed to alter envi- ronmental cues for drinking by avoiding the cue, rear- ranging it, or implementing different responses in the same environment. Stimulus control strategies are com- patible with the AA suggestion to be attuned to “peo- ple, places, and things.” Work with Suzanne illustrates stimulus control strategies.
With Suzanne, stimulus control strategies served a major function early in treatment. She developed spe- cific strategies to deal with a number of the environ- mental high-risk situations identified in her functional
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FIGURE 14.6. Suzanne’s functional analysis.
Alcohol Use Disorders 583
analysis. Her first approach was to avoid such situations whenever possible. She suggested to Josh that they eat only at restaurants without liquor licenses, and asked that they decline several social invitations to places where alcohol would be the main focus of the evening (e.g., cocktail parties). The one situation that she could not avoid was the end of the day, after the children had gone to bed. Her usual routine had been to complete the dinner dishes while Josh helped the girls get ready for bed, then sit down in the den with her wine and the television after reading the children a story. She decided that she needed to disrupt this pattern and thought that if she got ready for bed herself, then curled up on the couch with a book and a cup of herbal tea, she would experience less urge to drink. It took her 3 weeks to get to a bookstore to buy some light novels, but once she had the books, Suzanne was able to implement this plan with success, except when she was upset.
Dealing with Urges
As individuals decrease their drinking or initiate absti- nence, they may experience urges or cravings for alco- hol. It is helpful to provide the client with a framework for understanding that urges are learned responses to drinking situations, and that urges abate if unfulfilled. Imagery may help clients cope with urges; images may be acceptance-oriented imagery (e.g., surfing with the urge), action-oriented imagery (e.g., attacking the urge with a samurai sword), or they may incorporate imagi- nal retraining procedures that have been found to lead to decreased alcohol consumption (e.g., Moritz et al., 2019).
Suzanne struggled with urges to drink, particular- ly when anything reminded her of her twin brother’s death. During therapy, we focused on a variety of as- pects of her feelings about her brother’s death and also addressed the urges more directly. Suzanne initially reacted to the imagery techniques negatively, saying that she was not a person who imagined things much. She clearly needed some way to cope with these rather strong urges, so I pushed her a bit to try:
THERAPIST: I appreciate that you don’t think of your- self as imaginative, but maybe I can help you out. Just humor me for a minute, and let’s see if we can come up with an image that grabs you. It doesn’t matter what the image is—you could imagine climb- ing a mountain and coming down the other side, or spraying the urge with a fire extinguisher.
SUZANNE: (smiling) I know what I can imagine— I could picture you jumping out of the bottle and shaking your head at me.
THERAPIST: OK. Should I look mean? SUZANNE: No, just having you there would help me
deal with it. THERAPIST: All right, I can live with that. SUZANNE: In fact, I could picture a row of wine bot-
tles—with you coming out of the first one, then showing me all the disgusting things in the other ones.
THERAPIST: So, what would be disgusting? Ticks? SUZANNE: Ticks would be good, and maybe cock-
roaches, too. THERAPIST: Let’s try this out.
At that point, I had her practice using the imagery in an imagined urge situation. Remarkably, she used the imagery frequently and found it helpful.
A second technique for coping with urges is to en- list the assistance of a family member or friend. Persons involved with AA are told to call someone in the AA program when they feel an urge to drink, and they usu- ally receive telephone numbers from several members. Clients not involved with AA can seek other sources of support. Suzanne, for example, asked her husband to help her when she had the urge to drink. She asked Josh to remind her of why she had stopped drinking and to say, “Of course, it has to be your decision.”
Addressing Beliefs about Alcohol
People who drink heavily hold stronger positive ex- pectancies about the effects of alcohol than do people who drink more lightly (Pabst, Baumeister, & Kraus, 2010). Clients may believe that drinking facilitates social interactions, enhances sexual responsiveness, al- lows them to forget painful events or feelings, or makes them more capable. These beliefs often are deeply held and difficult to challenge, particularly if a client con- tinues to drink. Several cognitive strategies may help. First, effecting a period of abstinence allows the client to experience many situations without alcohol—an experience that often leads to reevaluation, with little input needed from the therapist. At some point, many clients are impressed with the vacuous nature of drunk- en conversation; the undesirable physical appearance, behaviors, and odors that accompany high BALs; and
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the shallow nature of drinking relationships. The wise therapist watches carefully for these observations and reflects their importance and self-relevance. If a client does not have such experiences spontaneously, the ther- apist facilitates new views of drunken comportment by developing a relatively safe way for the client to observe intoxicated behavior—through either movies or video- tapes, or visits to a local bar (accompanied by someone who is aware of and supports the client’s abstinence).
A second set of cognitive strategies involves clients evaluating the impact of drinking on themselves and others and using that reevaluation to support change in their drinking. Research suggests that greater use of these strategies is associated with more positive treat- ment outcomes (Roos & Witkiewitz, 2016). The ther- apist and client can generate a list of negative conse- quences of drinking and use imaginal rehearsal in the session to help the client pair positive thoughts about alcohol with the list of negatives. Continued rehearsal in the natural environment is then important. Third, some clients develop a set of erroneous beliefs about their drinking that sets them up for drinking. Common beliefs include “I’ve been doing so well, I can just drink tonight,” or “I’ll have just one.” (See https://boozemus- ings.com/top-ten-lies-drinkers-tell-themselves-and-others for other examples.) Although moderate drinking is possible for some clients, others have histories of drink- ing until they lose control, which is in direct opposition to a belief in control, and they need to learn to recog- nize and counter these beliefs.
Work with Steve provides a simple illustration of cognitive strategies to address positive expectations about drinking. Steve had a long history of loss-of-con- trol drinking. After a period of abstinence, he began to think, “I could have just one beer, and that would be fine.” His therapist questioned the accuracy of that belief. Steve readily acknowledged that he had never been able to control his drinking in the past, that if his girlfriend found out she would be very upset and probably leave him, and that relapses to heavy drinking usually led him to use heroin. Steve and his therapist developed a simple cognitive formula to use when he thought about drinking: “1 = 32 = 10,” meaning that for him, one drink would lead to a quart of liquor (32 ounces), which would lead to heroin use (10 bags a day).
Alternative/Distracting Behaviors
Drinking is a time-occupying activity, and clients may see few alternatives to help them through times when
they previously would drink. Discussion of specific be- havioral alternatives to drinking that are both time-oc- cupying and mentally or physically absorbing is another helpful strategy early in treatment.
Steve’s experiences provide a particularly powerful example of the alternatives that highly motivated clients may find. After Steve found space in a rooming house and had begun the detoxification process, he was faced with the daunting prospect of filling his completely un- structured days. Some of his time was occupied with the time-consuming work of being poor—getting back and forth to the soup kitchen, waiting at the free clinic for medical services, getting an appropriate identifica- tion card, so that he was eligible for other charitable programs, such as clothing distribution. But even with these necessary activities, Steve had hours and hours of free time. Steve began to address this challenge by cre- ating his own activities. He obtained a library card and scheduled times for himself at the library. Instead of reading randomly or recreationally, he decided to read about the Crusades, which sparked an interest for him in medieval Christianity. A lapsed Catholic, he decided to attend Mass again, and began to attend daily. His daily attendance led to involvement in a Bible study group, and he became a thoughtful and passionate par- ticipant. A creative man, Steve then began to write short stories with religious themes.
Identifying Alternative Ways to Obtain Positive Experiences
Among the more compelling aspects of alcohol and drug use are the psychoactive properties of the substances. In the short term, large quantities of alcohol effectively deaden negative affect, decrease obsessional thoughts, and decrease muscle tension, although these effects do not endure over the long term. Alcoholic beverages also have distinctive and sometimes desirable tastes that are difficult to replace with other beverages. An important aspect of the functional analysis is articulating the cli- ent’s perception of positive consequences of drinking. The clinician can address the power of these perceived reinforcing consequences in several ways: helping the client develop alternative means of obtaining the same types of positive experiences; challenging the client’s belief that the desirable consequences will occur (e.g., questioning whether the client is in fact more socially adept and appealing after consuming a quart of vodka); helping the client reevaluate the importance of these consequences; and/or helping the client identify other
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classes of reinforcers that might be valued more highly in the long run (e.g., valuing spirituality more highly than hedonism).
Drink Refusal Skills
Some drinkers find the interpersonal aspects of absti- nence difficult. For them, identification of interpersonal situations that are high risk for drinking, development of effective responses, and rehearsal of these responses all form an important component of treatment. Early research (Chaney, O’Leary, & Marlatt, 1978) suggested that giving a quick response is strongly associated with successful change. More recent research has found that drink refusal training makes a unique positive contri- bution to treatment outcome (Witkiewitz, Donovan, & Hartzler, 2012) and that the quality of these skills is important (Kiluk, Nich, Babuscio, & Carroll, 2010). Suggested components of effective drinks refusal in- clude indicating clearly that the one does not want an alcoholic beverage, requesting an alternative beverage, communicating confidence and comfort with the re- quest, and being persistent in the face of social pressure. In addition, clients who face excessive social pressure may be advised to consider avoiding certain social situ- ations or persons.
Although the guidelines for refusing drinks appear simple, client beliefs and expectations often make the drink refusal process difficult. Common cognitions in- clude “Everyone will think I’m an alcoholic,” “My host will be offended if I don’t drink,” or “People will think I’m too good for them if I don’t drink.” As with other distorted beliefs, the clinician can provide alternative frameworks for thinking about drink refusal situations, suggesting that most people really are uninterested in others’ drinking, or that hosts are most concerned that guests are enjoying themselves. Many clients also expe- rience ambivalence about not drinking and find that the most difficult part of the drink refusal process is internal rather than interpersonal. Another complicat- ed aspect of drink refusal is how much personal infor- mation the client wishes to divulge. Most people share different levels of personal information, depending on the closeness of the relationship and their knowledge of the other person’s behavior and attitudes. For persons to whom a client does not want to disclose his/her drink- ing problem, we encourage use of a simple “No, thank you,” or, if pressed, a simple response that would dis- courage pushing without being revealing, such as “I’m watching my weight and can’t afford the calories,” “I’m
on medication that doesn’t allow me to drink,” or “My stomach’s been acting up—I better pass.” None of these replies protects the client against future offers, but each is effective in the moment. For closer relationships, the client makes a decision about when, where, and how much to reveal. Two clinical examples illustrate these points.
Steve was living in a boarding house and had friend- ly, sociable neighbors who liked to drink on the front porch. These neighbors were from the Portuguese Azores and spoke virtually no English. After accepting a beer from them one day, he insisted to his therapist that he could not refuse, because he did not speak Por- tuguese. The therapist suggested that perhaps the word “No,” spoken with a smile and a hand gesture, might be understood even in Portuguese. Steve acknowledged that his difficulty with refusing the drink came from his desire to drink, and that a friendly “No” would cer- tainly work.
Suzanne did not want anyone to know that she had a drinking problem, or that she was abstaining. This stance posed problems for an upcoming cocktail party. Strategizing, Suzanne decided ahead of time that she would drink seltzer water that evening, and that she would attempt to forestall offers of drinks by keeping a glass of seltzer in her hand at all times. If offered a drink, she decided to tell people that she had had some health problems that might be made worse by her drinking, so she was sticking to seltzer. Although she was concerned that one of her friends (a social worker) might surmise that she had an alcohol problem, the evening progressed uneventfully.
Coping Strategies
Clients with AUD face common life difficulties stem- ming from dysfunctional thoughts, negative affect, and interpersonal conflicts. As clients develop a greater abil- ity to maintain abstinence or moderated drinking, the clinician may devote increasing attention to other prob- lems clients are facing. General clinical techniques to deal with dysfunctional thoughts or social skills deficits can be used readily with clients with drinking prob- lems.
Dealing with Negative Affect
There are multiple sources of negative affect in per- sons with an AUD. As noted earlier in the chapter, co- occurrence of AUD with other psychiatric disorders is
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high (particularly mood and anxiety disorders). Rates of sexual and physical abuse are also elevated among those with AUD (Cisler et al., 2011), and the sequelae of these problems often include a strongly negative af- fective component. In addition, persons who have used alcohol to cope with negative affect over an extended period of time may simply have limited experience and limited skills to cope with the pain that is a part of ev- eryday life.
In focusing on negative affect, a careful assessment of the causes is essential. Negative affect associated with another disorder should be treated in accord with the appropriate approach for that disorder or through use of the unified protocol for treating emotional dis- orders (Barlow et al., 2017). In treating negative affect associated with AUD, certain common principles are of value. When clients first reduce or stop drinking, they may experience all emotions as unfamiliar and intense. Cognitive reframing to help clients view these intense emotions as a natural part of the change process may be useful. For clients pursuing a moderation goal, avoidance of drinking at times of intense negative af- fect provides the opportunity to learn alternative cop- ing strategies. Coping strategies may vary with the type of negative emotion and may include relaxation, yoga, prayer or meditation; exercise; paced breathing and other strategies, such as the diving response to manage emotion dysregulation, anxiety, and depression; behav- ioral activation; increasing the experience of pleasurable events to decrease depression; use of anger management and assertiveness skills to cope with angry feelings; cognitive strategies to address beliefs that contribute to distressing affect; and/or consultation with an addic- tion psychiatrist to begin nonaddictive antidepressant, mood stabilizer, or anxiety medication.
Work with Suzanne illustrates several of these princi- ples. Most difficult for Suzanne were any situations that reminded her of the death of her twin. Their birthday, the anniversary of his death, the celebration of Father’s and Mother’s Days, holiday celebrations, and special celebratory events for her children, in which he would have been importantly involved (e.g., a bat mitzvah) all elicited intense negative affect and a strong desire to drink. Given that Suzanne had begun drinking heav- ily right after her twin’s death, she had spent little time experiencing grief or even discussing his death and her feelings about it. My initial approach in therapy was to give her opportunities to be exposed to these negative feelings by simply talking about him in the therapy ses-
sion. The second approach was to discuss and identify ways to approach events that reminded her of him. I saw her over a 6-month period, during which a number of these situations arose naturally. For example, in the week prior to the anniversary of his death, we discussed ways that she could focus on his death and memories. Suzanne took one of her children to his gravesite, and they cleaned it up and planted flowers together. On the Saturday of the anniversary of his death, she went to temple with her family, then cooked what had been her twin’s favorite dinner. The day was sorrowful, and Suzanne cried several times, but it was the first anni- versary that she felt she had honored him rather than shaming his memory by getting drunk. We also ad- dressed her repetitive, self-blaming thoughts about his death by using cognitive restructuring techniques. She found it difficult not to blame herself for his death, and few cognitive strategies had much impact on the self- blame. Suzanne finally was able to begin to think, “I cannot torture myself forever with this blame. If I don’t let go of it, I won’t be a good mother. He’d be disap- pointed with me if I let my children down.” In addi- tion to cognitive-behavioral trauma-informed therapy described here, which worked very well for Suzanne, if necessary, clinicians may also consider incorporating other evidence-based trauma treatments to formally address the trauma underlying drinking behavior, such as prolonged exposure therapy or cognitive process- ing therapy. Diagnosing and treating or referring for evidence-based treatment of comorbid psychiatric dis- orders is an important and sophisticated aspect of the CBT model presented in this chapter given the high prevalence of other psychiatric problems in AUD popu- lations and the negative reciprocal relationship among other psychiatric problems and alcohol use.
Lifestyle Balance and Positive Activities
Long-term success is supported by lifestyle changes that enhance positive experiences and allow for a bal- ance between responsibilities and pleasure. As they begin to change, some of our clients believe that they need to make up for their previous lack of responsibility with a very high level of responsibility to family, job, and home. Taking on major redecorating or remodel- ing projects, trying to spend every free moment with their children or cleaning out 10 years’ worth of messy drawers and cabinets is not uncommon. This zeal for responsibility can be a double-edged sword for both cli-
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ent and family. Unrelenting attention to responsibilities may be simultaneously satisfying and exhausting and unrewarding, and may lead the client to question the value of not drinking. Family members may be thrilled that the client is taking on responsibility but leery of the stability of the change and unwilling to give up re- sponsibilities they have assumed for him/her. They also may experience the client’s enthusiasm as an intrusion on their own independent lives and schedules. Clients should be prepared for such reactions, and the clinician can help reframe the family’s response as understand- able. With most clients, it is important for the clinician to suggest the importance of leisure time, pleasurable activities, and self-reinforcement for positive changes made.
Helping Suzanne identify a half-hour per day dur- ing which she could relax, read, or exercise was a chal- lenge. She believed that she should devote herself to her daughters—a belief that resulted in her being with them virtually all the time when they were home. When they were at school, she focused on housecleaning, cooking, errands, paying bills, and other chores. She was ex- hausted and tense at the end of the day, and commented that alcohol had been a good way to “come down.” We finally agreed on a half-hour block before lunch, during which she would use her exercise bike, read a book of daily meditations, or take a walk. She was only partially successful in these efforts, often citing other responsi- bilities that took precedence. The clinician should keep in mind that the positive consequences of sobriety are what tend to maintain continued abstinence, so it is im- portant to help clients achieve a balanced lifestyle that substitutes the time and energy spent drinking with pleasant, rewarding activities and experiences instead.
Partner/Family Involvement and the Social Context of Treatment
The literature on the treatment of AUD suggests that the involvement of some significant social system is associated with positive treatment results (reviewed in McCrady & Flanagan, in press). Because of these find- ings, the clinician’s first inclination should be to involve the client’s spouse/partner or some significant other in the treatment. There are a number of ways to involve significant others: using them as sources of informa- tion, having them provide differential reinforcement for drinking and abstinence, helping them to provide emotional or practical support, involving them in re-
lationship-focused treatment, providing treatment to them without the person who drinks, and/or helping them access new social systems.
Information
Folklore suggests that persons with AUD minimize or lie about their drinking and its consequences. The em- pirical literature suggests that such individuals provide relatively accurate data when sober, and when there are no strong negative consequences for telling the truth (e.g., Sobell & Sobell, 2003). Despite these results, a number of clinical considerations suggest that obtain- ing information from a family member may be useful in the assessment phase of treatment.
Clients who are referred to or coerced into treatment may be reluctant to provide full information about their drinking. Collecting data from the referring agent helps both client and clinician understand the reasons for the referral. Even with self-referred clients, significant oth- ers can provide information that may be unavailable to the clients because of problems with memory or recall. In addition, an intimate significant other usually has observed the drinker over a long period of time and in multiple environments, and may have valuable observa- tions to contribute to the conceptualization of anteced- ents to drinking.
Responses to Drinking and Abstinence
Clients with AUD often face the challenge of establish- ing a social network that provides differential reinforce- ment for abstinence and applies negative consequences for drinking. Such reinforcement may be relatively simple, such as positive comments and encouragement from friends and family, or may involve the negotiation of detailed contracts that specify the consequences of drinking and abstinence. The community reinforcement approach (CRA; Meyers & Smith, 1995) helps clients access potential reinforcers (jobs, families, social clubs), teaches clients and partners behavioral coping skills, and may involve the development of contingency con- tracts to make access to reinforcers contingent on sobri- ety. In addition, clients may be prescribed disulfiram or naltrexone, and compliance may be monitored by a significant other. Evaluations of the CRA suggest that clients are significantly more successful than controls in maintaining abstinence and employment, avoiding hos- pitalizations or jail, and maintaining a stable residence.
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In addition to formal treatments that focus on ma- nipulation of environmental contingencies, the thera- pist also may teach spouses/partners and other fam- ily members how to allow the client to experience the naturally occurring negative consequences of drinking. Many spouses/partners protect the drinker from these consequences by covering for him/her at work, doing his/her chores, or lying to friends and family about the drinking (Orford et al., 2010). Experience of these neg- ative consequences may increase the client’s awareness of the extent and severity of his/her drinking problem, and provide further motivation for change.
Decreasing Cues for Drinking
Significant others also may engage in behaviors that cue further drinking. A wife who wants her husband to stop drinking may nag him repeatedly about the problems his drinking is causing, hoping that her concerns will motivate him to change. Or a husband may try to get his wife to stop drinking by limiting her access to alco- hol or tightly controlling their money. Such behaviors may have an unintended negative effect, eliciting anger or defensiveness from the person with the drinking problem, and leading to further drinking. Helping fam- ily members learn to identify such behaviors, recognize the results of these actions, and find alternative ways to discuss concerns about drinking may be helpful.
Support for Abstinence
Significant others can provide many kinds of support to clients. Support may involve helping a client to imple- ment behavior change, discussing urges to drink, sup- porting a client’s plan to avoid high-risk situations for drinking, or (upon the request of the client) assisting in the implementation of other coping skills that support sobriety.
Relationship Change
For many clients, interactions with their spouses/part- ners, children, parents, or close friends cue drinking. Thus, treatment that focuses on changing these inter- personal relationships is another way that significant others may become involved. These interventions may include couple or family therapy, or parent skills train- ing. Data (McCrady et al., 2009; McCrady, Stout, Noel, Abrams, & Nelson, 1991) suggest that a focus
on changing the couple relationship during conjoint AUD treatment results in greater stability of drinking outcomes, fewer separations, and greater couple satis- faction.
Accessing New Social Systems
Some clients have either no social support system or one that strongly supports heavy drinking. For such clients, it is important to access new systems that either rein- force abstinence or are incompatible with heavy drink- ing. Mutual-help groups such as AA and SMART Re- covery are potential sources of such support. Because many religious groups are against the use of alcohol, serious involvement in a religious organization also may support abstinence. Many group activities are in- compatible with drinking: Running, hiking, or cycling groups are examples. Unfortunately, alcohol can be in- volved in almost any activity, and therapist and client need to look carefully at activity groups to determine whether the group norm includes drinking.
In summary, decisions about the social context of AUD treatment are complicated. The initial assessment should involve at least one significant other. The results of the assessment should reveal persons who are most available for treatment, and who might be sources of support and reinforcement. For some clients with no readily accessible supports, new support systems need to be developed.
Long‑Term Maintenance
Relapse Prevention
Marlatt and Gordon’s (1985) RP model and Witkiewitz and Marlatt’s (2004) and Hunter-Reel et al.’s (2009) re- vised RP models are comprehensive treatment models; Epstein and McCrady’s (2009) CBT manual provides specific RP exercises in the last several treatment ses- sions. Many elements of the RP treatment model al- ready have been described—identifying high-risk situ- ations for drinking, developing alternative strategies to cope with high-risk situations, enhancing self-efficacy for coping, dealing with positive expectancies about the use of alcohol, and facilitating the development of a bal- anced lifestyle. An additional and important part of the RP model is addressing the possibility of relapse and developing preventive and responsive strategies related to relapse.
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RP can be introduced to clients by letting them know that use of alcohol after treatment is not uncommon, and that is helpful to discuss this possibility during treatment. Two basic strategies are used. First, a client is helped to develop a list of warning signs of an impending relapse, including behavioral, cognitive, interpersonal, and affective signs. If a client’s spouse/partner is part of the treatment, he/she contributes to the list. After the client and therapist have developed this list, they then can generate a set of possible responses. Most important is for the client to recognize that these warning signs should trigger action rather than inaction and fatalistic cognitions about the inevitability of relapse. A second set of strategies involves response to actual drinking or heavy drinking. The clinician attempts to address the possibility of the AVE by calling attention to the possi- bility that a client may have catastrophic thoughts if he/ she drinks and helping him/her consider and practice al- ternative ways of thinking about having drank. Marlatt and Gordon (1985) also suggested a series of behavioral steps: Introduce a behavioral delay (1–2 hours) between an initial drink and any subsequent drinks; get out of the immediate drinking situation; conduct a functional analysis of the drinking situation during that time; re- view possible negative consequences of drinking; and call someone who might be helpful. Some research evi- dence supports the use of such RP approaches, as well as newer approaches that integrate RP with mindfulness training (e.g., Bowen et al., 2014).
Continuing Care/Maintaining Contact with Clients
Time-limited treatment is appropriate and effective for many clients, and there is good evidence of long-term, sustained improvement following a course of outpatient treatment (Project MATCH Research Group, 1998). However, periods of relapse are common. The clini- cal strategies we have described for RP are intended to minimize periods of problem use and to maximize posi- tive outcomes. For some clients, however, AUD must be viewed as chronic, relapsing disorder (McLellan et al., 2000). As with other chronic health problems, such as diabetes or rheumatoid arthritis, acute care models that treat individuals and send them on their way may be inappropriate and ineffective. An alternative strategy provides longer-term, low-intensity contact over an ex- tended time interval (McKay et al., 2011).
During the initial treatment of a client with a history of severe AUD, multiple treatment episodes, and diffi-
culty maintaining successful change, the clinician may elect to set a different expectancy with that client—that some form of contact will be ongoing and long term.
“Leonard,” a 54-year-old married man, came to treatment with problems with severe AUD and agora- phobia. Treatment focused on both disorders, and he was successful in becoming abstinent from alcohol and in gradually increasing the distances that he could drive by himself. Leonard’s home was an hour’s drive from my (B. S. M.) office, and treatment had gone on for almost 12 months before he could drive to office with- out his wife accompanying him. By the end of the year, we were meeting every 2 to 3 weeks. Given that Leon- ard had been abstinent for a year and was functioning well, we discussed the possibility of termination. His response was instructive:
LEONARD: Doctor, I’ve been drinking a long, long time. One year is just a drop in the bucket in com- parison. I think that I need to keep seeing you.
THERAPIST: Leonard, I understand your concerns, but you’ve been doing well for quite a long time now. Maybe we should just cut down more on how often you come in. How about an appointment in a month, and making it a bit shorter—a half-hour instead of an hour?
LEONARD: I think that’s a good idea. Let’s try it.
I gradually tapered the frequency and length of my sessions with Leonard, and saw him twice per year, 15 minutes per session, for the last 3½ years of his 5-year course of treatment. He described the importance of the sessions: “I just know I’ll have to see you and tell you what I’ve been doing. It keeps me honest.”
Management of Complicating Conditions
As described earlier in the chapter, clients with AUD may present with myriad other complicating condi- tions. The clinician must assess and develop a treat- ment plan for the multiple needs of such clients. At a minimum, clinicians should consider possible problems related to housing, transportation, income, occupation/ employment, the legal system, the family, child care, medical conditions, and comorbid psychological disor- ders. Knowledge of services and agencies in the local community and the development of working relation- ships with a range of agencies are essential to the treat-
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ment of complicated clients. Rose, Zweben, Ockert, and Baier (2013) provide a comprehensive framework for interfacing with other health and social systems.
The Role of Mutual‑Help Groups
Types of mutual-help groups were described in an ear- lier section of this chapter. Various therapeutic strate- gies may facilitate involvement in a mutual-help group, when appropriate. The clinician should first assess whether a client may be a good candidate for mutual- help group involvement. Clients with very high social anxiety or social phobia, clients who believe that a person should take care of problems alone, and those with a history of negative experiences with mutual-help groups may be poorer candidates. Conversely, affilia- tive clients, those who are used to solving problems with assistance from others, those who are particularly anx- ious and concerned about their drinking, those whose social support systems strongly support continued heavy drinking, and those with more severe AUD are particularly good candidates for AA. Persons who are interested in the social support aspects of mutual help but explicitly reject some of the constructs associated with AA (e.g., powerlessness or spirituality) may be best served by referral to an alternative mutual-help group such as SMART Recovery.
As with all aspects of the therapy, the clinician should use a client-centered approach to the introduction of AA or other mutual-help groups. Such an approach sug- gests a dialogue between client and therapist, acknowl- edgment and discussion of the client’s perceptions and concerns, and development of a mutually agreed-upon plan. Because many clients have misconceptions about AA and are unfamiliar with alternative mutual-help organizations, the clinician should be prepared to de- scribe the organizations and answer questions. It also is helpful for the clinician to have some basic publications from each group available in the office. At times, we may encourage a reluctant client to try a few meetings to sample firsthand what actually occurs. We negotiate a very short-term agreement for a specified number of meetings in a specified length of time (e.g., six meetings in 3 weeks); we agree that if the client continues to be negative or reluctant after trying the groups, then we will abandon this idea; and we discuss the client’s expe- riences and perceptions of the mutual help group meet- ing in each therapy session. We use behavioral sampling with other aspects of therapy as well: Clients often can- not visualize how a strategy might work without try-
ing it—be it a relaxation technique, an AA meeting, or an assertive response—and we encourage clients to be open to new strategies. In AA, newcomers may be told, “Your best thinking got you here,” which suggests that their own coping strategies have been ineffective. Behavioral sampling is based on this same construct.
Therapist Variables
As with any form of therapy, the therapist’s relation- ship and the therapeutic stance he/she assumes with the client are important. Empathy, active listening, instillation of hope, flexible application of therapeutic principles and techniques, and establishment of a sense that therapist and client are working toward mutually agreed-upon goals are essential. Research suggests that in contrast to a confrontational style, an empathic, motivational style is associated with better treatment outcomes, and that confrontational behaviors by the therapist tend to elicit defensive and counteraggressive behaviors by the client (Miller, Benefield, & Tonigan, 1993). Such responses are hardly conducive to a con- structive therapeutic alliance.
Working with a client with an AUD often is diffi- cult because of both the client’s behavior during treat- ment and his/her history of drinking-related behaviors that the therapist may find repugnant or upsetting. The client may lie about or minimize drinking during treatment. If the spouse/partner is also involved in the treatment, the therapeutic relationship becomes even more complicated. By treating a client with a drinking problem along with a spouse/partner who wants that client to stop or decrease drinking, the therapist is al- lied de facto with the spouse/partner. The partner may attempt to enhance his/her alliance with the therapist by echoing the therapist’s comments, expressing anger at the client’s behavior, being confrontational, or, alter- natively, being submissive and allowing the client to be verbally aggressive or dominant.
Certain therapist attitudes and behaviors appear to be conducive to successful treatment. First is a sense of empathy with the client. The therapist must develop some understanding of the client’s subjective experi- ence of entering therapy and the difficulty of admitting behaviors that are personally embarrassing and often not socially sanctioned. In addition, the therapist needs to have some appreciation of the incredible difficulties involved with long-term change in drinking behavior. He/she may develop this appreciation by attempting to change his/her own deeply ingrained behavior pattern
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(e.g., eating sugar) or by attending meetings of some mutual help group (e.g., AA, SMART Recovery) and listening carefully to clients.
A second important therapist skill is the ability to distinguish between the person and the drinking-re- lated behavior. The client needs to be able to describe drinking-related actions without feeling that the thera- pist either feels repulsed or condones or accepts such be- haviors. This is a delicate balance to achieve, especially when a client describes drinking episodes in a joking manner that may hide embarrassment or disgust with the behavior. The client’s motivation to change may be enhanced by discussing negative, drinking-related be- haviors and experiencing the negative affect associated with thinking about those actions. The therapist also should communicate a sense of hope to the client by anticipating positive changes that might be associated with changes in drinking, and by emphasizing that it is possible to change. Thus, the implied message to the client is as follows:
“You have done many things when drinking that are distressing to you and to the people around you. The fact that you are in treatment is a statement that you want to change. It is important to talk about things you have done when drinking because being aware of them will strengthen your desire to stop drink- ing and to stop doing these things. Making changes will take time and a lot of work on your part, but I believe that you will be successful if you stick with treatment.”
In other words, the therapist’s message is positive about change but negative about drinking-related be- havior.
A third important therapist quality is integrity. Be- cause of both their discomfort and their reinforcement history, it is difficult for some clients to honestly report their drinking episodes, failed homework assignments, or their feelings and attitudes about being in treat- ment. The therapist can acknowledge how difficult it is to be honest given that lying was probably adaptive in the past, but he/she must make it clear that part of therapy involves learning how to be honest. The thera- pist also must provide a positive model of integrity. He/she should not ignore the smell of alcohol on a cli- ent’s breath, and he/she should review the homework assigned each week. Attending to the client’s behavior teaches the client the importance of following through on commitments and increases the chances that ther-
apist and client will be able to identify problems and blocks to progress in treatment.
The therapist also must set clear expectations about both the client’s and his/her own responsibilities to the therapy, and must be able to set appropriate limits. The therapist should set clear expectations for the client: coming to scheduled sessions on time, calling if unable to attend, paying the bill for therapy sessions, com- ing in sober, and completing assigned homework. The therapist also should make his/her own commitment to therapy clear by being at sessions on time, being reason- ably available by telephone, providing coverage when unavailable, and providing treatments with demon- strated empirical support for their effectiveness. Being clear about expectations for the client’s behavior and his or her own behavior during therapy emphasizes the therapist’s commitment to therapy as a serious process.
Client Variables
Only a few client characteristics are consistent predic- tors of treatment outcome (Haaga, McCrady, & Lebow, 2006). Clients who have positive expectancies about the outcomes of treatment tend to have better outcomes. Additionally, clients with greater readiness to change have more positive outcomes. Finally, clients with more severe problems have poorer outcomes. Both treatment expectancies and readiness to change can be influenced by the therapist.
The clinician must be aware of and sensitive to a number of issues that persons with drinking problems bring to treatment. The client’s emotional experience, beliefs, attitudes, physical state (described in the section on treatment settings), and the social context of drink- ing (described in the section on the social context of drinking) are all important aspects of the therapeutic plan.
A person has a variety of reactions to the initial real- ization that his/her drinking is causing problems. Most commonly, as negative consequences accumulate, an individual begins to feel out of control and ashamed of the behavior. The person’s actions may be unac- ceptable to his/her self-definition. Thus, financial or work irresponsibility, neglecting family members, en- gaging in physical violence, or verbal abuse all may be actions about which the individual feels intense guilt and self-blame. The prospect of admitting these ac- tions to a stranger is frightening and embarrassing, making it difficult for a client to discuss drinking-as- sociated problems. Because many clients ascribe their
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problems to weakness or lack of willpower and believe that if they were only “stronger” these events would not occur, they blame themselves. Thus, clients are unusu- ally sensitive to implied criticisms from the therapist. The therapist can attenuate this difficulty by making empathic comments while asking questions, letting clients know that their actions are common among people who drink heavily, and listening to clients’ de- scriptions of drinking-related actions in an accepting manner. Clients also hold a number of beliefs and at- titudes about alcohol and their ability to change that make change difficult. People with AUD have positive expectancies about the effects of alcohol on feelings and behavior, and they hold these more strongly than do people without drinking problems. They may attribute their drinking to reasons external to themselves and be- lieve that they are not personally responsible for either drinking or changing. They may have low self-efficacy beliefs about their ability to change their drinking or to handle alcohol-related situations without drinking, or they may have unrealistically high self-efficacy beliefs that are not grounded in actuality. Finally, if people who stop drinking then consume alcohol again, cog- nitive dissonance may occur; they may experience the AVE (Marlatt & Gordon, 1985), characterized by an excessively negative reaction to initial alcohol consump- tion, and a self-perception that they have “blown” their abstinence and will inevitably relapse to the previous drinking pattern.
CASE STUDY
In the preceding sections, we have presented case ex- amples to illustrate the application of parts of our treat- ment model. In this section, we present a complete out- patient therapy case to illustrate a number of the issues described earlier in the context of ongoing treatment. The couple was part of a research project evaluating different approaches to the maintenance of change fol- lowing conjoint behavioral AUD treatment (McCrady, Epstein, & Hirsch, 1999), and seen by one of us (B. S. M.).
Couples in the study had to have been married or cohabitating for at least 6 months; neither partner could have a primary problem with the use of illicit drugs or show evidence of gross cognitive impairment or psy- chosis; and only the male partner could show evidence of alcohol abuse or dependence. All couples were seen by a therapist for 15–17 sessions of weekly outpatient
treatment, and agreed to a baseline assessment and 18 months of posttreatment follow-up.
“Carl” and “Maria” were married, and both were 32 years old. They came to treatment because of Carl’s drinking. Maria was of average height, had long, black, wavy hair and was heavy. Carl was also of aver- age height, had blond hair, and was slim but showed the beginnings of a “beer belly.” Both were neat and attractive. The couple had been married 5 years and had known each other for 12 years. They had two boys, ages 2 and 3. Both came from intact families, although Carl’s father had died a number of years previously. Carl’s family was primarily Polish; Maria’s was Italian.
At the time of treatment, Carl and Maria had been separated for 5 months. He was living with his mother in her home; Maria was renting a one-bedroom apart- ment in a poor community, where she lived with the two boys. Maria was a trained cosmetologist; Carl was an electrician who worked out of the union hall. Carl was not working at the time, because he did not want to establish a pattern of support for Maria or the children in case she filed for divorce. In addition, if he did not work for a certain period of time, Carl would be able to withdraw his money from the union’s pension plan, and he thought that would be an easy way to obtain money. Maria was not working, because she had decided that Carl would have to babysit while she worked, and she did not think that he would be reliable about coming to her apartment to care for the children. She was sup- ported by Aid to Families with Dependent Children; Carl worked odd jobs “under the table.” Both were high school graduates.
The couple came to treatment at Maria’s urging. She was very concerned about Carl’s drinking and cited it as the primary reason for their marital separation.
Behavioral Assessment and Case Conceptualization
Carl and Maria were assessed using several approaches. Their assessment was somewhat more extensive than is usual in clinical practice because of their involvement with the treatment research project. However, the main elements of the assessment are applicable to clinical practice as well.
Drinking Assessment
To assess his drinking, we used a clinical interview to ask Carl about his drinking history and perceptions of his current drinking. A handheld Breathalyzer was used
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at the beginning of each session to assess his current BAL. In addition, we used two structured interviews, the TLFB (Sobell & Sobell, 1995) and the Alcohol sec- tion of the Composite International Diagnostic Inter- view—Substance Abuse Module (CIDI-SAM; Robins et al., 1988), to obtain a more complete picture of his drinking. Maria was present for all interviews and con- tributed additional information.
The TLFB assesses drinking behavior on each day in a set window of time before treatment. For this study, we asked about Carl’s drinking in the prior 6 months, cue- ing his recall of drinking by noting other salient events in his and Maria’s lives, such as social events, medical appointments, holidays, and other celebrations. The TLFB revealed that Carl had drunk alcohol virtually every day of the previous 6 months. His only abstinent day was when he and some friends were arrested for at- tempted breaking and entering. His preferred beverages were beer and vodka, and he reported that the most he drank on any single day was about 32 drinks. His usual consumption was in the range of 10–12 drinks daily. Carl met DSM-IV (the system in effect at the time of assessment) and DSM-5 criteria for a diagnosis of se- vere AUD with physiological dependence. He had been drinking since high school and reported having his first problems as a result of alcohol at the age of 25. Carl had experienced a variety of problem consequences of his use: three arrests for DWI, one arrest for breaking and entering, warnings from job supervisors for intoxication on the job, problems in his relationship with his wife, and the feeling that he had neglected his responsibili- ties to his wife and sons. He had experienced numerous blackouts and reported many signs of physical depen- dence, including morning drinking, a sense of “panic” when he thought he would not be able to obtain a drink when he wanted one, and drinking throughout the day. However, Carl said that he had never experienced any of the physical symptoms of alcohol withdrawal. He also reported no health or emotional problems associ- ated with his drinking. When asked about his goals for treatment, Carl indicated that his own preference was to cut down and to drink moderately, but that his wife insisted on abstinence, and he was willing to work to- ward that goal.
We used two assessment techniques to identify an- tecedents to Carl’s drinking, the DPQ (Menges et al., 2008) and self-monitoring cards. The DPQ was used to assess Carl’s and Maria’s perceptions of drinking an- tecedents. Carl completed the DPQ by checking off all antecedents that applied to his drinking in the previous
6 months, and Maria completed the measure as well, to indicate her views of his drinking. They also were asked to indicate what they thought were the most influential antecedents. Both perceived environmental influences as being most important to Carl’s drinking, citing as the most salient settings bars and his home, afternoons when he was not working, any celebratory occasions, and being around others who were drinking.
The second most important set of drinking cues per- tained to their relationship, with Carl citing arguments, anger, feeling nagged, or having a good time together as antecedents. The third area of concern that both Carl and Maria cited was physiological antecedents, primar- ily restlessness and fatigue.
Carl used daily self-monitoring cards throughout the treatment to record drinks and drinking urges. Review- ing the information he recorded and discussing events associated with drinking or drinking urges made it clear that being with heavy-drinking friends was an impor- tant component of Carl’s drinking. The self-monitoring cards also clarified factors associated with his feelings of “restlessness.” When Carl and Maria were together and the children were being active, if he wanted to leave or go somewhere, then he would get restless and irritable, and want to drink to “take the edge off.” Finally, it was apparent that Carl felt like drinking whenever Maria reminded him of a commitment that he had made (even something simple; e.g., bringing a book to her apart- ment), when she tried to get him to commit to any re- sponsible course of action, or when he felt “trapped.”
We used questionnaires and self-monitoring cards to assess how Maria coped with Carl’s drinking. She re- corded her perceptions of his drinking each day on a Lik- ert scale (None, Light, Moderate, or Heavy) and recorded her daily marital satisfaction as well. Her responses ante- cedent to and consequent to drinking episodes were dis- cussed in the therapy sessions. In addition, both partners completed a modified version of the Coping Question- naire (Orford, Templeton, Velleman, & Copello, 2005).
Data from these assessment sources made it appar- ent that Maria often questioned Carl about his actions, threatened him, or pleaded with him not to drink. She had reacted to his drinking in a number of negative ways—by separating from him, calling the police, and refusing to have sex with him. At the same time, she had made serious efforts to support him and encourage his abstinence by doing positive things with Carl when he did not drink, doing nice things for him, or talking about positive things they could do together if he did not drink.
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Marital Relationship
We assessed the couple’s relationship by administering the ACQ (Margolin et al., 1983) and the DAS (Spanier, 1976), and by viewing a videotape of the couple discuss- ing a problem in their relationship. Maria had a number of major concerns about their relationship. In addition to Carl’s drinking, she was concerned about his appar- ent lack of responsibility, citing his unwillingness to work, to care for the children, or to be independent of his mother. In general, Maria felt that Carl could not be relied upon for concrete or emotional support. A second concern she expressed was their role definitions. She felt that Carl dictated her role to her, and that she allowed him to do so. She often felt angry and resentful as a result. Finally, she cited Carl’s mother as a problem, de- scribing her as an “enabler” who rescued Carl from his problems and made no demands upon him. She stated that when she and Carl first dated, they liked to drink, stay out late, ride motorcycles, and have a good time, but she felt that it was now time to “move forward” with their lives and “get somewhere.”
Carl had fewer marital concerns. He disliked Ma- ria’s “nagging” him or discussing his drinking, stating at one point, “If I had a different wife, I wouldn’t have a drinking problem.” He also disliked her “persistence” in wanting to discuss topics at length and her “attitude change” when he drank.
A videotape of their interactions revealed several communication problems. Carl and Maria interrupted each other frequently and did not listen to each other’s comments. Each made frequent sarcastic and biting comments about the other, usually stating these with a smile and a funny comment. Maria complained about her excessive responsibilities, and Carl criticized her for not fulfilling her responsibilities but refused to ac- knowledge any responsibilities of his own.
Despite these considerable marital problems, they enjoyed each other’s company, shared many activities and pleasures (e.g., fishing, going to parks with the chil- dren), and had a very positive sexual relationship. Maria said of their relationship, “We get along great when I don’t demand anything.”
Behavioral Formulation
Carl’s drinking appeared to have developed in a social context, with virtually all his drinking occurring with- in social groups with similar drinking patterns. The pattern was reinforced by these positive social interac-
tions, both with friends and (early in their relationship) with Maria. He had developed significant tolerance for alcohol, so that he could consume increasingly large amounts, resulting in a pattern of daily drinking with some signs of physical dependence on alcohol. For Carl, alcohol provided a number of positive consequences: He enjoyed the tastes and sensations associated with drinking, the social context of drinking, and the feel- ings of relaxation that drinking engendered. Although he had accumulated a number of significant negative consequences of drinking, none had affected his inter- nal perceptions of himself or of alcohol. From his per- spective, negative consequences were imposed on him by others—the police, job supervisors, and his wife. In addition, Carl had been able to avoid responsibility for his actions in many areas of his life. When he did not work, he was able to live with his mother, who shielded him from the negative consequences of not working by providing shelter and food for him. When Carl’s wife made demands that he experienced as aversive, he avoided or ignored her. To some degree, his problems with alcohol were accentuated by their different devel- opmental stages: Maria was ready to move to a more adult stage of life, with increased responsibilities and long-term goals; Carl, in contrast, wanted to maintain the lifestyle and behavior patterns of his early 20s.
Despite Carl’s externalizing attributions for his prob- lems and his tendency to avoid negative consequences and responsibility, his wife and children were impor- tant to him, and he did not want to lose them from his life. Therefore, he came to treatment to maintain these desired reinforcers, but not necessarily to make the behavior changes his wife saw as necessary for them to have a successful long-term marriage.
As treatment progressed (see below), Carl engaged in a variety of maneuvers to maintain the relationship but avoid behavior change, and his wife, and at times the therapist, reinforced these behaviors. Maria had a lim- ited repertoire of effective ways to obtain positive rein- forcers for herself. She appeared to expect most positive feelings to come from external sources, and nagging and criticizing were the only verbal behaviors she used to try to get what she wanted. She reinforced Carl’s drinking by continuing to have contact with him but engaged in aversive negative verbal behavior at the same time. She placed responsibility for her happiness with Carl, stating that she could not work (something she enjoyed a great deal) until he stopped drinking and was more responsible, and that she could not lose weight until he stopped drinking and she was less upset.
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As a couple, Carl and Maria lacked the verbal skills to discuss these very major problems. Aversive control, avoidance of responsibility, and lack of empathic com- munication characterized their interactions.
Preparing the Client for Change
Carl and Maria were seen together for all phases of the evaluation. In the initial evaluation, both partners were asked to describe their perceptions of Carl’s drinking, their relationship, and how each had attempted to cope with Carl’s drinking. By seeing the couple together, I communicated my view that the drinking was inti- mately connected to their relationship, and that each partner would need to examine his/her own behavior to effect positive changes. At the end of the evaluation, I provided them with feedback about the main difficul- ties that I perceived (as summarized earlier), and ori- ented them to the plan for treatment. In discussing the treatment plan, I covered the following:
“We have asked you to come to treatment as a cou- ple. This is because drinking affects many areas of your life, including your marriage and your family. I know from what you have said, Maria, that you have tried many different ways to cope with Carl’s drink- ing, and that you have been angry and frustrated at times. It is clear that you have tried to help, but it seems, Carl, that you mostly have resented it when Maria has said anything about your drinking. Dur- ing treatment we will look at your drinking, how you have tried to cope with it, and how the two of you are getting along as a couple. Right now, the two of you are separated, and you have a lot of concerns about your relationship. As we go along in the therapy, I will help you improve your communication, and I will ask you to try new ways to spend time together and discuss problems. The therapy will focus on three main topics—your drinking, Carl, how you, Maria, have coped with it, and how to cope in ways that work better for both of you, and for your rela- tionship with each other.”
In addition to this overall orientation, which both Carl and Maria felt captured their goals for the treat- ment, we discussed Carl’s drinking goals in more de- tail and made plans for how to achieve those goals. As indicated earlier, Carl’s preferred drinking goal was moderate drinking. However, Maria felt strongly that she wanted him to abstain, and he had agreed to that
goal prior to coming to treatment. Since he had been drinking daily and showed evidence of tolerance to al- cohol, I was concerned that he would not be able to stop drinking without assistance. I therefore discussed with him the possibility of being detoxified under medical supervision:
“I am concerned, Carl, that it will be difficult for you to stop drinking on your own. You drink every day and have been drinking a lot. On the questionnaires, you indicated that you ‘panic’ if you think that you will not be able to get any alcohol, and you typically drink throughout the day. All of these things suggest to me that you may be ‘hooked’ on alcohol, and that your body will have a strong reaction to going with- out any alcohol at all. The easiest way to get through the first few days without drinking is to check into a hospital detoxification program, and I would like you to consider it.”
Carl had a very negative reaction to the thought of being hospitalized. He was afraid of being “locked up,” and said, “I know that I would go crazy. I can’t stand being confined. After 24 hours, I would just have to leave. It’s not a good idea.” I wanted to engage Carl in treatment, so I thought that pushing Carl to enter a detoxification center would decrease his motivation for treatment and have a negative effect on our therapeutic relationship. I was certain that if I made brief hospi- talization a prerequisite to further treatment, he would leave treatment completely. Therefore, we developed a plan to achieve abstinence. The plan had two major components: (1) Carl was to come to therapy sessions sober, and his BAL would be verified by breath alcohol test reading, and (2) Carl would set goals to reduce his drinking gradually, with a target date for abstinence 6 weeks hence. If he was not able to achieve either goal, then we would reevaluate the need for supervised de- toxification. He was amenable to this agreement, as was Maria.
Process of Treatment
The course of treatment is described sequentially to provide the reader with the clearest picture of the progress and pitfalls of this therapy case. The treat- ment covered several major areas: (1) helping Carl to reduce, then stop his drinking; (2) teaching Carl skills to maintain abstinence; (3) enhancing Carl’s perception of his drinking as problematic; (4) teaching Maria more
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constructive coping strategies; (5) teaching the couple how to engage in positive interactions; and (6) teach- ing the couple mutual problem-solving techniques. In addition, as treatment progressed, we focused on some other areas of individual behavioral change for Maria.
Intake and Sessions 1 and 2
At the initial intake session, Carl had a BAL of greater than 400 mg%. Although he did not show gross signs of intoxication, he was belligerent, and the clinician doing the intake did not feel that he could conduct a reason- able intake interview. He suggested that Carl receive medical attention because his BAL was so high, but Carl refused, and the clinician rescheduled the intake. At the rescheduled appointment, Carl was sober and able to provide information, to give informed consent for the research aspects of the program, and to schedule the baseline data collection session.
At the first treatment session, however, Carl again had an elevated BAL (120 mg%). He reported only having had “a couple of beers” and insisted that he was fine. We briefly discussed Carl’s and Maria’s concerns and goals, but I suggested that we would not be able to have a very productive session with Carl’s BAL so high. (Our general policy is to reschedule a treatment session if the client’s BAL is greater than 50 mg%.) Carl agreed to come to the next session sober and to have no more than four drinks per day. I gave Carl and Maria self-monitoring cards, on which I asked them to record drinks, drinking urges, and relationship satisfaction on a daily basis. Carl was given one card for each day and was asked to record each drink he actually consumed, to note urges to drink not followed by drinking, and to note on the back of the card the situations in which he drank or had urges to drink (see Figure 14.3).
Maria received one card to use for the entire week. I asked her to write on the card a daily estimate of Carl’s drinking (None, Light, Moderate, or Heavy) and also to record her estimate of the strength of his urges to drink that day. She also made a daily rating of her relationship satisfaction (see Figure 14.4).
When Carl and Maria came to the second session, his BAL was again elevated, at 60 mg%. He reported drinking about four beers during the day. We contin- ued the discussion of detoxification, and Carl said that he felt he was addicted to alcohol. He said that he would consider detoxification, and we scheduled a phone con- versation to discuss detoxification further. After we
spoke twice by phone, Carl again decided that he did not want to be hospitalized. He did not use the self- monitoring cards during these first 2 weeks, although Maria completed his cards for him while they drove to the treatment session. I did not think that I had a full picture of Carl’s drinking, but it was clear that he was continuing to drink daily.
Sessions 3–5
Carl came to the third session with a BAL of 0 mg%. He again reiterated his desire to stop drinking without hospitalization, and we worked out a plan for him to reduce his number of drinks gradually to zero over a 6-week period. In addition to setting drinking goals, we began to discuss a behavioral-analytic view of drinking. To introduce the couple to a behavioral way of thinking about their drinking, I said:
“Together we are going to observe carefully and analyze all the factors that seem to be part of your drinking. I think that we can look at your drinking and figure out what kinds of situations lead you to feel like drinking. If we can figure this out, then we can work together to come up with alternatives for these situations. We will be using these sheets, called ‘triggers’ sheets, to analyze your drinking. Let’s go through one of these together.”
I then asked Carl to identify a recent drinking situa- tion. He indicated that he liked to drink when he went fishing. As we spoke, I completed the boxes on the “trig- gers” sheet, illustrated in Figure 14.7. Carl had a fairly unpsychological view of his drinking. He described his thoughts as “I want to get some beer” and his feelings as “happy.” He viewed drinking when fishing as hav- ing positive consequences—“I have a blast.” He felt that the only negative consequences came from Maria, who would be angry when he came home.
Carl and Maria grasped the behavioral analysis quickly and found it a comfortable way to conceptualize his drinking. As homework, I then asked both of them to complete the DPQ and bring it to the next treatment session. I gave them additional self-monitoring cards to use for the week.
Carl also came to the fourth session sober but re- ported heavy drinking over the weekend. The graph of his weekly alcohol consumption during treatment is reproduced in Figure 14.8. Carl’s and Maria’s average
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weekly marital satisfaction ratings are reproduced in Figure 14.9. Carl expressed no concern about his con- tinued heavy drinking, and showed no evidence that he was trying to cut down.
“I am glad that you have come to the last two sessions sober—I know that’s not easy for you, and it does show that you want treatment to succeed. However, I am concerned that you have not cut down at all between sessions. If anything, your drinking seems a bit heavier. It’s not clear to me whether you don’t really want to cut down, or whether you just don’t know how.”
Carl said that it was hard to cut down, but that he was committed to stopping drinking because he wanted to have Maria and the boys back again. We then discussed a number of potential strategies to help him avoid drinking, such as sleeping (his suggestion) or having alternative beverages available in the house (my suggestion), or going back to work (Maria’s sug-
gestion). He was reluctant to commit to any plans, and Maria challenged whether he was really willing to stop drinking.
To respond to Carl’s ambivalence, I suggested that we examine consequences of his drinking other than Maria’s disapproval and the couple’s arguments about his drinking. Carl was unable to think of any other ad- verse consequences. I asked him about his legal prob- lems from the DWIs and the arrest for breaking and entering, but Carl said that he did not believe alcohol had anything to do with the latter charge, and that DWI laws were “ridiculous.” He also indicated that he was still driving, even though he did not have a driver’s license, and that he would continue to drive even if his license was revoked for 10 years (a real possibility given that he had had three DWIs in less than 10 years, with two in the same month). Carl expressed a similar lack of concern about any other aspects of his drinking but again said that he was willing to stop because of his commitment to the marriage and his children. I made a list of the negative consequences that he or Maria had
FIGURE 14.7. Triggers sheet.
Negative consequencesTrigger
Thoughts & Feelings Behavior
Positive consequences
Triggers sheet
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reported at various times and asked him to review the list at least twice daily, and to think about which of these consequences were of concern to him. Carl re- ported looking at the list “once or twice” between ses- sions, but he was relatively indifferent to the content.
Despite my concern about Carl’s relative lack of motivation to change, I decided to proceed with a be- havioral analysis of his drinking. I thought that if we
could identify a discrete set of antecedents to drinking, and if Carl could successfully avoid drinking in some of these situations some of the time, his motivation to change might increase as his self-efficacy increased. We discussed two other drinking situations in the session and, as homework, I had him complete two behavioral chains at home. A complete summary of the behavioral analysis of his drinking is provided in Figure 14.10.
0
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ce s
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Week in Treatment
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at is
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a
a
FIGURE 14.8. Carl’s weekly alcohol consumption during treatment. aNo self-monitoring during this time.
FIGURE 14.9. Average weekly marital satisfaction ratings for Carl and Maria. aNo self-monitoring during this time.
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FIGURE 14.10. Sample behavioral analysis of Carl’s drinking.
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Carl came to the next treatment session with a BAL of 118 mg% and reported drinking heavily for the last several days prior to the treatment session. After a lengthy discussion, he agreed to go for detoxification. Carl said he was afraid of the hospitalization and con- cerned that he would not be able to be abstinent after detoxification. I tried to emphasize that detoxification was only the first step in treatment, and that we would be working together to help him learn ways of coping without drinking.
He also expressed his belief that life would not be fun if he did not drink. Maria oscillated between en- couraging Carl to get detoxified and saying to me that he was only agreeing to the detoxification to get out of my office. Because he was so concerned, I had him call the detoxification center from my office to ask any questions he had. He did so, and scheduled himself for admission the next day.
Sessions 6–8
Carl did not admit himself for detoxification and stated again that he could not face being “locked up.” He was still drinking daily, making minimal efforts to decrease his drinking. I suggested outpatient detoxification and gave him the phone number of a physician colleague who supervised outpatient detoxification, but I had little expectation that he would follow through with that referral either. Carl continued to express willing- ness to be in treatment and to change his drinking, and I decided to continue despite my doubts about whether he had sufficient incentives to change. We completed the behavioral analysis of his drinking during Session 6 and identified several of Maria’s actions that were antecedents to his drinking, including reminding him about responsibilities, her slow pace when they had an appointment and there was a lot to do to get themselves and their children ready to go out, and her comments about his drinking.
At one point during Session 6, Carl said, “You know, Maria has a real temper. You should ask her what she did to me at the beach.” Maria responded immediately by saying, “Show Barbara your arms.” Carl rolled up his sleeves, revealing a number of scratches and bruises covering his lower forearms. Maria then explained that she had been intensely frustrated with Carl because of his drinking, and often grabbed him, scratched him, or tried to hit him in the chest or abdomen when she was angry. The behavior had started in the last 4 months, and she found it very upsetting. She also indicated her
concern that she might become abusive toward her children and admitted that she sometimes used physi- cal punishment when she was angry at them. Although Maria’s anger and frustration were not surprising and are common reactions of partners of people with AUD, the physical aggression, particularly in the absence of any physical abuse from Carl, was less usual. We dis- cussed her behavior toward the children in great detail, because I was concerned about the possibility of child abuse. She reported, and Carl confirmed, that she had never bruised, cut, or injured the children in any way, and that they had never had to take either of the chil- dren to a physician or emergency room because of her discipline. Both reported the belief that physical pun- ishment, in the form of “swats on the bum” or physi- cally removing the child from a dangerous situation, was an appropriate form of discipline. However, Maria felt that she did not always discipline the children ra- tionally, and that she would occasionally hit them on the arm, or pull too hard when removing them from a situation. From the couple’s reports, I did not believe that Maria was abusing the children, but I thought it was important to address her concerns in the therapy. I instructed Maria to use the self-monitoring cards to write down any times in the next 2 weeks when she felt that she was reacting too strongly to the children, or when she was physically aggressive toward Carl.
Over the next two sessions, Carl began to decrease his drinking substantially and was abstinent for each treatment session. Carl and Maria had begun to spend more time together, and they reported that their time together was more positive. They had a family barbecue and went fishing at the beach with the children.
Maria had been faithful in recording her reactions to her children, noting two times each week when she either slapped one of the children on the arm or felt that she grabbed one of them too hard. We discussed the antecedents to these incidents and identified several salient aspects: Maria was tired, the child was tired, and she attempted to tell him to do something when she could not enforce it (she was across the room or had her hands full). In each situation, she repeated her verbal instructions to the boy several times to no avail, then felt angry and stomped across the room and grabbed him. We discussed alternative strategies, and I empha- sized the importance of being able to follow through on a verbal instruction immediately rather than allow- ing herself to get frustrated. She quickly picked up on my suggestions and also expressed relief at being able to discuss her concerns. After the 2-week period, Maria
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reported no further instances of excessive physical reac- tion to the boys, and reported feeling more in control of herself as a parent again. Carl’s observations confirmed her reports.
At the same time that we discussed Maria’s problems with disciplining the children, we began to implement some self-management planning techniques for Carl. I suggested to Carl that it would be easier not to drink if he had ideas about how to handle certain triggers without alcohol. He could avoid situations or rearrange them to minimize the importance of alcohol in the situ- ation. We used a self-management planning sheet to as- sist in the process (see Figure 14.11).
We selected fishing as a topic for self-management planning, because it was a high frequency, high-drink- ing activity for him. Carl had a number of ideas about how to fish without alcohol. These included taking his older son, taking his wife, or inviting an older friend, who was an excellent fisherman and did not drink at all. In addition, Carl thought that if he bought soft drinks the night before he went fishing and filled his cooler with the sodas before he left the house, he would be less tempted to stop by the liquor store at the end of his block. For homework, I asked Carl to implement this plan and to develop another self-management plan for getting together with a friend without drinking.
FIGURE 14.11. Self-management planning sheet.
Trigger Plan +/– Consequences Difficulty (1–10)
1.
2.
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Carl implemented the fishing plan successfully and also planned to ask his friend Scott to play tennis, then go to a fast-food restaurant to eat, because alcohol would not be available there. Although Carl saw no obstacles to implementing this latter plan, he never used it, and could provide no reasons for not following it up. He did, however, tell Scott that he was trying not to drink, and his friend reacted positively and supportively.
The other major topic of these several sessions was reinforcement for changes in Carl’s drinking. Because Carl was so ambivalent about changing his drinking, I thought it particularly important that he experience some positive consequences for decreased drinking and for abstinence. I also wanted to help Maria learn some positive rather than coercive ways to interact with Carl about his drinking. In introducing this topic, I sug- gested that they both should think about ways to make abstinence and reduced drinking more positive. I first suggested that Maria might give Carl positive feedback when he was not drinking, but he reacted quite nega- tively to this suggestion, saying, “I would just think it was another one of her sneaky ways to try to pres- sure me to stop. I don’t want her to say anything.” In continuing with this discussion, I asked whether there was anything that Maria could do that would make ab- stinence worthwhile to him, and Carl suggested that she could refrain from talking about alcohol and spend time with him without being “picky.” They decided on several mutually enjoyable activities to share when he was not drinking, such as having a shrimp dinner, and having Maria tell Carl when she was enjoying their time together. They were able to implement these plans successfully, and although Carl drank while they were together, the amount was substantially less on these oc- casions.
Sessions 9–11
By this point in the treatment, Carl had reduced his drinking to approximately three to six drinks per day, but he had not abstained from drinking at all. His reports of urges to drink had also begun to decrease. Maria reported high relationship satisfaction almost every day (a rating of 7 on a scale of 1–7), and they were spending most of their free time either at her apartment or at the home of Carl’s mother. However, in the ther- apy sessions, they began to argue more frequently, with their conflict revolving around two major topics—Ma- ria’s desire to move to North Carolina and her feeling that Carl was not emotionally supportive of her. I began
to implement some structured communication training with them, teaching them skills that included allowing the other to finish before speaking, reflective listening, and making specific positive requests. These sessions were supplemented with handouts about communica- tion. After reading the first handout, which covered basic topics, such as the value of being polite and re- spectful of one’s partner, and some of the sources of bad communication, they came into the session absolutely surprised at the notion that calling each other names (e.g., “idiot,” “asshole,” or “shithead”) could have any negative impact on their relationship. They had begun to use positive rather than negative communication at home and were pleased with the impact it had on their conversations.
Although we were making progress in the treatment, I was concerned that Carl was still drinking every day, and I relayed this concern to him. Carl stated that he believed he could now stop, and he agreed to be absti- nent for 2 days in the following week. The first week that he agreed to this contract, Carl did not want to discuss strategies for abstinence, and he was unsuccess- ful. The second week we discussed very specific plans for how he would abstain. He planned to be with Maria and the children for part of each day, and he decided not to buy more beer to have in his mother’s house those days. In addition, he would stock up on soft drinks and plan to go to bed early. I also suggested that he might use Maria as a support in his attempts to abstain. I often encourage a client to find someone with whom to discuss urges, and the partner can be a good source of support. He again was resistant to involving Maria, saying, “I wouldn’t tell her that I wanted to drink—all I’d get is a lecture.” I suggested that he usually disliked her comments because they were unsolicited, but in this situation, he would be in charge, because he would be the person concerned about his drinking. He responded positively to this reframing. I then asked him whether there was anything Maria could say that would be help- ful to him, and he suggested that she tell him it was his choice. Maria indicated that it would be difficult not to lecture, but she agreed to a role play. They imagined that they were driving to the beach, and Carl said, “I want to stop to pick up a six-pack on the way down.” Maria answered, “It’s your choice if you want to, but we could stop to get some sodas instead, if you want.” Carl was amazed at how much he liked her response, and although Maria acknowledged that it was very dif- ficult to be that neutral, she liked feeling that it was not her responsibility to prevent him from drinking.
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They agreed to try out such a discussion once during the coming week.
Carl was not successful in maintaining any abstinent days, although he did implement most of the rest of the plans and drank only one beer on each of the 2 target days. However, he did not tell Maria about any of his urges to drink. He again expressed little concern about not meeting his goals. During the session, Carl and Maria announced that they were going to North Caro- lina for a 2-week trip. Carl knew a contractor who had offered him work there, and Maria was intrigued with the possibility of moving to an area with a lower cost of living and more rural environment in which to raise the children. Maria stated that she would not move while Carl was still drinking, but they both decided that a trip to explore the possibilities was appealing.
Sessions 12–15
Carl and Maria returned from their 2-week trip very enthusiastic about North Carolina. They believed that work was available, the cost of living was clearly lower, and both liked the area they had visited. Maria said again that she would not move unless Carl had been abstinent for a considerable length of time, because she did not want to leave her family if she could not depend on Carl. He again said that he would stop drinking. I had taken advantage of the break in the therapy to review all of my progress notes and to think about the couple with a bit more detachment. It was clear to me that although Carl had agreed to abstinence because of Maria’s pressure, he wanted instead to reduce his drinking. However, he had dealt with this conflict by providing verbal reassurances that his behavior would change, without accompanying behavior changes. He had implemented only a few of the behavioral plans that we had developed, and I did not think that the lack of implementation reflected a skills deficit. I had decided to point out Carl’s behavioral inconsistencies at this treatment session.
To initiate this discussion, I told Carl and Maria that I wanted to discuss their progress so far. I emphasized the positive changes that they had made so far: Carl had decreased his drinking substantially; he had developed some skills to assist him in drinking less; their com- munication had begun to improve; they were spend- ing time together that was mutually enjoyable; and they had begun to consider possible long-term plans together. I noted, however, that Carl had made a series of promises about his drinking on which he had not
followed through. I read them several passages from my progress notes, noting Carl’s initial target date for absti- nence, and his broken agreements about detoxification and abstinent days. I suggested two alternative explana- tions to them: Either Carl did not want to stop drinking completely but felt that he had to agree to abstinence to keep Maria happy or he really could not stop drinking and needed further assistance to do so. By framing my explanations this way, I tried to avoid labeling Carl as dishonest or unmotivated to change. I also suggested that Maria had helped Carl to keep drinking by report- ing high marital satisfaction even though he was still drinking, and that perhaps reduced drinking really was acceptable to her as well. Both reacted quite strongly to my feedback. Carl said, “At first I didn’t want to stop, but now it doesn’t seem that bad. I’m not drinking enough now for it to mean anything, so I’ll just quit. It’s no big deal, and I don’t want to disappoint you.” Maria said, “I always feel like Carl is just saying whatever he has to say to get me or you off his back. But I have been so much happier since he cut down that I kind of lost sight of that fact that he’s still drinking. I am afraid to move anywhere with him while he’s still drinking at all. It was so bad before. I don’t want to go back to that.”
After this conversation, Carl denied that he preferred moderate drinking and announced that he was going to “quit for good.” Over the next 2 weeks, Carl had one drinking day each week—one beer the first week and two beers the second week. Although we discussed a variety of behavioral coping strategies, such as devel- oping behavioral alternatives for drinking situations, rehearsing strategies for refusing drinks, and using vari- ous strategies for coping with urges, Carl deemphasized their importance. Instead, he focused on cognitive cop- ing strategies: When he had urges to drink, he would think about reasons not to drink (“It’s not worth it— Maria and the kids are more important”). Or he would use delay tactics (“I won’t have anything right now—if I still feel like drinking at 5:00 [or some other, later time during the day], then I’ll have a beer”). Or he would de- emphasize the positive aspects of alcohol (“One or two beers won’t do anything for me, and I don’t want to get blasted”).
Carl and Maria also began to discuss their long-term goals. I asked them to write down how they would like their lives to be in 5 years. Carl wrote down the follow- ing4:
Comfortable place to live for Maria and this kids. Good schools, backyard. Get finances in order; save money,
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consolidate bills, improve credit. Maintain stable income ie. steady construction work or other. Obtain a loving re- lationship with Maria. Self improvement: manage money better, listen to Maria more objectivly, secure steadier employment. Maria: better self discipline, controll tem- per, improve self confidence, weight loss, less pestimistic in dialy matters. ie. scared of bugs, traffic, mishaps, etc.
Maria wrote down remarkably similar 5-year goals:
Five years from now—37 years old; Jonathan 8 years, Marc 7 years. We are living in North Carolina in a rented house. I’m working, Carls working the boys are in school. We have two cars. Carl is 5 yrs sober. I’m 4 years thin. We are two yrs away from getting credit back from filing bankruptcy. Some nights we will be together as a family to relax or to go to a baseball or soccer game of Jonathan’s or Marc’s. Other nights I will be out to socialize or run errands. Other nights Carl will do the same. We will be somewhat financialy comfortable. Three things I want out of life:
Maria: Carl: calmness, thinness, to feel secure, a car, money, independence, control over my life
motivation, sobriety, responsibility, contentedness
Because Carl and Maria’s goals were so similar, I asked them if I could read them aloud. Both were ame- nable to this suggestion, and I did so. They reacted quite positively and felt encouraged; because their long- term goals were so similar, they could work together to achieve these goals. I began to teach them skills related to assertiveness and problem solving, discussing ways to implement these skills both in their relationship and in other interpersonal situations.
Sessions 16–18
Carl abstained from drinking from Session 15 to the end of the treatment. He reported a few urges to drink, but these soon decreased. However, he discussed very strong reactions to not drinking. He felt sad, saying that he missed drinking and felt that he had lost something important to him. He also said that it was frustrating, because he always had been able to drink when he felt bad, but now he could not do so. I tried to reframe his feelings for him, noting that his ability to recognize that he missed alcohol was an important step toward being able to reorganize his life without it, and that his reac- tion suggested that he was serious about his intentions
not to drink. Carl seemed to find the reframing helpful, but he continued to find abstinence uncomfortable.
As Carl remained abstinent, his relationship satisfac- tion ratings decreased. Previously, Carl had reported fairly high relationship satisfaction, but as he stopped drinking, he became increasingly unhappy. When I asked him about his ratings, he said that he felt they were “going nowhere” in terms of reconciling. We had begun assertiveness and problem-solving training, and I suggested that Carl could use these skills to express his feelings to Maria more directly. They had a positive dis- cussion during the session about his feelings and about wanting to reconcile, and her concerns about how dif- ficult that would be, with each using some of the posi- tive skills on which we had worked. Both agreed that they now wanted to live together again, but it would be difficult to develop a plan to do so. We used struc- tured problem-solving techniques over two treatment sessions to develop a plan. The major impediment to reconciliation was financial. Maria was receiving wel- fare, but if either she or Carl began to work, they would receive less public assistance. However, to be able to live together, they would have to save sufficient money for a security deposit and first month’s rent. They finally decided that Maria would begin to work a few hours a week as a hairdresser, working “under the table,” and that Carl would care for the children while she worked. If that worked well, then Carl would begin to look for work again; once both were working, they would move in with his mother for a limited period of time to save money for the deposits and rent, then either obtain an apartment together in New Jersey or find a trailer to rent in North Carolina and move. They also used prob- lem-solving techniques to develop a plan to deal with their other debts.
Termination
Because Carl and Maria were part of a clinical research study, we had to terminate treatment after 18 sessions (including the sessions when he was intoxicated). They had made significant progress during treatment: Carl had been abstinent for more than a month; Maria had learned more effective ways to discipline the children and no longer reported concerns about being overly punitive to them; the couple’s relationship was signifi- cantly improved; and they had a constructive plan for reconciliation. I was concerned that Carl was still un- comfortable with abstinence, and I thought that he had acquired only a few effective coping strategies to deal
Alcohol Use Disorders 605
with triggers for drinking. We had not worked directly on Carl’s style of avoiding responsibility except by fol- lowing through on his commitment to abstinence and long-term goal setting. Whether Carl would implement his part of these agreements was relatively untested. The couple was fairly comfortable with termination but asked about possible follow-up treatment, inquir- ing specifically about AA or other support groups that focused on couples or on behavioral approaches to change. I referred them to SMART Recovery, and to a couples’ AA group. The constraints of the clinical research protocol precluded any longer-term treatment with me, even though I thought continued treatment would be beneficial.
Comment
Carl and Maria were a fairly typical couple. Carl’s am- bivalence about change, his entry into treatment solely because of an external agent, and his resistance to many behavioral interventions are not uncommon. I believe that he began to engage in treatment when he stopped feeling that he was the sole focus of the treatment, after Maria began to discuss her aggressive behavior and feelings. The second critical point in treatment was ad- dressing his continued drinking. I was willing to allow them to renegotiate for a goal of moderate drinking, but I did not think it therapeutic for Carl to feel that he could verbally agree to abstinence but then avoid the agreement. Addressing Carl’s behavior directly forced him either to be assertive and renegotiate treatment goals or to follow through on his commitment.
The role of behavioral skills training in facilitat- ing abstinence was less important with Carl than with some clients. He tried various skills introduced during the treatment but relied primarily on cognitive cop- ing strategies. The role of reinforcement was probably more important in understanding his changed drinking behavior. Carl’s marital relationship was important to him at the beginning of treatment, and focusing in the therapy on ways to improve that relationship increased its reinforcement value to him. Maria’s consistency in saying that they could reconcile only if he were absti- nent, in discussing long-term goals for the relationship, and in seeing the possible positive life they could live in North Carolina all contributed.
Finally, my relationship with the couple probably contributed to the positive changes they made. I found them a likable, appealing couple despite their challeng- es. At times, I would tease or cajole Carl into compli-
ance, and he commented at the end of the treatment, “At first I didn’t know if I liked you or not, but then I decided you were kind of cute, and then I realized that you weren’t going to let up on me, so I decided that I’d give it a try.” I tried to reinforce Maria’s ability to take care of herself, and I suspect that she saw me as a female role model in some ways. She often asked me personal questions (whether I was married, how old my son was), and gave me a desk calendar as a thank-you gift at ter- mination. Our research suggests that our more experi- enced therapists are more successful at keeping clients in treatment (Epstein, McCrady, Miller, & Steinberg, 1994; Raytek, McCrady, Epstein, & Hirsch, 1999), and I suspect that being able to deal with these complex re- lationships is one skill that our more experienced thera- pists have acquired more fully.
Typical Problems
The problems presented in this case are not atypical— coming to treatment sessions intoxicated, continued drinking during treatment, ambivalence about change, noncompliance with assignments, and discovering new and major problems as the therapy progresses. Lying and failing to come to scheduled treatment sessions are other obstacles that some clients with drinking problems present. By working with Carl and Maria to- gether, I was able to minimize these particular difficul- ties, because Maria was highly motivated for treatment and very responsible about keeping scheduled appoint- ments. Also, by having them both record Carl’s drink- ing and drinking urges, I had a clearer picture of his drinking and was able to maintain a clear idea of our progress (or lack thereof).
CLINICAL PREDICTORS OF SUCCESS OR FAILURE
A number of factors predict the success or failure of therapy. However, before we address these factors, it is important to discuss definitions of success. In any treat- ment, a minority of clients maintain long-term, unin- terrupted successful change (abstinence or nonproblem drinking). The proportion varies with the demographic characteristics of the population, and persons who have a stable relationship and stable employment, a stable residence, and no comorbid psychopathology have the best treatment outcomes. In addition, a person’s post- treatment environment plays an important role in deter- mining long-term outcomes. Observations of the long-
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term instability of drinking outcomes have led many to consider AUD as a chronic, relapsing disorder, and to reconceptualize “success” as a process rather than a static outcome; that is, the client who learns not only effective skills to avoid drinking or heavy drinking but also ways to cope with relapses by minimizing their length and severity should be considered “successful” as well. In treatment outcome studies, investigators look at percentage of abstinent or moderate drinking days and length of periods of abstinence compared to periods of heavy drinking as ways to assess relative rather than ab- solute “success.” From the individual clinician’s perspec- tive, certain client characteristics and behaviors bode well for the course of treatment. The client who has im- portant incentives to change (either internal or external) and some recognition of a relationship between his/her drinking and life problems is easier to treat. Complying with early homework assignments, coming to sessions sober, and being honest about behavior outside of the treatment are also positive indicators. However, clini- cian behavior is another important predictor of success. Various studies have pointed to different aspects of clini- cian behavior—empathy, matching clinician therapeu- tic behaviors to the client’s ambivalence versus readiness to change, specific goal setting and treatment planning, developing drinking goals with the client rather than imposing goals, and providing the client with options for treatment—as all being associated with better com- pliance with treatment.
CONCLUSION
Providing treatment to persons with drinking problems is a complex and continuously fascinating process. The clinician is faced with decisions about matching each client to the appropriate level of care, the setting for treatment, and treatment modalities and techniques. Diagnostic skills to identify concomitant medical, psy- chological, psychiatric, and cognitive problems are chal- lenged by these clients. Therapy requires knowledge of a range of treatment techniques, the ability to be able to form a positive therapeutic relationship with sometimes frustrating and difficult clients, and the ability to “think on your feet.” Recognition of diversity among individu- als with AUD demands a personalized approach to each case, based on a multivariate assessment; the therapist treats the whole person, not the disorder.
From the briefest, one-session treatments to motivate heavy drinkers to reduce their drinking to the complex
and longer treatment provided to individuals with severe AUD, treatment is never dull or routine. The clinician has a large body of empirical literature to guide the se- lection of treatments and a significant clinical literature as well to illustrate clinical techniques and problems. And although many persons with drinking problems change successfully on their own or with minimal as- sistance, treatment also can provide an effective means for persons to change a major life problem.
So this chapter concludes as it began—as a “sales pitch” for clinicians to be knowledgeable about and re- ceptive to providing thoughtful, informed treatment to persons with drinking problems.
NOTES
1. A standard drink is equal to one 12-ounce domestic beer with about 5% alcohol, one 5-ounce glass of wine, or a 1.5- ounce shot of 86-proof liquor. India pale ale (IPA) and for- eign beers have more alcohol in them. It is important for the clinician to be educated and to educate clients on calcula- tion of standard drinks for alcoholic beverages discussed.
2. All dialogue in this chapter is paraphrasing of actual thera- pist or client comments.
3. Although we generally discourage the use of the terms alco- holic or alcoholism as excessively labeling, at times it is help- ful to adopt a client’s own language as a way to establish an initial therapeutic bond. Within the Minnesota model, the term is used to facilitate an acceptance of an identity in which the AUD is central.
4. These verbatim transcripts include the clients’ spelling of all words.
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One of the great and ongoing tragedies of the last decade has been the opioid crisis in North America. This chapter describes in extremely useful detail the latest approach to treating opioid abuse by one of the most prominent groups in the world working on substance abuse, headed up by Stephen T. Higgins. This intervention, based on a successful clinical trial recently published in the New England Journal of Medicine, focuses on the importance of starting treatment immediately, as soon as a case presents, with a streamlined approach that allows clinicians to reduce wait-list time and reach many more people. Data show that mortality drops to the low level of 0.42 per 100 person-years if patients are afforded immediate entry into treatment versus 5.0 per 100 person-years if patients are placed on a wait list for certain amounts of time. In this chapter, we follow the case of “Joe,” an actual patient in a rural area struggling with this addiction. Using the latest technological innovations in behavioral treatment and describing an integration of psychological and pharmacological treatment for opioids, which is the recommended standard of care, this case illustrates very nicely the most current, up to date, and largely successful approach to these disorders. Even clinicians or students not working directly with addictive behaviors will benefit from being familiar with this new generation of successful approaches to drug use. —D. H. B.
substance use disorders represent a highly prevalent and costly public health problem in the United States
and virtually all other industrialized countries. To get a sense of the scope of the U.S. problem, an estimated 139.8 million persons 12 years and older (51.1%) report current alcohol use (past 30 days), 58.8 million (21.5%) report current tobacco use, and 31.9 million (11.7%) report current use of illicit drugs (Substance Abuse and Mental Health Services Administration [SAMHSA], 2019). Among those who report current illicit drug use, 2.9 million report prescription pain reliever misuse and 354,000 report heroin use in the past 30 days. Of course, not all current users experience adverse effects, but a sizable proportion incur substantial problems. An estimated 20.3 million (7.4%) of Americans 12 years and older met formal diagnostic criteria for a substance
use disorder within the past year, and 3.7 million (1.4%) report being treated for a substance use disor- der within the past year (SAMHSA, 2019). The annual costs to the U.S economy associated with these prob- lems are estimated to exceed $740 billion (National In- stitute on Drug Abuse [NIDA], 2020). The U.S. opioid epidemic has had a sufficiently extraordinary impact to be declared a national emergency, with overdose deaths (~350,000 between 1999 and 2016) contributing to a reduction in life expectancy (Walsh & Long, 2019). As might be expected, the epidemic has also had a trans- formative impact on U.S. treatment services for sub- stance use disorders, which is reflected in this chapter.
Clearly there is a tremendous need for effective treatments for substance use disorders. This chapter provides an overview of evidence-based psychosocial
C H A P T E R 15
substance Use Disorders
Stephen T. Higgins Sarah H. Heil Kelly R. Peck
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treatments for illicit substance use disorders but devotes considerable space to integrated psychosocial and medi- cation treatment for opioid use disorder, what is now the widely recognized standard of care for that prob- lem. Treatments for alcohol use disorders are covered by McCrady and Epstein (Chapter 14, this volume) and there are several excellent reviews on treatments for to- bacco use disorders (e.g., Fiore et al., 2008; Prochaska & Benowitz, 2019). Because the focus is on evidence- based interventions, our overview of psychosocial inter- ventions is largely devoted to behavioral and cognitive- behavioral therapies. Last, NIDA (2018) has published 13 principles of effective treatment for illicit substance use disorders based on more than 45 years of research (Table 15.1) and, when applicable, we underscore those principles throughout the chapter.
DEFINING THE CLINICAL DISORDER
Before proceeding to discussions about treatment, we briefly discuss criteria for diagnosing substance use dis- orders. We have used the fifth edition of the Diagnos- tic and Statistical Manual of Mental Disorders (DSM-5; American Psychiatric Association, 2013) in our research discussed below. This approach includes 11 criteria that examine whether the client has experienced a range of different problems from substance use, drug tolerance/ withdrawal, and expended considerable time and re- sources toward substance use. The presence of two to three symptoms is indicative of a mild substance use disorder; four to five, moderate; and six or more, severe. All of our research discussed below involves individuals who fall along the more severe end of this spectrum.
Evidence supports that, on average, more severe sub- stance use disorders are associated with poorer treat- ment outcome. Severity is influenced by frequency of use, amount of substance used, route of administration, and sociodemographics (e.g., educational attainment), among other factors. There seems little doubt that these factors will be positively correlated with the number of untoward signs and symptoms exhibited following a period of repeated substance use, and to that extent merit careful attention in a diagnostic assessment. For these and other reasons, we have found the spectrum approach of DSM-5 helpful in assessing the severity of substance use disorders.
ASSESSMENT
A comprehensive assessment is an essential first step in effective clinical management of substance use dis- orders. This section outlines the assessment practices we use in our outpatient clinic for individuals seek- ing treatment for opioid use disorder. The assessment framework is relatively generic and can be readily ap- plied to other types of substance use disorders by sub- stituting the opioid-specific information with pertinent information on whatever other type of substance use disorder is the presenting problem.
During the initial clinic contact, clinic staff members establish that the caller reports problems related to drug use, is age 18 years or older, and resides within driving distance of the clinic. During the initial clinic contact, staff members informally assesses factors that could po- tentially complicate treatment (e.g., pregnancy, pending legal issues, concurrent use of other substances). This in-
TABLE 15.1. Principles of Effective Treatment
1. Addiction is a complex but treatable disease that affects brain function and behavior.
2. No single treatment is appropriate for everyone. 3. Treatment needs to be readily available. 4. Effective treatment attends to multiple needs of the
individual, not just his/her drug abuse. 5. Remaining in treatment for an adequate period of time is
critical. 6. Behavioral therapies—including individual, family, or
group counseling—are the most commonly used forms of drug abuse treatment.
7. Medications are an important element of treatment for many patients, especially when combined with counseling and other behavioral therapies.
8. An individual’s treatment and services plan must be assessed continually and modified as necessary to ensure that it meets his/her changing needs.
9. Many drug-addicted individuals also have other mental disorders.
10. Medically assisted detoxification is only the first state of addiction treatment and by itself does little to change long-term drug abuse.
11. Treatment does not need to be voluntary to be effective. 12. Drug use during treatment must be monitored
continuously, as lapses during treatment do occur. 13. Treatment programs should test patients for the presence
of HIV/AIDS, hepatitis B and C, tuberculosis, and other infectious diseases, as well as provide targeted risk- reduction counseling, linking patients to treatment if necessary.
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formal assessment is typically conducted by phone and is important for identifying clients who may initially require more intensive treatment or a referral to another clinic. Although the buprenorphine maintenance pro- tocol that we use is less intensive than many treatment protocols for opioid use disorder, it does require daily clinic visits during the first week of treatment and an av- erage of one clinic visit per week during each subsequent week. Accordingly, persons living outside the county in which the clinic is located may require assistance with transportation (e.g., bus passes or transportation vouch- ers) or referral to treatment providers closer to home. The important matter is to have established the geo- graphical range that is practical for the treatment being offered. Those who do not satisfy these basic inclusion criteria are referred to an appropriate alternative clinic, while those who do meet criteria receive an appointment for a more comprehensive intake assessment.
Every effort is made to schedule the intake assess- ment as soon as is practicable (Principle 3, Table 15.1). Scheduling the interview within 24 hours of clinic con- tact significantly reduces attrition between the initial clinic contact and assessment interview, which is a sub- stantial problem among those with substance use dis- orders (Hoffman, Ford, Tillotson, Choi, & McCarty, 2011). When 24 hours is not possible, our secondary goal is to schedule the assessment within 48–72 hours.
Clients are informed that the intake interview will take about 3–4 hours. This initial session is one of the most important. Clinic staff members should be aware of the client’s potential uneasiness and try to make the person comfortable. Many patients may be reluctant to report behavior that is illegal or stigmatized. Dur- ing the intake assessment, clinic staff members must quickly attempt to establish an empathic and nonjudg- mental relationship with each new client. Being cour- teous, complimenting clients on taking this important first step toward change, anticipating that some clients might be physically ill or uncomfortable related to re- cent drug use or withdrawal and being respectful of that, being flexible with tardiness, and so forth, can help. The willingness of clinic staff members to accom- modate the need for brief breaks, food or drink, or a brief phone call can help as well. Throughout all inter- actions, we seek to be empathic and to convey a very upbeat “You can do it” message.
During the intake assessment, we collect detailed information on the presenting substance use disorder, while also assessing other drug use, psychiatric func- tioning, pain and chronic medical conditions, employ- ment/vocational status, recreational interests, current
social supports, family and social problems, and legal issues (Principle 4, Table 15.1). We discuss the instru- ments that we use to obtain such information in the order in which they are typically administered. Modi- fications can be readily made to our list, depending on the population being treated. We offer it only to provide an example of what we have found to be an effective assessment package, along with associated clinical ra- tionales.
Biochemical Monitoring
Biochemical verification via urine toxicology is the most objective method for evaluating recent drug use. Accordingly, urine specimens are collected at the intake appointment under observation of same-sex staff and immediately analyzed for opioids (e.g., buprenorphine, methadone, heroin) and other drugs (e.g., cocaine, am- phetamines, benzodiazepines, cannabinoids). Comor- bid alcohol use disorders are common; thus, we also obtain a breath sample to assess recent alcohol use.
Self‑Administered Questionnaires
We use several self-administered questionnaires that can be completed by the client upon arriving at the clinic for an initial intake assessment. The staff mem- bers who conduct the intake greet the client, introduce themselves, bring the client into a private office, and briefly but carefully explain what to expect during the intake process. It is essential to ask about clients’ reading ability prior to having them complete self-administered questionnaires. If there is doubt about reading capabil- ity, we discreetly ask clients to read several questions aloud to get an indication of whether they can complete the questionnaires without staff assistance. With poor readers, the questionnaires can be read aloud by a staff member in a private setting. This must be done with care and positive regard for the discomfort that poor readers may feel under such circumstances. Competent readers are given approximately 45 minutes to complete the questionnaires using pen and paper or an iPad, de- pending on their preference.
We have clients complete a routine, brief demo- graphics questionnaire. Obtaining a client’s current address and phone number is important, as is obtain- ing the number of someone who always knows the cli- ent’s whereabouts. This information is important for purposes of outreach efforts during treatment should the client stop coming to scheduled therapy sessions or should we need to contact him/her for other clinical
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purposes, and to contact clients for routine posttreat- ment follow-up evaluations.
All clients complete the Michigan Alcoholism Screening Test (MAST; Selzer, 1975), a widely used, brief alcoholism-screening instrument. Considering that one-third of individuals who receive buprenor- phine or methadone also misuse alcohol, and that al- cohol use is a risk factor for fatal overdose among in- dividuals prescribed opioids, the MAST is useful for flagging clients with alcohol problems.
Anxiety and depressed mood are also common prob- lems among those presenting for treatment for substance use disorders. We use the Beck Anxiety Inventory (BAI; Beck & Steer, 1993) and Beck Depression Inventory (BDI-II; Beck, Steer, & Brown, 1996) to screen for symp- toms of anxiety and depression and readminister these measures on a regular basis to monitor progress with those clients who score in the clinical range at intake. The average BAI and BDI-II scores of individuals with opioid use disorder entering treatment fall in the clini- cal range. For most clients, those scores decrease precipi- tously during the first few weeks in treatment. However, that is not true for all clients. Therefore, it is important to carefully assess and monitor symptoms of anxiety and depression, and to refer or intervene when symptoms do not remit. Assessing and monitoring for suicide risk is important as well. We use a protocol we developed in collaboration with our local mental health crisis service.
The Brief Symptom Inventory–II (BSI-II; Derogatis, 1993) is also used to screen for psychiatric symptom- atology more broadly and is helpful in determining whether a more in-depth psychiatric evaluation is war- ranted. The BSI-II also can be easily readministered to monitor progress or change in psychiatric status.
We use a Brief Pain Inventory—Short Form (Clee- land & Ryan, 1994) as an efficient means to collect specific information regarding pain intensity and pain- related interference in function. Persistent pain is com- mon among individuals with opioid use disorder, and patients with pain frequently cite pain as an impetus for substance use initiation and relapse. In addition to identifying patients who may benefit from treatment for chronic pain, prompt and expert assessment of pain is useful for treatment planning and in helping clients identify potential cues for substance use relapse during the course of treatment.
After clients complete these self-administered ques- tionnaires, staff members review them to ensure that all questions have been answered and the information appears consistent. Any obvious inconsistencies are re- solved with the client.
Program Description
We find it useful to break up the data-gathering aspects of the initial assessment between completion of the self- administered questionnaires and initiation of the struc- tured interviews. We provide a brief description of the treatment program and its rationale at this time. Clients are given the opportunity to ask questions or to express any concerns they may have. The goal here is to orient clients regarding what will happen in treatment, to create an atmosphere of optimism, and to help clients feel hope- ful that they can succeed in treatment. This description and interaction are typically brief (10–15 minutes). Senior staff members (e.g., prescribing physician or staff psychol- ogist) provide more detailed rationales and descriptions during this same intake session, but after the structured interviews are completed. When asked questions about the treatment process, staff members provide brief an- swers and reassure the client that a senior staff member will soon be meeting with him/her to provide much more information about the program and how it works.
In providing the brief description, staff members ex- plain that our program is confidential and specifically designed for persons who have opioid use disorder. For obvious reasons, users of illicit drugs are often quite concerned about confidentiality. Clients are informed about the overall duration of treatment, the recom- mended frequency and duration of clinic visits, and the general foci and orientation of our treatment approach (i.e., buprenorphine maintenance). We explain that the primary goals of treatment are to initiate and maintain abstinence from illicit opioids and make positive chang- es that result in greater life satisfaction and fewer drug- related consequences. Examples of what might occur during treatment are provided:
“As a patient in our clinic, you will receive buprenor- phine treatment. Buprenorphine is an opioid medi- cation that has been approved for treatment of opi- oid use disorder in this country. We will administer buprenorphine in accordance with standard practice. During the first week of treatment, you must attend daily clinic visits to get stabilized onto an appropri- ate buprenorphine dose. Following stabilization, you will visit the clinic every 1–2 weeks to provide a urine specimen and pick up your medication for the next week or two. We will test each specimen for all opioids and other commonly used drugs. This urine sample will allow us to confirm adherence to your medication regimen and that you’ve discontinued use of other drugs.
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“It will be very important for you to refrain from using other opioids, such as oxycodone, heroin, or methadone, during treatment as buprenorphine can cause withdrawal symptoms when given to someone who has recently used other opioid medications. For the duration of treatment, you will be required to notify clinic staff of any drugs (prescription, over- the-counter, and/or illegal) or supplements you are currently taking or begin taking during treatment.”
Semistructured Interviews
We developed a semistructured drug history interview in our clinic to facilitate collection of information on current and past drug use. Administration of this inter- view involves asking specific questions regarding recent patterns of opioid use, historical patterns of opioid use, prior instances of opioid abstinence, opioid treatment history, and other drug use history. The rationale here is to identify the individual’s typical pattern of opioid use, previous experiences in treatment, and concurrent use of other substances. Such detailed information is essential for proper treatment planning.
The goal in completing a drug-use history is to obtain detailed information regarding the duration, severity, and pattern of the client’s drug use. The ac- curacy of the client’s report of amount and frequency of drug use is facilitated by the use of an effective tech- nique for reviewing recent use known as the Timeline Follow-Back (Sobell & Sobell, 1992; for a review see Hjorthoj, Hjorthoj, & Nordendoft, 2012). Using a cal- endar as a prompt, clients are asked to recall on a day- by-day basis the number of days they used in the past month and the amount used per occasion. Milligrams are typically the best metric for determining amount of prescription opioids used, whereas “bags” are the best unit of measurement for assessing amount of heroin used. The same assessment is repeated for as far back in time as needed for diagnostic reasons. This technique results in a good overview of the client’s pattern of drug use during the past month and over their lifetime. The interviewer asks for as much clarification as possible to help obtain an accurate assessment of drug-use history. Diagnoses are made later by the staff psychologist.
We use the Addiction Severity Index (ASI; McLel- lan, Cacciola, Alterman, Rikon, & Carise, 2006) to obtain reliable, valid assessments of multiple problems commonly associated with drug use and a quantitative, time-based assessment of problem severity in the fol- lowing areas: alcohol and drug use; employment; and
medical, legal, family, social, and psychological func- tioning. The information obtained with the ASI is quite useful for developing treatment plans. It is also a use- ful instrument for assessing progress at follow-up, in that it is time-based and yields quantitative composite scores for the seven problem areas. Training on ASI ad- ministration is necessary to ensure that the interviewer conducts a reliable ASI interview (for information on training in the use of the ASI, see www.phmcresearch. org/2-uncategorised/235-addiction-severity-index).
After completing these interviews, the staff member who is conducting the intake assessment informs the client that he/she will be meeting with the prescribing physician in a few minutes. A brief break (5–10 min- utes) is given, during which the staff member who is conducting the assessment completes an intake sum- mary sheet for the prescribing physician, along with all of the supporting intake information. The staff member meets briefly with the physician to review the case. Clients are then introduced to their physician. We try never to allow a client to leave the intake interview without a brief meeting with the physician, so that he/ she can depart feeling that treatment has begun and with concrete plans for abstaining from illicit opioid use until the next clinic visit. The next clinical visit is typi- cally scheduled for the following morning, as clients are required to present in mild to moderate withdrawal in order to receive their first buprenorphine dose.
In many ways, the intake appointment is an orien- tation session used to establish rapport with the client and to provide further rationales for our treatment ap- proach. Doing so permits clients to develop clear ex- pectations about treatment. We continue with the “can- do” approach, acknowledging how hard the client and clinic staff members will have to work to succeed but conveying a very confident message that success can be achieved by working together. Following this brief meeting with the physician, patients often meet with a staff psychologist or counselor to collaboratively begin formulating an initial treatment plan. As part of this conversation, clients are encouraged to ask questions and to voice concerns. The staff psychologist orients clients to the urinalysis testing protocol and provides information regarding take-home dosing. We also ask clients to sign a Buprenorphine agreement form (Figure 15.1), which describes each component of the treatment program, clinic rules, and expectations for subsequent visits. The psychologist also uses this conversation to reiterate the importance of refraining from using other opioids during treatment.
Substance Use Disorders 617
This is an agreement between and the UVM Substance Abuse Treatment Center (SATC), for 6 months of interim buprenorphine treatment. By signing this agreement, I understand and agree to the following:
I agree to give the treatment team a phone number that I will answer or will accept phone messages from the clinic regarding a callback. I agree to be reachable at all times at this number. I will also leave a second phone number for messages as a backup. I will check both phone numbers for messages frequently. Regarding the Med-O-Wheel device, I will:
Keep it in a safe, dry location at all times. It will stay at home in a secure location at all times unless I must transport it to the clinic for a scheduled or random callback visit.
When transporting the device to/from the clinic, I will carry it in a safe backpack or bag.
Keep it and all medication doses away from children at all times.
Keep the device safe from theft.
Take my medication as instructed—no sharing, skipping, or storing doses.
• I will attend the clinic ON TIME on scheduled days to receive buprenorphine during my scheduled visit. • I will leave a valid urine sample at each visit. • I understand that buprenorphine can be toxic and caution must be taken to safeguard others from
intentional or accidental ingestion of buprenorphine. If my medication is ingested by another person, I must IMMEDIATELY CALL 911.
• I understand that I must have an appropriate bag/backpack to transport the device to and from the clinic. • I realize that I must take extra precautionary measures to keep the device and medication secure from
others in my household, especially children. • I understand that I must bring the device with all unused medications to the clinic at each random
callback and scheduled visit days. • I understand the seriousness of lost or stolen medication or device. I realize that I may not be
remedicated if this occurs. If my medication or device is stolen, I MUST call clinic staff immediately, notify the police immediately, and bring the resulting police report to the clinic.
• I understand that if there is any evidence of diversion, device tampering, or not adhering to the medication regimen, my participation in treatment will be terminated.
• I understand that failure to present at the clinic for a random callback could result in treatment discharge. • I understand that I am expected to attend ALL clinic visits ON TIME and that if my schedule changes for
any reason, I will notify clinic staff immediately. • I understand that if I arrive late to my visit, I may have to wait while clinic staff meets with other clients who
are scheduled after my original appointment time. • I understand that if I am planning to be out of town, I must notify clinic staff at least 2 weeks in advance
and bring appropriate documentation upon my return. • I understand that I am expected to follow all clinic policies and procedures.
My signature below indicates that I understand and agree to follow the conditions of this contract.
Participant signature Date
Clinic Staff Member signature Date
FIGURE 15.1. Buprenorphine agreement form.
618 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
BEHAVIORAL AND COGNITIVE‑BEHAVIORAL THERAPIES FOR ILLICIT SUBSTANCE USE DISORDERS
Conceptual Framework
Behavioral and cognitive-behavioral therapies are based largely on the concepts and principles of operant and respondent conditioning and social learning theory. Within this conceptual framework, drug use is con- sidered learned behavior that is maintained, at least in part, by the reinforcing effects of the pharmacological actions of drugs in conjunction with social and other nonpharmacological reinforcement derived from the drug-abusing lifestyle (Bickel, Moody, & Higgins, 2016; Higgins, Heil, & Lussier, 2004). The reliable empirical observation that abused drugs function as reinforcers in humans and laboratory animals provides sound scientific support for that position (Griffiths, Bigelow, & Henningfield, 1980; Higgins et al., 2004). Cocaine, other psychomotor stimulants, ethanol, opi- oids, nicotine, and sedatives serve as reinforcers and are voluntarily self-administered by a variety of species. Moreover, through operant and respondent condition- ing, environmental events that have been paired with drug use acquire the ability to engender drug seeking. Physical dependence is not necessary for these drugs to support ongoing and stable patterns of voluntary drug seeking and use in otherwise healthy laboratory animals or humans. Commonalities do not end there. Effects of alterations in drug availability, drug dose, schedule of reinforcement, and other environmental manipulations of drug use are orderly and have generality across differ- ent species and types of drug use (Griffiths et al., 1980; Higgins et al., 2004). These commonalities support a theoretical position that reinforcement and other prin- ciples of learning are fundamental determinants of drug use, and the emergence and maintenance of substance use disorders.
Within this conceptual model, then, drug use is considered a normal, learned behavior that falls along a frequency continuum ranging from patterns of little use and few problems to excessive use and many untow- ard effects, including death. The same processes and principles of learning are assumed to operate across the continuum. All physically intact humans are assumed to possess the necessary neurobiological systems to experience drug-produced reinforcement; hence, they have the potential to develop patterns of drug use and eventually a substance use disorder. Said differently, individuals need not have any exceptional or pathologi- cal characteristics to develop a substance use disorder.
Clearly genetic or acquired characteristics (e.g., fam- ily history of substance dependence, other psychiatric disorders, delay discounting) affect the probability of developing a substance use disorder (i.e., risk factors), but this model assumes that those special characteristics are not necessary for these disorders to emerge (Bickel et al., 2016; Higgins et al., 2004).
Treatment is designed to assist in reorganizing the physical and social environments of the patient. The goal is to weaken systematically the influence of re- inforcement derived from drug use and the related drug-using lifestyle, and to increase the frequency of reinforcement derived from healthier alternative activi- ties, especially those that are incompatible with contin- ued drug use. Below we describe the basic categories of empirically tested and efficacious behavioral and cognitive-behavioral therapies for achieving these over- arching goals.
Prototypical Behavioral and Cognitive‑Behavioral Interventions and Empirical Support for Efficacy
Behavioral and cognitive-behavioral therapies are the most common psychosocial interventions for substance use disorders (Principle 6, Table 15.1). At least four em- pirically based interventions are used in the treatment of illicit substance use disorders (Kiluk & Carroll, 2013). First is cognitive-behavioral/relapse prevention therapy, which has been shown to be effective with cocaine, methamphetamine, opioids, and other types of sub- stance use disorders (Magill & Ray, 2009). Typically, this approach entails training in functional analysis, through which clients learn to identify environmental antecedents and consequences that influence their drug use. Functional analysis is typically accompanied by skills training on how to rearrange one’s environment to alter the probability of drug use by either avoiding high-risk settings or managing them effectively when contact cannot be avoided. Strategies are often used to identify and modify unrealistic expectations about drug use, cope with craving for drug use, and change thinking patterns that increase the likelihood of drug use. Additionally, social skills training is often incorpo- rated when clients have used drugs to cope with social anxiety or when particular skills deficits limit clients’ access to alternative, healthier sources of reinforcement (e.g., Monti, Rohsenow, Michalec, Martin, & Abrams, 1997). Systematic training is included to prevent relapse, with sufficient emphasis that the terms cognitive-behav- ioral therapy and relapse prevention therapy are often used interchangeably. There is good evidence that this
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approach is efficacious in treating illicit substance use disorders (for a meta-analysis, see Magill & Ray, 2009).
Second, contingency management (CM) is an effi- cacious behavioral treatment strategy used to treat co- caine, opioids, and other types of illicit substance use disorders (Higgins, Silverman, & Heil, 2008), as well as other behavioral health problems (see Supplemental Issue of Preventive Medicine, “Incentives and Health”; Higgins, Silverman, Sigmon, & Naito, 2012). With CM, reinforcement and punishment consequences are systematically used to increase abstinence from drug use or to improve other therapeutic goals, such as treatment attendance or medication compliance (e.g., Heil, Davis, Arger, & Higgins, 2018). Most typically, when using CM to treat substance use disorders, clients receive vouchers that are exchangeable for retail items or other monetary-based reinforcement contingent on objective evidence of recent abstinence from drug use or other target behaviors (Higgins, Kurti, & Davis, 2019). Our group has published three comprehensive literature re- views, including a meta-analysis on voucher-based CM, that support the efficacy of this approach (Davis et al., 2016; Higgins, Sigmon, & Heil, 2011; Lussier, Heil, Mongeon, Badger, & Higgins, 2006).
Third, community reinforcement approach (CRA) therapy is another empirically based behavioral inter- vention used in the treatment of illicit substance use disorders. It was originally developed for the treatment of alcohol use disorder (Hunt & Azrin, 1973) and was later extended to the treatment of cocaine and opioid use disorder (Abbott, Moore, Weller, & Delaney, 1998; Higgins et al., 1991; see Budney & Higgins, 1998, for a therapist manual combining CRA with voucher-based CM for cocaine use disorder). Based in conditioning and social learning theory, CRA encourages clients to rearrange their lifestyle so that healthy, drug-free living is more rewarding and can compete with the reinforce- ment derived from drug use. This typically involves helping clients get involved in alternative non-sub- stance-related, pleasant social activities and increasing the enjoyment they derive from their family and their job. There is also good evidence to support two exten- sions of CRA: adolescent CRA, which targets adoles- cents with substance use disorders and their parents/ guardians (e.g., Godley et al., 2017); and community reinforcement and family training (CRAFT), which works through family members to facilitate getting treatment-resistant individuals into treatment (Kirby, Marlowe, Festinger, Garvey, & LaMonaca, 1999). No fewer than seven systematic reviews and one meta-anal- ysis provide evidence supporting the efficacy of CRA
(Finney & Monahan, 1996; Holder, Longabaugh, Mill- er, & Rubonis, 1991; Meyers, Roozen, & Smith, 2011; Miller et al., 1995; Miller, Andrews, Wilbourne, & Bennett, 1998; Miller, Wilbourne, & Hettema, 2003; Miller, Zweben, Johnson, 2005; Roozen et al., 2004).
Fourth, motivational-based interventions, including motivational interviewing and motivational enhance- ment therapy, were originally shown to be efficacious in treatment of problem drinkers (see review by Miller, 1996) and subsequently extended to treatment of to- bacco and illicit substance use disorders as well. These motivational-based interventions are typically brief and designed to facilitate behavior change by helping cli- ents to identify personal values and goals, to examine whether drug use may conflict with those values and goals, and to explore how to resolve any ambivalence or conflict between personal goals and values and ongoing drug use (Miller & Rollnick, 2002). There is extensive evidence that motivational interventions reduce alco- hol use; a more modest but still robust literature sug- gesting reductions in marijuana use; mixed or negative evidence for tobacco, cocaine, and methamphetamine use disorders; and insufficient evidence with regard to opioid use disorder (see DiClemente, Corno, Graydon, Wiprovnick, & Knoblach, 2017).
MULTIELEMENT TREATMENTS
It is a common practice to provide multielement inter- ventions when treating illicit substance use disorders, incorporating some or all of the interventions outlined earlier (e.g., Bellack, Bennett, Gearson, Brown, & Yang, 2006). The CRA + vouchers intervention that our group developed for the treatment of cocaine use disorder is an excellent example (Higgins et al., 1991, 1993, 1994, 2003; for a therapist manual, see Budney & Higgins, 1998). This combination intervention has been demonstrated to be highly efficacious. Indeed, a recent meta-analysis examining the efficacy of all psychosocial treatments for cocaine use disorder that have been tested in controlled trials ranked the CRA + vouchers intervention as producing the best during- and post-treatment outcomes (De Crescenzo et al., 2018; see also Lussier et al., 2006). A meta-analysis supports the efficacy of CRA in the treatment of substance use disorders when delivered alone or in combination with vouchers (Roozen et al., 2004), and separate random- ized trials have demonstrated that the voucher-based CM (Higgins et al., 1994) and CRA (Higgins et al., 2003) components of the CRA + vouchers intervention
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are each active contributors to outcomes when treating cocaine use disorder.
Combining‑Behavioral Interventions with Medications
The CRA + vouchers multielement treatment combines behavioral treatments with minimal use of medications save for disulfiram therapy for those with comorbid co- caine and alcohol use disorder. For patients with opi- oid use disorder, however, medications are a mainstay of evidence-based treatment. Combining medications with psychosocial treatments is the recommended stan- dard of care for opioid use disorder (Principle 7, Table 15.1) as outcomes are generally superior compared to those obtained with medication alone. It is important to note that withdrawal (“detoxification”) alone can be a first step, but it is not a primary treatment for opioid use disorder and should only be considered as part of a longer, more comprehensive treatment plan (Kampman & Jarvis, 2015) (Principle 10, Table 15.1).
Three medications are U.S. Food and Drug Admin- istration (FDA)-approved for the treatment of opioid use disorder: methadone, a full opioid agonist; bu- prenorphine, a partial opioid agonist; and naltrexone, an opioid antagonist. There is ample evidence for the safety and efficacy of all three medications, although treatment with methadone or buprenorphine is far more common than that with naltrexone (Comer et al., 2006; Krupitsky et al., 2011; Mattick, Breen, Kimber, & Davoli, 2009, 2014; Syed & Keating, 2013).
Methadone can only be dispensed by federal and state-licensed opioid treatment programs, and typically requires daily clinic attendance for supervised dosing. An increasing number of these highly regulated programs also offer the option of daily supervised dosing of bu- prenorphine. Office-based opioid treatment (OBOT), which allows for dispensing of medication via regular outpatient prescriptions filled in a retail pharmacy like any other prescription medication, is available for bu- prenorphine but not for methadone. Physicians in private practices, or other private and public sector clinics, can be authorized to prescribe buprenorphine. Naltrexone can be prescribed in any setting by any clinician with the author- ity to prescribe medications, and there are no regulations of facilities or prescribers like there are for methadone and buprenorphine. The reason for fewer regulations with na- ltrexone is there is little risk of overdose should the medi- cation be diverted and it has no psychoactive effects (i.e., addiction potential), which translates into little demand for the medication on the black market.
It is imperative that clinicians consider a client’s treat- ment history, psychosocial circumstances, co-occurring disorders, opportunities for treatment retention, and risks of medication diversion when determining which medication and setting are most appropriate.
Interim Dosing to Reduce Risk
The U.S. opioid epidemic of the past several decades has created a situation in which demand for treatment far exceeds treatment capacity or availability, especially in rural communities, where opioid use disorder was historically relatively uncommon. The gap between treatment need and availability has often resulted in lengthy wait lists for individuals in many areas of the country (Andrews, Shin, Marsh, & Cao, 2013; Sigmon, 2014). During delays to treatment entry, wait-listed in- dividuals are at significant risk for continued illicit drug use, criminal activity, psychiatric distress, infectious disease, overdose, and mortality (Scholl, Seth, Kariisa, Wilson, & Baldwin, 2019; Schwetz, Calder, Rosenthal, Kattakuzhy, & Fauci, 2019; Sigmon et al., 2016). In one evaluation of survival rates among individuals with opi- oid use disorder who received wait list versus immedi- ate entry into treatment, for example, the mortality rate was 5.0 and 0.42 per 100 person-years for wait-listed versus admitted patients, respectively (p < .0005; Peles, Schrieber, & Adelson, 2013). Extended waits are also associated with reduced likelihood of treatment entry when a slot does become available (Donovan, Rosen- gren, Downey, Cox, & Sloan, 2001; Festinger, Lamb, Marlowe, & Kirby, 2002; Chawdhary et al., 2007; Pol- lini, McCall, Mehta, Vlahov, & Strathdee, 2006).
These developments impacted the types of treat- ments being offered for opioid use disorder in our clin- ics and in most treatment settings throughout the Unit- ed States. Indeed, we transitioned from a long-standing practice of offering relatively intense interventions com- bining buprenorphine with CRA (e.g., Bickel, Amass, Higgins, Badger, & Esch, 1997; Sigmon et al., 2013) to more streamlined efforts to increase treatment capacity and provide care for those lingering on wait lists. Where feasible, we recommend the intensive therapy. Howev- er, in the context of the current U.S. opioid crisis, that is not always practicable.
Interim Buprenorphine Treatment
To address this tremendous need for streamlined inter- ventions to bring treatment to wait-listed individuals,
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our group developed a novel interim buprenorphine treatment (IBT) that is designed to mitigate the risks associated with treatment delays, while surmounting the considerable regulatory constraints associated with use of methadone (Sigmon et al., 2015, 2016). As de- scribed below, this intervention has four components, each strategically chosen to deliver potentially life- saving pharmacotherapy to wait-listed individuals with opioid use disorder, while minimizing the risk of medi- cation nonadherence and diversion.
Buprenorphine with Computerized Dispensing
The partial opioid agonist buprenorphine has a pharma- cological profile that is associated with reduced abuse liability and overdose risk (Bickel & Amass, 1995; John- son, Strain, & Amass, 2003; Walsh, Preston, Stitzer, Cone, & Bigelow, 1994; Walsh, Preston, Bigelow, & Stitzer, 1995). This treatment approach builds on prom- ising results from two studies in Scandinavian countries in which buprenorphine was provided in an interim treatment paradigm (Krook et al., 2002; Abrahamsson et al., 2016). Our effort represented the first to develop an IBT intervention in the United States and the first to involve take-home doses (Sigmon et al., 2016).
Although buprenorphine’s pharmacological profile reduces overdose risk, concerns about possible nonad- herence and diversion could still limit its widespread use (Alho, Sinclair, Vuori, & Holopainen, 2007; Johanson, Arfken, di Menza, & Schuster, 2012; Lofwall & Walsh, 2014; Wright et al., 2016). Thus, for this intervention, we use a computerized medication dispenser to facilitate mobile buprenorphine dispensing while reducing the risk of nonadherence or diversion. While electronic dispens- ers (e.g., Medication Event Monitoring System, Aprex Corporation, Fremont, California) have long been used to support medication adherence in clinical populations in which compliance is often poor (e.g., antiretroviral therapy in patients with HIV), they have substantive lim- itations. Patients can access all of their doses each time they open the bottle, and the cap only records a time- date stamp for each opening rather than the amount of medication removed. A patient could, therefore, remove more than the prescribed amount at one time, replacing it with illicitly obtained medication at a subsequent open- ing if he/she is called in for a pill count. While this risk may be reasonable when dealing with HIV medications, these limitations raise special concerns for pharmaco- therapies with potential for abuse (e.g., taking more than prescribed) or diversion (e.g., sharing or selling doses).
A promising advance is the development of portable, computerized devices that hold multiple doses for con- trolled daily dispensing. We use the Med-O-Wheel Secure device (Addoz, Forssa, Finland), which accom- modates doses for up to 28 days, with each day’s dose secured in separate compartments and only available during a predetermined 3-hour window (programmed by staff). The Med-O-Wheel also includes locks and alarms to prevent tampering and access to tablets out- side the preset time window (Figure 15.2).
Monitoring via Interactive Voice Response
An intensive clinical support package is impractical for resource-constrained settings. Accordingly, we devel- oped a mobile health (mHealth) platform for monitoring patients on a daily basis. mHealth platforms can extend the reach of health care by permitting delivery of moni- toring, education, point-of-care diagnostics, and treat- ment beyond the confines of the medical office (Boyer, Smelson, Fletcher, Ziedonis, & Picard, 2010). Interactive voice response (IVR) systems are particularly promising in that they can provide customized content or monitor- ing via phone and offer advantages of low-cost, consis- tent delivery, expanded access, 24-hour availability, pri- vacy, and convenience (Crawford et al., 2005; Helzer et al., 2008; Kim, Bracha, & Tipnis, 2007; Rose, MacLean, et al., 2010; Rose, Skelly, et al., 2010; Stacy, Schwartz, Ershoff, & Shreve, 2009). IVR is an ideal mHealth plat- form choice for IBT. Phone-based systems are compat- ible with resource-constrained settings, as they require no specialized equipment or extensive training. They also provide broad access for marginalized populations, as phones are familiar, easy to use, and more widely avail-
FIGURE 15.2. Computerized e-pill Med-O-Wheel secure device for safe medication dispensing.
622 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
able than computers. Furthermore, IVR uses an auditory interactive process that is not hampered by low literacy. Our system calls clients nightly to assess any opioid or other drug use, as well as opioid craving and withdrawal. It includes information about self-help meetings in the community, as well as immediate connection with staff, if needed. To maximize client convenience and adher- ence, we designed the system to automatically call clients each day rather than requiring them to call into the sys- tem; however, it also accepts inbound calls, if the client prefers, or anticipates missing the incoming call.
Random Callbacks via IVR
Biochemical verification via urine toxicology is the most objective method for evaluating recent drug use (Chermack et al., 2000; Fendrich, Johnson, Wislar, Hubbell, & Spiehler, 2004; Kilpatrick, Howlett, Sedg- wick, & Ghodse, 2000; Preston, Silverman, Schuster, & Cone 1997; Wish, Hoffman, & Hemes, 1997). Our long-standing protocol involves thrice-weekly urinaly- sis monitoring during the early months of treatment, followed by a reduction to twice weekly once clients are stable in treatment (Higgins et al., 2003; Sigmon et al., 2013). While this rigorous protocol maximizes detection of even low levels of drug use (Cone & Dick- erson, 1992), thrice-weekly visits are incompatible with resource-constrained settings and with reaching rural communities in which daily travel to treatment is chal- lenging. To balance the rigor of this procedure with the less-intensive schedule necessary for IBT, we developed a random callback protocol wherein patients are con- tacted by the IVR system at random times and instruct- ed to return to the clinic for urinalysis. Random sam- pling increases the effectiveness of urine monitoring, as patients remain unaware of when the next drug screen will be requested, reducing the possibility that they can tailor drug use to subvert monitoring (Harford & Kle- ber, 1978; Manno, 1986). For each random callback, the IVR system contacts clients and instructs them to visit the clinic (typically within 12 hours, but this can be individualized as needed) to provide a staff-observed urine specimen and present their Med-O-Wheel for inspection to ensure there is no evidence of tampering or nonadherence. This component provides a rigorous yet efficient way to support abstinence and adherence over an extended period of lower-frequency clinic visits. These random callbacks also provide an important op- portunity for brief counseling, as is illustrated in the case study below.
HIV and Hepatitis Education
Finally, while IBT is intended as a low-intensity, ex- tended-reach paradigm, we believe it is essential to in- clude an evidence-based intervention to enhance HIV and hepatitis knowledge in individuals awaiting entry into treatment for opioid use disorder. HIV and hepati- tis are responsible for more than 30,000 annual deaths in the United States (Centers for Disease Control and Prevention, 2013), and deaths from hepatitis-related liver complications are increasing in this population (Larney, Randall, Gibson, & Degenhardt, 2013). Thus, efforts to reduce disease transmission among those with opioid use disorder are critically important.
Our team has developed a single-visit intervention that produces significant and sustained improvements in HIV and hepatitis knowledge in adults with sub- stance use disorders (Ochalek, Heil, Higgins, Badger, & Sigmon, 2018). Briefly, the client completes an ini- tial assessment of HIV and hepatitis knowledge using a modified version of the HIV/AIDS Knowledge Test (Marsch et al., 2005) and a hepatitis C knowledge test (Dunn et al., 2013) delivered via an interactive iPad application developed by our group (application avail- able from the University of Vermont Center on Rural Addiction at uvmcora.org). Immediately following this pre-test, the application provides corrective feedback and explanations for any incorrect responses. Clients then watch a 15-minute video (“What Is Hepatitis C and How Is It Diagnosed?” [amfAR, The Founda- tion for AIDS Research]), both administered via iPad and monitored by study staff. The HIV and hepatitis C knowledge assessments are then readministered im- mediately following delivery of the educational content, with feedback provided for any incorrect answers. A staff member then offers condoms, as well as informa- tion for free HIV and hepatitis testing resources.
Efficacy Testing
To begin evaluating the efficacy of IBT (Sigmon et al., 2016), 50 wait-listed adults with opioid use disorder were randomly assigned to an IBT (n = 25) or wait- list control (WLC; n = 25) condition, each 12 weeks in duration. IBT participants received the multicom- ponent intervention described earlier, while WLC par- ticipants remained on the wait list of their local clinic. Participants randomized to IBT provided significantly more illicit opioid-negative urine specimens than WLC at Weeks 4 (88 vs. 0%), 8 (84 vs. 0%), and 12 (68 vs. 0%) (Figure 15.3). IBT participants also demonstrated
Substance Use Disorders 623
FIGURE 15.3. Abstinence from illicit opioids and intravenous opioids over 12 weeks with interim buprenorphine. From Sigmon et al. (2016). Copyright © 2016 Massachusetts Medical Society. Reprinted by permission.
624 CliniCal Handbook of PsyCHologiCal disorders
significantly greater reductions in self-reported past- month frequency of illicit opioid use and intravenous drug use vs. WLC participants (Figure 15.3). Adher- ence with IBT treatment components was also excel- lent. These promising data suggest that providing technology-supported interim buprenorphine dosing to waitlisted adults with opioid use disorder may reduce individual and societal risks during delays to compre- hensive treatment. In order to further examine the ef- ficacy of this approach, a larger-scale, longer-duration randomized controlled trial is currently underway.
Of course, IBT is only the first step. From there, the goal is to transition the client into longer-term care or what is referred to as maintenance therapy. Over the past decade, Vermont has developed a statewide program to expand treatment for individuals with opioid use disor- der. The effort has prioritized the expansion of medica- tion-based treatments, because they have strong empiri- cal support (Comer et al., 2006; Krupitsky et al., 2011; Mattick et al., 2009, 2014; Syed & Keating, 2013). The strategy for expanding access to these medications has employed an innovative treatment network, which has become known as the “hub-and-spoke” system (Brook- lyn & Sigmon, 2017; Simpatico, 2015). Vermont’s hub- and-spoke system is organized by geographic region. Each region has a “hub,” which is a licensed specialty out- patient treatment program with the authority to dispense buprenorphine and methadone for opioid use disorder. “Spokes” are medical practices that provide OBOT. Pa- tients are initially assessed using the Treatment Needs Questionnaire (Brooklyn & Sigmon, 2017) to deter- mine the most appropriate treatment placement (i.e., in the hub with methadone or buprenorphine treatment or with spoke providers for treatment with buprenorphine). Hubs have an extensive staff of addiction-trained MDs, nurses, and counselors who provide intensive specialty care addiction treatment. Spokes are primary care set- tings staffed by at least one buprenorphine-prescribing physician who is supported by a “medication-assisted treatment (MAT) team” comprising a registered nurse and a master’s-level, licensed counselor. Patients transfer between hubs and spokes when appropriate. Research has shown that delivering medications for opioid use disorder in the hub and spoke system is highly effective in reducing opioid use and overdose and in improving functioning in many life domains (Rawson, Cousins, McCann, Pearce, & Van Donsel, 2019). Given that this innovative and expansive model is in place in our state, it is always our goal to assist and support clients as they transition from our clinic into maintenance therapy via the Hub-and-Spoke system.
CASE STUDY: IMPLEMENTING BUPRENORPHINE MAINTENANCE TREATMENT
In this section, we review the case of a client who had no previous history of opioid treatment. He enrolled in treatment through our clinic given that he lived in a rural and medically underserved community, where his treatment options were limited. Following 6 months of treatment with the IBT intervention, he eventually transitioned into OBOT with a primary care physician in a spoke. We chose this case because it illustrates well a number of different aspects of using this treatment approach. The case also illustrates the multifaceted problems with which clients with opioid use disorder present. Outcome was quite good but highlights the system-level barriers that many individuals face when attempting to access treatment for opioid use disorder.
“Joe,” a 36-year-old, single (never married), male, was self-referred to the clinic for help with opioid use disor- der. He was a high school graduate who had been em- ployed full-time for the past 10 years as a supervisor for a local construction company. Joe lived with his girlfriend, who also used illicit opioids. Joe had not engaged in treatment previously because of concerns about stigma, and he lived in a rural county where few treatment op- tions were available. Because his work schedule required that he be present at work sites early in the morning, he was also unable to enroll in treatment in his designated hub, where clients are required to attend daily or near- daily dosing visits for an extended time period.
Joe had a history of criminal justice involvement, with two prior arrests for drug charges. He was con- victed and fined for one of those charges but never in- carcerated. He was not under criminal justice supervi- sion at the time he sought treatment. He reported no major medical issues but did live with mild to moderate back and elbow pain that occasionally interfered with his work and relationships. However, his pain was rela- tively well managed with rest and ibuprofen.
Presenting Complaint
Joe reported using opioids regularly for 14 years. As part of his intake assessment, he reported that he used illicit buprenorphine during the year prior to intake and wanted help with stopping illicit opioid use. Joe esti- mated that he spent between $700 and $900 monthly on opioids and was tired of this financial burden. De- spite these substantial financial costs, he had managed to keep his opioid use a secret from almost everyone in his life except his girlfriend. He also expressed serious
Substance Use Disorders 625
concerns about the consequences if his family or em- ployer learned about his drug use and related lifestyle. He was once able to stop using opioids for 2 years on his own but resumed use in an attempt to cope with work- related stress and fatigue.
Assessment
Opioid Use
Joe met DSM-5 criteria for opioid use disorder, severe. He first used illicit opioids as a teenager and progressed to regular use during his early 20s. He reported a 13- year history of intranasal oxycodone and hydrocodone use. However, within the year prior to presenting for treatment, he transitioned to illicit sublingual bu- prenorphine use. During the 7 days prior to intake, Joe used 8 milligrams of buprenorphine daily and reported this to be his typical pattern of use. He reported illicit buprenorphine use during each of the prior 30 days. He typically split his dose, using 4 milligrams in the morning and an additional 4 milligrams in the evening after work. Although Joe reported intermittent heroin use, he denied ever using intravenously. He reported a number of serious consequences as a result of his illicit opioid use, including financial problems and multiple drug charges.
Other Drug Use
Joe’s first use of alcohol was at age 15. He reported drink- ing 14 days out of the past 30 prior to intake. On most occasions, he would ingest two to three beers; however, it was not uncommon for Joe to drink to the point of intoxication on weekends. Joe also initiated tobacco and marijuana use at age 15. He reported 20 years of daily use of both substances. However, he reported that he quit smoking 9 months prior to beginning treatment and denied marijuana use during the prior 30 days. He reported a lifetime history of cocaine, amphetamine, benzodiazepine, hallucinogens, and inhalant use but no regular or current use of those substances. Joe reported no previous treatment episodes for substance abuse.
Other Psychiatric Problems
Joe denied a history of anxiety, depression, or suicidal- ity. His BAI score was 8, his BDI score was 15. These scores were indicative of mild symptoms of anxiety and depression, respectively (Beck & Steer, 1993; Beck et al., 1996), without suicidal ideation. In addition, Joe
reported a score of 0.32 on the Global Severity Index (GSI) of the BSI-II (respondents rank each BSI item on a 5-point scale ranging from 0 [not at all] to 4 [extreme- ly] and the GSI is the mean for all 53 items) (Derogatis, 1993).
Pain Intensity and Pain‑Related Interference
Joe reported back and elbow pain on the day of his in- take appointment and rated the intensity of his pain as a 3 on a 0- to 10-point scale. He indicated that his pain was well managed with rest and ibuprofen. Nonethe- less, he noted that his pain interfered with mood, work, sleep, concentration, and enjoyment of life.
Conceptualization of the Case
Joe worked long hours, often traveling to construction sites located throughout the state. His work schedule and the shortage of treatment providers in the rural county in which he resided made it difficult for Joe to engage in treatment, particularly in his designated hub, where clients were required to attend daily or near-daily appointments. Given these barriers to treatment, Joe resorted to self-treatment strategies. These strategies in- cluded at-home detoxification and switching from illic- it oxycodone and hydrocodone to illicit buprenorphine. Though well intentioned, these self-treatment strategies put Joe at risk for other negative outcomes, including a higher risk for overdose following prolonged abstinence from opioids and potential adverse legal consequences. Considered together, these factors suggested that Joe was an ideal candidate for IBT. Although we deemed Joe’s work schedule as a barrier to treatment, his full- time employment also likely provided some protection against opioid use gaining even greater control over his behavior. Full-time employment is a positive prognostic indicator for opioid use disorder, as was his lack of in- travenous use of opioids or other drugs.
Treatment Plan, Implementation, and Outcomes
Abstinence from illicit opioids was the first priority in Joe’s treatment plan and is always the main focus in this IBT treatment model. Buprenorphine is efficacious for reducing illicit opioid craving, use, and overdose, with- out producing the euphoric effects commonly seen with full opioid agonists. Buprenorphine has a long duration of action and is typically combined with naloxone to re- duce the risk for diversion and abuse. For these reasons, maintaining Joe on buprenorphine was a high prior-
626 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
ity. Additionally, we recommended alcohol abstinence given that the combination of buprenorphine and alco- hol placed Joe at increased risk for sedation and respira- tory depression. Furthermore, alcohol has disinhibitory effects that could increase risk for relapse to illicit opi- oid use. As mentioned earlier, Joe lived in a rural town in which opioid treatment was not readily accessible. Accordingly, our long-term goal was to help Joe iden- tify an OBOT provider near his home and help him successfully navigate this transition into maintenance therapy, so that he could continue treatment without the requirement of daily dosing and maintain full-time employment. Here, we detail how this treatment plan was recommended to Joe:
PSYCHOLOGIST: As you may already know, illicit opioid use places people at risk for all sorts of negative out- comes, including legal problems, significant finan- cial costs, the risk for HIV and hepatitis C, overdose, and premature death. Buprenorphine maintenance is one of the most widely used and efficacious treat- ments for opioid use disorder. It seems that you are an ideal candidate for buprenorphine maintenance treatment given that you’ve been buying illicit bu- prenorphine off the street for the past year and have clearly demonstrated signs of physical dependence.
JOE: Right. I was really proud of myself for switching from oxy to bup. It made a big difference, because I can take one 4 mg dose in the morning after break- fast and make it until I get home, without having to use anything else. Before, I was having to take breaks every couple of hours to run off and use or buy oxy from my dealer. So, bup definitely works for me. It’s just gotten to the point where I’m spending half of my paycheck to pay for my habit and to keep from getting sick. Being prescribed bup will really make a big difference for me financially and I won’t have to worry about buying off the street and all the ways that that can go wrong.
PSYCHOLOGIST: That’s a pretty common report. Even though buprenorphine places you at a lower risk for overdose than opioids like oxycontin or heroin, buy- ing buprenorphine off the street, as you know places, you at risk for all sorts of negative legal consequences and, as you already noted, it has taken a financial toll. The good news is that you have demonstrated the ability to modify your drug use in the past, whether that’s quitting smoking or making the switch from oxycontin to buprenorphine. I think that’s a strength you’ll be able to build upon during treatment.
JOE: Good, I haven’t felt like I’ve had too many strengths lately. But how do we do this? What would treatment look like? I’ve tried to get into treatment, but every time I try, the doctor tells me that I have to come into the clinic every day to dose for a couple of months before they will give me take-home medica- tions. Treatment is really important to me, but that kind of schedule just won’t work with all of the ob- ligations I have at work. A lot of days I have to be at the job site by 7 A.M.
PSYCHOLOGIST: That’s a really good question. By en- rolling in our treatment program, you will receive buprenorphine treatment for a 24-week period. Dur- ing the first week of treatment, we ask you to attend appointments in the clinic every day, so that we can get you stabilized on a buprenorphine dose that will not cause sedation but will keep you from craving opioids or experiencing withdrawal symptoms. After that, we will only see you once every 1–2 weeks on average. As part of these visits, you will provide a urine specimen and receive your remaining doses in a computerized medication disk called a Med-O- Wheel. We expect each visit to take about 30 min- utes. I’ll meet with you briefly during those visits to assess how things are going. While you work on maintaining abstinence from illicit opioids, we want to support your continued employment, because it sounds like your job is an important part of your life. Accordingly, we want to be flexible with scheduling. Do you think that your work schedule will allow you to attend clinic visits every 1–2 weeks for check-ins?
JOE: Yeah, even though it will be a pain to come into the clinic every day at first, it’s only 1 week. And it sure beats doing that every day for months on end. My boss is usually pretty understanding about these things as long as it’s not an everyday thing. It really helps that you’re willing to be flexible with schedul- ing these appointments. That means a lot. Getting into treatment is really important to me, but with these construction projects I’m supervising in all of these little country towns, I will need to get into the clinic early, so that I can get on with my day.
PSYCHOLOGIST: OK, our goal is to make treatment eas- ily accessible and reduce the burden as much as possi- ble. In an effort to make treatment more convenient, you will take most of your daily doses at home using the Med-O-Wheel, which holds multiple doses in separate secure cells. Each day’s dose is secured in its own locked compartment. Each day’s dose is available for a 3-hour window around a predetermined dosing
Substance Use Disorders 627
time. Because we won’t see you every day for dosing, we will use a confidential automated telephone sys- tem to check in with you each day about how you are doing. Each day, you will receive a call from our automated phone system and will be asked to com- plete a brief check-in. Throughout treatment, you will also be contacted by the automated phone system at random times and instructed to return to the clinic the next morning to provide a urine specimen. You will also present your Med-O-Wheel for inspection by study staff members to confirm your adherence to your medication regimen. It will be very impor- tant that you refrain from using other opioids, such as oxycodone, as buprenorphine can cause withdrawal symptoms when given to someone who has recently used these other opioids. We really have to think carefully about situations that might arise that could potentially put you at risk for relapse. Although the medication will help reduce the likelihood of illicit opioid use, it will be important for you to identify and avoid people, places, and situations that could tempt you to use. If this all sounds like it will work for you, let’s get your next appointment scheduled.
Alcohol Use
As noted earlier, another high priority was to assist Joe in controlling his alcohol consumption. Our pri- mary clinical recommendation was abstinence, but Joe quickly acknowledged that he was not going to fol- low that recommendation. Hence, we felt that work- ing to systematically decrease the likelihood of abusive or harmful drinking was the best approach. Some of these skills include identifying the circumstances (loca- tion, people, times, feeling states) associated with heavy drinking. Others are specific to alcohol consumption (e.g., providing information about the alcohol content of common drinks: relationship between drinks con- sumed, body weight, and the blood alcohol curve). Joe and the psychologist discussed controlled-drinking strategies during the first week of treatment while he was being stabilized on an appropriate buprenorphine dose, then revisited these strategies on several occasions during the 24 weeks that Joe was enrolled in treatment through our clinic. During the first session, the psy- chologist discussed with Joe the rationale for reducing his drinking during buprenorphine treatment:
PSYCHOLOGIST: Joe, we want to go over a few reasons for you to give alcohol abstinence a try. First, your history indicates that if you drink, you are more like-
ly to use opioids. You’re not alone in that regard. The scientific evidence is very clear that, for many indi- viduals who seek treatment for opioid use disorder, alcohol and opioid use are closely linked. Specifi- cally, alcohol reduces your ability to think rationally, impairs your inhibition, and distorts your judgment. In other words, after a few drinks, you are more like- ly to engage in risky behaviors, like opioid use, than you would if you were to abstain from alcohol.
JOE: I don’t want to get drunk any more. What about just a few drinks? Is that a problem?
PSYCHOLOGIST: Use of even modest doses of alcohol, even just a few drinks, can significantly decrease your chances of successfully abstaining from illicit opioid use. Our experience, and the experience in other clinics elsewhere around the country, is that you can make greater progress with opioid absti- nence if you abstain from alcohol use than if you continue to drink.
JOE: How long are you suggesting I stop drinking? Are you saying I can’t drink again?
PSYCHOLOGIST: I’m not saying that you can never go back to drinking. We can cross that bridge down the road. But for now, we want you to consider taking a total break from drinking, so that you give yourself the best chance to succeed with remaining abstinent from illicit opioids.
JOE: I’m not sure how much of a problem drinking is for me. I know it’s caused some problems in the past, but I’m just not so sure it’s an issue right now.
PSYCHOLOGIST: Joe, the second thing I wanted to emphasize is that people who use alcohol and opi- oids together are at increased risk for overdose. Both opioids and alcohol are central nervous depressants, which means that they work by slowing down parts of the brain. When combined, opioids and alcohol can depress the central nervous system to the point of respiratory failure, coma, or death. A period of abstinence will put you at a lower risk for overdose and may help you get a better sense of the effect that your current buprenorphine dose has on your body and brain. And still another point to consider is that agreeing to remain abstinent from alcohol represents a concrete demonstration of your commitment to opioid abstinence and substantial lifestyle changes.
JOE: Hey, I’m looking to make some progress here. When I’ve tried to quit opioids on my own, I do well for a while and then I get burnt out, my drinking in- creases, and next thing I know, I’m using pills again.
628 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
Maybe there is something to this idea that drinking affects my opioid use, I’m not sure. But I know I can’t continue like this. How about I agree to cut down to two drinks once or twice a week? That’s a pretty good commitment.
Joe agreed to reduce his drinking for the duration of treatment. An agreement was made for Joe to leave a breath sample and complete a Timeline Follow- Back Interview assessment every time he came to the clinic. The psychologist made it clear that abstinence from drinking was not a requirement for enrollment in treatment. However, regular assessment of alcohol consumption was a tool that could be used to help Joe be successful in maintaining his abstinence from illicit opioids.
In addition to setting goals to reduce his alcohol con- sumption, the therapist worked with Joe to functionally analyze his alcohol use (Figure 15.4). They reviewed specific circumstances under which Joe was more likely to drink or less likely to drink, and listed the negative consequences he had previously experienced from his alcohol use. The therapist and Joe then began to devel- op a plan for finding alternative ways to relax that did not involve the bar or drinking, as well as skills train- ing and role playing on how to refuse alcohol when it was offered (Table 15.2), and how to identify times and places Joe might be tempted to have a drink.
Joe was moderately successful in reducing the num- ber of drinks he consumed each week. He continued to
drink three nights per week on average. However, he met his goal of consuming only two beers each time he drank. Over the course of treatment, he reported only one instance when he drank to the point of intoxica- tion, on Labor Day, when he had friends and family at his house for a cookout. During his subsequent clinic visit, the psychologist completed a functional analysis with Joe, as detailed below, to identify what set up the occasion for him to drink excessively. Joe recommitted to reducing his alcohol consumption for the duration of treatment.
FIGURE 15.4. Form for functional analysis of substance use.
Trigger Thoughts
and feelings Behavior
Consequences
Positive Negative
TABLE 15.2. Components of Effective Refusal
1. No should be the first thing you say. 2. Tell the person offering you drugs or asking you to go
out not to ask you now or in the future if you want to do cocaine. Saying things like “maybe later,” “I have to get home,” or “I’m on medication,” and so forth, just make it likely that he or she will ask again.
3. Body language is important: a. Making good eye contact is important; look directly at
the person when you answer. b. Your expression and tone should clearly indicate that
you are serious. 4. Offer an alternative, if you want to do something else
with that person. Make sure that it is something that is incompatible with cocaine use (taking your children for a walk or to the park, going to work out, etc.).
5. Change the subject to a new topic of conversation.
Substance Use Disorders 629
Psychologist: So it looks like you consumed four drinks on Monday?
Joe: Yep, I had a bunch of friends and family over to my house for a cookout on Labor Day. I was catching up with a bunch of guys who I haven’t seen in years and lost track of how many drinks I had. I had a good time and didn’t do anything stupid. I don’t think it was a big deal.
Psychologist: Joe, you’ve done really well so far with buprenorphine, as well as with this current plan to reduce your drinking. Most folks are not as success- ful as you’ve been in stopping opioid use.
Joe: Oh, I agree. I just feel like I’ve done really well in treatment and I’ve been working long hours, I’d like to be able to relax and unwind with a few drinks if I want to.
Psychologist: It sounds like alcohol consistently helps you relax on the weekends or on evenings after you’ve been working really hard. Although I don’t doubt that’s the case, I wonder if you can identify any other activities that could help you wind down when you have time off from work and don’t put you at risk for relapse to illicit opioid use?
Joe: Hmm, that’s a really good question. For the past few years, my day-to-day life has been so wrapped up in using opioids and making enough money to maintain my use that I’ve really given up most of my hobbies. I used to really enjoy spending time with my family and neighbors, fishing, and even some wood- work, but it’s been years since I’ve spent time doing any of these things.
Psychologist: Joe, that’s a really common report. Many people who are maintained on buprenorphine have to do some work to rediscover healthy activities that they enjoy. You described a couple of really great examples of potentially healthy alternatives to drink- ing. Do you think it’s possible to make time during the upcoming week to go fishing or to spend time on a woodworking project? It might be particularly helpful to think about whether you could engage in either of these activities during the evenings or on weekends when you’ve noticed you’re more likely to drink.
Joe: Well, it’s funny that we’re talking about this today. My dad invited me to go fishing with him this week- end. My dad doesn’t know that I’m in treatment. He’s a real teetotaler, so we never drink while we’re out fishing. Maybe I could make plans to go with him this weekend. It would mean a lot to him if we
were able to spend time together. Plus, it would give me something fun to do. I used to really enjoy fish- ing. I just haven’t had the time or energy over the past few years to plan a trip or to follow through when my dad has invited me.
Psychologist: Joe, that’s a fantastic idea. Making plans ahead of time to engage in meaningful and enjoyable alternatives to drinking are important to continuing your success. Let’s talk a bit more about other activities that you would like to engage in dur- ing the next month and how you can make a plan to make it more likely that you will follow through. By that, I mean let’s really think about what activities you think you can actually engage in during the next month and put concrete plans into place regarding when, where, and how long you will engage in each. This kind of planning might seem a little bit exces- sive, but similar to your drinking goals, if you put make commitments and set concrete goals, it might increase the odds that you follow through, particu- larly if you’re faced with the temptation to drink. Does this sound reasonable to you?
Joe: Yeah, sure, that sounds really good.
As part of this conversation, Joe identified circum- stances that increased the likelihood that he would drink, including spending time with certain friends, long work weeks, experiencing stress or physical ex- haustion, and weekends where he had no healthy activi- ties planned. He identified fishing and woodworking as activities that decreased his likelihood of drinking. Around this time, Joe’s girlfriend was also able to suc- cessfully enroll in treatment. Accordingly, he reported a renewed interest in spending time with her and with a small group of family members and neighbors. That information was updated and used throughout Joe’s course of treatment in self-management planning and in planning for recreational and social activities.
Transition to a New Provider
Shown in Figure 15.5 is a cumulative record of Joe’s illicit opioid use and urinalysis results during the 24- week treatment. Joe was abstinent for illicit opioids at every clinic visit. Although buprenorphine is highly ef- ficacious for the treatment of opioid use disorder, slip- ups are not uncommon. Joe’s success in treatment is notable in that there was not a single instance of illicit opioid use over the 24-week course of treatment.
Once Joe had established a sustained period of illicit
630 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
opioid abstinence, the treatment team began working with him to find an OBOT provider near his home. Although many treatment providers require patients to attend daily or near-daily dosing visits, Vermont’s hub- and-spoke model of care allows stabilized patients like Joe to transition from our clinic to a spoke provider for continued treatment with less intensive dosing require- ments. To facilitate this transition, we obtained a release of information that allowed us to contact a OBOT pro- vider in Joe’s community. Here, we detail how a staff member approached this important transition with Joe.
PSYCHOLOGIST: Hi, Joe. How have things been going? JOE: Pretty good. PSYCHOLOGIST: I wanted to take a couple of minutes
to congratulate you for how well you’ve done in our treatment program. You’ve made it 16 weeks without using illicit opioids.
JOE: Wow. I can’t believe it’s already been that long. Thank you for all of the help that you and the rest of the team have given me. There’s no way I could have done this by myself.
PSYCHOLOGIST: Joe, you’ve done the heavy lifting. Not everyone who enrolls in this program is successful.
You’ve had to change the way that you spend your free time, the people you hang out with, and how you respond to stress and other negative emotions. All of the work that you’ve done so far seems to suggest that you will continue to be successful in treatment, and I think it’s time that we start thinking about what’s next for you.
JOE: That’s true. I guess I have done a lot of work. But thinking about what happens once I’m done with this program makes me a little bit nervous. I’ve really gotten comfortable with you and the rest of the team, and I worry that if I transition to a different provider, they might not be as understanding.
PSYCHOLOGIST: It’s understandable that you feel ner- vous about this transition. Would it make you feel better if we helped you identify a treatment provider who we think would be a good fit?
JOE: Definitely. PSYCHOLOGIST: Do you currently have a primary care
physician? JOE: No, I haven’t been to see a doctor in years. Even
though my job pays well, the benefits aren’t great. I re- ally only go to the doctor when there’s an emergency.
FIGURE 15.5. A cumulative record of Joe’s urinalysis test results (y axis) across 24 consecutive urinalysis tests (x axis) con- ducted during 24 weeks of treatment. Solid symbols indicate scheduled visits, and empty symbols indicate random visits.
0
5
10
15
20
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24
C um
ul at
iv e
Ill ic
it O
pi oi
d- N
eg at
iv e
Sa m
pl es
Treatment Week
Illicit Opioid Abstinence
Substance Use Disorders 631
PSYCHOLOGIST: There are physicians who can pre- scribe buprenorphine to their primary care patients. If I gave you the information for a provider who is located near where you live, would you be willing to call them from my office to set up an appointment for primary care? As part of this conversation, you could also mention your interest in continuing bu- prenorphine treatment with them.
JOE: Sure. I can do that. They will probably ask for my drug screens, huh?
PSYCHOLOGIST: Most likely. The good news is that you’ve been 100% abstinent from illicit opioids dur- ing your time in treatment in our clinic. If you’re willing to sign a release, I can send the provider doc- umentation of how well you’ve done in treatment. It’s also important that you continue to remain abstinent from illicit opioids and other drugs. If you’re able to continue maintaining abstinence from these sub- stances, the transition to this new program should go smoothly. In fact, many patients find that this tran- sition, while unnerving initially, is a really great op- portunity in the long-term. Because you’ve demon- strated a sustained period of abstinence from opioids and other substances, this provider is likely to take a less intensive treatment approach and require fewer clinic visits. Plus visits would be more similar to what you would expect from a family physician and less like a substance use treatment clinic.
JOE: Yeah, that would be perfect. Like I told you before, my boss and my family don’t know that I’m on bup. I’ve never wanted to go to other treatment clinics, because they make you wait in line each morning to dose and I’m always worried that I will see someone I know. If I could get it from a doctor, that would make my life way easier.
PSYCHOLOGIST: Great! If you’re willing to sign this release and set an appointment to see a provider to establish primary care before your next appointment with us, I can go ahead and send a recommendation letter and as well as information documenting your success in our program.
JOE: OK, that sounds like a good plan. PSYCHOLOGIST: In fact, why don’t you go ahead and
call from my office? That way, we will have the ap- pointment set up and you won’t have to worry about remembering to call during a break at work.
JOE: That’s probably a good idea. I’m not always good at remembering to do things like that.
Our experience is that transitions in treatment pro- viders can be destabilizing, even for patients who are doing quite well in treatment. Accordingly, we work with our patients to make this process as smooth and stress-free as possible. By collaboratively developing a transition plan that takes into account the individu- alized needs of each patient, we seek to foster a sense of autonomy and personal investment in the process. However, rather than assuming that patients will know how to independently navigate complex medi- cal systems, we assist each participant in putting this transition plan into place as part of regularly scheduled clinic visits. By doing so, we ensure that patients have established care with a new provider by the end of our 24-week treatment protocol. In this case, Joe was suc- cessful with enrolling in care with an OBOT provider. He established continued buprenorphine treatment, as well as a relationship with a primary care physician who could also help him manage his back and elbow pain and other medical needs.
Illicit Opioid Use Summary
Joe achieved abstinence from illicit opioids throughout the entire 24-week period that he was enrolled in treat- ment through our clinic. He was initially inducted on 8 mg of buprenorphine during the first week of treatment and remained stable on this dose throughout the course of treatment. Regularly scheduled clinic visits were used as opportunities to discuss situations that placed Joe at increased risk for relapse as well as potential coping strategies.
During treatment, Joe’s nephew was hospitalized for a prolonged period. Joe maintained a close relationship with his brother and his brother’s family. Unsurpris- ingly, Joe reported increased emotional distress and cravings for opioids during this time. Treatment staff members worked with Joe to develop a plan for coping with this distress by engaging in activities that helped him unwind and relax without the use of opioids, alco- hol, or other substances.
Other Drug Use
In addition to maintaining abstinence from illicit opi- oids, Joe also remained abstinent from tobacco, mari- juana, cocaine, amphetamines, and benzodiazepines. This is particularly remarkable given the high rates of co-occurring substance use that we see in individuals with opioid use disorder.
632 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
Family/Social Issues
During the intake assessment, Joe noted that he had managed to keep his opioid use a secret from almost ev- eryone in his life except for his girlfriend. Although he never disclosed his treatment status to family or friends, the flexibility of our treatment protocol allowed Joe to engage in enjoyable and meaningful activities that might not have been possible in the context of tradi- tional treatment protocols. For example, Joe initially expressed anxiety about a weekend fishing trip with his father, because he was concerned that his father would learn that he was prescribed buprenorphine. Because Joe was not required to attend daily clinic visits, he was able to go on this trip with his father. Furthermore, a treatment staff member was able to adjust the timing of his dosing window and the volume of the alarm so that Joe was able to dose discretely while out of town and staying in the same house as his father.
Joe disclosed at the intake assessment that his girl- friend also used illicit opioids. This was concerning given that it placed Joe at increased risk for illicit opioid use and diverting his medication. During treatment, our staff provided Joe with a list of treatment provid- ers in his community. His girlfriend successfully en- rolled in treatment and Joe eventually established care through the same clinic following completion of our treatment program.
Employment/Education
Joe entered treatment with a history of full-time em- ployment, which is a good prognostic indicator in itself. However, his demanding schedule precluded enroll- ment in most treatment programs. Because our treat- ment program did not require daily clinic visits after the first week of treatment and allowed for flexibility in scheduling subsequent clinic visits, Joe was able to en- roll and succeed in treatment. Treatment staff members also worked with Joe to avoid working excessive hours and to establish engagement in enjoyable and meaning- ful activities that did not involve substance use.
Joe also described the substantial financial costs as- sociated with buying illicit buprenorphine. He recalled that he initiated illicit buprenorphine use because it was cheaper and safer than oxycontin. Because he was uninsured, treatment through a primary care physician would be costly, and treatment through his designated hub would require him to miss work. Accordingly, he identified illicit buprenorphine use as his most viable financial option. Because he was able to establish treat-
ment for free through our research clinic, Joe was able to save a substantial amount of money and paid off several bills. During treatment, our staff members also worked with Joe to complete the necessary paperwork to obtain health insurance that would cover a substantial portion of his treatment costs following completion of our treat- ment program and alleviate a source of stress.
Psychiatric Monitoring
Joe’s progress is reflected in the pre- to posttreatment changes in BDI-II, BAI, BSI-II, and ASI scores shown in Table 15.3. For example, Joe’s BDI-II score at intake was 15. His BDI-II scores decreased steadily over the course of treatment and reached a score of 5 by the end of treatment. Although his scores on the BAI and BSI-II also decreased over the course of treatment, it is interesting to note that Joe experienced a temporary increase in psychiatric distress between his 4- and 16- week assessments that is reflected by his scores on the BAI, BSI-II, and ASI Psychiatric composite score (com- posite scores range from 0, representing no problems in the past 30 days, to 1, representing severe problems) in Table 15.3. During this time, Joe was coping with his nephew’s hospitalization. He also reported that his girl- friend frequently experienced conflict with her parents, and these stressors made him feel anxious. Although Joe never reported suicidal ideation at any point during treatment, staff members assessed him for symptoms of depression and suicidality at each clinic appointment as part of the routine care that we provide as part of IBT. Furthermore, when Joe reported the presence of stressors and crises, the psychologist and treatment staff worked with him to establish a plan for implementing healthy coping skills that did not involve substance use.
Summary of Treatment Progress
Joe achieved sustained abstinence from illicit opioids and other illicit substances. This progress is reflected in the decrease in his ASI Drug composite score after he began treatment (Table 15.3). In addition, Joe increased his involvement in enjoyable and meaningful activities that did not involve substance use, improved his finan- cial situation, reported decreased symptoms of anxiety and depression, and secured treatment with a local pro- vider for himself and his girlfriend. Joe continued to drink throughout treatment; however, he rarely drank to the point of intoxication and worked with treatment staff members to implement controlled-drinking strate- gies.
Substance Use Disorders 633
Follow‑Up
Following completion of the 24-week treatment proto- col, Joe was eligible for treatment in a spoke as part of Vermont’s hub-and-spoke system for opioid use disor- der. With the help of the treatment team, he was able to establish continued treatment through an OBOT provider close to his home. This transition was possible because Joe was able to demonstrate stability in treat- ment and 24 weeks of abstinence from illicit opioids. At the time of this writing, Joe had continued in treat- ment through the spoke for 5 months; thus, we have some information pertaining to his progress following his completion of our treatment program.
Joe largely sustained the excellent progress he made during treatment in our clinic. As part of his new treat- ment program, he completed urine toxicology tests once monthly. All urine toxicology tests conducted dur- ing follow-up were negative for illicit opioids, and Joe also denied any illicit opioid use during this time. Fur- thermore, his urine toxicology tests were negative for all other illicit substances. He continued to report moder- ate use of alcohol throughout follow-up; however, his rate of drinking was similar to what he reported during participation in our treatment program.
Regarding other areas of functioning, depression and anxiety symptomatology remained well below clinical levels throughout the follow-up period. Joe remained healthy and reported no medical problems during the 5 months. He sustained full-time employment through- out the first 4 months of the follow-up period. Unfortu-
nately, he was laid off from his job due to the COVID- 19 pandemic. This change in his employment status did not precipitate a relapse back to opioid or other drug use, which underscores the substantial progress he made with those problems. Joe’s current treatment provider continues to check in with Joe frequently and commended him on his sustained progress in abstain- ing from opioids during this challenging time.
CONCLUDING COMMENTS
In this chapter we have presented the most up-to-date scientific information available on effective clinical management of illicit substance use disorders, plac- ing special emphasis on opioid use disorder, which has been at crisis levels in the United States for the past de- cade or more. In the process, we have tried to illustrate what have come to be considered principles of effective treatment for illicit substance use disorders in general, using opioid use disorder as a specific exemplar. We have reviewed evidence-based practices, including ef- ficacious, multielement treatments approaches such as the CRA + vouchers intervention for cocaine use disorder, which has an outstanding record of efficacy. However, we also shared how the current opioid crisis has altered treatment practices in our own clinics and many others throughout the United States. We hope that this information offers insights into the important elements of effective treatment for illicit substance use disorders generally, including the special features that
TABLE 15.3. Scores on the BAI, BDI‑II, Global Severity Index of the BSI‑II, and ASI over the 24 Weeks That Joe Was Enrolled in Treatment
Score Intake 4 weeks 8 weeks 12 weeks 16 weeks 20 weeks 24 weeks
BAI 8 4 5 6 3 4 1
BDI-II 15 7 10 7 4 4 5
BSI-II 0.32 0.19 0.32 0.17 0.17 0.17 0.06
ASI subscales Medical 0.00 0.00 0.00 0.00 0.00 0.00 0.00 Employment 0.00 0.00 0.00 0.00 0.00 0.00 0.00 Alcohol 0.00 0.00 0.00 0.00 0.00 0.00 0.00 Drug 0.34 0.00 0.00 0.00 0.00 0.00 0.00 Legal 0.00 0.00 0.00 0.00 0.00 0.00 0.00 Family/Social 0.00 0.00 0.00 0.00 0.00 0.00 0.00 Psychiatric 0.00 0.178 0.711 0.00 0.244 0.00 0.00
634 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
treatment for opioid use disorder entails. We also hope that this information makes the job of clinicians who are out there in the trenches treating opioid and other substance use disorders a little easier and, we hope, their practices more effective.
ACKNOWLEDGMENTS
Preparation of this chapter was supported in part by Na- tional Institute on General Medical Sciences Grant No. P20GM103644 and National Institute on Drug Abuse Grant Nos. DA042790, DA036670, 1DA047867, and DA050283.
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Perhaps the best-kept secret among health and mental health practitioners everywhere is the marked superiority of brief psychological treatments for insomnia compared to popular and frequently adver- tised medications. With approximately 6% of members of the adult population suffering from insom- nia to the degree that they meet diagnostic criteria, and as many as 10–15% reporting that insomnia interferes significantly with their daytime activities, the problem is significant and most often poorly treated. Insomnia very frequently accompanies other psychological disorders, and recent evidence indicates that insomnia predates and may contribute to or even cause these comorbid disorders, which is all the more reason why every health and mental health practitioner should be aware of the cutting-edge brief interventions presented in this chapter. Indeed, the American Academy of Sleep Medicine and the American College of Physicians recommend these protocols as a first-line treat- ment for people with all forms of insomnia, including those currently using hypnotic drugs. Among the leaders in this burgeoning field, Kaplan and Harvey outline a state-of-the-art integrated behavioral and cognitive approach, with strong evidence for both efficacy and durability, that should be in the armamentarium of every health professional. —D. H. B.
s leep disorders are common and associated with con- siderable morbidity and functional impairment. In
this chapter, we focus on insomnia given its high preva- lence and public health impact. We also briefly discuss hypersomnolence disorder given the rising possible role of psychological treatments for patients with this disorder, along with transdiagnostic approaches, given the realization that insomnia is often comorbid either subclinically or clinically with other sleep and circadian problems. A wide range of other sleep disorders, which are beyond the scope of this chapter, are each prevalent and impairing. For example, obstructive sleep apnea/ hypopnea involves transient closure of the upper airway during sleep that results in pauses in breathing, often leading to daytime sleepiness and cardiovascular prob-
lems. Restless legs syndrome involves an involuntary urge to move one’s legs during sleep that leads to partial or full awakenings, resulting in sleep fragmentation and daytime sleepiness. It is important for clinicians to have a working knowledge of these and other sleep disorders. These clients should be referred to a sleep center, neu- rologist, or other health professional who can offer a diagnostic assessment and treatment (Kryger, Roth, & Dement, 2017).
Insomnia is a prevalent sleep disturbance that in- volves difficulty with falling asleep, staying asleep, or waking too early in the morning. It is associated with considerable functional impairment and health-related costs. Insomnia is often comorbid with, and predicts the development of, numerous psychological and medi-
C H A P T E R 16
Treatment of sleep Disturbance
Katherine A. Kaplan Allison G. Harvey
Sleep Disturbance 639
cal conditions. As such, insomnia represents an impor- tant target for intervention. We begin this discussion with a brief overview of human sleep, along with di- agnostic and theoretical considerations, because this knowledge provides the basis for delivering cognitive- behavioral therapy for insomnia (CBT-I), which is the focus of this chapter.
SLEEP AND INSOMNIA
Sleep Stages
Human sleep can be divided into (1) non-rapid-eye- movement (NREM) sleep that can be subdivided into three stages (N1, N2, and N3) through which sleep pro- gressively deepens, and (2) rapid-eye-movement (REM) sleep. In adults, each NREM–REM cycle spans 70–120 minutes (Kryger et al., 2017). NREM sleep is thought to be important for conservation of energy and resto- ration. This phase of sleep is associated with the most rapid cell division in some tissues, as well as increased protein synthesis (Kryger et al., 2017). The functions of REM sleep are understood to include a role in learning (Karni, Tanne, Rubenstein, Askenasy, & Sagi, 1994) and in the unlearning of irrelevant information (Crick & Mitchison, 1983), as well as memory consolidation, emotional processing, and mood/emotion regulation (Krause et al., 2017). Sleep promotes the clearance of toxic waste by-products that build up throughout the day (Xie et al., 2013). It is well established that sleep deprivation has detrimental effects in many domains of health (Zee & Turek, 2006), including the immune system, the neuroendocrine system, and the cardiovas- cular system (Van Someren et al., 2015). Given these important functions, disorders of sleep have major pub- lic health implications.
Two‑Process Model of Sleep
The two-process model of sleep regulation (Borbély, 1982) is important in that it underpins the treatment we describe later. In fact, many clinicians describe this model to clients as part of the rationale for delivering stimulus control and sleep restriction described below. The model proposes that sleep and wakefulness are de- pendent on two processes, a homeostatic process and a circadian process (Achermann & Borbély, 2017). The homeostatic process influences sleep likelihood. Sleep pressure increases with time spent awake, resulting in
an increased tendency to sleep when a person has been sleep-deprived, and a decreased tendency to sleep after having had a substantial amount of sleep or a substan- tial nap. The circadian rhythm is an internal biological clock that operates on roughly a 24-hour basis. It is re- sponsible for variations in melatonin, temperature, and other biological functions, including levels of alertness throughout the day (Lack & Bootzin, 2003). These two processes work together such that sleep is likely to occur when sleep pressure (the homeostatic process) is high and level of alertness (the circadian process) is relatively low. Thus, if a person naps in the afternoon, he/she may have difficulty falling asleep that evening because homeostatic sleep pressure is low; likewise, if a person goes to bed early following a poor night of sleep, even if sleep pressure is high, circadian arousal may prevent sleep onset from occurring.
Some, but not all, studies have found impaired sleep homeostasis in persons with insomnia (e.g., Besset, Villemin, Tafti, & Billiard, 1998; Stepanski, Zorick, Roehrs, & Roth, 2000). Likewise, sleeping at odds with the endogenous circadian pacemaker is suspected to contribute to some, but not all, cases of insomnia (Flynn-Evans et al., 2017). Environmentally induced phase shifts, such as those occurring as a result of shift work or jet lag, can cause acute insomnia. There is also evidence that hyperarousal, a central notion in theories of insomnia that we discuss below, may not be a 24- hour issue for some but rather may fluctuate according to circadian influences (Perlis, Smith, & Pigeon, 2005).
Sleep across the Lifespan
Sleep changes across the lifespan. This is very impor- tant, because it impacts therapists’ expectations of sleep outcomes when working with clients of different ages. With age, slow-wave sleep decreases, while lighter sleep and awakenings become more common across the night (Ohayon, Carskadon, Guilleminault, & Vitiello, 2004). Moreover, both circadian and homeostatic processes are influenced by age. For example, with age, the circadian system grows increasingly less sensitive to zeitgebers such as melatonin and morning light (Hood & Amir, 2017; Van Someren, 2000). Throughout adolescence, there is a well-documented circadian shift in favor of later bedtimes and rise times, with a more slowly build- ing homeostatic pressure to fall asleep (Jenni, Acher- mann, & Carskadon, 2005). This pattern can result in initial insomnia (difficulty falling asleep at night). In
640 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
middle to older adulthood, circadian shifts can again favor early bedtimes and rise times, resulting in termi- nal insomnia (early morning awakening with difficulty falling back asleep (Ancoli-Israel, 2009). Along with circadian rhythms, the homeostatic process also shows age-dependent changes across the lifespan. Individu- als in their 60s and 70s showed reduced homeostatic pressure to sleep and achieve less total sleep time (TST) relative to members of a comparison group in their 20s (Klerman & Dijk, 2008).
THE INSOMNIA DIAGNOSIS
We describe in this section diagnostic considerations, reviews prevalence, and comorbidity, and present sev- eral models of insomnia that have been influential in conceptualizing CBT-I treatment targets.
There are three main classification systems that may be used to define insomnia: the third edition of the International Classification of Sleep Disorders (ICSD-3; American Academy of Sleep Medicine, 2014), the Re- search Diagnostic Criteria (RDC; Edinger et al., 2004), and the Diagnostic and Statistical Manual of Mental Disorders (DSM-5; American Psychiatric Association, 2013). Within DSM-5 criteria, a diagnosis of insom- nia may be given when there is a subjective complaint of trouble falling or staying asleep at least 3 nights per week for a period of 3 months or more. These difficul- ties must be associated with daytime impairment and must not be better accounted for by another medical or psychiatric condition.
These insomnia diagnostic criteria have been further clarified with quantitative criteria, which require that self-reported sleep-onset latency (SOL) and/or wake after sleep onset (WASO) must be greater than 30 minutes for at least 3 nights per week over a period of at least 6 months (Lichstein, Durrence, Taylor, Bush, & Riedel, 2003). Note that self-reports of insomnia complaints are sufficient for the diagnosis, without ob- jective evidence for sleep disturbance (see “Assessment” below).
Insomnia Prevalence and Comorbidity
It is estimated that about 6–10% of the general adult population meet diagnostic criteria for a formal diag- nosis of insomnia. Approximately 33% of the general population report some significant symptoms of insom- nia. Additionally, as many as 10–15% of individuals in
the general adult population suffer from the daytime sequelae of sleep disturbance (Ohayon, 2002). Other surveys suggest that health-related costs of insomnia are considerable, regardless of the diagnostic system used to define it (Roth et al., 2011).
Because insomnia can be associated with a wide range of medical illnesses and psychological disorders, the previous DSM edition (i.e., DSM-IV-TR; Ameri- can Psychiatric Association, 2000) made distinctions between primary and secondary, or comorbid, insom- nia. The distinction between primary and secondary insomnia was blurred, however, by epidemiological re- search suggesting that insomnia may predate, and pre- dict, psychological disorders (Breslau, Roth, Rosenthal, & Andreski, 1996; Ford & Kamerow, 1989). Indeed, a National Institutes of Health (2005) state-of-the- science conference concluded that the term secondary should be replaced with comorbid on the basis of evi- dence that insomnia that is comorbid with another dis- order likely contributes to the maintenance of the dis- order (Harvey, 2001; Smith, Huang, & Manber, 2005). These conclusions were recognized in DSM-5, which does not distinguish between primary and secondary insomnia, but has only one insomnia disorder.
For older adults, insomnia is often accompanied by medical illnesses that may complicate issues of assess- ment and treatment, further compounding burden and cost (Morin et al., 2006). In a large epidemiological study, Ford and Kamerow (1989) found that there is ap- proximately a 50% comorbidity rate between insomnia and other psychological disorders or medical illnesses; these high rates of comorbidity have been replicated in subsequent research (Budhiraja, Roth, Hudgel, Budhi- raja, & Drake, 2011; Sarsour, Morin, Foley, Kalsekar, & Walsh, 2010). In cases of comorbid insomnia, ad- ditional empirical and clinical attention may be espe- cially important, because there appears to be a cyclical influence of sleep disturbance and medical illness or psychological disorders, with worsening sleep problems leading to a decline in general health and increased psy- chiatric symptoms that, in turn, worsen sleep problems. Fortunately, evidence suggests that insomnia responds to CBT-I treatment even if the accompanying disorder is not under control (Rybarczyk, Lopez, Schelble, & Stepanski, 2005). Treatment effects are generally mod- erate to large for CBT-I administered in the context of accompanying disorders or illnesses (Geiger-Brown et al., 2015; Wu, Appleman, Salazar, & Ong, 2015), with some benefit for the comorbid illness observed (Wu et al., 2015).
Sleep Disturbance 641
Models of Insomnia
We begin this section with a discussion of an influen- tial overarching framework, the Spielman model. We then move on to describe several behavioral, cognitive, and combination models of insomnia that help to ex- plain particular facets of the disorder that should be ad- dressed and treated in CBT-I.
Spielman’s Three‑Factor Model
This diathesis–stress model is often referred to as the three-factor, or the three-P, model. According to Spiel- man, Caruso, and Glovinsky (1987), acute or short- term insomnia occurs as a result of predisposing factors (e.g., traits) and precipitating factors (e.g., life stressors). This acute form can then develop into a chronic or lon- ger-term disorder as a result of perpetuating factors (e.g., poor coping strategies). Predisposing factors (e.g., a ten- dency to worry) constitute a vulnerability for insomnia, and this vulnerability remains across the life of the dis- order. Precipitating factors trigger acute insomnia, but their influence tends to wane over time. In contrast, perpetuating factors take hold of and maintain insom- nia. CBT-I targets these perpetuating factors, seeking to reduce the additive effects of predisposing, precipi- tating, and perpetuating factors below the threshold for insomnia diagnosis.
Behavioral Models
One of the most important behavioral models for in- somnia, the stimulus control model (Bootzin, 1972), is based on the conditioning principle that insomnia oc- curs when the bed or bedroom ceases to be paired spe- cifically with sleep, but has become paired with many possible responses (e.g., being awake and anxious about not sleeping). As will become evident later in this chap- ter, this theory has led to the development of “stimulus control,” an intervention with strong efficacy (Morin et al., 2006).
Cognitive Models
Some of the earliest research on cognitive processes in insomnia indicated that individuals with insomnia tend to overestimate wakefulness and underestimate TST (Bixler, Kales, Leo, & Slye, 1973; Carskadon et al., 1976), and researchers began to explore the role of cog- nitive arousal in insomnia (Borkovec, 1982; Lichstein
& Rosenthal, 1980). Seminal work in the 1990s high- lighted the importance of unhelpful beliefs about sleep (Morin, 1993) and delineated the content of presleep intrusive thoughts (Watts, Coyle, & East, 1994; Wick- low & Espie, 2000). The 2000s ushered in an increase in empirical attention to other cognitive mechanisms in insomnia, including attention to threat and the use of safety behaviors to allay perceived threats (Espie, 2002; Harvey, 2005; Harvey, Tang, & Browning, 2005).
One cognitive model of insomnia aims to specify the cognitive processes that serve to perpetuate insomnia (Harvey, 2002a) and represents an important com- ponent of CBT-I as outlined here. According to this conceptualization, contributors to the maintenance of insomnia include the following cascade of cognitive processes that operate at night and during the day: (1) worry and rumination, (2) selective attention and mon- itoring, (3) misperception of sleep and daytime deficits, (4) dysfunctional beliefs about sleep (based on Morin, 1993), and (5) counterproductive safety behaviors that serve to maintain beliefs. Many of the specific predic- tions generated by this model have been empirically tested, leading to refinement of the model (Harvey, 2005) and a cognitive therapy treatment approach sup- ported by both an open trial (Harvey, Sharpley, Ree, Stinson, & Clark, 2007) and a randomized controlled trial (RCT; Harvey et al., 2014).
Combination Models
Morin’s (1993) cognitive-behavioral model of insomnia incorporates cognitive, temporal, and environmental variables as both precipitating and perpetuating factors, with hyperarousal as the key precipitating factor of in- somnia. Conditioning can then exacerbate this arousal. For example, a person may associate temporal (e.g., bed- time routines) and environmental (e.g., bedroom) stim- uli with fear of being unable to sleep. Worry and rumi- nation may then result. Additional perpetuating factors may ensue, including, as in the cognitive model, daytime fatigue, worry, and emotional distress about sleep loss and maladaptive habits (e.g., excessive time in bed).
In summary, adequate treatment of insomnia tar- gets both cognitive and behavioral processes to address their mutually maintaining effects. Each of the models reviewed earlier has been influential in conceptualiz- ing the insomnia diagnosis and identifying treatment targets. In the next section, we review evidence for the effectiveness of CBT-I as a multicomponent treatment for insomnia.
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EVIDENCE FOR CBT‑I TREATMENT
CBT-I has been established as an effective treatment in multiple meta-analyses (Irwin, Cole, & Nicassio, 2006; Montgomery & Dennis, 2003; Morin, Culbert, & Schwartz, 1994; Trauer, Qian, Doyle, Rajaratnam, & Cunnington, 2015) and in a updated review by the Stan- dards of Practice Committee of the American Academy of Sleep Medicine (Morin et al., 2006). Moreover, the effects of CBT-I appear to persist over time (van der Zweerde, Bisdounis, Kyle, Lancee, & van Straten, 2019). As such, CBT-I is currently recommended over pharma- cotherapy as the first-line treatment by the American College of Physicians (Qaseem et al., 2016).
A number of RCTs have compared one or more components of CBT-I to each other and/or to placebo. One review indicated that CBT-I is highly effective and has sustainable gains over long-term follow-up, up to 24 months in adult and older adult samples (Morin et al., 2006). This review used the American Psychologi- cal Association’s Society of Clinical Psychology crite- ria for well-supported, empirically based treatments (Chambless & Hollon, 1998) and concluded that these criteria are met by stimulus control, paradoxical inten- tion, relaxation, sleep restriction approaches, and the administration of multiple components in the form of CBT-I. The sleep hygiene intervention alone has not been found to be effective as a treatment for insom- nia. Likewise, a recent dismantling RCT comparing cognitive therapy, behavior therapy, and combined cognitive-behavioral therapy (CBT) to treat insomnia demonstrated significant improvements across all three conditions on measures of insomnia symptom severity, nighttime sleep disturbances, and daytime function- ing, and these improvements were generally sustained at 6-month follow-up. Combined CBT was associated with greatest improvements, the improvements associ- ated with behavior therapy were faster but not as sus- tained, and the improvements associated with cognitive therapy were slower and sustained (Harvey et al., 2014).
There are multiple classes of medications, both pre- scribed and over the counter, that can be used to treat insomnia (Sateia, Buysse, Krystal, Neubauer, & Heald, 2017), including benzodiazepines, nonbenzodiazepine hypnotics (e.g., zolpidem, zaleplon, and eszopiclone), antidepressants (e.g., trazodone and doxepin), and over- the-counter antihistamines (e.g., diphenhydramine and doxylamine). However, there is evidence that nonphar- macological interventions for insomnia are more ac- ceptable to clients (Morin, Gaulier, Barry, & Kowatch,
1992) and produce more durable effects (Morin et al., 2009; Sivertsen et al., 2006) than do hypnotic medica- tions alone. Perhaps recognizing this, CBT-I is current- ly recommended over pharmacotherapy as the initial treatment approach by the American College of Physi- cians (Qaseem et al., 2016). In the case of comorbid insomnia, the optimal intervention would alleviate in- somnia without causing adverse interactions with other prescribed medication; therefore, a nonpharmacologi- cal intervention may be the best choice for these cases of insomnia (Harvey, 2008).
In summary, CBT-I appears to be an efficacious and promising intervention to address sleep disturbance, particularly in treating comorbid insomnia. In the next section, we discuss treatment objectives, setting, and client–therapist variables that are considered when ad- ministering CBT-I.
THE CONTEXT OF THERAPY
Treatment Objectives and Structure
CBT-I aims to target and reverse the behavioral and cog- nitive processes that maintain insomnia. This is done in a time-limited format. Treatment usually comprises six to eight sessions, each 50 minutes in length. Because there are multiple targets to address in a limited period of time, it is essential that treatment be agenda-driven, goal-oriented, and center around an individualized case formulation derived for each client.
The overall treatment structure is illustrated in Fig- ure 16.1. The first session of treatment focuses on ex- plaining treatment rationale and objectives, deriving a case formulation, and providing psychoeducation on sleep and insomnia. This is generally followed by two to three sessions with a behavioral emphasis, and two to three sessions with a cognitive emphasis. However, the therapist will decide whether to pursue behavioral targets or cognitive targets, or some combination of both, based on the individualized case formulation (Manber & Carney, 2015). For example, a client who presents with excessive worry, rumination, unhelpful beliefs about sleep, and myriad safety behaviors is likely to benefit from treatment that begins with cognitive targets. A client whose sleep disturbance is character- ized by schedule irregularity, daytime napping, and ex- cessive time in bed is likely to benefit from treatment that begins with behavioral targets. The final session summarizes tools learned, and anticipates and plans for sleep setbacks.
Sleep Disturbance 643
Setting
The CBT-I overview presented here is an outpatient- based treatment delivered in an individual rather than group setting. Sessions are typically held weekly. The therapist will find it helpful to have a table on which to spread out materials (diaries, handouts, thought re- cords), along with a calculator to derive weekly sleep averages and sleep efficiency scores. The client is en- couraged to keep all treatment-related materials in a binder or folder and reinforced for bringing this weekly to session.
Though treatment is conducted on an individual basis, the social and familial context of the sleep en- vironment should not be ignored. Clients may have bedmates, children, or pets that disrupt sleep, and
often the therapist has to improvise to adapt treatment guidelines to the lives of individual clients. Social con- texts, when used strategically, can also facilitate treat- ment adherence and behavior change. Encouraging the use of friends, family, and technology to aid in adher- ence to sleep principles—for example, in regularizing sleep–wake times, sleep restriction, and stimulus con- trol, each of which is described below—can be help- ful. Many clients use cell phone alarms as reminders to begin a wind-down period or to wake up at the same time each morning. Likewise, recruiting the support of family and friends to call or visit in the morning so as to prevent oversleeping, or to respect a “no-calls” period in the hour before bed to promote a relaxing wind down, can be crucial to the success of the strategies.
• Treatment overview • Case formulation • Goal setting • Motivational interviewing • Sleep and circadian education
Session 1: Introduction
• Sleep restriction • Stimulus control • Sleep hygiene • Wind-down routine • Wake-up routine
3 Sessions: Behavioral Targets
• Worry • Attention and monitoring • Unhelpful beliefs about sleep • Safety behaviors • Daytime energy
3 Sessions: Cognitive Targets
• Treatment review • Anticipate obstacles • Lapse vs. relapse • Review goal attainment
Session 8: Relapse Prevention
FIGURE 16.1. Treatment flow diagram. Note the practitioner’s discretion in beginning with behavioral or cognitive targets as indicated by case conceptualization.
644 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
Client Variables
The treatment described here is for individuals who ex- perience insomnia, defined as difficulty falling or stay- ing asleep at least 3 nights per week. This treatment is equally suitable for men and women. Though we present a treatment here that is suitable for adults, ad- aptations can be readily made for teenagers (Clarke & Harvey, 2012; Harvey, 2009; Kaplan et al., 2019). This treatment is effective in clients who present with a va- riety of comorbid diagnoses, including anxiety, depres- sion, and other psychological conditions, along with a variety of medical comorbidities. Special considerations are needed for clients with concurrent alcohol and sub- stance use disorders given their myriad effects on sleep.
Many clients who present for treatment are taking concurrently a sleep medication, either prescribed or over the counter, and many of these medications are taken nightly. Clients may wish to reduce or cease their use of these medications. There is an evidence base for how to approach discontinuation of prescribed medi- cation, and readers are referred to several protocols for more information (Belleville, Guay, Guay, & Morin, 2007; Hintze & Edinger, 2018; Lichstein et al., 1999). Any change to a prescribed medication regimen is made in collaboration with the prescribing provider. Over- the-counter sleep agents do not appear to have substan- tial discontinuation effects (Morin, Koetter, Bastien, Ware, & Wooten, 2005) and may be stopped without physician collaboration.
Therapist Variables
It is essential to establish a collaborative working re- lationship between clinician and client. Along with genuine empathy and support, a strong therapist– client alliance is necessary, because much of the treatment depends on the client’s compliance with implementing different clinical recommendations. In this context, the therapist’s role is one of facilitator and problem-solver. He/she provides specific guidelines, instructions, and corrective feedback. Therapy is directive, task-oriented, and teaches clients problem-solving skills to improve sleep and to cope with residual insomnia after complet- ing treatment. In turn, the client is also actively en- gaged in the therapeutic process and is responsible for implementing clinical procedures.
The treatment is highly structured and requires time, effort, and diligent adherence with homework as- signments. This cannot be overemphasized. Although
some procedures may initially appear simplistic and straightforward, the client is cautioned that regular and consistent adherence to the entire program, including homework, is the key to successful outcome.
It is often necessary to contrast the CBT-I approach with medication treatment for insomnia. It is essential to point out that with CBT-I, there is no “quick fix” for chronic insomnia. To avoid premature termination, the client is cautioned that no immediate results should be expected after one or two office visits. A time com- mitment of 6–8 weeks is required. This time-limited format is emphasized to maximize compliance. Consid- ering that most clients will have suffered with insomnia for years, this represents a very short investment of time.
It is also important to convey a sense of hope and model a positive yet realistic attitude regarding out- come. An occasional poor night of sleep, particularly associated with a stressor, is normal and should be an- ticipated. Also, it is important to emphasize that a goal of treatment is to equip the client with tools and meth- ods to continue making sleep gains once therapy is over.
Finally, therapists work with clients to encourage a system of regular rewards and positive reinforcement to facilitate behavior change. Clients can be motivated to comply with treatment recommendations with use of small daily rewards, such as a morning trip to the coffee shop or taking an enjoyable bath. Likewise, therapists are encouraged to highlight successes in sessions rather than failures. For example, if a client’s weekly sleep diary reveals that naps were taken on 4 of 7 days, praise the client for the 3 days naps were not taken, and per- haps do a functional analysis of how naps were avoided. Point out positive nighttime sleep parameters (e.g., re- duced time to fall asleep or nighttime wakefulness) on days that naps were not taken.
ASSESSMENT
Subjective Estimates
As is evident from DSM-5 criteria, insomnia is defined subjectively. As such, three levels of self-reported sleep data are collected from clients during an assessment for insomnia (see Buysse, Ancoli-Israel, Edinger, Lichstein, & Morin, 2006, for further information on insomnia assessment). First, a clinical sleep history is taken to as- sess for diagnostic criteria and the presence of comorbid problems. Information gathered includes the duration, frequency, and severity of nighttime sleep disturbance, including estimates of the key sleep parameters: SOL,
Sleep Disturbance 645
number of awakenings after sleep onset, total amount of time awake after sleep onset, TST, and an estimate of sleep quality (SQ). Information about the onset and duration of the insomnia and type of symptoms (i.e., sleep onset, sleep maintenance, early morning waking problem, or combinations of these) is collected. A de- scription of the daytime correlates and consequences of insomnia is key. In addition, obtaining information about medications (prescription and over the counter) and screening for the presence of comorbid psychologi- cal disorders and medical problems (including other sleep disorders) are also important.
Second, one or more validated measures can be used to index global SQ (e.g., the Pittsburgh Sleep Quality Index; Buysse, Reynolds, Monk, Berman, & Kupfer, 1989), insomnia (e.g., the Insomnia Severity Index; Bas- tien, Vallieres, & Morin, 2001), and daytime sleepiness (e.g., the Epworth Sleepiness Scale; Johns, 1991). The Duke Structured Interview for Sleep Disorders (Eding- er et al., 2009), a semistructured interview that assesses research diagnostic criteria for sleep disorders, may also be used to establish sleep disturbance diagnoses.
Third, asking the client to complete a sleep diary (Carney et al., 2012) each morning as soon as possi- ble after waking for 2 weeks can provide prospective estimates of sleep. A sleep diary provides a wealth of information, including night-to-night variability in sleeping difficulty and sleep–wake patterns, and can be used to determine the presence of circadian rhythm problems, such as a delayed sleep phase or an advanced sleep phase. Also, sleep diaries reduce several problems associated with the methods just discussed that rely on retrospective report, such as answering on the basis of saliency (i.e., the worst night) or recency (i.e., last night) (Smith, Nowakowski, Soeffing, Orff, & Perlis, 2003). Interestingly, the “enhanced awareness” of sleep patterns facilitated by diary keeping can reduce anxi- ety over sleep loss and thus contribute to better sleep (Morin, 1993, p. 71). A sample sleep diary is illustrated in Figure 16.2. Clients who prefer to track sleep on mo- bile devices may wish to download the free app CBT-I Coach (Koffel et al., 2018) to track and graph sleep.
Objective Estimates
Polysomnography (PSG) is used to classify sleep into various stages. It involves placing surface electrodes on the scalp and face to measure electrical brain activity, eye movement, and muscle tone. The data obtained are used to classify each epoch by sleep stage and in terms
of sleep cycles (NREM and REM). Disadvantages as- sociated with PSG include its expense, discomfort for participants, and labor-intensive nature. Although PSG is not needed for the routine assessment of insomnia (Reite, Buysse, Reynolds, & Mendelson, 1995), it is important if the client is suspected of having a comor- bid sleep disorder, such as sleep apnea or periodic limb movement disorder.
Actigraphy is an alternative means of providing an objective estimate of sleep. An actigraph is a small, wrist- worn device that contains a sensor, a processor, and memory storage. The sensor samples physical motion and can be downloaded and analyzed to generate various estimates of sleep parameters, though it cannot differen- tiate stages of sleep. When compared to PSG, actigraphy is reasonably accurate and highly sensitive to detecting sleep (Marino et al., 2013). It is worth noting, however, that actigraphy validation for insomnia patients has had variable success. Actigraphy appears to be less accurate in populations with fragmented sleep (Paquet, Kawinska, & Carrier, 2007) and in periods of quiet wakefulness, such as the sleep-onset period (Lichstein et al., 2006). Numerous studies have documented that actigraphy has a tendency to overestimate TST and underestimate wake time during sleep in insomnia (Lichstein et al., 2006; Vallieres & Morin, 2003). Thus, although actigraphy is not required for the assessment of insomnia and may be subject to overestimation of TST, it nonetheless provides an overview of the sleep–wake cycle in a way that is mini- mally intrusive (Smith et al., 2018).
INTRODUCING TREATMENT
Following an assessment of insomnia history, severity, and collection of 7–14 days of diary data, a first treat- ment session with the client should be scheduled. This first session has several critical treatment components: to provide a treatment overview and rationale, to derive an individualized case formulation, and to educate the client about basic sleep processes. After this initial ses- sion, behavioral and cognitive processes are selectively targeted. The treatment concludes with a review of tools and a focus on relapse prevention.
Treatment Overview
As a first introduction to treatment, the therapist pres- ents an overview of the therapy in the first session. This can take the following format:
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Sleep Disturbance 647
“The treatment that you will receive is called ‘cog- nitive-behavioral therapy’ for sleep (CBT for short). CBT is a psychological intervention that is designed to help you change some behaviors (sleep habits, sleep schedules) and thoughts and beliefs (worries about sleeplessness and its consequences) that con- tribute to and perpetuate your sleep problem. These are selected as the target, because research shows this is an effective strategy. The main characteris- tics of CBT for insomnia are that it is sleep-focused, relatively brief compared to other types of psycho- therapy, and you take a very active role in your own treatment. Your treatment will involve six to eight weekly, 50-minute individual therapy sessions. The main agenda of each of these sessions will include reviewing your sleep diary from the previous week, providing practical recommendations and home projects to facilitate changes sleep habits, schedules, beliefs, thoughts, and so forth, and to help you solve problems that may interfere with your progress and homework assignments. The main objective is to help you improve your sleep and your daytime func- tioning. To achieve these goals, you will be provided with direct guidance, but you will be responsible for implementing the recommendations at home.”
After presenting this overview, the therapist provides additional information about how this intervention was developed and about its clinical effectiveness. This information is useful to enhance treatment credibility and to induce a sense of hope in clients who have long- standing insomnia, and at the same time cautions oth- ers against expecting rapid changes in sleep.
“This treatment has been developed by psychologists as an alternative to medication therapies. It is based on clinical research and has been tested extensive- ly throughout the world. This treatment has been shown effective with thousands of individuals suffer- ing from insomnia problems similar to yours. This treatment will help improve your sleep and, most im- portantly, develop self-management skills to regain control of sleep and cope more adaptively with occa- sional sleep difficulties you may encounter even after completing this program. Although it may take more time to improve your sleep with this approach than with medication, research has shown that CBT pro- duces sleep improvements that are well maintained long after completing treatment.”
Therapists are encouraged to emphasize the collab- orative nature of the treatment and the importance of homework as core foundations in treatment. The cor- nerstone of this approach, which is common to most CBTs, is that the client assumes an active role in his/ her treatment. As such, he/she is encouraged to develop new skills to achieve better control of his/her sleep.
Maintaining a daily sleep diary is an essential require- ment of treatment, and this is made very clear during the first therapy session. Therapists explain that a daily diary is important to (1) document the nature and sever- ity of the initial sleep problem; (2) assess night-to-night variations in sleep patterns and identify factors that con- tribute to improved or worsened sleep; (3) monitor treat- ment progress; and (4) evaluate compliance with treat- ment procedures. The treatment can become difficult if a client fails to monitor his/her sleep or forgets to bring in his/her diary. As noncompliance with self-monitoring is likely related to noncompliance with treatment proce- dures, therapists are encouraged to address this issue up front if it becomes a problem. There is no need for the client to monitor the clock in order to provide accurate times. Only one’s “felt sense” of the timing of sleep is needed. If self-monitoring is overlooked on a particu- lar day, clients should be discouraged from going back and estimating sleep parameters retrospectively. Com- pliance with the diary daily is often enhanced when completion time and place is identified. For example, the client and therapist can discuss a time (breakfast) and location (kitchen) for filling in the diary.
Functional Analysis and Case Formulation
To derive a case formulation, the therapist and client discuss frequency, intensity, and duration of insomnia and its antecedents. Sleep-related behaviors and conse- quences are assessed before bed (e.g., bedtime routine), during the night (e.g., cell phone left on), on waking (e.g., sleepiness, lethargy), and during the day (e.g., caf- feine use, napping). The relationship between sleep- specific thoughts, emotions, and behaviors is charted across the night and day. Figure 16.3 is an example of a case conceptualization form for the nighttime period.
The case formulation is designed to elicit the client’s curiosity about his/her sleep and to start forming a pic- ture of what is going on. The therapist can introduce the exercise as follows:
“It will be helpful in planning our sessions together to get a very detailed picture of what the experi-
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FIGURE 16.3. Case conceptualization form completed for the night.
Antecedents
Situation
Thoughts
Feelings and Arousal
Monitoring Safety Behaviors/Responses
Outcome:
Typical Thursday, nothing unusual
Woke up at 2:00 am
Oh my God, it’s 2:00 am. I won’t be
able to cope tomorrow, and I’ve
got such a big day ahead, with
so much to do!
Anxious
Frustrated
Scared
Look at clock
Notice tension in neck
Notice eyelids not heavy
Stayed in bed
Turned on TV
All of this made it hard to get back to sleep!
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ence of insomnia is like for you, almost like putting your sleep under a microscope. The way we do this is by identifying together a recent typical night and then after that a recent typical day. I’ll ask you lots of questions about each, so that I can get a sense of the kind of things that are going on. It’s like a fin- gerprint, everyone is a bit different so the treatment needs to be a bit different. Would that be all right?”
The first step is to help the client to choose a very specific recent example of an “insomnia episode” dur- ing the night. Make sure you work on deriving only one model (i.e., either the day or the night) at a time. A very specific episode is a situation that happened on one particular day and at a particular time. Be sure to check in regularly to ensure that the night was typi- cal. Sometimes a selected night or day is not typical or it was not very distressing. The therapist should stop that model as soon as this becomes apparent and start again with a typical, distressing night. Examples of some very specific recent episodes may include “Last Tuesday night I worked until 1:00 A.M. and then I couldn’t get to sleep” or “On Friday at work I had a terrible day, I felt sick, looked terrible and performed badly.” Spend a few minutes asking information-gath- ering questions to explore the content of the nighttime or daytime model. The aim of this initial discussion is to obtain a very detailed description of exactly what happened, along with the consequences of it. The fol- lowing is an example of a client who awoke at 2:00 A.M. (Figure 16.3):
THERAPIST: What woke you up? CLIENT: Don’t know. THERAPIST: How did you know what time it was? CLIENT: I looked at my clock and saw it was 2:00 A.M.
THERAPIST: When you looked at the clock and noticed it was 2:00 A.M., what ran through your mind?
CLIENT: I thought, “Oh my God.” THERAPIST: OK, so you looked at the clock and no-
ticed it was 2:00 A.M. and you thought “Oh my God.” Could you tell me more? What do you mean by “Oh my God?”
CLIENT: Oh my, I won’t cope tomorrow, I’ve got such a big day ahead with so much to do.
THERAPIST: So when you thought, “Oh my, I’ve got
such a big day ahead with so much to do,” how did you feel?
CLIENT: Really anxious.
Drawing on classic treatment development work by David M. Clark’s team (Clark et al., 1999, 2006), the following are useful questions to ask when deriv- ing the model. The following illustrates questions for nighttime models, with analogous daytime questions in brackets [ ]:
For identifying negative thoughts • “What went through your mind/what were you
thinking before getting into bed [on waking], as you got into bed [as you got ready for the day], and as you noticed you weren’t getting to sleep [weren’t performing well]?”
• “What did you think would happen as a result?” • “What would that mean? What would be so bad
about that?”
For identifying safety behaviors • “When you thought X might happen, did you do
anything to try to prevent it from happening?” • “Is there anything you do to ensure you get to sleep
[perform well during the day]?”
For identifying feelings • “When you are afraid that X will happen, what do
you notice happening in your body?” • “What kind of emotions do you have as you think
X?” • “How about your energy level?”
For identifying monitoring • “How did you know that X would happen?” • “How did you determine or measure how close to
falling asleep you were or what the time was [that you were feeling so tired]?”
• “How do you monitor/measure when the insomnia is back?”
• “How do you know that you hadn’t fallen asleep [were still tired]?”
It is important for the therapist to ask questions to illustrate the cyclical relationship among thoughts, feel- ings, and behaviors that is often evident in insomnia.
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These questions focus on the arrows. It is often impor- tant to connect “monitoring” and “safety behaviors” back to thoughts. Here are some questions that will help:
For connecting thoughts, feelings, and behaviors • “When you are concentrating on (give examples
of monitoring, like looking at the clock), what thoughts occur to you? Anything run through you mind?”
• “When you are concentrating on (give examples of safety behaviors, like remaining in bed for long periods of time), what is its impact on your getting back to sleep?”
• “When you monitor these things (when you cope by doing X ), does that help you worry less or does it trigger more worries?”
Drawing out the consequences • “Does watching out for fatigue and tension have
any consequences [for your day]?” • “Were there any consequences of these thoughts,
emotions or behaviors for getting back to sleep [how the rest of your day went]?”
Once the model has been derived, the therapist shares the personalized version with the client, asking for feedback and reactions. The therapist might say the following:
“This has been very helpful. Let me show you what I have been scribbling here, and I’d like for you to give me feedback about which parts I understand and which parts I have got wrong. This is so similar to what we very often find. These kinds of thoughts [name some] seem to lead to these kinds of feelings [name them]. Both put together make it difficult to sleep. On top of that, the thoughts and feelings can put us into a state of vigilance. Then we start moni- toring the environment and our bodies [name some examples of the kinds of monitoring in which client engages], which often triggers more thoughts, which triggers more feelings. Then, very understandably, we try to cope by doing things like [name some of the safety behaviors]. Now some of these really are likely to be helpful in getting us back to sleep, but some- times during the treatment we will test out the extent to which they are helpful by doing an experiment,
to double check. That’s why we call them safety be- haviors. Safety behaviors are things that people do in order to try and fix the problem they have but which, inadvertently, sometimes contribute to the problem. We may test out whether these behaviors are helpful or unhelpful. How does this model fit for you?”
Once the model has been completed, it is important to ask clients if they can think of ways to intervene. If an area is identified, draw a double line across the maintaining arrows to visually represent cutting into the cycle. Most often, clients are not able to come up with ways to intervene, so the therapist can help them by saying something like the following:
“I suggest that one of our targets be these thoughts. . . . If we can change them, we will change your feelings. This alone will be very helpful for helping you get back to sleep. In addition, we’ll also target the moni- toring. When we change the monitoring people typi- cally feel much more relaxed and sleep much better. Then, as I have already said, if you are interested, we’ll test with experiments the things you are doing to cope right now, just in case some are feeding into the cycle.”
Summarize by pointing out that a change in one or more parts of the perpetuating cycle will shift the sys- tem.
Goal Setting
Once the case conceptualization/insomnia models are derived, specific goals are collaboratively identified and written down in session. Goals are clearly stated (e.g., “falling asleep within 30 minutes each night” instead of “falling asleep more quickly at night”) and feasible (e.g., “sleeping through the night with only several brief awakenings” instead of “sleeping through the night without waking,” as the latter is not biologically fea- sible). Practitioners and clients can establish goals for both the nighttime (falling asleep, staying asleep, ad- vancing bedtime) and the daytime (increasing energy, reducing caffeine consumption). Goals are revisited briefly midway through treatment and at the conclu- sion of treatment.
Therapy goals are set in Session 1 but may need to be reevaluated and readjusted periodically as the inter- vention unfolds. It is important to set realistic, opera-
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tional, and well-defined goals. Goal setting is useful to keep the therapy focused. By setting well-defined goals, the therapeutic alliance remains oriented to the client’s needs and desires, and minimizes diversion to irrelevant materials. It also provides useful information about the client’s sleep expectations, which sometimes need to be adjusted during the goal setting process.
Motivational Interviewing
Motivational interviewing (MI) is a communication method that emphasizes accepting the client as an indi- vidual, avoiding argumentation/lectures, and focusing on the process of eliciting and shaping language in favor of change (Miller & Rollnick, 2002). MI also includes regular, straightforward reviews of perceived pros and cons of change, because many sleep-incompatible/inter- fering behaviors are rewarding.
A straightforward review of perceived pros and cons of the change is conducted. For example, clients often struggle with waking up at around the same time on both weekdays and weekends. Allowing the client to generate advantages and disadvantages with therapist guidance facilitates behavior change. MI is revisited in future sessions as additional strategies are introduced.
Sleep and Circadian Education
Education on the circadian system and homeostatic sleep drive (see the earlier “Sleep and Insomnia” sec- tion) is presented to the client. This underscores the following three points: (1) Waking up at the same time each day helps the circadian system adapt to the 24- hour sleep–wake cycle; (2) daytime napping disrupts the natural buildup of homeostatic sleep pressure; and (3) going to bed early is inadvisable, as circadian arousal may still be high; likewise, sleeping in in the morning is inadvisable, as it delays the circadian clock and de- lays buildup of homeostatic sleep pressure for the next night. Individuals across the age range may also benefit from education about specific changes in sleep across the lifespan. In adolescence and young adulthood, un- derstanding the biological shift toward later bedtimes and rise times with puberty is helpful for later inter- vention. Likewise, explaining to adults that sleep grows lighter and more fragmented with age, and that sleep needs change with age, such that 7 hours of sleep per night may be sufficient, can go a long way to normalize and lay the foundation for intervention.
BEHAVIORAL COMPONENTS
Sleep Restriction
Sleep restriction, as developed by Spielman and col- leagues (1987), rests on the general premise that time in bed should be limited to maximize the sleep drive, so that the association between the bed and sleeping is strengthened. This behavioral treatment begins with a reduction of time spent in bed, so that time in bed is equivalent to the time the client estimates he/she spends sleeping. Thus, for instance, if an individual gets ap- proximately 6 hours of sleep per night (an average across the week based on sleep diaries), but usually spends about an additional 2 hours trying to get to sleep, the sleep restriction therapy would begin by limiting his/ her time spent in bed to 6 hours. This initial reduction in time spent in bed is intended to heighten a person’s homeostatic sleep drive (Perlis, Aloia, & Kuhn, 2010) and reduce the association between the bed and wake- fulness. Following this restriction, sleep gradually be- comes more efficient, at which point time spent in bed is gradually increased.
Practitioners begin sleep restriction by calculat- ing TST, time in bed, and sleep efficiency based on the prior week’s sleep diary. Sleep efficiency is defined as TST divided by time in bed, multiplied by 100 to form a percentage. So, in the previous example, if a client sleeps an average of 6 hours per night over the week and spends an average of 8 hours in bed, sleep efficiency for the week will be (6 ÷ 8) × 100, or 75%. The goal is to increase sleep efficiency to more than 85–90%. The therapist would set a “sleep window” equal to the prior week’s TST (6 hours), choosing a bedtime and rise time with the client (e.g., 12:00 A.M. to 6:00 A.M.). Once sleep efficiency reaches 85%, client and therapist can gradually expand the window (e.g., by 30 minutes per week) toward an optimal sleep time.
Clients are often hesitant about implementing sleep restriction. Many individuals with insomnia believe that they need to spend a great deal of time in bed in order to “catch” a minimum amount of sleep. Still oth- ers worry about the short-term sleep deprivation that sleep restriction is likely to impart—after all, clients are presenting with the desire to get more sleep, and sleep restriction is a strategy that, in the short term, is likely to give them less. Explain to the client that his/her brain and body have developed habits that lead to time awake in bed and poor sleep efficiency. Sleep restriction is the most effective way to improve sleep efficiency by
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consolidating sleep time. Tell the client that although, initially, he/she may not get more sleep, his/her sleep quality and sleep efficiency will likely improve. These are the first steps to remedying sleep problems. Reas- sure the client that as his/her sleep efficiency improves, you will be expanding the “sleep window” to allow for more time in bed.
Stimulus Control
The rationale for stimulus control therapy lies in the notion that insomnia is a result of conditioning that occurs when the bed becomes associated with inabil- ity to sleep. The bed, bedtime, and bedroom have lost their properties previously associated with sleep, and the main therapeutic goal is to reestablish or strengthen the associations between sleep and the stimulus condi- tions under which it typically occurs. As described by Bootzin, Epstein, and Wood (1991), stimulus control requires clients to comply with a series of specific be- havioral recommendations. These recommendations, along with suggestions for introducing them, are out- lined below.
• Only go to bed when sleepy. To reestablish the asso- ciation between the bed and sleep, clients are instruct- ed to go to bed and to stay in bed only when sleepy and when sleep is imminent. Therapists explain that “sleepy” is different from “tired,” and that although an individual may feel tired in the evening, he/she must wait until he/she feels sleepy before getting into bed. Note that if a sleep window has been set as part of sleep restriction (described earlier), the client is instructed to remain awake until the start of the sleep window, even if he/she feels sleepy.
• Get out of bed if unable to fall asleep. Because time spent awake in bed can often be associated with worry, rumination, and arousal, clients are instructed to leave the bed if they do not fall asleep within 15–20 minutes, returning to bed only when they feel sleepy. This may be introduced in session as follows:
“If you are unable to fall asleep or return to sleep with- in 15–20 minutes, get out of bed, go into another room, and engage in a quiet activity that you find re- laxing. You can read, listen to music, do a crossword puzzle, or find something else that is nonarousing. Return to bed only when sleepy, and repeat this step as often as necessary throughout the night—so that anytime you wake up and are awake for more than
20 minutes, you will be getting out of bed and going to another room. This regimen will help reassociate your bed/bedroom with falling asleep quickly.” • Brainstorm relaxing activities with clients and write
them down in session, listening carefully for and discour- aging potentially stimulating activities (social media use, watching certain TV programs, cleaning the house). Emphasize to clients that it will be difficult to comply with this recommendation. Encourage clients to put warm clothing by the bed to increase the desire to get out of bed. Brainstorm with clients who live in studios or single rooms to find an alternate place (a chair or pillow on the floor) to go to when getting out of bed.
• Keep the bedroom for sleep and sex. Eliminate all sleep-incompatible activities (upsetting conversations, studying, watching TV) from the bed and bedroom. Many individuals get into bed early and read or watch TV in order to facilitate sleep onset. Remind clients that this time in bed spent awake, however, dilutes the association between the bed and sleep.
• Discourage napping. Explain to clients that napping can offset homeostatic sleep pressure, making it more difficult to fall asleep or stay asleep at night. Often it can be helpful to point to specific examples in the sleep diaries where a daytime nap led to greater difficulty fall- ing asleep, or more wakefulness throughout the night, to illustrate this point. If clients regularly nap at a cer- tain time, brainstorm activities that can be scheduled as an alternative. Tell clients that although naps may feel helpful in the short term, they can disrupt sleep–wake rhythms and perpetuate insomnia in the long term.
Sleep Hygiene
Information about sleep and sleep-incompatible be- haviors, and the daytime consequences of sleep distur- bance, is often given to inform clients of basic steps they can take to improve their sleep. Interventions targeting sleep hygiene are behavioral in nature and target sleep- incompatible routines. Sleep hygiene interventions typically include the following components (Morin & Espie, 2007): (1) Education on the sleep-disrupting ef- fects of alcohol, tobacco, and caffeine use are introduced to the client, who is encouraged to avoid caffeine in the evening and alcohol/tobacco at bedtime; (2) clients are encouraged to have a small snack before bedtime but to avoid heavy meals; (3) exercise is known to enhance sleep continuity and quality, and is recommended to
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client; exercising within several hours of bedtime, how- ever, can delay sleep onset; (4) clients are encouraged to keep the bedroom environment quiet, dark, and cool. Although sleep hygiene education is typically included as one component of CBT-I, its use as the sole interven- tion in treating insomnia has not been empirically sup- ported (Morin et al., 2006).
Wind Down, Wake Up, and Regularity
Wind‑Down Routine
Clients need assistance to devise a “wind down” of 30–60 minutes in which relaxing, sleep-enhancing activities are introduced in dim lighting conditions. A regular wind-down routine is beneficial across multiple domains: It promotes relaxation, increases positive asso- ciations with the bed/bedtime, and, when done in dim lighting conditions, helps the circadian phase advance in clients who are evening types, maintaining entrain- ment (Wyatt, Stepanski, & Kirkby, 2006). Activities that are encouraged in the wind-down routine include reading, grooming/hygiene, bathing, completing a light crossword, listening to soft music, and other relax- ing activities of the client’s choosing. A central issue is the use of interactive electronic media (Internet brows- ing, cell phone use, social media use). Though clients may acknowledge that these activities are stimulating, they may be reluctant to surrender them in the period before sleep. MI can often be helpful given that many clients are socially isolated and rely on prebedtime, digi- tally based social interaction. A behavioral experiment stretching across the week (e.g., 3 nights of bedtime “as usual” followed by 3 nights with a “wind-down rou- tine,” with daily ratings of prebedtime relaxation and SOL) can be helpful to illustrate the sleep-promoting effects of a good wind-down routine (Harvey & Tal- bot, 2012). Many clients voluntarily choose an elec- tronics curfew and time at which the wind down will commence, opting to set an alarm on a cell phone as a reminder.
Wake‑Up Routine
As mentioned earlier, clients benefit from education about sleep inertia upon waking, and about behav- iors that can increase or decrease sleep inertia. Help- ful behaviors to curb sleep inertia include not hitting “snooze,” exposure to sunlight upon waking (e.g., opening the curtains to let sunlight in, eating breakfast
outside), encouraging morning physical activity, show- ering, listening to upbeat music, and encouraging social contact (Kaplan, Talavera, & Harvey, 2018). Behavioral recommendations may be introduced to combat the de- sire to sleep in, including placing an alarm away from the bed so that it is necessary to rise to turn it off, and making the bed, so that the incentive to get back in bed is reduced. Encouragement from family and friends can also help a person to comply with morning rise times.
Regularizing and Shifting Sleep and Wake Times
Regularizing sleep and wake times across the week can be a helpful intervention, particularly if schedule vari- ability appears to be a prominent feature of the sleep disturbance. Building motivation for the client to wake at the same time, including on weekends (Crowley & Carskadon, 2010), is a key focus. This promotes con- sistent sleepiness in the evening, particularly when naps are avoided.
Often it is helpful to frame schedule variability around the phenomenon of “jet lag” as follows:
THERAPIST: Have you ever experienced jet lag? CLIENT: Yes, I have. THERAPIST: When was the last time? CLIENT: Oh, I guess the last time was flying out East
to visit relatives. THERAPIST: What did you notice? CLIENT: Let’s see . . . I felt kind of out of it, like I
couldn’t focus. It was difficult to fall asleep, even more than it usually is for me!
THERAPIST: And flying out East . . . that’s a 3-hour time difference from here, correct?
CLIENT: Yes. THERAPIST: Let’s take a look at your sleep diary from
last week. What do you notice from weekday to weekend?
CLIENT: Well . . . I went to bed at 2:00 A.M. on Friday and Saturday, because I went out both nights. And I guess I slept in as a result.
THERAPIST: And what time did you go to bed on Sun- day and Monday?
CLIENT: Looks like I tried to sleep at 11:00 P.M., be- cause I have to get up for work.
THERAPIST: So you just went from 2:00 A.M. on the
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weekend to 11:00 P.M. on the weekday. You just flew across the country!
CLIENT: Huh. I guess I never thought of it that way. THERAPIST: No wonder you had difficulty falling
asleep on Sunday and Monday. Your body was jet lagged, and with the “time change,” it was hard to fall asleep.
CLIENT: No wonder I have so much trouble on Sunday nights!
For clients who wish to advance their sleep schedules, we work to achieve behavioral adjustments to adapt to earlier bedtimes. We do this in small, systematic shifts (e.g., by advancing bedtime by 20–30 minutes each week) to ensure mastery. We encourage exposure to light upon waking, which will help the circadian sys- tem advance, and work with clients to minimize vari- ability around wake times. We reassure clients that any sleep pressure (i.e., sleep loss) accumulated initially with bedtime advancement will actually help the sleep schedule align by increasing likelihood of earlier sleep onset on subsequent nights.
COGNITIVE COMPONENTS
Worry
It is well established that individuals with chronic in- somnia worry while in bed about a range of topics, including the failure to fall asleep (Harvey, 2002b; Wicklow & Espie, 2000). Cognitive models implicat- ing worry (Harvey, 2002a) posit that worry activates the sympathetic nervous system and corresponding physiological arousal, which hinders sleep onset (Espie, 2002). Therefore, an intervention targeting worry is an important clinical area in the treatment of insomnia.
Following well-established cognitive therapy ap- proaches (Beck, 2021; Young, Ward-Ceisielski, Rygh, Weinberger, & Beck, Chapter 7, this volume), the first step in addressing worry involves education on negative automatic thoughts (NATs) and mistakes in thinking. NATs can be introduced to clients as follows:
THERAPIST: Imagine there are two people outside of a movie theater, each waiting for a friend to arrive. The friend is late, and these two people have been waiting. Person 1 is thinking, “Gosh, I wonder why she is late. I hope everything is all right with her! Did she get into an accident on her way over?” Person 2 is
thinking, “Gosh, I can’t believe she is late. She always does this. She has no respect for my time. She is not a good friend.” What kinds of emotions do you think Person 1 is feeling?
CLIENT: Probably some fear and concern. THERAPIST: Right. And what about Person 2? CLIENT: (chuckling) Anger, and maybe resentment. THERAPIST: Exactly! So two people in the same situa-
tion can have very different emotional responses to an event based on what they were thinking. In other words, our thoughts can directly influence our emo- tions. Often, we have dozens of thoughts in rapid succession, and we don’t even realize it. We accept them at face value without stopping to look at them. We’re going to look for, and respond to, some sleep- related automatic thoughts over the next few weeks.
The therapist then provides further education on au- tomatic thoughts: (1) They are often a train of thought that runs parallel with spoken thought; (2) we are often not fully aware of them; (3) automatic thoughts are ex- tremely rapid, and sometimes only a few words rather than sentences; (4) they do not arise as a result of delib- eration but just happen like a reflex; (5) they are often difficult to turn off; (6) we often accept their validity without stopping to question them; and (7) they often precede a powerful emotion. The therapist should un- derscore the point that we have hundreds and hundreds of NATs each day, and it is often helpful to look for NATs by paying attention to changes in emotion.
The therapist next works with a client to identify a recent powerful emotion from the previous 2 days, and use the emotion as the starting place to uncover related NATs. These are written down on a simple three-col- umn form (Situation–Thoughts–Emotions). The client is asked to practice identifying additional NATs over the week by paying attention to changes in emotion and writing them down on the three-column form, emphasizing insomnia-related NATs (“I’m exhausted” or “I won’t be able to cope today”). The therapist also provides psychoeducation on common cognitive distor- tions (black-and-white thinking, catastrophizing, per- sonalizing, mistaking feelings for facts, etc.) and asks clients to categorize some of the NATs they spot over the week.
At the following session, the practitioner reviews the client’s three-column NAT form and has a brief discus- sion/review of NATs and NAT themes. The practitioner
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then introduces an extended thought record that guides the client in evaluating the validity of the thought with a series of questions, including evidence for–against the thought, alternative ways of interpreting the thought, considering the worst that could happen and whether the client would be able to live through it, the helpful- ness of the thought and the effect of thinking in this manner, how others might see the situation, how im- portant the thought will be when the client is 80, and whether the thought falls into one of the “mistakes in thinking.” Client and therapist pick a NAT together and work through the form together in session.
Once the client has fully grasped this procedure, the therapist assigns as homework completing one extended record daily or, at the very least, several examples each week. This is continued for several weeks. The therapist provides the following rationale for continuing to fill out the extended record on a daily basis: (1) By observ- ing, reporting, and evaluating NATs, it is easier to see them objectively and to get some distance from them; (2) observing, reporting, and evaluating NATs presents an opportunity to test their reality/logic and recognize that thoughts can be unreliable; and (3) most impor- tantly, because it takes a long time to change thinking habits that have been around for many years, reversing the old habits will take practice. Completing one form daily over a period of weeks will make the new style of thinking habitual.
Helpful and Unhelpful Worry Strategies
A menu of other worry interventions is offered, so that the client gets to create a personalized list of helpful and unhelpful strategies to manage worry. Unhelpful strate- gies might include suppression (Harvey, 2003a), posi- tive beliefs about worry (Harvey, 2003b), and “why” questions (Watkins & Baracaia, 2001). For suppression, introduce the adverse consequences of thought suppres- sion whenever it becomes relevant, sometimes as early as Session 1. For example, as soon as the client men- tions something along the lines of “I try to suppress my thoughts” or “I clear my mind,” the therapist can do an in-session “white bear experiment” (“For the next min- ute, let’s close our eyes and think about whatever we’d like, anything except a big white fluffy bear”) to illus- trate paradoxical effects of thought suppression. This helps the client become aware that suppression often leads to “thought rebound” or monitoring for the sup- pressed thought, which makes it more likely to occur. A helpful assessment for suppression and other thought
control strategies is available (Ree, Harvey, Blake, Tang, & Shawe-Taylor, 2005). Therapists should also be on the lookout for clients who hold positive beliefs about the utility of presleep worry. Therapists can use Socratic questioning to discuss the pros and cons of pre- sleep worry, or consider doing behavioral experiments to collect data on whether positive beliefs about worry- ing in bed are helpful or not. Finally, “why” questions are often implicated in the presentation of insomnia. Many clients ask questions such as “Why am I awake?” or “Why don’t I sleep as well as my partner?” Give your client the rationale that experimental studies suggest that “why” questions block processing and promote ru- mination.
After reviewing what not to do to manage worry, consider alternative, more helpful thought manage- ment strategies with the client. First, suggest the idea of not controlling or suppressing thoughts. Do the op- posite—let them come. Let them drift in and out. Let- ting the thoughts come and go may give the thoughts less strength and power, and may even move them into the category of being boring. Another helpful al- ternative involves catching the thoughts and evaluat- ing them with the extended thought record described earlier. Introducing the importance of a wind-down or buffer zone to process and disengage from the day can be a helpful response to worry. Finally, practice savor- ing to focus on the positives in the client’s life. Savor- ing involves attending to, appreciating, and enhancing positive experiences the client has had during the day. It can be a small/everyday event such as looking out the window and noticing the lovely trees and flowers, remi- niscing over a favorite vacation, or anticipating a family reunion or a date with one’s spouse/partner. Encourage the client to focus on the positive experience, and when negative thoughts arise, return to the positive experi- ence and savor it. The rationale is to associate bedtime with positive thoughts. Work with your client in the session to identify times in the present, past, and future that he/she can savor. Practice savoring together in the session, and allow the client to reflect on the experience.
Set one or more of these alternative strategies as home- work, introducing it as a behavioral experiment. Behav- ioral experiments, explained in Table 16.1, are powerful methods used across all of the cognitive components of CBT-I (for further reading on behavioral experiments, see Perlis, Aloia, & Kuhn, 2012; Ree & Harvey, 2004a). The goal is to give the client some experience and prac- tice with each. Feel free to follow up with additional experiments in subsequent sessions if needed.
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TABLE 16.1. Steps Involved in Creating, Testing, and Processing Behavioral Experiments
Steps and description Example
• Step 1. Identify the thought, belief, behavior, or process the experiment will target. The rationale for completing the experiment, along with the target or aim, should be clear. Targets can include challenging an unhelpful belief/behavior or testing a new belief/behavior. The target is written down in session.
Victor is unsure as to whether looking at the clock as he falls asleep is helpful. He believes that knowing the time, and calculating how much time he has left to sleep, may increase his anxiety at night; however, he also feels that not knowing the time could increase worry and anxiety throughout the night. Victor and his therapist set out to test the following: “Is looking at the clock at night helpful or harmful to my sleep?”
• Step 2. Collaborate to brainstorm ideas for an experiment. Encourage clients to be specific, defining a place and time for the experiment. Get creative and arouse clients’ curiosity. Be open and flexible to ideas the clients have, as this may increase motivation to complete the experiment. Clients sometimes enjoy giving their experiments creative titles.
Victor and his therapist agree to set up an experiment to test the impact of clock watching on sleep. They agree to spend 3 nights watching the clock as usual, followed by 3 nights without looking at the clock. Victor states that he will be tempted to turn the clock around on the “no-clock” nights, so he and his therapist collabora- tively brainstorm to move the clock across the room to reduce this temptation.
• Step 3. Write down predictions about the outcome and devise a method to record the outcome as soon as possible after the experiment is completed. This is very important: A delay in recording the outcome could lead to vague and inaccurate memory of the experiment itself.
Victor has the following prediction: “Not looking at the clock at night will increase my anxiety and keep me up longer because I’ll be won- dering what time it is all night.” He and his therapist decide to record “last night’s anxiety” on a scale of 1–10 immediately upon waking and use the sleep diary to look at time it takes to fall asleep.
• Step 4. Anticipate problems and brainstorm solutions. Ask your client what might prevent him/her from completing this experiment. Identify obstacles and collaborate on how to overcome them. If the experiment centers around a new skill, practice the skill together in session before making it a part of the experiment.
Victor and his therapist discuss obstacles to completing the experi- ment. Victor has a party to attend on one of the nights, which will delay his bedtime slightly; he and his therapist decide to skip the clock-watching experiment on this “nontypical” night and complete it the other six nights of the week.
• Step 5. Conduct the experiment. Victor spends 3 nights looking at the clock and 3 nights not looking at the clock, recording anxiety and standard sleep variables on his sleep diary.
• Step 6. Review the experiment. Ask your client to summa- rize main points he/she has learned from the experiment. Assist him/her in filling in gaps, and write out conclusions together. Remind your client of the conclusions drawn from each experiment in future sessions. If the outcome is other than anticipated, ask follow-up questions to review any fac- tors (mood, behavior, cognitions) that may have influenced the outcome in a manner other than expected. Typically, via careful questioning, learning can be derived from an experi- ment regardless of the outcome.
Clock nights: Anxiety ratings (on a scale of 1–10): 8, 6, 7 Time to fall asleep (in minutes): 120, 45, 60
No-clock nights: Anxiety ratings (on a scale of 1–10): 10, 6, 4 Time to fall asleep (in minutes): 140, 50, 15 At first glance, the numbers above do not appear to “solve” the experiment one way or the other. However, with careful questioning, a subsequent testable hypothesis is generated. Victor reports that his anxiety levels and length of time to fall asleep were consistent on the clock-watching nights. On the no-clock nights, Victor reports that his anxiety was initially very high as he wondered what time it was; by the third day, however, he acknowledged hardly thinking about the time. Victor and his therapist discuss the possibility that he was experienc- ing initial anxiety with the new behavioral change, and speculate that he may need more time in the no-clock condition to “get used to” the shift.
• Step 7. Identify follow-up experiments if needed. If the experiment was not completed in full, or if the outcome was ambiguous and/or raised another question, return to Step 1 and devise a further experiment.
Victor and therapist decide to extend the “no-clock” condition for another week, still rating anxiety and time to fall asleep immediately upon waking.
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Attention and Monitoring
As noted earlier, a number of studies have documented that individuals with insomnia underestimate their sleep time and overestimate time spent awake at night (Harvey & Tang, 2012). Individuals may become more anxious about their perceived sleep problem, and with increased vigilance toward the sleep state, may draw in- accurate conclusions about their prior sleep. Likewise, individuals may monitor for signs of daytime fatigue. A helpful measure of sleep-related monitoring is available (Neitzert Semler & Harvey, 2004). Behavioral experi- ments, both in and out of session, can be introduced to illustrate the effects of attentional bias and monitoring (Harvey & Talbot, 2012; Ree & Harvey, 2004a).
To introduce the concept of monitoring, the thera- pist may wish to do the following:
THERAPIST: Close your eyes and focus on your knee joints and the sensations that are there. I’ll do it, too. Let’s both take 2 minutes to do this. (after 2 minutes) What did you notice?
CLIENT: Hmm . . . some tingling, and pins and nee- dles. Mild pain, maybe.
THERAPIST: Imagine for a moment there was a lot of research to indicate that the things you mention are soft signs of a serious immune system disease. If you believed this were true, how would this impact your attention for the rest of the day?
CLIENT: I’d be paying attention to my knee all day! THERAPIST: And how would you feel about those sen-
sations? CLIENT: Well, concerned, I guess. Wondering if they
had gotten worse. THERAPIST: What if your sleep is like that knee? And
the more you look out for symptoms of tiredness or fatigue, the more they appear?
The therapist can use this dialogue to brainstorm with the client about the monitoring in which he/she may engage during the day and night. Then, the thera- pist can introduce one or more of the following behav- ioral experiments to assess monitoring.
Monitoring for Fatigue
Go for a brief walk together in session. Instruct the cli- ent to spend 5 minutes focusing internally to monitor how his/her body feels, paying particular attention to
signs of tiredness and fatigue. Ask your client to rate how tired he/she feels. Then spend 5 minutes focusing externally on the trees, flowers, and sky. Ask your client to again rate how tired he/she feels. Go back to your office to debrief.
Monitoring for Sounds
To instruct the client about monitoring at night, it is often helpful to use the metaphor of a “radar.” One cli- ent who monitored for the garbage truck had her “radar” on all night for the sound of the garbage truck. She would wake up to many sounds during the night and think, “Oh no, it is the garbage truck, it must already be 5:00 A.M. I’m never going to get enough sleep.” This thought led to anxiety that made it difficult for her to get back to sleep. We used multiple strategies to address this monitoring: (1) evaluating whether hearing the gar- bage truck was really an indication of wakefulness or whether the truck could have caused the client to wake from a light sleep; (2) discussing the pros and cons of having a “radar” on during the night; and (3) asking the client to listen to sounds in the room, and further away, in the adjacent room, and still further away, to sounds on the road, and to sounds further away yet again, en- couraging habituation to the full range of sounds.
Monitoring Physical Appearance
One client with whom we worked used to complain about her physical appearance on the days following poor nights of sleep. She would wake up and immedi- ately look in the mirror, noticing bags under her eyes. When asked how bad the bags were on days when she had not slept poorly, the client admitted she never really looked for them. We devised a behavioral experiment whereby she was to look at the bags under her eyes upon waking every day of the week, regardless of how she had slept, and rate the appearance of baggy eyes. The client found that her bags did not really change from morning to morning, and that she had really just ignored them on days when her sleep was not poor.
Monitoring the Clock
Paying attention to the clock throughout the night can increase anxiety and vigilance, interfering with sleep. Client and therapist can create an experiment whereby the clock is displayed in full view 3 nights of the week, then hidden from view (i.e., turned to face the wall or
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placed under the bed) for 3 nights. Ask the client to rate overall anxiety about the prior night’s sleep in the morning and record it on the sleep diary. The sleep diary can then be reviewed in the following session to compare anxiety and wakefulness on clock-watching nights versus clock-hidden nights.
Unhelpful Beliefs about Sleep
In seminal research on insomnia from the 1990s, Morin (1993) highlighted the role of unhelpful beliefs about sleep. It has been suggested that these unhelp- ful beliefs may exacerbate intrusive and worrisome thoughts throughout the day and night, contributing to the development and maintenance of sleep distur- bance (Harvey, 2002a). An unhelpful belief about in- somnia might take the form of an individual believing that he/she needs to sleep through the night with no awakenings to feel refreshed. Such a belief is unhelpful, in that awakenings are a natural part of nocturnal sleep (e.g., Akerstedt et al., 2002); worry related to this belief might take the form of an individual who, once awak- ened at night, believes that this fragmented sleep will result in impaired work performance the following day. One large-scale correlational study (Jansson & Linton, 2007) surveyed unhelpful beliefs about sleep, depres- sion, anxiety, and arousal at two time points spaced 1 year apart. The researchers found that unhelpful be- liefs about sleep—in particular, beliefs about the long- term negative consequences of insomnia—predicted a chronic pattern of poor sleep over and above arousal, depression, anxiety, and beliefs about short-term con- sequences, suggesting that targeting unhelpful beliefs about sleep is important for reversing chronic insomnia. Subsequent research has similarly shown that reducing unhelpful sleep beliefs may play a mechanistic role in improving insomnia symptoms in a digital CBT-I pro- gram (Lancee, Eisma, van Straten, & Kamphuis, 2015).
In addition to thought records, unhelpful beliefs about sleep can commonly be addressed in two ways: (1) gentle Socratic questioning to explore an unhelpful belief, and (2) creation of a survey to collect data related to the belief (Harvey & Eidelman, 2012). The following vignette il- lustrates how the therapist can use Socratic questioning to guide the client to explore and correct some unrealistic expectations about sleep needs and morning energy:
THERAPIST: Some of your responses suggest that you believe quite strongly about the need for 8 hours of sleep every night.
CLIENT: Well, I’ve always thought that we need 8 hours of sleep to stay healthy.
THERAPIST: Do all people you know have the same height?
CLIENT: Of course not! THERAPIST: What is the normal height for an adult? CLIENT: Well, there is no norm that applies to every-
one. It varies . . . THERAPIST: It is similar for sleep. There are individual
differences in the amount of sleep we need to feel rested and function well during the day. Although most people report about 7 or 8 hours of sleep, some can get by with less than that and still feel rested in the morning. It is possible that 6.5 hours of uninter- rupted sleep be more satisfying and refreshing than 8 hours of broken sleep. So, it will be important to experiment with various sleep durations to determine what the optimal duration is for you. What do you think happens if you assume that you need 8 hours of sleep but you really only need 7?
CLIENT: I guess I’m awake an hour . . . and I spend that hour worrying about why I’m not sleeping!
THERAPIST: Exactly. Pursuing unrealistic goals is coun- terproductive and may actually make you anxious and, as a consequence, perpetuate the underlying sleep difficulties. I also noted that you are very con- cerned when you are not fully rested in the morning.
CLIENT: Well, this concerns me, because I assume that if I am not well rested in the morning, it must mean that I have not slept well the night before.
THERAPIST: This may be a valid assumption. How- ever, even the best sleepers do not always arise in the morning feeling well rested and full of energy.
CLIENT: So you’re telling me that when I wake up in the morning feeling tired, it is not necessarily an in- dication of poor sleep.
THERAPIST: What I am suggesting is that you need to be careful with your expectations and interpreta- tions. Even with good-quality sleep, you simply can- not expect to always feel refreshed and energetic dur- ing the day. There are day-to-day variations in how we feel and how energetic we are.
CLIENT: I guess I have noted that for myself. THERAPIST: So, what alternative thoughts should you
have the next time you catch yourself setting stan- dards that may be unrealistic?
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CLIENT: That 8 hours of sleep is not necessarily a “gold standard” that applies to everyone, and that even if on some days I am not fully rested, I may simply need to accept that and not jump to the conclusion that I slept poorly the night before and won’t be able to function the next day.
THERAPIST: Very good! This should reduce your anxi- ety about sleep as well.
As this vignette illustrates, many clients have unre- alistic expectations about their sleep requirements and their daytime energy level. An important goal is to help these clients realize that diminished sleep and daytime energy are not always pathological, and that even good sleepers do not always get 8 hours of sleep or feel com- pletely refreshed every morning. With gentle Socratic questioning, clients may benefit from reappraising their expectations regarding both sleep requirements and daytime energy.
Surveys can also be designed to evaluate unrealis- tic beliefs about sleep. Before the session, the therapist should have an idea of unrealistic beliefs to target (e.g., “Good sleepers get 8 hours of sleep,” “Only people with insomnia feel tired in the daytime,” or “I am not nor- mal for waking up four times a night”). Dysfunctional Beliefs and Attitudes about Sleep (Morin, Vallieres, & Ivers, 2007) is a terrific measure to assess and document change in unhelpful beliefs about sleep. The therapist can introduce the survey by saying:
“One of the components of this treatment that we have found to be very effective is for us to collabo- rate together to create and administer a survey. There are a number of things we get from this: advice from good sleepers about why they sleep so well; a remind- er as to how well good sleepers really sleep; and data on our beliefs about sleep. Most of us have developed our ideas about sleep from magazine articles, from a parent, or on the basis of our own experience. What or who has most influenced your ideas about sleep? [Allows the client to respond.] In order to start to become more data driven, we are going to devise a survey together and administer it to people in your age group. This is always an interesting exercise and an opportunity to learn from others about how they manage their sleep. We focus on people around your age given that sleep changes so much across the lifes- pan. Here are some questions we have found to be helpful in the past.”
At this point, the therapist asks questions that per- tain specifically to the client’s unhelpful beliefs about sleep. Survey questions may include the following:
• “Are you a good sleeper or someone with insom- nia?” This question can be particularly useful to illustrate that individuals who regard themselves as “good sleepers” often feel tired in the morning, wake up at night, and feel sleepy in the afternoon.
• “How many hours of sleep per night do you get?” • “How long does it take to fall asleep at night?” • “How many times do you wake up at night?” • “How alert do you feel upon waking, on a 1- to
10-point scale? What have you found helpful to increase alertness?”
• “How often do you nap? Does it affect your sub- sequent sleep?”
• “Do you have a bedtime routine? A morning rou- tine?”
• “Do you feel tired in the daytime? When? What do you do to increase energy when you feel tired?” This question often generates many strategies sug- gested by others, and only a small proportion of the strategies involve resting or sleeping. Common alternatives include changing the environment, getting fresh air, going for a walk, drinking cold water, or having a snack. Clients often realize that energy can be increased by things other than rest and sleep, and that boredom is a big trigger for feeling tired.
Be sure to add questions of the client’s choosing as well, so that the survey is truly collaborative and gener- ates enthusiasm and interest. Clients are often curious about dreams, nightmares, or sleep patterns that can be added as questions to the survey. Also, questions about mood (“How often do you feel sad?” or “Have you no- ticed a relationship between your daytime mood and nighttime sleep?”) can provide normalizing evidence that sleep and mood are interrelated, even in good sleepers.
Safety Behaviors
Closely related to unhelpful beliefs are so-called “safety behaviors,” which are actions taken to avoid feared out- comes that are maladaptive in two ways: (1) They pre- vent disconfirmation of the unhelpful beliefs, and (2) they increase the likelihood that the feared outcomes will occur. Individuals with insomnia, in an attempt
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to cope with anxiety related to unhelpful beliefs about sleep, often employ safety behaviors (Salkovskis, 1991). In the previous section, we described an individual who endorsed the unhelpful belief that only solid, unin- terrupted sleep would allow unimpaired work perfor- mance the next day. To prevent nocturnal awakenings, this individual might develop a routine of safety behav- iors that include never going out in the evening, wear- ing earplugs, and using a sound machine as she sleeps. Engaging in these behaviors, while understandable in a general way, will clearly prevent her from learning that she can get adequate sleep even if the routine is broken. Paradoxically, these behaviors may make the feared outcome more likely to occur. Not going out in the evening increases the chance that she will become pre- occupied with her sleep, and may contribute to rumi- nation/worry and sad mood. Earplugs can be effective in certain circumstances, but they can also contribute to sleep problems if they are uncomfortable, or if they cause her to strain to try and hear things in the envi- ronment. Daily use of a sound machine may increase sleep-related distress and perceived sleep disturbance in situations in which the sound machine is not available, such as while traveling.
To work with safety behaviors, a helpful assessment tool is available (Ree & Harvey, 2004b). Behavioral experiments are designed in which the safety behavior is selectively adopted and then dropped, providing an often-stunning demonstration of their adverse impact. For example, if a client avoids going out in the evenings because of feared impact on sleep, the practitioner and client can set up a behavioral experiment in which two of the evenings in the week are spent at home (the “con- trol” condition), and two evenings in the week are spent outside the home (socializing with others, going to a movie, etc.; the “experimental” condition). The practi- tioner instructs the client to rate not only standard sleep variables on the weekly diary (SOL, TST, etc.) but also to add a simple scale to measure evening satisfaction or mood each night. Often, it is helpful to point out that mood and satisfaction increased on nights the client left the home, as well as to emphasize minimal (or incon- sistent) changes in sleep as a result of leaving the home.
Daytime Energy
Individuals with disturbed sleep often monitor them- selves for signs of fatigue upon waking or throughout the day. Normalizing feelings of grogginess upon wak- ing (so-called “sleep inertia”), and introducing behav-
ioral experiments and attention strategies for daytime monitoring can reduce anxiety and preoccupation with sleep. Often, clients believe the only way they can feel less tired in the daytime is to sleep more. Hence, a be- havioral experiment is devised to allow the client to ex- perience the energy-generating effects of activity (Ree & Harvey, 2004a). This is also an opportunity to develop a list of energy-generating and energy-sapping activities that can be used to manage daytime tiredness and in- evitable bouts of occasional sleep deprivation.
Many clients believe that energy progressively drains away throughout the day, and that the only way to gen- erate energy is to sleep or rest. Accordingly, many cli- ents work particularly hard at conserving energy after a poor night’s sleep. As such, a behavioral experiment targets the following cognitions: “Energy is increased only by rest or sleep” and “I don’t have much energy, so I need to take care to conserve it.” We hope to use the experiment to illustrate that factors other than sleep influence energy levels.
To set up this behavioral experiment, client and therapist begin by using the sleep diary as a basis for discussing sleep and energy during the day. They note examples in which nighttime sleep was good but energy levels in the day were poor, or in which nighttime sleep was poor but energy levels during the day were good. The therapist may wish to say something like “That is really interesting. So, if sleep isn’t the full account of how you feel during the day, then there must be other things that can account for it.” Set up a 2-day experi- ment to test energy as follows: On the first day, spend one 3-hour block conserving energy, then a 3-hour block using energy. After each 3-hour block, the client rates his/her energy and mood. The following day, the client does this in the reverse order. Be careful to define what conserving energy means for your client. Examples in- clude avoidance of socializing with colleagues, setting work tasks at a slow pace, attempting only mundane tasks, not going out for lunch with work friends, and not returning phone calls. Also, spend time in the ses- sion brainstorming strategies for using energy. These might include going for a 10-minute walk, returning all phone calls, arranging to have a coffee with a col- league, getting on top of the paperwork, going to the water cooler to get a drink, or walking to a local shop to buy a magazine or snack. Ask the client to rate his/ her mood and fatigue on a form developed collabora- tively in the session. The client typically finds that his/ her mood and energy were improved by “using” energy, and using energy then becomes synonymous with gen-
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erating energy. The therapist may comment that energy levels are like elastic that can be stretched quite easily.
TREATMENT SUMMARY AND RELAPSE PREVENTION
The final treatment session is oriented around consoli- dating skills and preparing for setbacks. Relapse pre- vention is designed to build skills to minimize or pre- vent the reoccurrence of sleep disturbance in the long term. At the end of treatment, the therapist guides the participant in identifying potential high-risk situations for insomnia in the future and discusses skills to pre- vent or cope with these high-risk situations. Client and therapist together discuss potential obstacles to main- taining gains, and they problem-solve around areas of future sleep disturbance. An individualized summary of learning and achievements guides relapse prevention work. Areas needing further intervention are addressed by setting specific goals and creating plans for achiev- ing each goal.
In the final session, therapist and client distinguish between a lapse (an occasional night of insomnia), which is normal even for good sleepers, and relapse (re- turn of frequent and chronic insomnia). Discuss with the client the inevitability of having an occasional poor night’s sleep and caution against interpreting this as ev- idence that chronic insomnia has returned. Identifying situations that have been problematic in the past, and reviewing a “new” response to temporary setbacks, can be critical in maintaining gains.
The therapist can guide the client in imagining a typical scenario in which insomnia is present for 2 or 3 nights, then follow up by exploring strategies the client might use to handle this situation in the future. This is a good opportunity to check, once again, whether the client has integrated the necessary skills to cope with such insomnia nights. Discuss how he/she can avoid falling back in the old patterns of poor sleep.
Clients are strongly urged to review their materi- als from treatment and do their own assessment of the problem, and identify the best course of action. Thera- pists also encourage clients to continue using tools after treatment has concluded. They work with clients to review tools, along with how the tools can be used to prevent insomnia reemergence. For example, the thera- pist can give the client multiple copies of the extended thought record or materials that the client found par- ticularly helpful in session.
COMMON PROBLEMS IN TREATMENT
There are at least three common problems practitioners may encounter in delivering CBT-I for treatment of in- somnia: difficulty regularizing the sleep–wake sched- ule, opposition to sleep restriction, and beliefs about the cause of insomnia that can hinder treatment com- pliance. We briefly discuss solutions to each problem below.
Clients are often reluctant to go to bed and wake up at the same time every day, including on weekends. This can be particularly problematic for teenagers or young adults, who often socialize and/or schedule pleasurable activities in the weekend evening hours. As described earlier, MI that honestly reviews the pros and cons of regularizing a sleep schedule can be one way to clarify ambivalence and prepare clients for change. Therapists may also find it helpful to guide clients in some general behavioral activity scheduling (e.g., encouraging clients to schedule a brunch, a hike, or a social visit on week- end mornings instead of weekend evenings, to enhance motivation). Finally, family members and friends can be instrumental to encouraging change. One client found it helpful to have a parent come in and turn on the overhead bedroom lights every morning, including weekends; another agreed to have a friend call at the same time every morning, and to keep her phone by the bed, so that she knew to answer it. Clients may also be encouraged by establishing reinforcement for making a target rise time, such as treating oneself to a special breakfast item or a nice walk in the first week of sched- ule adoption.
In addition to regularizing sleep schedules, clients are often resistant to implementing sleep restriction. It is helpful to allow clients to voice their concerns with this component of treatment (e.g., fear of reduced sleep), then follow up with basic education and problem solv- ing to address specific areas noted. Often it is helpful to characterize the mild sleep deprivation engendered by sleep restriction as a “tool” that will allows sleep pres- sure to build and the system to get back on track, or as a short-term side effect on the road to long-term, lasting gains. It can be helpful to validate clients’ fears associ- ated with restricting time in bed opportunity while at the same time encouraging clients to experiment with their sleep.
Finally, clients may have a variety of beliefs about the cause of their insomnia that may shape treatment expectations and compliance. Some clients see their insomnia as purely biological; others recognize psy-
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chological components; and still others attribute emer- gence of their insomnia to environmental causes (e.g., the birth of a child, or experiencing a trauma). Each of these may influence motivation to implement com- ponents of CBT-I. The therapist can acknowledge the client’s beliefs about his/her insomnia while explaining the Spielman model (see the earlier “Models of Insom- nia” section), highlighting the fact that regardless of the predisposing/precipitating factors that initiated insom- nia, perpetuating factors (excessive time in bed, worry, napping) are currently maintaining the insomnia. These perpetuating factors will be the focus of CBT-I treatment.
CONCLUSION AND FUTURE DIRECTIONS
CBT-I is established as an effective treatment option for insomnia. Administered as a brief, structured outpatient treatment, CBT-I targets behavioral, cognitive, and at- tentional processes that mutually maintain insomnia. Though it is structured, we wish to underscore the idea that CBT-I can be adapted flexibly according to the in- dividualized conceptualizations of clients. Clinicians can use assessment data, sleep diaries, and clinical intu- ition to formulate a plan that emphasizes and addresses particular areas of concern (e.g., erratic sleep schedules, worry and rumination, or reliance on safety behaviors). Finally, CBT-I can be adapted for clients with comorbid conditions and even be used as a platform for address- ing sleep problems such as hypersomnolence disorder. In this concluding section, we consider client–therapist variables that predict success or failure in treatment, is- sues specific to treating insomnia in mood disorders, and use of CBT-I principles to treat hypersomnolence as well as transdiagnostic considerations.
Predictors of Clinical Outcome
There is limited research on factors that predict success or failure with CBT-I, though this represents an excit- ing area of future research. Evidence suggests that cli- ent factors predicting dropout from treatment include short or long sleep duration and elevated levels of base- line depressive symptomatology (Ong, Kuo, & Man- ber, 2008; Yeung, Chung, Ho, & Ho, 2015), though, in those who complete treatment, more severe insomnia and functional impairment at baseline actually predict clinical improvement (Van Houdenhove, Buyse, Ga- briels, & Van den Bergh, 2011). Clinical improvement
is also predicted by changes in unhelpful beliefs about sleep (Edinger, Wohlgemuth, Radtke, Marsh, & Quil- lian, 2001; Lancee et al., 2015; Morin, Blais, & Savard, 2002). Better therapeutic alliance has been linked to improved outcomes in some (Constantino et al., 2007) but not all (Trockel, Karlin, Taylor, & Manber, 2014) research. In our own clinical experience, we have found that fostering a sense of curiosity and experimentation, and providing a clear rationale for homework comple- tion, makes a big difference in client motivation and treatment outcome. Finally, though adherence to CBT-I components is an important predictor of suc- cess (e.g., Trockel et al., 2014), research has shown that individuals in CBT-I programs have surprisingly poor memory for the content of therapy sessions (Lee & Har- vey, 2015), suggesting outcomes may be improved by enhancing memory for therapy.
Treating Insomnia in Mood Disorders
Sleep disturbance is commonly comorbid with other mood disorders (Armitage, 2007), and CBT-I may be a particularly useful intervention to stabilize sleep and circadian rhythms. For example, two recent me- ta-analyses suggest sleep in the interepisode phase of bipolar disorder is characterized by long SOL, long WASO, longer sleep durations and, consequentially, impaired sleep efficiency (Geoffroy et al., 2015; Ng et al., 2015)—all of which may respond favorably to sleep restriction and stimulus control, two components sug- gested to be safe in this population (Kaplan & Harvey, 2013). Studies confirm that CBT-I effectively reduces insomnia in patients with comorbid depression (e.g., Manber et al., 2016). However, results from trials that concomitantly treat insomnia and depression have not consistently shown improved depression outcomes in adults (Carney et al., 2017; Manber et al., 2016) or in adolescents (Clarke et al., 2015).
For practitioners who wish to address sleep problems in the context of depression or bipolar disorder, we offer the following recommendations. First, routinely moni- tor depression, anxiety, and/or mania symptoms, as ap- plicable, at the start of each session. Negotiate a safety plan with the client prior to the start of therapy should his/her mood grow unstable during treatment. If symp- toms of depression or mania emerge, evaluate changes in TST that may be contributing to decline and con- sider modifying or temporarily suspending sleep re- striction or stimulus control if necessary. Finally, we encourage practitioners to monitor sleepiness regularly,
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using an instrument such as the Epworth Sleepiness Scale (Johns, 1991). When Epworth levels reach clini- cal significance (a score of 10), discourage clients from driving or engaging in other potentially unsafe behav- iors during periods of drowsiness.
Adapting CBT‑I to Treat Hypersomnolence
As with insomnia, several authors have raised the possi- bility that psychological mechanisms may contribute to the maintenance of hypersomnolence, generally defined via excessive daytime sleepiness or excessive sleep (Bil- liard, Dolenc, Aldaz, Ondze, & Besset, 1994; Jacobson, Martell, & Dimidjian, 2001; Nofzinger et al., 1991). If these hypotheses are supported empirically, there may be utility in developing a psychological intervention for hypersomnolence. We have been developing a four- to eight-session multicomponent psychological interven- tion, briefly described below, though we emphasize that this approach awaits empirical evaluation. A number of the components used to treat hypersomnolence are ad- aptations or extensions of the interventions for insom- nia reviewed earlier.
As in insomnia treatment, hypersomnolence treat- ment begins with a functional analysis and case formu- lation. Clinicians probe for the frequency, intensity, and duration of the hypersomnolence, as well as its ante- cedents, behaviors, and consequences. Clients complete a daily sleep diary, supplementing standard sleep diary questions with additional probes for energy, activity levels, and other contextual/psychological data of note. The first session also involves MI, including a straight- forward review of pros and cons of working toward managing the hypersomnolence (Miller & Rollnick, 2002). Practitioner and client then set goals for treat- ment. The first and most obvious goal we set is for sleep (typically reducing sleep to approximately 8 hours per night), though we find it is equally critical to set goals for life. The latter is based on our clinical experience that “having nothing to get up for” is a key contribu- tor to hypersomnolence in clients with mood disorders. Often the combination of the mood disorder and the sleep disorder has led to unemployment and disrupted social networks. Without work to get up for and family/ friends to see, some individuals’ motivation to reduce sleep seems to waver. After setting the “sleep” and “life” goals for the treatment, the client is asked to identify one small step toward these goals for the coming week. We engage in problem solving to limit the impact of these obstacles on reaching the goal, and a method is
developed for monitoring the extent to which the goal is achieved (e.g., activity scheduling).
Clients with hypersomnolence also benefit from ed- ucation about a range of issues relating to sleep. Two domains have been particularly important. The first involves education about the operation of the circa- dian system, the stimulating environmental influences acting on it (e.g., light), and the tendency, if left un- checked, to move toward a delayed phase. The second involves education about sleep inertia described earlier. Finally, we work with clients to establish a wind-down period, a “wake-up protocol” (e.g., not hitting “snooze” on the alarm; making the bed, so that the incentive to get back in is reduced; heading for the shower; taking a quick brisk walk; getting sunlight), and to minimize fluctuation in the sleep–wake schedule across the nights of the week.
Finally, many of the same behavioral experiments and surveys described in this chapter appear to effec- tively treat the decreased energy and fatigue that we see in hypersomnolence. For example, clients benefit from completing an “energy experiment” to experience how spending energy can be a useful way to generate energy. Other times, we structure an experiment in which cli- ents are asked to rate their mood and energy before and after engaging in a social activity or leaving the house, to illustrate contextual variables that can improve mood and sleepiness. Creating a survey that emphasizes col- lecting data on what others do to generate energy, to get out of bed, or to fill their time when bored can offer helpful strategies. Finally, education and experiments on monitoring fatigue versus external stimuli can help to break attentional biases in hypersomnolence. As al- ways, we conclude with a session on relapse prevention in which progress is reviewed, gains are consolidated, and possible setbacks are discussed. In this manner, many of the treatment principles useful for insomnia may also be used to treat hypersomnolence.
Transdiagnostic Approaches
One only needs to work in a sleep clinic for a few days to realize the complexity of real-life sleep and circadian problems, particularly when sleep problems are accom- panied by mental and physical illness. Specifically, it is not uncommon to encounter clients who present with subsyndromal or syndromal systems of one or more sleep or circadian problems, including insomnia, hy- persomnia, advanced and delayed phase, sleep conti- nuity problems, irregular sleep–wake schedules, night-
664 CliniCal Handbook of PsyCHologiCal disorders
mares, and sleep apnea. At this point in history, there is a problem of “too many empirically supported treat- ments” (Weisz, Ng, & Bearman, 2014). In some ways, it is wonderful that our field has been so productive. However, too many treatments and continuing to de- velop more single-disorder treatments would likely cre- ate confusion for clinicians and exacerbate the existing challenges in disseminating and sustaining treatments in routine practice settings. Hence, the transdiagnostic sleep and circadian intervention (TranS-C; Harvey & Buysse, 2017) has been offered as one way to address the need for one short protocol to address the broad- est range of sleep and circadian dysfunction, and in a way that might be useful across mental and physical illness, and maybe even across some stages of develop- ment. TranS-C is grounded in basic science and the sleep health framework (Buysse, 2014) and combines principles from CBT-I, interpersonal and social rhythm therapy (Frank et al., 2005), chronotherapy (Wirz- Justice, Benedetti, & Terman, 2009) and MI (Miller & Rollnick, 2002). A key advantage of one treatment that tackles multiple problems is the substantial cost advantage to training providers (McHugh & Barlow, 2010). TranS-C takes a modular approach. It comprises crosscutting core and optional modules, which allows the treatment sessions to be more time efficient and “personalized” to the specific sleep problem(s) experi- enced by each client. As such, it is more time efficient and focused on each individual client’s presenting prob- lem. To date, two RCTs have supported the approach ( Harvey et al., 2018; Harvey et al., in press). The ap- proach awaits more comprehensive evaluation.
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670
Chronic pain represents the most common single disorder presenting to our health care systems, costing approximately $600 billion annually in direct treatment and lost productivity costs. This easily outranks cancer, cardiovascular disease, and every other psychological disorder described in this book. In this chapter John D. Otis, one of the foremost authorities on the treatment of chronic pain in the world, with decades of clinical experience, presents in a very detailed fashion his own approach to this problem, illustrated in his treatment of “Scott.” Here, clinicians can see how a variety of psycho- logical procedures, including several different calming interventions, activity pacing, pleasant event scheduling, cognitive restructuring, as well as anger management and sleep hygiene skills, all with strong empirical support, are all woven together in the context of expertly delivered motivational and educational messaging to facilitate compliance. Clinicians will find the necessary information in this chapter to begin treating the common and difficult problem of chronic pain that is so often ignored in health care delivery settings. —D. H. B.
over the last century, the conceptualization and treat- ment of chronic pain has evolved significantly. For
example, chronic pain was once viewed and treated by health providers in much the same way as acute pain; patients were frequently prescribed opiate pain medi- cations, and there were few other options for pain re- lief. Furthermore, health providers believed that once an injury healed, pain should resolve, and if it failed to resolve, the problem was deemed “psychological” in nature rather than “physical.” For patients whose pain persisted, this conclusion was understandably quite dis- tressing, as these patients felt their pain was real and not simply “in their heads. Our current understand- ing of the etiology of chronic pain has significantly changed and become much more nuanced, and we cur- rently have more varied treatment options to provide patients rather than relying solely on opiate medications for pain relief. In fact, research on evidence-based psy- chological approaches to pain management has grown tremendously over the past few decades. We now rec-
ognize that biological, psychological, and social factors can all contribute to the experience of pain, and we are much better equipped to address these factors to alle- viate patients’ suffering. Cognitive-behavioral therapy (CBT), now considered the “gold standard” psychologi- cal treatment for chronic pain, has substantial empiri- cal support. Cognitive-behavioral treatment approaches focus on changing certain target behaviors that appear to be problematic and teaching adaptive ways of coping. CBT for chronic pain is widely used as a stand-alone treatment or as part of multidisciplinary pain treat- ment programs. Importantly, decades of research have now contributed to our understanding of the various factors that should be considered when providing CBT to patients with chronic pain, and on ways therapists can tailor CBT to the specific needs of each patient in order to maximize treatment efficacy. The application of the cognitive-behavioral model to the management of chronic pain is based on the understanding that pain is a complex experience that is influenced by not only
C H A P T E R 17
Cognitive-behavioral Therapy for Chronic Pain
John D. Otis
Cognitive‑Behavioral Therapy for Chronic Pain 671
the presence of underlying pathology but also an indi- vidual’s thoughts, emotions, and behaviors. Thus, we have come a long way from old simplistic models that considered pain as either “physical” or “psychological,” and, as a result, patients with chronic pain now have in- creased hope for improved daily functioning and qual- ity of life.
The primary aim of the chapter is to provide a com- prehensive overview of the nature, etiology, and current theoretical conceptualizations of chronic pain, while focusing in detail on its evidence-based assessment and treatment. Given that many factors can impact the de- livery of chronic pain treatment, treatment variables such as treatment setting (e.g., inpatient, outpatient, specialty pain clinic, primary care setting) and treat- ment format (e.g., individual, group, or telehealth), are discussed and their clinical relevance highlighted. Given that the presence of comorbid diagnoses such as posttraumatic stress disorder or depression can further exacerbate the experience of chronic pain, the chapter includes a section on diagnoses that are frequently co- morbid with pain and their impact on treatment. The chapter then turns to a comprehensive overview of vari- ous evidence-based treatment components that are all important parts of evidence-based CBT for chronic pain (e.g., relaxation training, cognitive restructuring, stress management, time-based activity pacing, sleep hygiene). The final portion of the chapter describes a case example of a patient with chronic low back pain, and a detailed, session-by-session outline illustrates how cognitive-behavioral treatment for chronic pain treat- ment is conducted. Throughout the case, transcriptions of dialogue between therapist and patient illustrate how to deliver each of the treatment components. By provid- ing a thorough review of the process of assessing and treating a patient with chronic pain, along with a re- view of most recent clinical research, it is my hope that that this chapter will equip therapists with the tools to help patients return to healthier, happier, and more pro- ductive daily lives. The CBT protocol described in this chapter has been developed through decades of clinical research and practice, and the full protocol is detailed in available treatment manuals (e.g., Otis, 2007a, 2007b).
THE NATURE OF CHRONIC PAIN
The sensation of pain is defined as an unpleasant sen- sory and emotional experience associated with actual or potential tissue damage or described in terms of such
damage (Merskey & Bogduk, 1994). Pain is typically an adaptive sensation and serves to alert the individual that some type damage has happened or that time is needed to allow healing to occur following an injury. This type of pain would be experienced with a burn, bruise, fracture, or following a surgical procedure and is often referred to as acute pain. Typically, this type of pain resolves on its own after a period of rest, healing, or moderate physical activity; however, for some people, the experience of pain persists longer than would be an- ticipated and is out of proportion to the scope of an injury. When pain persists for more than 3 months, it is considered chronic pain (Merskey & Bogduk, 1994), which differs from acute pain because it often persists, sometimes for years, when there is no longer an un- derlying physical cause and can even occur in cases in which there was no precipitating injury.
Pain can present in a number of ways and combina- tions depending on the type of injury. There are two basic types of pain that can present as both acute and chronic in nature: nociceptive and neuropathic pain. Nociceptive pain is generally more common and can occur as either somatic, meaning activation of pain re- ceptors on the surface of the body or musculoskeletal tissues, or visceral, referring to the activation of pain receptors located in internal organ systems. Nocicep- tive pain can occur from injuries such as bumping one’s head, burning one’s skin, or pulling a muscle in the back. For example, a common patient description of nociceptive back pain is “It feels like a dull throb or ache in my back.” The damage can be from mechani- cal, thermal, or chemical stimuli, and can be focally located and somatic (e.g., a pain in your stomach after eating something that does not agree with you) or dif- fuse or referred in the case of visceral pain (e.g., an in- tense and painful feeling of pressure in the abdomen after surgery). Neuropathic pain occurs as the result of damage to the nervous system, either central or pe- ripheral, and may be described as “burning” “shooting” or “electrical” sensation. It is important to elicit from patients a description of their pain as part of an initial intake.
THERAPIST: Can you describe your pain to me? PATIENT: Ever since the accident, my arms feel like they
have pins and needles all the time. My back pain is always there, but when I move the wrong way, it feels like a bolt of electricity shoots down my leg. I lay there at night and I don’t even want to move.
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THERAPIST: That’s sounds tough. How are you coping with this change?
PATIENT: Not well. I can’t play with my kids, hug my wife, or work in the yard. I can’t do anything, be- cause I never know when it’s going to hit me.
In this case, the experience of neuropathic pain is being felt both physically and emotionally by this pa- tient. Neuropathic pain is most commonly caused by conditions such as diabetes, alcoholism, shingles, HIV infection, stroke, spinal cord injuries, nerve injuries, or multiple sclerosis (Bouhassira, Lantéri-Minet, Attal, Laurent, & Touboul, 2008). It is not uncommon for neuropathic or nociceptive pain to present in various combinations with one another, making diagnosis and treatment more complex.
THE PREVALENCE AND COST OF PAIN
Chronic pain is one of the most frequent reasons that people seek health care in the United States. A survey conducted by the Centers for Disease Control and Pre- vention indicated that 19.6% of adults endorsed having “pain most days or every day” for the past 6 months (QuickStats, 2017). Chronic pain conditions affect at least 116 million U.S. adults at a cost of $560–635 bil- lion annually in direct medical treatment costs and lost productivity due to pain (Institute of Medicine, 2011; Gaskin & Richard, 2012). Higher rates of chronic pain are found in women (34.3%) compared to men (26.7%), although men may have chronic pain for longer dura- tions than women (Manchikanti et al., 2006). Com- mon types of chronic pain conditions include low back pain, headache, arthritis, multiple sclerosis, fibromyal- gia, and shingles. The cost of chronic pain exceeds the economic costs of the six most costly major diagnoses: cardiovascular diseases ($309 billion); neoplasms ($243 billion); injury and poisoning ($205 billion); endocrine, nutritional, and metabolic diseases ($127 billion); diges- tive system diseases ($112 billion); and respiratory sys- tem diseases ($112 billion) (Gaskin & Richard, 2012).
There is a particularly high prevalence of chronic pain among U.S. veterans. Within the U.S. Depart- ment of Veterans Affairs (VA) health care system, al- most 50% of patients in primary care endorse experi- encing pain on a regular basis (Kerns, Otis, Rosenberg, & Reid, 2003). Chronic pain is also a significant prob- lem among soldiers returning from deployment, with
44% reporting chronic pain (Toblin, Quartana, Riv- iere, Walper, & Hoge, 2014).
THE FEAR–AVOIDANCE MODEL OF PAIN
One of the patient factors that often plays a significant role in the development of chronic pain is avoidance. People tend to avoid situations that are considered un- pleasant or painful. While avoidance may be consid- ered an adaptive reaction to dealing with situations that could elicit acute pain, it tends to not be an adaptive way of coping with chronic pain. Another patient factor that contributes to the experience of pain is catastroph- izing. A substantial literature shows that a tendency to catastrophize during actual or anticipated pain is one of the most important predictors of the pain experience (Sullivan et al., 2001; Riddle, Wade, Jiranek, & Kong, 2010). The cognitive-behavioral fear–avoidance model of chronic pain was proposed by Vlaeyen and Linton (2000) to explain how fear and avoidance play a role in the transition from acute pain to the development of chronic pain. According to this model, if a person inter- prets the experience of pain as overly threatening (cata- strophizing), it may lead him/her to fear the experience of painful sensations and avoid activities that he/she be- lieves have the potential to cause pain. For example, if a person believes that going for a walk with a friend will increase his/her back pain, he/she may cancel the plan with the friend or engage in the activity with height- ened caution. This interpretation can result in guarding behaviors, such as tensing or rubbing muscles in prepa- ration for movement, walking cautiously, or altering posture in preparation for pain. This heightened level of alert to any pains based on the incorrect belief that they are a sign of damage being done or of some type of underlying pathology that has yet to be identified may cause some people to become hypervigilant to painful sensations, and may cause even low-intensity painful sensations to be perceived as extreme and unbearable. As the fear and avoidance of physical activity grows, the world in which the individual functions becomes more and more restricted. The avoidance of physical activ- ity limits the individual’s opportunity to test and cor- rect pain expectations. Pain may begin to interfere with everyday function and cause increased disability. Once engagement in reinforcing activities (e.g., interacting with friends, exercise, cooking) begins to decline, the individual may become down or depressed. Depres- sion, inactivity, fear, and avoidance interact with one
Cognitive‑Behavioral Therapy for Chronic Pain 673
another to make pain seem more intense. However, in the absence of serious somatic pathology, individuals who interpret pain as nonthreatening, and who engage in adaptive problem solving rather than catastrophiz- ing, are more likely to have quicker recoveries due to their participation in daily activities. Thus, catastroph- izing may play a mediating role in the development of chronic pain (Flink, Boersma, & Linton, 2013; Racine et al., 2016; Ramírez-Maestre, Esteve, Ruiz-Párraga, Gómez-Pérez, & López-Martínez, 2016). Since the in- troduction of this model, studies have shown that fear and avoidance of movement is an even better predic- tor of disability than underlying biomedical pathology (Crombez, Vlayen, Heuts, & Lysens, 1999). This model has served as the basis of research and clinical practice for decades and has helped in our formulation of treat- ments designed to help patients adaptively cope with the experience of chronic pain.
CBT FOR CHRONIC PAIN
CBT is considered the “gold-standard” psychological treatment approach for chronic pain. CBT for chronic pain is aimed at changing patients’ negative thoughts and behaviors that serve to maintain and exacerbate the experience of pain, and teaching ways of safely reintroducing enjoyable activities into their lives. Key components of CBT for chronic pain include relaxation training (e.g., diaphragmatic breathing, visual imagery, progressive muscle relaxation, and meditation), cogni- tive restructuring focused on thoughts related to pain (e.g., “This pain is going to kill me”), time-based activ- ity pacing (i.e., teaching patients how to become more active without overdoing it), and graded homework as- signments designed to decrease patients’ avoidance of activity and reintroduce a healthy, more active lifestyle. CBT also focuses on promoting patients’ increased ac- tivity and productive functioning using techniques such as exercise homework, activity scheduling, and graded task assignments. A substantial literature documents the efficacy of CBT for a variety of chronic pain condi- tions, including osteoarthritis, chronic back and neck pain (Linton & Ryberg, 2001), diabetic neuropathic pain (Otis et al., 2013), and tension headache (Hol- royd et al., 2001). In a meta-analysis of 22 randomized controlled trials of psychological treatments for chronic low-back pain, cognitive-behavioral and self-regulatory treatments specifically were found to be efficacious (Hoffman, Papas, Chatkoff, & Kerns, 2007).
Given that pain occurs across the lifespan, a sub- stantial amount of research has focused on evaluating the efficacy of CBT for particular subpopulations of patients, such as children or older adults. For example, a number of studies have documented the efficacy of CBT for children with a variety of painful conditions (Eccleston, Morley, Williams, Yorke, & Mastroyan- nopoulou, 2002; Palmero, Wilson, Peters, Lewandows- ki, & Somhegyi, 2009; Kashikar-Zuck et al., 2013). A meta-analysis of review of 25 randomized controlled trials concluded that CBT, relaxation, and biofeedback all produce significant positive improvements in pain reduction in youth with headaches, fibromyalgia, and abdominal pain (Palermo, Eccleston, Lewandowski, Williams, & Morley, 2010). Chronic pain is common in older adults, and while there are fewer studies ex- amining the effectiveness of CBT with this population, research suggests that the skills taught in CBT can be effective at helping older adults with chronic pain. One pilot study found that CBT significantly reduced pain intensity and pain-related disability in older adults with chronic low-back pain (Reid, Otis, Barry, & Kerns, 2003), and a randomized control trial in older adults with a range of chronic pain conditions demonstrated that a CBT-based pain self-management program was effective in reducing pain distress, pain disability, and unhelpful pain beliefs (Nicholas et al., 2013).
Treatment Variables
It is important for therapists to take into consideration variables that could affect treatment delivery, such as the context or format in which treatment for chronic pain will be delivered. Factors such as the setting of treatment can impact aspects treatment delivery, as different settings (e.g., inpatient or outpatient settings) might focus on treatment of particular types of pain, and some settings might differ in the amount and ways that therapists work in conjunction with a multidisci- plinary care team. Furthermore, therapy format is also important to consider given that treatment for chronic pain can be implemented in either group or individual sessions, with each format having its advantages and challenges. I discuss each of these issues in turn.
Therapy Setting
Opportunities exist for therapists to practice CBT for pain in a variety of clinical settings. Therapists who have been trained to deliver CBT for pain may offer
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this approach as one of several evidence-based treat- ments available in an individual outpatient or group practice setting. Opportunities also exist for therapists to join multidisciplinary pain management programs that include disciplines such as physical therapy, occu- pational therapy, nursing, psychiatry, neurology, phys- iatry, rheumatology, and so forth. In multidisciplinary pain management programs, providers work together in a coordinated manner to provide care that is inte- grated and tailored to the needs of the patient. Given the high prevalence of pain complaints in the primary care setting, therapists who are integrated into primary care have an opportunity to disseminate needed pain management skills to a broad sample of the population. Therapists may also find opportunities to practice in specialty programs, including surgical centers, facial pain clinics, dental clinics, burn units, or orthopedic surgical centers, as skills learned in CBT for pain help patients in these programs achieve reduced pain and disability, and higher rates of benefit from treatment interventions. The inpatient setting also provides many opportunities for therapists to help patients to develop pain management skills. While some inpatients may have existing painful medical conditions, others may be engaged in rehabilitative services, such as physical or oc- cupational therapy, that require regular participation in order to maximize functional gains. Although patients may be experiencing a combination of both acute and chronic pain sensations, many patients can potentially benefit from learning skills that allow them to cope more effectively, reduce distress, and fully participate in rehabilitation efforts. Regardless of the clinical setting, therapists should strive to establish open communica- tion with all providers involved in a patient’s pain care. This effort helps to ensure that the patient is receiving a consistent message across providers and facilitates a coordinated overall plan for the patient’s recovery.
Therapy Format
CBT for pain management can be facilitated in indi- vidual or group formats, and both of these formats have potential benefits and challenges that are important to consider. There are situations in which individual therapy is the treatment approach of choice. Individ- ual therapy allows a therapist more time to address the specific issues and challenges of the patient, to tailor the treatment to the specific needs of the patient, and to engage in patient-specific problem solving and goal setting. There is more flexibility in timing of sessions
when providing individual therapy, as sessions only need to be scheduled for one person rather than an en- tire group. Patients may request individual therapy if they feel uncomfortable sharing personal information with a group. However, there are also several advantages to group treatment. First, a group therapy approach is more resource-efficient and allows one therapist to help several patients at the same time. Second, group treat- ment provides an opportunity for patients to learn cop- ing skills from other group members. Third, interacting with others in a group may enable patients to develop a positive social support network that lasts well beyond the end of therapy.
While a substantial literature documents the effi- cacy of CBT for chronic pain, there are sizable barriers that prevent patients from receiving therapy, including physicians’ lack of familiarity with behavioral therapy modalities, limited geographic access to therapists with specialized training in CBT for pain, stigma associated with psychotherapy, and lack of sufficient insurance to cover these modalities. In addition, patients with chronic pain and comorbid health conditions (e.g., pa- tients with spinal cord injuries, dialysis patients) often encounter physical and logistical barriers that interfere with mobility and transportation to appointments. As a result, many patients do not receive adequate care for their pain. Given the wide availability of smartphones and Internet accessibility, the development of telehealth or mobile application “app”-based CBT programs offer an opportunity to expand the “reach” of evidence- based treatment for pain. Preliminary research on the development and use of apps to teach pain manage- ment skills show promise (Friesen et al., 2017; Jamison, Mei, & Ross, 2018; Jamison, Jurcik, Edwards, Huang, & Ross, 2017) and data suggest that the use of apps is feasible and well-tolerated by patients (Jamison et al., 2017). An app-based CBT program is likely to be most successful if it includes reminders to use pain manage- ment skills throughout the day and to take medications as prescribed, and if it provides the opportunity for patients to have two-way communication with provid- ers to elicit a sense of support. All of these features are likely to increase patients’ engagement with learning and increase their use of pain management skills. Using this technology could facilitate the delivery of CBT approaches to pain management and the development of adaptive coping skills. Future continued research is needed to develop and test novel approaches to make evidence-based pain treatment available to large num- bers of patients.
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Patient Variables
In addition to treatment variables, it is important to consider a number of patient-centered variables prior to engaging a patient in treatment. This may include the presence of comorbid conditions, such as anxiety, depression, posttraumatic stress disorder, substance use disorders, or whether the patient is receiving pharmaco- logical treatment for pain.
Comorbidities
Chronic pain is a stressful condition that can be caused by a variety of precipitating events (e.g., injury, trauma, illness) and can impact nearly every aspect of a person’s life. Thus, it is not uncommon for individuals with chronic pain to experience related mental health prob- lems (e.g., mood problems, traumatic stress, or sub- stance use disorders). It is possible that the presence of chronic pain then increases a patient’s vulnerability to experience other psychological disorders; alternatively, it is also possible that the presence of co-occurring psy- chological conditions such as mood problems make the recovery from chronic pain much more difficult. Either way, the interaction between pain and other mental health comorbidities can impact symptom presentation and should be considered by the clinician when devel- oping a treatment plan.
Emotional Disorders: Anxiety and Depression
Given the impact that chronic pain can have on all aspects of a person’s life, it is not uncommon to find high rates of comorbidity between pain and emotional disorders such as anxiety and depression. Studies in- dicate depression prevalence rates ranging from 30 to 54% in chronic pain samples (Banks & Kerns, 1996; Elliott, Renier, & Palcher, 2003), and depression is as- sociated with more frequent pain complaints and im- pairment (Bair, Robinson, Katon, & Kroenke, 2003). Although data indicates that women are more likely to have chronic pain than men, men and women with chronic pain are equally likely to be depressed (Miller & Cano, 2009). Co-occurring pain and depression are common in primary care, with one study revealing that two thirds of patients with a major depressive disorder also had chronic pain (Arnow et al., 2006). Rates of anxiety are reported be as high as 45% in pain pop- ulations (Kroenke et al., 2013; Staerkle et al., 2004). Anxiety and fear play an important role in the experi-
ence of pain, with one study indicating that for patients with low-back pain, anxiety accounted for 32% of the disability and 14% of the severity of the pain (Staerkle et al., 2004). The presence of emotional disorders can complicate the delivery of many elements of CBT, in- cluding goal setting, activity engagement, challenging negative thinking, and motivation to participate (Kerns & Haythornthwaite, 1988). For example, patients with pain and anxiety may catastrophize and worry about the meaning of pain, avoid activities that have the po- tential to cause pain, or withdraw and socially isolate themselves. Similarly, patients with depressed mood may report that they understand the benefits of goal setting but lack the motivation to take the first step. There is accumulating evidence that pain and emo- tional disorders share common neurobiological path- ways (Bär et al., 2007; Wiech & Tracey, 2009; Han & Pae, 2015). Studies using functional MRI investigated the impact of pain catastrophizing on central nocicep- tive processing and found that during intense pain, prefrontal cortical modulation impedes patients from disengaging from and suppressing pain (Seminowicz & Davis, 2006). Experimental studies of pain indi- cate that inducing a depressed mood state and negative pain-specific cognitions is associated with increased pain unpleasantness and increased activity in the pre- frontal cortex, subgenual anterior cingulate cortex, and hippocampus (Berna et al., 2010). This body of re- search is currently evolving, but evidence of overlapping structures involved in pain and cognitions may explain how the presence of an emotional disorder may impact processing of painful stimuli.
Posttraumatic Stress Disorder
Over the past 20 years, interest has grown in examin- ing the interaction between chronic pain and posttrau- matic stress disorder (PTSD), as clinical observation and research suggest that these disorders co-occur at high rates and often negatively impact a patient’s re- sponse to treatment focused on either condition (Otis, 2019). Research indicates that individuals with co- morbid chronic pain and PTSD report greater pain, PTSD symptoms, depression, anxiety, disability, and opioid use than those with only one of these condi- tions (Asmundson, Wright, & Stein, 2004; Sullivan et al., 2009; Jenewein, Wittmann, Moergeli, Creutzig, & Schnyder, 2009; Outcalt et al., 2015). Studies esti- mate that between 20 and 34% of patients referred for the treatment of chronic pain have significant PTSD
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symptomatology or are diagnosed with PTSD (Geisser, Roth, Bachman, & Eckert, 1996; Asmundson, Nor- ton, Allerdings, Norton, & Larsen, 1998). In patients for which pain is secondary to motor vehicle accidents, PTSD rates have been found to range from 30 to 50% (Hickling & Blanchard, 1992; Chibnall & Duckro, 1994; Taylor & Koch, 1995). Given the types of inju- ries sustained in military combat, pain and PTSD are common comorbidities faced by military veterans (Seal, Bertenthal, Miner, Sen, & Marmar, 2007; Clark, Bair, Buckenmaier, Gironda, & Walker, 2007). Lew et al. (2009) reviewed the medical records of 340 Operation Enduring Freedom/Operation Iraqi Freedom (OEF/ OIF) veterans seen at a Level 2 Polytrauma Resource Center. Analyses indicated a high prevalence of chronic pain (81.5%), PTSD (68.2%), and mild traumatic brain injury (66.8%). Integrated treatments for chronic pain and PTSD have shown promise in reducing symptoms of both conditions by targeting shared psychological vulnerabilities (Otis, Keane, Kerns, Monson, & Scioli, 2009).
Substance Use
When working with a patient who has chronic pain, it is important to determine whether he/she is using substances as a way to cope with pain or other mental or physical comorbidities. Given the fact that problem- atic use of substances will interfere with the acquisi- tion of skills taught in CBT, in those cases in which a substance use disorder is present, treatment of the sub- stance use disorder should take precedence over engage- ment in CBT for pain. Although there are a number of different types of substances that have the potential for abuse (e.g., alcohol, cannabis, street drugs), the use of opioids for pain has gained great attention, because it is considered a starting point for many people who subse- quently develop addiction to drugs such as heroin (see Higgins, Heil, & Peck, Chapter 15, this volume). Data indicate that 21–29% of patients prescribed opioids for pain misuse them (Vowles et al., 2015), and 80% of people who use heroin first misused prescription opi- oids (Muhuri, Gfroerer, & Davies, 2013). In fact, some of the highest rates of opioid abuse and illicit drug use are found in patients who sustain injuries from auto- mobile accidents, in those with multiple pain locations, and in those with a history of past illicit drug use or pain. Other predictors of substance use in patients with chronic pain are family history of substance abuse, his- tory of legal problems, higher doses required to manage
pain, dependency on cigarettes, psychiatric treatment history, multiple car accidents, and fewer reported ad- verse symptoms of opioids (Michna et al., 2004).
Concurrent Pharmacological Treatment for Pain
There are many appropriate and necessary forms of pain medications that allow individuals with acute and chronic pain to participate in rehabilitation, regain function, and lead productive lives. Patients should be reassured that participation in CBT does not mean that medications will be “taken away” from them. It is important to allay patients’ fears and apprehensions by talking openly about the ways that psychological thera- pies might work in conjunction with pharmacological approaches. For example, learning and practicing cog- nitive and behavioral skills to manage pain can actually help prescribed pain medications to work more effec- tively. Furthermore, patients who learn psychological skills to manage pain have another method for decreas- ing pain during pain flare-ups, rather than only having the option of reaching for a pill. By coordinating care with a physician who is prescribing pain medication, the patient is provided with a consistent message about the ways that medication and psychological treatments can complement one another. This might help patients to be less resistant to trying psychological approaches. Furthermore, patients who consider learning psycho- logical approaches to pain management in conjunction with taking medication can be reminded that the psy- chological approaches do not have “side effects,” and that many patients have found the combination of these treatment approaches to be effective in reducing pain. Finally, given that many patients report that they want to stop taking pain medications, it can be helpful to remind patients that after learning psychological ap- proaches to managing pain, many patients have been able to successfully reduce or eliminate their need for pharmacological forms of pain management.
CASE STUDY
“Scott Davis” is a 64-year-old, married male with chronic back pain. He and his wife have three daugh- ters who are in college but live nearby. The onset of his back pain was associated with an injury 9 months ago, when he tripped while walking down a flight of steps at a friend’s house. After 1 month of constant pain, Scott started attending sessions with a physical therapist.
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The physical therapist worked with Scott weekly, and although Scott was able to gain strength and flexibility, his back pain did not resolve. Scott sought a consul- tation with a neurologist and an orthopedic specialist at a local hospital, but they we not able to offer him additional information to account for why his chronic pain was persisting and informed him that he was not a candidate for corrective surgery. Scott was referred to the outpatient psychology clinic by his orthopedist, with the recommendation that he might benefit from learning CBT skills for assistance with managing his chronic back pain.
Engaging the Patient in Treatment Prior to the Interview
When speaking with the patient for the first time, it is important to explain why it has been suggested that he/ she meet with a therapist regarding his/her pain. This initial contact with the patient, whether completed over the phone, by video, or in person, should be handled tactfully, since patients with chronic pain may feel that they are being referred to a see a therapist because no one believes their pain is real, or because the pain is only psychological in nature and thus “in their head.” Also, for some patients with severe pain, the effort it takes to transport themselves to attend the initial appointment can itself be painful. Patients need to feel that the ap- pointment will have some perceived benefit, or else they may not show up for the interview. For these reasons, it is important to reassure the patient and acknowledge that while pain is certainly felt physically, it can also be influenced by many other factors. It is also impor- tant to clearly explain the value of the assessment. The interviewer should engage the patient in a discussion of the ways that pain has impacted his/her life, relay the importance of considering all of these areas when developing a plan for treating pain, and explain that the interview is an important step toward gaining a greater understanding of the pain in order to tailor treatment. The following scenario exemplifies the way to conduct the introductory phone call when a patient is referred to a pain therapist.
THERAPIST: Hi, Mr. Davis. This is Dr. Jones from the Central Pain Clinic. The reason I’m calling you today is because your medical provider thought you might be interested in speaking with me about learn- ing some strategies for managing your pain. Do you have a minute to talk right now?
SCOTT: Hi, Doctor. It’s nice to meet you. Please call me Scott. Yes, my provider brought this up at our last appointment, so I thought you might be calling, but I really don’t know if there is anything you can do for me. This is real pain and I feel it every moment of the day—it’s not in my head. So, I’m not sure how talking to you about it is going to do me any good.
THERAPIST: Well, seeing a therapist doesn’t mean we think that your pain is in your head. We know your pain is real. There are a number of approaches that can be used for managing pain, such as physical therapy, medications, and surgical procedures, but we also need to make sure that we are doing every- thing we can do to manage our pain ourselves. That’s where pain psychology comes in.
SCOTT: I’m not interested in surgery and I don’t like taking pain medication. I’ve been working with a physical therapist and I’m exercising at home, but I feel like I have reached a point where I’m not improv- ing and I’m still in pain. So, what are you offering?
THERAPIST: When you have had pain for a long time, it can affect everything you do—relationships, fam- ily, work—it affects your whole life—and it can be stressful. Have you experienced this?
This is an important moment in the call, because the therapist is demonstrating interest in the issues that are likely faced by Scott, and allowing him an opportunity to reveal the ways that pain has impacted his life.
SCOTT: Yes. I feel like I’m constantly thinking about my pain and it has affected everything I do. I feel like I’m falling apart, and it’s really frustrating.
THERAPIST: Sometimes people report that pain affects their mood and makes them feel anxious, down, or less tolerant of even minor annoyances. People even say sometimes that when they are feeling stressed it makes pain seem even more intense. Have you ever noticed this? [Patients typically agree with this.]
SCOTT: I worry about hurting my back again. On days when the pain is bad, I don’t feel like doing anything. I just want to stay inside, not go to work, and be away from people. I’m also having a hard time sleeping at night. I definitely see how my mood and pain are related.
THERAPIST: Health care providers know that in order to provide effective pain management, it’s important to treat the whole person, not just your back. The
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goal of our first meeting would be for me to develop a complete history of your pain and understand how it affects all the areas of your life. We’ll sit down and talk for about an hour, and then I’ll ask you to fill out some questionnaires about your pain. After I have reviewed the information, we will speak again to develop the best plan for your treatment. How does that sound?
SCOTT: I don’t see how talking about my pain is going to help me.
THERAPIST: This is not talk therapy. If we decide to move forward with treatment, I will be teaching you some actual skills that you can use to manage your pain more effectively. I will teach you skills such as how you can manage your thoughts and emotions to reduce pain, how to relax, how to improve your sleep, how to pace yourself during activities, and how to reduce stress in your life. Many people have found these skills to be very effective in managing pain. In fact, these skills have been well supported by lots of different clinical trials that show that they are effec- tive. This is a short-term, goal-oriented treatment, so you won’t be in therapy forever, and when we are done, you will have more tools in your “tool belt” that you can use to take the edge off your pain when- ever you need it. Unlike pain medication, there are no side effects, and once you learn the skills, they are yours for life. How does this sound?
SCOTT: Al right. I guess I don’t have anything to lose, since I don’t have many other options. But these skills you are talking about actually do sound some- what promising. I’ll meet with you and see what you have to offer.
Conducting a Pain Assessment
There are a number of components that typically comprise a pain assessment. In most settings, a clini- cal pain interview is conducted to assess specifically a patient’s pain history and experience of pain. Often, this interview is supplemented by the administration of self-report questionnaires that assess domains that are relevant to the experience of pain. In addition, it is also important for therapists to communicate with other providers who are involved in the patient’s pain care, such as medical providers and physical thera- pists, in order to develop a coordinated plan for treat- ment.
The Clinical Pain Interview
Prior to engaging a patient in treatment, it is important to conduct a clinical interview in order to gather in- formation about the patient’s experience of pain. This information helps the therapist determine the elements of CBT that will likely be of greatest benefit to the pa- tient. Information obtained in the clinical interview can be supplemented by the completion of self-report questionnaires. In addition, if the patient is currently receiving care for his/her pain from other providers (e.g., neurologists, physical therapist, family physician), then an authorization for the release of medical infor- mation should be obtained, so that the therapist can communicate with other providers for input about the treatment approach they are developing with the pa- tient, any limitations on movement, and to ensure that treatment goals are consistent across providers. The clinical interview should assess the etiology of the pa- tient’s pain condition, along with psychological, social, and environmental factors that may serve to maintain or intensify a person’s experience of pain.
After meeting for the assessment, the therapist can remind the patient that the goal of the meeting is to obtain a complete history of his/her pain and how it has impacted his/her life, so that a more tailored plan for treatment can be developed. Specifically, the inter- view begins with obtaining a pain history that includes a thorough description of the patient’s pain condition; how and when the pain started; a description of the pain in the words of the patient (e.g., “sharp,” “burn- ing,” “aching”); location(s) of pain; and pain intensity ratings, both current and average over the previous week, using a numeric rating scale (where 0 = no pain and 10 = worst pain imaginable). Many patients report experiencing pain in several locations, and information regarding pain frequency, intensity, and duration may be different for each pain site. It can be helpful to ask the patient to rank the pain sites, beginning with the site that most negatively affects his/her functioning. There are a number of additional pain-related factors to carefully evaluate, such as pain-related functional in- terference (e.g., pain interferes with ability to perform at work or school, when socializing, when doing house- hold chores). It is important to gain an understanding of strategies the patient has tried in the past and is cur- rently using to manage the pain. For example, ask the patient about things he/she has discovered that make the pain increase (e.g., lifting boxes, bending, sitting
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for long periods of time) and things he/she has identi- fied that tend to reduce pain (e.g., taking a hot shower, yoga, pain medication, or using a heating pad). The patient is the “expert” on his/her pain, and the thera- pist’s job is to find out what the patient already knows about his/her pain and ways he/she has tried to manage it. Personal coping strategies, beliefs and expectations, and other cognitive processes are important to assess in order to understand a person’s strengths and vulner- abilities. Thoughts, beliefs, and reactions to pain can have a large impact on the way pain is processed. Nega- tive thoughts (e.g., “I can’t deal with this any longer” “What did I do to deserve this?”; “My life is miserable”) can lead to exacerbation of existing pain, difficulty in coping with pain, and a downward spiral, leaving the patient feeling unable to manage the pain effectively. However, positive thoughts (e.g., “I can control my pain”; “This will not last forever”; “I have coped before and I can do it again”) can have just the opposite ef- fect. In addition, adaptive coping skills that the patient has already developed and used successfully in the past can be reinforced and utilized to cope with the current pain episode. Questions about treatment modalities the patient has tried previously to address the pain (e.g., acupuncture or physical therapy) and their effective- ness, and goals for pain management (e.g., returning to work vs. receiving disability) can provide information about the patient’s motivation to engage in pain self- management approaches.
During the interview, Scott described the onset of his injury in detail. He was forthcoming and stated that he appreciated the opportunity to describe how pain had impacted his life—he said that it was the first time a provider had allowed him time to “tell his story.” This is not an uncommon observation by patients, as many providers are not allowed sufficient time in their appointment schedule to gather this level of detailed information. This discussion also facilitated the devel- opment of the therapeutic alliance, because Scott was able to see that the therapist was genuinely interested in his perspective on his experience of pain. Scott rated his back pain as a 6 out of 10 on average over the past week. He described his pain as “constant” but also re- ported that it tends to increase with activity as the day progresses. He reported that long walks, bending, and standing “too long” cause his pain to increase, while resting and sitting allow his pain to decrease. Scott re- ported that he had a similar back injury 2 years prior to his most recent accident of falling down the stairs.
He had fully recovered from that injury, and expected to recover from his current injury. Scott used the same rehabilitation strategy that helped him to recover from his back pain the previous time; however, this time, the pain persisted. Scott used words such as excruciating, burning,and debilitating to describe his pain, which was an important observation, as some of these words were more affectively laden and suggested an emotion- al component to his pain. Scott reported that he was prescribed pain medication by a provider, but he did not like the way it made him feel, or the idea of tak- ing something that was “just covering up the issue.” He reported that he wanted to know what was causing his pain, and that was why he had sought consultation with the neurologist and orthopedic physicians.
After obtaining the pain history, a brief psychosocial assessment should be conducted, including information such as marital status, living situation, education, cur- rent employment/school, interpersonal relationships, hobbies, and daily activities. This provides information about the patient’s potential sources of social support, level of activity, and potential targets for behavioral activation. It is helpful to inquire about other health behaviors, such as sleep, sex, weight, and substance use, each of which may have an impact on the patient’s expe- rience of pain. Finally, a mental health history should be obtained, including a review of past and present mental health diagnoses and treatment, with special attention given to past and present depressive symptoms, anxiety, posttraumatic stress symptoms, and substance use (in- cluding aberrant use of medications and substances use to manage pain). Therapists should always ask about the use of substances (e.g., alcohol, marijuana, cocaine, heroin), pain medication obtained from other sourc- es (e.g., obtained from friends, spouse, medications bought off the street, or prescriptions), and whether the patient takes pain medication as prescribed. This last question is important, because some patients take medication according to their own schedule, which can reduce the medication’s effectiveness or contribute to addiction.
Scott described a positive and supportive relationship with his wife of 25 years and loving relationships with his three daughters. He stated that he had missed many important occasions over the past few months due to his pain, including many of his daughters’ sports games, due to his pain with standing or sitting. In terms of his educational and vocational accomplishments, Scott stated that he had completed a college degree, found a
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job as a professional in the community, and had been very successful in his career. He described himself as “highly efficacious” and recognized by his peers as a person who was very productive at work. Scott reported that he enjoyed working and felt driven to succeed. Prior to the injury, Scott had been in good health and had no other significant health issues. He was physi- cally active and enjoyed activities such as riding his bike to work, shopping for groceries at the local market, and performing chores and home maintenance. He enjoyed having friends over for dinner, being a host, and prepar- ing for social events. However, since the onset of his pain, Scott’s active life had become far more limited. Scott described that he never was a cigarette smoker, and he only consumed alcohol on occasion. He denied the use of recreational drugs since college, although he indicated that a friend had suggested he try marijuana for pain relief.
When asked about how he had been coping with his pain, Scott paused for a moment, then became tearful. He reported, “I pretty much live in fear of hurting my- self again. I’m not the man I use to be.” He described an event while walking on a sidewalk when he felt as though he was in so much pain that his back was going to give out, and he caught himself before falling to the ground. After this happened, Scott started to become very cautious when walking on sidewalks or any uneven surfaces where he might step in a way that could cause increased pain. Scott stopped many of the activities he once enjoyed at home, including maintaining the house, doing laundry, emptying the dishwasher, and grocery shopping. He stopped socializing with friends, because he worried about what they would think of him. He bought a cane at a local drug store and started using it when walking. Scott reported feeling guilty for asking his wife to do the chores that he used to do, and he felt that she was becoming impatient with him. He report- ed being far less productive at work since his injury. He reported difficulty with concentration and reduced mo- tivation to complete jobs. On the occasional “good day” when pain is lower than usual, Scott reported that he does “as much as he can,” but this often backfires and he ends up in pain again. When asked about how his pain affects his sleep, Scott sighed and remarked that he has difficulty falling to sleep at night, because he thinks about all the things he has to do, and he worries about how he will feel the next day if he does not sleep. He denied any thoughts of hurting himself. Scott denied a history of psychological treatment. Scott stated that he was never an anxious person, and prior to his injury, he
was always able to look on the bright side of things, but lately his thoughts were more focused on his pain and all of the things he was no longer going to be able to do.
A typical pain interview such as the one conducted with Scott may take an hour to complete, depending on the level of detail the patient provides and number of pain sites and/or comorbid conditions reported. Fol- lowing completion of the interview, the therapist should provide some immediate feedback to the patient if there are domains of functioning that could serve as targets for intervention, such as relaxation training, activity pacing, or sleep hygiene.
Standardized Pain Inventories
The selection of standardized pain inventories depends on a number of factors, including the type of informa- tion desired and the amount of time a therapist has to meet with the patient. Completing questionnaires is a burden on patients and can be distressing; thus, the data obtained from those questionnaires must be clini- cally useful. Therapists should carefully consider the validity and reliability of each measure that they ask a patient to complete, and choose only well-validated and standardized measures. Depending on the information that is revealed in the clinical interview, other measures that assess the presence or severity of comorbid psycho- logical conditions (e.g., substance use, anxiety, depres- sion, sleep disorders, or posttraumatic stress disorder) can be added as needed.
While the clinical interview is the best source of data about a person’s experience of pain, a number of self-report inventories have been developed in an ef- fort to supplement information obtained in the inter- view. These assessments are meant to evaluate the level of subjective pain, interference, coping strategies, and depressive symptoms that are relevant to pain. The fol- lowing are some of the “gold standard” pain assessment inventories that are commonly used in both inpatient and outpatient pain clinics.
The Brief Pain Inventory—Short Form (BPI; Clee- land & Ryan, 1994) is a 9-item, self-report question- naire that allows patients to rate the severity of their pain and the degree to which their pain interferes with common dimensions of feeling and function. Two do- mains measured by the BPI—pain intensity (severity) and the impact of pain on functioning (interference)— have been recommended for inclusion as outcomes in all chronic pain clinical trials (Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials
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[IMMPACT]; Turk et al., 2003). Pain intensity is rated on a 0- to 10-point scale, with 0 = No pain and 10 = Pain as bad as you can imagine. The IMMPACT panel specifically recommended the interference items of the BPI, rated on a 0- to 10-point scale, for assessment of pain-related functional impairment (Dworkin et al., 2005). It has excellent reliability and validity, and it has been used widely in research with medical populations.
In situations in which therapists have limited time for assessments, such as in primary care or when seeing a patient who is hospitalized, brief measures of pain are more appropriate. The PEG (Krebs et al., 2009), a brief, 3-item scale, comprises items assessing average pain in- tensity (P), interference with enjoyment of life (E), and interference with general activity (G). The PEG was de- rived from the BPI and has been shown to be a reliable and valid measure of pain among primary care patients with chronic musculoskeletal pain and diverse VA am- bulatory patients.
The McGill Pain Questionnaire (MPQ; Melzack, 1975), a self-report questionnaire, comprises 102 words separated into three major classes: the sensory, affec- tive, and evaluative aspects of pain. It also includes a pain drawing. Each word is grouped into one of 20 sub- classes of words, and respondents are asked to circle one word from each subclass as a description of the pain. Scores range from 0 to 78, based on the rank value of the words circled. The scores are interpreted in terms of quantity of pain, determined by the number of words circled, and quality of pain, determined by the rank- ing of particular words circled. The short-form MPQ can be used to cut down on administration time (Mel- zack, 1987). The MPQ does have some limitations, as it requires a solid grasp of the English language and a sophisticated vocabulary. The stability, reliability, and validity of the MPQ have been established (Reading, Everitt, & Sledmere, 1982).
The Pain Catastrophizing Scale (PCS; Sullivan, Bishop, & Vivek, 1995) is a self-report measure that asks patients to reflect on past painful experiences and to indicate the degree to which they experienced each of 13 thoughts or feelings when experiencing pain on a 5-point scale from 0 (not at all) to 4 (all the time). A total score is yielded (ranging from 0 to 52), along with three categories including Rumination (persistent thoughts about pain), Magnification (worrying that something serious may happen), and Helplessness (complete lack of control in reducing the pain). A total PCS score of 30 corresponds to the 75th percentile of the distribu- tion of PCS scores in clinic samples of patients with
chronic pain and represents clinically relevant levels of catastrophizing. The information gathered about cata- strophizing can help to predict disability, identify areas for restructuring during therapy, and facilitate posi- tive rehabilitation outcomes (Osman, Barrios, Kopper, Hauptmann, Jones, & O’Neill, 1997).
Given the potential contribution of depression to the experience of pain, it is helpful to have an assess- ment measure that can directly assess the extent to which depressed mood is present. The Patient Health Questionnaire–9 (PHQ-9) is the self-report component of the Primary Care Evaluation of Mental Disorders (PRIME-MD) inventory designed to screen for depres- sive symptoms. Respondents are asked to report how often they have been bothered by “problems” using a 4-point scale ranging from Not at allto Nearly every day. Item 9 indicates “Thoughts that you would be better off dead or of hurting yourself in some way.” Its brevity, reliability, and validity make the PHQ-9 an ideal mea- sure to include in pain assessment (Kroenke, Spitzer, & Williams, 2001).
Scott completed several assessment measures as part of his pain assessment, and his scores on these measures were very consistent with the data obtained during his clinical interview. On the BPI, he endorsed an average pain intensity of 7 out of 10, and an interference score of 7.6, suggesting that pain was significantly interfer- ing in activities, including walking, relations with oth- ers, sleep, and enjoyment in life. His score of 10 on the PHQ-9 was consistent with his report of symptoms of depressed mood during the interview, including prob- lems with sleep, concentration, low energy, and feeling down. He did not endorse thoughts of self-harm. In addition, his total score of 32 on the PCS indicated a clinically relevant level of catastrophizing in response to pain.
Medical Evaluation
Scott’s completion of the release of medical information form allowed the therapist to speak with two of Scott’s healthcare providers. During a telephone call, Scott’s physical therapist reported that Scott had actively par- ticipated in therapy but he had reached a plateau of im- provement due to his fear of reinjury. She reported that she had noticed high levels of muscle tension through- out his body whenever he was engaged in physical therapy. She commented that he “always looked tense.” Although she had encouraged him to approach move- ment with less fear, she was unable to decrease his level
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of hypervigilance to painful sensations. Scott’s physical therapist cleared him to perform exercise to tolerance. From her perspective, all healing associated with his injury had been achieved and the experience of pain was no longer serving an adaptive purpose. The thera- pist had a similar conversation with Scott’s orthopedic physician, who had told Scott at their last appointment that his back was completely healed, the pain was not an adaptive signal, there was no pathology to account for it, and no damage was being done during activity. All providers agreed that pain management efforts that involved increasing Scott’s level of activity were highly recommended.
Case Conceptualization
Based on the information obtained in the clinical in- terview, the completion of self-report questionnaires, and conversations with Scott’s other healthcare pro- viders, a conceptualization of his case was developed. Although Scott’s injury had healed and he was cleared to participate in physical activities, he continued to be hypervigilant to all painful sensations. His attention to bodily sensations, feelings of lack of control, and his interpretation that the experience of any pain was a sign of pathology (catastrophizing) had led to his fear and avoidance of engaging in activities that had the poten- tial to cause pain. His avoidance and withdrawal from reinforcing physical and social activities interfered with his rehabilitation and contributed to depressed mood, which further intensified his experience of pain. Scott was informed of this conceptualization and agreed with the findings. Scott was offered treatment at the Central Pain Clinic, and Scott agreed to start a course of treat- ment of CBT for chronic pain.
COMPONENTS OF CBT FOR CHRONIC PAIN
The components of the CBT described in this section are integrated into a session-by-session treatment pro- gram in the next section.
Defining Treatment Goals
Although a number of skills can be incorporated into CBT pain management, one of the first objectives is to define overall treatment goals. Patients with chronic pain often report that pain has interfered with their ac- tivity and contributed to declines in social role func-
tioning. As a result, goals that include increased activity and productive functioning are often the target of treat- ment. There are three types of goals that are set over the course of therapy. During the first therapy session, the therapist should work with the patient to identify the specific overall treatment goals toward which they will work over the course of therapy. The goals should be designed to decrease the patient’s avoidance of activity and reintroduce a healthy, more active lifestyle. Regard- less of the specific target of treatment, goals should be behavioral and quantifiable rather than general, such as “experiencing less pain” or “having a better outlook on life.” Goals should be chosen in areas in which the patient can reasonably expect change over the course of therapy. Goals do not have to focus on exercise; rather, goals can include performing valued activities such as updating a resumé, working on a project or other hobby, or spending more time with a significant other. Goals should be flexible so that if a goal achieved before the end of treatment it can be updated or another goal can take its place. A second type of treatment goal is called weekly behavioral goals. These goals are small, achiev- able goals set at the end of each therapy session that help the patient take steps toward achieving the overall treat- ment goal. For example, if a patient has set an overall treatment goal of walking daily during her lunch break by the end of the treatment program, she could begin by setting the goal of walking twice a week and gradually increasing the number of times walked with each visit to the therapist. A third type of treatment goal is home- work goals, which are associated with the content of the material present in each therapy session. For example, while a patient might have the behavioral goal of having lunch with a friend, he/she may also have the homework goal of practicing diaphragmatic breathing daily.
Therapy Homework
Each therapy session should begin with a review of the goals assigned during the previous session and a collab- orative evaluation by patient and therapist to determine the extent to which the patient achieved the assigned goals. Making homework evaluation an expected part of treatment communicates to the patient that home- work is essential, increases the likelihood of homework completion, keeps the session focused on goal-oriented therapy (rather than spending session time catching up with the patient), and builds into therapy an opportu- nity to positively reinforce the patient for goal accom- plishment.
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Teaching Relaxation
One of the first strategies often taught to patients with pain is focused on learning how to relax and reduce stress. There are a number of ways that this can be taught, including diaphragmatic breathing, progressive muscle relation (PMR), and visual imagery.
1. Diaphragmatic breathing, a core component in meditation, yoga, Tai Chi, and mindfulness-based practices, focuses on the breath and teaches people to reduce stress in the body and clear the mind. Diaphrag- matic breathing involves contracting the diaphragm, which pulls air into the lungs, expanding the belly, and taking slow deep inhalations and exhalations. Research indicates that breathing practice can be an effective nonpharmacological intervention that can result in re- ductions in anxiety (Brown & Gerbarg, 2005), reduc- tions in workplace burnout (Salyers et al., 2011), and have positive health effects, including reductions in oxi- dative stress (Martarelli, Cocchioni, Scuri, & Pompei, 2011) and decreases in cortisol (Ma et al., 2017).
2. PMR is a widely used relaxation strategy that can help people to achieve a deep state of relaxation by al- ternating the tensing and relaxing of muscle groups. Research indicates that implementing PMR can have a number of positive effects (Carlson & Hoyle, 1993) including immunoenhancement (Pawlow & Jones, 2005), and significant decreases in stress in the work- place (Sundram, Dahlui, & Chinna, 2016). PMR can be particularly helpful for patients who carry muscle tension in particular parts of the body but are unaware of it.
3. Visual imagery, the purpose of which is to help the patient to create a relaxing image that he/she can use to relax and reduce stress, has been shown to be an effective treatment component for pain related to ar- thritis (Baird & Sands, 2004), fibromyalgia (Hadhazy, Ezzo, Creamer, & Berman, 2000), and other chronic pain conditions (Ilacqua, 1994; Akerman & Turkoski, 2000). Although some patients report prior experience with one or more relaxation strategies, it is important to review all the strategies with the patient to ensure that his/her previous experience is truly consistent with evidence-based practices.
Regardless of which relaxation technique the patient prefers, the practice of taking time to slow the mind and notice thoughts helps to pave the way for the cog- nitive interventions that takes place in subsequent ses-
sions of therapy. In the treatment section below, I re- view the implementation of these relaxation techniques with Scott.
Changing Negative Thinking
Given the relationship between thoughts and the expe- rience of pain, teaching patients to challenge maladap- tive thoughts related to pain is a core skill taught in CBT for pain. One of the first steps in teaching this skill is to provide education on the role of thoughts in the experience of emotions. Patient are taught to be aware of categories of automatic thoughts called cogni- tive errors, including catastrophizing. For patients with chronic pain, common automatic thoughts may include “I can’t cope with my pain,” “I’m disabled for life,” or “I can’t do anything.” Patients are taught to notice the connection among thoughts, feelings, and behaviors using ABC Worksheets (activating event, belief, con- sequences). They are taught to use cognitive restructur- ing to recognize automatic thoughts that give rise to negative emotions, to evaluate thoughts by gathering evidence for and against the thought, then to replace negative thoughts with more adaptive thoughts that are based on the evidence.
Time‑Based Activity Pacing
Activity pacing is a behavioral strategy in which people learn to balance being active with resting in order to ac- complish daily activities. It is a key component of treat- ment used by physical therapists when treating patients with chronic pain (Beissner et al., 2009). Learning to pace appropriately is an important skill, because pa- tients who have pain, but who are accustomed to being active, tend to push themselves to get things done when they are having a day with less pain. This can result in a flare-up of pain symptoms afterwards, which reduces one’s function and productivity. Time-based activity pacing is a process in which physical activity breaks are based on time intervals, not on how much of the job is completed. For example, a patient is asked to identify a job he/she frequently does that can result in increased pain. The patient is asked to estimate how long he/she can perform the job before the pain increases (active time) and how long he/she will need to rest before be- coming active again (rest time). This active–rest sched- ule is then used when completing the entire project. Although different jobs require different active–rest cycles, using a time-based activity pacing strategy re-
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duces time spent recovering from pain flare-ups due to over activity.
Pleasant Activity Scheduling
In pleasant activity scheduling, the goal is to identify pleasant and reinforcing activities that the patient can include in her life. This can be achieved by speaking with the patient about enjoyable hobbies or activities he/she likes to perform. If some activities are no longer possible due to the nature of a person’s injury or other factors, alternative ways to engage in activities that were enjoyable in the past can be discussed. In addition, therapist and patient can generate new choices of pleas- ant activities that were not considered in the past. Once selected, these activities are then scheduled into the pa- tient’s week. Activity scheduling is a core component to evidence-based treatment of depression, and a substan- tial literature demonstrates the positive effects of sched- uling social and pleasant activities on depressed mood (Lewinsohn & Atwood, 1969; Cuijpers, van Straten, & Warmerdam, 2007). For patients with chronic pain, en- gaging in pleasant activities can have the added benefit of increasing healthy behaviors.
Anger Management
Anger, a natural emotional response that we all have from time to time, can range from mild irritation to intense rage. Anger is common in patients who have chronic pain (Okifuji, Turk, & Curran, 1999), and research sup- ports an association between anger and pain intensity (Gaskin, Green, Robinson, & Geisser, 1992), unpleas- antness (Wade, Price, Hamer, Schwartz, & Hart, 1990), and emotional distress (Duckro, Chibnall, & Tomazic, 1995). There are three main steps to anger management. The first step involves developing an awareness of the environmental triggers for anger (e.g., verbal/physical abuse, annoyances, frustrations, injustices), the physical changes that can occur when we are becoming angry (e.g., heart racing, muscle tension, stiff posture), and the behavior changes that we demonstrate when we are be- coming angry (e.g., tightening muscles or pacing). The second step of anger management involves modifying the internal responses of anger using relaxation strate- gies (e.g., diaphragmatic breathing, PMR, imagery) or cognitive interventions to change our own thinking about a situation. The third step to anger management involves learning to respond in constructive ways that allow the patient to express an opinion. Patients are
taught how to respond assertively rather than aggres- sively or passively, and they are provided with guidelines for effective communication with others.
Sleep Hygiene
Although a number of health issues can result in im- paired sleep, insomnia is the most common sleep dis- order, with almost 30% of Americans reporting insom- nia (Ohayon, 2002). Studies suggest that patients with chronic pain experience problems with sleep (Finan & Smith, 2013), and there are indications that these two conditions can serve to maintain and exacerbate one another (Ohayon, 2005; Raymond, Nielsen, Lavigne, Manzini, & Choiniere, 2001). In one meta-analysis ex- amining the association between chronic low-back pain and sleep, it was found that pain is consistently associ- ated with greater sleep disturbance, reduced sleep dura- tion and sleep quality, increased time taken to fall asleep, poor daytime function, and greater sleep dissatisfaction and distress (Kelly, Blake, Power, O’Keeffe, & Fullen, 2011). While some research implicates dopamine as a neurobiological factor associated with symptoms of insomnia and pain, the exact nature of the association has yet to be elucidated (Finan & Smith, 2013). CBT for insomnia (CBT-I) is considered the “gold standard” psychological treatment for insomnia and includes in- structions such as sleep restriction, stimulus control, relaxation, and thought restructuring (Trauer, Qian, Doyle, Rajaratnam, & Cunnington, 2015). Given the high rates of comorbidity between pain and insomnia, and the strong research support of CBT-I, efforts to im- prove sleep by teaching components of CBT-I are in- cluded as an essential part of pain management. Given Scott’s difficulties with sleep, teaching sleep hygiene was one important component of his treatment proto- col, as described in detail in the section below.
TREATMENT DESCRIPTION: PROTOCOL
What follows is a description of an 11-session CBT for chronic pain that has been tailored to Scott.
Session 1: Pain Education
The goals of Session 1 are to discuss the impact that pain has had on the person’s life, explain the cycle of pain, present the general goals of treatment, set behav- ioral goals for therapy, and help the patient to notice
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things that tend to increase and decrease his/her pain. Therapy begins with a discussion of the ways in which pain has impacted the patient’s life in the domains of activities and thoughts and feelings.
THERAPIST: Can you tell me how pain has affected your activities?
SCOTT: Well, I was a really active person before all this started. I enjoyed doing things for myself. I liked to go on walks, bike ride, fix things around the house. Now it seems like I don’t do any of those things be- cause of pain.
THERAPIST: I recall you mentioning in the interview that pain has had an effect on your thoughts and mood as well?
SCOTT: Yes, I use to think about future plans, what my wife and I would be doing when we retire, but now I don’t want to go anywhere. I’m thinking of how I can cancel plans I have already made.
THERAPIST: How has your thinking changed? SCOTT: I was always ready to try new things and ex-
plore. Now I just want to stay home, where I know I’m not going to get bumped into on the street or make a wrong step.
Generally, patients have no difficulty describing the activities that have been negatively impacted by pain, including socializing with friends and family, perform- ing work, engaging in hobbies, or participating in sports. The therapist can use this information to begin to generate a list of potential behavioral goals that can be gradually implemented over the course of therapy.
When speaking with the patient about his/her ex- perience of chronic pain, it is often helpful to discuss the cycle of pain, which includes pain, disability, and distress (see Figure 17.1). This figure can be presented
to the patient or drawn by the therapist while discussing the interaction of the components.
THERAPIST: The cycle I’m going to show you explains how pain, disability, and distress tend to interact with one another. When pain persists over an ex- tended period of time, some people may develop neg- ative and catastrophic beliefs about their pain, such as “Why me?”; “This is never going to get better”; or a negative view themselves, such as “I’m worthless to my family because I can’t work.” When this pat- tern of thinking persists, people may start to report feeling down and depressed. As pain and depressive symptoms continue, people may withdraw or avoid doing everyday activities for fear of further injury or increased pain. They may also withdraw because they are tired of answering questions from other peo- ple, like “Why aren’t you working?”
SCOTT: Well, that sounds familiar. I stopped doing lots of things because I’m worried about hurting myself. I know this is not good for me, and I know my doctor told me that my back is healed, but it still hurts and I just get tensed up every time I move.
THERAPIST: So, you can see how this works. As a per- son withdraws and become less active, their muscles may become weaker, they may begin to gain weight, and their overall physical conditioning may decline. This, in turn, increases the experience of pain. This cycle of pain is quite common for people who have had chronic pain for an extended period of time.
SCOTT: This is me. This is exactly what I’m doing. THERAPIST: [Now that the Scott understands the cycle
of pain, it is time to set goals for treatment.] Now that you know how important your thoughts and ac- tivities are in the experience of pain, it is important to realize that your thoughts and the things you do in response to pain are all under your control. By learning ways of addressing negative thoughts and emotions associated with pain, and ways of keeping active, you can take greater control over your pain.
Time was spent working with Scott to develop overall behavioral goals that he could work on over the course of therapy. This step is important, because the overall goals serve as the basis for some of the weekly therapy goals. Using a Goal-Setting Worksheet, Scott was asked to think of between three and five behavioral goals for therapy, and to write down a description of what some improvement, moderate improvement, and maximum
Disability
Distress
Pain
FIGURE 17.1. The pain cycle.
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improvement would look like for each of the goals (see Figure 17.2). Having these performance benchmarks al- lows the patient to see the extent to which he/she has achieved the goals. Scott’s goals were focused on in- creased walking, going grocery shopping, and increased time riding his bicycle.
THERAPIST: These are great goals. Now that we have an idea of things you want to work on, let’s pick one of your goals for this week.
SCOTT: That sounds great. Which one should I do? THERAPIST: Why don’t we start with a small goal and
work our way up. Where do you think you would like to begin?
SCOTT: I would really like to be able to do my own shopping again.
THERAPIST: What happens now when you go shop- ping?
SCOTT: I don’t even go at all. I loved to go shopping before all this happened. I would go pick out what I wanted, and I knew all the people who worked there and they would say hello to me. It was a nice feeling to be there, but I haven’t been in so long and I know
it’s going to hurt, and I know the people there are going to wonder where I have been.
THERAPIST: What if we started by just having you get one item from the store. That’s all. How would that feel?
SCOTT: It would feel strange, because I always bought lots of items and had a full basket.
THERAPIST: There is a saying that “the journey of a thousand miles begins with a single step.” How would it feel to be able to go into the store again?
SCOTT: It would feel great. I would feel like myself. THERAPIST: Then perhaps this would be a good place
to start.
In addition to this assignment, Scott’s homework for the week included completing the Things That Af- fect My Pain form, on which he would list things that make his pain increase, and things that make his pain decrease. Both homework assignments were written down on a Weekly Goal Completion Form, on which he would rate the level of goal accomplishment at the beginning of the next week’s session. The process of completing this form and rating goal completion at the
FIGURE 17.2. Goal-Setting Worksheet.
We would like you to set some goals that you can work toward over the next few weeks. These should be goals that you can reasonably achieve over the course of therapy. Goals can be any positive behavior that you would like to increase. For example, they can be something you have done in the past but would like to do more often, something you have been meaning to do but have been putting off, or something you have never done but would like to try. Use the goal-setting form below to come up with at least two to three goals for treatment.
Goal Some Improvement Moderate Improvement Maximum Improvement
1. Walking
Walking once a week Walking three times a week Going on a walk once a day
2. Riding my bike
Riding my bike once a week Riding my bike three times a week; one time to work
Riding my bike to work three times a week
3. Going grocery shopping
Going to the grocery store once a week
Going to the grocery store twice a week
Going to the grocery store three times a week and helping to put groceries away
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beginning of the following session is repeated for every session of therapy.
Session 2: Theories of Pain and Diaphragmatic Breathing
The goals of Session 2 were to review the patient’s homework completion, review an educational compo- nent designed to inform the patient of our current un- derstanding of pain, and to teach the first relaxation strategy. Scott’s completion of his Things That Affect My Pain form indicated that there were many things related to movement that increased his pain, but he had few active strategies that he used to cope with pain (see Figure 17.3). The therapist discussed with Scott how they would be working on things he could do person- ally to control his pain rather than relying on rest. Im- portantly, Scott reported that he went to the grocery store one day the previous week and picked up vegeta- bles for that night’s dinner. He stated that it felt great to be there even though he felt some pain afterward. Scott was praised for his practice, and he and the therapist rated his completion of the goals for the week (see Fig- ure 17.4). Even though Scott had done well with both of his goals, he rated his goal completion in the “3 to 4”
range. Underrating of goal accomplishment is not un- common for patients early in therapy, particularly pa- tients with low self-efficacy. Thus, therapists should be ready to provide patients with feedback and give them credit for their efforts. After discussing his goal comple- tion with his therapist, Scott was able to recognize that he had completed the assigned goals and he agreed to rate his goal completion at a higher level.
Pain education included information about the adap- tive purpose of pain, different types of pain fibers, and how the transmission of pain signals works in the body. One of the most useful theories for describing the inter- action between the mind and the body in pain percep- tion is the gate control theory (Melzack & Wall, 1965). The theory had a significant impact on the study of pain, because it recognized that psychological factors can have important roles in the experience of pain. The theory suggests that a type of “gate mechanism” exists in the dorsal horn of the spinal cord that modulates the pain signal. The gate opens and closes depend- ing on feedback from other nerve fibers in the body. This includes descending neural impulses from the brain related to an individual’s thoughts or mood (e.g., anxiety or depression). The opening and closing of the gate modify how much information is sent to the brain from an injured area. Negative thoughts open the gate, which lets more pain information through, while posi- tive thoughts close the gate and restrict the pain mes- sage. The result is that pain signals can be intensified, reduced, or even blocked on their way to the brain. This information was incredibly helpful for Scott, because it allowed him to visualize that what he was trying to do was learn strategies that would reduce his focus on pain and help to close the gate.
Next, Scott was taught diaphragmatic breathing. Breathing is the first skill taught, because it is easily learned, highly effective, and gives the patient early suc- cess. The diaphragm is a dome-shaped muscle located underneath the ribcage. When a person breathes in cor- rectly, the diaphragm moves down, the stomach moves out, and air is drawn into the lungs. When instructing a patient on how perform breathing, it is important to set him/her up for success.
THERAPIST: One of the most effective ways we can lean to relax is by noticing our breathing. Over time, many of us have become accustomed to taking short, shallow breaths . . . just enough to survive. You’ve probably noticed that when you are stressed, it feels good to stop, stretch, and take a deep breath.FIGURE 17.3. Things That Affect My Pain.
Your assignment for this session is to make a list of all the things you can think of that you believe affect your pain. Can you think of things that make your pain decrease? How about things that make your pain increase? These can be things you did or thoughts you had during the day. Write down these things in the spaces below.
Things that can make my pain INCREASE:
Walking
Bending when I need to pick something up
Staying on my feet for a long time
Lifting anything heavy
Things that can make my pain DECREASE:
Taking a break by sitting on the couch
Resting and limiting movement
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SCOTT: Yes, I do this sometimes when I have been working on the computer. My wife told me she does this at her yoga classes. It feels good.
THERAPIST: You can breathe this way all the time, but you just have to get into the habit of doing it. Here is how to practice diaphragmatic breathing: First, start by sitting in a comfortable position.
SCOTT: Can I practice while lying down in bed? THERAPIST: Eventually, but right now you should prac-
tice while you are seated, because we want you to learn what it feels like to relax and not fall asleep. Next, place one hand on your chest and the other hand on your stomach. This will help you to check that you are breathing correctly. Slowly inhale through your nose for 3 seconds. As you inhale, the hand on your chest should remain as still as possible, but the hand on your stomach should move out.
SCOTT: Why should my stomach go out?
FIGURE 17.4. Weekly Goal Completion form.
Session Number: 2
Rate goal accomplishment for the week by marking the scale below: 0 (not at all accomplished) to 10 (completely accomplished). Complete for each established goal.
Goal 1 Complete “Things That Affect My Pain” Worksheet
0——1——2——3——4——5——6——7——8——9——10
Notes:
Goal 2 Go to the grocery store and get 1 item
0——1——2——3——4——5——6——7——8——9——10
Notes: It felt really good to be back in the store
Goal 3
0——1——2——3——4——5——6——7——8——9——10
Notes:
Goal 4
0——1——2——3——4——5——6——7——8——9——10
Notes:
Goal 5
0——1——2——3——4——5——6——7——8——9——10
Notes:
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THERAPIST: When you breathe effectively, the dia- phragm moves down and pulls air into the lungs. When this happens, everything below the dia- phragm, like your stomach, has to move outward, because there is nowhere else to go. Slowly exhale through your mouth for 3 seconds and notice how the hand on your stomach now goes inward. A rate of 3 seconds to inhale, and 3 seconds to exhale is a good place to start, but you can adjust your rate of breath- ing to a pace that feels good for you. Choose a time and place to practice where you won’t be bothered, and make practice part of your daily routine. Where and when do you think you could practice?
SCOTT: Probably in the morning before work. I could go on my porch and it would be nice and peaceful.
THERAPIST: Great. Don’t make phone calls, read the news, or text while you practice. Just focus on how it feels to breathe.
SCOTT: This is going to be hard. I never stop. THERAPIST: If you are not accustomed to stopping for
more than a minute, this might feel strange and your mind is likely to wander—but when that happens, just let the thoughts go, refocus on your breathing, and don’t give up—it gets easier.
Scott was assigned diaphragmatic breathing for homework four times a week for 10 minutes each time. Although he would have agreed to practice daily, reduc- ing the goal increased the chances of compliance should he miss a day of practice and provided an opportunity for early success. In addition, Scott decided to try shop- ping again and take his bike for a ride around the block once the next week.
Session 3: PMR and Visual Imagery
The goals of Session 3 were to review the patient’s homework completion, and to teach PMR and visual imagery. Scott indicated that he went to the grocery store twice the previous week. On both occasions, he felt pain, because there was no place to rest, but he enjoyed the experience and was able to say hello to a cashier he had not seen in months. Scott also reported that riding his bike was enjoyable, but he could tell that he had not ridden in a while. Scott was praised for his practice, and he and the therapist rated his completion of the goals for the week. Scott reported that doing the breathing was challenging at times.
SCOTT: I was able to try the breathing every day. THERAPIST: Wow, you exceeded your goal, great job! SCOTT: Yeah, but it was harder than I thought. Ten
minutes seems to go slow. I kept feeling like I should be doing something else, and I was having of all kinds of thoughts. What do you do with that?
THERAPIST: That’s a perfectly normal reaction. When you are breathing and you start to think about other things, don’t beat yourself up about having the thoughts. Just let the thought go and try to bring your attention back to your breathing, and notice how that feels. If the thought comes back, which it likely will at first, you can remind yourself that if the thought is “that important,” it will be there in 10 minutes when you are done, but for now, just focus back to your breathing. The more you practice this the easier it gets.
When instructing patients on how to perform PMR, the therapist should perform the technique with the pa- tient. If there are areas of the body in which increasing muscle tension would result in pain or harm, then those areas should be avoided. A form listing all of the muscle groups to be targeted in PMR, along with instructions, should be given to the patient to take home from the session.
THERAPIST: One of the most common responses to pain is to tighten the muscles. The tightening acts to limit movement, protect the body.
SCOTT: That’s just what I do. I feel like I have to be ready for it.
THERAPIST: Tightening muscles might be protective for acute pain, but it actually makes chronic pain feel more intense. Tension in your muscles can build slowly throughout the day, and we may not even no- tice how tense we are until we stop what we are doing and stretch. The purpose of PMR is to help you learn to notice when your muscles are becoming tense and to relax your muscles throughout the day. Here is how to practice: First, make yourself as comfortable as possible in a seated position. Start by taking a few deep breaths and allowing yourself to relax. In PMR, you will tense a specific muscle group for 3 seconds, take a deep breath, and, as you exhale, release the tension slowly, while noticing the different sensa- tions. Perform this twice for each muscle group and then move along to the next group of muscles. After a
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few times practicing PMR, you will start to be more aware of when your muscles are getting tense and how your body feels. You will be able to practice this technique anywhere—at your desk, while waiting in traffic, or while watching TV.
In addition to PMR, Scott was also taught how to perform visual imagery as a way to enhance relaxation practice. Before beginning visual imagery, the therapist should take a few minutes to gather information on the image the patient wishes to imagine. Collect informa- tion on the place, such as what the patient sees, smells, hears, feels, and tastes. As the patient begins to describe the image, the therapist should write down as many de- tails as possible. The therapist is responsible for weaving this information together to guide the patient in imag- ining the chosen image. The patient can be instruct- ed to close his/her eyes and perform diaphragmmatic breathing while the therapist describes the image he/ she just provided. While guiding the patient through the image, the therapist can include suggestions such as “As you take a deep breath notice how your body feels, and any tension that you are holding back just let go of now.” Scott visualized walking on his favorite beach at sunset. He imagined the cool breeze, the smell of the salty air, the feeling of the sand on his toes, and the sounds of the seagulls in the distance. Scott seemed to very much enjoy the addition of visual imagery to his breathing practice.
The therapist ended visual imagery by counting backward and giving Scott the suggestion that he be- come more aware of surroundings. Scott was assigned PMR and visual imagery practice. He was encouraged to continue with the diaphragmmatic breathing, and homework practice was increased to 6 times a week for 10 minutes each time. Goals included grocery shopping and going for a walk with his wife.
Session 4: Automatic Thoughts
The goals of Session 4 were to review the patient’s homework completion, and to teach him about the connection among thoughts, emotions, and pain. Scott indicated that he tried all of the techniques from the previous week. He preferred diaphragmatic breath- ing for relaxing and felt that he was getting better at relaxing and letting go of thoughts. He also reported that practicing PMR had made him more aware of his tension levels throughout the day. Scott completed the behavioral goals for the week and reported that he went
twice to the grocery store and bought a few more items. He and his wife were unable to schedule a time for the walk, but hoped to do it this week. Scott was praised for his practice, and he and the therapist rated his comple- tion of the goals for the week.
During this session, therapy begins to focus on no- ticing the relationship among thoughts, emotions, and pain. First, the connection between emotions and thoughts is made. Scott was able to discuss examples in which he did not notice his pain when he was involved in enjoyable activities such as talking with his wife or watching a movie. He was also able to recall times when frustration and stress led to an increase in his pain. His observations were related back to the gate control theory discussed in the previous session, and it was pointed out that since emotions can affect our experience of pain, and emotions are caused by how we think, we need to make sure that our thinking is accurate. The concept of “automatic thoughts” was reviewed, and examples were provided to demonstrate how automatic thoughts can be adaptive and help us to make sense of the world. In order to help develop an awareness of thoughts that are not adaptive, a list of cognitive errors was read aloud by Scott. As each of the cognitive errors was reviewed, he was asked if this was a type of error that he recognized, and if he could provide an example of a situation where it occurred. Scott was able to identify a number of rel- evant cognitive errors including “catastrophizing,” the “fortune-teller,” and “should” statements.
SCOTT: (laughing) Yikes, I think I make a lot of these thinking errors—especially the “fortune-teller”! I think a big reason I avoid going places in my life is that I always think I will definitely not feel well if I go. But of course, I really can’t predict what is going to happen. Sometimes I actually do feel OK. I also think I catastrophize. I usually think that if I have pain somewhere, like at the grocery store, that it will really be the worst thing in the world. But I guess I can actually think of many worse things, and I have coped with this pretty well when it has happened in the past.
THERAPIST: Many people make these errors, and notic- ing them is an important first step.
SCOTT: So, how do you change the way you think? THERAPIST: Before we can learn to change these types
of thoughts, we have to be more aware of them. Your job this week is to be an observer of your own thoughts. If anything stressful happens this week,
Cognitive‑Behavioral Therapy for Chronic Pain 691
your job will be to notice it and ask yourself, “What am I thinking right now that’s making me feel this way?” You are going to write down what you are thinking and then notice the consequences, includ- ing your emotions, how you feel physically, and things you do as a result.
SCOTT: So, this week I’m a detective? THERAPIST: That’s right. You are not a victim of your
emotions, you are an observer. You want to notice how all the pieces fit together, so we can make some changes.
Scott was assigned the ABC Worksheet in order to monitor his thoughts daily during the week. He was encouraged to continue with the diaphragmatic breath- ing. For behavioral goals, Scott requested focusing on riding his bike around the neighborhood this week, in addition to going for a walk with his wife and grocery shopping.
Session 5: Cognitive Restructuring
The goals of Session 5 were to review the patient’s homework completion, and to teach the patient how to perform cognitive restructuring. Scott completed four ABC Worksheets the previous week and brought them to session for review. He was praised for his home- work completion, and time was spent reviewing the worksheets and noticing repeated themes in the types of thoughts he was having, such as “Why me? This is never going to get better”; “Something is wrong with me”; and “I will be living with this pain for the rest
of my life.” Next, Scott and the therapist discussed the consequences of the automatic thoughts reported on his ABC Worksheets. Scott was able to notice that when he was having negative thoughts about his pain and the future, it caused his mood be become down, his pain to become more apparent, and his movements to become more guarded (see Figure 17.5). Scott reported that he went to the grocery store three times, biked in the neighborhood, and went for a walk with his wife.
THERAPIST: Scott, I noticed that you have already reached the “maximum improvement” indicated on your Goal-Setting Worksheet for grocery shopping.
SCOTT: I know, it seems that I was avoiding going to the grocery store, and my avoiding it was making it seem like it was something that I really couldn’t do.
THERAPIST: When we avoid things, it deprives us of the opportunity to collect competing information. If we never try, we will never know what we are capable of.
After reviewing the ABC Worksheets, the therapist then walked Scott through the process of how to engage in cognitive restructuring. Scott was provided with a Cognitive Restructuring Worksheet and was asked to complete the form himself while the discussion with the therapist continued (see Figure 17.6).
THERAPIST: Let’s take one of the examples from your ABC Worksheets and try to go through it using the restructuring form.
FIGURE 17.5. ABC Worksheet.
Activating Event (Stressful Situation)
Beliefs (Automatic Thoughts)
Consequences (My Reactions)
Going to the grocery store and I wanted to pick up a case of water and put it in the cart, but I couldn’t.
Why me?
This is never going to get better.
Something is wrong with me.
I will be living with this pain for the rest of my life.
Emotional:
Down and frustrated
Physical:
Face feels hot and flushed, body tensed up, pain increased
Behavioral:
Walk slowly so I don’t cause more pain
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SCOTT: That would be helpful. One of the situations that was the most stressful that I described on my worksheet was walking on the sidewalk when com- ing home from the office.
THERAPIST: Can you identify the emotions you were experiencing and rate how intense they were?
SCOTT: Yes, I was feeling anxious 90% and worried 75%
THERAPIST: And can you remember what you were thinking at the time that was making you feel those emotions?
SCOTT: Yes, I was worried that I was going to step on a crack or a break in the sidewalk, which would throw my body off balance and cause my pain to increase, or someone was going to bump into me as I was walking and I would get knocked down and go fly- ing to the ground in a lot of pain.
THERAPIST: OK. Great job noticing the thoughts. Now, our job is to evaluate or challenge the thoughts. Remember the rule—you can have any kind of
thought, but just because you think it doesn’t mean it is necessarily true. If there is sufficient evidence to support a thought, then you can keep it. If there is evidence against a thought, then you have to get rid of it—it is like spam, or fake news. If there is evidence for and against the thought, then you have balance in the way you want to think. The reason this technique works so well is that our conclusion is based on your actual experience.
SCOTT: (laughing) It’s funny to think about my nega- tive thoughts as “fake news” or “spam.” I can almost visualize pressing “delete” on them from my “inbox”! I know it won’t be quite that easy, but I like the meta- phor and now I really want to learn how to challenge a thought!
THERAPIST: Great! So let’s take the thought that you are going to definitely step in a way that would in- crease your pain, or get knocked to the ground if you are walking on the sidewalk—what evidence do you have to support that thought?
FIGURE 17.6. Cognitive Restructuring Worksheet.
Situation Emotion Automatic Thought Evidence for
Evidence against
Positive Coping Thought
Describe the event that led to the unpleasant emotion.
Specify and rate the emotion from 0 to 100%.
Write the automatic thought that preceded the emotion.
What is the evidence that this thought is true?
What is the evidence that this thought is false?
What else can I say to myself instead of the automatic thought?
Walking on the sidewalk when coming home from the office
Anxious 90%
Worried 75%
I will step in a way that’s going to cause my pain to increase.
Someone is going to bump into me, knock me down, and cause pain.
None
I have been bumped by a person two times in the past.
I have walked down the street a thousand times and I have never fallen.
When I have been bumped in the past I didn’t get knocked down. We just brushed by each other.
I have walked this way many times and I have always been fine. No one is going to knock me down and even if they bump me, I will most likely be fine.
Emotion
Rerate the emotion from 0 to 100%.
Anxious 30%
Worried 20%
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SCOTT: Well, I injured myself by stepping down a flight of stairs.
THERAPIST: Yes, but just because that happened once, is that evidence that you will trip and fall in the street walking home?
SCOTT: Well, it’s not evidence. It’s just a worry. THERAPIST: What cognitive error are you making? SCOTT: I think I’m fortune-telling and catastrophizing. THERAPIST: That’s exactly right. There is no crystal
ball and we can’t tell the future. What is the evidence against that thought? Have you walked down that street before, and have you been fine?
SCOTT: Yes, I have walked down that street a thousand times, and I have never fallen.
THERAPIST: Have you ever been bumped by a person walking in the opposite direction?
SCOTT: Yes, a couple of times, but I didn’t go flying to the ground. I just turned my shoulder and we just brushed by each other.
THERAPIST: So, based on the facts we just reviewed, it doesn’t sound like we have any substantial evidence to support your thought that you will definitely get knocked to the ground or step in a way that will ex- acerbate your pain if you are walking on the side- walk. What do you think is a more positive coping thought that you could have which is consistent with the evidence?
SCOTT: I could tell myself that I have walked this way many times, and I have always been fine. No one is going to knock me down, and even if they bump me, I will most likely be fine.
THERAPIST: How does that thought impact your expe- rience of anxiety and worry?
SCOTT: That thought brings my anxiety and worry way down. I would say my anxiety decreases to 30% and my worry to 20%.
Scott was assigned the Cognitive Restructuring Worksheet to complete daily during the week. He was encouraged to continue with the diaphragmmatic breathing. For behavioral goals, Scott chose the goals of riding his bike for 10 minutes twice a week and walking with his wife. Given that he had already made signifi- cant gain in going to the grocery store, he requested to start adding other tasks to his goals, such as helping to empty the dishwasher.
Session 6: Stress Management
The goals of Session 6 were to review the patient’s homework completion, and to teach the patient stress management techniques. Scott completed five Cogni- tive Restructuring Worksheets and brought them to session for review. The therapist praised Scott for his thorough homework completion, and time was spent reviewing the worksheets. The therapist pointed out re- peated themes in the types of thoughts Scott reported. Scott noted that completing the forms was making him aware that many of his worries about pain were future- oriented, yet lacked supporting evidence. Scott com- pleted the behavioral goals for the week and reported that he tried to empty the dishwasher four times. He reported having a pain flare-up during the week and noticed that was also engaging in some negative think- ing. Scott reported that he achieved both his biking goal and walking with his wife prior to his pain flare- up. The following illustrates how the therapist helped Scott put his pain flare-up in perspective:
SCOTT: Last week I was doing pretty well, not a lot of pain, but I woke up one morning and the pain was just incredible. I don’t know what I did, but the pain was there first thing in the morning and lasted for hours.
THERAPIST: Tell me what happened next? What were you thinking?
SCOTT: I took it easy the rest of the day. I felt really down and disappointed that it came back. I started having thoughts like “Here we go again” and “This is never going to end.” I really wanted it to be over, and I thought I was making progress.
THERAPIST: It’s tough when we have days that are going well, and then, out of nowhere, we have a day where pain increases.
SCOTT: Yeah, I thought I was done with this. THERAPIST: I know it’s frustrating, but there are going
to be days when you have more pain than others. Recovery is not linear. There are going to be bumps along the way, but what is important to notice is your overall trajectory. For example, how did things go in the days following your pain flare-up?
SCOTT: It took a day or so to feel back to normal, but now I’m doing much better.
THERAPIST: It’s important to remember that even though you can have a pain flare-up, it doesn’t mean
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that all is lost. We can focus on what may have caused it and remember that these are just bumps in the road to recovery.
Next, the discussion turned to the primary focus of the session: stress management. Time was spent review- ing psychoeducation on the fight-or-flight response, the effects of acute and prolonged stress on the body, and the interaction between stress and pain. The therapist and Scott reviewed a list of common categories of exter- nal and internal sources of stress, and Scott was able to identify both kinds of stressors in his own life. Scott re- ported noticing that when his job was more demanding and he had less time to relax, his stress level increased and he seemed to have less tolerance for things, includ- ing his pain. He also remarked that he recognized that pain could be a source of stress.
THERAPIST: How has your pain been stressful? SCOTT: You know, one of the most stressful things
about pain is I keep wondering what I did wrong. I tell myself that I should be better by now and these thoughts just start spinning and grinding away in my head, and it feels overwhelming. I feel myself tensing up right now just talking about it.
THERAPIST: Look, this is good. You are noticing some- thing right now that is causing stress. Now, given what we just reviewed, where do you think you could make some changes?
SCOTT: Well, I know a big part of this stress is coming from me and how I’m talking to myself.
THERAPIST: What tools do you have to deal with that? SCOTT: I can notice my thoughts and use my cognitive
restructuring to push back on thoughts that don’t make sense.
THERAPIST: You mentioned feeling tense. What other tools do you have?
SCOTT: Right, I can use the relaxation skills I have been practicing to notice the muscle tension, like I just did, and then take steps to relax my body.
Scott was assigned the My Life Changes Worksheet to complete during the week, which helped him to de- velop a list of changes he could make to reduce stress in his life. Diaphragmmatic breathing had now become a regular part of his morning routine. For behavioral goals, Scott asked to continue the goals of riding his bike twice a week and walking with his wife.
Session 7: Time‑Based Activity Pacing
The goals of Session 7 were to review the patient’s homework completion and to teach the patient time- based pacing skills. Scott completed the My Life Changes Worksheet and was able to identify several areas in which he would like to make modifications in order to reduce his stress (see Figure 17.7). He was praised for his homework completion. Scott completed the behavioral goals for the week, including riding his bike and walking with his wife. In addition to helping with the dishes, Scott also helped move laundry out of the dryer, which he said made him feel very helpful. He stated that his wife often thanked him for how much he was contributing to the household chores even despite his pain, and that made him want to do as much as he could. The following transcript illustrates how the therapist taught Scott the concept of time-based activ- ity pacing:
THERAPIST: Today we are going to talk about how to pace yourself. When some people begin a project, it’s hard for them to stop working on it before it is completed, even if it is a very big project. As a result of “working through” the pain, the level of pain be- comes higher and higher. This can sometimes result in severe pain that requires rest for an extended peri- od, sometimes days, before being able to work again.
SCOTT: That’s always been an issue for me. Just the other day I was having a pretty good day—not a lot pain—so I started moving some furniture and doing a bunch of other things around the house. Before I knew it, I had been moving around for hours and my back was killing me. I didn’t want to move at all the next day.
THERAPIST: One method for breaking this cycle is called time-based pacing. Time-based pacing is a process in which activity breaks are based on time intervals, not on how much of the job is completed.
SCOTT: So how would that work? THERAPIST: Here’s an example. What is a job you do
that can cause pain if you do it for a long period of time?
SCOTT: Mowing the lawn and doing other yardwork can cause pain sometimes.
THERAPIST: Suppose you decide to do yardwork this weekend and you tell yourself that you don’t want to overdo it, so you’re going to pace yourself by taking a break when half of the job is done. Now, imagine
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that the yard takes longer than you thought, and by the time you are halfway finished, you have spent hours on your feet and you are in a lot of pain. If you had paced yourself by the amount of time spent active, for example, taking breaks every few minutes before the pain starts, rather than taking a break only after half the job was completed, you might have been able to avoid the onset of pain.
SCOTT: That sounds logical, but I hate the idea of stop- ping to rest. I want to get things done and I am going to have a hard time walking away from a project.
THERAPIST: Actually, by taking breaks before pain be- gins (not after pain gets bad), you will be able to re- turn to activity sooner, and you will actually get more done. By using time rather than pain as an indicator,
you will not need long periods of rest to recover from pain, because the pain flare-up will never happen. Think about it this way, what is your favorite sport?
SCOTT: I’m a big football fan. THERAPIST: Professional athletes (e.g., basketball,
hockey, football) all take regular water breaks on the sidelines during games in order to perform at peak efficiency. Their coaches and trainers know that if players are kept in the game until they are tired or dehydrated, then they have waited too long, and they will not be performing at their best. The same rea- soning should apply to you.
SCOTT: That makes a lot of sense. THERAPIST: By pacing yourself, you will be able to get
FIGURE 17.7. My Life Changes Worksheet.
In the spaces provided, indicate the types of changes you would like to make in your life in order to help decrease stress. Be as specific as possible.
Lifestyle Habits:
Diet: Eat well. Start my day with a good breakfast. Not just coffee.
Exercise: I can maintain my exercise routine like walking and riding my bike.
Sleep: Use my relaxation skills to let my thoughts go before I go to bed.
Relaxation: Take time to practice my breathing and PMR every day.
Approaches to Situations:
Time management: Don’t pack my schedule too tight with appointments. Take breaks!
Money management: Don’t take on too much debt.
Assertiveness: Tell people how I feel and don’t just keep it inside.
Problem-solving coping skills: Try to recognize the things I can change.
Ways of Thinking:
Realistic expectations: Don’t hold myself up to unrealistic expectations about what I “should” be doing.
Sense of humor: I’m a funny guy and I can laugh at things I sometimes think to myself.
Support system: Remember that my family cares about me.
Positive thinking: I can give myself credit for how far I have come already.
Challenge negative thinking: I will use my restructuring skills to push back on thoughts that don’t make
sense or thoughts that are just bringing me down.
Other Changes:
Remind myself that there is no such thing as a “bad day.”
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the job done, and you will be ready to play again tomorrow.
Work with the patient on two other tasks that cause an increase in pain, remembering that different types of activities require different activity/rest schedules. The therapist should remind the patient that activity/ rest estimates are not always accurate the first time, so the patient may need to adjust the schedule as he goes. If flare-ups do occur, the patient should cut the activ- ity level in half at first and over 3 days build back up to the previous level of activity. Encourage the patient to expand the activity/rest schedule to other activities and slowly build up the active time. Emphasize that the patient should not stop practicing time-based pacing skills, even when he is feeling good or pain-free. Pac- ing needs to be consistent in order to be an effective pain-reducing strategy. Scott was assigned the Activ- ity Pacing Worksheet to complete during the week. In addition, he was encouraged to continue cognitive re- structuring, so that the process of challenging thoughts could become automatic. His behavioral goals for the week included riding his bike three times, walking with his wife three times, and pacing himself while doing yard work.
Session 8: Pleasant Activity Scheduling
The goals of session 8 were to review the patient’s homework completion, and the importance of includ- ing pleasant activities in one’s life. Scott completed the Activity Pacing Worksheet and reported that he tried pacing himself while doing yardwork and cleaning out
his garage over the weekend. Scott reported that it felt strange taking a break before the pain started, and he brainstormed with the therapist some of the different activities he could perform while he was on a break, such as calling a friend, making lunch, or reading a book (see Figure 17.8). Scott completed the behavioral goals for the week, including biking three times. He reported that he and his wife had a regular walking rou- tine in the neighborhood and were considering getting a dog. All of this activity was increasing his confidence in his ability to ambulate, even if he was still experienc- ing pain. By not avoiding activity, Scott was gathering evidence that he could then use to challenge his previ- ous automatic negative thoughts that he was disabled. The therapist praised Scott for meeting his behavioral goals, and Scott appeared to be very appreciative of the support of his progress.
The experience of pain can be associated with reduced activity and social withdrawal. The reductions may be the result of physical limitations related to structural pathology or fears of injuring oneself. Alternatively, they may be self-imposed for reasons such as not want- ing to answer questions about pain (e.g., “Why aren’t you working?”), feeling embarrassed, or feeling frustrat- ed over limitations. Consequently, the patient may stop doing enjoyable activities, which can lead to depressed mood, increased disability, an increased pain. Scott had fallen into this pattern of behavior; he had stopped so- cializing with friends and stopped doing many of the hobbies he once enjoyed. The therapist helped Scott to think about how pain and feelings of low mood might be helped by scheduling pleasant activities, which is il- lustrated in the following interchange:
Activity Estimate Day 1 Day 2 Day 3 Day 4 Day 5 Day 6 Day 7
Doing yard work Active: Active: Active: Active: Active: Active: Active: Active:
10 minutes
15 minutes
20 minutes
none 25 minutes
30 minutes
none 20 minutes
Resting: Resting: Resting: Resting: Resting: Resting: Resting: Resting:
5 minutes
10 minutes
10 minutes
none 15 minutes
15 minutes
none 10 minutes
Comments: This was hard to do, but I kept reminding myself to take breaks.
FIGURE 17.8. Activity Pacing Worksheet.
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SCOTT: When this all happened, I stopped doing so many things I enjoyed. I avoided going to games, working in the yard, having friends over to the house, even going out to dinner with my wife.
THERAPIST: Sometime people think that if they can’t do fun things the exact way they did them before, then they can’t do them at all.
SCOTT: Why bother trying? Yeah, I know that’s not a helpful way to think.
THERAPIST: When we stop doing the things we enjoy most in life, we naturally get down, we stop mov- ing, and that feeds right back into pain. Even if there are some fun activities that you can’t do the way you could before, does that mean that you have to remove them entirely from your life?
SCOTT: No, of course it doesn’t. THERAPIST: So, let’s take look at some of the things
that perhaps you pulled back from, and see if there is a way to start putting some of those activities back in your life.
After more discussion, Scott agreed on a plan to in- vite friends over to his house for a barbeque. This plan was created in session, and specific dates for e-mailing the friends were solidified. This was done in session be- cause plans that can be enjoyable have a higher likeli- hood of occurring if they are scheduled. In addition to the specific assignment related to inviting friends over to his house, Scott was assigned the task of identifying other pleasant and enjoyable activities to include in his week. Scott’s behavioral goals for the week included rid- ing the bike three times around the neighborhood and once to work, and walking with his wife three times.
Session 9: Anger Management
The goals of Session 9 were to review the patient’s homework completion and the importance of learning anger management skills. Scott completed the pleasant activity assignment and reported that he contacted his friends as planned, and they were excited to find a time to get together. In addition, he chose to read a book that had been on his shelf for months. He also called an old high school classmate with whom he had not spoken in years, and Scott expressed that they had a very enjoy- able conversation. Scott also said that he made a plan to take a walk with his daughter, who was home from college for a brief break. Scott completed his behavioral
goals for the week, including biking three times. He reported feeling nervous about his bike ride to work; however, he used a restructuring form the night before to challenge thoughts related to crashing his bike and experiencing more pain. His ride went without an issue, and although he felt some pain sensations in his back, Scott was able to tell himself that these were the sen- sations of muscles being used and brought back into shape. All other weekly goals were achieved.
The focus of this session was learning about ways that anger and frustration can interact with the expe- rience of pain. The therapist and Scott engaged in a discussion on how anger can be adaptive in some cir- cumstances, yet less adaptive in others.
SCOTT: I’m really good at controlling my anger in some situations, like with my coworkers, but not as much when it comes to some of my siblings.
THERAPIST: What’s the situation with your siblings? SCOTT: I don’t have a good relationship with my older
brother, and he knows just how to frustrate me. Every time I get off the phone with him, I’m angry and seriously want to punch something. I get tense, my face turns red, and my wife just sends me out of the house to cool down.
THERAPIST: How do these feelings of anger impact your pain?
SCOTT: I really hadn’t thought about it much, but now that we are talking about it, I know it makes it worse. My whole body tightens up and I feel stressed out whenever we talk. He has always been this way—we have to talk about family matters on occasion, but he is just a jerk and he is not going to change.
THERAPIST: It sounds like you are frustrated but you are dealing with the best you can. How would you feel about going over a few strategies you could use to manage your anger the next time he calls?
SCOTT: Well, that would be awesome.
Next the therapist and Scott discussed steps that he can take to cope more effectively with his anger. First, Scott was taught how to become more aware of trig- gers in his environment, in addition to his brother, that tend to cause anger. Scott recalled that he has similar anger reactions when dealing with the dealership that does the maintenance on his car. The therapist encour- aged Scott to notice his own physiology and behav- iors as a cue that he is starting become angry. Second,
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Scott was reminded that he has already learned some skills to modify the internal processes that contribute to anger, including using relaxation skills to reduce muscle tension, and cognitive coping to challenge his own thinking. Third, Scott and the therapist reviewed ways of responding assertively rather than passively or aggressively in response to his brother’s comments, and in response to his interactions with people at the car dealership.
Scott was assigned the task of reviewing the three steps toward anger management and restructuring any thoughts related to anger. For behavioral goals, Scott indicated that he wanted to maintain his current bik- ing goal for another week. He increased his goals of walking with his wife to four to five times per week and helping with chores around the house. Scott reported that he was regularly helping with grocery shopping. In addition, Scott indicated that he might reach out to his gym to see if he could start his membership up again, along with some sessions with a personal trainer.
Session 10: Sleep Hygiene
The goals of Session 10 were to review the patient’s homework completion, and the importance of learn- ing sleep hygiene skills. Scott completed the anger management assignment, and even though he report- ed there were no issues that caused anger last week, he used the time to practice restructuring other thoughts. Scott reported that he contacted his gym and signed up for several sessions with a personal trainer. He completed the behavioral goals for the week, including biking to work once and walking with his wife five times a week.
The session started with an educational component on the necessity of sleep, and how sleep is an opportu- nity for the body to repair itself both physically and mentally. Reviewing the phases and function of sleep engages the patient and helps to reinforce the impor- tance of practicing good sleep hygiene. Based on in- formation collected in the assessment, the therapist was aware that Scott had problems falling asleep. The therapist asked Scott a series of questions to determine the types of problems he was having and to explore pos- sible reasons for the sleep difficulties. While insomnia is quite common in patients with chronic pain, patients may report waking at night due to pain and afterward having difficulty returning to sleep. By reviewing the patient’s sleep behaviors, the therapist can determine the behaviors that are likely contributing to sleep diffi-
culties and create a plan with the patient for improving sleep behaviors.
THERAPIST: Looking over our assessment, I know that sleep has been an issue in the past. Can you tell me more about that?
SCOTT: My sleep is all over the place. Sometimes I can fall asleep with no problem, but other nights I just lay there and I can’t seem to turn my brain off.
THERAPIST: What do you do when that happens? SCOTT: I’ll get up and look for something to do. I fig-
ure I might as well be productive, so I will get out the laptop and read an article in bed, or I will go downstairs and turn on the TV and watch the news.
THERAPIST: How long do you stay there? SCOTT: It depends. After a while I might get sleepy and
go back to bed, but sometimes I just fall asleep on the couch and I end up crawling back to bed around 6 A.M. and sleeping for an hour or so before I have to get up.
THERAPIST: That sounds tough. How do you feel the next day when that happens?
SCOTT: I feel like a mess. It’s hard to focus, I’m grumpy, and I just feel like I can’t keep up. Plus, when I wake up after sleeping on the couch, my back is killing me.
THERAPIST: If you do fall asleep when you first go to bed at night, are you able to sleep through the night?
SCOTT: Some of the time. But sometimes I wake up because my back is hurting, or I have to go the bath- room, and once I look at the clock, I can be up for hours.
THERAPIST: What happens at that point? SCOTT: I start thinking about the day ahead, how
much pain I will feel, and how I’m going to feel so tired because I’m not sleeping.
THERAPIST: So, it sounds like “thoughts” are some- times keeping you awake, and sometimes those thoughts are worries about the effects of not getting sleep. Can I ask you, what do you generally do before bed? Do you have a regular routine?
SCOTT: Sometimes my wife and I will watch some TV or a movie, or I do some work in the office after din- ner.
THERAPIST: Do you work in bed? SCOTT: Sure, I have my laptop and an iPad, so I might
do some reading in bed in order to get tired.
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THERAPIST: Have you ever taken medication for sleep? SCOTT: I took some over-the-counter melatonin a few
times but it didn’t work, and my PCP prescribed some medication for sleep, but it made me feel really groggy the next day, so I stopped taking that. I’m not taking anything now.
THERAPIST: Based on what you have told me so far, there might be some things that we can try to help you sleep get back on track.
SCOTT: Well, that would be a life-changer!
Time was spent reviewing with Scott the compo- nents of sleep hygiene, including the timing of sleep, sleep behaviors, environmental tips, timing of eating meals, reducing caffeine, and mental control. Scott was very interested in finding ways to improve his sleep, so he and the therapist collaborated to develop a plan that included small changes to his bedtime routine in order to improve his chances of getting sleep. For example, a plan was made for Scott to create a presleep ritual that included refraining from the use of electronic devices for 30 minutes before bed, and not using electronic de- vices in bed, as this type of behavior teaches the brain that the bed is a place to work. In addition, regular sleep and wake times were set, which also included the rule of no daytime naps. His alarm was placed away from the bed, so he could not look at it at night when going to the bathroom. Importantly, Scott was reminded of the relaxation skills he had learned earlier in therapy, and he was encouraged to use his skills, so that he could let go of unwanted thoughts at night. In addition, the ther- apist suggested that Scott notice the types of thoughts he is having at night, and spend time during the day restructuring them.
SCOTT: What do I do if I can’t go to sleep? THERAPIST: Place a chair by your bed and find some-
thing incredibly dull to read. SCOTT: (laughing) So, like one of my wife’s travel maga-
zines? THERAPIST: Precisely. If you are unable to fall asleep
after 15 minutes, then get out of bed, sit in the chair, and read the magazine. Once you get tired, you can get back into bed. However, if you can’t sleep, after 15 minutes get out of bed and repeat the process. You want to train your brain that the bed is not a place you struggle. When you feel the pillow against your head its “lights out.”
All of this information was used to create a plan for Scott, and he was assigned the sleep hygiene module to review. For behavioral goals, Scott indicated that he would try to bike to work twice over the next week. He maintained his goal of walking with his wife five times, and helping with chores around the house.
Session 11: Relapse Prevention
The goals of Session 11 were to review the patient’s homework completion and the relapse prevention module. Scott reported that he used the sleep hygiene checklist to ensure that he was practicing good sleep behaviors. He also shared the sleep information with his wife and daughters. Scott found the most challeng- ing part of sticking to the plan was putting down his electronic devices before bed. However, he solved the issue by leaving his phone in an entirely different room. Even though he still had to wake up at night to go to the bathroom, he reported being more conscious of not looking at the time or engaging his brain in a line of thought that would keep him awake. He also used imagery of imagining himself immersed in a beauti- ful winter scene, overlooking snow covered mountains. The combination of these techniques really helped Scott to fall back asleep. Scott completed the behavioral goals for the week, including biking to work once and walking with his wife almost daily.
During the final session of therapy, time should be spent reviewing the skills the patient has developed, problem-solving pain flare-ups, summarizing gains made, and developing a plan for continuing to work to- ward treatment goals. Pain flare-ups are likely to occur in the future, so it is important to openly discuss this with the patient, so that he does not abandon every- thing learned when pain flare-ups occur. The following discussion is an example of how to engage a patient in a conversation about pain flare-ups.
THERAPIST: You’ve done such an incredible job at learn- ing so many skills in therapy, and it seems you have really learned how to make your daily life a lot more pleasant while controlling your pain effectively! Let’s talk about what happens from here. Even though you have developed some really great tools for managing your pain, there are probably going to be days in the future where you will experience a pain flare-up.
SCOTT: Yes, I’ve had a few of those already. THERAPIST: Since we know this is likely to happen in
700 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
the future, you can prepare for flare-ups in advance so they don’t catch you off guard.
Scott was instructed on how prepare for pain flare- ups by being aware of cues that pain may be increas- ing and rehearsing positive self-statements rather than engaging in negative thoughts or thoughts related to being helpless (e.g., “I can’t deal with this,” “I thought I was done with this”). The therapist reviewed how to confront pain by using the self-management strategies Scott learned in therapy (e.g., breathing, imagery, cog- nitive restructuring, time-based activity pacing) and switching strategies as necessary. Finally, it was sug- gested that, after a pain flare-up, Scott reflect on strate- gies that worked best and positively reinforce himself for using his coping skills. By reviewing his efforts and picking out the strategies that worked best, Scott could create a plan for how to manage the flare-up next time.
The final part of the session was spent reviewing the progress Scott made over the course of treatment. Scott was asked to complete the same set of brief self-report questionnaires he completed at the time of the assess- ment. By asking Scott to complete the questionnaires in session, the therapist was able to show Scott actual data demonstrating the changes he had made of the course of therapy (see Table 17.1). Scott and the thera- pist reviewed the Goal-Setting Worksheet, on which he had written his overall treatment goals, and the Weekly Goal Completion forms, on which goal achievement was tracked each week. This comprehensive review al- lowed Scott to visually see the progress he had made on each of his goals. Scott was proud of his progress and commented that he had achieved many of the goals set and had actually added additional goals along the way. Time was spent reflecting each of the skills Scott learned over the course of therapy. It is important for
therapists to engage patients in taking stock of all they have accomplished, which is illustrated in the following transcript between Scott and the therapist:
THERAPIST: Scott, you’ve done a great job in treatment. You put a great deal of effort into learning the skills and now they are paying off for you. As I mentioned when we first met, once these skills are learned, they are yours for life. In addition to learning the skills, you also achieved many of your behavioral goals.
SCOTT: One of the things I leaned from his program was that “avoidance” doesn’t make pain go away. I made the gains I did because I took one step at a time, confronted my fears about movement, and I started taking better care of myself on so many dif- ferent levels.
THERAPIST: You did. You deserve absolute credit. I showed you the skills, but you learned them and ap- plied them to your life.
SCOTT: You know, I met most of the goals I set for myself. Even though I still have some back pain, I’m taking walks with my wife almost every day, which I enjoy tremendously. We are even planning to ex- plore new neighborhoods together. I’m shopping for groceries while being mindful of what I carry, and I’m doing fun stuff like riding my bike, spending time with friends and my daughters, and doing little projects around the house. I still have a few things I want to work toward, but I feel like I have my life back.
As with any relationship, therapy termination may be difficult for some patients. It’s important to take time in the final session to openly address how the patient is feeling about ending treatment. For example, some pa- tients may feel that they are losing a source of support or will miss the opportunity to have undivided attention paid to their issues. Normalize these feelings, and reas- sure the patient that he or she is ready to end treatment. Reinforce to the patient how many skills are now part of his/her “toolkit” in facing pain. It is also important to point out to the patient how the/she will continue to benefit from this program long after it has ended. Leave the patient with a feeling of hope and encouragement that he/she is now able to be his/her own “coach.” Fi- nally, congratulate the patient for completing the pain management program and for making the commitment to learning skills to help him/her take greater control of his pain.
TABLE 17.1. Pain Assessment Measures Completed Pretreatment and Posttreatment
Measures Pretreatment Posttreatment
Brief Pain Inventory Average severity 7 3
Interference 7.6 2
Pain Catastrophizing Scale 32 7
Patient Health Questionnaire–9
10 2
Cognitive‑Behavioral Therapy for Chronic Pain 701
CONCLUSION
Because chronic pain is such a prevalent problem that is faced by so many patients, it is my hope that this chap- ter has provided a “road map” for how to effectively implement cognitive behavioral treatment for chronic pain. While all patients may have slightly different circumstances, these tools can be used with patients with varying types of pain (e.g., back pain, knee pain, or headache) and with patients of varying ages. Some of the clinical tools that comprise the 11-session pain management program may resonate more with some patients than with others; while one patient may re- port that relaxation and imagery was their “go to” skill, others may report that time-based activity pacing was the key to helping them become more active. Scott’s particular case illustrated how it is possible, even with- out medication, for patients to utilize concrete tools to gradually regain confidence in their ability to move, to reduce avoidance, and to take the important steps nec- essary to restore the joy in their lives.
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The fifth edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) clearly defines and separates anorexia nervosa and bulimia nervosa, and for the first time recognizes binge-eating disorder as a specific diagnosis. But many people with serious eating disorders do not quite fit these diagnostic criteria and would be lumped into an “other specified feeding or eating disorder” category. It is also the case that individuals with eating disorders change from one category to another over time. The authors of this chapter, involved over the years in the creation of the DSM eating disorder categories, are also among the originators of the most successful treatment yet devised for these disorders. Thus, it is significant that Cooper and Murphy and their colleagues have moved ahead of the curve and created a “transdiagnostic” unified theory and treatment protocol applicable to all eat- ing disorders, including those falling into the “other specified” category. (For a similar approach to emotional disorders, see Payne, Ellard, Farchione, & Barlow, Chapter 6, this volume.) In this chapter Cooper and Murphy describe this state-of-the-art treatment, along with its empirical support. In what to some readers may be a surprising departure, the authors’ note that the central problem requir- ing intervention is not necessarily dieting, bingeing, low weight, or purging, but rather the culturally reinforced abnormal attitudes and beliefs regarding shape and weight. The recommendation for ap- plying various treatment components in a “modular” fashion speaks to the art of administering this treatment, as illustrated very nicely in the case of “Anna.” The detailed explication of this approach as applied across the full range of eating disorders should be extraordinarily useful to clinicians working with these difficult problems. —D. H. B.
feeding and eating disorders are serious disorders, characterized by persistent disturbances of eating or
eating-related behavior, and may also be accompanied by altered consumption and absorption of food. The three main eating disorders recognized by the fifth edi- tion of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5; American Psychiatric Association, 2013), are anorexia nervosa (AN), bulimia nervosa (BN), and binge-eating disorder (BED). DSM-5 also describes variants that do not meet the thresholds for the main disorders or contain a mix of their features.
These eating disorders and their variants are the cause of substantial physical and psychosocial morbidity, in- cluding significant impairment in quality of life. They typically begin in adolescence and, once established, are difficult to treat, with longer duration of disorder predicting worse outcome (Vall & Wade, 2015). They are less common among men than among women, al- though recent evidence suggests that more men than previously thought are affected (Mangweth-Matzek & Hoek, 2017). In particular, they represent a significant source of morbidity among adolescent girls and young
C H A P T E R 18
eating Disorders A Transdiagnostic Protocol
Zafra Cooper Rebecca Murphy
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women (Hoek, 2017). Both AN and BN are associated with increased mortality, and BED is associated with an increased risk of obesity (Smink, Van Hoeken, & Hoek, 2013). Despite the existence of evidence-supported spe- cialist interventions for eating disorders (Cooper & Bailey-Straebler, 2015; Kazdin, Fitzsimmons-Craft, & Wilfley, 2017), there is a well-documented unmet need for treatment. The majority of those with diagnosable disorders do not receive appropriate treatment (Hart, Granillo, Jorm, & Paxton, 2011), and even fewer receive evidence-based treatments (Waller, 2016).
In this chapter we focus on the main eating disorders and their variants and describe their psychopathology and the mechanisms that are involved in their persis- tence. We then describe a transdiagnostic cognitive- behavioral treatment designed to disrupt these mecha- nisms. The feeding disorders, avoidant/restrictive food intake disorder, pica, and rumination disorder newly included in DSM-5 do not share the distinctive core psychopathology of most of the other eating disorders and tend to be associated with anxiety and in some cases neurodevelopmental disorders. As such, they are beyond the scope of this chapter.
CLASSIFICATION AND DIAGNOSIS
The DSM-5 scheme for classifying and diagnosing eat- ing disorders recognizes three specific disorders: AN, BN, and BED. Clear inclusionary and exclusionary cri- teria are provided for establishing the presence of these disorders and distinguishing them from each other. In addition, there are “other eating disorders” (OEDs) that DSM-5 has grouped in two residual categories termed other specified feeding or eating disorder and unspecified feeding or eating disorder, respectively (American Psy- chiatric Association, 2013).
No diagnostic criteria are specified for the two resid- ual eating disorder diagnoses in DSM-5, but examples of the other specified feeding or eating disorder presen- tations are listed. Conceptually, it is helpful to distin- guish two subgroups within the OEDs, although there is no sharp boundary between them. The first com- prises cases that closely resemble AN, BN, or BED but just fail to meet their diagnostic criteria; for example, body weight may be marginally above the threshold for AN, or the frequency of binge eating may be just too low for a diagnosis of BN or BED. These cases may be viewed as “subthreshold” forms of AN, BN, or BED,
respectively. The second subgroup comprises cases in which the clinical features of the specific eating disor- ders are combined in a different way to that seen in the prototypical disorders. Such states may be described as “mixed” in character.
CLINICAL FEATURES
AN, BN, BED, and the OEDs share a variety of dis- tinctive features. AN and BN share a core psychopathol- ogy, the overevaluation of shape and weight and their control; this is also present in the majority of those with BED (Grilo, 2013) and those with the OEDs. This core psychopathology is very similar in females and males, adults and adolescents. Whereas most peo- ple evaluate themselves on the basis of their perceived performance in a variety of life domains (e.g., the qual- ity of their relationships, their work performance, their sporting prowess), people with eating disorders judge their self-worth largely, or even exclusively, in terms of their shape and weight, and their ability to control them. This psychopathology is peculiar to the eating disorders and is rarely seen in the general population. It should be distinguished from body shape dissatisfac- tion, which refers to the dislike of aspects of one’s ap- pearance. Some degree of body shape dissatisfaction is widespread, and its presence is sometimes referred to as normative discontent (Rodin, Silberstein, & Striegel- Moore, 1984).
The overevaluation of shape and weight results in the pursuit of weight loss and/or shape change, and an intense fear of weight gain and fatness. Most other features of these disorders are secondary to this core psychopathology and its consequences (e.g., undereat- ing, driven exercising, becoming severely underweight). In AN, there is a sustained and successful pursuit of weight loss that results in patients becoming severely underweight. In BN, equivalent attempts to restrict food intake are disrupted by repeated episodes of loss of control over eating (binges).
Many patients mislabel adverse physical and emo- tional states as “feeling fat” and equate this with actu- ally being fat. In addition, many repeatedly scrutinize their bodies, focusing on parts that they dislike. This may contribute to patients’ overestimation of their size. Others actively avoid seeing their bodies, assuming that they look fat and disgusting. Equivalent behavior is seen with respect to weighing (weight checking), with many
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patients weighing themselves frequently. As a result, these patients become preoccupied with trivial, day-to- day fluctuations. Others actively avoid knowing their weight and, with no information to disconfirm their worst fears, remain highly concerned about it.
Anorexia Nervosa
In AN, the pursuit of weight loss leads patients to en- gage in a severe and selective restriction of food intake, avoiding foods viewed as fattening. Generally, there is no true “anorexia” (loss of appetite) as such. The un- dereating may also be an expression of other motives, including asceticism and competitiveness. In the early stages of the disorder, undereating may be a goal in its own right, with the patient valuing the sense of self- control that it confers. Some patients also engage in a driven type of exercising that contributes to their weight loss. This is characterized by a strong drive to exercise, a tendency to overexercise, and giving exercise precedence over other aspects of life. Self-induced vom- iting and other extreme forms of weight control (e.g., the misuse of laxatives or diuretics) are practiced by a subgroup of these patients, and patients in an overlap- ping group have episodes of loss of control over eating, although the amount eaten may not be objectively large (“subjective binge eating”). Depressive and anxiety fea- tures, irritability, lability of mood, impaired concentra- tion, loss of sexual appetite, and obsessional features are also frequently present. Typically, these features get worse as weight is lost and improve with weight regain. Interest in the outside world also wanes as patients be- come underweight, with the result that most become socially withdrawn and isolated. This, too, tends to re- verse with weight regain.
Bulimia Nervosa
The eating habits of those with BN resemble those seen in AN. The main distinguishing feature is that the at- tempts to restrict food intake are disrupted by repeated episodes of binge eating. The frequency of these epi- sodes ranges from once a week (the DSM-5 diagnostic threshold) to several times a day. The amount eaten per episode varies but is typically between 1,000 and 2,000 kilocalories (kcal, although larger amounts have been reported (Forbush & Hunt, 2014; Keel, 2017). In most cases, each binge is followed by compensatory, self-induced vomiting or laxative misuse. There is a
subgroup of patients who do not “purge” but instead severely restrict their eating and/or exercise excessively to compensate for having overeaten. The weight of most patients with BN is in the healthy range (body mass index [BMI] between 18.5 and 25.0) due to the effects of undereating and overeating balancing each other.1 As a result, these patients do not experience the secondary psychosocial and physical effects of maintaining a very low weight. Depressive and anxiety features are promi- nent in BN—indeed, more than in AN—and there is a subgroup of patients who engage in substance misuse or self-injury, or both (Keski-Rahkonen & Mustelin, 2016). This subgroup, which is also present among some patients with AN who binge-eat, tends to attract the diagnosis of borderline personality disorder.
Binge‑Eating Disorder
Patients with BED report recurrent binge eating, much as in BN, but the binge eating is not associated with the recurrent use of compensatory weight control behavior. Thus, regular self-induced vomiting and laxative mis- use are not present, nor is there a tendency to overex- ercise. Overevaluation of shape and weight and their control is present in over 50% of those with BED (e.g., Grilo, White, Gueorguieva, Wilson, & Masheb, 2013). However, there remain a significant proportion who do not present with this feature (overevaluation is not a di- agnostic criterion for BED), although it may serve as a useful specifier for formulation and treatment (Grilo et al., 2009) in addition to severity (Coffino, Udo, & Grilo, 2019).
Although BED occurs in those who are in the healthy weight range, it is reliably associated with overweight and obesity (BMI ≥30.0) in those who seek treatment (Kessler et al., 2013; Udo & Grilo, 2018). In contrast to BN where there is a high level of dietary restraint and adherence to a highly restricted diet when not binge eating, those with BED do not show high levels of sustained dietary restriction, although they do report frequent attempts to diet. These attempts are largely unsuccessful, and there is in fact a tendency to overeat outside the binges. Despite this eating pattern, patients with BED differ from those with obesity in experienc- ing episodes of binge eating precipitated by negative af- fect, interpersonal stressors and dietary restraint, and in laboratory studies, those with BED and obesity eat more than individuals of similar weight without BED (Engel et al., 2009).
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BED is a serious health problem (Kessler et al., 2013) and the cause of substantial impairment and reduced quality of life (Kornstein, 2017). It is associated with significant psychiatric and physical health comorbid- ity including depressive disorders, anxiety disorders, substance abuse disorders, and obesity with its associ- ated potential secondary medical complications and in- creased health care costs (Ágh et al., 2015; Guerdjikova, Mori, Casuto, & McElroy, 2019; Udo & Grilo, 2018).
Other Specified and Unspecified Eating Disorders
As discussed earlier, the psychopathology of the OEDs, “specified and unspecified disorders” in DSM-5 closely resembles that seen in AN, BN, and BED. It is also of comparable severity, and disorders are of comparable duration (Fairburn et al., 2007).
THE “TRANSDIAGNOSTIC” PERSPECTIVE
The DSM-5 scheme, with its proliferation of eating disorder diagnoses, encourages the view that AN, BN, and BED are distinct clinical states, each requiring its own form of treatment. It also obscures the important fact that the eating disorders, including the OEDs, have much in common. In fact, a study of their clinical fea- tures indicates that AN, BN, and most cases of BED and the OEDs share a distinctive core psychopathology not seen in other psychiatric disorders.2 As described earlier, this is the overevaluation of shape and weight and their control, which refers to patients’ tendency to judge their self-worth largely or even exclusively in terms of weight and shape, and their ability to control them. The trans- diagnostic cognitive-behavioral theory proposes that this distinctive scheme for self-evaluation is of central importance in maintaining the eating disorders. Other clinical features can be understood as stemming directly from this psychopathology, albeit at somewhat varying frequencies or in different combinations.
Further support for the transdiagnostic perspective comes from studies of the course of the various eating disorders that suggest that, over time, patients move between the various diagnostic categories. When classi- fied using the earlier DSM-IV scheme, a third of those who initially received a diagnosis of AN subsequently met diagnostic criteria for BN (Eddy et al., 2008) and a substantial minority of those who were in the residual category “not otherwise specified disorders” met crite-
ria for AN or BN in the past (Fairburn et al., 2007). A review of studies of the course and outcome of AN and BN show that no significant differences exist whether DSM-IV or DSM-5 definitions are used, while noting that much less is known about the course and outcome of BED (Smink et al., 2013). Although some changes might be expected in the detailed proportions of those who move within DSM-5 categories, given the rela- tively small changes made in the new system, it seems likely that further new research will continue to show a similar pattern of movement as shown in a recent study (Forbush et al., 2018). If this temporal movement con- tinues to be the norm in the case of the eating disorders, it does call into question the claim that these various forms of disorder are indeed separate and distinct states. In summary, the shared but distinct psychopathology of the eating disorders, together with the phenomenon of temporal movement between the diagnostic catego- ries, suggests that transdiagnostic mechanisms may be responsible for maintaining these disorders (Fairburn, Cooper, & Shafran, 2003). If correct, this implies that treatments capable of successfully addressing these maintaining mechanisms should be effective with all forms of eating disorder rather than just one.
TRANSDIAGNOSTIC COGNITIVE‑BEHAVIORAL THEORY
In common with most evidence-based cognitive-behav- ioral treatments, the theory that underpins cognitive behavior therapy for BN (CBT-BN) is primarily con- cerned with the processes that maintain the disorder rath- er than those responsible for its development. Accord- ing to the theory, these patients’ dysfunctional scheme for self-evaluation is central to the maintenance of the disorder. As noted earlier, whereas most people evalu- ate themselves on the basis of their perceived perfor- mance in a variety of life domains, people with eating disorders judge themselves largely, or even exclusively, in terms of their shape and weight, and their ability to control them. Consequently, their lives become focused on shape, weight, and eating, with dietary control, thinness, and weight loss being actively pursued, while overeating, “fatness,” and weight gain are assiduously avoided. Most of the other features of BN can be un- derstood as stemming directly from this “core psycho- pathology,” including the weight control behavior, the various forms of body checking and avoidance, and the
Eating Disorders 709
preoccupation with thoughts about shape, weight, and eating. Figure 18.1 provides a schematic representation (or “formulation”) of the main processes involved in BN.
The only feature of BN that is obviously not a direct expression of the core psychopathology is these patients’ binge eating. Cognitive-behavioral theory proposes that the binge eating is largely a product of the par- ticular way that these patients attempt to restrict their eating (i.e., their form of dietary restraint), irrespective of whether they actually undereat. Rather than adopt- ing general guidelines about how they should eat, these patients try to adhere to multiple extreme, and highly specific, dietary rules. An accompanying tendency— one that involves reacting in an extreme and negative fashion to the frequent and almost inevitable breaking of these rules—leads to interpreting even minor dietary slips as evidence of lack of self-control. The result is that patients respond by temporarily abandoning their at- tempts to restrict their eating and instead give in to the urge to eat. This produces a highly distinctive pattern of eating in which attempts to restrict eating are repeat- edly interrupted by episodes of binge eating. The binge eating maintains the core psychopathology by intensi- fying patients’ concerns about their ability to control
their eating, shape, and weight, and it encourages yet greater dietary restraint, thereby increasing the risk of further episodes of binge eating.
It should be noted that these patients’ dietary slips and binges do not come out of the blue; rather, they are particularly likely to occur in response to life difficul- ties and any associated mood change, in part because binge eating temporarily ameliorates negative mood states, and in part because it distracts patients from thinking about their difficulties.
A further process maintains binge eating in those pa- tients who practice compensatory “purging” (i.e., those who induce vomiting or take laxatives in response to specific episodes of binge eating). Patients’ mistaken belief in the effectiveness of purging in preventing calorie (i.e., energy) absorption undermines a major de- terrent against binge eating. They do not realize that vomiting only retrieves part of what has been eaten, and laxatives have little or no effect on energy absorption (Fairburn, 2013).
This well-established cognitive-behavioral account of the maintenance of BN has clear implications for treatment. It suggests that if treatment is to have a last- ing impact on binge eating and purging, then it also needs to address these patients’ extreme attempts to restrict their eating, their overevaluation of shape and weight, and their tendency to eat in response to adverse events and negative moods.
The cognitive-behavioral account of the mainte- nance of BN can be extended to all eating disorders. As noted earlier, the transdiagnostic theory highlights the fact that AN and BN have much in common (Fair- burn et al., 2003). They share essentially the same core psychopathology, and express this psychopathology in similar attitudes and behavior. Thus, patients with AN restrict their food intake in the same rigid and extreme way as patients with BN and they, too, may vomit, mis- use laxatives or diuretics, and exercise in a driven way. The presence of binge eating does not distinguish the two disorders, because there is a subgroup of patients with AN who binge-eat (with or without compensa- tory purging). The major difference between the two disorders lies in the relative balance of the undereating and overeating, and its effect on body weight. In BN, body weight is usually unremarkable, whereas in AN undereating predominates, resulting in body weight that is extremely low, with features of starvation con- tributing to the clinical picture and its maintenance. Particularly important in this regard is the pronounced
Binge eating
Compensatory vomiting/laxative
misuse
Events and associated mood change
Overevaluation of shape and weight and their control
Strict dieting; noncompensatory
weight-control behavior
FIGURE 18.1. The cognitive-behavioral theory of the maintenance of BN. From Fairburn (2008, p. 19). Copy- right © 2008 The Guilford Press. Reprinted by permission. This figure may be downloaded from www.credo-oxford. com.
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social withdrawal seen in starvation, since this encour- ages self-absorption, while isolating patients from exter- nal influences that might diminish their overconcern with eating, shape and weight. Figure 18.2 shows the cognitive-behavioral formulation of the classic “restrict- ing” form of AN.
The processes that maintain BN and AN also appear to maintain the clinical presentations seen in BED and their variants. Figure 18.3 shows a composite transdi- agnostic formulation. In our experience, this composite formulation represents the core processes that maintain any eating disorder, whatever its exact form. The specif- ic processes operating in any individual patient depend on the nature of the eating disorder psychopathology present. In some cases, only a limited number of these processes are active (as in some cases of BED), whereas in others (e.g., cases of AN in which there is binge eat- ing and purging), most of the processes are operating. This transdiagnostic account highlights the processes that need to be addressed in treatment, thereby helping the clinician design a bespoke treatment to fit the indi- vidual patient’s psychopathology.
TRANSDIAGNOSTIC COGNITIVE BEHAVIOR THERAPY
A transdiagnostic form of cognitive behavior therapy (CBT) has been developed that is designed for the full range of clinical eating disorders seen in adults, includ- ing other specified eating disorders (Fairburn, 2008; Fairburn et al., 2003). It is based on the transdiagnostic theory outlined and was derived from CBT-BN. The treatment—enhanced CBT (CBT-E)—is described as “enhanced” because it uses a variety of new strategies and procedures intended to improve treatment adher- ence and outcome. In addition, it has modules de- signed to address certain obstacles to change that are “external” to the core eating disorder, namely, clinical perfectionism, low self-esteem, and interpersonal diffi- culties. Thus, there are two forms of CBT-E, a focused form that focuses exclusively on the eating disorder psychopathology, and a broad form that also addresses the three external obstacles to change.3 The treatment also exists in two lengths, a 20-week version for pa- tients who are not significantly underweight, defined as having a BMI of 18.5 or more, and a version that can be up to double this length for patients with a BMI below 18.5.
FIGURE 18.2. The cognitive-behavioral theory of the maintenance of AN. From Fairburn (2008, p. 21). Copy- right © 2008 The Guilford Press. Reprinted by permission. This figure may be downloaded from www.credo-oxford. com.
FIGURE 18.3. The “transdiagnostic” cognitive-behavior- al theory of eating disorders. From Fairburn (2008, p. 21). Copyright © 2008 The Guilford Press. Reprinted by per- mission. This figure may be downloaded from www.credo- oxford.com.
Strict dieting; noncompensatory
weight-control behavior
Significantly low weight • preoccupation with eating • social withdrawal • heightened fullness • heightened obsessionality
Overevaluation of shape and weight and their control
Strict dieting; noncompensatory
weight-control behavior
Binge eating
Compensatory vomiting/laxative
misuse
Significantly low weight
Events and associated mood change
Overevaluation of shape and weight and their control
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CBT-E, primarily an outpatient treatment, is de- signed to be delivered on an individual rather than a group basis, although day patient and inpatient versions have been developed (Dalle Grave, 2012a). It has also been adapted for adolescents (Cooper & Stewart, 2008; Dalle Grave & Calugi, 2020; Dalle Grave, Calugi, Doll, & Fairburn, 2013).
RESEARCH ON CBT AND CBT‑E
Consistent with the current way of classifying eating disorders, much of the research on their psychological treatment has focused on the particular disorders in iso- lation. Over the past two decades, significant progress has been made in developing treatments for eating dis- orders, and evidence for their efficacy has been docu- mented in both narrative and systematic reviews. In particular, CBT, a guided self-help form of CBT (CBT- GSH), CBT-E, and interpersonal psychotherapy (IPT) are recommended for the treatment of BN, BED, and to a lesser extent (due to less robust evidence) the OEDs (Brownley, Berkman, Sedway, Lohr, & Bulik, 2007; Hay, 2013; Kass, Kolko, & Wilfley, 2013; National In- stitute for Health and Care Excellence [NICE], 2017; Peat et al., 2017; Shapiro et al., 2007) with further sup- port for CBT-E from two more recently published stud- ies comparing CBT-E to active comparison treatments. In samples that did not include those who were sig- nificantly low weight, CBT-E was superior to IPT and psychoanalytic psychotherapy respectively (Fairburn et al., 2015; Poulsen et al., 2014). In addition, recently published meta-analyses and systematic reviews have confirmed support for manual-based CBT as superior to both alternative active psychological treatments and third-wave behavioral treatments (Linardon, Fairburn, Fitzsimmons-Craft, Wilfley, & Brennan, 2017; Linar- don, Wade, de la Piedad Garcia, & Brennan, 2017).
Treatment for adults with AN is less well supported (Bulik, Berkman, Brownley, Sedway, & Lohr, 2007; Hay, 2013; Kass et al., 2013; Watson & Bulik, 2013), although the evidence base is improving (Brockmeyer, Friederich, & Schmidt, 2018). Currently, three main approaches for AN are recommended (NICE, 2017): CBT-E (Fairburn et al., 2013) and other forms of evi- dence-based CBT for eating disorders (CBT-ED); spe- cialist supportive clinical management (SSCM; Carter et al., 2011; McIntosh et al., 2006; Touyz et al., 2013); and the Maudsley model AN treatment for adults
(MANTRA; Schmidt et al., 2015), with eating-disor- der-focused focal psychodynamic therapy (FPT; Zipfel et al., 2014) as a subsequent consideration. As yet, no one specialist treatment has emerged as clearly supe- rior to the others, with studies comparing a variant of CBT-E with FPT (Zipfel et al., 2014) and a study com- paring CBT-E with SSCM and MANTRA (Byrne et al., 2017) being broadly consistent with this conclusion.
For adolescents with AN, family-based treatment (FBT) has received the most support (Agras et al., 2014; Couturier, Kimber, & Szatmari, 2013; Lock, 2018; NICE, 2017) with evidence, although not derived from controlled studies, for CBT-E (Dalle Grave, El Ghoch, Sartirana, & Calugi, 2016).
Four recently published meta-analyses and system- atic reviews that include both controlled and uncon- trolled trials have provided robust support for CBT-E in transdiagnostic samples (Atwood & Friedman, 2020; Dahlenburg, Gleaves, & Hutchinson, 2019; de Jong, Schoorl, & Hoek, 2018; Groff, 2015), with the latest and most comprehensive review (Atwood & Friedman, 2020) concluding that there is support for the efficacy and effectiveness of CBT-E for the full spectrum of eat- ing disorders, with respect to reducing eating disorder behaviors and core psychopathology, and increasing BMI in individuals with AN. Superiority over compari- son treatments, especially in the longer term, has not been conclusively demonstrated.
Two main points emerge from the research on CBT-E to date:
1. CBT-E can be used to treat all forms of eating disorder in adults and adolescents. Thus, CBT-E is transdiagnostic in its scope.
2. There are good data on the use of CBT-E to treat adults and older adolescents, including those with low weight and AN. For these patients, the avail- ability of CBT-E may make the need to learn a va- riety of different treatments for each of the eating disorders (Fairburn & Wilson, 2013) redundant.
The remainder of this chapter is devoted to a descrip- tion of the main form of CBT-E, the focused version. This is the core version of the treatment that forms the basis of the variants of CBT-E. It is the version used to treat the great majority of adults with an eating disorder, so long as they can be managed on an outpatient basis. A full description of the focused treatment is provided in the complete treatment guide (Fairburn, 2008; Fair-
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burn et al., 2008b) together with details of the broad version (Fairburn, Cooper, Shafran, Bohn, & Hawker, 2008a). CBT-E may be modified to make it suitable for inpatient, day patient, and intensive outpatient settings (Dalle Grave, 2012a, 2012b), and a recently published book describes the treatment for young people (Dalle Grave & Calugi, 2020).
THE CONTEXT OF TREATMENT
The Patient
CBT-E is a treatment for patients with an eating dis- order of clinical severity (i.e., the eating disorder psy- chopathology is persistent and significantly interferes with the patient’s psychosocial functioning or physi- cal health). It was originally designed for patients aged 18 years or older, and it is equally suitable for men or women. Because it is an outpatient-based treatment, it is essential that it be safe for the patient to be man- aged this way, both in physical terms and from the psy- chiatric point of view. In practice, this means that the patient’s physical state must be stable and that he/she must not be at risk of suicide. The treatment is designed for patients with a BMI between 15 and 40. Although some patients with a BMI below 15 can be treated using outpatient CBT-E, this is probably best left to experi- enced therapists. The management of such patients is discussed by Dalle Grave (2012a). Management of pa- tients with a BMI over 40 is addressed by Mitchell and de Zwaan (2012).
The Therapist
There are no specific professional qualifications needed to practice CBT-E, but certain background knowledge and experience are desirable. First, ideally, therapists should be well informed about psychopathology in general and about eating disorder psychopathology in particular, and they should have experience working with patients with eating disorders. Second, therapists should also be aware of the medical complications of eating disorders and be able to manage them appro- priately (Fairburn, Cooper, & Waller, 2008c, 2008d). Third, therapists should be happy to implement a short-term, psychopathology-focused treatment and, preferably, should have some experience working this way.
In contrast with many other applications of CBT, the gender of the therapist is of some relevance to the
treatment of patients with eating disorders. Most of these patients are female; as a result, female therapists may have certain advantages. They may be viewed by patients as being more likely to understand their dif- ficulties and, in addition, may serve as role models in terms of the acceptance of shape and weight. These considerations are minor, however, in comparison with being competent at delivering the treatment. Our ex- perience indicates that being an excellent CBT-E thera- pist does not depend on gender.
ASSESSING PATIENTS AND PREPARING THEM FOR TREATMENT
The Initial Evaluation Interview(s)
The initial assessment interview has three interrelated goals. The first is to put the patient at ease and begin to forge a positive therapeutic relationship. This is impor- tant for a number of reasons. First, many patients with an eating disorder are highly ambivalent about treat- ment because of the “ego-syntonic” nature of their psy- chopathology (especially true of underweight patients), because of shame (especially true of those who are binge eating), or because they have had adverse treatment ex- periences in the past. The assessing clinician needs to be sensitive to the patient’s attitude to the assessment interview and ask directly about it. The goal is that it be a collaborative enterprise, ending with the clinician being able to give patients an expert opinion as to the nature of their problems and, if indicated, the treatment options.
The second goal is to establish the diagnosis. An ap- parent eating disorder may, for example, turn out to be an anxiety disorder (e.g., difficulty eating with others due to a social phobia), a presentation of a mood dis- order (e.g., severe weight loss resulting from a clinical depression), or a weight problem (in cases of obesity). It is therefore critical to diagnose the problem or problems (if there is comorbidity) accurately and evaluate their severity in order to decide on the most appropriate next step.
The third goal is to ensure that the patient is safe to manage on an outpatient basis. This requires checking that there are no reasons to be concerned about the pa- tient’s physical health or the risk of suicide. Guidance for doing so is provided in the complete treatment guide (Fairburn et al., 2008b; Fairburn, Cooper, & Waller, 2008d).
Patients are invited to bring others to the appoint-
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ment if they wish. They may simply provide moral support (and stay in the waiting area) or also serve as informants. The informant’s view is of interest, since it can provide a different perspective on the patient’s difficulties. Problems may be described that were not disclosed by the patient (e.g., that the patient takes an inordinate time to eat meals or has extremely small portions). However, it is not appropriate to insist that informants attend given that some adult patients will have kept their eating problem hidden from others and would not attend if disclosure were required. The situ- ation is different with younger patients, in which in- volvement of the parents is generally essential.
Toward the end of the first interview, we weigh pa- tients and measure their height. This is an extremely sensitive matter for most patients, and some are re- sistant to it. As the patient must be weighed for the assessment to be complete, we explain this. We do not regard it as appropriate to rely on patients’ self- reported weight or height, which can be inaccurate. In our experience, patients expect their weight to be measured, although many prefer that this not happen. At this stage, we do not insist on patients knowing their weight if they do not wish to, but we like to tell them their BMI when discussing the outcome of the assessment.
We are not in favor of lengthy assessment appoint- ments, because they are exhausting for the patient. On the other hand, we routinely see patients twice as part of the assessment process, since we find that a second appointment, a week or two later, often adds new infor- mation of value. On the second occasion, patients are more relaxed; they sometimes disclose material previ- ously withheld; and there is an opportunity to pursue matters that require particularly careful exploration (e.g., the nature and extent of any comorbid depressive features). The second appointment is also a good time to discuss treatment options.
We routinely ask patients to complete certain ques- tionnaires prior to the initial appointment. This is use- ful, since it gives us standardized information on the nature and severity of patients’ eating problems. The two questionnaires we favor are the Eating Disorder Ex- amination Questionnaire (EDE-Q; Fairburn & Beglin, 2008) and the Clinical Impairment Assessment (CIA; Bohn & Fairburn, 2008). The EDE-Q provides a mea- sure of the severity of current eating disorder features, and the CIA assesses the impact of this psychopathol- ogy on psychosocial functioning. Both questionnaires are short and easy to fill in, and both focus on the previ-
ous 28 days and are sensitive to change. In addition, we include one of the well-established measures of general psychiatric features.
Outcome of the Evaluation
By the end of the second appointment, it should be pos- sible to decide on the best course of action. Generally there are five possible next steps:
1. Do “nothing.” This is appropriate with minor eat- ing problems that are likely to be self-limiting.
2. Observe. This is appropriate if the nature or sever- ity of the problem is not clear; for example, if it seems to be remitting.
3. Recommend outpatient-based CBT-E. This is ap- propriate for the vast majority of patients. We rec- ommend CBT-E for virtually all patients with an eating disorder who have a BMI between 15 and 40.
4. Recommend more intensive treatment. We recom- mend more intensive treatment (mainly day pa- tient or inpatient treatment) for patients whose BMI is below 15 and for those whose physical state is not stable. This can be followed by out- patient-based CBT-E. We may also recommend more intensive treatment when CBT-E fails to be of benefit.
5. Recommend referral elsewhere. This is appropriate when the problem is not an eating disorder (e.g., an anxiety or mood disorder).
If patients have not benefited from CBT for their eating disorder in the past, it merits thought whether it is appropriate to offer them the same treatment a second time. On the other hand, it is possible that a patient’s circumstances may now be more conducive to a good outcome than in the past, or the patient may be more motivated than before. It is important to note that while patients may report having had CBT before, it often emerges that it was quite different in charac- ter from CBT-E. It is always worth finding out exactly what the prior treatment involved.
Contraindications to Starting CBT‑E Immediately
There are certain contraindications to embarking on CBT-E right away. Most of these apply to any psycho- logical treatment for an eating disorder. The main con- traindications follow.
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Comorbid Clinical Depression
Most patients with an eating disorder have secondary depressive features, but a sizable subgroup has an inde- pendent, but interacting, clinical depression. The iden- tification and management of clinical depression in pa- tients with eating disorders is discussed in detail in the complete treatment guide (Fairburn, Cooper, & Waller, 2008c). The presence of a clinical depression interferes with psychological treatment in a number of ways. De- pressive thinking results in patients being unduly nega- tive about the possibility of change, and the reduction in drive has a similar effect. Concentration impairment is also a problem, since it results in information not being retained. Once the depression has been treated, however, CBT-E can start, and such patients are often particularly highly motivated.
It is important to add that other, co-occurring forms of psychopathology (e.g., anxiety disorders, personality disorders) are not necessarily contraindi- cations to CBT-E. To date, there is little research to guide how best to address comorbid psychiatric and physical conditions in patients with eating disorders (NICE, 2017).
Significant Substance Misuse
Intoxication in treatment sessions renders the sessions virtually worthless, and persistent intoxication outside sessions severely undermines the patient’s ability to uti- lize CBT-E. Once the substance misuse has been ad- dressed, CBT-E can start.
Major Life Difficulties or Crises
These are distractions that interfere with treatment. It is often best to delay treatment until the crisis has passed.
Inability to Attend Regularly
A central feature of CBT-E is establishing and main- taining “therapeutic momentum.” This requires that appointments be frequent (especially in the early stages) and regular. We ask patients to guarantee that there will be no breaks in their attendance in the first 6 weeks and no breaks of longer than two consecutive weeks throughout the rest of treatment. If this is impossible, say, because of a prebooked vacation, we prefer to defer starting treatment. Patients generally understand and
respect the rationale behind this stance. They can see that we are taking their treatment seriously and do not want them to have a “false start.”
Therapist Absence
The need to establish and maintain therapeutic mo- mentum also places an obligation on the therapist. If the therapist is going to be away in the first 6 weeks of treatment, it is best to delay its start. Ways of minimiz- ing the impact of therapist absence are discussed in the treatment guide (Fairburn et al., 2008b).
Describing CBT‑E to the Patient
If CBT-E is to be recommended, it is important that it be accurately portrayed. A description by the thera- pist may be supplemented by providing an informa- tion sheet about CBT-E (obtainable, along with other resources, from www.cbte.co/for-professionals/cbt-e- resources-and-handouts). Then, and once patients have had an opportunity to ask questions, it is our practice to ask them to think over what has been proposed and let us know within a week what they have decided. In our experience, virtually all of them say that they would like to proceed with the treatment.
Case Study: Assessing Patients and Preparing Them for Treatment
“Anna” was a 22-year-old college student referred by her primary care physician for the treatment of an eat- ing disorder. She attended the initial assessment on her own and reported that her family were unaware of her problems. She gave a clear account of her eating dif- ficulties and their development. Assessment indicated that she was suffering from an eating disorder that met DSM-5 diagnostic criteria for BN. She had been dis- satisfied with her weight since early adolescence and began dieting to lose weight during her final year at high school. Initially, she lost about 15–16 pounds (7 kilograms [kg]) in weight but then found it more dif- ficult to stick to her diet and began binge eating and subsequently inducing vomiting. She described her daily food intake as consisting of a very small bowl of cereal for breakfast with nonfat milk and a small salad for lunch. She often tried to delay these meals as long as possible and sometimes skipped them entirely. She reported large episodes of binge eating every night (typical binge episodes including some combination of
Eating Disorders 715
a loaf of bread, a large family-size bag of chips, a pack- age of cookies, a large tub of ice cream). Occasionally, she also took more than the recommended dose of a laxative to further compensate for the binge eating. During the evening she would vomit up to four times. Anna described a range of rigid dietary rules about how much she should eat at each meal, and she reported avoiding many foods that she regarded as fattening and likely to trigger binges.
Anna found her body “repulsive” and had avoided weighing herself for the past 6 months. She did not know her weight but believed it to be unacceptably high. She frequently checked her body (to see “how fat I am”) and had missed important lectures as a result of her ensuing low mood. At assessment she weighed 140 pounds (63.5 kg), giving her a BMI of 24.9. Although she was reluctant to be weighed, she understood that it was needed to complete the assessment and, after some discussion, agreed to being told her BMI but not her weight. At the time she was first assessed, Anna had a number of work deadlines to meet and her mood ap- peared low. She was also drinking a bottle or more of wine each night.
Aside from the eating difficulties, two issues were of concern and were possible contraindications to im- mediate CBT-E: her apparently persistently low mood, together with a range of features suggestive of a co- morbid depression (reduced interest and socializing, negative thinking, hopelessness) and her alcohol intake. Her scores on the EDE-Q and the CIA were consistent with her account of her eating difficulties and resul- tant impairment, and standardized assessment of gen- eral psychiatric features confirmed the concern about depressed mood. The assessing clinician explained how these two issues might interfere with treatment. The patient responded by acknowledging that she was drinking too much and saying that she would like to reduce it. She added that she wished to overcome her eating disorder but feared weight gain. She had a num- ber of work deadlines in the following 2 weeks, so a second appointment was arranged after these and it was agreed that she would attempt to reduce her alco- hol intake. At her second appointment, Anna was more relaxed having completed her work. Her mood seemed considerably improved, and she was no longer report- ing other depressive symptoms. She had greatly reduced her alcohol intake, confining her drinking to no more than two glasses of wine on weekday evenings and up to three on weekend evenings. It was agreed that 20 weeks of CBT-E would begin.
OVERVIEW OF TREATMENT
Length of Treatment
CBT-E, a short-term, time-limited, individualized psy- chological treatment, is best delivered on a one-to-one basis. For patients who are not significantly under- weight (which may be defined in this context as having a BMI above 18.54), an initial assessment appointment followed by 20 fifty-minute treatment sessions over 20 weeks is generally sufficient. For patients below this weight, treatment needs to be longer, often involving about 40 sessions over 40 weeks. In this chapter, we de- scribe the 20-week treatment first, then the adaptations needed for underweight patients.
The fact that CBT-E is usually time-limited might be thought not to be entirely consistent with the claim that it is individualized. Our experience is that the recommended number of treatment sessions is suf- ficient but not excessive for the great majority of pa- tients. There are major advantages to working within a fixed time, the major one being that it concentrates the minds of both patient and therapist. It both encour- ages the establishment of therapeutic momentum and helps to ensure that therapist and patient keep working hard to help the patient change. It also makes it much more likely that treatment will have a formal ending rather than fizzling out, as sometimes happens when treatment is open-ended. Having a definite endpoint is important, as it ensures that important future-oriented topics (e.g., how to minimize the risk of relapse) are cov- ered in the final part of treatment.
There are circumstances under which it is appropri- ate to adjust the length of treatment. It rarely needs to be shortened, although this does apply in occasional cases in which change is so profound and rapid that there is little or no remaining psychopathology to ad- dress. Somewhat more often, there is a case for extend- ing treatment. The indications for doing this are de- scribed briefly toward the end of the chapter.
Structure of Treatment
The 20-week version of the treatment has four stages. These are illustrated in the treatment map (see Figure 18.4):
• Stage 1. The aims are to engage the patient in treat- ment and change, jointly create a formulation of the processes maintaining the eating disorder, pro- vide education, address weight concerns, and in-
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troduce a pattern of regular eating. Following the initial preparatory session, the appointments are twice weekly for 4 weeks.
• Stage 2. The aims are to take stock, review prog- ress, identify barriers to change, modify the for- mulation as needed, and plan Stage 3. This stage generally comprises two appointments, each a week apart.
• Stage 3. This is the main body of treatment. The aim is to address the key mechanisms that are maintaining the patient’s eating disorder. There are eight weekly appointments.
• Stage 4. This is the final stage of treatment, and the focus is on the future. There are two aims: The first is to ensure that the changes made in treat- ment are maintained over the following months, and the second is to minimize the risk of relapse in
the long term. Typically, there are three appoint- ments, each 2 weeks apart.
In addition, there is a single review appointment 20 weeks after treatment has finished.
The Implementation of CBT‑E
CBT-E is designed to be a complete treatment in its own right. In our view, it should not be combined with other forms of therapy, nor should it coexist with them. Both can detract from the treatment.
CBT-E should remain focused on the eating disor- der, more or less, whatever happens. If the patient expe- riences a crisis during treatment that cannot be ignored, we arrange one or more “crisis sessions,” in addition to the CBT-E sessions to address the problem in ques-
FIGURE 18.4. Treatment map for CBT-E.
Stage 3 – Body Image Self-evaluation
Developing other domains Body checking, body avoidance,
and feeling fat
Stage 1 – Starting Well An overview of Stage 1 and the initial session
Creating a formulation Self-monitoring
Weight, weight concern, and psychoeducation Regular eating
Stage 2 – Taking Stock Taking stock and planning ahead
An overview of Stage 3
Stage 3 – Events, Moods, and Eating Events, moods, and eating,
and proactive problem solving
Stage 3 – Dietary Restraint
Dietary restraint and dietary restriction
Stage 3 – Relapse Prevention
Manipulating mindsets
Stage 4 – Ending Well An overview of Stage 4
Preventing relapse in the long term Maintaining progress
Eating Disorders 717
tion. This rarely happens, however. Very occasionally, we suspend CBT-E for a few weeks if continuing seems inappropriate.
We have observed that some therapists are tempted to change therapeutic tack if progress is slow or diffi- cult. We think that this is rarely appropriate. Although it might be tempting to switch over to another thera- peutic modality, or to add or try to “integrate” other techniques, we recommend that the therapist continues to work within the framework of CBT-E, while using the formulation of the patient’s difficulties (see below) to try to understand the basis of the relative lack of progress. Indeed, this is the strategy that led to the de- velopment of CBT-E and its broad form in particular (Cooper & Fairburn, 2011).
THE TREATMENT PROTOCOL
Stage 1: Starting Well
This is the initial intensive stage of treatment. There are a number of interrelated goals, all of which apply, regard- less of the exact nature of the patient’s eating problem.
The Initial Preparatory Session
The initial session is typically up to 2 hours long and has four major goals.
ENGAGING THE PATIENT IN TREATMENT AND THE PROSPECT OF CHANGE
A particular challenge in working with patients with eating disorders is engaging them in treatment. Many come to treatment with misgivings and varying degrees of reluctance. It is essential that the therapist under- stand this and be sensitive at all times to the patient’s likely ambivalence.
The initial session is especially important in this regard. The patient is evaluating the therapist just as much as the therapist is evaluating the patient. Some clinicians advocate an initial phase of “motivational en- hancement.” We agree that engagement in treatment, and more especially, in change, is crucial, but con- tend that competently administered CBT-E enhances motivation for change and overlaps significantly with the strategies of motivational interviewing (Wilson & Schlam, 2004). We do not view special non-CBT pro- cedures as being required.
Integral to engaging patients is explaining what treatment will involve. With this in mind, it is impor- tant that patients be fully informed about the treatment on which they are embarking. Various topics need to be covered:
1. The nature and style of the treatment. Clearly, pa- tients need to be told the name, nature, and style of the treatment.
2. Treatment practicalities. They should also be told the number, duration, and frequency of the treat- ment sessions.
3. In-session weighing. Patients need to be forewarned about the in-session weighing that is an element of treatment from Sessions 1 or 2 onward. The rationale needs to be explained (see “Establish- ing Collaborative Weighing”). We are often asked whether patients ever refuse to be weighed even after this rationale is given and once an oppor- tunity to discuss this further has been provided. The occasional patient is very reluctant, but in the context of an “engaging” initial session and the ra- tionale being well explained, we find that refusal is not a problem. Our experience is that if one ac- cedes to the patient’s fear of in-session weighing, it is difficult to introduce the procedure later.
4. Instillation of “ownership,” enthusiasm, and hope. The notion that it is the patient’s treatment, not the therapist’s, also needs to be stated. Through- out treatment, patients should feel clear about what is happening and why. While many patients are keen to overcome their eating problem and eager for treatment to start, it is important to maximize enthusiasm and hope. Part of this in- volves conveying that one is knowledgeable about eating disorders in general and the patient’s type of eating problem in particular.
Not infrequently, we come across patients who have been told that they will never overcome their eating disorder. Rarely have we felt that such a statement was warranted. Saying something like this sets up a self- fulfilling prophecy, because it undermines any hope of recovery that the patient might have had. Research has not generated reliable predictors of treatment outcome, and our experience over the years has taught us not to trust our clinical judgment in this regard. We are con- tinually surprised (usually favorably) at our patients’ response to treatment.
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ASSESSING THE NATURE AND SEVERITY OF THE PSYCHOPATHOLOGY PRESENT
Depending on the context within which one works, the person who conducts the initial evaluation interview(s) may or may not be the person who subsequently treats the patient. In our context, the therapist is often seeing the patient for the first time. This means that a second assessment of the eating disorder needs to take place, so that the therapist is fully in the picture. Inevitably, this assessment overlaps to an extent with the initial one. This cannot be avoided.
This particular assessment is treatment-oriented rather than diagnostic, so it differs somewhat from the one conducted when the patient was first seen. While a broad range of topics is covered, the main focus should be on the patient’s current state.
JOINTLY CREATING THE FORMULATION
The next step is the creation of the formulation, that is, a personalized visual representation (i.e., a diagram) of the processes that appear to be maintaining the pa- tient’s eating problem. This is done in the initial ses- sion, unless the patient is significantly underweight (see below) or the eating disorder is unusual and difficult to understand, in which case it is best delayed until the next session, so that the therapist has ample time to think over its likely form.
The creation of the formulation has a number of purposes: It helps to engage the patient in treatment; it involves “decentering,” which is central to helping patients change; it conveys the notion that eating prob- lems are understandable and maintained by a variety of interacting self-perpetuating mechanisms; and by highlighting the maintaining mechanisms, it provides a guide to what needs to be targeted in treatment.
A composite transdiagnostic formulation (see Figure 18.3) should be used by the therapist as a template from which the personalized formulation can be derived, one that matches the particular clinical features pres- ent. The more familiar the therapist becomes with the template formulation, the easier it is to create an indi- vidualized one.
The formulation should focus on the main mecha- nisms that appear likely to be maintaining the patient’s eating problem. It does not need to be comprehensive (as this risks the formulation being overdetailed and confusing), and it is not concerned with the origins of the problem.
The formulation, usually referred to as the “diagram” or “picture,” should be drawn out, step by step, in an unhurried manner, with the therapist taking the lead but with the patient’s active involvement. It is best to start with something that the patient wants to change (e.g., binge eating) or something that is clearly agreed to be a problem (e.g., very low weight). Whenever possible and appropriate, the patient’s own terms should be used. Since the formulation is based on information only just obtained, the therapist should make clear that it is provi- sional and will be modified as needed during treatment. It is important that patients accept the formulation as a credible explanation of their eating problem.
Once the formulation has been created, the thera- pist should discuss its implications for treatment. The points to be made are that to overcome the eating disor- der, the patient will need to address not only the things that the patient would like to change (e.g., loss of con- trol over eating) but also the mechanisms responsible for maintaining them (the “vicious circles”). Thus, for example, with patients who binge-eat, treatment com- monly needs to focus on more than simply stopping binge eating; instead, it may also need to address pa- tients’ various forms of dieting, their ability to deal with adverse events and moods without binge eating, and their concerns about shape and weight. Not addressing the range of maintaining processes markedly increases the likelihood of relapse.
ESTABLISHING REAL-TIME SELF-MONITORING
The final task in the initial session is to establish re- al-time self-monitoring. This is the ongoing, “in-the- moment” recording of relevant behavior, thoughts, feel- ings, and events. It needs to be initiated from the outset of treatment and fine-tuned in Session 1. It continues throughout treatment and is central to it. It has two main purposes: First, it helps patients identify precisely what is happening on a day-to-day basis; second, by gaining such awareness of their thoughts, feelings, and behavior at the time it happens, patients learn that they have choices, and that many things they thought were automatic and beyond their control can be changed.
The monitoring record that we employ is simple for patients to complete and to use. Exactly what is re- corded evolves during treatment. At the beginning, the emphasis is largely on the patient’s eating habits. When describing how to monitor eating habits, it is our prac- tice to go over an example (created for this purpose) that roughly matches in form the eating habits of the
Eating Disorders 719
patient in question. Table 18.1 shows our instructions for monitoring, and Figure 18.5 shows a completed monitoring record.
Fundamental to establishing accurate real-time re- cording is going over the patient’s records in detail, especially in Session 1, when the patient brings them back for the first time. Reviewing the records should be a joint process, with the patient taking the therapist through each day’s record in turn. There are two as-
pects to the review in Session 1: assessing the quality of monitoring and assessing the information gained about the patient’s eating habits. In subsequent sessions, the focus is largely on what has been recorded, although the therapist should intermittently ask the patient about the process of recording and the accuracy of the records. In these subsequent sessions the review of the records generally takes no longer than 10 minutes. Therapists need to remember not to address identified problems
TABLE 18.1. Instructions for Self‑Monitoring
During treatment, it is important that you record everything that you eat or drink, and what is going on at the time. We call this “self-monitoring.” Its purpose is twofold: First, it provides a detailed picture of how you eat, thereby bringing to your attention and that of your therapist the exact nature of your eating problem; and second, by making you more aware of what you are doing at the very time that you are doing it, self-monitoring helps you change behavior that may previously have seemed automatic and beyond your control. Accurate “real-time” monitoring is central to treatment. It will help you change.
At first, writing down everything that you eat may be irritating and inconvenient, but soon it will become second nature and of obvious value. We have yet to encounter anyone whose lifestyle made it truly impossible to monitor. Regard it as a challenge.
Look at the sample monitoring record to see how to monitor. A new record (or records) should be started each day.
• The first column is for noting the time when you eat or drink anything, and the second is for recording the nature of the food and drink consumed. Calories should not be recorded: Instead, you should write down a simple (nontechnical) description of what you ate or drank. Each item should be written down as soon as possible after it is consumed. Recalling what you ate or drank some hours afterwards will not work, since it will not help you change your behavior at the time. Obviously, if you are to record in this way, you need to carry your monitoring sheets with you. It does not matter if your records become messy or if the writing or spelling is not good. The important thing is that you record everything you eat or drink, as soon as possible afterwards.
• Episodes of eating that you view as meals should be identified with brackets. Snacks and other episodes of eating should not be bracketed.
• The third column should specify where the food or drink was consumed. If this was in your home, the room should be specified.
• Asterisks should be placed in the fourth column, adjacent to any episodes of eating or drinking that you felt (at the time) were excessive. This is your judgment, regardless of what anyone else might think. It is essential to record all the food that you eat during “binges.”
• The fifth column is for recording when you vomit (write “V”) or take laxatives (write “L” and the number taken) or diuretics (water tablets; write “D” and the number taken).
• The last column is used in various ways during treatment. For the moment it should be used as a diary to record events and feelings that have influenced your eating: For example, if an argument precipitated a binge or led you not to eat, you should write that down. Try to write a brief comment every time you eat, recording your thoughts and feelings about what you ate. You may want to record other important events or circumstances in this column, even if they had no effect on your eating. The last column should also be used to record your weight (and your thoughts about it) each time you weigh yourself.
Every treatment session will include a detailed review of your latest monitoring sheets. You must therefore remember to bring them with you!
Note. From Fairburn (2008, p. 61). Copyright © 2008 The Guilford Press. Reprinted by permission. This table may be downloaded from www.credo-oxford.com.
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while doing this, but to acknowledge the problems and put them on the session agenda.
The Main Body of Stage 1
Following the initial preparatory session, there are eight twice-weekly appointments. We find that twice-weekly appointments are helpful in building therapeutic mo- mentum. Stage 1 has four distinct elements.
ESTABLISHING COLLABORATIVE WEIGHING
The collaborative weighing intervention has a num- ber of purposes. First, as patients’ eating habits will be
changing in treatment, they are likely to be anxious about any resulting change in their weight. In-session weighing provides good, week-by-week data on their weight. Second, regular in-session weighing provides an opportunity for the therapist to help patients inter- pret the number on the scale, which they otherwise are prone to misinterpret. Third, collaborative weighing addresses one form of body checking, namely, weight checking. Many patients with eating disorders weigh themselves at frequent intervals, sometimes many times a day. As a result, they become concerned with day-to- day weight fluctuations that would otherwise pass un- noticed. Others actively avoid knowing their weight but remain highly concerned about it. Often, these patients
FIGURE 18.5. A completed self-monitoring record. V, vomiting. A blank monitoring record may be downloaded from www.credo-oxford.com.
Day ......Thursday........... Date .....March 21...........
Time Food and drink consumed Place * p Context and comments
]ssorgyllaer—sdnuop811[nehctiKretawssalG03.7 Thirsty after yesterday
8:10 Whole cinnamon raisin bagel Light cream cheese Black coffee
Cafe * Should have only had half the bagel. Must not binge today.
10:35 Half banana Black coffee
Work—at desk Better—on track
11:45 Smoked turkey on wheat bread Light mayo Diet coke
hcnullausUefaC
6:40 to 7:30
Piece of apple pie Kitchen * Help—I can’t stop eating. I’m completely out of control. I hate myself.
*maercecinollag2/1 *rettubtunaephtiwtsaotfosecils4
VekocteiD *legabnisiaR *rettubtunaephtiwtsaotfosecils2
Diet coke *rajmorfrettubtunaeP *legabnisiaR *rabsrekcinS
odIodyhW.gnitsugsidmaIVegral—ekocteiD this? I started as soon as I got in. I’ve ruined another day.
9:30 Rice cake with fat-free cheese Diet coke
Kitchen Really lonely. Feel fat and unattractive. Feel like giving up.
Eating Disorders 721
weighed themselves frequently in the past but switched to avoidance when they found frequent weight checking too aversive. Avoidance of weighing is as problematic as frequent weighing, since it results in patients having no data to confirm or disconfirm their fears about weight gain.
Patients need to learn how to assess and interpret their weight. They should be informed that body weight fluctuates throughout the day and from day-to- day according to their state of hydration, the state of their bowels and bladder, their point in the menstrual cycle, and other factors, too. (All this information may be found in the second edition of Overcoming Binge Eating [Fairburn, 2013]; see the next section.) Frequent weighing results in preoccupation with inconsequential weight fluctuations that tend to be misinterpreted. This leads many patients to restrict their eating, whatever the reading on the scales. This important maintaining pro- cess is disrupted by the collaborative weighing interven- tion.
Collaborative weighing involves the therapist and patient together checking the patient’s weight at the outset of the session. This is done once a week (for un- derweight patients, see below). The latest data point is then plotted on an individualized weight graph that is jointly interpreted, with particular emphasis on trends over a period of at least 4 weeks. A crucial element of the intervention is that patients do not weigh them- selves outside these times.
Patients are also educated about BMI. They are told their BMI and its significance from a health point of view. They are advised against having an exact desired weight, since this does not allow for natural, day-to- day fluctuations. Instead, they are advised to accept a weight range of approximately 6 pounds (3 kg) in mag- nitude.
Almost all patients are anxious about the effects of treatment on their weight. Patients with BN, BED, and the other specified eating disorders (who are not un- derweight) generally do not experience much weight change in treatment. Patients should be told that the aim of treatment is to give them control over their eat- ing, and thus, they will have as much control over their weight as possible. It is best that patients postpone de- ciding on a specific goal weight range until near the end of treatment, when their eating habits should have stabilized and they should be less sensitive about their weight and shape. Later in treatment, patients are ad- vised against having a goal weight (range) that neces- sitates anything more than slight dietary restraint, since
dietary restraint will maintain preoccupation with food and eating, and increase their risk of binge eating.
EDUCATING PATIENTS ABOUT EATING PROBLEMS
To ensure that patients have a reliable source of infor- mation, we recommend that they read one of the au- thoritative books on eating disorders. We use Overcom- ing Binge Eating (Fairburn, 2013), which provides the information needed and has a CBT-E orientation that is compatible with the treatment. It should be noted that, despite its title, Overcoming Binge Eating is relevant to all patients with eating disorders, because it discusses and addresses all eating disorder psychopathology and not just binge eating.
It is our practice to provide patients with a copy of the book; this way, we can ensure that they have it at exactly the right point in treatment (generally, Week 2). We ask patients to annotate the book in the margins to facilitate subsequent discussion in the session. This “guided reading” allows patients to be educated in an efficient, thorough, and personalized way.
ESTABLISHING “REGULAR EATING”
Regular eating is fundamental to successful treatment, whatever the form of the eating disorder. It reliably re- sults in a rapid decrease in the frequency of binge eating (if present), and it addresses an important type of diet- ing, “delayed eating,” that is, putting off eating during the day. For patients who are underweight, it introduces regular meals and snacks that can be subsequently in- creased in size (see below).
Regular eating is introduced around Session 3. It is the first time that patients are asked to change the way they eat. There are two aspects to the intervention: First, patients should eat at regular intervals through- out the day (usually three planned meals each day, plus two planned snacks); second, patients’ eating should be confined to these meals and snacks. A number of points need to be stressed:
1. Patients should be encouraged to choose what they eat in their planned meals and snacks. The only condition is that the meals and snacks must not be followed by vomiting, laxative misuse, or any other compensatory behavior.
2. Patients should not be put under pressure to change what, or how much, they eat at this point in treatment. Doing so tends to be an obstacle in
722 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
their being able to adopt this pattern of regular eating.
3. If patients seek advice on what to eat, they should be told that the priority is their pattern of eating and not what they eat. Nevertheless, if patients want guidance, they should be told that it would be ideal if they adopted a varied diet with the minimum number of avoided foods.
4. While the new eating pattern should be adhered to whatever the patients’ circumstances or appe- tite, it should be adjusted to suit patients’ day-to- day commitments.
5. Patients should plan ahead. They should always know when they are going to have their next meal or snack, and there should rarely be more than a 4-hour interval between the meals and snacks. If the day is going to be unpredictable, they should plan ahead as far as possible and identify a time when they can take stock and, if necessary, replan the rest of the day.
6. Patients whose eating habits are chaotic or highly restrictive may need to introduce this pattern in stages. Patients should be told that their sensa- tions of appetite, hunger, and fullness are all likely to be disturbed at present and for the time being should not be used to determine what they eat. Instead, they should adhere to the agreed pattern of eating.
Two rather different strategies may help patients re- sist eating between the planned meals and snacks. The first is to help them identify activities that are incompat- ible with eating or that make it less likely. They should try to predict when difficulties are likely to arise and intervene early by arranging activities that are likely to help them adhere to the regular eating pattern. Advice on how to do this is contained in Overcoming Binge Eat- ing (Fairburn, 2013). The other strategy is very differ- ent. It involves asking patients to focus on the urge to eat, recognize that it is a temporary phenomenon, and note that they do not have to give in to it. In this way, patients can learn to decenter from the urge and simply observe it rather than try to eliminate it. As with feel- ings of fullness, they will find that the urge dissipates over time. This latter strategy is a difficult one for most patients, especially in the early stages of treatment. If it is to be used at all, it is best left until later on in treat- ment, when urges to eat between meals and snacks are intermittent and less overwhelming.
INVOLVING SIGNIFICANT OTHERS
CBT-E was developed as an individual treatment for adults; hence, it does not actively involve others. De- spite this, it is our practice to see “significant others” if this is likely to facilitate treatment and the patient is willing for this to happen. We do this with the aim of creating the optimum environment for the patient to change. There are two specific indications for involving others: (1) if others can be of help to the patient in mak- ing changes, and (2) if others are making it difficult for patients to change, for example, by commenting ad- versely on their appearance or eating.
Typically, the sessions with others last about 45 min- utes and take place immediately after a routine session. We hold up to three such sessions (with underweight patients, there may be more such sessions, as we dis- cuss below). Topics other than the eating disorder are not usually addressed. With adolescent patients, there is far greater involvement of others (Cooper & Stewart, 2008; Dalle Grave & Calugi, 2020).
Case Study: Progress through Stage 1
Anna was initially very quiet during treatment sessions and appeared to simply agree to everything the thera- pist suggested. The therapist actively encouraged her to ask questions and express any doubts she had in order to engage her collaboratively in treatment. The formula- tion was used to show her what was keeping her eating disorder going and to outline all the areas to address in treatment. The patient responded positively to the “diagram” as she felt it “explained” her eating disorder, but she was surprised and somewhat skeptical that her attempts to diet during the day were leading to binge eating at night. She was able to complete real-time monitoring records and responded well to the educa- tional material.
Two difficulties were encountered at this stage: (1) Anna was very reluctant to be weighed, arguing that she would only become more preoccupied with her weight, and (2) she did not think she would be able to eat regular meals and snacks, because she had never eaten this way before and it would certainly lead to weight gain. Once the therapist had explained the ra- tionale for weekly weighing, Anna agreed to be weighed but was nevertheless very anxious and upset when she was informed of the “number on the scales.” However, she agreed to persist with weighing and soon discovered
Eating Disorders 723
that she was much less anxious about her weight and that her preoccupation had not increased. With regard to regular eating, the therapist explained, with refer- ence to the formulation, that adopting this pattern of eating would help to protect her from binge eating and hence to begin to overcome her eating problem. Anna’s reluctance to eat meals and snacks for fear of weight gain was tackled by reassuring her that this rarely oc- curs, since the change is concerned with the timing of eating rather than the amount or types of food eaten. Also, it was pointed out that regular eating results in a decrease in the frequency of binge eating and thereby a significant reduction in overall energy intake (since even when she vomited, she was absorbing a significant amount of energy from each binge).
Stage 2: Taking Stock
Stage 2, a transitional stage in treatment, has three aims:
1. To conduct a joint review of progress. 2. To revise the formulation, if necessary. 3. To design Stage 3.
At the same time, the therapist continues to work with the patient to implement the procedures intro- duced in Stage 1. The sessions are now held once weekly.
The reason for conducting this formal review of progress is that there is strong evidence across all eating disorders that the degree of change during the first few weeks of treatment is a potent predictor of outcome (Li- nardon, Wade, et al., 2017). Thus, if progress is limited, this needs to be recognized early on, and its explanation sought, so that treatment can be adjusted as needed.
Conducting a Joint Review of Progress
The review of progress is best done systematically, with the patient once again completing the EDE-Q, the CIA, and the measure of general psychiatric features. In this way, patient and therapist can both review the extent of change. Reviewing the patient’s monitoring records can also be helpful. In addition, patient and therapist should consider the degree to which the pa- tient has been able to carry out or comply with the vari- ous elements of treatment.
Generally, patients’ views on their progress are undu- ly negative. An important task for the therapist is there-
fore to help the patient arrive at a balanced appraisal of what has changed and what has not. Typically, there will have been a decrease in the frequency of any binge eating and compensatory purging, and an improvement in the pattern of eating, whereas concerns about shape will not have changed (to a large extent because they have not been addressed).
One important, and sometimes overlooked, reason for progress not being as good as might be expected is the presence of a clinical depression. Ideally, such de- pressions should be detected and treated before treat- ment, but inevitably some are missed and others devel- op afresh. If there appears to be a clinical depression, it is our practice to treat it with antidepressant medication (Fairburn, Cooper, & Waller, 2008c, 2008d) and con- sider suspending CBT until the patient has responded.
Revising the Formulation
It is important to review the formulation in light of what has been learned during Stage 1. Often, no change is indicated, but sometimes problems and processes are detected that were not obvious when the formulation was originally created. For example, it may emerge that overexercising is a far greater problem than had been thought. If so, the formulation may need to be re- vised. Also, if the patient is to receive the “broad” form of CBT-E, it is at this point that the contribution of clinical perfectionism, core low self-esteem, and inter- personal difficulties is considered (see Fairburn et al., 2008a).
Designing Stage 3
Last, Stage 2 is the time when Stage 3 should be de- signed. At this stage, the treatment becomes highly individualized. The therapist should decide which ele- ments of Stage 3 will be of most relevance to the patient and in what order they should be implemented (see below).
Case Study: Progress through Stage 2
A review of progress conducted in Stage 2 with Anna revealed that she was making good use of the treat- ment procedures and carrying out agreed “next steps” between sessions. She was keeping records as agreed, eating regular meals and snacks most of the time, and she was no longer extremely anxious about weighing,
724 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
nor had she become more preoccupied with her weight. There was a marked reduction in the frequency of her binge eating and vomiting, although she still experi- enced episodes of binge eating and vomiting once or twice a week. Problems that still needed addressing in Stage 3 included her dieting, stress-related binge eating, and her overevaluation of the importance of weight and shape. It was decided that there was no need for the broad form of CBT-E.
Stage 3: Addressing the Key Maintaining Mechanisms
This is the main part of treatment. The focus is on ad- dressing the key mechanisms that are maintaining the patient’s eating problem. These may be categorized under six headings:
1. Overevaluation of shape and weight 2. Overevaluation of control over eating 3. Dietary restraint 4. Event- and mood-related changes in eating 5. Dietary restriction 6. Being underweight
The relative contributions of these mechanisms vary from individual to individual. Relatively fewer mecha- nisms tend to operate in those with binge-eating disor- der, whereas most operate in cases of anorexia nervosa in which there is binge eating and purging. The first four are considered here. Dietary restriction and being underweight are addressed separately, when we discuss the adaptations required for those who are underweight. The order in which these mechanisms are addressed de- pends on their relative importance in maintaining the patient’s psychopathology and the length of time it takes to address them. Generally, it is best to start by address- ing the concerns about shape and weight, because this is the most complex mechanism, and it takes the longest.
At the same time, the therapist needs to continue implementing the procedures introduced in Stage 1. If the patient is receiving the broad form of CBT-E, one or more of the additional treatment modules will also be employed (Fairburn et al., 2008a).
Addressing the Overevaluation of Shape and Weight
At the heart of most eating disorders is the distinctive “core psychopathology,” the overevaluation of shape and weight, that is, the judging of self-worth largely,
or even exclusively, in terms of shape and weight, and the ability to control them. As described earlier, most of the other features of these disorders are secondary to this psychopathology and its consequences. This psy- chopathology occupies a central place in most patients’ formulation and is a major target of treatment. Clini- cal experience and research evidence suggest that unless this psychopathology is successfully addressed, patients are at substantial risk of relapse. There are five aspects to this process:
1. Identifying the overevaluation and its conse- quences
2. Developing marginalized domains of self-evalua- tion
3. Addressing body checking 4. Addressing body avoidance 5. Addressing “feeling fat”
Other than the initial identification of the overevalu- ation and its consequences, these topics are not neces- sarily addressed in the order listed above. In addition, toward the end of Stage 3, it is important to develop patients’ skills at dealing with setbacks.
IDENTIFYING THE OVEREVALUATION AND ITS CONSEQUENCES
The starting point is educating patients about the no- tion of self-evaluation and helping them to identify their schemes for self-evaluation. The implications of such schemes are discussed, and plans for addressing the expressions of the overevaluation are devised. Be- cause therapists are often unsure how to broach the subject of self-evaluation, the complete treatment guide (Fairburn, 2008) provides a detailed dialogue demon- strating how to explain this to patients.
Briefly the therapist starts by explaining that most people tend to judge themselves on the basis of meet- ing personal standards in the areas of life they value. Patients are then encouraged to generate a list of areas in their lives that make an important contribution to their self-evaluation. Almost invariably, this will in- clude appearance and perhaps also controlling eating. The therapist explores the relative importance of these domains of self-evaluation; the clue to their relative im- portance is the magnitude (in terms of intensity and duration) of patients’ responses to things going badly in the area. The various areas of life that have been listed can then be ranked and represented by means of a pie
Eating Disorders 725
chart, which the therapist and patient draw together. The pie chart of someone without an eating disorder is shown in Figure 18.6, and this may be contrasted with one that is typical of someone with an eating problem (Figure 18.7), in which there is a large “slice” represent- ing the overevaluation of shape and weight.
It is useful for patients to review their pie chart on several occasions before their next session, so that it can be discussed further and adjusted as needed. Generally, any revision takes the form of expanding the size of the slice representing the importance of shape and weight.
Patients are asked to consider the implications of their scheme for self-evaluation (as represented by the pie chart) and to reflect on whether there might be any problems inherent in such a scheme. Discussion gener- ally leads to the identification of three main problems:
1. Having a pie chart with a dominant slice is “risky.” A dominant slice makes people particu- larly vulnerable should anything threaten their ability to meet their personal standards in the area concerned.
FIGURE 18.6. The pie chart of a young woman without an eating problem. From Fairburn (2008, p. 99). Copyright © 2008 The Guilford Press. Reprinted by permission.
FIGURE 18.7. The pie chart of a young woman with an eating problem. From Fairburn (2008, p. 98). Copyright © 2008 The Guilford Press. Reprinted by permission.
Family
Work
Shape, weight and eating
Other
Family
Work
Shape, weight, and eating
Other
Friends
Sport
Music
726 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
2. Judging oneself largely on the basis of appear- ance is particularly problematic, because this as- pect of life is only controllable to a limited extent. It makes people prone to feeling that they have failed or are a “failure.”
3. Placing great importance on shape and weight drives people to pursue unhelpful behavior such as dieting, purging, and body checking, and these behaviors maintain eating problems.
Such a discussion naturally leads to the final step in the examination of self-evaluation, namely, the cre- ation of a formulation that includes the consequences of the overevaluation (the “extended formulation”). A discussion of what the patient experiences and does as a result of the importance placed on shape and appear- ance leads to a diagram resembling that in Figure 18.8. The therapist generally needs to add the upward feed- back arrows and explain that the consequences of the overevaluation also serve to maintain the overevalua- tion.
The next step involves the therapist and patient de- vising a plan to address the concerns about shape and weight. There are two overarching strategies: (1) to de- velop new domains for self-evaluation and (2) to reduce the importance attached to shape and weight.
Both are important, and they complement one an- other.
DEVELOPING MARGINALIZED DOMAINS FOR SELF-EVALUATION
Tackling expressions of the overevaluation of shape and weight gradually reduces the extent of the overevalu- ation: The shape and weight-related “slice” of the pie chart begins to shrink. At the same time, it is impor- tant to increase the number and importance of other domains for self-evaluation to diminish the relative im- portance of shape and weight. To achieve this, patients need help to begin to get actively involved with other aspects of life. The six steps to this process should con- tinue to be on the agenda throughout the rest of the treatment:
1. Explaining the rationale for developing new do- mains for self-evaluation.
2. Helping the patient identify new activities that might be engaging.
3. Agreeing on one, or possibly two, activities that the patient can try.
4. Ensuring that the patient actually does try the activity identified, often using a problem-solving approach (described later in the chapter).
5. Reviewing progress each week, with the therapist being encouraging and facilitative.
6. Simultaneously, directly targeting the patient’s overevaluation of shape and weight, usually start-
FIGURE 18.8. The overevaluation of shape and weight: an “extended” formulation. From Fairburn (2008, p. 101). Copy- right © 2008 The Guilford Press. Reprinted by permission. This figure may be downloaded from www.credo-oxford.com.
Overevaluation of shape and weight and their control
Dietary restraint
Shape and weight checking and/or avoidance
Preoccupation with thoughts about shape and weight
Marginalization of other areas of life
Mislabeling adverse states as “feeling fat”
Eating Disorders 727
ing with body checking, which is often of central importance in maintaining the patient’s concerns.
ADDRESSING BODY CHECKING AND AVOIDANCE
The importance of body checking and avoidance has only recently been appreciated. The reason is quite simple: Few clinicians know about it. This is because patients do not disclose the behavior unless asked, and many are not fully aware of it.
The first step involves providing information about body checking, body avoidance, and their consequenc- es, stressing the following two points:
1. We all check our body to some extent, but many people with eating problems repeatedly check their bodies, and often in a way that is unusual. Such checking can become “second nature,” so that patients may not be aware they are doing it. In people with eating problems, this checking can maintain dissatisfaction with appearance.
2. Some people with eating problems avoid seeing their bodies and also dislike having other people seeing them. Usually, these people engaged in body checking in the past but switched over to avoidance, because the repeated checking became intolerable. Body avoidance is problematic, be- cause it allows concerns and fears about shape and appearance to persist in the absence of any accu- rate information. It, too, needs to be tackled.
The therapist and patient first need to identify any checking and avoidance that is present. A specific mon- itoring record may be used for this purpose (see www. cbte.co). Since recording body checking is highly dis- tressing for some patients, it is best to ask patients to do it for only two 24-hour periods, often, one on a working day and the other on a day off work. It may be useful to forewarn patients that it might be distressing, but it will yield information that is helpful in overcoming their eating disorder. It is common for patients to be taken aback by how often they check their shape.
Once various forms of body checking have been identified, they are best divided into two groups, ac- cording to whether they are “normative.”
Unusual Forms of Body Checking. Unusual forms of body checking are best stopped altogether. Examples include frequent measuring and pinching of certain body parts. Patients can usually do this if the rationale
is well explained and they are provided with support. There are two points to emphasize:
1. Body checking usually involves focusing on as- pects of one’s appearance that one dislikes, and it generally has adverse effects.
2. Stopping unusual forms of checking is generally experienced (after a week or so) as a relief.
Addressing More Normative Forms of Body Check- ing. A different strategy needs to be adopted with more normative forms of body checking. Here, the problem is the frequency of checking, the way that it is done, and patients’ interpretations of what they find. The thera- pist needs to help patients consider the following ques- tions each time that they are about to check themselves:
• What are they trying to find out? • Can checking in this way produce the information
they are seeking? • Might there be adverse effects from such checking? • Is there a better alternative?
Mirror use deserves particular attention, because mirrors have the potential to provide credible but highly misleading information, and as a result, they are likely to play an important role in the maintenance of many patients’ body dissatisfaction. Education about mirrors and mirror use is therefore of importance. One point to stress is that apparent flaws that would nor- mally go unnoticed become more salient when people focus in detail on aspects of their appearance that they dislike. Another is that scrutiny is prone to magnify ap- parent defects. Patients therefore need to question their use of mirrors, as they are the main way that we de- termine how we look. Mirrors are useful for applying makeup, brushing/styling hair, shaving, and so forth. Full-length mirrors are helpful to see whether clothes go well together. But the therapist should ask patients whether there is ever a case for looking at themselves naked in a full-length mirror. If they are already dis- satisfied with their appearance, doing so is likely to risk increasing their dislike of their shape through the mag- nification process mentioned earlier. This is not to say that total avoidance of mirrors is recommended; rather, the advice is (for the time being) to restrict the use of mirrors to the purposes listed earlier.
Another form of body checking that actively main- tains dissatisfaction with shape involves comparing one- self with other people. The nature of these comparisons
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generally results in patients concluding that their bodies are unattractive relative to those of others. As we noted earlier, patients’ appraisals of their bodies often involve scrutiny and selective attention to body parts that are disliked. The scrutiny is liable to result in the magnifi- cation of perceived defects, and the selective attention increases overall dissatisfaction with shape. In contrast patients’ assessment of others is very different. They tend to make superficial and often uncritical judgments about other people. Furthermore, when making these comparisons, they tend to choose a biased reference group, generally people who are thin and attractive.
The steps involved in addressing comparison making are as follows:
1. The therapist helps patients identify when and how they make comparisons.
2. The therapist encourages patients to consider whether the comparisons are inherently biased—in terms of the person chosen and how their shape was evaluated. Two points are worth highlighting:
• Body checking provides patients with a per- spective on their bodies that is difficult, if not impossible, to get when viewing someone else’s body. For example, what they see when looking at themselves in the mirror is quite unlike what they see when looking at someone else.
• Comparing themselves with people portrayed in the traditional media or social media (mod- els, film stars, celebrities, or friends’ and ac- quaintances’ social media profiles) is problem- atic, since they may be an unrepresentative subgroup, and images may well have been care- fully selected or manipulated, or both.
3. Certain homework tasks usefully complement these discussions; for example, patients may be asked to be less selective when choosing targets for comparisons. Instead of selecting thin people, the therapist may ask them to select every third person (of similar age and gender) they walk past in a busy street. They can also experiment with scrutinizing other people’s bodies. One way of doing this is to select someone of about the same age and gender who at first glance seems at- tractive, then to unobtrusively scrutinize their body, focusing exclusively on the parts that the patient is per- sonally most sensitive about. What patients discover is that even attractive people have apparent flaws when scrutinized.
4. Assuming that patients’ comparison making is biased (as it almost invariably is), the therapist should explore the implications of these biases. The goal is that patients become aware that their checking and making comparisons yields misleading information about other peoples’ bodies and their own.
ADDRESSING BODY AVOIDANCE
“Exposure” in its technical and literal sense is the strat- egy here. Therapists need to help patients get used to the sight and feel of their bodies and to learn to make evenhanded comparisons of their own bodies with those of others. They need to get used to seeing their own bodies and letting others see them, too. Dressing and undressing in the dark needs to be phased out, and patients should gradually abandon wearing baggy, shape-disguising clothes. Participation in activities that involve a degree of body exposure can be helpful (e.g., swimming, both seeing their image on social media and allowing others to do so). Depending on the extent of the problem, tackling body avoidance may take many successive sessions. As there is a risk of a patient return- ing to repeated body checking, the therapist needs to help the patient adopt normative and risk-free forms of checking.
ADDRESSING “FEELING FAT”
“Feeling fat” is an experience reported by many women, but the intensity and frequency of this feeling appears to be far greater among people with eating disorders. It is an important target for treatment, since it tends to be equated with being fat, whatever the patient’s ac- tual weight or shape. Hence, feeling fat is not only an expression of overconcern with shape and weight, but it also maintains it.
There has been almost no research on feeling fat, and little has been written about it. What is striking is that it tends to fluctuate markedly from day to day and even within a single day. This is quite unlike many other as- pects of these patients’ core psychopathology, which is relatively stable. It is our impression that in people with eating disorders, feeling fat is a result of the mislabeling of certain emotions and bodily experiences. It is impor- tant to stress that “feeling fat” and having overweight or obesity are quite different, but they can co-occur. Some people with obesity are not troubled by “feeling fat,” de- spite being dissatisfied with their shape or weight, while others experience both “feeling fat” and dissatisfaction.
Eating Disorders 729
Since “feeling fat” contributes to the maintenance of body dissatisfaction, it is essential that this be addressed in all patients who have this experience.
In general, it is best to focus on “feeling fat” once one has begun to make inroads into body checking and avoidance, but this is not invariably the case. In patients in whom “feeling fat” is a particularly prominent fea- ture, it is advisable to address it before tackling body checking and avoidance.
There are five steps in addressing “feeling fat”:
1. The therapist should first explain that “feeling fat” should not be equated with “being fat,” and that “feeling fat” may mask other feelings or sensations oc- curring at the same time.
2. Patients should be asked to record times when they have particularly intense feelings of fatness. This can be done as part of the normal recording process, using the right-hand column of the recording sheet for this purpose. This requires accurate real-time record- ing. When patients record “feeling fat,” they should also think (and record) what else they are feeling at the time.
3. Once patients have mastered this, they should ask themselves two questions each time they “feel fat”:
• “What has happened in the last hour that might have triggered this feeling?”
• “What else am I feeling just now?” 4. It usually emerges that the patient’s experiences
of “feeling fat” are triggered either by the occurrence of certain negative mood states or physical sensations that heighten body awareness. Examples of these two types of stimulus include the following:
• Feeling bored, depressed, lonely, or tired. • Feeling full, bloated, or sweaty; feeling one’s
body wobble or one’s thighs rubbing together; clothing that feels tight.
Over subsequent weeks, patients should continue to do this whenever they have strong feelings of fatness. In addition, they should address any masked problem (e.g., feeling bored) using the problem-solving approach (described later in this chapter). In some patients, prob- lem solving will already have been taught in the context of addressing event-triggered changes in eating. In oth- ers, the approach needs to be introduced at this point. When tackling patients’ response to heightened body awareness, therapists should help them appreciate that
the problem is their negative interpretation of these sen- sations rather than the sensations themselves.
Addressing “feeling fat” typically takes many weeks and will be a recurring item on the session agenda. Gen- erally, the frequency and intensity of “feeling fat” pro- gressively declines, and patients’ “relationship” to the experience changes, such that it is no longer equated with “being fat.” This metacognitive change is impor- tant, since once it happens, “feeling fat” ceases to main- tain body dissatisfaction.
Addressing Dietary Restraint and Food Avoidance
Dieting is one of the most prominent features of pa- tients with eating disorders. A major goal of treatment is to reduce or, if possible, eliminate the strong tendency of these patients to diet. As noted earlier, attempts to restrict eating (“dietary restraint”) may or may not be successful. Thus, it is far from inevitable that they result in true undereating in physiological terms (“dietary re- striction”) and weight loss. In this section, we focus on addressing dietary restraint and dietary rules. Tackling of dietary restriction is addressed in a later section on treatment of those who are underweight.
The dietary restraint of patients with eating dis- orders is both extreme in intensity and rigid in form. These patients set themselves multiple demanding di- etary rules. These may concern when they eat (e.g., not before 6:00 P.M.), how much they should eat (e.g., less than 600 kcal per day) and, most especially, what they should eat, with most patients having many foods that they attempt to avoid (“food avoidance”). Many have all three types of dietary rule. As a result of these rules, patients’ eating is inflexible and restricted in nature. Despite this, dietary restraint is valued, and patients tend to be oblivious to its adverse effects.
When addressing dietary restraint, an important first step is for the therapist to help patients to see that their dieting is indeed a problem. This can be done with ref- erence to their formulation, which in most cases shows that dieting plays a central role in the maintenance of their eating problem. If this is the case, it will need to be addressed to overcome the problem. Second, their dieting may well have many adverse effects on their day-to-day life. These may be uncovered using the CIA (Bohn & Fairburn, 2008); for example, it may preclude eating out; it may result in tension at mealtimes; and it may cause preoccupation with thoughts about food and eating.
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Once it has been agreed that dietary restraint is a problem, therapist and patient need to identify the vari- ous dietary rules present. Many will be evident by this stage in treatment. The principles that underlie address- ing these rules are as follows:
1. Identifying specific rules and their motivation. 2. Exploring the likely consequences of breaking the
rule. The patient may believe that breaking the rule will lead to weight gain or invariably result in binge eating.
3. Devising and implementing a plan to break rules in order to explore the consequences of doing so.
4. Analyzing the implications of planned rule break- ing.
5. Planning further breaking of rules until they cease to have significance.
With patients who binge-eat, it is important to pay particular attention to food avoidance. First, avoided foods should be identified. A good way of doing this is to ask patients to visit a local supermarket and note all foods they would be reluctant to eat because of their possible effect on their shape or weight, or because they fear that they might trigger a binge. The patient and therapist should rank these foods (often a large number) according to the difficulty the patient would experience eating them. Patients should be encouraged to intro- duce these foods progressively into their diet, starting with the easiest and gradually moving on to the most difficult. The amount eaten is not important, although the eventual goal is that the patient should be capable of eating normal quantities without difficulty. The sys- tematic introduction of avoided foods should continue until patients are no longer anxious about eating them. Often, this will take the remainder of treatment and sometime beyond it.
Other dietary rules should be tackled in a similar fashion, with a focus on both the belief that is main- taining the rule and breaking the rule itself. It is es- pecially important to address rules that interfere with social eating.
Addressing Event‑ and Mood‑Related Changes in Eating
In patients with eating disorders, eating habits may change in response to outside events and moods. The following are common:
• Binge eating or vomiting, or both, to cope with negative events or adverse moods. Binge eating has two relevant properties: It is distracting and may take the patient’s mind off aversive thoughts, and it has a direct mood-modulatory effect, in that it dampens strong mood states. The latter property is also true of vomiting and intense exercising.
• Eating less or avoiding eating to gain a sense of personal control when external events feel outside the patient’s control. This is seen most often in un- derweight patients.
• Eating less to influence others; for example, it may be a way of exhibiting feelings of distress or anger, or it may be an act of defiance.
If in Stage 3 events and moods appear to contribute to the maintenance of the eating disorder, their contri- bution needs to be assessed and addressed, with the goal of helping patients deal with events and moods directly and effectively. With most patients, the first step is to identify such changes in eating through real-time re- cording, and in subsequent sessions examine in detail particular examples in an attempt to identify the trig- gers involved. Then, patients should be introduced to a variant of the standard cognitive-behavioral technique of problem solving, termed proactive problem solving. The distinctive feature of this approach is its empha- sis on spotting problems early. It is described in detail in the complete treatment guide, and it is also covered from the patient’s perspective in Overcoming Binge Eat- ing (Fairburn, 2013). The approach, if well taught, is remarkably effective in most cases. One exception is for patients who have difficulty tolerating mood states that involve arousal. These patients (who tend to attract the diagnosis of borderline personality disorder) have what we term mood intolerance. They benefit from pro- active problem solving, but they also need more direct help coping with their moods. To this end we use an approach that overlaps with elements of dialectical be- havior therapy (Linehan, 1993; see Neacsiu, Zerubavel, Nylocks, & Linehan, Chapter 10, this volume) and is described in the treatment guide.
Setbacks and Mindsets
The core psychopathology of eating disorders may be viewed as a mindset, or frame of mind. While normally one’s “mind-in-place” varies with changing circum- stances, in people with eating disorders, it tends to get
Eating Disorders 731
locked in, and patients’ thinking becomes persistently dominated by eating disorder thoughts. It leads patients to filter both internal and external stimuli in a distinc- tive way; it leads to the forms of behavior characteristic of eating disorders; and it results in the mislabeling of various physical and emotional experiences as “feeling fat.”
The cognitive-behavioral strategies used in CBT-E are designed to address both the key features of the eating disorders and, most importantly, the processes that are maintaining them. In patients who are mak- ing good progress, these mechanisms gradually erode during Stage 3, with the result that healthier and situ- ationally more appropriate mindsets start to move into place, albeit temporarily at first. Such shifts in mindset usually become evident toward the end of treatment. Patients often report these shifts with surprise, noting that they suddenly realize that for a period of time they have not had their usual eating disorder thoughts. At first, the eating disorder mindset is prone to come back into place with even minor provocations (e.g., a friend discussing a diet). These “setbacks” can readily esca- late into full-blown relapse unless they are addressed as quickly as possible. It is therefore important to raise the topic of mindsets at this stage in treatment, so that pa- tients can learn to identify their eating disorder mind- set coming into place by being aware of characteristic early changes in their behavior. Once patients can de- tect these early behavior changes, they can learn how to change or “eject” the mindset, thereby preventing the setback from becoming established. Practice in becom- ing aware of the mindset returning and dealing with it effectively is of great value, as this skill—intervening very early at the beginnings of a setback—may account for the low relapse rates following CBT-E. Experienc- ing occasional setbacks later in treatment can be help- ful, because it gives patients an opportunity to utilize the strategies and procedures for controlling mindsets while still in treatment. Full details of how to help pa- tients manipulate their mindset and address setbacks are provided in the treatment guide.
Case Study: Progress through Stage 3
The first issue tackled in Stage 3 was Anna’s overevalu- ation of weight and shape. When she and the therapist completed a pie chart, Anna was distressed to see that controlling eating, weight, and shape, filled three quar- ters of her chart. She was also able to see, after discussion,
that other areas in her life had become marginalized— largely as a result of her shape and weight concerns. As a first step toward “increasing” the domains in her pie chart, Anna agreed to pursue her previous interest in drawing and to investigate and subsequently join an art class. In discussion with the therapist, Anna was able to recognize that her body checking and “feeling fat” were an expression of her shape and weight concerns, and she was able to understand, using the extended formulation, how these expressions were maintaining her concerns. She was much less convinced by the therapist’s sugges- tion that dieting was also playing a role in the mainte- nance of her disorder. Thus, while the patient was able to reduce her body checking (and remove all but one of the six mirrors in her room) and relabel “feeling fat” successfully, she was very reluctant to tackle her dieting. Her dieting involved numerous rules about eating and a long list of avoided foods. Anna did not see dieting as a problem and thought that she would definitely feel better about herself if she were to reduce her weight to the lower, rather than higher, end of the healthy weight range. She also thought that strictly avoiding foods she usually ate during her binge-eating episodes was the best strategy to prevent these episodes occurring. The thera- pist addressed this difficulty in treatment by returning to the formulation and explaining how this form of di- eting maintained her binge eating in the same way her delayed eating had done at the beginning of treatment. In addition, the therapist initiated a discussion about the major adverse effects of such dieting, stressing pre- occupation with food and eating, anxiety about eating generally, and an inflexible eating pattern that often makes eating socially impossible. Anna was eventually able to begin to break some of her dietary rules and to start eating previously avoided foods without the feared consequences of weight gain or more binge eating. With encouragement from the therapist, Anna was also able to reconsider the advantages and disadvantages of losing weight given that her weight was already in the healthy range. By this stage, Anna had almost stopped binge eat- ing, but an analysis of remaining residual binge-eating episodes revealed that they were more likely to happen if she had been drinking alcohol. As a result, she decided to further reduce her alcohol consumption.
Toward the end of this stage in treatment, Anna could see that the eating problem was beginning to re- solve and that she was at times able to distance herself from it and the eating disorder mindset. Minor setbacks during treatment had helped her identify that delaying
732 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
eating, skipping snacks, and going back to certain diet foods were likely early warning signs of the return of her eating disorder mindset.
Stage 4: Ending Well
This is the final stage in treatment. With patients who are receiving 20 sessions of treatment, it comprises three sessions over 5 weeks (i.e., the sessions are 2 weeks apart). It has two broad aims:
1. To ensure that the changes made in treatment are maintained and built upon
2. To minimize the risk of relapse in the future
At the same time, patients discontinue self-monitor- ing and transfer from in-session weighing to weighing themselves at home.
Ensuring That the Changes Made in Treatment Are Maintained
The first step in doing this is to review patients’ progress and identify remaining problems. This can be done in much the same way as in Stage 2, using the EDE-Q and CIA as a guide. On the basis of this review, the therapist and patient jointly devise a specific short-term plan for the patient to follow until the posttreatment review ap- pointment in 5 months’ time. Typically, this includes further work on body checking and food avoidance, as well as encouraging the patient to maintain efforts to develop new interests and activities.
Minimizing the Risk of Relapse in the Future
Relapses are not all-or-nothing phenomena. They occur in degrees and may start as a “slip” or setback that then becomes established. Commonly, the slip comprises the resumption of dietary restraint, often triggered by an adverse, shape-related event (e.g., a critical comment, clothes feeling tighter than usual). In patients who were previously prone to binge-eat, this return of dietary re- straint may lead to an episode of binge eating through the mechanisms described earlier, which in turn will encourage yet greater dietary restraint, thereby increas- ing the risk of further episodes of binge eating. Within days, most aspects of the eating disorder may have re- turned. The patient’s reaction to this sequence of events is crucial in determining what happens. If it is detected
early on, as discussed earlier, it is relatively easy to in- tervene, but if it is not, it becomes progressively more difficult to deal with the setback.
To minimize the risk of relapse in the long term, the therapist needs to do the following:
1. Educate the patient about the risk of relapse, high- lighting common triggers and the likely sequence of events in the patient’s case. Some patients hope that they will never have an eating problem again. This is especially common in those who have ceased to binge-eat, but it is seen in other patients, too. Without casting a nega- tive light on patients’ hopes for the future, therapists need to ensure that patients’ expectations are realistic; otherwise, there is a risk that they will be vulnerable to react negatively to any emerging setback. Patients should learn to view their eating disorder as their Achil- les’ heel: that is, their responses to stress in general and to certain triggers.
2. Stress the importance of detecting problems early, be- fore they become entrenched. Therapist and patient should identify likely early warning signs of an impending re- lapse. For patients who are prone to binge or purge, these forms of behavior often occur early on in the course of any setback and are readily noticeable. Patients whose eating disorder is primarily characterized by dietary re- striction may need help to spot ominous signs.
3. Construct with the patient a plan of action (a writ- ten personalized “ long-term maintenance plan”) for use in the future should problems arise. There are two impor- tant elements: focusing on an emerging eating problem and correcting it, and addressing the trigger of the set- back. In general, the former is achieved by doing what was learned in treatment (doing the right thing), pos- sibly following the guidance in Overcoming Binge Eat- ing (Fairburn, 2013) while the latter is achieved using problem solving.
4. Discuss when the patient should seek further help. It is important that patients seek further help if it is needed. If patients are not able to get back on track within a few weeks using what they learned in treat- ment and their maintenance plan, we suggest that they seek outside help.
Ending or Extending Treatment
It is unusual not to end CBT-E as planned. So long as patients have got to the point where the central main-
Eating Disorders 733
taining mechanisms have been disrupted, treatment can and should finish. Otherwise, patients (and thera- pists) are at risk of ascribing continued improvement to the ongoing therapy rather than natural resolution of the eating disorder. In practice, this means that it is acceptable to end treatment with patients who are still dieting to an extent, perhaps binge eating and vomit- ing occasionally, and those who have residual concerns about shape and weight.
At times, there are grounds for extending treatment. In our view, the main indication for doing this is the presence of eating disorder features that continue to in- terfere significantly with the patient’s functioning and are unlikely to resolve of their own accord. Another reason to extend treatment is to compensate for the del- eterious impact of disruptions to treatment, generally due to the emergence of a clinical depression or the oc- currence of a life crisis.
The occasional patient benefits little from CBT-E. It is our practice to refer such patients for day patient or inpatient treatment rather than to extend outpatient CBT-E.
Case Study: Progress through Stage 4
Anna was able to end treatment on time. By the end of treatment, she was eating regularly and was no longer binge eating and vomiting. Somewhat to her surprise, her weight had remained unchanged during treatment. She identified regular eating, not avoiding certain foods and taking up new activities as the most help- ful aspects of treatment, and planned to work on main- taining these changes until the posttreatment review. To prevent further problems, she identified two early warning signs: dieting (for her, skipping meals or snacks and avoiding certain foods) and increasing her alcohol intake. Although she was still somewhat dissatisfied with her shape, Anna was resolved that trying to diet as she had done before was not helpful. She planned to continue to find other ways of accepting and valuing herself and her body.
The Posttreatment Review Appointment
We routinely hold a posttreatment review appointment about 20 weeks after the completion of treatment. Dur- ing the intervening period, patients do not receive any further therapeutic input. The review session has sev- eral purposes:
1. To reassess the patient’s state and need for further treatment. If residual eating disorder features are significantly interfering with the patient’s func- tioning, then further treatment should be con- sidered. If there has been a setback, a few brief sessions may be needed to get the patient back on track.
2. To review the patient’s implementation of the short-term maintenance plan. The therapist should review the plan with the aim of identifying residual eating disorder features that the patient needs to continue to address.
3. To discuss how any setbacks have been handled. The patient’s ability to detect and address setbacks should be reviewed in detail.
4. To review and amend the long-term maintenance plan if necessary.
Case Study: Progress at the Posttreatment Review Appointment
At the review appointment Anna described several occasions when, under stress, she had experienced a “lapse.” On these occasions, she was able to implement the strategies she had learned in treatment to prevent a “relapse.”
CBT‑E FOR UNDERWEIGHT PATIENTS
The great majority of patients with an eating disorder undereat at some stage, and many may become under- weight for a time. Generally, this does not last, and they regain the lost weight, but a minority maintain strict control over their eating and stay underweight. A pro- portion of these patients meet current diagnostic crite- ria for AN, whereas others are eligible for one or other of the two residual eating disorder diagnoses.
CBT-E for underweight patients does not require major modifications, because the core psychopathology and behavior of these patients is very similar to that of the majority of patients with an eating disorder. How- ever, it does need to be adjusted to accommodate three problems seen in this group, but not necessarily con- fined to it:
1. Limited motivation to change 2. Being underweight 3. Undereating (“dietary restriction”).
734 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
To do this, CBT-E needs to be extended, because it takes time to engender motivation to change and even more time to regain weight. Hence, as mentioned earlier, for those with a BMI between 15.0 and 18.5, treatment generally takes up to 40 weeks, with sessions generally held twice weekly until the patient is consis- tently gaining weight. Once this is happening, sessions are weekly; then, toward the end of treatment, sessions are every 2–3 weeks.
Patients’ health and safety are always of paramount importance, and this is especially true of patients who are underweight, because their physical health is invari- ably compromised. Therapists need to be aware of po- tential physical complications, and those who are not medically qualified should have good access to a phy- sician who can advise on the management of medical problems.
Overview
The four stages of the 20-week version of CBT-E do not neatly map onto the version for underweight pa- tients. Treatment for these patients may be thought of as having three phases (see Figure 18.9 showing these phases and their relation to the four stages of the 20- week treatment):
• Phase I. This lasts up to 8 weeks, and the focus is on engaging patients and helping them arrive at the decision that they need to regain weight.
• Phase II. This is the weight-gain phase. The goal is that patients gain weight at the rate of about 0.5 kg per week. Therefore, the length of this phase is de- termined by the amount of weight to be regained. During this phase, the patient’s eating disorder psychopathology is addressed.
FIGURE 18.9. The four stages of CBT-E shown in relation to the three steps of weight regain. From CREDO (2017). Copyright © 2017 CREDO. Reprinted with permission.
Deciding to regain weight
Regaining weight
Maintaining weight
150
140
130
120
110
100
90
80 0 2 4 6 8 10 12 14 16 18 20 22 24 26 28 30 32 34 36 38 40
Stage 1: Starting Well
Stage 2: Taking Stock
Stage 3: Body Image
Dietary Restraint Events, Moods, and Eating
Stage 3: Setbacks and
Mindsets
Stage 4: Ending Well
Eating Disorders 735
• Phase III. This is the weight-maintenance phase, in which patients practice maintaining their new healthy weight. It lasts about 8 weeks.
Consistent with these phases patients’ weight graphs generally have a distinct three-phase pattern to them, as shown in Figure 18.10.
Phase I
The first two treatment sessions are similar to those of the 20-week treatment, although there are certain modifications to accommodate education about the ef- fects of being underweight and to incorporate this in- formation in the formulation. In practice this involves the following:
• Inquiring carefully in the initial assessment about the features that are likely linked to being under- weight. This inquiry should be embedded within the usual assessment.
• Providing personalized education about the effects of being underweight before jointly creating the for-
mulation. This involves delaying the formulation to the second treatment session rather than creating it in the initial session as in the 20-week version.
• Jointly creating a formulation that highlights the likely contribution of being underweight to the maintenance of the patient’s eating problem (e.g., preoccupation with food and eating, increased need for routines and predictability, indecisive- ness, heightened feelings of fullness, low mood, social withdrawal). A patient-oriented description of these features is provided in the second edition of Overcoming Binge Eating (Fairburn, 2013).
• Discussing the implications of the formulation for treatment. The major point is that many features identified will resolve if patients regain weight, and at the same time patients will discover that their true personalities have been masked by being underweight. Simultaneously, it is emphasized that treatment will involve much more than mere weight regain.
The emphasis then moves on to helping patients decide to change. The goal is that patients make this
FIGURE 18.10. The weight graph of a patient with anorexia nervosa. From Fairburn (2008, p. 180). Copyright © 2008 The Guilford Press. Adapted by permission.
100
110
120
130
140
150
160
170
0 2 4 6 8 10 12 14 16 18 20 22 24 26 28 30 32 34 36 38 40
BMI 20.0 (126 lbs)
BMI 25.0 (157 lbs)
Weeks
Weight (lbs)
BMI 19.0 (120 lbs)
736 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
decision themselves rather than having the decision im- posed on them. The aim is to interest the patient in the benefits of change and the possibility of a “fresh start.” There are five steps in this process:
1. Creating a “Current Pros and Cons of Change” table.
2. Creating a “Future Pros and Cons of Change” table.
3. Creating a “Conclusions” table. An example is shown in Table 18.2.
4. Helping the patient identify and accept the impli- cations of these conclusions.
5. Helping the patient decide to act and “take the plunge.”
At the same time, collaborative weighing and regu- lar eating are also introduced, much as in the 20-week treatment. One difference is that weighing takes place every session, because patients’ low weight is a signifi- cant health problem and a major target of treatment. Another is that the pattern of regular eating should include three meals and three snacks; that is, patients should have six episodes of eating rather than five, as in the 20-week treatment.
If the patient decides to regain weight, then Phase II begins. If, however, the patient never reaches this de- cision despite extensive nondirective exploration of the topic (over at least 8 weeks), then CBT-E has failed and other treatment options should be considered. This ap- plies in about one in five cases.
Phase II
In Phase II, the focus is simultaneously on weight regain and addressing the patient’s eating disorder psychopathology in much the same way as described earlier. Thus, there is an emphasis on modifying the overevaluation of shape and weight, dietary restraint, and event- and mood-related changes in eating.
Weight regain is very difficult for these patients. It is a long and laborious process. It requires that patients maintain an energy surplus each day of about 500 kcal if they are to regain weight at a rate of about 0.5 kg per week.
It is our practice to have a weight goal correspond- ing to a BMI over 19. This figure ensures that the great majority of patients are free from the psychobiological effects of being underweight, while still being slim. It is important not to compromise on this figure. Many
patients want to stop regaining weight when their BMI is in the range of 17–18, possibly because this is when their shape begins to change and some of the worst ef- fects of undereating are ameliorated. This is a mistake, because they are still experiencing many of the adverse effects of being underweight and have not experienced the full advantages of weight regain. It is also an un- stable condition, with many patients with a BMI at this level tending to lose weight again.
Full details of how to help patients regain weight are provided in the complete treatment guide.
TABLE 18.2. Pros and Cons of Change: A Patient’s “Conclusions”
I want to get better and regain weight because . . .
• I will be able to have a full-life not one that is just about eating and weight.
• I will be healthier: my bones and heart will be stronger; I won’t be cold and faint and will be able to sleep properly. I won’t be ill!
• I will be able to have good relationships with other people and hopefully a partner and children who I can be a good role model to.
• I will be able to enjoy my job and be successful at it.
• At the moment the eating problem stops me from being able to do things well. When I am better I won’t need an excuse.
• Regaining weight will mean that I will become slim and healthy. It does not mean that I will become fat.
• Getting better won’t be giving in. Not getting better would be giving in. Getting better is about choosing to give myself a life.
• I want to show how strong I can be by eating as right now not eating is the easy thing.
• Eating enough food to be a healthy weight isn’t greedy. It is being normal.
• Being a healthy weight and eating enough will help to give me true control over my eating. I will be able to make choices about what I eat. At the moment the eating problem has control over me. Becoming well will protect me from out-of-control eating and uncontrolled weight gain.
• Being well will enable me to develop my talents as a person and to discover my true self.
• Getting better will give me choices in life. The eating problem has been holding me back. Change can only be good.
Note. From Fairburn (2008, p. 167). Copyright © 2008 The Guilford Press. Reprinted by permission.
Eating Disorders 737
Phase III
The goal of this phase is to help patients maintain a weight, such that their BMI fluctuates between approx- imately 19 and 20. Patients and therapists have opposite concerns at this point. While patients are afraid that their weight will continue to rise, therapists fear that it will fall. The therapists’ fears are usually the more real- istic ones. The risks and dangers of weight loss should be discussed openly with patients.
This phase of treatment usually runs smoothly, and certainly so in comparison with Phase II. Therapists should encourage patients to live life fully now that they are free from the debilitating effects of being un- derweight. Patients should be helped to flourish, take risks, and enjoy themselves, while not forgetting the importance of maintaining their new healthy weight.
The final few sessions need to cover the same topics as those covered in the 20-week version. Thus, they ad- dress (along the same lines) (1) mindsets and setbacks, (2) ensuring that achieved changes are maintained, and (3) procedures for minimizing the risk of relapse in the future.
CONCLUDING REMARKS
Treatment with CBT-E is guided by a highly individu- alized formulation. This is based on patients’ eating dis- order psychopathology, not their diagnosis. Moreover, this formulation is modified and further personalized as treatment progresses and the patient’s psychopathol- ogy evolves. CBT-E specifies the strategies and proce- dures used to bring about change, but how and when they are applied varies markedly from case to case. As a result, CBT-E is more of a challenge to learn than more prescriptive treatments, but the compensation is that it is more rewarding to implement, not least because of its effectiveness.
Despite its successes, CBT-E does not help everyone. There is an urgent need to identify predictors and mod- erators of treatment response in order to understand for whom, and under what conditions, the treatment is likely to be helpful. There is also a need to improve the treatment further in order to extend the range of patients who might be helped by the approach. A bet- ter understanding of how the treatment works is likely to contribute to this goal. Greater knowledge of the mechanisms of change would provide the basis for fur- ther enhancing the active components of treatment and
omitting redundant ones. It might also suggest ways to simplify treatment, generally, or in particular cases.
Another urgent challenge concerns the dissemina- tion and implementation of CBT-E. Despite empirical support, few patients with eating disorders are receiving it. In part, this is due to individuals not seeking treat- ment or eating problems not being correctly detected in primary care. However, even when treatment is sought and offered, many do not receive empirically supported interventions. The barriers to wider dissemination and implementation include clinician attitudes toward such treatment and the lack of sufficient numbers of suit- ably trained therapists. One way to begin to address this is to use a highly scalable method of training large numbers of geographically dispersed therapists simul- taneously. A Web-based training program for CBT-E has been developed for this purpose. The evaluation of this program has revealed it to be popular and effective (Cooper et al., 2017; Fairburn, Allen, Bailey-Straebler, O’Connor, & Cooper, 2017; O’Connor, Morgan, Bai- ley-Straebler, Fairburn, & Cooper, 2018).5 However, it is still unlikely that there will be sufficient numbers of therapists to meet the need for treatment. Direct- to-sufferer treatments, which are wholly program-led, are urgently needed to increase the reach of CBT-E. To this end, a programme-led digital version of CBT-E is currently under development (www.cbte.co/self-help- programmes/digital-cbte).
ACKNOWLEDGMENTS
We are grateful to the Wellcome Trust for its support over many years for our research on eating disorders, CBT-E, and training. Zafra Cooper was supported by a strategic award (No. 094585). Rebecca Murphy is supported by the NIHR Oxford Biomedical Research Centre. Charandeep Khera provided valuable assistance with preparation of the manu- script.
NOTES
1. BMI is a widely used way of representing weight adjusted for height. It is weight in kilograms divided by height in meters squared [i.e., wt/(ht)2]. The BMI applies to adults of both sexes between ages 18 and 60. The healthy range is 18.5–25.0.
2. If there is a difference in their core psychopathology, it is that some patients with AN are primarily concerned with controlling their eating per se, rather than their shape and
738 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
weight. This is especially true of younger cases of short dura- tion.
3. Originally, the broad version of the treatment addressed a fourth obstacle to change, termed mood intolerance. This has subsequently been incorporated into the focused form of CBT-E.
4. Our research on the 20-week version of CBT-E included pa- tients with a BMI over 17.5, but our clinical experience sug- gests that patients who are somewhat underweight do better with a longer treatment. We therefore recommend a BMI threshold of over 18.5 for the 20-week treatment and that patients with a BMI of 18.5 or lower should be offered the longer treatment.
5. The website www.cbte.co provides up-to-date information on the empirical status of CBT-E. All the materials needed to implement CBT-E may be downloaded free of charge from this website. Details about training opportunities and a digital self-help program currently under development are also available on the website.
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de Jong, M., Schoorl, M., & Hoek, H. W. (2018). Enhanced cognitive behavioural therapy for patients with eating dis- orders: A systematic review. Current Opinion in Psychiatry, 31(6), 436–444.
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Fairburn, C. G. (2008). Cognitive behavior therapy and eating disorders. New York: Guilford Press.
Fairburn, C. G. (2013). Overcoming binge eating (2nd ed.). New York: Guilford Press.
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Fairburn, C. G., Bailey-Straebler, S., Basden, S., Doll, H. A., Jones, R., Murphy, R., et al. (2015). A transdiagnos- tic comparison of enhanced cognitive behaviour therapy (CBT-E) and interpersonal psychotherapy in the treatment of eating disorders. Behaviour Research and Therapy, 70, 64–71.
Fairburn, C. G., & Beglin, S. J. (2008). Eating Disorder Examination Questionnaire (EDE-Q 6.0). In C. G. Fairburn, Cognitive behavior therapy and eating disorders (pp. 309–313). New York: Guilford Press.
Fairburn, C. G., Cooper, Z., Bohn, K., O’Connor, M. E., Doll, H. A., & Palmer, R. L. (2007). The severity and status of eating disorder NOS: Implications for DSM-V. Behaviour Research and Therapy, 45(8), 1705–1715.
Fairburn, C. G., Cooper, Z., Doll, H. A., O’Connor, M. E., Palmer, R. L., & Dalle Grave, R. (2013). Enhanced cogni- tive behaviour therapy for adults with anorexia nervosa: A UK–Italy study. Behaviour Research and Therapy, 51(1), R2–R8.
Fairburn, C. G., Cooper, Z., & Shafran, R. (2003). Cognitive behaviour therapy for eating disorders: A “transdiagnos- tic” theory and treatment. Behaviour Research and Therapy, 41(5), 509–528.
Fairburn, C. G., Cooper, Z., Shafran, R., Bohn, K., & Hawk- er, D. M. (2008a). Clinical perfectionism, core low self-es- teem and interpersonal problems. In C. G. Fairburn, Cog-
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Grilo, C. M., Crosby, R. D., Masheb, R. M., White, M. A., Peterson, C. B., Wonderlich, S. A., et al. (2009). Overvalu- ation of shape and weight in binge eating disorder, bulimia nervosa, and sub-threshold bulimia nervosa. Behaviour Re- search and Therapy, 47(8), 692–696.
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The second edition of this book presented, for the first time, a substantially different approach to couple therapy—different both in conceptualization and in treatment strategies. It was noted that these changes in technique and conceptualization were profound enough to warrant a new name for the approach: integrative behavioral couple therapy (IBCT). As described in this sixth edition, IBCT has matured into a sophisticated and intuitively appealing set of strategies. These strategies are very nicely illustrated in this chapter in the context of the comprehensive treatment of one couple in substantial distress. Because these strategies require considerable clinical skill and talent, beginning therapists in particular should learn much from the case descriptions presented in this very readable and engaging chapter. —D. H. B.
Unlike other chapters in this volume, the term couple distress does not refer to a specific clinical or person-
ality disorder. In both the International Classification of Diseases, 10th Revision, Clinical Modification (ICD- 10-CM; American Medical Association, 2017) and the 11th edition of the International Classification of Diseases (ICD-11; World Health Organization, 2018), couple distress is not considered a mental or behavior- al disorder but is relegated to the category of “factors influencing health status and contact with health ser- vices” and assigned a lesser code for “problems in rela- tionship with spouse or partner” (Z63.0; ICD-10-CM) or for “relationship distress with spouse or partner” (QE51.0; ICD-11). Couple distress is handled similarly in DSM-5 (American Psychiatric Association, 2013). Yet the evidence suggests that couple distress creates as much psychological and physical pain as many, if not most, of the ICD and DSM disorders (e.g., Beach et al., 2006). Furthermore, couple distress can initiate, ex- acerbate, and complicate underlying disorders such as
depression and anxiety, or trigger a relapse of symptoms (Whisman, 2007; Whisman & Bruce, 1999; Whisman & Uebelacker, 2009). Additionally, couple distress can have a significant impact on children, and can trigger or exacerbate externalizing and internalizing disorders (Shelton & Harold, 2008). Indeed, there was a push to give relationship processes such as couple distress greater attention in DSM-5, and perhaps include some relationship problems as disorders; however, such ef- forts seem to have faltered (American Psychiatric As- sociation, 2013; Beach et al., 2006). Whatever the mer- its and outcome of these efforts, there is no doubt that couple distress has serious psychological consequences and is deserving of therapeutic attention.
In this chapter we describe one promising approach to the treatment of couple distress called integra- tive behavioral couple therapy (IBCT; Christensen & Jacobson, 2000; Christensen, Doss, & Jacobson, 2020; Jacobson & Christensen, 1998). We first review how IBCT differs from two conceptually similar approaches:
C H A P T E R 19
Couple Distress
Andrew Christensen Jennifer G. Wheeler Brian D. Doss Neil S. Jacobson
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traditional behavioral couple therapy (TBCT; formerly called behavioral marital therapy) and cognitive-behav- ioral couple therapy. Then we describe IBCT, including its stages of therapy and its specific interventions. Final- ly, we discuss the empirical support for IBCT, describe current efforts at implementation and dissemination through the U.S. Department of Veterans Affairs (VA) and through an online adaption of IBCT (ourrelation- ship.com), and provide a case study.
TRADITIONAL BEHAVIORAL COUPLE THERAPY
The term couple therapy (as opposed to “individual” or “group” therapy) refers to clinical approaches for im- proving the functioning of two individuals within the context of their romantic relationship to one another.1 Although couple therapy is unique in its emphasis on a specific dyad, by its very definition, it is a contextual approach to the treatment of two individuals. Accord- ingly, successful treatments for couple distress have emphasized the assessment and modification of each individual’s contribution and response to specific inter- actions in their relationship (e.g., Gurman, 2015).
The most investigated approach for the treatment of couple distress has been behavioral couple therapy. First applied to couple distress by Stuart (1969) and Weiss, Hops, and Patterson (1973), TBCT uses basic behav- ioral principles of reinforcement, modeling, and behav- ioral rehearsal to facilitate collaboration and compro- mise between partners. With an eye toward facilitating changes in the partners’ behavior, TBCT teaches them how to increase or decrease target behaviors (behavior exchange), to communicate more effectively (commu- nication training), and to assess and solve problems (problem solving) to improve overall relationship sat- isfaction. The monograph by Jacobson and Margolin (1979) has been a commonly used treatment manual for TBCT.
Clinical trials in the United States and several other countries repeatedly demonstrated the positive impact of TBCT (see reviews by Shadish & Baldwin, 2005; Snyder, Castellani, & Whisman, 2006) on relationship satisfaction. Research also showed the positive impact of TBCT for couples in which one partner has an indi- vidual disorder, such as depression (Gupta, Coyne, & Beach, 2003), alcoholism (McCrady & Epstein, 2015), or anxiety (Baucom, Shoham, Kim, Daiuto, & Stickle, 1998). Recent meta-analyses have shown that TBCT has effects comparable to those of the most studied
nonbehavioral treatment, emotionally focused couple therapy (Rathgeber, Bürkner, Schiller, & Holling, 2019; Roddy, Walsh, Rothman, Hatch, & Doss, 2020).
Despite the apparent success of TBCT, however, outcome research early on revealed some limitations in its efficacy and generalizability. For example, ap- proximately one-third of couples failed to show mea- surable improvement in relationship quality following treatment with TBCT (Jacobson, Schmaling, & Holtz- worth-Munroe, 1987). Furthermore, many couples who initially responded to treatment relapsed within 1 or 2 years after therapy (Jacobson et al., 1984, 1987). Snyder, Wills, and Grady-Fletcher (1991) found a di- vorce rate of 37% in couples treated with TBCT 4 years after therapy.
Findings about the limited effectiveness of TBCT encouraged the development of additional therapeutic approaches. Various modifications and enhancements have been made to TBCT in an effort to improve its effectiveness (e.g., Baucom & Epstein, 1990; Epstein & Baucom, 2002; Halford, 2001), yet existing treatment studies have failed to demonstrate any incremental ef- ficacy in various enhancements to TBCT. For example, the addition of cognitive strategies created a treatment that was as good as but not better than TBCT (e.g., Baucom et al., 1998).
In addition to examining treatment outcome, couple therapy research has examined how “treatment success- es” differ from “treatment failures.” Early research on treatment response identified several factors that appear to affect the success of TBCT. Compared to couples who responded positively to TBCT, couples who were regarded as “treatment failures” or “difficult to treat” were generally older, more emotionally disengaged, more polarized on basic issues, and more severely dis- tressed (see Jacobson & Christensen, 1998, for a re- view). Despite the fact that these couples arguably had the greatest need for effective treatment, each of these factors has an obvious deleterious effect on their abil- ity to collaborate, compromise, and facilitate behavioral change. Older couples, for example, have had more time than younger couples to become “stuck” in their destructive behavioral patterns; couples who are more polarized on fundamental issues (e.g., how traditional they are with respect to their gender roles) may never be able to reach a mutually satisfying compromise; and extremely disengaged couples may be unable to collabo- rate. Each of these factors is likely to be associated with long-standing, deeply entrenched, and seemingly “un- changeable” behavioral patterns. Thus, it should come
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as no surprise that the change-oriented techniques of TBCT are ineffective for these couples.
INTEGRATIVE BEHAVIORAL COUPLE THERAPY
These findings served as the impetus for the devel- opment of IBCT. Evidence on the limited success of TBCT, particularly during follow-up, spurred an effort to find a treatment with more enduring effects. Evi- dence of TBCT’s failures spurred efforts to find treat- ments that would be applicable even to these difficult cases. Four developments in IBCT are directed toward making treatment more enduring and more broadly ap- plicable: (1) a focus on the couple’s relational “themes” and patterns rather than on specific target behaviors; (2) a focus on historical and distal causal variables, as well as proximal causal variables; (3) an emphasis on “contingency-shaped” versus “rule-governed” behavior; and (4) a focus on emotional acceptance.
The first aspect that is intended to make IBCT’s ef- fectiveness more broadly applicable and more enduring is its focus on a couple’s relational “themes,” that is, their long-standing patterns of disparate yet function- ally similar behaviors. Although this focus is similar to TBCT in that it requires a comprehensive assessment of the couple’s behavioral patterns, it differs from TBCT in that multiple and complex behavioral interactions— and not just specific behavioral targets—are considered for therapeutic intervention.
A highlight of all behavioral approaches, and cer- tainly of TBCT, is an assessment process that trans- forms broad, global complaints into specific, observable behaviors. For example, a wife may come into therapy complaining that her husband does not love her, while her husband complains that his wife does not believe in him. The TBCT therapist would assist the wife in defining her general complaint into specific behavioral targets for her husband, such as kissing and hugging her more often. The therapist would also assist the hus- band in defining his general complaint into specific behavioral targets for his wife, such as complimenting his achievements more often. However, IBCT suggests that valuable information may be lost in the transfor- mation of a global complaint into a specific behavioral target. By quickly narrowing down global complaints into specific behavioral targets, TBCT inadvertently limits the means by which partners may satisfy each other. For example, if “feeling loved” is defined solely in terms of physical affection and the husband has dif-
ficulty in increasing and/or sustaining a higher level of physical affection, then his wife’s desires to feel loved will not be satisfied. Indeed, the husband could per- form a variety of other behaviors in addition to physical affection that function to make his wife feel loved, such as calling her during work to see how she is doing, lis- tening to her troubles with her family, or noticing that the air in her car tires is dangerously low. She may not be able to articulate many behaviors that might func- tion in ways to make her feel loved, either because she is not aware of the desired behaviors or perhaps she feels too vulnerable to express this need. Without more elaborate exploration of and functional analysis of the wife’s and husband’s thoughts, feelings, and behaviors, such important opportunities for facilitating therapeu- tic change may be lost. Furthermore, these very specific behavioral definitions may have iatrogenic effects. In the previous example, the wife may begin to define her husband’s love more and more in terms of his limited ability to be affectionate because this is how “love” was operationalized in the context of the TBCT interven- tion. If the husband is unable to make her feel “loved” via physical affection alone, then her anger and sense of loss could be heightened rather than ameliorated by the treatment.
In contrast to TBCT’s emphasis on specific behav- ioral targets, IBCT focuses on broader “themes” in the couple’s history, that is, developing a shared under- standing of the many circumstances in which the wife has felt loved and unloved, and in which the husband has felt that his wife believed or did not believe in him. Certainly, this shared understanding includes some specific behavioral examples illustrating what makes the wife feel unloved and what would make her feel loved, and what makes the husband feel that his wife does not believe in him and what would make him feel that she does. However, IBCT tries to keep open all possibilities of behaviors that function to provide each spouse with his/her desired emotional state. Thus, if one partner has difficulty performing a particular be- havior (e.g., physical affection), he/she may still be able to perform other, perhaps less obvious behaviors that serve the same function (e.g., calling one’s wife from work). By focusing on the broader emotional “theme” (her history of feeling unloved, his history of feeling not believed in), rather than attempting to operation- alize that theme completely into one or more specific behaviors, IBCT maintains its functional roots, while increasing the chances that each partner is able to meet the other’s needs.
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A second development that may make IBCT appli- cable to more couples and create more enduring change has to do with its assessment and conceptualization of relationship distress. Traditional behavioral approaches rely on a functional analysis of behavior, or an ABC (an- tecedent–behavior–consequence analysis), to determine the proximal controlling variables that influence behav- ior. For example, Susan criticizes Bill (antecedent), Bill reacts strongly (behavior), and Susan shuts down, refus- ing to talk to him for the rest of evening (consequence). IBCT incorporates that analysis but expands it to in- clude historical variables, such as Bill’s history of pa- rental criticism that has made him particularly sensitive to criticism. IBCT also includes distal variables, such as cultural norms that may proscribe certain behaviors. Perhaps Bill is from a culture that values privacy within the family, so that when he hears that Susan has told her friends of her complaints about him, he feels betrayed and shamed. In IBCT, we assume that such a broader analysis better captures the roots of distress and may facilitate partners’ understanding of each other and willingness to accommodate each other.
A third development that is designed to make IBCT applicable to more couples and to create more enduring change is based on the distinction between “rule-gov- erned” versus “contingency-shaped” behavior (Skinner, 1966). In the former, an individual is provided with a rule to guide his/her behavior and is then reinforced when he/she follows the rule. Using the previous ex- ample of affection, a therapist could develop a list of possible affectionate behaviors for the husband, such as giving his wife a kiss when he leaves for work and when he returns, then encourage the husband to imple- ment these behaviors. Upon implementing them, the husband would be reinforced by both his wife and the therapist. TBCT is largely based on employing “rule- governed” strategies to create positive change. Not only is behavioral exchange a rule-governed strategy, but even more importantly, the TBCT strategies of com- munication training and problem-solving training are also dominated by rule-governed strategies. In both, the TBCT therapist teaches the partners certain rules of good communication or good problem solving to use during their discussions of problems. The guidelines to use “I statements” and to “define the problem clearly before proposing solutions” are examples.
With “contingency-shaped” behavior, naturally oc- curring events in the situation serve to elicit and rein- force the desired behavior. For example, the husband would be affectionate with his wife when something in
their interaction triggered a desire for him to hug or kiss her; the experience of closeness or physical contact in the affectionate gesture itself, or his wife’s response to his gesture, would serve to reinforce his affectionate behavior. In contrast to TBCT, IBCT engages in con- tingency-shaped behavior change. IBCT therapists try to discover the events that function to trigger desired experiences in each partner, then attempt to orches- trate these events. For example, IBCT therapists might hypothesize that a wife’s criticisms push her husband away, but that her expressions of loneliness could bring him toward her. The IBCT therapist listens to her criti- cisms (e.g., that her husband ignores her), suggests that she may be lonely (as a result of feeling “ignored”), and, if she acknowledges such a feeling, encourages her to talk about it. The therapeutic goal is that this “shift” in her conversation (from criticism to self-disclosure) might also “shift” her husband’s typically defensive posture in listening to (or ignoring) his wife. Although such a strategy of emphasizing contingency-shaped be- havior makes intervention more complicated and less straightforward than a purely rule-governed approach, IBCT suggests that a contingency-shaped approach leads to more profound and enduring changes in the couple’s relational patterns.
A fourth development in IBCT that is designed to make it applicable to more couples and to create more enduring change is its focus on emotional acceptance. In TBCT, the approach to solving couple problems is to create positive change. If the husband in the couple we discussed could be more physically affectionate, and the wife more verbally complimentary, then the couple’s problems would presumably be solved. However, if the husband is unable or unwilling to be more physically affectionate, and if the wife is unable or unwilling to be more complimentary, then the case will be a treatment failure. If the husband and wife are able to make these changes initially but are unable to maintain them over the long run, then the case becomes a temporary suc- cess followed by relapse.
In contrast to TBCT, the focus of IBCT is on emo- tional acceptance, as well as change. Unlike the change- oriented goal of TBCT, the primary goal of IBCT is to promote each partner’s acceptance of the other and their differences. Rather than trying to eliminate a couple’s long-standing conflicts, a goal of IBCT is to help cou- ples develop a new understanding of their apparently irreconcilable differences, and to use these differences to promote intimacy, empathy, and compassion for one another. With its focus on acceptance rather than change,
746 CliniCAl HAnDbook of PsyCHologiCAl DisorDers
IBCT creates an environment for couples to understand each other’s behavior before deciding whether and how they might modify it. In the earlier example, IBCT would explore the husband’s difficulties in expressing affection and the wife’s difficulties in giving him com- pliments—difficulties that may have little to do with how much love they feel for one another. Through this exploration of the individuals, the partners may come to a greater understanding of one another and experience more emotional closeness, thus achieving the feelings of love they previously pursued by requesting changes in each other’s behavior (i.e., increased physical affection and verbal compliments).
While there is an expectation of “change” in IBCT, this expectation differs significantly from that of TBCT in regard to which partner and what behavior is expected to change. In TBCT, the “change” involves Partner A changing the frequency or intensity of a spec- ified behavior in response to a complaint from Partner B. But in IBCT, the therapeutic “change” also involves Partner B modifying his/her emotional reaction to Part- ner A’s “problem” behavior. When a difference between partners is identified to be “irreconcilable,” the thera- peutic strategy of IBCT is to change the “complaining” partner’s response to the “offending” partner’s behavior rather than directing all therapeutic efforts at attempt- ing to change what has historically been an essentially “unchangeable” behavior. Ideally, through exploration of the thoughts and feelings underlying Partner A’s behaviors, Partner B develops a new understanding of Partner A’s behavior, and the “complaint” about Part- ner A’s behavior is transformed into a less destructive response. In turn, this change in Partner B’s reaction often then has a salutary impact on the frequency or intensity of Partner A’s behavior. Using this approach, as opposed to an exclusively change-focused approach, even the most polarized, disengaged, and “unchange- able” couples have an opportunity to increase their overall marital satisfaction.
It is important to note that in this context, accep- tance is not confused with resignation. Whereas resig- nation involves one partner grudgingly giving in and giving up on the hope for a better relationship, accep- tance involves one partner letting go of the struggle to change the other. Ideally, partners let go of the struggle not grudgingly but as a result of a new appreciation for the partner’s experience. By understanding their couple distress in terms of their individual differences, and by learning to accept each other’s differences, it is hoped that the distress that has historically been generated by their struggle to change one another will be reduced.
Thus, for IBCT to be effective in treating couple dis- tress, it is important for partners to understand the factors that have contributed to the development and maintenance of their distress.
THE ETIOLOGY OF COUPLE DISTRESS
According to IBCT, relationship distress develops as a result of two basic influences: decreases in reinforc- ing exchanges, such as through reinforcement erosion, and the development of punishing exchanges, such as through conflict development. Reinforcement erosion refers to the phenomenon whereby behaviors that were once reinforcing become less reinforcing with repeated exposure. For example, demonstrations of physical af- fection may generate powerful feelings of warmth and pleasure for each partner during the early stages of their relationship. But after partners have spent many years together, the reinforcing properties of these affection- ate behaviors may diminish. For some couples, once- reinforcing behaviors may become “taken for granted,” whereas for others, once-reinforcing behaviors may ac- tually become aversive. In some cases, behaviors that were once considered attractive, endearing, or pleasing become the very same behaviors that generate or exacer- bate the couple’s distress. For example, Frank may have found Jeremy’s extraversion appealing in the beginning of their relationship because it was such a contrast to his own shy approach to life but over time, he often saw Jeremy’s extraversion as boisterous and overbearing.
As with the erosion of reinforcing behaviors, con- flicts may emerge as couples spend more and more time together. In the early stages of a relationship, dif- ferences in partners’ backgrounds, goals, and interests may initially be downplayed or ignored. For example, if Partner A prefers to save money and Partner B prefers to spend money, this difference may not be apparent dur- ing courtship, when spending money is a tacit expecta- tion of both partners. If this difference is detected early on, perhaps it is regarded as a “positive” difference, in that each partner is encouraged to be a little more like the other in his/her spending habits. Or perhaps each partner expects the other to eventually compromise or change to his/her way of doing things. But over time, these incompatibilities and their relevance to the rela- tionship are inevitably exposed. Differences that were once regarded as novel, interesting, or challenging may ultimately be perceived as impediments to one’s own goals and interests. Furthermore, in addition to any extant incompatibilities, other unanticipated incom-
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patibilities may emerge with new life experiences (e.g., having children, changing careers). Thus, even those couples who had initially made a realistic appraisal of their differences may discover unexpected incompat- ibilities over time.
These incompatibilities, while challenging in their own right, can be further exacerbated by each partner’s emotional sensitivities or vulnerabilities. Returning to our earlier example, if our “saver” comes from a back- ground of economic deprivation and has developed a justifiable fear of being destitute, then the issues related to saving may be motivated by powerful emotions that may impair his/her ability to understand the partner’s desire to spend and enjoy what they have. Incompat- ibilities can also be exacerbated by external stressors. For example, if one member of our “saver–spender” couple loses his/her job, then that might put their dif- ferences into even sharper relief. Efforts by the partners to deal with their struggle over money might paradoxi- cally make the problem worse. If the saver, for example, engages in behaviors such as investigating and interro- gating the spender, while the spender avoids and hides his/her purchases from the other, their problem might increase in intensity. One goal of IBCT is to help the partners identify and reframe their incompatibilities in a way that minimizes the destructive nature of these incompatibilities, by encouraging a more effective way of communicating about them, while maximizing their level of intimacy and relationship satisfaction.
DESCRIPTION OF IBCT
The Formulation
The most important organizing principle of IBCT is the formulation, a term used to describe how the thera- pist conceptualizes the couple’s problems and describes them to the couple. The formulation comprises three basic components: a theme, a DEEP analysis, and a mu- tual trap. The therapist refers back to the formulation and its components throughout the treatment process, when couples have conflicts during or between therapy sessions.
One of the most basic goals of IBCT is for the part- ners to adopt the formulation as part of their relation- ship history. From that point forward, they can use the formulation as a context for understanding their rela- tionship and their conflicts. The formulation also gives couples a language to discuss their problems, and allows partners to distance themselves from their problems. It is important to remember, however, that the formula-
tion is a dynamic concept that may require alteration and modification (or “reformulation”) throughout treatment.
The Theme
The theme is the description of the couple’s primary conflict and is usually described by a word or phrase that captures the issues with which the couple strug- gles. For example, a common theme of many distressed couples is that of “closeness–independence,” in which one partner seeks greater closeness, whereas the other seeks greater independence. Other common themes center around trust, sexuality, money, and parenting. Sometimes a broad theme comprises two separate is- sues. For example, perhaps the couple is struggling over intimacy, with one partner focused on sexual intimacy, while the other is focused on emotional intimacy.
The DEEP Analysis
In IBCT, therapists conduct a DEEP analysis of the couple’s theme or issue/s. This acronym outlines the four major factors contributing to a couple’s problems: Differences, Emotional sensitivities, External circum- stances, and Patterns of interaction. IBCT suggests that partners have their primary conflict, or theme, because of differences between them and each part- ner’s emotional sensitivities or vulnerabilities linked to those differences, both of which can be exacerbated by external circumstances. For example, in the theme of closeness–independence, Partner A may want more closeness and connection, and Partner B may want more independence simply because they are different people with different genes and different social learning histories. Perhaps this difference was not readily appar- ent early on, because both partners were enchanted by their developing relationship. Or perhaps there really was little difference in their desires for closeness and independence until they had children, or until one partner’s career took off. Whatever the basis for the dif- ference, it creates problems for the couple, as differences are perceived as deficiencies. For example, the closeness seeker may see the other as being “afraid of intimacy”; the independence seeker may see the other as being “ex- cessively needy.” Partners find that they cannot both get their needs fully satisfied. Compromise may still be relatively easy unless emotional sensitivities or vulner- abilities are also present, which provide emotional fuel for the differences. If Partner A wants greater closeness than Partner B and is emotionally vulnerable to easily
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feeling abandoned, then negotiations about closeness may be threatening to Partner A. Similarly, if Partner B wants greater independence and is emotionally vulner- able to easily feeling controlled and restrained, then ne- gotiations about closeness may be threatening for Part- ner B. External circumstances may conspire to make the problem even greater. If the couple lives in an area where Partner A, who wants more closeness, is far away from other sources of social support, and where Partner B, who wants more independence, is close to leisure ac- tivities in which he/she wants to engage independently, the struggle between them will be even greater. The combination of their differences (D), their emotional sensitivities (E), and the external circumstances (E) may lead the two to engage in a destructive pattern (P) of interaction that can polarize them even further.
The pattern of interaction refers to the often frustrat- ing and destructive communication that ensues when a distressed couple enters into a theme-related conflict. A natural response for partners confronted with their dif- ferences is for each partner to try to change the other. In many cases, these efforts at changing each other may be successful. However, many times, the result may be that their differences are exacerbated and the two partners become polarized in their conflicting positions. When partners have become polarized on an issue, further at- tempts to change each other only increase the conflict and perpetuate their polarized stance. For example, in a couple whose theme is closeness–independence, the polarization process is likely to occur when the inde- pendence-seeker “retreats” from attempts by the close- ness-seeker to gain more intimacy, which then creates more “intrusive” efforts by the closeness-seeker. The more the one partner “advances,” the more the other partner “retreats”; the more that partner “retreats,” the more the other partner “advances.” Furthermore, being deprived of a desired goal can make that goal seem even more important: Partners can become desperate, esca- lating their futile efforts, and their differences become magnified. It can begin to look like the closeness-seeker has no needs for independence and the independence- seeker has no needs for closeness. Through their inter- action, they have become more different than they were originally.
The Mutual Trap
The mutual trap, which describes the outcome of the polarization process, is called a trap because it typi- cally leaves the partners feeling “stuck” or “trapped” in
their conflict. Partners in a mutual trap feel that they have done everything they can to change the other, and nothing seems to work. But they are reluctant to give up their efforts to change each other, because this would mean resigning themselves to a dissatisfying relation- ship. As a result, they become more entrenched in their respective positions.
The experience of partners who are so polarized is one of helplessness and futility, and this experience is rarely discussed openly between them. As a result, each partner may be unaware that the other partner also feels trapped. Making each partner aware of the other’s sense of entrapment is an important part of acceptance work, and encouraging each partner to experience the other’s sense of “stuckness” can sometimes be the first step toward promoting empathy and intimacy between partners.
Stages of Therapy
In IBCT, there is a clear distinction between the assess- ment/feedback phase and the active treatment phase. The assessment phase comprises at least one conjoint session with the couple, followed by individual ses- sions with each partner. These sessions are followed by a conjoint feedback session, during which the therapist describes his/her formulation of the partners and their problems, as well as the therapist’s plan for their treat- ment. The feedback session is followed by the treat- ment phase that typically comprises conjoint sessions, the exact number of which should be determined on a case-by-case basis depending on each couple’s treat- ment needs. However, the protocol used in a recent clinical trial of IBCT for seriously and chronically dis- tressed couples (discussed below) was a maximum of 26 sessions, including both the assessment and treatment phases.
The Use of Objective Measures
Objective assessment instruments (see Table 19.1) are useful for both initial assessment and for monitoring a couple’s progress at various points throughout treat- ment. Such objective measures may provide additional information about areas of disagreement that have not been covered in the session, or they may provide objec- tive data about a couple’s levels of distress and satisfac- tion. Additionally, research has shown that sharing and actively discussing a couple’s progress (or lack thereof) in therapy can improve therapy outcomes (e.g., Halford
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et al., 2012). For example, a couple’s relationship satis- faction can be assessed using the Couples Satisfaction Index (Funk & Rogge, 2007); partners’ commitment to the relationship and steps taken toward separation or divorce can be assessed using the Marital Status Inventory (Crane & Mead, 1980; Weiss & Cerreto, 1980); partner’s areas of conflict and troubling behav- iors can be assessed with the Problem Areas Question- naire (Heavey, Christensen, & Malamuth, 1995) and the Frequency and Acceptability of Partner Behavior Inventory (Christensen & Jacobson, 1997; Doss & Christensen, 2006), and the couple’s level of physi-
cal violence, with the Revised Conflict Tactics Scales (CTS2; Straus, Hamby, Boney-McCoy, & Sugarman, 1996). The Couple Questionnaire (Christensen, 2009) includes a brief assessment of commitment, intimate partner violence, and relationship satisfaction (a four- item version of the Couples Satisfaction Index).
We recommend that, at a minimum, clinicians ad- minister measures that assess relationship satisfaction, intimate partner violence, commitment, and problem areas. To assess these areas, we typically recommend three questionnaires that are short, easy, and cost-free: the Problem Areas Questionnaire, the Couple Ques- tionnaire, and the 16-item version of the Couples Sat- isfaction Index (see Table 19.1). Measures of violence, commitment, and problem areas are needed, because partners may indicate concerns on a questionnaire that they do not bring up spontaneously. Typically, partners are given questionnaires at their first session to com- plete then return at their individual sessions. In addi- tion to being part of the assessment phase, a relation- ship satisfaction questionnaire should be administered repeatedly throughout treatment and follow-up to as- sess changes from partners’ presenting baseline levels of satisfaction. We briefly assess not only satisfaction each session with the Weekly Questionnaire (to be discussed below) but also satisfaction periodically with the 16- item Couple Satisfaction Index.
Assessment of Domestic Violence
Objective measures are particularly useful in assess- ing a couple’s history of physical violence. Assessing for domestic violence is a critical part of every couple’s intake—not only to determine whether the personal safety of either partner is in imminent danger but also because couple therapy may actually be contraindicated for some violent couples (Jacobson & Gottman, 1998; Simpson, Doss, Wheeler, & Christensen, 2007). Couple therapy requires that both partners take some degree of responsibility for their problems, but such a perspective is inappropriate when a couple’s problems include do- mestic violence, because perpetrators of violence must assume sole responsibility for their behavior. Further- more, because therapy sessions can elicit strong emo- tions, the couple therapy itself may trigger postsession violence in some couples. In such cases, treatment that focuses on the violent behavior of the perpetrator—and not the interactive distress of the couple—is indicated. The Couple Questionnaire (Christensen, 2010) and the CTS2 (Straus et al., 1996) are useful screening tools
TABLE 19.1. Useful Assessment and Screening Instruments
• Couples Satisfaction Index (Funk & Rogge, 2007): Measures relationship distress. (To obtain this freely available measure, go to www.courses.rochester.edu/surveys/funk and scroll down to “Research Tools.”)
• Couple Questionnaire (Christensen, 2009): Brief screening assessment for couple satisfaction, intimate partner violence, and commitment, as well as open-ended descriptions of typical positive and negative interactions. (To obtain this freely available measure, go to the “Questionnaires” tab on the IBCT website: https://ibct.psych.ucla.edu.)
• Frequency and Acceptability of Partner Behavior Inventory (Christensen & Jacobson, 1997; Doss & Christensen, 2006): Assesses frequency and acceptability of behavior for 24 categories of spouse behavior. (To obtain this freely available measure, go to the “Questionnaires” tab on the IBCT website: https://ibct.psych.ucla.edu.)
• Marital Status Inventory (Crane & Mead, 1980; Weiss & Cerreto, 1980): Assesses commitment to the relationship and steps taken toward separation or divorce. (To access this measure, go to https://darkwing.uoregon.edu/~rlweiss/ msi.htm.)
• Problem Areas Questionnaire (Heavey, Christensen, & Malamuth, 1995): Assesses common problem areas or areas of disagreement in couples. (To obtain this freely available measure, go to the “Questionnaires” tab on the IBCT website: https://ibct.psych.ucla.edu.)
• Revised Conflict Tactics Scales (Straus, Hamby, Boney- McCoy, & Sugarman, 1996): Assesses domestic violence. (To purchase this measure, go to www.wpspublish.com/ cts-conflict-tactics-scales.)
• Weekly Questionnaire (Christensen, 2010): Assesses significant positive and negative events since the last session and includes a brief form of the Couples Satisfaction Index. (To obtain this freely available measure, go to the “Questionnaires” tab on the IBCT website: https://ibct.psych.ucla.edu.)
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for evaluating the frequency and severity of a couple’s physical aggression, and to determine whether couple therapy is contraindicated. Finally, a couple’s history of violence should be directly addressed during the assess- ment phase, primarily during the individual sessions, when each partner can talk freely without fearing con- sequences from the other.
Assessment Phase
The assessment phase typically comprises one joint ses- sion with the partners (Session 1), followed by indi- vidual sessions with each partner (Sessions 2 and 3). The primary goal of the assessment phase is for the therapist to evaluate whether the couple is appropri- ate for therapy and, if so, to develop the formulation. However, the therapist should also use the assessment period to orient the couple to the therapy process. In addition, although the IBCT therapist is not actively intervening during the assessment phase, it is possible for the therapist to have a therapeutic impact in these first few sessions.
Orientation (Session 1)
After introductions and general orientation to therapy (e.g., informed consent, billing), the couple is oriented to the specific process of IBCT. Therapists should ex- plain the difference between assessment, feedback, and treatment phases of therapy, and explain why an assess- ment period and feedback are needed before therapists can provide active treatment interventions.
Also during the first session, couples are introduced to the self-help book Reconcilable Differences (Chris- tensen, Doss, & Jacobson, 2014; Christensen & Jacob- son, 2000). Couples are encouraged to complete Parts I and II of this book prior to the feedback session. Al- though reading this book is not a necessary component of treatment, it can benefit that treatment. Ideally, the reading in Parts I and II helps couples begin to concep- tualize their problems in a way that is similar to how their therapist will frame them during the feedback ses- sion.
Therapists should be aware that at least one partner, if not both, may likely be ambivalent about participat- ing in therapy. Such ambivalence should be normalized and validated, and the therapist should explain to part- ners that the assessment period is also their opportunity to get to know the therapist and to determine whether this treatment is going to be a “good match” for them.
Problem Areas (Sessions 1–3)
After the couple has been oriented to the therapy pro- cess, the therapist begins the evaluation by reviewing the couple’s presenting problem(s). Much of this infor- mation can be gathered from objective measures and also during each partner’s individual session, so this discussion during Session 1 should not consume the entire session. However, it is important during the first session that the partners feel heard and validated, and that their problems and distress are clearly understood by the therapist.
From the information gathered from objective mea- sures and during the evaluation sessions, therapists should be able to describe the partners’ problem areas and develop their formulation. The following six ques- tions provide a guideline for this assessment, and each should be answered by the end of the assessment period.
1. How distressed is the couple? 2. How committed is this couple to the relationship? 3. What issues divide this couple? 4. Why are these issues a problem for them (the
DEEP analysis)? 5. What strengths keep this couple together? 6. What can treatment do to help them?
The first three questions can be addressed with ob- jective questionnaires. However, even questions that can be addressed with questionnaires should usually be explored in further detail in interviews. For example, the individual sessions may be particularly useful for assessing whether distress is so great that separation is imminent, each partner’s level of commitment to the relationship and the possible presence of affairs, and the couple’s history of physical violence.
The assessment of problem areas should also include a determination of the couple’s collaborative set (Jacob- son & Margolin, 1979). This term refers to the couple’s joint perspective that they share responsibility for the problems in their relationship, and that both will have to change if the relationship is to change. The strength of this set determines whether change- or acceptance- oriented interventions are indicated. The stronger the couple’s collaborative set, the more successful initial change-oriented interventions are likely to be.
The fourth question—why the partners’ issues are a problem for them—requires a functional analysis along the lines of the DEEP analysis described earlier. It is usu- ally possible to obtain initial information about all four
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aspects of the DEEP analysis in the joint interview, but more nuanced understandings about these factors, par- ticularly emotional sensitivities and patterns of interac- tion, are typically best left to the individual interviews. Because adults are often unaware of the contingencies controlling their behavior, or may be embarrassed to admit those contingencies even if they know them, a functional analysis of emotions and patterns involves much more than a simple, straightforward inquiry. The therapist must be particularly sensitive to the emotional reactions of partners, which may indicate important re- inforcers and punishers. For example, let us assume that our partners with the closeness–independence theme argue frequently about the amount of time they spend together. However, that specific issue may not be where the most powerful contingencies are found. Perhaps the wife’s history includes having been abandoned by her family members at a time when she was in particu- lar need of their support and comfort. Her fear in her marital relationship is that her husband may do likewise. For her, the time they spend together is simply a poor proxy for her concerns that he may not always be there when she needs him. If she felt confident of that, then she could tolerate much less time together. For her husband’s part, let us assume that his social learning history has led him to be especially sensitive to being controlled or re- stricted by another person. Therefore, he battles his wife over their time together not so much because he does not want the time together, but because he feels controlled by her and naturally resists. In such a situation, the IBCT therapist needs to move the discussion away from the re- petitive arguments about time spent together, toward the more important contingencies that affect each spouse’s behaviors, for example, the emotional sensitivities that each partner brings to the relationship and the pattern of interaction that triggers their emotional responses.
Answers to the fifth question, about the couple’s strengths, also come from the joint and individual in- terviews. It is helpful for partners to keep their strengths in mind even as they focus on their difficulties. Some- times there is an interesting relation between partners’ strengths and their problems, in that the latter may in- volve some variation of the former. For example, let us assume that two partners were initially attracted to each other in part because of their different approaches to life. He is much more spontaneous; she is more delib- erate and planful. Those differences may be attractive and helpful at times, but they can also be a source of irritation and conflict, since they are in effect “two sides of the same coin.”
In answering the final question, about what treat- ment can do to help, the therapist must first be sure the couple is appropriate for couple therapy. If the couple has a serious violence or a substance dependence prob- lem, for example, then couple therapy as usual will not be the recommendation. Treatment directed at those particular problems will be necessary. If the couple is appropriate for couple therapy, the therapist will need to outline the focus of the therapy and what it com- prises.
The Couple’s History (Session 1)
After the partners have been oriented to therapy and their problem areas have been assessed, the therapist then takes the history of the couple’s relationship. The therapist’s obvious objective for taking this history is to gain a good understanding of the partners’ attach- ment to one another. Often the distress has escalated to the degree that it has overshadowed the reasons the two became a couple in the first place. In addition, this history can provide some immediate therapeutic ben- efit to the couple. Generally, when partners discuss the earlier (and usually happier) stages of their relationship, their affect is likely to become more positive. They have been focused for so long on the negative aspects of their relationship that they probably have not thought about their early romance, courtship, and attraction to each other for a very long time. In this way, having couples describe the evolution of their relationship can be thera- peutic in and of itself. Although some couples may be in too much pain to discuss their history without blam- ing and accusatory remarks (in which case the therapist should abandon the following guidelines and instead use the session to validate their pain), most couples enjoy reminiscing about their happier times.
The following series of questions provides the thera- pist with useful information about the couple’s history and allows the partners an opportunity to reflect on the reasons they fell in love in the first place:
• “How did you get together?” • “What was your courtship like?” • “What attracted each of you to the other?” • “What was your relationship like before your prob-
lems began?” • “How is your relationship different now on days
when you are getting along?” • “How would the relationship be different if your
current problems no longer existed?”
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These and other, related questions may also reveal useful information about each partner, such as his/her hopes and dreams for the future. Information about the couple’s history is useful for the therapist in develop- ing the couple’s formulation, which is presented to the partners during their feedback session.
Individual History (Sessions 2 and 3)
Each partner’s individual history can often provide use- ful information for the formulation, in that it provides a context for each partner’s behavior and illuminates possible emotional vulnerabilities in each. For example, perhaps the husband experienced his mother as very de- manding of him and learned to cope with this through withdrawal, and this defensive withdrawal continues in response to his wife’s demands. Or perhaps the wife had two previous boyfriends who cheated on her, so she is sensitive to any indication of betrayal by her husband.
The following questions may be useful in guid- ing a discussion of each partner’s individual history: What was your parents’ marriage like? What was your relationship with your father like? What was your re- lationship with your mother like? What were your re- lationships with your siblings like? What were your re- lationships with previous important romantic partners like? Each of these questions could potentially take an inordinate amount of time. The IBCT therapist tries to elicit features of these early relationships that are similar to or may inform the current relationship. For example, if the therapist were aware of a difference between hus- band and wife in terms of how comfortable they are with conflict, he/she would guide the husband away from details about where his family lived and focus on the expression of conflict that occurred in his family.
Feedback Session
The feedback session (usually Session 4) comprises two parts: (1) explanation of the formulation and (2) dis- cussion of the treatment plan. From the information gathered during the assessment sessions and from the questionnaires, the therapist has developed a tentative formulation of the couple’s problems. After checking in with the couple and seeing if there have been any major changes since the assessment sessions, the therapist shares that formulation with the couple. The feedback session can follow the outline of the six earlier questions used to assess the couple’s problem areas. It is impor- tant that the feedback session be a dialogue and not a
lecture from the therapist—with the therapist continu- ally checking in with the couple about the formulation being presented. The partners are the experts on their relationship and should be treated as such.
The feedback session is also used to describe the pro- posed treatment plan for the couple, based on the thera- pist’s formulation. The therapist describes the goals for treatment and the procedures for accomplishing these goals. The goals for treatment are to create an in-ses- sion environment in which the couple’s problems can be discussed constructively and ameliorated through some combination of acceptance and change. In rela- tion to the DEEP analysis, IBCT promotes emotional acceptance for the partners’ differences and emotional sensitivities, in that these factors are likely to change only slowly, if at all. External stressors can sometimes be changed, but often they, too, require acceptance. It is the pattern of interaction that can be changed and is the focus of change efforts in IBCT. The procedures for meeting these goals of acceptance and change are usually (1) in-session discussions of incidents and is- sues related to the formulation, and (2) homework to be conducted outside the session to further the in-session work.
During the feedback session, the therapist introduces the couple to the Weekly Questionnaire (Christensen, 2010), goes over it, and asks that each partner complete it prior to each session. This questionnaire provides in- formation on the couple’s experiences since the last ses- sion and serves as the basis for treatment sessions. It in- cludes the four-item version of the Couples Satisfaction Index (Funk & Rogge, 2007) so the therapist can mon- itor the couple’s relationship satisfaction on a regular basis. The questionnaire asks whether there have been any major changes in the couple’s life, and whether any incidents of violence, or any problematic incidents of substance/drug use have occurred. Then the question- naire asks each partner to describe the most positive or meaningful interaction they had since the last session, the most difficult or negative interaction since the last session, and whether they anticipate any upcoming, challenging events in the near future. Partners then rank what they think would be most important to dis- cuss: the positive, negative, or upcoming event, or some issue not tied to a particular incident (e.g., finances). Finally, there is a place for any homework assignment. These positive, negative, and challenging upcoming events, as well as the general issues the partners indicate on their questionnaires, provide the usual content for the therapy sessions.
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The goals of the feedback session are (1) to help part- ners think of their problems in terms of the formula- tion; (2) to orient them to the twin goals of change and acceptance through open communication; and (3) to explain the processes of the active phase of therapy. Thus, the feedback session gives partners some idea of what they can expect from therapy, and it elicits their willingness to participate. If one or both partners are reading the book Reconcilable Differences (Christensen & Jacobson, 2000; Christensen et al., 2014), the thera- pist can assign Part III, which specifically addresses the topic of acceptance. After the formulation and treat- ment plan have been described, partners are asked to go home and discuss the treatment and make a joint decision to participate in the active phase of IBCT.
Treatment Phase
Format for a Typical Treatment Session
A typical treatment session begins with the collection of the Weekly Questionnaire. A brief glance at the first four items in which partners rate their satisfaction with each other since the last session gives the thera- pist a sense of how the week has gone and can lead to brief general discussion about that week. If the couple marked any issues with violence, drug/alcohol prob- lems, or major changes in their life, that is the first order of business. Fortunately, most couples will not have ex- perienced those events. If the partners are not angry at each other, the therapist usually debriefs the positive incidents they report first. If the positive incident was significant, considerable attention is given to it, with the therapist trying to learn and in so doing helping the partners learn how they were able to bring about such a positive experience. Significant positive incidents are usually those in which the partners were able to handle a difficult interaction in a better way, recover from a difficult interaction in a more effective way, or experi- ence some connection that they had not experienced for some time (e.g., sex for the first time in a while, an emo- tionally meaningful discussion, an experience of emo- tional closeness with each other). If the positive incident was not significant, such as a pleasant visit with some friends, the therapist might acknowledge how they are able to have good times together despite their problems but not spend much time discussing the event, since there may not be much useful to learn from it.
After the discussion of the positive event, the ther- apist typically sets an agenda for discussion based on
what the partners listed as their difficult incidents, chal- lenging upcoming events, or problematic issues, even if no relevant incident occurred. It is often not possible to discuss all the events that partners mention on the Weekly Questionnaire, so it is important to ensure that (1) the most important topics are discussed (partners’ rankings of these topics on the Weekly Questionnaire can assist with this determination) and (2) that both partners get attention to what they believe is important. Once an agenda has been set, the therapist can help the partners discuss these topics using the strategies de- scribed below.
Toward the end of the session, the therapist should alert the couple that the session is almost over so that there can be a wind-down and summary phase. Such a phase is particularly important if strong emotions were aroused by the discussion. The therapist can note that the problem is not going to be solved in the remaining time and give each partner a chance to make a final statement so that they have some closure on the topic. If the discussion was intense and the couple is likely to continue a discussion after therapy that will not go well, the therapist can do brief problem solving. Can the couple leave the problem for discussion at the next therapy session? If they want to continue the discus- sion, would it make sense to have a break so they can calm down first? The therapist can then capture some of the important points mentioned in the discussion to provide a kind of “take-home message” for the partners. Important points might be some revelation a partner has made (e.g., why some comment is so triggering for them), a partner’s realization of what the other is expe- riencing, or a recap of the pattern that keeps occurring between partners.
Goals for Treatment Sessions
The goal for an IBCT treatment session is to help the couple have a constructive interaction about an emo- tionally salient and often difficult topic. Since the inci- dents and issues from the Weekly Questionnaire reflect the most emotionally salient material in the couple’s life, they provide the content for the discussion. For ex- ample, a couple with a closeness–independence theme might discuss a difficult incident in which the inde- pendence-seeker wanted to spend the night out with friends and the closeness-seeker protested. Discussions also may be centered around upcoming events listed on the Weekly Questionnaire, such as a weekend trip for the couple, in which the independence-seeker fears that
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there will not be space for him/her to be alone. Broad issues related to the formulation and listed on the ques- tionnaire are also appropriate for discussion, such as whether separate weekend trips apart with friends are acceptable for the couple.
Partners usually revert back to their usual pattern of interaction as they deal with these emotionally charged topics. For example, the independence-seeker turns away as the closeness-seeker gets emotionally agitated during a discussion or partners discuss an argument they had the previous Sunday evening and get into a pattern of blame and defend, similar to how they inter- acted on Sunday. In these situations, the therapist can focus on the current interaction going on in the room. This interaction provides the therapist with an oppor- tunity to intervene as the problem is unfolding in the moment.
The goal of the IBCT therapist is to move couples away from their usual dysfunctional pattern of discus- sion toward one or more of the following meaningful discussions: (1) a compassionate discussion in which partners reveal their feelings, some of which may not have been revealed before, and experience some un- derstanding and empathy for each other (empathic joining); (2) an analytic discussion in which partners look at their problem from a distance and attempt to mindfully describe what goes on without judgment or blame (unified detachment); or (3) a practical discus- sion in which partners discuss concrete changes they might each make to improve their relationship (joint problem solving). These conceptually distinct inter- actions are often mixed in practice. The first two are acceptance-oriented interventions, in that the focus is not on what should be changed or who should change. These first two types of discussions can and often do bring about spontaneous change as partners come to understand each other and their dynamics better, but the focus is not on change. The last intervention, joint problem solving, is a change-focused intervention.
How the therapist intervenes depends to a large extent on which one of these strategies is being used. However, the therapist is active in all three strategies, only sitting back and observing when the interaction is going well. When the interaction begins to derail, typically reverting back to the couple’s usual style of dysfunctional interaction, the therapist intervenes to redirect the interaction. Often, the therapist has the partners talk to him/her rather than to each other, so the therapist can highlight certain aspects of what each is saying, translate what each is saying so the other can
understand it, or redirect the conversation toward more constructive territory. As emotions heat up for partners, they have a tendency to talk faster and louder. The therapist tries to slow down the interaction so that each partner has a chance, with the therapist’s help, to ex- press a meaningful message to the other, and the other has a chance, with the therapist’s help, to respond with a meaningful message.
IBCT Strategies for Fostering Emotional Acceptance
Typically, treatment begins with a focus on promoting acceptance. The exception is when partners are able to collaborate with one another (“the collaborative set”) and both want to make specific changes in their re- lationship. In that case, the therapist may begin with change strategies.
In the context of acceptance work, the actual con- tent of each session is determined by the partners and what they “bring in” every week. The therapist looks for emotionally salient material that is relevant to the formulation. Recent negative or positive events listed on the Weekly Questionnaire and related to the formula- tion are often the topics of discussion. Sometimes sa- lient events relevant to the formulation occur between partners during the session, and the therapist should generally make these the top priority, because the emo- tions involving events during sessions tend to be more accessible than events that occur between sessions. At other times, clients may indicate on the Weekly Questionnaire some issue of concern that they wish to discuss even though no incidents around this issue oc- curred in the last session. All of these topics are useful means for implementing the three acceptance-building strategies of empathic joining, unified detachment from the problem, and tolerance building. Because they can create greater closeness, as well as greater acceptance, the first two strategies are more commonly employed than the last one.
EMPATHIC JOINING
The goals of empathic joining are to engage partners in a compassionate discussion regarding their struggles as a way to bring about greater emotional closeness between them, reduce the intensity of their negative emotional reactions to each other, increase their acceptance of each other, and increase their support and helpfulness to each other. As noted in our DEEP analysis, partners have struggles in part because of their emotional sensi-
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tives; these struggles therefore provide a window into these sensitivities, as well as the ways partners often in- advertently trigger those sensitivities. In empathic join- ing, the therapist shifts the partners away from blame and defense, and toward open expression of feelings, particularly feelings of vulnerability. Initially, partners may express “hard feelings” such as anger, resentment, and frustration. The therapist validates these feelings but shifts the focus from the pain that each has deliv- ered to the pain that each partner is experiencing. This shift can lead into expression of softer feelings, such as embarrassment, shame, fear, and guilt, which usually exist alongside those hard feelings. As partners label some of their emotions, particularly the emotions they have often not voiced, these emotions may diminish in intensity (Torre & Lieberman, 2018). As partners hear less blame from the other and more revelation of emo- tional distress, they may increase their understanding and empathy for the partner. This understanding and empathy can lead to greater intimacy between partners (Laurenceau et al., 2004), less blame and greater accep- tance of the partner (Davis, 2018), and facilitate spon- taneous helpfulness and support by the partner (Pavey, Greitemeyer, & Sparks, 2012).
The process of creating empathic joining is anything but straightforward. Partners may be only dimly aware of some of their most vulnerable feelings, may feel em- barrassed to voice them, and may fear the partner will react negatively to these feelings or use the feelings against them in the future. Thus, the therapist should acknowledge the surface emotions that people express verbally or display nonverbally but consider the hidden emotions that may also exist. For example, Ben may re- port on his Weekly Questionnaire an incident where he “caught Susan flirting with another man.” His surface emotion of anger might be easy to detect. However, the therapist should consider the possible hidden emotions Ben might also experience in regard to that incident— fear that Susan is not attracted to him, concern that she might leave him, or even dismay that he is so upset by something relatively innocent that she did. For her part, Susan’s initial response may be defensiveness about her behavior or anger that Ben interprets “anything I do with another man as flirtatious.” Susan’s surface emo- tions of anger and defensiveness are readily apparent, but the therapist should consider the possible hidden emotions that she might also experience—embarrass- ment at her own behavior, regret that she hurts Ben so often, and discomfort about interacting with other men in Ben’s presence. The therapist’s goal in empathic join-
ing is to shift Ben and Susan from angry accusation and angry defense and counteraccusation toward more open, fuller expression of all the emotions that this in- cident aroused in each of them.
In discussing the incidents and issues that partners report on the Weekly Questionnaire, as well as discuss- ing the incidents that take place in the therapy session, partners usually focus on the provocations of the other, the wrongs done to them, and what is messed up in their relationship. We can shift to the pain that each has experienced, the wounds that each suffered, and what they feel is missing in their relationship. If they whine about the relationship, we can identify the wish that lies behind that whining. If they express hopelessness about the relationship, we can help them identify what they hoped for in the relationship. Thus, we help the couple shift away from the fruitless interactions they usually have into more constructive interactions that ideally bring about mutual empathy.
We do not expect that partners will easily achieve empathic joining, particularly with a very distressed couple. Instead, they may want to focus on the egre- gious acts that their partner did rather than the emo- tions that led to those acts or the emotions those acts elicited, or they may be too hurt and angry to empa- thize with their partner’s pain. However, IBCT thera- pists should not only elicit the less revealed emotions that partners are experiencing but also show their own empathic responses to those emotions. Even though partners may not join the therapist in his/her empathic response to the other, they will be influenced by a val- ued and credible third party who sees the partner’s ex- perience in a less judgmental and more understandable and sympathetic light. Perhaps not in the moment, but they will be influenced.
UNIFIED DETACHMENT FROM THE PROBLEM
The goal of unified detachment is to engage partners in an analytic discussion about their struggles. Unlike empathic joining, which focuses on having partners express their emotional reactions, the focus in unified detachment is on having partners express their dispas- sionate, objective scrutiny of an incident or issue. Rath- er than a close-up view of their difficulties, we engage them in a more distanced view of these struggles. We encourage partners to “step back” from their problems and describe them in a nonjudgmental, mindful way, without placing blame—or responsibility for change— on either partner.
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This strategy can be used to engage a couple in a DEEP discussion about their differences (how these differences resulted from their backgrounds), their emotional sensitivities (what past experiences may have understandably led to these sensitivities), their external stressors (how these stressors came to be), and their pat- terns of interaction (how each interacts in ways that make sense from his/her perspective). However, most often, it is used to help the partners discuss their pat- terns of interaction. For example, the therapist may engage partners in a dialogue in which they try to ob- jectively describe the sequence of a particular conflict from their Weekly Questionnaire, such as what factors triggered their reactions, how specific events were con- nected to one another, how things escalated between them, and how they attempted to resolve the conflict or return to normal. The therapist can engage the couple in an analysis of why similar conflicts were either more or less intense than this one. The therapist can also use metaphor and humor to distance the couple emotion- ally from the problem, as long as the humor does not in any way belittle either partner. Through it all, the therapist treats the problem, and encourages the couple to treat the problem, as a third-party “it” rather than a personal “you” or “me.” When possible, the therapist can encourage the partners to give their theme, their pattern of interaction, or their mutual trap a name, and thus define the problem further as an “it.” By detach- ing themselves from the problem in this way, partners have an opportunity to discuss their conflict without becoming emotionally “charged” by it. In this way, they can understand the conflict from a more neutral, objec- tive stance. They engage in a kind of joint mindfulness about their problem, which can lead to an acceptance of each other’s experience and of the problem, and reduce their adversarial stance toward each other.
At an individual level, mindfulness-based interven- tions have been shown to reduce negative and increase positive affect, reduce negative thinking, and increase emotional clarity (Cooper, Yap, & Batalha, 2018; Gu, Strauss, Bond, & Cavanagh, 2015). Joint mindfulness may have similar but perhaps even larger effects. Al- though there is little research on joint mindfulness, one recent intervention study with nondistressed couples showed the benefits of an intervention that captures some of what we mean by unified detachment inter- ventions. Partners were asked to write an analysis of specific disagreements that they had “from the perspec- tive of a neutral third party who wants the best for all involved; a person who sees things from a neutral point
of view. How might this person think about the dis- agreement? How might he or she find the good that could come from it?” (Finkel, Slotter, Luchies, Walton, & Gross, 2013, p. 1597). The study revealed that doing this task repeatedly had beneficial effects on the cou- ples’ relationship quality compared to couples who just described the conflicts without taking this perspective.
TOLERANCE BUILDING
Building acceptance may be most challenging when one partner experiences intense emotional pain as a result of the other partner’s behavior. In these circum- stances, the IBCT therapist must help one partner build tolerance for the other partner’s “offending” behavior. By building tolerance, the partner ideally experiences a reduction in the pain caused by the behavior. To build tolerance, however, the partner must cease efforts to prevent, avoid, or escape the “offending” partner’s be- havior. Instead, by exposing him/herself to the behavior without the associated struggle, the partner reduces his/ her sensitivity to the behavior and, ideally, experiences the “offending” behavior as less painful.
One strategy for building tolerance is through “posi- tive reemphasis,” or focusing on the positive aspects of a partner’s negative behavior. This strategy may be rel- atively easy when a negative behavior is in some way related to a quality the partner once found attractive about the other. For example, what she sees as her part- ner’s “uptightness” might be the “stability” that first at- tracted her. Alternatively, what he sees as her “flakiness” or “irresponsibility” might be the “free-spiritedness” or “rebelliousness” that so attracted him in the beginning of their relationship. The positive reemphasis does not deny the negative qualities of the behavior in question, but it helps partners gain the perspective that any qual- ity often has both good and bad features.
Another strategy for building tolerance for differ- ences is to focus on the ways these differences complement each other, and to present these differences as part of what makes the relationship “work.” One partner’s sta- bility might balance the other’s free-spiritedness. The therapist might describe for the partners the ways they would be “worse off” if those differences did not exist. The differences can become a positive aspect of the re- lationship, something in which the partners take pride rather than something they see as a destructive threat.
A third technique for building tolerance to a part- ner’s behavior is to prepare couples for inevitable slipups and lapses in behavior. This is especially important
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when the partners first begin to detect changes in their behavior and begin to feel positive about the progress they are making in therapy. It is during this time that the therapist should congratulate them for their hard work and progress, then warn them that “backsliding” is still a likely occurrence. The partners should be asked to imagine some of the circumstances in which a slipup is likely to occur, and to consider possible responses to the slipup in advance. Working out how they will face such lapses helps partners build their tolerance for them.
A related strategy for building tolerance is to instruct couples to fake negative behavior while they are in ses- sion or at home. Each partner is instructed to engage in a designated “bad behavior”—with the stipulation that he/she is to engage in this behavior only when he/she does not feel like doing so. The instructions are given to the couple, so that each partner knows that a bad behavior he/she is about to witness in session or may see in the future might actually be faked. Ideally, this in- troduces an ambiguity about future negative behaviors that may mitigate the partner’s emotional response to them. More importantly, however, is that faking behav- ior gives both partners an opportunity to observe the effects of their negative behavior on the other. Specifi- cally, because they are performing the “bad behavior” during a time when they do not feel like it, they make these observations when they are in a calm emotional state that allows them to be more sympathetic. When done in session, the therapist can help debrief the reac- tions to the “bad” behavior. When done at home, the faker is instructed to let the other partner know about the faked behavior soon after is it performed, so the situation does not escalate and the partners have an op- portunity to “debrief” following their “experiment.”
One unavoidable source of pain for many partners is the feeling that the other fails to meet their needs in some important way. However, rarely is a partner able to fulfill all of the needs of the other or to fulfill the other’s needs when he/she is distressed and focused on his/her own needs. An important aspect of accep- tance building is for partners to increase their own self- reliance, or self-care, in getting their needs met. They should be encouraged to find alternative ways to care for themselves when their partners are not able to do so. Partners may need to seek support from friends and family in times of stress, or to find new ways to define and solve a problem on their own. As their self-reliance increases, reliance on partners to meet all of their emo- tional needs decreases. Ideally, this results in decreased
sensitivity to their partners’ failure to meet their needs, thereby reducing conflict. This discussion of alternative means of need fulfillment must be done sensitively, so that it does not exempt the partner from any role in need fulfillment or lead to emotional distance between them.
THE IMPACT OF EMOTIONAL-ACCEPTANCE-FOCUSED DISCUSSIONS ON CHANGE
The IBCT strategies described earlier for fostering emo- tional acceptance can also instigate autonomous, self- initiated change by partners. During empathic joining, partners express more clearly their own, often compli- cated emotional reactions to the other and hear the other’s emotional reactions. Neither partner intention- ally wants to hurt the other, so they may, with greater empathy for the emotional impact of their behavior on the other, alter their behavior without being asked or pressured to do so. During unified detachment, partners describe in detail the process by which they inadvertently trigger each other or escalate a normal disagreement into an intense argument. In so doing, they indirectly suggest alternative behaviors in which each partner could engage that might make the inter- action go better or at least not escalate it so intensely. As a result, partners sometimes spontaneously engage in change. In a similar way, tolerance interventions can indirectly suggest change. For example, when partners fake their triggering behaviors, in session or out of ses- sion, they become more acutely aware of what these triggering behaviors are and that they have some con- trol over them. In IBCT, this is the best kind of change, because it is initiated spontaneously by clients. They do it not because of pressure from the partner or from the therapist, but because they care about the partner and the relationship and do not want to hurt the partner or the relationship. Thus, we believe that this kind of change is more likely to endure.
Clients may follow these acceptance-based interven- tions not with spontaneous change on their own part, but requests of change to their partner. They may say, in effect, “Now that you know what hurts me, why don’t you stop doing it?” or “Now that you understand what you do to escalate our conflicts, why don’t you stop it or do something better?” Since therapists want to be helpful and facilitate change, they too have a nat- ural tendency to follow these acceptance-based inter- ventions with suggestions for change. They may point out that if one did X rather than Y, then things would
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go better between them. In these ways, an acceptance- based intervention can be hijacked into a change-based discussion, complete with the pressure and resistance that is similar to the couple’s dysfunctional pattern of interaction. Therefore, the IBCT therapist is care- ful not to suggest changes as an immediate follow-on to an acceptance-based discussion and guides couples away from such a change-focused discussion. When the acceptance-based discussions we have described go well, it is often helpful to stretch them out and to give clients time to process them. For example, the IBCT therapist may say something like “Let’s not discuss the changes that either of you could or should make. Change is often hard. I think that it would be help- ful for each of you just to hear what the other said and think about what you both have said.” Often, these acceptance-based discussions lead to a softening in each partner toward the other and, as a result, a greater con- nection between them. This kind of change may be the most important change that happens to them and we do not want to interrupt a natural process that could bring about this change, or autonomous changes in the focal problem, by shifting to a discussion of “what each of you should do differently.”
IBCT Strategies for Fostering Deliberate Change
A focus on deliberate change is often necessary and helpful for couples. Although the previously discussed acceptance-based strategies may bring about enhanced emotional connection and autonomous change, they may still leave the partners with dysfunctional interac- tion patterns that prevent them from addressing con- structively the problems they face and thus bring about repeated frustration. Although IBCT therapists usually start with acceptance-focused strategies and typically postpone change-based discussions until acceptance- based interventions have had an impact, they focus on change as it happens naturally throughout the therapy. On the Weekly Questionnaire, partners are asked to in- dicate their most important positive interaction since the last session. IBCT therapists always debrief these interactions and give them special attention when they reflect positive changes by one or both partners (e.g., handling a problem in a better way, doing something different to enhance the relationship). This debriefing is a way of highlighting and thus reinforcing what each is doing to improve the relationship. In addition to this focus on change as it happens naturally, IBCT thera- pists facilitate practical discussions about change when
clients have understood their issues and patterns, and have developed a collaborative attitude toward change based on the acceptance-based interventions. The fol- lowing strategies are ways that IBCT therapists foster change.
FOSTER CLIENT-INITIATED, CHANGE-BASED DISCUSSIONS
As partners discuss a problem with the strategies dis- cussed earlier, they may indicate that they would like to change something about themselves or their behavior. IBCT therapists then facilitate an exploration of that topic, such as the impact on the partner, the possible difficulties in making the change, and so forth. Thera- pists want to encourage change, but without promoting unrealistic expectations for change. Similarly, partners may request change by the other in the context of a con- structive discussion. IBCT therapists then facilitate an exploration of that topic, such as the partner’s reaction to the request, the impact that the change might have, and the possible barriers to implementation. During these discussions, IBCT therapists keep in mind the two areas in which change is likely to be most impor- tant: (1) a change in partners’ pattern of interaction and (2) a change in the underlying core problem. A change in the pattern of interaction can focus on the begin- nings of the pattern, before things have escalated (e.g., Sue comes home stressed from work and complains about her job, and Bill tries to help by giving her sug- gestions, which make her even more upset), the things that partners do during escalation that are painful for the other (e.g., Sue saying they are incompatible and that she wished she had married a more sensitive man), and the way they recover from conflict (e.g., Bill insist- ing that Sue apologize and her resisting, which often continues the struggle). A change in the core conflict refers to change in the underlying issue (e.g., Sue’s stressful job), but sometimes the problem is more in the pattern than in the core issue (e.g., Sue’s job is stressful, but she does not want to quit it or look for other jobs). At other times, there is a core issue that partners want to change (e.g., Sue does want to quit her job and go back to school, but that would have a big impact on their finances). In these discussions about the pattern or the core conflict, IBCT therapists try to elicit part- ners’ ideas about change before suggesting their own. When partners generate their own changes, they likely feel more ownership of them and may be more likely to implement them. IBCT therapists can also suggest
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changes if clients have difficulty coming up with pos- sibilities. If these discussions lead to constructive ideas for change, therapists can encourage the partners to attempt these changes in the following week, then de- brief them in future sessions. However, if this practi- cal discussion about change becomes adversarial, with partners pressuring and/or resisting, therapists can slip back into more acceptance-based discussions, such as empathic joining based on the emotional reactions that were triggered by the discussion or unified detachment around that pattern that just unfolded in the discussion about change.
REPLAY INTERACTIONS THAT DID NOT OR DO NOT GO WELL AND MAKE THEM BETTER
Clients report on their Weekly Questionnaire interac- tions that did not go well, interactions that are usu- ally variations of their usual dysfunctional patterns of communication. During difficult therapy discussions, clients may also return to their default modes of dys- functional communication. IBCT therapists can have clients replay those specific interactions, or replay a typical interaction, but ask them to “do it better” or “do it more constructively.” Often, therapists give these instructions after reviewing the pattern in which the couple got stuck. The initial instruction is general (“Do it better”) to see if the clients, with knowledge of how they got stuck, can use their existing repertoire of com- munication skills to have a more constructive interac- tion. If the clients have difficulty with doing the re- play in a better way, therapists can provide additional prompts, such as encouraging each to reveal more of what is going on with him/her emotionally. The idea is to provide limited instruction, just enough to get them into a more constructive interaction. After replay of an interaction, therapists debrief that experience with the clients, going over how they felt, and what they thought each did that made it go better. If clients are able to improve with limited instruction, reliance on what they already know, and review of what they did or do that makes difficult interactions go better, they are more likely to maintain any improvement.
USE CHANGE STRATEGIES FROM TBCT AS NEEDED
IBCT therapists can use all the deliberate change strat- egies of TBCT but usually employ them only as back- ups, when the strategies discussed above prove lacking.
These TBCT strategies are behavioral exchange, com- munication training, and problem solving training. Be- cause these strategies are not first-line interventions in IBCT and because there are lengthy discussion of them in multiple sources (Baucom, Epstein, Kirby, & LaTail- lade, 2015; Epstein & Baucom, 2002; Christensen et al., 2020), we only describe them briefly.
In behavior exchange (or guided behavior change, Baucom, Epstein, et al., 2015), partners try to bring about change in areas where there is not controversy and therefore do not require much communication and negotiation. Therapists may help partners specify simple actions that each might do that would bring pleasure to the partner and would not be complicated to enact. Once these possible acts have been generated, therapists may try to instigate them through a variety of assignments, such as a simple encouragement to do more of these acts during the following week or to set aside a particular day on which partners focus on doing these acts. At the subsequent session, therapists debrief the assignment and revise as needed.
The goal of communication training is to enable partners to express their feelings to each other about a significant issue or event, to understand each other’s feelings, and to do this without getting into an argu- ment. Therapists train partners in the speaker–listener technique, in which they take turns in these two roles. In the speaker role, they are trained to express their feel- ings about a topic using “I statements,” in which they describe their feelings (“I feel disappointed and upset”) about a specific partner behavior (“when you don’t call me”) in a particular situation (“when you have to work later than usual”). In the listener role, they are trained to summarize their partner’s message without evaluat- ing it or giving their response. When the speaker has come to a natural stopping point but has not talked very long, the speaker switches roles with the listener. Thera- pists use didactic instruction, modeling, and behavior rehearsal to train these skills, often starting with more innocuous topics and progressing toward more difficult ones.
Once partners are able to share and understand each other’s feelings about an issue, they are taught problem-solving techniques to bring about positive change. Therapists train the couple to generate possible solutions to the problem, to generate pros and cons of each solution, to negotiate over the possible solutions, to come to an agreement to try a solution or set of solu- tions, and then to evaluate the effect of those solution/s and, as needed, to renegotiate solutions. Therapists also
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use didactic instruction, modeling, and behavior re- hearsal to train these skills.
Termination Phase
There is no fixed number of sessions in IBCT. When partners have achieved some success in handling their difficulties and creating a closer emotional connection with each other, they may indicate a desire to termi- nate, or the therapist may suggest possible termination. Whenever that point occurs, the IBCT therapist initi- ates a termination session, in which he/she leads a dis- cussion of how the couple has improved, based on the DEEP analysis. They also discuss future challenges and dealing with possible setbacks. Therapists always leave the door open for future sessions if the couple so desires.
More detailed information on all the phases and strategies of IBCT can be found in Christensen et al. (2020).
Therapist and Client Variables Relevant to IBCT
As in any therapy, it is important that IBCT therapists maintain a nonjudgmental stance toward their clients. But in the context of IBCT, it is particularly important that the therapist practice acceptance with both part- ners in the same way that partners are asked to practice acceptance with one another. The IBCT therapist must validate the experiences and responses of both partners, and find ways to develop empathy and compassion for each of them, no matter how challenging this may be.
In addition to practicing acceptance, it is impor- tant that IBCT therapists listen carefully to couples’ in-session interactions and look for the functions of their various problematic behaviors. IBCT therapists must be particularly attentive to subtle verbal and nonverbal cues that may be relevant to the formula- tion of couples’ problems. IBCT therapists must also be prepared to abandon any prescribed agenda to ad- dress the immediate needs of the couple at any given time. When destructive interactions occur in session, the IBCT therapist must not only be able to maintain a nonconfrontational demeanor but also stop the interac- tion effectively. Other important IBCT skills include using the partners’ language and jargon when making interventions. Finally, it is not a goal of IBCT thera- pists to necessarily “cheerlead” for the success of the re- lationship; rather, they create an environment in which couples can experience the hope of finding a different way of being together, and safely discuss and evaluate their own relationships.
EFFICACY, DISSEMINATION, AND IMPLEMENTATION OF IBCT
Efficacy of IBCT
Three clinical trials attest to the efficacy of IBCT—two small pilot investigations and one major outcome study. Wimberly (1998) randomly assigned eight couples to a group format of IBCT and nine couples to a wait-list control group, and found superior results for the IBCT couples. Jacobson, Christensen, Prince, Cordova, and Eldridge (2000) randomly assigned 21 couples to ei- ther IBCT or TBCT. At the end of treatment, 80% of couples who had received IBCT showed clinically sig- nificant improvements in relationship satisfaction com- pared to 64% of couples who received TBCT.
To date, the largest study of couple therapy in general and of IBCT in particular was reported by Christensen and colleagues (2004). In a two-site clinical trial con- ducted at UCLA and the University of Washington, Christensen and colleagues randomly assigned 134 seri- ously and chronically distressed couples to either IBCT or TBCT. Couples received a maximum of 26 sessions of couple therapy delivered by professional PhD-level therapists, who provided both IBCT and TBCT treat- ments and were carefully supervised in both. Adher- ence and competence data provided evidence that treatments were delivered as expected. At termination, 70% of IBCT couples and 61% of TBCT couples had clinically significant improvements in relationship sat- isfaction. Pre- to posttreatment effect sizes on marital satisfaction were d = 0.90 for IBCT and d = 0.71 for TBCT (see Christensen, Atkins, Baucom, & Yi, 2010). Although the termination results were not significantly different, the trajectory of change was significantly different for IBCT and TBCT couples. IBCT couples improved steadily in satisfaction throughout treatment, but TBCT couples improved more rapidly early on in treatment, with their gains flattening out more than those of IBCT couples later in treatment.
Doss, Thum, Sevier, Atkins, and Christensen (2005) analyzed the mechanisms of change in this study of couple therapy. Early in therapy, changes in the fre- quency of targeted behaviors were associated with in- creases in satisfaction for both treatment conditions. However, later in therapy, changes in the acceptance of targeted behaviors were associated with increases in sat- isfaction for both treatment conditions. TBCT generat- ed significantly greater increases than IBCT in targeted behaviors early in treatment. However, IBCT generated significantly greater increases in the acceptance of tar- geted behaviors throughout treatment. Thus, the study
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validated some of the putative mechanisms of change and differences between the treatments in their impact on these mechanisms.
Subsequently, studies have examined these couples over follow-up: Christensen, Atkins, Yi, Baucom, and George (2006) looked at relationship satisfaction data in couples every 6 months over a 2-year follow-up; K. Baucom, Sevier, Eldridge, Doss, and Christensen (2011) looked at observational data at 2-year follow-up; and Christensen and colleagues (2010) examined re- lationship satisfaction and relationship status approxi- mately every 6 months over a 5-year follow-up. Couples generally maintained their treatment gains in satisfac- tion over 2 years, and IBCT couples had significantly superior relationship satisfaction compared to TBCT couples at each time point during the first 2 years of follow-up. Although TBCT couples, having been trained explicitly in communication, showed greater improvements in observed communication at termina- tion than IBCT couples (Sevier, Eldridge, Jones, Doss, & Christensen, 2008), IBCT couples showed greater maintenance of gains over 2 years (K. Baucom et al., 2011). Over the subsequent 3 years, couples lost some of their gains, and results from IBCT and TBCT con- verged. At 5-year follow-up, results for marital satisfac- tion relative to pretreatment revealed effect sizes of d = 1.03 for IBCT and d = 0.92 for TBCT; 50.0% of IBCT couples and 45.9% of TBCT couples showed clinically significant improvement. Relationship status, obtained on all 134 couples, revealed that 25.7% of IBCT cou- ples and 27.9% of TBCT couples were separated or di- vorced. None of these findings at 5-year follow-up were statistically significant. These follow-up data compared favorably to other, long-term results of couple therapy.
Three studies have looked at predictors of outcome at termination (Atkins et al., 2005), 2-year follow-up (Baucom, Atkins, Simpson, & Christensen, 2009), and 5-year follow-up (Baucom, Atkins, Rowe, & Chris- tensen, 2015). The only consistent predictor across these three time points was length of marriage: Couples who had been married longer tended to benefit more from couple therapy. Since this study included only moder- ately to severely distressed couples (almost 100 mildly distressed couples were excluded from participation), the couples who were married longer probably had more at stake and had weathered previous difficulties, so they were better able to benefit from couple therapy. It is im- portant to note that this sample, although designed to include seriously and chronically distressed couples, ex- cluded couples in which one or both partners (1) were experiencing bipolar disorder, schizophrenia, or serious
suicidality; (2) met criteria for current drug or alcohol abuse or dependence; (3) met criteria for borderline, an- tisocial, or schizotypal personality disorders; or (4) had a history of severe physical violence. The rationale for these exclusionary criteria is that for such individuals, a primary treatment other than couple therapy is likely to be indicated. However, the sample did not exclude couples in which one or both partners suffered from other psychological disorders, such as anxiety or depres- sion. The rationale for including these couples is that their relationship can still be treated despite partners having such individual problems. Furthermore, some of the couples’ relationship problems may even be contrib- uting to these individual problems. Thus, preliminary data suggest that IBCT can be successfully applied to many couples, including those in which a partner has certain other psychological disorders. For example, the preceding predictor studies found that indices of men- tal illness, including Structured Clinical Interview for DSM-IV diagnoses, were not related to improvements during couple therapy. Furthermore, Atkins, Dimidji- an, Bedics, and Christensen (2009) found that depres- sion in this sample improved as relationship satisfaction improved.
Dissemination and Implementation of IBCT in the VA
In 2010, the VA adopted IBCT as one of its evidence- based treatments. Since that time, the first author (A. C.)—along with Dr. Shirley Glynn of the VA and Dr. Peter Fehrenbach, a therapist and supervisor in two of the earlier clinical trials, as well as a psychologist in the VA—have instituted a training program for therapists in the VA. This training program consists of a 3-day workshop followed by 6–8 months of clinical super- vision. The workshop includes didactic instruction, videotaped demonstrations of IBCT, and role playing. During the workshop, trainees are organized into small groups of three to six therapists and a trained IBCT consultant. Following the workshop, therapists return to their home setting and start seeing couples under the supervision of their consultant, who talks to them in their small group weekly by phone. The trainees must audio-record at least 20 therapy sessions across at least two couples and covering the major stages of IBCT. The consultant not only listens to the recordings and provides feedback but also rates the sessions on fidelity and competence, based on rating scales used in Jacob- son et al. (2000). Trainees must achieve a specified level of competence before they can be certified as having successfully completed the IBCT training. Recently,
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the VA trainers have successfully substituted online training, which includes webinars and online role play- ing through programs such as Adobe Connect, in place of the three day in-person workshop.
To date, 21 trainings have been conducted (19 start- ing with in-person workshops and two starting with online training). Based on data from the first 18 co- horts, over 500 therapists, primarily social workers and psychologists, have entered training, and about 80% successfully completed training. The most common reason that therapists do not complete training is dif- ficulty finding appropriate cases. Over 1,000 couples have been seen by these therapists. These couples were mostly married, and usually included a male veteran in his mid-40s and a similar-age female nonveteran. Many of these couples have challenging individual circum- stances in addition to their relationship problems. For example, 22% of the veterans are disabled; 47% were diagnosed with posttraumatic stress disorder (PTSD); 20% were diagnosed with depression. These couples experience significant improvement during therapy but participate in fewer sessions (average of about 10) and evidence somewhat less improvement than what occurred in our earlier clinical trials. For example, on the four-item version of the Couple Satisfaction Index (Funk & Rogge, 2007), the last nine cohorts of couples showed significant improvement after the feedback ses- sion (d = 0.49 for veteran; 0.40 for partner), after eight sessions (d = 0.62 for veteran; 0.52 for partner), and after 12 sessions (d = 0.65; 0.51 for partner). The train- ing program and its ongoing evaluation continues (for more detail, see Christensen & Glynn, 2019).
Dissemination and Implementation of IBCT through an Online Program
The OurRelationship program (Doss, Benson, Georgia, & Christensen, 2013) is an online, self-help program based on IBCT principles that we created to increase the reach of IBCT to couples who would otherwise be unable or unwilling to seek in-person couple therapy. It is a stand-alone online program but, like the IBCT self- help book Reconcilable Differences (Christensen, Doss, & Jacobson, 2014), can be used as homework to intro- duce or reinforce many of the concepts couples learn during sessions. It can also form the foundation for an abbreviated form of IBCT (Christensen et al., 2020).
The OurRelationship program has been shown to improve relationship functioning in three separate ran- domized clinical trials (Doss et al., 2016, 2020; Roddy,
Rothman, & Doss, 2018)—more couples than have been involved in all randomized controlled trials of in- person couple therapy combined (Roddy et al., 2020). Compared to a control group, couples experienced sig- nificantly greater improvements during the OurRela- tionship program in relationship satisfaction (d = 0.53– 0.69), communication conflict (d = –0.78), emotional support (d = 0.46), relationship confidence/break-up potential (d = 0.47–0.53), and intimate partner violence (d = –0.10). Furthermore, these effects lasted for at least a year after the end of the program (Doss, Roddy, Now- lan, Rothman, & Christensen, 2019; Roddy, Knopp, Georgia Salivar, & Doss, 2020).
The OurRelationship program has also been shown to significantly improve both mental and physical health when compared to a control group. In both na- tionally representative samples (Doss et al., 2016) and samples of low-income couples (Roddy, Rhoades, & Doss, 2020), the OurRelationship program has im- proved depressive symptoms (all individuals: d = –0.36 to –0.50; initially distressed individuals: d = –0.42 to –0.71), as well as anxious symptoms (all individuals: d = –0.21 to –0.36; initially-distressed individuals: d = –0.42 to –0.94). Participants also reported decreases in perceived stress (all individuals: d = –0.42; initially dis- tressed individuals: d = –0.48), anger (all individuals: d = –0.23; initially distressed individuals: d = –0.39), and problematic alcohol use (all individuals: d = –0.11; initially distressed individuals: d = –0.33).
Couples participating in the OurRelationship pro- gram, compared to couples in a control group, expe- rience significantly greater improvements in perceived health (all individuals: d = 0.14–0.23; initially dis- tressed individuals: d = 0.51–0.54), insomnia (all indi- viduals: d = –0.17; initially distressed individuals: d = –0.40); quality of life (all individuals: d = 0.18; initially distressed individuals: d = 0.44); and work functioning (all individuals: d = 0.19; initially distressed individuals: d = 0.57).
CASE STUDY
We describe the case example of “Anne” and “Mark”2 to demonstrate the application of IBCT. Anne and Mark, a middle-aged couple, had been married for 10 years at treatment onset and lived with Anne’s three children from her previous marriage. We include excerpts from the assessment, feedback, and intervention sessions with Dr. S to illustrate acceptance-building interventions.
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Assessment and Feedback Sessions
The three assessment sessions provided clear informa- tion on the couple’s problems and revealed no intimate partner violence and no affairs. During this assessment phase, opportunities for open disclosure and building ac- ceptance presented themselves. At one point during Ses- sion 1, Anne made a soft disclosure when she discussed a time when she had initially rejected Mark (who had asked her to dance). Anne said that when Mark did not get angry with her after she rejected him, she felt safe with him, because she could be herself and he would not get mad at her. She reported that this quality about Mark attracted her to him. Mark, who had initially reported feeling humiliated by Anne’s rejection, responded to Anne’s soft disclosure by saying, “I’m kind of surprised by that. I know that is an important feeling for her, but I didn’t realize she was feeling that back then.” Anne said that she had not realized she felt that way either, until describing the incident in the therapy session.
During the feedback session, Dr. S summarized their levels of relationship satisfaction (both scored in the distressed range) and their level of commitment (both were highly committed to the relationship). Then Dr. S described their areas of difficulty, emphasizing the emotional reactions these difficulties aroused in each of them:
“So let’s talk about the areas of your relationship that are troubling. One area is finances; that tends to be an area of dispute. For you, Anne, feeling resentful sometimes, feeling the burden of the responsibility, and for you, Mark, feeling guilty about how things are financially. This area really brings out lots of dif- ferent feelings—feelings of resentment, feelings of guilt, feelings of burden—and rather than feelings of closeness and togetherness, feelings of control. Does that sound accurate? Are there any other aspects of finances that the two of you can think of?
“The other area I saw was with regard to Anne’s children. You both feel very differently about the subject of Anne’s children: Anne, you feel like Mark is not involved with your children, and Mark, you feel as though you have not been invited. For you, Mark, the experience of being rejected [by the chil- dren] is Anne’s fault. This is an area that brings out very strong feelings for both of you, whether it gets expressed directly or not. You may not talk about it, but I definitely got the sense that this is a real pres- sure cooker for both of you. This is an area that I
imagine will come up in different ways, especially with the holidays coming up.
“The third area I saw concerns responsiveness (‘How responsive are you to me?’). Whether you are being physical (‘You’re not responsive enough’ or ‘You’re too responsive’), listening (‘Are you listening to me?’), touching, or asking a question, your actions can carry a message of what you want to express, or a feeling that you are having. So part of what we will work on is expressing those feelings you are having. Those may be a surprise for each of you.”
Throughout each of his descriptions, Dr. S checked in with Anne and Mark for their feedback about each problem area, and the ways that they might add to his description.
Even during this part of the feedback session, an op- portunity for acceptance work presented itself. When Mark discussed his relationship with Anne’s children, he was initially making only “hard” disclosures, by de- scribing her children as rude and only able to talk about themselves. Because Mark made such critical state- ments about Anne’s children, Dr. S elicited from Mark some softer disclosures about his emotions with regard to Anne’s children:
DR. S: Besides them being rude, what is the feeling you are left with when [Anne’s children] don’t talk to you?
MARK: The feeling I’m left with is being ignored. DR. S: Besides being ignored, how did it feel? MARK: Like I don’t matter, like I am only there to serve
them. DR. S: Like you are not a part of the family. MARK: Yeah. I think I’ve just resigned myself to hoping
that they’ll show their love for their mother. DR. S: So it upsets you that they don’t take an interest
in their mother? So it isn’t just about you, you have some feelings about how Anne’s sons interact with her?
MARK: Yeah, yeah, I do. DR. S: And that upsets you? MARK: Yeah, it does. I feel protective. I’d like them to
show more appreciation to her. But then, I’d like my- self to show more appreciation to her. I don’t think I show enough appreciation to her. Maybe they’re relat- ed . . . it’s a reminder of the things I’m not doing well.
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By moving Mark from criticizing Anne’s children to making softer statements about his feelings, Dr. S gave Mark an unexpected opportunity to make important realizations about his own behavior—his emotional sensitivity.
After reviewing their problem areas, Dr. S proceeded to describe the two themes he had observed from his assessment of Anne and Mark. In both themes, he em- phasized the emotions that each partner was experienc- ing:
“I think the first theme is that you both have feel- ings of being unloved and unappreciated. You have an idea of what it means to be loved. You have an idea of what it means to be appreciated. But your definitions are different. And because of those dif- ferent definitions, because of your different experi- ences, if something does happen, it leaves you feeling unappreciated and unloved. Within the arguments about finances or children, there is something about that—about feeling unappreciated. How does that sound to you?
“The second theme is that you both have your in- securities. You both have feelings of insecurity, for whatever reason. Some of the arguments, the differ- ences, the conflicts, the big fights, come from that also. That feeling comes up and can create the whole battle. A concrete example is that you, Anne, de- scribed feeling insecure about yourself in relation to some of your family members. That affects how you feel about yourself in comparison to other women. Mark, you described feeling insecure about the fact that Anne has not annulled her previous marriage. That may affect how confident you feel in compari- son to other men. Again, these feelings of insecuri- ty, feeling not loved, unappreciated—these are the themes.”
After Dr. S described each theme—and some of the related differences, emotional sensitivities, and external stressors—and received feedback from Anne and Mark about these themes, he moved on to discuss their pat- tern of communication or polarization and the resul- tant mutual trap:
“Now, what is this thing we call the ‘trap’ that you both get into? You each have different ways of re- sponding to feeling unloved and insecure. The sense that I get is that, Mark, when you start to feel those things, you use distance. The sense I get from you,
Anne, is that you become critical. Put the two of you together, and you have a cycle: The feelings come up, Mark gets distant, and Anne gets critical. Mark feels criticism, he gets distant. Anne experiences the dis- tance, she gets critical. Distance, criticism, criticism, distance. That’s what we call the trap. It may be that you take turns being critical and distant, and that each response makes the other person feel even more insecure.”
After reviewing the polarization process and mutual trap, Dr. S proceeded to explain to Anne and Mark what to expect from the upcoming therapy sessions. In the brief excerpt below, he describes the goals of open disclosure as a way of preparing the couple for empathic joining:
“What I hope to do is create in here a place of com- fort, enough that you can both take risks in open- ing up, in sharing—sharing some of your reactions, your questions, your experiences. There is a desire for closeness here that is going to take some sharing and some risk taking. Now, there’s no guarantee about how the other person is going to react. It may not always be pleasant. But on the other hand, that’s the price we have to pay to get there, to open up. You can do some more thinking about this and from week to week we can reformulate, and we’ll keep getting a clearer, better picture.”
Intervention Sessions
Most of Anne and Mark’s subsequent intervention sessions were focused on building acceptance using empathic joining, unified detachment, and tolerance building. Below are excerpts from two sessions in which Dr. S helped Anne and Mark to increase acceptance by using techniques such as empathic joining, unified de- tachment, and tolerance building.
A Richer Man, a Younger Woman?
The content of this session was about Anne and Mark’s search for a condominium, but that led to an explora- tion of both of their insecurities:
MARK: If we settle for a condominium that we don’t really want, it will forever be a monument to my in- ability to get the condo she wants.
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DR. S: I’m wondering if there’s another part that won- ders, “Will I ever really be able to give her what she wants?”
MARK: Yeah. If she married somebody who had a lot of money, she could get whatever condo she wanted.
ANNE: But if you married someone who was gorgeous, who was 20 years younger, you could have a trophy wife, but that’s not what happened. (Both laugh.)
DR. S: So that may be part of your insecurity. If you looked the way that you experience as “the way he wants things,” then maybe he’d be happier.
MARK: (to Dr. S) I think that’s how she feels about herself at her worst moments. Like maybe all men are attracted to younger women and that you have to harness yourself not to lose what’s important to you . . . (to Anne) Maybe that’s how you look at your desire to have your dream condo. How do you keep from saying, “There’s that rich lawyer who looks at me all of the time”? . . . (to Dr. S) I think that would be a pretty natural thing for her to think about.
This dialogue also reveals the unified detachment Anne and Mark are developing, when they both laugh at Anne’s comment about a “trophy wife.” What has previously been a very painful subject for Anne is be- coming something about which they can joke. The discussion then moved to exploring Anne’s insecurities about Mark’s relationships with other women:
DR. S: So what in your eyes is Mark’s ideal “bill”? You made reference to a “bill” that is his ideal.
ANNE: Well, probably someone younger, who is able to have children, someone who plays tennis, who goes running and also cooks and cleans, makes a good living, is very good in bed . . .
DR. S: (to Mark) Because this is comparable to the rich- er man that you view with Anne. (to Anne) For you, it’s the woman who . . .
ANNE: But that woman’s out there. A lot of women are like that.
DR. S: And the way that you see and experience Mark talking to women. And at times you kind of wonder to what extent he enjoys it, and you think it’s just a matter of time if you’re not willing to live up to it . . .
ANNE: Right, that some other women is going to be able to step right in there without a problem.
DR. S: When the insecurities come up for both of you.
For you, Mark, it’s the rich man who could come along and provide what Anne longs for, and for you, Anne, it’s that you don’t compete physically—with the workout—so it’s just a matter of time until a woman comes along and decides, “I’m going after him.” Anne, can you tell me some of the things Mark does that make you feel threatened?
ANNE: When he makes comments about how attractive a woman is, like I’m one of the guys. When he tells me I’m fat, or makes comments like I have a double chin . . .
DR. S: Which then tells you that you’re not cutting it. ANNE: Yeah.
Dr. S then brought back the subject of condomini- um buying, and used this as a metaphor for Anne and Mark’s concerns about “settling” for less than what they want in making a major commitment:
DR. S: When you make a commitment, whether it’s committing to a condo, committing to a relation- ship—it’s settling, you’re settling—you’re saying, “This is it.”
ANNE: That’s a good way of looking at it. I hadn’t thought of that. That’s what we’re having trouble with . . . the reality that we’re not going to get ev- erything that we want. The insecurity, the scariness of making the purchase, is knowing that we’re never going to get what we want.
MARK: Part of it is our concern that the next condo- minium we see is going to be the one we want.
ANNE: Right, it’s the condo over the next hill. MARK: So you have to think, “Is 60% of what we want
what we should settle for?” I’m thinking, 60? I was thinking it’s more like 90. So I don’t know when you’re supposed to cut your losses and say we have to go for this—this is what reality dictates.
DR. S: And if we can take it a step further, it might be that when you both decided to get married, you both made a settlement. You both start to wonder whether the other settled for 60 or 90%. You wonder, “What did I settle for? Did I settle for 60 or 90%?”
MARK: Yeah. ANNE: Right. DR. S: Now let’s put yourselves in a situation where
you’re insecure. What’s gonna happen? When you’re in an insecure place, that 90% might feel like . . .
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ANNE: 50%. DR. S: Exactly. When you’re feeling good, you think,
“She got 90% of what she wanted in me,” or “I got 90%.” But when you’re in an insecure place, you think, “I settled for 50%.” Then when you look at your own insecurity, you think, “My God, she set- tled for 35 or 40%.” You both made a settlement when you married each other. You decided, “This is it, we’re gonna get married,” and you settled.
MARK: But “settled” has such negative connotations. DR. S: I think there’s some feelings associated with
that. And a parallel to the word “settlement” is “ac- ceptance.”
MARK: Oh, I see. DR. S: When you go through the settlement, you think,
“This is who this person is.” Whether it’s 90, 80, 60, or 35%, you’ve settled—you’ve basically said, “I ac- cept this.”
By using condominium buying as a metaphor, Dr. S has underscored how Anne and Mark’s theme of insecurity feeds itself, and how it leads them both to question whether each has “settled” for less than he/she wanted in the relationship. Adding the additional com- ponent of “insecurity about settlement” to their theme helped Anne and Mark understand the things each of them do that “threaten” the other (e.g., when Mark talks about his attraction to younger women), and also build a bridge toward working on acceptance.
The Emotional Underpinnings of Fights over Advice
In this session, Dr. S continues to process the theme of insecurity with Anne and Mark. In this particular part of the dialogue, when Anne and Mark are discuss- ing a familiar polarization process, Mark suggests to Anne that she work out more. Anne interprets Mark’s suggestion as a criticism about her appearance, which makes her feel insecure and threatened. Anne then “fights back” against Mark’s suggestions by becoming depressed and “doing nothing,” which in turn makes Mark more critical of her.
Here Dr. S uses two IBCT acceptance-building tech- niques. The first technique is empathic joining. As Dr. S tries to “get to the bottom of” Mark’s suggestions/ criticisms of Anne’s appearance, Mark makes the fol- lowing soft disclosure about his own insecurities:
DR. S: This is a real, central question. There are some basic limits that you have, where you say, “Up to here, I accept you, but beyond that, you’d better change.” On the other hand, this is who you are. This is who you are. But the irony of it is, that once we accept, change can come about. But there’s that push to de- termine within ourselves not only the other person’s limits but also our own. I get the sense that you’re both exploring yourselves and your own limits.
ANNE: Perhaps, yes. DR. S: You’re both looking at your own limits. With
you, Anne, it’s about your looks, your appearance. And for you, Mark, it’s about you as a financial pro- vider. And the temptation is, when that gets uncom- fortable, that’s where your partner comes in kind of, to redirect your focus from that versus being able to talk about how you’re feeling.
ANNE: Yeah. MARK: Yeah, I think I’ve noticed, since we’ve started
therapy, that’s what I do. When I get insecure about myself, I start looking outwards, saying, “You should do this,” and that makes me feel better.
DR. S: Right, it’s active. It can be advice giving—it can be a real male thing, “Do this, do that.”
MARK: Right, I do that with her kids, too. I know I do.
Instead of focusing on the critical nature of Mark’s suggestions, Dr. S has placed an emphasis on why Mark becomes critical. Mark is encouraged to consider the reasons for his behavior, and as a result discloses that he becomes critical when he himself is feeling insecure. Mark recognizes that this happens not only with regard to his attempts to direct Anne’s behavior but also in his interactions with Anne’s children.
The second acceptance-building technique Dr. S uses in this portion of the session is a tolerance inter- vention: emphasizing the positive aspects of a partner’s negative behavior. Dr. S continues:
DR. S: In some situations it might work really well [to give advice]. People might like that—like in your work as a counselor, Mark. You feel really produc- tive.
MARK: Yeah, I change people’s lives. I know I do. DR. S: On the other hand, there might be some circum-
stances where it’s experienced as being critical, and I
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think of this in terms of the two of you. It feeds into Anne’s feeling criticized.
ANNE: Yes. DR. S: And then it feels threatening, like “If you don’t
do something about it, then . . . ”
Here, Dr. S has positively reemphasized Mark’s sug- gestions to Anne as his attempts to give her guidance or advice. Mark, an employment counselor, is used to giving such suggestions to others as a way of being constructive or helpful. Dr. S underscores this aspect of Mark’s be- havior—that this same “counselor” quality makes Mark very good at what he does in his career. However, Dr. S does not try to reframe Mark’s behavior as completely positive. Dr. S also underscores how Mark’s “advice” is experienced by Anne as critical and threatening.
At the end of the session, Dr. S recharacterizes Anne and Mark’s polarization process in terms of the infor- mation that has emerged from these two interventions:
DR. S: I think you put it really well, Mark. When you start to feel uncomfortable, this is your process, this is what you do. You start to look outside yourself. From your end, it might be like you’re being a coun- selor when you start with Anne. You want to advise. But from her end, it might be like you’re being au- thoritarian, the drill sergeant rather than the coun- selor. And you, Anne, start to feel you’re being be- rated. You start to feel worse about yourself.
ANNE: Yeah. DR. S: So you feel like you’ve gotta either take it, or
you’ve gotta fight back. MARK: I think I can . . . the fighting back is . . . well, I
can understand that. I really can.
Termination Session
In their final session, Anne described a recent insight she had had about feeling “undeserving” of happiness, and her belief that happiness comes at a cost of some kind. She said that happiness made her feel guilty, be- cause she felt that someone else must be suffering for her happiness, or that somehow she would suffer negative repercussions for being happy. Anne connected some of these feelings to her bout with an eating disorder as a teenager, and to the depressive episodes she sometimes experienced as an adult.
In the dialogue below, Dr. S uses several IBCT tech- niques to discuss Anne’s insights and the way that her feelings contribute to the couple’s polarization process. First, Dr. S uses empathic joining to help Mark under- stand the experience Anne is having when she gets de- pressed (a time when Mark regularly makes suggestions about how Anne “should” think, feel, or behave). Then Dr. S detaches Anne and Mark from their problem— that Anne feels criticized whenever Mark makes these suggestions. Rather than engaging Anne and Mark in their emotional responses to each other’s behavior, Dr. S framed this problem as a consequence of basic com- munication problems. By describing their problem in terms of their methods of communication, Dr. S de- taches Anne and Mark from the problem itself, and pro- vides each with a new way of reacting to an old problem (without doing any formal communication training):
DR. S: I think the idea around the conflict over hap- piness—having the happiness—is like savoring a good meal, and that it will cost you: “OK, so it has some high fat, but I’m going to enjoy it because I deserve this, I deserve this moment—the same way that I deserve this moment of happiness, even if so- and-so doesn’t have it together. I deserve this happi- ness.” And that’s going to be the struggle, to be able to react to Mark in a way that expresses, “God, I’m really feeling guilty.”
ANNE: When I’m on the couch, and I’m totally immo- bile in my depression, that’s a lot of what’s going on. I’m beating myself up.
DR. S: And so Mark needs to listen, to just listen and say, “Gee, that must be really hard.” Now there may be a pull, Mark, to problem-solve, to say, “Well, you shouldn’t feel that way,” or “So-and-so is that way because . . . ,” but that will only bring out Anne’s self- criticism and it could become argumentative. When you sense the pain, Mark, and what it’s costing Anne, the reaction that you have is “Let me show you what to do.” But that is only going to bring out in Anne the feeling of “You see, you idiot, you’re not doing it right,” which will then feed into the self-criticism. So it’s going to help to just listen, and simply to para- phrase, and she will hear that it’s not reasonable. If, rather than criticizing, you just say, “Gee, you really don’t feel worthy of these things,” if you just para- phrase those themes of her insecurity, her self-crit- icalness, that is kind of maintaining a connection.
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Finally, Dr. S uses tolerance interventions to allow Anne and Mark to see their problem as a difference in their communication styles. As he continues to describe their problem in terms of communication difficulties, Dr. S describes Anne as responding to situations based on how she feels, while Mark is more likely to use logic or reason to determine his responses to situations. Dr. S also points out how Anne and Mark’s problem is often a result of this difference, and that these differences actu- ally complement one another:
DR. S: (to Mark) And that’s what I want to encourage, maybe a new way of responding rather than using reason when you start to feel like Anne’s feelings don’t make sense. Rather than saying, “This doesn’t make sense,” say instead, “What I’m hearing you say is that you don’t deserve this”—whatever it is. And what I’m expecting, Anne, is that to hear Mark ex- press that he understands you would make you feel close to him.
ANNE: Yeah, and it would definitely not be the wedge of “you should.” (Mark laughs.)
DR. S: Anne, you talk about things from the emotional experience, and Mark, you talk about things from the rational experience—and both are needed, both are important.
This section of the dialogue also reveals how Anne and Mark have developed unified detachment from their problem. Anne uses the phrase “the wedge of ‘you should’ ” to describe what had previously been the “hot topic” of feeling criticized by Mark, and Mark is able to laugh about his own behavior.
Even when couple therapy is successful in improving a couple’s relationship satisfaction, as it did with Mark and Anne, the therapy does not completely resolve their problems or even come close to such complete resolu- tion. Mark and Anne will continue to have struggles triggered by their long-standing insecurities. However, therapy helped them manage those struggles better at times through empathy for the other and through humor. It also helped them accept their struggles and thus not be as emotionally jolted by them and to be better able to recover from them. And finally, through the empathic and repeated exploration of each one’s emotional experience, Mark and Anne grew emotion- ally closer to each other. Those are the outcomes we seek in IBCT.
CONCLUSION
Although a single case study is useful for illustrative purposes, it obviously does not establish generalizable conclusions about treatment outcome. However, the studies we have described provide strong evidence for the efficacy of IBCT. They also provide extensive evi- dence for its effectiveness in a broad-scale implementa- tion through the VA and through an online program.
IBCT is part of what Hayes (2004) has called the “third wave” of behavior therapy. The “first wave” en- compassed traditional classical and operant condition- ing approaches. The “second wave” incorporated cogni- tive strategies. The third wave emphasizes “contextual and experiential change strategies in addition to more direct and didactic ones” (p. 6). Acceptance and mind- fulness are key aspects of these third-wave therapies. Although these therapies have generated considerable enthusiasm and confirming data, only additional out- come research will establish whether these therapies in general or IBCT in particular will work to alleviate human suffering, including the substantial suffering that occurs in couple relationships, in more powerful ways than the first two waves of behavior therapy.
RESOURCES FOR LEARNING AND IMPLEMENTING IBCT
Treatment Manual for IBCT
Christensen, A., Doss, B. D., & Jacobson, N. S. (2020). Inte- grative behavioral couple therapy: A therapist’s guide to creat- ing acceptance and change. New York: Norton. (This is a revision of Jacobson & Christensen, 1998.)
Self‑Help Book on IBCT
Christensen, A., Doss, B. D., & Jacobson, N. S. (2014). Rec- oncilable differences (2nd ed.). New York: Guilford Press. (This is a revision of Christensen & Jacobson, 2000.)
Online Intervention Based on IBCT
www.ourrelationship.com Information on how to integrate the online interventions into
individual and couple therapy: www.ourrelationship.com/ therapists
Video Illustrations of IBCT
Heterosexual couple seen by Andrew Christensen: www.apa. org/pubs/videos/4310904.aspx
Couple Distress 769
Gay couple seen by Christopher Martell: www.apa.org/pubs/ videos/4310939.aspx
Website on IBCT
This website contains resources on IBCT, including a list of therapists throughout the country who have been trained in IBCT: https://ibct.psych.ucla.edu
Couple Therapy Resources for Veterans
Treatment Works for Vets website: www.treatmentworksforvets.org
Description of IBCT and videos on IBCT on this website: www.treatmentworksforvets.org/proven-treatment-for- relationship-distress
NOTES
1. We use the more inclusive term couple therapy rather than the more limited marital therapy, because the former can refer to unmarried couples as well as married couples.
2. Identifying information has been changed to protect con- fidentiality, but clinical dynamics are accurately portrayed, and quotations are taken directly from tapes of the therapy sessions but altered slightly to increase readability.
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773
Aaronson, C. J., 16 Aaronson, S. T., 263 Aasland, O. G., 564 Abbott, M. J., 113, 185 Abbott, P. J., 619 Abel, G. G., 66 Abela, J. R. Z., 274 Abrahamsson, T., 621 Abramowitz, J. S., 11, 134, 135, 139, 140,
142, 144, 146, 152, 153, 159 Abrams, D. B., 588, 618 Abramson, L. Y., 448 Achermann, P., 639 Acierno, R., 341, 342, 355 Adamson, G., 526 Addington, D., 531 Addington, J., 531 Addis, M. E., 341, 342, 344 Adelson, M., 620 Aderka, I. M., 108, 109 Adler, C. M., 484 Adler, G., 384 Ágh, T., 708 Agras, W. S., 2, 4, 13, 226, 318, 390, 711 Ahern, 144 Ahrens, A., 191 Aikins, D., 24 Akerman, C. J., 683 Akerstedt, T., 658 Akiskal, H. S., 134, 495 Aksut, D., 135 Alarcon, R., 72 Albano, A. M., 219 Albert, I., 383 Albon, J. S., 260
Alcaine, O. M., 185 Aldao, A., 118 Aldaz, C., 663 Alden, L. E., 110, 112 Aldinger, F., 485 Alford, B. A., 259 Alho, H., 621 Allen, E., 737 Allen, J. J., 146 Allen, L. B., 14, 185, 221, 223, 384 Allerdings, M., 676 Allgulander, C., 190 Allmon, D., 388 Allot, K., 531 Alloy, L. B., 486 Alneas, R., 5 Aloia, M., 651, 655 Alonso, J., 109 Alpers, G., 221 Alterman, A. I., 616 Altman, B., 71 Altshuler, L. L., 485 Amass, L., 620 American Academy of Sleep Medicine, 640 American Foundation for Suicide
Prevention, 444 American Medical Association, 742 American Psychiatric Association, 1, 2,
3, 4, 5, 19, 69, 184, 219, 297, 318, 327, 382, 383, 418, 444, 450, 481, 523, 556, 613, 640, 705, 706, 742
American Psychological Association, 75, 449
American Society of Addiction Medicine, 572
Amering, M., 4, 5 Ametaj, A. A., 218, 451 Amick, A. E., 74 Amir, S., 639 Amiri, M., 343 Amole, M. C., 320 Amrhein, C., 9 Ancoli-Israel, S., 640, 644 Anderson, B. P., 486 Anderson, D. A., 463 Anderson, D. J., 4 Anderson, L. M., 463 Anderson, R. A., 143 Andersson, G., 11, 261 Andover, M. S., 446, 447 Andreski, P., 640 Andrews, B., 549 Andrews, C. M., 620 Andrews, G., 6, 11, 14, 25, 140, 188, 220,
264 Andrews, N. R., 619 Angst, J., 135 Annis, H. M., 569 Ansell, E. B., 382 Anstee, J. A., 10 Antonuccio, D. O., 263, 264, 340 Antony, M. M., 8, 9, 14, 109, 110, 135,
189, 223 Appelbaum, A. H., 384 Appelo, M. T., 387 Appleman, E. R., 640 Appleton, C., 268 Arancio, C., 9 Arbid, N., 189 Arch, J. J., 31, 187
Author Index
774 Author Index
Arendt, M., 11 Arfken, C. L., 621 Arger, C. A., 619 Arias, B., 119 Arkowitz, H., 233, 455 Armento, M. E. A., 343, 355 Armey, M. F., 448, 449 Armitage, R., 662 Armstrong, H. E., 388 Arnow, B. A., 13, 286, 675 Arntz, A., 13, 15, 27, 268, 274 Arrindell, W., 13 Arsenault-Lapierre, G., 446 Asarnow, J. R., 445 Asbahr, F. R., 143 Asberg, M., 153 Asher, M., 109, 119 Askenasy, J. J. M., 639 Asmundson, G. J. G., 675, 676 Asnaani, A., 108, 109 Asselmann, E., 7 Atkins, D. C., 388, 760, 761 Attal, N., 672 Atwoli, L., 64, 65 Atwood, G. E., 684 Atwood, M. E., 711 Auchterlonie, J. L., 66 Auerbach, R. P., 126, 274 Austin, D. W., 11 Austin, S. B., 444 Aveneoli, S., 220 Averill, P. M., 26 Avery, L. M., 492 Aviram, R. B., 381 Axelrod, R., 66 Axelson, D. A., 482, 484, 491, 495 Ayduk, O., 121 Azrin, N. H., 619
B
Babat-Zinn, J., 210 Babeva, K. N., 445 Babor, T. F., 564 Babuscio, T., 585 Baca-Garcia, E., 444 Bachman, J. E., 676 Bachofen, M., 11, 142 Badger, G. J., 619, 620, 622 Baer, L., 135, 136, 159 Baetz, M., 448 Bagby, R. M., 260 Bagge, C. L., 382 Baier, A., 590
Bailey, E., 354 Bailey-Straebler, S., 706, 737 Baillie, A., 109 Bair, M. J., 675, 676 Baird, C. L., 683 Baity, M. R., 74 Baker, J. P., 112 Baker, M., 523 Balbuena, L., 448 Baldessarini, R. J., 485 Baldwin, D. S., 14, 190, 191 Baldwin, G., 620 Baldwin, L. E., 26 Baldwin, S. A., 743 Baler, R. D., 557 Ball, J. R., 275 Ballenger, J. C., 184, 185 Bandelow, B., 7, 190 Banks, S. M., 675 Bär, K., 675 Baracaia, S., 655 Barbee, J. G., 185 Barber, J. P., 120, 265, 268, 335 Barbui, C., 385 Barlow, D. H., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10,
13, 14, 15, 16, 19, 21, 23, 26, 28, 29, 31, 32, 33, 35, 112, 119, 187, 188, 189, 191, 217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 230, 234, 235, 237, 258, 384, 403, 446, 447, 449, 450, 453, 454, 455, 460, 462, 463, 465, 586, 664, 705
Barnhart, R., 383 Barnhofer, T., 266 Barnicot, K., 383 Barnoski, R., 390 Barns, T. R. E., 531 Barraca, J., 343 Barrantes-Vidal, N., 487 Barratt, S., 532 Barrera, M., Jr., 341 Barrera, T. L., 121 Barrett, L. F., 112 Barrett, M. S., 275 Barrett, P., 143, 144 Barrios, F. X., 681 Barrowclough, C., 523, 530, 549, 550 Barry, L. C., 673 Barry, T., 642 Barsky, A. J., 2, 144 Barth, S. K., 66 Barthel, A. L., 190 Baruch, D. E., 354 Basco, M. R., 275 Basoglu, M., 17, 28, 135, 150 Bastien, C. H., 644, 645
Batalha, L., 756 Bateman, A., 384, 385, 445 Bates, M., 464 Baucom, B. R., 760, 761 Baucom, D. H., 743, 759, 761 Baucom, K. J. W., 761 Bauer, M. S., 482, 488 Baumeister, H., 261 Baumeister, R. F., 448 Baumeister, S. E., 583 Beach, B. K., 275, 390 Beach, S. R. H., 742, 743 Bearden, C., 485 Bearman, S. K., 664 Beauchaine, T. P., 393, 449 Beaulieu, S., 482 Bebbington, P. E., 526, 530 Bechara, A., 556 Beck, A. T., 31, 111, 119, 144, 225, 234,
235, 257, 258, 259, 264, 269, 275, 281, 296, 319, 323, 341, 343, 346, 351, 362, 386, 387, 416, 445, 446, 448, 523, 524, 615, 625, 654
Beck, J. G., 26, 27, 28 Beck, J. S., 259, 654 Becker, E. S., 7 Becker, J. V., 66 Bedics, J. D., 388, 761 Beekman, A. T. F., 262 Beem, C., 569 Beens, H., 144 Beesdo-Baum, K., 4, 7 Beglin, S. J., 713 Behar, E., 185, 186 Beidel, D. C., 119 Beissner, K., 683 Bekman, N. M., 563 Belanger, L., 184 Bell, J. L., 355 Bellack, A. S., 619 Belleville, G., 644 Bellgrove, M. A., 557 Bellino, S., 260, 386 Bellivier, F., 483 Bellodi, L., 9, 135 Belluardo, P., 262 Belnap, B. H., 230 Bender, D. S., 382 Bendit, N., 389 Benedetti, F., 664 Benefield, R. G., 590 Benger, M., 110 Benjamin, L. S., 343, 382, 395, 495 Bennett, C. B., 128 Bennett, M. E., 560, 619
Author Index 775
Bennett, S., 5 Bennett, S. M., 218 Bennett-Levy, J., 342 Benowitz, N. L., 613 Benson, L. A., 762 Bentley, K. H., 225, 229, 443, 446, 447,
448, 450, 451, 455, 458, 460, 461, 464, 465, 466, 468
Ben-Zeev, D., 448, 449 Berchick, R. J., 416 Berenbaum, H., 112 Berger, A., 191 Berger, M., 110 Berglund, P., 4, 64, 65 Bergman, R. L., 146 Berkman, N. D., 711 Berle, D., 222, 450 Berlin, K. S., 343 Berliner, L. A., 75, 383 Berman, B. M., 683 Berman, S. R., 645 Berna, C., 675 Berndt, E. R., 258 Berra, Y., 497 Berry, C., 317 Berry, K., 522, 523, 528, 530, 532 Bertani, A., 9 Bertenthal, D., 676 Bertollini, R., 264 Bertolote, J. M., 446 Besset, A., 639, 663 Best, C. L., 64, 66 Bhangoo, R. K., 481 Bhaskara, L., 25, 26 Bianchi-Salguero, J. M., 343 Biancosino, B., 385 Bickel, W. K., 618, 620 Biederman, J., 4 Bieling, P. J., 110 Biesheuvel-Leliefeld, K. E. M., 263 Bigda-Peyton, J. S., 126, 274 Bigelow, G. E., 618, 621 Biggs, M. M., 259 Biglan, A., 340 Billiard, M., 639, 663 Biondi, F., 8 Birchwood, M., 524, 547, 548 Bird, V., 526, 530 Birmaher, B., 481, 482, 491, 515 Birnbaumer, N., 9 Bisdounis, L., 642 Bishop, F. M., 560 Bishop, S., 259, 681 Bisson, D. I., 383 Bisson, J. I., 75, 76
Bittencourt, J., 191 Bittner, A., 4 Biuckians, A., 487 Bixler, E. O., 641 Björgvinsson, T., 126 Black, D. W., 5, 386, 446 Blackburn, I. M., 259, 262, 342 Blain, L. M., 76 Blairy, S., 343 Blais, F., 662 Blake, C., 684 Blake, R., 655 Blakey, S. M., 139 Blanchard, E. B., 71, 73, 676 Blanco, C., 258 Bland, J. M., 354 Bland, K., 13 Blatt, S. J., 335 Blazer, D., 381 Bleiberg, K. L., 72, 317, 318, 319, 320, 326 Blevins, D., 189 Bliss, P., 354 Block, R. I., 8 Blonigen, D. M., 558 Blum, N., 386, 387, 446 Blumenthal, R., 230 Bobb, K., 74 Boccagno, C., 444 Bockting, C. L. H., 263 Bodden, D., 144 Bode, K., 382 Boden, M. T., 112 Bodenlos, J. S., 355 Boelen, P. A., 221 Boergers, J., 448 Boersma, K., 673 Boesky, L., 390 Boettcher, H., 230, 446, 455 Bogduk, N., 671 Bogels, S. M., 144 Bogenschutz, M., 577 Bogetto, F., 260 Bohlmeijer, E. T., 230 Bohn, K., 712, 713, 729 Bohn, P., 9 Bohni, M. K., 11 Bohus, M., 382, 383, 385, 389, 403 Boland, R. J., 258, 262, 266, 306 Bollini, P., 259 Bolton, E., 523 Bolton, J. M., 468 Bond, F. W., 192 Bond, R., 756 Boness, C. L., 568 Boney-McCoy, S., 571, 749
Bonn, J. A., 28 Bonnin, C. M., 488 Bootzin, R. B., 639 Bootzin, R. R., 641, 652 Borbély, A. A., 639 Borden, J. W., 159 Bordin, E. S., 120 Borge, F. M., 109 Boritz, T., 383 Borkovec, T. D., 185, 186, 187, 188, 191,
225, 235, 342, 641 Bos, E. H., 387 Boschloo, L., 259 Boswell, J. F., 221, 344, 451, 463, 465 Bothwell, S., 343 Bottlender, R., 481 Bouchard, S., 11, 27 Bouhassira, D., 672 Boulougouris, J. C., 141 Boulter, N., 144 Bouman, T. K., 4 Bourke, M. E., 381, 382, 383 Bouton, M. E., 7, 8, 9, 17, 29, 139, 219,
221 Bowen, G. R., 72 Bowen, R., 448 Bowen, S., 589 Bowers, W., 5 Bowers, W. A., 259, 262 Bowlby, J., 319 Bowler, K., 276 Bowman, J., 109 Boyd, J. L., 501 Boyer, E. W., 621 Bozzatello, P., 386 Brabban, A., 523, 531 Bracha, Y., 621 Bradford Reich, D., 382 Bradley, R. G., 384, 390, 393 Bradwejn, J., 110, 259 Brausch, A. M., 448, 453 Breen, C., 620 Brennan, L., 711 Brennan, M. B., 77 Brenner, C. A., 523 Brent, D. A., 382 Brereton, A., 448 Breslau, N., 640 Breuer, P., 8 Brevers, D., 556 Brewin, C. R., 17, 68, 69, 383 Brick, L., 448 Briere, J., 383, 444 Bright, P., 9 Brockmeyer, T., 711
776 Author Index
Brodsky, B. S., 381 Broekaert, E., 559 Brom, D., 72 Bromet, E., 64 Bromet, E. J., 257 Bronisch, T., 109 Broocks, A., 28 Brooker, C., 523 Brooklyn, J. R., 624 Brooks, G., 451 Brouillard, M., 4 Brouwers, C., 15 Brown, C. H., 619 Brown, G., 416 Brown, G. K., 119, 225, 319, 343, 386,
445, 446, 452, 453, 615 Brown, J. M., 568 Brown, L., 29 Brown, L. A., 189 Brown, M. Z., 388, 449 Brown, R. P., 683 Brown, S. A., 563 Brown, S. M., 221 Brown, T. A., 2, 5, 6, 7, 8, 9, 10, 14, 15, 19,
23, 28, 31, 32, 112, 119, 135, 188, 191, 218, 219, 220, 221, 222, 223, 225, 226, 230, 447, 453
Browne, J., 532 Browning, L., 641 Brownley, K. A., 711 Bruce, M. L., 742 Bruce, S. E., 184 Bruce, T. J., 31 Brunner, R., 447 Bruno, A., 482 Bryan, C. J., 445 Bryant, R. A., 383 Bryson, S. W., 318 Bucci, S., 528 Buckenmaier, C. C., III, 676 Buckley, T. C., 71 Budhiraja, P., 640 Budhiraja, R., 640 Budney, A. J., 619 Buelens, T., 444 Buglass, P., 12 Buie, D. H., 384 Buitelaar, J. K., 143 Bulik, C. M., 711 Bullis, J. R., 5, 7, 218, 222, 446, 447, 448 Buntrock, C., 264 Burgess, N., 68 Bürkner, P., 743 Burns, A. M. N., 523 Burns, D. D., 275, 284
Burns, T., 523 Busch, A. M., 343, 355 Busch, K. A., 446 Bush, A. J., 640 Butler, A. C., 31 Bux, D. A., 146, 563 Buyse, B., 662 Buysse, D. J., 642, 644, 645, 664 Byrne, S., 711 Bystritsky, A., 9, 12
C
Caballo, V. E., 119 Cacciola, J. C., 616 Caddell, J. M., 66 Cahill, S. P., 139 Cain, C. K., 29 Cain, S. M., 185 Calam, R., 541 Calder, T., 620 Calloway, A., 186, 190 Calugi, S., 711, 712, 722 Calvete, E., 274 Cameron, O. G., 4 Campanella, S., 556 Campbell, L., 135 Campbell, L. A., 5, 19, 220, 223, 226 Campbell, M., 355 Campbell, W., 580 Campbell-Sills, L., 10, 30, 112, 218, 221,
225, 229, 447 Canestrari, R., 262 Cannon, T. D., 497 Cano, A., 675 Cao, D., 620 Caputo, G., 9, 23 Cardoso, A., 222 Carey, R., 159 Carise, D., 616 Carl, E., 109, 343 Carl, J. R., 5, 7, 218, 225, 447, 453 Carlbring, P., 11 Carlson, C. R., 683 Carlson, E., 383 Carlson, E. B., 70 Carlson, G. A., 495 Carlson, J. G., 66 Carney, C. E., 642, 645, 662 Carpenter, J. K., 109 Carpenter, K. M., 344 Carr, A., 261 Carr, A. C., 384 Carrier, J., 645
Carroll, K. M., 585, 618 Carskadon, M. A., 639, 641, 653 Carson, A. J., 268 Carson-Wong, A., 445 Carter, F. A., 711 Carter, G. L., 389 Carter, M. M., 16 Carter, R., 264 Caruso, L. S., 641 Carvalho, J. P., 343 Carver, C. S., 486 Caspi, A., 221 Cassiello-Robbins, C. F., 222, 446, 450,
451, 460 Castellani, A. M., 743 Castle, D., 445 Castonguay, L. G., 268, 286, 342 Castriotta, N., 4 Castro, F. G., 563 Casuto, L. S., 708 Cath, D. C., 137 Cavanagh, K., 756 Cavanaugh, M. M., 390 Cellucci, T., 448 Centers for Disease Control and
Prevention, 444, 557, 622 Cerny, J. A., 13, 31 Cerreto, M. C., 749 Ceulemans, E., 112 Chadwick, P., 524 Chakrabarti, S., 485 Chalkley, A., 25 Chambers, C. D., 557 Chambers, W. J., 495 Chambless, D. L., 5, 8, 9, 12, 13, 15, 23,
109, 135, 186, 191, 642 Chan, K. K., 577 Chaney, E. F., 585 Chang, C. M., 263 Chapman, A. L., 444, 448, 449 Chapman, D. P., 258, 266 Chapman, J. E., 31 Chaput, Y., 11 Chard, K. M., 64, 67, 83, 89, 91, 92, 95,
98 Charlesworth, S. E., 386 Charney, D. S., 2, 481 Chartier, M., 266 Chatkoff, D. K., 673 Chawdhary, A., 620 Cheavens, J. S., 448 Chelminski, I., 381 Chemtob, C., 66 Chen, E., 9 Chen, H., 382
Author Index 777
Chen, W. J., 185 Cheng, Y., 317, 515 Chermack, S. T., 622 Cherry, S., 318 Chesham, R. K., 109 Cheslow, D., 134 Chevron, E. S., 317, 319 Chevron, R. S., 488 Chiang, K. J., 275 Chibnall, J. T., 676, 684 Chinna, K., 683 Chittenden, E. H., 136 Chiu, W. T., 4, 5, 64, 109 Chmielewski, M., 192 Choate, M. L., 384 Chodron, P., 188 Choi, D., 614 Choi-Kain, L. W., 384 Choiniere, M., 684 Chorpita, B. F., 6, 219 Chowdhary, N., 353 Christensen, A., 742, 743, 749, 750, 752,
753, 759, 760, 761, 762, 768 Christiansen, J., 5 Christie, J. E., 259 Christopher, M. S., 342 Christopher, P. J., 560 Chu, B. C., 354 Chung, B. D., 488 Chung, K. F., 662 Cichon, J., 66 Cifu, A. S., 72 Cimilli, C., 493 Cipriani, A., 385, 492 Cisek, E., 355 Cisler, J. M., 188, 384, 586 Cissell, S. H., 225, 453 Claes, L., 464 Clancy, J., 4 Clark, D., 27 Clark, D. A., 138, 259 Clark, D. M., 5, 9, 10, 12, 25, 26, 31, 67,
68, 69, 73, 110, 111, 144, 217, 641, 649
Clark, L. A., 6, 219, 229, 258, 265 Clark, M. E., 676 Clarke, D., 261, 275 Clarke, G., 644, 662 Clarke, J., 12 Clarke, S. B., 384 Clarkin, J. F., 384, 389 Cleary, P. D., 2 Cleeland, C. S., 615, 680 Clifton, J., 121 Cloitre, M., 72, 383
Clougherty, K. F., 317 Clum, G. A., 11 Cobb, A. M., 144 Cobb, J., 140 Cocchioni, M., 683 Coffino, J. A., 707 Cohen, A. N., 487 Cohen, D. J., 136 Cohen, L. R., 72 Cohen, P., 382 Cohen, S., 13, 275 Cole, D., 448 Cole, J. C., 642 Collins, N., 445 Colom, F., 485, 488 Comer, J. S., 142, 218 Comer, S. D., 620, 624 Comings, D. E., 136 Comtois, K. A., 388, 445, 452 Cone, E. J., 621, 622 Conelea, C. A., 136 Cong, E., 266 Conklin, C. Z., 383 Conklin, L. R., 230, 465 Connolly, K. R., 264 Connor, K. M., 119 Connors, G. J., 580 Conrad, A. M., 389 Conrad, B. E., 17 Constantino, M. J., 344, 662 Conte, H. R., 259 Conti, S., 262 Conway, C. C., 139 Conwell, Y., 446 Cook, M., 9 Cook, S., 576 Cooper, D., 756 Cooper, Z., 705, 706, 708, 711, 712, 714,
717, 722, 723, 737 Copello, A., 571, 593 Cordova, J., 760 Cormac, I., 523 Cormier, H. J., 11 Cornelius, J. R., 557 Corno, C. M., 619 Correll, C. U., 526 Corry, J., 31, 264 Cory, S. E., 30 Costello, E., 185 Côté, G., 11 Cottraux, J., 144, 145, 262, 342, 386 Courbasson, C., 389 Courtois, C. A., 383 Cousins, S. J., 624 Couturier, J., 711
Covin, R., 185 Cowley, D. S., 5 Cowpertwait, L., 261, 275 Cox, B. J., 2, 4, 8, 11, 390 Cox, G. B., 620 Cox, W. M., 555, 556, 557 Coyle, K., 641 Coyle, T. N., 382 Coyne, A. E., 344 Coyne, J. C., 743 Craighead, L. W., 390 Craighead, W. E., 275, 355 Cramer, V., 382 Crane, C. A., 561 Crane, D. R., 749 Cranford, J. A., 557 Craske, M. G., 1, 2, 3, 4, 6, 7, 8, 9, 10, 11,
12, 13, 14, 15, 16, 17, 21, 23, 24, 25, 28, 29, 30, 31, 32, 33, 35, 109, 139, 141, 186, 220, 226, 234, 237, 463
Crawford, A. G., 621 Crawford, M. J., 386 Creamer, P., 683 Creutzig, J., 675 Crick, F., 639 Crino, R., 140 Cristea, I. A., 384 Crits-Christoph, P., 386 Croft, J., 526 Crombez, G., 673 Crome, E., 109 Cronholm, B., 153 Crosby, A. E., 444 Crouch, T. A., 185 Crowell, S. E., 393, 449 Crowley, S. J., 653 Crowther, J. H., 449 Cucherat, M., 262, 342 Cuellar, A. K., 483 Cuijpers, P., 11, 109, 185, 186, 259, 261,
264, 275, 318, 343, 523, 684 Culbert, J. P., 642 Cullen, J. M., 354 Culver, N., 29, 30 Cunnington, D., 642, 684 Curran, J., 354, 355 Curran, S. L., 684 Curran, S. R., 531 Currier, G. W., 453 Curry, S. J., 318 Curtis, G. C., 4 Curtiss, J. E., 121 Cusack, K., 75, 77 Cutajar, M. C., 526 Cutler, N. R., 484
778 Author Index
Cutter, C. J., 386 Cutter Jr., C. J., 446
D
Dadds, M., 144 Dagöö, J., 110 Dahlenburg, S. C., 711 Dahlin, M., 187, 189 Dahlui, M., 683 Daiuto, A. D., 743 Daley, S. E., 487 Dalgleish, T., 68, 69 Dalle Grave, R., 711, 712, 722 Dalrymple, K. L., 109, 112 Dalsgaard, S., 134 Dammen, T., 267 D’Anci, K. E., 445 Dancu, C. V., 230 Danitz, S. B., 189 Dansky, B. S., 64 Danton, W. G., 263, 264 Darlington, N., 523 Darnell, D. A., 354 Dattilio, F. M., 19 Daughters, S. B., 341, 342, 355 Davey, G. C. L., 185 Davies, M. C., 676 Davies, S., 9 Davila, J., 266 Davis, A. K., 580 Davis, C. G., 7 Davis, C. S., 569 Davis, D. R., 619 Davis, K. D., 675 Davis, K. L., 393 Davis, L., 223 Davis, M., 30 Davis, M. H., 755 Davis, N. R., 29 Davison, G. C., 393 Davison, M. R., 269 Davoli, M., 620 Dawson, M. S., 354 de Almeida Sampaio, T. P., 187, 189 De Araujo, L. A., 141, 142 de Beurs, E., 17, 25, 28 De Cort, K., 9 De Crescenzo, F., 619 de Geus, F., 135 de Graaf, R., 262 de Haan, E., 135, 143 de Jong, M., 711
de Jong, M. G., 4 de Jonge, P., 4, 5 de Jongh, 383 de la Fuente, J. R., 564 de la Piedad Garcia, X., 711 de Oliveira, I. R., 258 de Ornelas Maia, C. A. C., 222 de Ruiter, C., 25 de Waart, R., 564 de Zwaan, M., 712 Deacon, B., 11, 28 Deagle, E. A., 26 Deale, A., 141 Debiec, J., 30 Deckert, J., 6 DeCola, J. P., 9, 11 DeCou, C. R., 445, 448 Defares, P. B., 72 Degenhardt, L., 622 Degnan, A., 532 Dekel, R., 69 Del, A. C., 119 Delaney, H. D., 580, 619 DelBello, M. P., 484 Deldin, P., 121 Delsignore, A., 135 DeLuca, A., 572 Delucchi, K., 265 DeMartini, K. S., 580 Dement, W. C., 638 Demler, O., 4, 64, 109 Demyttenaere, K., 263 Den Boer, J. A., 6 DeNelsky, G. Y., 263 Dengler, W., 9 Dennis, C. L., 318 Dennis, J., 642 Denson, L. A., 265 Denys, D., 135 Department of Defense, 75, 76 Department of Veterans Affairs, 75, 76 Depp, C. A., 448 Derbidge, C. M., 449 Derogatis, L. R., 615, 625 DeRubeis, R. J., 259, 260, 263, 265, 268 DeSilva, P., 148 DeVeaugh-Geiss, J., 145 Dewey, D., 13 di Menza, S., 621 Di Nardo, P. A., 19, 222 Diaferia, G., 135 Diamond, D., 445 Diaz, M. L., 235 Dickerson, S. L., 622
DiClemente, C. C., 560, 569, 619 Diefenbach, G. J., 153 Diels, L., 13 Dijk, D. J., 640 Dillon, K. H., 76 DiMarco, I. D., 186 Dimeff, L. A., 343, 382, 383, 385 Dimidjian, S., 235, 339, 341, 342, 343,
354, 355, 375, 663, 761 Dinger, U., 120 Dingle, G., 268 Diniz, J. B., 135 Dixon, L., 389 Dixon, L. B., 523 Dizén, M., 112 Dobson, K. S., 258, 259, 263, 264, 341, 342 Doebler, P., 261 Doering, S., 385 Dohn, D., 8 Dohrenwend, B. P., 65 Dolenc, L., 663 Doll, H. A., 711 Doll, R., 523 Dollard, J., 138 Dombeck, M. J., 9 Domínguez-Martínez, T., 487 Domschke, K., 6 Donaldson, D., 448 Donisi, V., 264 Donnelly, M., 31 Donovan, D. M., 562, 568, 569, 577, 585,
620 Donovan, S., 335 Dorahy, M. J., 526 Doran, N., 354 Doss, B. D., 742, 743, 749, 750, 760, 761,
762, 768 Dougherty, D. D., 145 Dougherty, D. M., 486 Dougherty, L. R., 266 Dow, M., 31 Downey, L., 620 Downie, F., 135 Downs, M. F., 453 Doyle, J. S., 642, 684 Doyle, S. R., 569 Dozois, D. J. A., 185, 233 Drabant, E. M., 221 Drake, C. L., 640 Drayton, S. J., 492 Dreessen, L., 15 Dryman, M. T., 112 Dube, S. R., 266 DuBois, D. L., 276
Author Index 779
Duckro, P. N., 676, 684 Duff, K., 7 Duffy, A., 484 Dugas, M. J., 138, 185, 186 Dukes, E. M., 184 Dunlop, B. W., 263 Dunn, G., 525 Dunn, J., 274 Dunn, K. E., 622 Dunn, T. D., 258 Dunner, D. L., 482 Dupuis, G., 14 Durrant, J. D., 9 Durrence, H. H., 640 Dursa, E. K., 66 Dutra, L., 384 Dvir, S., 355 Dworkin, B. R., 8 Dworkin, R. H., 681 Dworkin, S., 8 Dyck, I., 135, 184 Dykman, B. M., 266
E
East, M. P., 641 Eaton, W. W., 8 Eaves, L. J., 6 Eberhart, N. K., 274 Eberle, J. E., 390 Eberle, J. W., 381 Ebert, D., 261 Ebner-Priemer, U. W., 383 Eccleston, C., 673 Echiverri, A. M., 30 Eckert, T. A., 676 Eddy, K. T., 708 Edge, M. D., 486, 532 Edinger, J. D., 640, 644, 645, 662 Edwards, R. R., 674 Eells, T. D., 275 Efthimiou, O., 487, 491 Egan, S. J., 342 Egede, L. E., 355, 526 Ehlers, A., 2, 5, 7, 8, 9, 10, 67, 68, 69, 73,
226 Ehlers, C. L., 486 Eidelman, P., 658 Eifert, G. H., 10, 30, 275 Eisemann, M., 274 Eisen, J. L., 134, 135, 136, 137 Eisenberg, D., 453 Eisendrath, S., 265, 266
Eisma, M. C., 658 Eken, S., 140 Ekers, D. M., 343, 354 Ekselius, L., 11 El Ghoch, M., 711 Elbert, T., 72 Elbogen, E. B., 72 Eldridge, K. A., 760, 761 Eley, T. C., 6 Elkin, I., 259, 260, 264, 268, 320, 334 Ellard, K. K., 5, 6, 7, 8, 187, 217, 218, 221,
403, 447, 449, 705 Elliott, T. E., 675 Ellis, A., 144, 416 Ellis, T. E., 448 Emery, G., 111, 234, 258, 341 Emmelkamp, P. M. G., 5, 13, 109, 135,
142, 143, 144, 152 Emmerson, L. C., 531 Endicott, J., 230, 317 Endler, N. S., 4 Engel, S. G., 707 Engelman, J., 355 Engels, M. L., 7 Ennis, N., 76 Epstein, A. M., 2 Epstein, D., 652 Epstein, E. E., 555, 560, 563, 569, 576,
588, 592, 605, 613, 743 Epstein, N., 743, 759 Erbas, Y., 112 Erickso, D. H., 523 Erickson, T. M., 185 Erisman, S. M., 186 Ershoff, D., 621 Esch, R. A., 620 Espel-Huynh, H., 451 Espie, C. A., 641, 652, 654 Esposito-Smythers, C., 260 Esteve, R., 673 Etherton, J. L., 355 Etkin, A., 185, 384 Eustis, E. H., 184, 187, 189 Evans, D. L., 146 Evans, L., 11 Evans, M. D., 259, 260, 262, 263 Evans, S., 189 Everitt, B., 523 Everitt, B. S., 681 Evershed, S., 389 Ewbank, M. P., 117 Eynan, R., 382 Eysenck, H. J., 6, 219 Ezzo, J., 683
F
Fadardi, J. S., 557 Faedda, G. L., 484, 515 Fagiolini, A., 258 Fairburn, C. G., 318, 354, 708, 709, 710, 711,
712, 713, 714, 717, 719, 721, 722, 723, 724, 725, 726, 729, 730, 732, 735, 736, 737
Fairholme, C. P., 449 Falbo, J., 27 Falloon, I. R. H., 501 Fals-Stewart, W., 140, 143 Fama, R., 557 Fan, B., 276 Fang, C., 381 Farach, F. J., 447 Faragher, B., 534 Faraone, S. V., 4 Faravelli, C., 8 Farchione, T. J., 187, 217, 221, 403, 446,
449, 705 Farley, R., 355 Farmer, A. S., 112, 126 Farmer, C. C., 77 Farrell, J., 267 Farrell, J. M., 387 Farrell, L. J., 136, 144 Fauci, A. S., 620 Fava, G. A., 4, 262, 263 Fava, M., 266, 390 Favazza, A. R., 443 Favrod, J., 523 Fawcett, J., 446 Fazel, S., 549 Feeley, M., 268 Feeny, N. C., 146, 384 Fehm, L., 109 Feigenbaum, J. D., 389 Feigenbaum, W., 11, 27 Feinstein, B. A., 563 Feldman, G., 266, 390 Feldner, M. T., 384 Fendrich, M., 622 Feng, C. Y., 261 Fergus, K. D., 11 Fergusson, D. M., 7 Ferre, F., 190 Ferrell, E. L., 355 Ferris, R., 276 Ferster, C. B., 340, 341, 342 Festinger, D. S., 619, 620 Fiebach, C. J., 221 Fiedeldij Dop, M., 25
780 Author Index
Fiedorowicz, J. G., 481 Fiegenbaum, W., 8 Field, A. P., 185 Field, M., 556 Fillmore, H. H., 355 Finan, P. H., 684 Finch, E. F., 384 Findler, M. N., 70 Findling, R. L., 482 Fink, C. M., 11 Fink, E. B., 572 Finkel, E. J., 756 Finney, J. W., 558, 559, 619 Fiola, L. A., 342 Fiore, M., 613 First, M. B., 70, 225, 343, 382, 453, 481,
495, 568 Fischer, S. C., 141 Fitzmaurice, G., 382 Fitzsimmons-Craft, E. E., 706, 711 Flament, M., 134, 135 Flanagan, J. C., 557, 576, 587 Fleck, D. E., 484 Fleischmann, A., 446 Fleming, J. E., 109, 121, 189 Fleming, R., 185 Fletcher, R., 621 Flink, I. L., 673 Flint, D. D., 355 Flint, J., 448 Flückiger, C., 119 Flynn-Evans, E. E., 639 Foa, E. B., 29, 66, 67, 69, 70, 71, 72, 73,
133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 144, 145, 146, 149, 150, 152, 158, 230, 342, 384, 403, 416
Fokas, K., 563 Foley, K., 640 Follette, V. M., 10, 112, 188 Follingstad, D., 390 Fonagy, P., 384, 385, 445 Fontana, A., 72 Foote, J., 572 Foran, H., 275 Forbes, D., 75, 77, 383, 384 Forbush, K. T., 707, 708 Ford, D. E., 640 Ford, J. D., 383 Ford, J. H., 614 Forgue, D. F., 71 Forman, E. M., 31 Forsyth, J. P., 7, 23, 118, 384 Forte, A., 258 Fortgang, R. G., 444
Fossati, A., 394 Fournier, J. C., 260, 263 Fowler, D., 526 Fowles, D. C., 8 Fox, K. R., 444, 446, 448 Fox, M. G., 259 Francis, J. L., 276 Frank, E., 261, 263, 275, 306, 317, 320,
325, 481, 486, 488, 495, 515, 664 Frankenburg, F. R., 382, 386, 446 Franklin, G., 268 Franklin, J. C., 447, 448 Franklin, M. E., 133, 134, 135, 140, 142,
144, 145, 146, 152, 153, 159, 176 Fredman, S. J., 69, 72, 76 Free, M. L., 268 Freed, S., 9 Freedy, J. R., 70 Freeman, A. M., 259, 269, 386 Freeman, D., 524, 526 Freeman, J. B., 144 Freeman, S. M., 259 Freeston, M. H., 138, 144 French, P., 525 Frenkel, M., 386 Fresco, D. M., 185, 186, 221, 384 Freyer-Adam, J., 569 Friborg, O., 260, 261 Friederich, H. C., 711 Friedman, A., 711 Friedman, B. H., 185 Friedman, E. S., 265 Friedman, M. A., 259 Friedman, S., 15, 16 Friedrich, M., 258 Friesen, L. N., 674 Friez, E. J., 7 Fristad, M. A., 491 Fritzler, B. K., 11 Frost, N. D., 75 Frueh, B. C., 526 Fruzzetti, A. E., 390, 464 Fry, W., 12 Fuchs, C. H., 189, 190 Fuetsch, M., 109 Fullen, B. M., 684 Fulton, J. J., 66 Funk, J. L., 749, 752, 762 Furman, J. M., 9 Furmark, T., 109 Furr, J., 159 Furr, J. M., 342 Futterman, A., 276 Fyer, A. J., 19, 318
G
Gabel, J., 5 Gabriels, L., 662 Gallagher, M. W., 222, 225, 453 Gallagher, R., 9 Gallagher-Thompson, D., 276 Gallop, R. J., 388, 390 Galovski, T. E., 76, 77 Gámez, W., 192 Garavan, H., 557 García-Soriano, G., 135 Gard, D., 121 Garety, P. A., 525, 526, 531 Garfinkel, R., 317, 335 Garnaat, S. L., 121 Garner, M., 190 Garssen, B., 25 Garvert, D. W., 383 Garvey, K. A., 619 Garvey, M., 563 Garvey, M. J., 4 Garyfallos, G., 266 Gaskin, D. J., 672 Gaskin, M. E., 684 Gastfriend, D. R., 572 Gaughran, F., 531 Gaulier, B., 642 Gauthier, J. G., 11 Gawrysiak, M., 354 Gearson, J. S., 619 Geddes, J. R., 263, 487, 492 Geiger-Brown, J. M., 640 Geisser, M. E., 676, 684 Gelder, M. G., 10, 141, 306 Gelernter, J., 221 Geller, B., 483 Gelles, R. J., 390 Gentes, E. L., 185 Geoffroy, P. A., 662 George, E. L., 482, 487, 489 George, L., 381 George, W. H., 761 Georgia, E. J., 762 Georgia Salivar, E., 762 Gerbarg, P. L., 683 Germer, C. K., 188 Gershenfeld, H., 265 Gershuny, B. S., 7, 136 Gfroerer, J., 444 Gfroerer, J. C., 676 Ghesquiere, A., 355 Ghodse, A. H., 622 Ghoneim, M. M., 8
Author Index 781
Ghosh, A., 11 Giasson, H. L., 66 Gibb, B. E., 447 Gibbons, M., 343 Gibbons, R. D., 260 Gibson, A., 622 Giesen-Bloo, J., 267, 387 Gifford, E. V., 10, 112, 188 Gignac, A., 484 Gil, E., 444 Gilbert, P., 110 Gilbody, S., 343, 354 Gilson, M., 259, 577 Giorgio, J., 74 Giradi, G., 445 Gironda, R. J., 676 Gitlin, M. J., 484, 494 Gleaves, D. H., 711 Gleeson, J., 525 Glen, A. I. M., 259 Glenn, D., 17 Gloaguen, V., 262, 342 Gloster, A. T., 4, 27, 31 Glover, D., 9 Glovinsky, P. B., 641 Glynn, S., 761, 762 Glynn, S. M., 530 Gobin, R. L., 76 Gochneaur, K., 342 Godley, M. D., 619 Goes, F. S., 483 Goetsch, V. L., 7 Goff, D., 523 Goghari, V. M., 483 Goisman, R. M., 4, 5 Goldberg, C., 391 Goldberg, D. P., 264 Goldenberg, I., 5 Goldfried, M. R., 268, 342 Goldin, P. R., 110 Goldstein, A. J., 8, 12 Goldstein, B. I., 484, 493 Goldstein, C., 5, 218 Goldstein, M. J., 487 Goldstein, R. B., 76 Goldstein, R. Z., 556 Golinelli, D., 15, 16, 32 Gollan, J. K., 341 Gollwitzer, P. M., 351 Gomez, A. F., 190 Gómez-Pérez, L., 673 González-Diez, Z., 274 Goodday, S., 484 Gooding, P., 445, 446
Gooding, P. A., 72 Goodman, M., 382 Goodman, W. K., 146, 230 Goodson, J., 76 Goodwin, G. M., 494 Goodwin, R. D., 7, 8 Gordon, J. R., 190, 409, 562, 588, 589,
592 Gore, K. L., 16 Gorman, B. S., 450 Gorman, J. M., 9, 16, 217, 224 Gorman, L. L., 317 Gortner, E. T., 341 Gosselin, P., 185 Götestam, K. G., 140, 144 Gottman, J., 749 Gould, R. A., 11, 523 Gournay, K., 355 Goyer, L. R., 14 Graap, K., 72 Gracely, S., 23 Gradus, J. L., 66, 446 Grady-Fletcher, A., 743 Graf, M., 343 Graham, J. M., 569 Grandi, S., 262 Granholm, E., 531 Granillo, M. T., 706 Grant, B. F., 76, 381, 382, 555 Grant, M., 564 Grant, P. M., 524 Grassi, L., 385 Gratz, K. L., 192, 445, 446, 449 Gray, J. A., 6 Graydon, M. M., 619 Grayson, J. B., 140, 141 Green, B., 70 Green, K. E., 563 Green, M., 485 Greenberger, D., 275, 276 Greene, A. F., 684 Greene, J., 384 Gregg, L., 549 Gregg, S. F., 31 Gregory, J. D., 68 Greist, J. H., 109, 135, 145, 146 Greitemeyer, T., 755 Grenyer, B. F. S., 381, 382, 383 Griez, E., 7, 9, 28 Griffiths, C., 385 Griffiths, R. R., 618 Grigoriadis, S., 318 Grilo, C. M., 15, 16, 382, 706, 707, 708 Grisanzio, K. A., 219, 220
Grisham, J., 135 Grisham, J. R., 5, 220 Grochocinski, V. J, 263 Grof, P., 484 Groff, S. E., 711 Groschwitz, R. C., 444 Gross, J. J., 112, 114, 188, 192, 221, 756 Grosscup, S. J., 340 Grossman, L. S., 483 Grubaugh, A. L., 526 Gu, J., 756 Guay, B., 644 Guay, C., 644 Gudmundsen, G., 355 Gueorguieva, R., 707 Guerdjikova, A. I., 708 Guilleminault, C., 639 Guiterrez, P. M., 72 Gumley, A., 525 Gunasekara, S., 390 Gunderson, J. G., 386, 418, 445, 446 Gupta, M., 743 Gur, S., 109 Gurman, A. S., 743 Gursky, D., 21 Gyulai, L., 259
H
Haaga, D. A. F., 559, 591 Haby, M., 31, 32 Haby, M. M., 264 Hacker, D., 523 Hackmann, A., 27, 110–111 Haddock, G., 523, 530, 534, 549 Hadhazy, V. A., 683 Haeny, A. M., 568 Hafeman, D. M., 484, 515 Hafner, J., 13, 230 Hafner, R. J., 13 Hagenaars, M., 141 Hainsworth, C., 109 Hajcak, G., 221 Hale, N., 446 Halford, W. K., 743, 748 Hall, G. C. N., 190 Hall, P., 564, 565 Hall, P. H., 528 Hallam, R., 13 Hallgren, K. A., 576 Halvorsen, M., 274 Hamada, R. S., 66 Hamblen, J. L., 70
782 Author Index
Hamby, S. L., 571, 749 Hamer, R. M., 684 Hamilton, M. A., 226, 319, 323, 343 Hamilton, S. P., 6 Hamman, M., 5 Hammen, C., 487 Hamza, C. A., 449 Han, B. H., 444 Han, C., 675 Han, H., 72 Hancock, K., 109 Hancock-Johnson, E., 385 Hand, I., 13 Handley, T. E., 448 Handmaker, N., 580 Hankin, B. L., 274 Hanks, D. L., 266 Hanna, G. L., 134 Hannan, S. E., 153 Hanrahan, F., 185, 186 Hanratty, D., 445 Hanseman, D., 484 Hansen, B., 140 Hanson, J. E., 72 Haradhvala, N., 189 Harden, T., 276 Hardeveld, F., 262 Harford, R. J., 622 Hariri, A. R., 221 Harley, R., 266, 390 Harned, M. S., 72, 76, 383, 384, 388,
399, 400 Harold, G. T., 742 Harrell, S. P., 190 Harrison, J., 28 Harrison, W., 230 Harrow, M., 483 Hart, L. M., 706 Hart, R. P., 684 Hartlage, S., 258 Hartnett, D., 261 Hartzler, B., 585 Harvey, A. G., 638, 640, 641, 642, 644,
653, 654, 655, 657, 658, 660, 662, 664 Harwood, D., 446 Hasin, D. S., 257, 318 Hasking, P., 444 Haslam, M. T., 28 Hatch, M., 16 Hatch, S. G., 743 Hatcher, R. L., 286 Hatcher, S., 445 Hatfield, A. B., 515 Hauptmann, W., 681 Hautzinger, M., 340
Havnen, A., 140 Hawke, L. D., 267, 274 Hawker, D. M., 712 Hawkins, R., 445 Hawley, L. L., 109, 189 Hawton, K., 445, 446, 448, 492 Hay, P., 711 Hayden, E. P., 266 Hayes, A. M., 268, 342 Hayes, N. A., 448 Hayes, S. A., 186, 447 Hayes, S. C., 10, 30, 31, 109, 110, 112,
113, 114, 115, 118, 119, 121, 126, 175, 186, 187, 188, 191, 195, 234, 266, 342, 768
Hayes-Skelton, S. A., 186, 187, 189, 190 Hayhurst, H., 264 Haynos, A. F., 464 Hays, P. A., 192, 193 Haythornthwaite, J. A., 675 Hayward, C., 4, 6, 7 Hayward, P., 275, 487 Hazlett-Stevens, H., 235 He, H., 190 Heald, J. L., 642 Healy-Farrell, L., 143 Heard, H. L., 388 Heath, A. C., 6 Heatherington, L., 189 Heavey, C. L., 749 Hecker, J. E., 11 Heckman, T. G., 317, 318 Hedley, L. M., 14, 26 Hedman, E., 11 Heffner, M., 10, 30 Heidenreich, T., 110 Heil, S. H., 612, 618, 619, 622, 676 Heim, C., 266 Heimberg, R. G., 9, 111, 112, 185, 186,
221, 224, 230, 384 Heinrichs, N., 110, 111 Heisel, M. J., 382 Heiser, N. A., 119 Hekler, E. B., 186 Helbig-Lang, S., 29 Held, P., 77 Heldt, E., 17 Heller, K., 569 Heller, W., 221 Hellström, K., 26 Helzer, J. E., 621 Hembree, E., 384 Hembree, E. A., 73 Henderson, A., 12 Henderson, L., 390
Hendriks, G. J., 17 Hennen, J., 386, 446, 485 Henningfield, J. E., 618 Henry, R. M., 487 Henry, T. R., 76 Henry, W. P., 286 Herbert, J. D., 109, 112 Herman, J. L., 383, 394 Herman-Dunn, R., 235, 339, 341 Hermans, D., 9, 17 Hermesh, H., 109 Hersh, R. G., 381 Hester, R. K., 580 Hettema, J. E., 619 Hettema, J. M., 221 Heuts, P. H., 673 Heuzenroeder, L., 17, 191 Hibbert, G., 25 Hickling, E. J., 71, 676 Hielscher, E., 464 Higgins, S. T., 612, 618, 619, 620, 622,
676 Hikida, I., 342 Hildebrandt, T., 562, 576 Hill, C. E., 320 Hill, C. L., 2 Hill, D. M., 390 Hill, E. M., 394 Hiller, W., 275 Himadi, W., 13 Himle, J., 4, 142 Himle, M. B., 142 Hinton, D. E., 108 Hintze, J. P., 644 Hirsch, C. R., 110 Hirsch, L. S., 592, 605 Hirvikoski, T., 390 Hiss, H., 135, 144, 158, 176 Hjorthoj, A. R., 616 Hjorthoj, C. R., 616 Ho, F. Y., 662 Ho, L. M., 662 Hoberman, H., 340 Hodges, L. F., 72 Hodgson, R. J., 141 Hodkinson, K., 524 Hoefler, M., 342 Hoehn-Saric, R., 185 Hoek, H. W., 705, 706, 711 Hoekstra, R., 27 Hoekstra, R. J., 144 Hoertel, N., 262 Hoes, D., 343 Hoffart, A., 11, 13, 14, 26, 27 Hoffman, B. M., 673
Author Index 783
Hoffman, D. L., 184 Hoffman, J. A., 622 Hoffman, K. A., 614 Hofmann, M., 262 Hofmann, S. G., 10, 15, 25, 26, 108, 109,
110, 111, 112, 113, 115, 119, 121, 123, 190, 221, 258, 447
Hoge, C. W., 65, 66, 71, 672 Hogg, L. I., 381 Hohagen, F., 145 Højgaard, D. R. M. A., 136 Holaway, R. M., 185 Holden, A. E. O., 10, 11, 13 Holder, H., 619 Holder, N., 77 Hollander, E., 386 Hollandsworth, J. G., 392 Holle, C., 268 Holliday, R., 77 Holling, H., 743 Hollon, S. D., 258, 259, 260, 262, 263,
268, 354, 642 Hollowell, B., 531 Holman, C. S., 446 Holmberg, E. B., 448, 453 Holmes, M. K., 486 Holmes, M. R., 66 Holmqvist, R., 321 Holopainen, A., 621 Holroyd, K. A., 673 Holt, C., 11 Holt, P., 25 Holtzworth-Munroe, A., 743 Holzhauer, C. G., 573, 580 Homish, G. G., 557 Hong, J. J., 190 Hood, S., 639 Hoogduin, C. A. L., 13, 15, 17, 15, 135,
137 Hoogduin, K. A., 143 Hooley, J. M., 444, 448, 486, 487, 496 Hooper, L., 70 Hope, D. A., 9 Hope, R. A., 318 Hope, T., 446 Hopko, D. R., 341, 343, 354, 355 Hopko, S. D., 341, 355 Hops, H., 743 Hor, K., 549 Hornsveld, H., 25 Horowitz, M. J., 67 Horvath, A. O., 119 Horwood, L. J., 7 Hou, R., 190 Houck, J. M., 560
Houck, P., 230 Hougaard, E., 11 Houghton, S., 354, 355 Howland, R. H., 258 Howlett, M., 622 Hoyer, J., 342 Hoyle, R. H., 683 Hu, S., 185 Huang, C. C., 674 Huang, L., 276 Huang, M. I., 640 Hubbell, A., 622 Hubley, S., 235, 339, 343 Hudgel, D. W., 640 Hughes, J. L., 445 Hughes, M., 64 Huh, G. A., 524 Huibers, M., 274 Huibers, M. J., 13 Huibers, M. J. H., 268 Huneke, N. T. M., 190 Hunsley, J., 13 Hunt, G. M., 619 Hunt, M. K., 355 Hunt, T. K., 707 Hunter, E. C. M., 527 Hunter-Reel, D., 562, 588 Huntley, A. L., 275 Huppert, J. D., 13, 14, 139, 146, 223 Hurtado, G. D., 355 Huta, V., 109, 189 Hutchinson, A. D., 711 Hutton, P., 525, 526 Hwang, I., 446
I
Ilacqua, G., 683 Ilgen, M. A., 580 Ince, P., 523 Infantino, A., 10 Ingram, R. E., 268 Insel, T., 448 Insel, T. R., 134, 218 Institute of Medicine, 672 International Society for the Study of Self-
Injury, 443 Irurtia, M. J., 119 Irving, C. B., 523 Irwin, M. R., 642 IsHak, W. W., 263 Islam, M. N., 386 Isometsa, E. T., 382 Issakidis, C., 14
ISTSS Guidelines Committee, 383 Ito, L. M., 28, 141 Ivanova, E., 109 Ivers, H., 659 Iverson, K. M., 76, 390 Izard, C. E., 2, 235
J
Jackson, R. J., 6 Jackson, S., 74 Jacob, K. L., 342 Jacob, M., 266 Jacob, R. G., 9 Jacobi, D., 140 Jacobo, M., 266, 390 Jacobs, C., 146 Jacobs, D. G., 446 Jacobsen, P. C., 524, 525 Jacobson, C. M., 382, 447, 448 Jacobson, N. S., 235, 341, 342, 663, 742,
743, 749, 750, 753, 760, 761, 762, 768 Jacoby, R., 446 Jager-Hyman, S., 445, 446, 453 Jakupcak, M., 355 James, L. M., 382 Jamison, C., 342 Jamison, R. N., 674 Janca, A., 386 Janelle, A., 445 Jang, K. L., 383 Janoff-Bulman, R., 67 Jansson, M., 658 Jardine, R., 6 Jarrett, R. B., 258, 259, 264, 265 Jarvis, M., 620 Jasin, E., 23 Jauhar, S., 523, 524 Jaycox, L. H., 141 Jefferson, J. W., 145 Jeffrey, J., 390 Jenewein, J., 675 Jenike, M. A., 136, 145, 159 Jenkins, J. A., 384 Jenni, O. G., 639 Jensen, N. K., 576 Jeste, D. V., 531 Jin, R., 4 Jiranek, W. A., 672 Jo, B., 389 Jobes, D. A., 445 Joffe, R., 268 Johanson, C. E., 621 Johansson, R., 261
784 Author Index
John, A., 448 Johnides, B. D., 76 Johns, M. W., 645 Johnsen, T. J., 260, 261 Johnson, M. R., 119 Johnson, R. E., 621 Johnson, S. L., 483, 486 Johnson, T. P., 622 Johnson, W. R., 619 Johnston, D. W., 141 Joiner, T. E., 72, 266, 274, 446, 448 Jones, C., 523 Jones, E. E., 260 Jones, F. W., 185 Jones, G. E., 683 Jones, J., 681 Jones, M., 355 Jones, M. K., 117 Jones, N., 76 Jones, R., 318 Joormann, J., 486 Jorm, A. F., 706 Jörnestedt, L., 153 Joseph, S., 68 Jowett, S., 383 Joyce, E. E., 389, 390 Joyce, P. R., 260 Judd, L. L., 484 Jurcik, D. C., 674 Jurkovich, G. J., 355
K
Kabat-Zinn, J., 194, 207 Kabela-Cormier, E., 562 Kadden, R. M., 562 Kahn, R. S., 6 Kalata, A. H., 342 Kales, A., 641 Kalsekar, A., 640 Kalsy, S., 159 Kamerow, D. B., 640 Kampfe, C. K., 10 Kamphuis, J. H., 658 Kampman, K., 620 Kampman, M., 15, 17 Kampmann, I. L., 109 Kane, R., 343 Kanter, J. W., 343, 355 Kanwar, A., 446 Kaplan, K. A., 638, 644, 653, 662 Kaplan, M. L., 453 Karamians, R., 263 Karasu, T. B., 259
Karatzias, T., 383 Karg, R. S., 70, 225, 343, 382, 453, 568 Kariisa, M., 620 Karlin, B. E., 217, 662 Karni, A., 639 Karyotaki, E., 261, 264, 343, 523 Kashdan, T. B., 112, 126 Kashikar-Zuck, S., 673 Kass, A. E., 711 Kasvikis, Y., 135 Kato, M., 263 Katon, W., 5, 675 Katschnig, H., 5 Kattakuzhy, S., 620 Katz, L. Y., 390 Katz, M. R., 390 Katz, R., 145 Katzelnick, D. J., 109, 145 Katzman, M. A., 190 Kaufman, J., 495 Kawinska, A., 645 Kay, B., 140 Kazarian, S. S., 146 Kazdin, A. E., 444, 706 Kean, Y. M., 109 Keane, T., 676 Keane, T. M., 66, 71 Keating, G. M., 620, 624 Keel, P. K., 707 Keeley, P., 355 Keen, N., 527 Kegan, R., 391 Keijsers, G. P., 13, 15, 17, 135, 137, 143 Kelemen, O., 268 Keller, M. B., 5, 184, 258, 262, 266, 267,
306 Keller, M. L., 23 Kellett, S., 354 Kellison, J. G., 563 Kellogg, S. H., 386 Kelly, G. A., 684 Kelly, J. F., 562 Kelly, T. M., 446 Kendler, K. S., 6, 7, 8, 221, 266, 448 Kennedy, B. L., 185 Kenny, M. A., 265 Keown-Stoneman, C., 484 Kéri, S., 268 Kerkhof, A. J. F. M., 453 Kernberg, O. F., 384 Kerns, R. D., 672, 673, 675, 676 Kerrigan, M., 266, 390 Keski-Rahkonen, A., 707 Kessler, R. C., 4, 5, 7, 64, 65, 109, 134,
184, 220, 257, 258, 381, 446, 707, 708
Keyes, C. L. M., 230 Keyl, P. M., 8 Khadivi, A., 534 Khan, S., 557 Kiekens, G., 447 Kikuchi, M., 4 Kilic, C., 17 Kilicaslan, J., 445 Killen, J. D., 6, 7 Kilpatrick, B., 622 Kilpatrick, D. G., 64, 66, 70, 74 Kiluk, B. D., 585, 618 Kim, C., 446 Kim, E., 9 Kim, E. Y., 483 Kim, H., 621 Kim, J. A., 8 Kim, S. H., 126 Kim, T., 743 Kimber, J., 620 Kimber, M., 711 Kindt, M., 30 Kinney, C., 531 Kirby, H, S., 759 Kirby, K. C., 619, 620 Kircanski, K., 2, 29 Kirkby, J., 653 Kiropoulos, L. A., 11 Kirsch, P., 221 Kiss, A., 318 Kitchens, J., 192 Klassen, B. J., 77 Kleber, H. D., 559, 622 Kleber, R. J., 72 Kleiger, J. H., 534 Kleiman, E. M., 449 Klein, B., 11 Klein, D. F., 19, 335 Klein, D. N., 266, 267 Kleindienst, N., 382, 385 Klerman, E. B., 640 Klerman, G. L., 317, 318, 319, 321, 488 Kliem, S., 445 Klinger, E., 557 Klonsky, E. D., 447, 449 Klosko, J. S., 13, 266, 273, 274, 296,
386 Kluetsch, R. C., 382 Knappe, S., 4 Knoblach, D. J., 619 Knopp, K., 762 Kobak, K. A., 135, 145 Koch, W. J., 7, 14, 676 Kocovski, N. L., 109, 121, 189 Kocsis, J. H., 317
Author Index 785
Koegl, C. J., 572 Koele, P., 17, 25, 28 Koenen, K. C., 64, 65, 72 Koenigsberg, H. W., 384 Koerner, K., 382, 434 Koeser, L., 264 Koetter, U., 644 Koffel, E., 645 Kogan, C. S., 134 Kohlenberg, R. J., 422 Kohn, R., 258 Kolko, R. P., 711 Kondel, T. K., 523 Kong, X., 672 Königbauer, J., 261 Koob, G. F., 556, 561 Koons, C. R., 388 Kopper, B. A., 681 Koran, L. M., 135 Korman, L. M., 383 Kornstein, S. G., 708 Korslund, K. E., 72, 384 Körük, S., 268 Kosanke, N., 572 Kosfelder, J., 445 Koster, E. H. W., 188 Koszycki, D., 110 Kothgassner, O. D., 72 Kotov, R., 192, 448 Kovacs, M., 259, 446 Koval, P., 112 Kowalski, R. M., 111 Kowatch, R. A., 642 Kozak, M. J., 29, 134, 135, 137, 138, 139,
140, 141, 142, 144, 403, 416 Kraemer, H. C., 6 Kraepelin, É., 480 Kraft, A. R., 25 Kramer, R., 390 Krause, A. J., 639 Krause, L., 583 Krebs, E. E., 681 Krebs, P., 560 Kretchman, J., 146 Kring, A. M., 383 Kringlen, E., 382 Kroenke, K., 343, 452, 468, 675, 681 Kroeze, S., 9 Kröger, C., 382, 445 Krook, A. L., 621 Kross, E., 121 Krumm, B., 385 Krupitsky, E., 620, 624 Krupnick, J., 70 Kruse, J., 262
Kryger, M. H., 638, 639 Krystal, A. D., 642 Krystal, J. H., 2, 30 Kubany, E. S., 70 Kuch, K., 8 Kuhn, B., 651, 655 Kuipers, E., 526, 530 Kulka, R. A., 64, 65 Kumar, A., 276 Kumar, V., 8 Kumari, V., 485 Kuo, T. F., 662 Kupelnick, B., 259 Kupfer, D. J., 261, 263, 486, 495, 645 Kupka, R., 482 Kuppens, P., 112 Kurlan, R., 136 Kurti, A. N., 619 Kurtz, M., 532 Kushner, M. G., 15 Kuyken, W., 265 Kvale, G., 140 Kwapil, T. R., 487 Kyle, S. D., 642 Kyokai, B. D., 409
L
Labelle, R., 445 Laberge, B., 11 Labus, J. S., 30 Lack, L. C., 639 Lacroix, D., 11 Ladoucer, R., 138 Ladouceur, R., 138, 184, 185, 186 Lafer, B., 482 Lake, R. I., 6 Lally, J., 531 Lam, D. C. K., 381 Lam, D. H., 275, 487 Lam, R. W., 484 Lamb, R. J., 620 Lambert, J. A., 72 Lamers, S. M., 230 Lammers, M. W., 13 LaMonaca, V., 619 Lamontagne, Y., 13 Lancee, J., 642, 658, 662 Landau, P., 145 Landes, S. J., 445 Lane, M. C., 381 Lang, A. J., 9, 24, 29, 31 Lang, P. J., 66, 74, 138 Lange, A., 17, 25, 28
Långström, N., 549 Lantéri-Minet, M., 672 Larimer, M. E., 577 Larney, S., 622 Larsen, D., 676 Larsson, B., 140 Laska, K. M., 75 Last, C. G., 5, 13 LaTaillade, J. J., 759 Latham, G. P., 351 Latimer, P., 140 Laudenslager, M. L., 9 Laurenceau, J. P., 755 Laurent, B., 672 Lavigne, G., 684 Laws, K. R., 523 Lawson, P., 355 Lax, T., 135 Lazarus, A. A., 297 Lazarus, C. N., 297 Lazzari, C., 342 Leahy, R. L., 259 Leary, M. R., 110, 111 Leavey, K., 445 Lebow, J., 559, 591 Leckman, J. F., 134, 135, 136 Leclerc, C., 530 Lecomte, T., 530 Lecrubier, Y., 109 Ledermann, T., 7 Ledley, D. R., 9, 135 LeDoux, J. E., 29, 30 Lee, C. W., 274 Lee, J. K., 185, 186, 187, 188, 190, 221 Lee, J. Y., 662 Lee, M. D., 453 Lee, S., 394 Lefave, K., 146 Leff, J. P., 486 Lehman, C., 135 Lehman, C. L., 5, 15, 19, 220, 226 Leibenluft, E., 481, 482 Leichsenring, F., 262 Lejuez, C. W., 341, 354, 355 Lelliott, P. T., 8, 11, 135, 150 Lenane, M., 134 Lenze, E., 4 Lenzenweger, M. F., 381, 383, 384 Leo, L. A., 641 Leon, A. C., 135 Leonard, H. L., 134 Leonard, K. E., 557, 561 LePage, J. P., 341 Lequesne, E. R., 381 Lerew, D. R., 6
786 Author Index
Letarte, H., 138 Letsch, J., 261 Levav, I., 258 Levendusky, P. G., 126 Levenson, H., 392 Levenson, J. C., 486 Levenson, R. W., 112, 192 Levine, J. C., 185 Levine, J. L., 262 Levis, D. J., 144 Levitt, A., 561 Levitt, J., 140 Levitt, J. T., 10, 30, 188 Levitt, K., 2 Levy, K. N., 384, 385, 445 Levy, R., 140, 446 Lew, H. L., 676 Lewandowski, A. S., 673 Lewin, M. R., 14, 25, 237 Lewin, T. J., 389 Lewinsohn, P. M., 340, 341, 342, 343,
355, 684 Lewis, D. C., 559 Lewis, E. L., 16 Lewis, J. A., 185 Lewis, S. W., 524, 548 Lewis-Fernandez, R., 4 Li, X., 448 Liao, B., 29 Lichner, T. K., 138 Lichstein, K. L., 640, 641, 644, 645 Licht, D. M., 487 Lichtenstein, P., 549 Lidren, D. M., 11 Lieb, K., 385, 386 Lieb, R., 7 Lieberman, M., 755 Liebman, R. E., 76 Liebowitz, M., 109 Liebowitz, M. R., 19, 119, 224, 230 Liepman, M. R., 564 Lilford, R. J., 523 Lim, L., 111 Lin, J., 261 Lin, Q., 318 Linardon, J., 711, 723 Lincoln, M., 524 Lindhiem, O., 128 Lindsay, M., 140 Linehan, M. M., 72, 186, 218, 235, 265,
266, 342, 353, 381, 382, 383, 384, 385, 388, 390, 391, 393, 394, 400, 403, 404, 408, 409, 412, 415, 434, 444, 445, 448, 452, 462, 730
Link, P. C., 531
Links, P. S., 382 Linton, S. J., 658, 672, 673 Lipp, O. V., 30 Lipsitz, J. D., 109, 318 Lipton, M., 68 Liss, A., 9 Lissek, S., 9 Litt, M. D., 562 Litz, B. T., 76, 109 Liu, L., 531 Liu, S., 448 Liverant, G. I., 189, 218, 221 Livesley, J. W., 383 Lizardi, H., 266 Llera, S. J., 185 Lobbestael, J., 268, 274 Lochner, C., 135 Lock, J., 711 Locke, E. A., 351 Lofwall, M. R., 621 Logue, M. B., 185 Lohr, K. N., 711 Lohr, N. E., 394 Long, Q. X., 612 Longabaugh, N., 576 Longabaugh, R., 562, 568, 572, 619 Lonsdorf, T. B., 221 Looney, S. W., 355 Loosen, P. T., 259 Lopatka, C., 2 Lopez, M., 640 Lopez, M. E., 218 López-Martínez, A. E., 673 Loranger, A. W., 381, 382 Lorenz, M., 9 LoSavio, S. T., 76 Losee, M. C., 11 Louro, C. E., 9 Lovell, K., 142, 355 Lovibond, P. F., 17, 29, 191, 220 Lovibond, S. H., 191, 220 Lowe, M. R., 451 Lozano Bleda, J. H., 343 Lubman, D. I., 555 Lucas, J. A., 2, 23 Luchies, L. B., 756 Lucock, M. P., 111 Ludäscher, P., 382 Ludman, E. J., 488 Lukach, B. M., 9 Luoma, J. B., 266 Lussier, J. P., 618, 619 Lustman, P. J., 259 Luttels, C., 15 Luty, S. E., 260
Luytens, P., 321 Lyddon, W. J., 67 Lydiard, R. B., 119 Lynch, D., 523 Lynch, K. G., 446 Lynch, S. M., 445, 448 Lynch, T. R., 389, 403, 448 Lysens, R., 673 Lytle, R., 342 Lyvers, M., 384
M
Ma, S. H., 265 Ma, X., 683 Machan, J. T., 184 MacLane, C., 390 MacLean, C. D., 621 Macmillan, F., 547 MacPherson, L., 354, 355 Madeddu, F., 394 Maercker, A., 383 Maes, H. H., 6 Maffei, C., 394 Magill, M., 618, 619 Mago, R., 258 Magura, S., 572 Mahoney, A., 126 Mahoney, M. J., 67 Maidenberg, E., 9, 12 Maier, S. F., 9 Maimone, J. S., 443 Mainguy, N., 14 Mairs, H., 355 Maitland, D. W. M., 342 Maki, K., 11 Malamuth, N. M., 749 Malan, J., 2 Malkoff-Schwartz, S., 486 Maller, R. G., 7 Malogiannis, I. A., 268 Malone, K. M., 446 Malouff, J. M., 109 Maltby, N., 153 Maltsberger, J. T., 448 Manber, R., 640, 642, 662 Manchikanti, L., 672 Mancill, R., 135 Mancill, R. B., 5, 220 Maner, J. K., 7 Mangweth-Matzek, B., 705 Manicavasagar, V., 265 Mann, D., 384 Mann, J. J., 446
Author Index 787
Manno, J. E., 622 Mannuzza, S., 19 Manos, R. C., 343 Manuel, J. K., 576 Manzini, C., 684 March, J. S., 136, 143 Marchand, A., 14 Marchione, K., 14 Marchione, N., 14 Marcus, S. C., 258 Margolin, G., 571, 594, 743, 750 Margraf, J., 2, 5, 7, 9, 21, 226 Mari, J. J., 530 Marin, N. W., 16 Marino, M., 645 Marker, C. D., 26 Markowitz, J. C., 72, 76, 258, 317, 318,
319, 320, 321, 322, 324 Marks, A. P., 140, 143 Marks, I. M., 8, 11, 17, 28, 135, 140, 141,
142, 145, 150, 230 Marks, L. M., 141 Marlatt, G. A., 409, 562, 577, 585, 588,
589, 592 Marlowe, D. B., 619, 620 Marmar, C., 676 Marmar, C. R., 65 Marom, S., 109 Marques, L., 77 Marrs, A., 4 Marsch, L. A., 622 Marsh, G. R., 662 Marsh, J. C., 620 Marshall, R. D., 318 Marsiglia, F. F., 563 Martarelli, D., 683 Martell, C. R., 235, 339, 341, 342, 343,
346, 352, 353, 355, 663, 768 Marten, P. A., 185 Martin, C., 445 Martin, G. E., 444 Martin, N. G., 6 Martin, T., 560 Martinez, J. H., 189 Martinsen, E. W., 26 Marx, B. P., 72 Marzol, P., 7 Masellis, M., 135 Masheb, R. M., 707 Masi, G., 483 Masland, S., 496 Masland, S. R., 384 Mastroyannopoulou, K., 673 Masuda, A., 175 Mataix-Cols, D., 11, 135
Mathew, K. L., 265 Mathews, A., 110 Mathews, A. M., 141 Mathys, M., 265 Matsunaga, H., 136 Mattick, R. P., 620, 624 Mavissakalian, M., 5 Mawson, D., 140 Mayers, A., 317 Mayfield, D., 564, 565 Mayo-Wilson, E., 109 Mays, V., 523 Mazumdar, S., 230 Mazzucchelli, T., 343 McBride, C., 260 McCall, L., 620 McCann, I. L., 67 McCann, M., 624 McCarron, J., 534 McCarthy, E., 531 McCarthy, K. S., 120 McCarthy, P. R., 142 McCarty, D., 614 McCauley, E., 355, 388, 389 McCracken, J. T., 146 McCrady, B. S., 555, 557, 559, 560, 562,
563, 569, 572, 575, 576, 587, 591, 592, 605, 613, 743
McCray, L. W., 259 McCrone, P., 264 McCullough, J. P., Jr., 266, 267 McDavid, J. D., 385, 388 McDonald, R., 140 McDonell, M. G., 390 McDowell, Y. E., 568 McEachran, A. B., 263 McElroy, S. L., 708 McEvoy, P., 11 McFall, M., 72 McGill, C. W., 501 McGinn, L. K., 258 McGirr, A., 484 McGlashan, T. H., 382 McGlinchey, E., 448 McGovern, J., 523 McHugh, R. K., 218, 449, 664 McIlhaney, K., 390 McIntosh, V. V. W., 711 McKay, D., 134 McKay, J. R., 589 McKenna, P. J., 523 McKnight, P. E., 112 McLane, M., 266 McLaughlin, K. A., 64, 447 McLean, C. P., 109
McLean, P. D., 14, 144 McLean, P. L., 144 McLear, C., 128 McLellan, A. T., 559, 568, 589, 616 McLeod, G., 564, 565 McMain, S. F., 383, 388 McManus, F., 111 McMillan, D., 354 McNally, R. J., 7, 9, 21, 29 McNamee, G., 8, 11 McNeil, D. W., 341 McQuaid, J. R., 531 McTeague, L. M., 221 Mead, D. E., 749 Meaden, A., 523 Meadows, E. A., 8 Meadows, G. N., 266 Means-Christensen, A. J., 225, 453 Medina-Pradas, C., 487 Medoro, L., 7 Meeks, S., 355 Meerwijk, E. L., 444, 445 Mehlum, L., 388, 389, 390 Mehta, M., 143 Mehta, S. H., 620 Mei, A., 674 Meichenbaum, D. H., 74 Meijer, J., 7 Mellman, T. A., 2 Melzack, R., 681, 687 Mendelson, T., 389 Mendelson, W., 645 Menges, D., 569, 593 Mennin, D. S., 185, 186, 187, 221, 384,
447 Menzies, R. G., 117 Merikangas, K. R., 64, 220, 482, 483 Merriam-Webster, Inc., 412 Merskey, H., 671 Mertens, J. R., 557 Messenger, C., 7 Meterissian, G. B., 259 Metzger, R. L., 191, 225 Meuret, A. E., 25, 26, 27, 30 Meyer, A., 319 Meyer, B., 486 Meyer, O. L., 190 Meyer, T. J., 191, 225 Meyer, V., 139, 140 Meyers, R. J., 564, 566, 576, 587, 619 Michalec, E., 618 Michel, B. D., 453 Michelson, L. K., 13, 14 Michelson, S. E., 186, 188 Michna, E., 676
788 Author Index
Miklowitz, D. J., 275, 480, 482, 483, 484, 487, 488, 489, 490, 491, 493, 494, 496, 497, 501, 503, 504, 515, 530
Miller, A. L., 15, 382, 390, 447 Miller, G. A., 221 Miller, I. W., 343, 446, 448, 449, 483, 485 Miller, K. J., 605 Miller, L. R., 675 Miller, M. L., 191, 225 Miller, N. E., 138 Miller, P. P., 4 Miller, S., 9 Miller, W. R., 128, 233, 239, 455, 560,
564, 568, 569, 576, 577, 590, 619, 651, 663, 664
Milliken, C. S., 66 Milliner, E., 136 Millner, A. J., 453 Millstein, D. J., 187 Milrod, B. L., 318, 320, 321 Milton, F., 13 Mineka, S., 7, 9, 17, 219 Miner, C. R., 676 Minhajuddin, A., 265 Minichiello, W. E., 136, 159 Mintz, J., 485, 487 Mintz, R. S., 397 Miranda, R., 448 Mitchell, B. G., 265 Mitchell, J. E., 712 Mitchell, K. M., 275 Mitchell, K. S., 76, 77 Mitchison, G., 639 Mitsopoulou, T., 11 Miyahara, S., 496 Moeller, F. G., 486 Moergeli, H., 675 Moffit, T. E., 221 Mohammadi, A., 343 Mohlman, J., 186 Mohr, D. C., 264 Moisan, D., 7 Mojtabai, R., 258 Molenberghs, G., 453 Molina, S., 185 Möller, H. J., 481 Monahan, P., 5, 386 Monahan, S. C., 619 Mondin, T. C., 268 Mongeon, J. A., 619 Monk, T. H., 486, 495, 645 Monson, C., 676 Monson, C. M., 64, 67, 69, 71, 72, 75, 76,
83, 89, 91, 92, 95, 98, 383 Montag, C., 221
Monteiro, W. O., 135, 150 Montgomery, P., 642 Monti, P. M., 618 Moody, L., 618 Moore, A., 448 Moore, B. A., 619 Moore, L. M., 261 Moore, M. T., 185 Moore, P., 4 Moos, B. S., 580 Moos, R. H., 558, 559, 580 Moran, P., 445 Moreau, D., 317 Moreira, A. L. R., 482 Morgan, K. E., 737 Morgenstern, J., 559 Mori, N., 708 Morin, C. M., 184, 640, 641, 642, 644,
645, 652, 653, 658, 659, 662 Morina, N., 109 Moring, J. C., 77 Moritz, S., 583 Morland, L. A., 76 Morley, S., 673 Morphy, M. A., 262 Morral, A. R., 141 Morris, B. W., 446 Morris, T. L., 355 Morrison, A. P., 525, 526, 531, 532 Morse, J. Q., 389, 448 Mortensen, P. B., 446 Moscovitch, D. A., 110, 123 Moser, J., 145 Mou, D., 449 Mowrer, O. H., 66, 137, 138 Moyers, T. B., 560 Muehlenkamp, J. J., 382, 447, 449, 453,
464 Muenz, L. R., 335 Mueser, K. T., 523, 530, 531 Mufson, L., 317 Muhlberger, A., 9 Mühlberger, A., 221 Muhuri, P. K., 676 Muijen, M., 523 Mulé, S., 486 Mulick, P. S., 343, 355 Mullen, K., 77 Müller, N., 109 Munafò, M. R., 221 Munizza, C., 259 Munoz, E. A., 342 Muñoz, R. F., 341, 342 Munroe, M. K., 343 Munshi, K., 265
Munz, L. M., 444 Munzinger, M., 261 Muran, J. C., 286 Murdock, T., 67 Murphy, D. L., 145 Murphy, G. D., 262 Murphy, G. E., 259 Murphy, M. T., 14, 27 Murphy, R., 705 Murphy, R. A., 76 Murray, A. L., 342 Murray, G., 485 Murray, H. W., 449 Murrell, A. R., 192 Murrell, E., 4 Mussell, M., 185 Mustelin, L., 707 Mystkowski, J. L., 14, 24, 30, 31, 220
N
Nader, K., 30 Nadort, M., 387 Nagendra, A., 532 Nahum-Shani, I., 470 Naito, N. A., 619 Najmi, S., 188, 192, 448 Napier, A. Y., 494 Naranjo, C. A., 573 Nardi, A. E., 222 Nardo, P. A., 226 Nathan, P. E., 217 National Institute for Health and Care
Excellence, 75, 523, 711, 714 National Institute of Health and Clinical
Excellence, 343 National Institute on Alcohol Abuse and
Alcoholism, 556, 562, 564, 577 National Institute on Drug Abuse, 612,
613 National Institutes of Health, 640 Nations, K. R., 12 Naugle, A. E., 355 Neacsiu, A. D., 218, 381, 383, 390, 391,
444, 445, 462, 730 Neale, J. M., 393 Neale, M. C., 221 Neary, T. J., 342 Nee, J., 230 Neely, J., 493 Neff, K. D., 191 Negt, P., 266, 267 Neighbors, C., 577 Neilson, E. C., 342
Author Index 789
Neitzert Semler, C., 657 Nelson, C. B., 64 Nelson, H. F., 588 Nelson, P., 2 Nelson Goff, B. S., 69 Nemeroff, C. B., 266 Nemes, S., 622 Néron, S., 11 Nesse, R. M., 4 Neubauer, D. N., 642 Neugebauer, R., 318 Neuhaus, E. C., 342 Neumann, D. L., 30 Neuner, F., 72 Newman, C. F., 259, 386 Newman, M. G., 185, 186, 342 Neziroglu, F., 134 Ng, M. Y., 664 Ng, T. H., 662 Nhat Hanh, T., 195 Nicassio, P. M., 642 Nich, C., 585 Nicholas, C., 354 Nicholas, M. K., 673 Nicholson, J. M., 560 Nielsen, T., 684 Nierenberg, A. A., 262 Niles, A. N., 15 Nisbett, R. E., 391 Nisenbaum, R., 382 Nishikawa, Y., 389 Nock, M. K., 443, 444, 446, 447, 448,
449, 450, 451, 452, 453, 459 Noel, N., 588 Noël, X., 556 Nofzinger, E. A., 663 Nolen, W. A., 262 Nolen-Hoeksema, S., 353 Norberg, M. M., 30 Norcross, J. C., 560 Nordahl, H. M., 186, 572 Nordentoft, M., 446, 447, 616 Nordgreen, T., 11 Noriega-Dimitri, R., 25, 237 Norman, S. B., 225, 229, 453, 468 Norris, F. H., 65 Norton, P. J., 27, 31, 121, 676 Nose, M., 385 Noshirvani, H., 28, 135 Noshirvani, H. F., 150 Nowakowski, S., 645 Nowlan, K. M., 762 Noyes, R., 4, 5 Nuechterlein, K. H., 487, 526 Nugent, N. R., 448
Nunes, E. V., 335 Nuzzarello, A., 31 Nylocks, K. M., 218, 381, 730
O
O’Brien, C. P., 559 O’Brien, G. T., 5, 10, 13 O’Brien, M. P., 497 Ochalek, T. A., 622 Ockert, D., 590 O’Connor, M. E., 318, 737 O’Donnell, L. A., 490 Oei, T. P. S., 11, 268, 275 O’Flaherty, A. S., 29 O’Grady, J., 448 O’Grady, K. E., 320 Oguz, M., 493 O’Hara, M. W., 317 Ohayon, M. M., 639, 640, 684 Okamura, N., 6 O’Keeffe, D., 684 Okifuji, A., 684 Olatunji, B. O., 7, 187, 384 O’Leary, K. D., 275 O’Leary, M. R., 585 Olendzki, B., 355 Olesnycky, O. S., 465 Olfson, M., 258 Ollendick, T., 136 Olmstead, T. A., 576 Oltmanns, T. F., 447 Olufs, E., 142 O’Mahen, H. A., 354 O’Malley, S. S., 562 Ondze, B., 663 O’Neill, E., 681 Ong, J. C., 640, 662 Onwumere, J., 530 Oomen, J., 15 Operskalski, B., 488 Oquendo, M. A., 444 Orff, H. J., 645 Orford, J., 571, 588, 593 Orme, W. H., 448 Ormel, J., 10 Orr, E., 110 Orr, S. P., 71, 72 Orrico, E. G., 447 Orsillo, S. M., 10, 184, 185, 186, 187, 188,
189, 190, 191, 207, 211, 221, 447 Ortega, L. A. G., 444 Orue, I., 274 Osborn, M., 448
Osman, A., 681 Öst, L., 140, 144, 145 Öst, L. G., 26, 27, 142 Ostacher, M. J., 72 O’Sullivan, G., 11, 135 Otis, J. D., 670, 671, 672, 673, 675, 676 O’Toole, M. S., 186 Otto, M. W., 7, 12, 17, 30, 496 Oud, M., 261, 276 Ougrin, D., 445 Ouimet, A. J., 185 Outcalt, S. D., 675 Overholser, J. C., 306 Özabaci, N., 268 Ozdemir, O., 135 Özdin, S., 274 Ozeki, S., 342 Ozerdem, A., 493
P
Pabst, A., 583 Padesky, C. A., 275, 276 Pae, C. U., 675 Page, A., 444 Page, B., 382 Pagoto, S. L., 341, 354, 355 Pagura, J., 383 Pai, A., 135 Palav, A., 7 Palcher, J. A., 675 Palermo, T. M., 673 Pallanti, S., 8, 190 Palmer, S., 264 Pampallona, S., 259 Panagioti, M., 72, 446 Pantelis, C., 531 Panting, H., 381 Papageorgiou, C., 267 Papas, R. K., 673 Paquet, J., 645 Parachini, E. A., 386 Paradis, C. M., 15, 16 Parag, V., 445 Pargament, K. I., 126 Paris, J., 381 Park, C., 268 Parker, G., 265 Parker-Guilbert, K., 77 Parks, S. E., 444 Parsons, T., 323 Patel, V., 354 Paterniti, S., 8 Paterson, C., 524
790 Author Index
Pathak, D., 8 Pato, M. T., 145, 153 Patterson, G. R., 743 Paul, L., 526 Pauli, P., 9, 221 Pauls, D. L., 136, 137 Pavey, L., 755 Pawlow, L. A., 683 Paxton, S. J., 706 Paykel, E. S., 262, 264 Payne, L. A., 187, 217, 403, 449, 454,
705 Pazzaglia, P. J., 486 Pearce, R., 624 Pearlman, L. A., 67 Peat, C. M., 711 Peck, K. R., 612, 676 Pedersen, C. B., 446 Pediatric OCD Treatment Study Team,
143, 146 Peeters, F. P. M. L., 260, 268, 274 Peles, E., 620 Pelissolo, A., 109 Peng, K., 391 Penn, D., 532 Pennebaker, J. W., 8 Pepper, C. M., 266, 447 Pérez-Álvarez, M., 343 Perich, T., 265 Peris, T. S., 144 Perissaki, C., 141 Perivoliotis, D., 524, 531 Perlick, D. A., 489, 490 Perlis, M. L., 639, 645, 651, 655 Perlis, R. H., 485 Perloff, J. M., 275 Perna, G., 9 Perry, G. S., 258 Perry, J. C., 394 Perry, S. W., 317 Persons, J. B., 120, 275 Peselow, E. D., 263 Petermann, F., 29 Peters, E., 524, 527 Peters, E. M., 448 Peters, E. R., 524 Peters, M., 673 Peters, S., 342 Peterson, A. L., 445 Peterson, R., 21 Pettit, J. W., 448, 449 Petukhova, M., 4, 184 Peveler, R. C., 318 Pezawas, L., 221 Pfohl, B., 386, 446
Pham, M., 486 Pharoah, F., 530 Phoenix Australia Centre for Posttraumatic
Mental Health, 75 Photos, V. I., 453 Piacentini, J., 140, 146 Picard, R. W., 621 Picchioni, M., 385 Piccirillo, M. L., 112 Piedmont, J. I., 185 Pieters, R., 126 Pietrzak, R. H., 76 Pigeon, W., 639 Pilkonis, P. A., 335 Pilling, S., 523 Pilsbury, D., 25 Pincus, A. L., 342 Pine, D. S., 4, 481 Piper, W. E., 286 Pisetsky, E. M., 464 Pistorello, J., 390, 445 Pitman, R. K., 71, 72 Pivik, J., 681 Pizano, D., 263 Pizzi, L. T., 355 Plamondon, J., 11 Plasencia, M. L., 112 Plate, A. J., 118 Plener, P. L., 444 Plotkin, D., 6 Plutchik, R., 259 Pocock, S. J., 523 Polanco-Roman, L., 448 Polat, A., 135 Pollack, M. H., 7, 17 Pollini, R. A., 620 Pols, H., 7 Pomini, V., 523 Pompei, P., 683 Pontillo, D. C., 11 Poplavskaya, E. V., 381 Porter, J. F., 354 Portera, L., 135 Posner, K., 452 Post, R. M., 484 Pothos, E. M., 557 Pouliot, L., 445 Poulsen, S., 711 Poulton, R., 6 Power, C. K., 684 Power, K. G., 10, 11 Preacher, K. J., 266 Premkumar, P., 531 Prenoveau, J. M., 6 Presley, A., 12
Preston, K. L., 621, 622 Pretzer, J., 386 Price, D. D., 684 Price, E., 27, 31 Priebe, S., 383, 523 Prince, S. E., 760 Prins, A., 71 Prinstein, M. J., 448, 449, 459 Prochaska, J. J., 613 Prochaska, J. O., 560 Procidano, M. E., 569 Project MATCH Research Group, 560,
576, 589 Proulx, J., 190 Provencher, M. D., 267, 274 Prusoff, B. A., 317 Przeworski, A., 185 Purdon, C., 138 Purgato, M., 263 Pusch, D., 258
Q
Qaseem, A., 642 Qian, M. Y., 642, 684 Qiang, C., 276 Quartana, P. J., 672 QuickStats, 672 Quigley, B. M., 561 Quijano, L. M., 342 Quillian, R. E., 662 Quilty, L. C., 260 Quinlan, D. M., 335 Quintero, J. M., 186
R
Rabavilas, A. D., 141, 159 Rabbitt, S. M., 444 Rachman, S., 2, 29, 138, 141, 144, 148 Racine, M., 673 Radomsky, A. S., 29 Radtke, R. A., 662 Raes, F., 343 Rafanelli, C., 262 Raffa, S. D., 224 Rains, J. C., 342 Rajaratnam, S. M., 642, 684 Rakfeldt, J., 390 Ramirez, C. L., 355 Ramírez-Maestre, C., 673 Ramnero, J., 27 Randall, D., 622
Author Index 791
Randolph, J. J., 266 Ransom, D., 317 Rapee, R. M., 4, 7, 8, 9, 21, 23, 111, 113,
185, 226 Rapoport, J. L., 134 Rapp, R. C., 559 Rappaport, L. M., 448 Raskind, M., 72 Rasmussen, S. A., 134, 135, 136 Ratcliff, C. G., 121 Rathbone J., 530 Rathgeber, M., 743 Rathus, J. H., 15, 390 Rauch, S., 73 Rauch, S. L., 145 Raue, P. J., 268 Ravitz, P., 318 Rawson, R., 624 Ray, G. T., 557 Ray, L. A., 618, 619 Raymond, I., 684 Raytek, H. S., 605 Razran, G., 8 Rea, M. M., 489 Reading, A. E., 681 Ready, D., 72 Rector, N. A., 121, 135, 523 Ree, M. J., 641, 655, 657, 660 Reed, G. E., 139 Rees, C. S., 143, 342, 343 Rees, W., 28 Rehm, L. P., 258 Reich, D. B., 446 Reich, J., 5, 14 Reichler, L., 261 Reichman, J. T., 8 Reid, M. C., 672, 673 Reilly-Harrington, N. A., 259 Reimer, S. G., 110 Reinares, M., 490 Reinecke, M. A., 276 Reinhard, M. J., 66 Reinholt, N., 222 Reiser, D. E., 392 Reiss, S., 7, 21 Reite, M., 645 Reitz, S., 382 Renier, C. M., 675 Renna, M. E., 186 Renneberg, B., 5 Renner, F., 268, 274 Rescorla, R. A., 29, 138 Resick, P. A., 66, 67, 73, 76, 77, 83, 89, 91,
92, 95, 98, 383, 384 Resnick, H. S., 64, 65, 70
Reuter, M., 221 Revicki, D. A., 185 Reynders, A., 453 Reynolds, C. F., 645 Reynolds, C. F., III, 317 Reynolds, E. K., 354 Rhéaume, J., 138 Rhoades, G. K., 762 Ribeiro, J. D., 444, 446 Richard, P., 672 Richards, D., 343, 354 Richards, J. A., 482, 487, 489 Richards, J. C., 11 Richardson, A., 523 Richardson, T., 531 Richter, M. A., 135 Riddle, D. L., 672 Ridley, J., 7 Riedel, B. W., 640 Riemann, B., 140 Riemann, B. C., 9 Riggs, D., 67 Riggs, D. S., 135, 152, 159, 230 Riise, E. N., 140 Rikoon, S. H., 616 Rinaldi, C., 260 Ringer, F. B., 446 Riper, H., 343 Riso, L. P., 274 Ritenour, A. M., 495 Rith-Najarian, L. R., 261 Ritschel, L. A., 355 Ritz, T., 25 Ritzert, T. R., 118 Riviere, L. A., 672 Rizvi, S. L., 382, 383, 384, 391, 445 Roberson-Nay, R., 11 Roberts, J. E., 258 Roberts, M., 192 Roberts, N. P., 76 Roberts, P. A., 76 Roberts, T., 8 Robichaud, M., 144 Robins, C. J., 389 Robins, L. N., 593 Robinson, A., 389 Robinson, M. E., 684 Robinson, R., 468 Robinson, R. L., 675 Robinson, T., 76 Roca, J. V., 189 Rocca, P., 386 Rodante, D. E., 446 Roddy, M. K., 743, 762 Rodin, J., 706
Roehrs, T., 639 Roemer, L., 184, 185, 186, 187, 188, 189,
190, 191, 192, 207, 211, 221, 447 Roepke, S., 389 Rogers, M. L., 72, 446 Rogge, R. D., 749, 752, 762 Rohsenow, D. J., 618 Roitblat, H. L., 66 Rollman, B. L., 230 Rollnick, S., 128, 233, 239, 455, 560, 564,
569, 619, 651, 663, 664 Roman, P., 556, 572 Romera, I., 185 Ronchi, P., 9, 135 Rondung, E., 470 Roos, C. R., 584 Roozen, H. G., 564, 619 Rose, G. L., 621 Rose, N. R., 135 Rose, S. J., 590 Rosen, C., 483 Rosenberg, H., 580 Rosenberg, N. K., 11 Rosenberg, R., 672 Rosenfield, D., 25, 26, 30 Rosengren, D. B., 620 Rosenheck, R., 72 Rosenthal, E., 620 Rosenthal, L., 640 Rosenthal, M. Z., 381, 448 Rosenthal, R. N., 577 Rosenthal, T. L., 641 Rosmarin, D. H., 126 Ross, E. L., 674 Roth, R. S., 676 Roth, T., 638, 639, 640 Roth, W. T., 2, 9, 25, 226 Rothbaum, B. O., 66, 67, 72, 73, 140, 230,
342, 384 Rothman, K., 743, 762 Rothschild, L., 381 Rotunda, R., 4 Rounsaville, B. J., 319, 488 Rowa, K., 110, 112 Rowe, L. S., 761 Rowe, M. K., 8, 25, 29, 141, 237 Roy-Byrne, P. P., 2, 5, 10, 12, 14, 15, 32,
220 Rubenstein, B. S., 639 Rubonis, A. V., 619 Rucci, P., 226 Rücker, G., 385 Rudaz, M., 7 Rudd, M. D., 445 Rufer, M., 135
792 Author Index
Rufino, K. A., 448 Ruggero, C., 192 Ruggiero, K. J., 355 Ruiz-Párraga, G., 673 Runeson, B., 549 Rusch, L. C., 343, 355 Rüsch, N., 383 Ruscio, A. M., 184, 185 Rush, A. J., 234, 258, 259, 262, 263, 265,
275, 341, 445 Rush, B. R., 572 Ruskin, J. N., 2 Russ, E., 384 Rutter, M., 221 Ruzek, J. I., 217 Ryabchenko, K. A., 447 Ryan, K. M., 615, 680 Ryan, N. E., 276 Ryan, S. M., 9 Rybarczyk, B., 640 Ryberg, M., 673 Rychtarik, R. G., 572 Rygh, J. L., 234, 257, 387, 445, 654 Rytwinski, N. K., 119
S
Sabatino, S. A., 17 Sabo, A. N., 384 Sacco, W. P., 259, 264 Sachs, A. D., 11 Sachs, G. S., 496 Sachs-Ericsson, N., 266 Safer, D. L., 389, 390 Safran, J. D., 276, 286 Safren, S., 266, 390 Safren, S. A., 7, 230 Sagi, D., 639 Sagon, A. L., 189 Sahlin, H., 446 Sakai, M., 342 Sakiris, N., 222, 450 Sala, R., 483 Salas-Auvert, J. A., 19 Salavert, J., 486 Salazar, I. C., 119 Salazar, R. D., 640 Salbach-Andrae, H., 389 Salcedo, S., 487, 488 Saleem, R., 487, 489 Salisbury, C., 275 Salkovskis, P. M., 10, 25, 27, 29, 111, 138,
144, 149, 258, 381, 523, 660 Sallaerts, S., 15
Salters-Pedneault, K., 186, 190 Salyers, M. P., 683 Sampson, N. A., 4, 184, 446 Samstag, L. W., 276, 286 Sanchez, L., 355 Sanchez-Moreno, J., 485, 488 Sancho, M., 558 Sanderson, W. C., 15 Sandoz, E. K., 192 Sands, L., 683 Sanislow, C. A., 382 Santiago-Rivera, A. L., 355 Santos, M. M., 342 Saraceno, B., 258 Sareen, J., 468 Sarin, F., 523 Sarnie, M. K., 2 Sarsour, K., 640 Sartirana, M., 711 Sateia, M. J., 642 Sato, T., 481 Satre, D. D., 563 Sauer-Zavala, S. E., 5, 7, 187, 218, 219,
221, 223, 446, 447, 450, 451, 455, 460, 465
Saunders, B. E., 64 Saunders, J. B., 564 Savard, J., 662 Saxena, S., 258 Saxon, D., 354 Sayrs, J. H., 388 Sbrocco, T., 16 Scala, J. W., 385 Scarpato, M. A., 8 Schaap, C. P., 13, 135 Schade, A., 15 Schafe, G. E., 30 Schafer, J., 140, 143 Schatten, H. T., 446, 448 Schatzberg, A. F., 185 Schauer, M., 72 Schelble, K., 640 Schiller, E., 743 Schindler, A., 275 Schippers, G. M., 388 Schlam, T. R., 717 Schloredt, K., 355 Schmaling, K. B., 743 Schmidt, N. B., 6, 7, 15, 25, 274, 464 Schmidt, U., 711 Schneck, C. D., 491, 515 Schneider, A. J., 11 Schneider, K. L., 355 Schneiderman, A. I., 66 Schneiderman, J., 573
Schnicke, M. K., 67, 73 Schnurer, A., 140 Schnurr, P. P., 70, 75, 77 Schnyder, U., 72, 675 Scholl, L., 620 Schoorl, M., 711 Schramm, E., 110 Schreiber, S., 620 Schröter, A., 481 Schruers, K. R., 7, 9 Schulberg, H. C., 10 Schulze, T. G., 485 Schumacher, J., 6 Schumacher, T. S., 444 Schuster, C. R., 621, 622 Schutte, N. S., 109 Schwab, J. J., 185 Schwartz, C., 159 Schwartz, D. M., 684 Schwartz, S. M., 621, 642 Schwetz, T. A., 620 Scioli, E., 676 Scogin, F., 342 Scott, J. G., 258, 259, 264, 464, 485, 488 Scuito, G., 135 Scuri, S., 683 Seal, K. H., 676 Sedgwick, P., 622 Sedivy, S. K., 343 Sedway, J. A., 711 Seeds, P. M., 185 Segal, Z. V., 186, 207, 210, 259, 265, 266,
268, 276, 353, 362 Seidel, A., 25, 26 Sellers, E. M., 573 Selzer, M. A., 384 Selzer, M. L., 615 Seminowicz, D. A., 675 Sen, S., 676 Serlin, R. C., 145 Serowik, K. L., 189 Seth, P., 620 Sevier, M., 760, 761 Sexton, H., 26 Shadish, W. R., 743 Shafran, R., 29, 138, 708, 712 Shahar, F., 140 Shalev, A. Y., 72 Sham, P., 275, 487 Shapero, B. G., 448, 465 Shapiro, D., 11 Shapiro, F., 74 Shapiro, J. R., 711 Sharon, C., 445 Sharp, D. M., 10, 11
Author Index 793
Sharp, P. B., 221 Sharpless, B., 186, 187, 188 Sharpley, A., 641 Shattock, L., 532 Shaver, J. A., 382 Shaw, B. F., 234, 258, 259, 260, 276, 341 Shaw, I. A., 267, 387 Shaw, P. M., 141 Shawe-Taylor, M., 655 Shaw-Welch, S., 382 Shea, M. T., 260, 262, 268, 335 Shean, G., 7 Shear, M. K., 10, 16, 21, 23, 26, 224, 226,
230 Shearin, E. N., 408 Sheehan, D. V., 119 Sheehan, T., 575 Shelton, K. H., 742 Shelton, R. C., 259 Sher, K. J., 381, 568 Sherbourne, C. D., 343 Sherman, M., 23 Shevlin, M., 526 Shi, Q., 448 Shian-Ling, M., 381 Shin, H. C., 620 Shipherd, J. C., 28 Shlik, J., 110 Shnaider, P., 64 Shneidman, E. S., 448 Shoham, V. M., 743 Sholomskas, A. J., 317 Shreve, M. S., 621 Shudo, Y., 342 Shulman, I. D., 8 Siegel, S., 8 Siev, J., 186 Siever, L. J., 393 Sigmon, S. C., 619, 620, 622, 624 Sijbrandij, M., 109 Sijercic, I., 76 Silberstein, L., 706 Silk, K. R., 394, 446 Silverman, K., 619, 622 Simeon, D., 386 Simmonds-Buckley, M., 354 Simmons, A. D., 259 Simon, G. E., 10, 488 Simoneau, T. L., 482, 487, 489 Simons, A. D., 262 Simpatico, T. A., 624 Simpson, H. B., 140, 145, 146, 153, 176 Simpson, J. A., 411, 412 Simpson, L. E., 749, 761 Simpson, R. J., 10
Sinclair, D., 621 Singer, W., 268 Singla, D. R., 354 Sivertsen, B., 642 Skelly, J. M., 621 Skinner, B. F., 745 Skinner, L. J., 66 Skodol, A. E., 318 Skutch, J. M., 464 Slade, M., 523 Slaymaker, V., 575 Sledmere, C. M., 681 Sloan, D. M., 72, 383 Sloan, E., 221 Sloan, K. L., 620 Sloan, T., 29 Slotter, E. B., 756 Slye, T. A., 641 Smelson, D., 621 Smeraldi, E., 135 Smink, F. R. E., 706, 708 Smit, F., 523 Smith, D. B., 69 Smith, J. E., 547, 564, 566, 576, 587, 619 Smith, K. E., 448 Smith, L. J., 223, 645 Smith, M. T., 639, 640, 645, 684 Smith, P. H., 557 Smith, R. H., 126 Smitham, S., 354 Smith-Janik, S. B., 26 Smits, J., 343 Snarski, M., 355 Snyder, D. K., 743 Snyder, K. S., 487 So, M., 275 Sobczak, L. R., 190 Sobell, L. C., 568, 572, 576, 577, 587,
593, 616 Sobell, M. B., 568, 572, 576, 577, 587,
593, 616 Soeffing, J. P., 645 Soeter, M., 30 Sokol, L., 259 Sokolowska, M., 8 Soler, J., 388 Soloff, P. H., 446 Solomon, P. L., 390 Solomonov, N., 265 Somhegyi, H., 673 Soneson, E., 526 Sonnega, A., 64 Sonntag, H., 109 Sood, J. R., 355 Sotres-Bayon, F., 29
Sotsky, S. M., 334, 335 Southward, M. W., 450 Southwick, S. M., 76 Spangler, D. L., 284 Spanier, C. A., 263 Spanier, G., 571, 594 Spaniol, L., 515 Sparks, P., 755 Spates, C. R., 342, 354, 355 Specht, M. W., 448 Spek, V., 342 Spencer, T., 189 Spiegel, D. A., 31 Spiehler, V., 622 Spielman, A. J., 641, 651 Spijker, J., 262 Spinazzola, J., 383 Spindler, H., 11 Spinelli, M., 317 Spirito, A., 260, 261, 448 Spiro, A., III, 70 Spitzer, R. L., 70, 225, 343, 382, 452, 453,
468, 495, 568, 681 Sprich, S., 266, 390 Spruyt, A., 9 St. John, D., 386 St John, N. J., 444 St. Lawrence, J. S., 66 Stacy, J. N., 621 Staerkle, R., 675 Stafford, J., 69 Stahl, D., 445, 532 Staines, G., 572 Stallvik, M., 572 Stampfl, T. G., 144 Stangier, U., 110 Stanley, B., 381, 445, 452, 453 Stanley, I. H., 72 Stanley, M. A., 4, 26, 159 Stanton, C. E., 342 Stapinski, L. A., 185 Staples, A. M., 186 Starcevic, V., 386 Steele, C., 523, 527, 532 Steele, S. J., 222, 223 Steer, R. A., 119, 225, 319, 343, 416, 615,
625 Steffel, L. M., 445 Steger, M. F., 112 Stein, A. T., 343 Stein, D. J., 64, 133, 134, 135, 136, 269,
386 Stein, M. B., 7, 15, 109, 220, 221, 225,
453, 675 Steinberg, M. L., 605
794 Author Index
Steinert, C., 262 Steinmetz-Breckenridge, J., 340 Steketee, G. S., 66, 135, 136, 140, 141,
142 Stepanski, E. J., 639, 640, 653 Stepp, S. D., 382 Sterba, S. K., 448 Stern, R. S., 140 Stetson, D., 10 Stevens, C., 286 Stevens, K. P., 134 Stevens, K. T., 450 Stewart, A., 711, 722 Stewart, B. L., 416 Stewart, D. G., 390 Stewart, J. W., 335 Stewart, R. E., 109 Stewart, S. H., 17 Stickle, T. R., 743 Stiles, T. C., 144 Stinson, K., 641 Stitzer, M. L., 621 Stöber, J., 191 Stockton, P., 70 Stockton, S., 492 Stoffers, J. M., 385 Stolar, N. M., 524 Storch, E. A., 136, 140, 142, 147, 153, 230 Stout, R., 588 Stowkowy, J., 531 Stoyanova, M. S., 30 Strain, E. C., 621 Strakowski, S. M., 484 Strathdee, S. A., 620 Straus, M., 571 Straus, M. A., 749 Strauss, C., 756 Strauss, J. L., 268 Street, A. E., 66, 69 Street, G. P., 135 Striegel-Moore, R., 706 Strine, T. W., 258 Strober, M. A., 491 Strong, D., 483 Strosahl, K., 112, 188 Strosahl, K. D., 30, 118, 186, 234, 342 Stuart, G. L., 14 Stuart, R. B., 743 Stuart, S., 259, 317 Sturges, L. V., 7 Styer, D. M., 448 Suarez, A., 388 Suárez, L., 5, 218, 221 Suarez-Jimenez, B., 321
Substance Abuse and Mental Health Services Administration, 444, 612
Suddath, R. L., 489 Sue, D. W., 192, 193 Suelzer, M., 5 Sugar, C. A., 445 Sugarman, D. B., 571, 749 Sullivan, H. S., 319 Sullivan, J. M., 340 Sullivan, J. T., 573 Sullivan, M. J. L., 672, 675, 681 Sundram, B. M., 683 Suppes, T., 481, 485 Surawy, C., 111 Surís, A., 77 Suvak, M., 189 Suvak, M. K., 76, 189 Svartberg, M., 320 Swain, J., 109 Swann, A. C., 486 Swannell, S. V., 444 Swanson, V., 10, 11 Swartz, H. A., 317, 320, 324, 515 Swartz, M., 381 Swartzentruber, D., 17 Swedo, S. E., 134, 135 Swick, D., 74 Swinson, R. P., 4, 8, 9, 11, 17, 135 Syed, Y. Y., 620, 624 Sykora, K., 573 Szabó, C., 268 Szafranski, D. D., 121 Szatmari, P., 711
T
Tabak, B. A., 221 Tacchi, M. J., 485 Taft, C. T., 69 Tafti, M., 639 Tai, S., 523, 531 Talavera, D. C., 653 Talbot, L., 653, 657 Talovic, S., 571 Tang, N. K., 641, 655, 657 Tanji, F., 448 Tanne, D., 639 Taplin, R., 390 Tarrier, N., 67, 72, 445, 446, 522, 523,
524, 525, 528, 530, 531, 532, 534, 541, 549
Taylor, A., 109 Taylor, A. E., 71
Taylor, C. B., 2, 4, 6, 7, 9, 13, 226, 662 Taylor, C. T., 112 Taylor, D. J., 640 Taylor, D. O., 482 Taylor, G., 274 Taylor, J., 382 Taylor, K., 445 Taylor, M., 549 Taylor, P. J., 525 Taylor, S., 7, 14, 21, 23, 676 Taylor Dryman, M., 112 Teachman, B. A., 26 Teasdale, J. D., 186, 210, 264, 265, 353 Telch, C. F., 4, 390 Telch, M. J., 2, 4, 11, 13, 23, 29, 274 Tellegen, A., 229 Templeton, L., 571, 593 ten Klooster, P. M., 230 Tennen, H., 562 Tenney, N., 135 Teri, L., 340, 355 Terman, M., 664 Testa, M., 561 Testa, S., 14 Tharp, R. G., 351 Thase, M. E., 258, 264, 265, 275, 276 Thayer, J. F., 185 Thomas, A. M., 185 Thomas, J. C., 140 Thomas, M., 264 Thomas, N., 523 Thomas, W. J., 276 Thompson, L., 276 Thompson, R. J., 112 Thompson-Brenner, H., 451 Thompson-Holland, J., 221 Thorberg, F. A., 384 Thordarson, D. S., 138, 144 Thorén, P., 153 Thorgeirsson, T. E., 6 Thulin, U., 27 Thum, Y. M., 760 Thyer, B. A., 4 Tibalbi, G., 259 Tiemens, B. G., 10 Tilders, F. J., 9 Tillotson, C. J., 614 Timko, C., 559 Timmer, A., 385 Timms, P., 531 Tipnis, A., 621 Tirpak, J. W., 450 Titov, N., 11 Tobena, A., 8
Author Index 795
Tobia, G., 263 Toblin, R. L., 672 Tolin, D. F., 30, 153, 159, 230, 260, 343 Tomasi, D., 557 Tomazic, T. J., 684 Tomko, R. L., 381, 382 Tondo, L., 485 Tonigan, J. S., 560, 568, 576, 590 Tordrup, D., 264 Torgersen, S., 5, 382 Torre, J., 755 Torrent, C., 488 Torres, A. R., 135 Touboul, C., 672 Touyz, S., 711 Towbin, K. E., 136, 481 Tracey, I., 675 Tran, G. Q., 135 Tranah, T., 445 Träskman, L., 153 Trauer, J. M., 642, 684 Treanor, M., 139, 186 Treat, T. A., 14 Trentacosta, C. J., 128 Trieu, V. H., 523 Trivedi, M. H., 265 Trockel, M., 662 Trower, P., 110 Truax, C. B., 275 Trull, T. J., 381, 382 Trupin, E. W., 390 Tsai, M., 422 Tsao, J. C. I., 2, 6, 14, 21, 31, 220 Tsuang, M. T., 134, 135 Tsypes, A., 448 Tucker, B., 142 Tukel, R., 135 Tull, M. T., 221, 354, 446, 447 Tune, G. S., 146 Tung, E. S., 19 Turecki, G., 446 Turek, F. W., 639 Turk, C. L., 221, 384 Turk, D. C., 681, 684 Turkheimer, E., 447 Turkington, D., 531 Turkoski, B., 683 Turksov, N., 135 Turner, B. J., 444 Turner, D. T., 523 Turner, J. B., 447 Turner, R. M., 140, 141, 388, 389 Turner, S. M., 119, 159 Tusa, N., 258
Tutek, D. A., 388 Twentyman, C. T., 66 Twisk, J., 343 Twohig, M., 142, 175 Twohig, M. P., 30, 175 Tyler, R., 390 Tyrer, P. J., 221
U
Udo, T., 707, 708 Uebelacker, L. A., 483, 742 Uhde, T. W., 2 Uhl, K., 260 Uhl, S., 445 Unruh, B. T., 384 Unutzer, J., 488 Uscinska, M., 386 Usmani, A., 187
V
Vajk, F. C., 275 Valderhaug, R., 140, 159 Valderrrama-Diaz, M. A., 343 Vall, E., 705 Valleni-Basille, L. A., 134 Vallieres, A., 645, 659 Vallis, T. M., 276 Valmaggia, L. R., 523 van Aalderen, J. R., 265 van Asselt, D. I., 387 Van Audenhove, C., 453 van Balkom, A. J., 17, 25, 144 van Beek, N., 7 van de Ven, N., 126 Van den Bergh, O., 662 Van den Bosch, L., 388 van den Brink, W., 388 van den Hout, M. A., 9, 15, 27, 28 Van Den Noortgate, W., 559 van der Gaag, M., 523 van der Kolk, B. A., 394 van der Kroft, P., 564 van der Zweerde, T., 642 Van Dijk, S., 390 Van Donsel, A., 624 van Dyck, R., 9, 17, 25, 28 van Gorp, W., 485 Van Gucht, D., 343 Van Haitsma, K., 355 Van Hoeken, D., 706
Van Houdenhove, L., 662 van Kraanen, J., 142 van Megen, H. J., 6 van Megen, J. G., 135 Van Meter, A., 482 van Minnen, A., 141 Van Someren, E. J., 639 van Spiegel, P., 25 van Straten, A., 275 van Straten, A., 343, 642, 658, 684 van Tulder, F., 221 Van Voorhees, B. W., 342–343, 355 van Wel, E. B., 387 van Zijderveld, G., 9 Vander Bilt, J., 226 Vanderplasschen, W. _, 559 Vansteenwegen, D., 30 Varese, F., 526 Vasile, R. G., 5 Vaughn, C. E., 486 Velleman, R., 571, 593 Veltman, D. J., 9 Vento, S., 460 Verbanck, P., 556 Verbraak, M. J., 387 Verburg, K., 7 Verdellen, C. W., 137 Verducci, J. S., 491 Verheul, R., 388 Vernon, P. A., 383 Verona, E., 266 Veronen, L. J., 64, 66 Versiani, M., 306 Vervliet, B., 29, 30 Vielhauer, M. J., 70 Vieta, E., 485, 488 Villalba-Garzon, J. A., 343 Villemin, E., 639 Vîslă, A., 344 Visser, H., 134 Visser, S., 144 Vitiello, M. V., 639 Vittengl, J. R., 258, 265 Vittorio, L., 446 Vlaeyen, J. W., 672, 673 Vlahov, D., 620 Vogel, P. A., 144 Vogel, R., 382 Vogt, D. S., 66 Volkow, N. D., 556, 557 Völlm, B., 385 Von, J. M., 64 Vos, S. P., 13 Vos, T., 31, 264
796 Author Index
Vowles, K. E., 676 Vrinssen, I., 221 Vuori, E., 621
W
Wachen, J. S., 67 Wade, D., 76 Wade, J. B., 672, 684 Wade, T. D., 705, 711, 723 Wade, W. A., 13 Wagener, A., 343 Wager, T. D., 384 Wagner, A. W., 355 Walford, L., 525 Walitzer, K. S., 580 Walker, D. L., 30 Walker, J., 382 Walker, R. L., 676 Wall, P. D., 687 Wallace, M. L., 486 Wallace, S. T., 110 Waller, D., 712, 714, 723 Waller, G., 354, 706 Wallin, L., 523 Walper, K. C., 672 Walser, R. D., 266 Walsh, J. K., 640 Walsh, L. M., 743 Walsh, S. L., 612, 621 Walters, E. E., 4, 64, 109 Walters, K., 491 Walters, S. T., 560 Walton, G. M., 756 Waltz, J., 389 Wamhoff, J., 261 Wampold, B. E., 75, 119 Wang, C. E., 274 Wang, G. J., 557 Wang, J., 258, 262 Wang, P. S., 184 Wang, S. B., 464 Ward-Ciesielski, E. F., 234, 257, 387, 445,
452, 654 Wardle, J., 17 Wardle, M., 526 Ware, J. C., 644 Ware, J. E., 343 Warmerdam, L., 275, 343, 684 Warren, R., 140 Warshaw, M., 135 Warwick, H. M., 144 Washburn, J. J., 448, 450 Wasser, T., 390
Waterloo, K., 274 Waters, A. M., 136, 186 Watkins, E., 655 Watkins, E. R., 275, 487 Watkins, L. E., 69 Watson, D., 6, 192, 219, 229 Watson, D. L., 351 Watson, H. J., 711 Watts, B. V., 75, 77 Watts, F. N., 144, 641 Weathers, F., 70 Weathers, F. W., 71 Webb, R. T., 549 Webber, M., 267 Webber, M. A., 387 Weck, F., 13, 14 Wedig, M. M., 382, 383, 448 Weems, C. F., 7 Wegner, D. M., 188, 192, 448 Weidt, S., 135 Weiller, E., 258 Weinberg, A., 221 Weinberg, I., 386, 387, 446 Weinberger, A. D., 234, 257, 387, 445, 654 Weiner, E. S., 411, 412 Weinstein, C. D., 571 Weinstock, L. M., 343, 483, 485 Weiser, M., 221 Weishaar, M. E., 266, 273, 274, 386 Weismann, T., 390 Weisner, C., 557 Weiss, B., 383 Weiss, C., 258 Weiss, R. L., 743, 749 Weissman, A., 446 Weissman, M. M., 135, 317, 318, 319, 320,
321, 322, 326, 329, 334, 335, 343, 488 Weisz, J. R., 664 Weitz, E. S., 259 Welch, K. A., 268 Welkowitz, L., 13 Weller, S. B., 619 Wells, A., 110, 111, 185, 187, 266, 267 Wells, H., 391 Wendel, J. S., 487 Wenzel, A., 114, 317, 445 Wergeland, G. J., 140 Wersebe, H., 109 Wesner, R., 5 West, A. E., 491 West, L. M., 190 West, P., 355 Westen, D., 383, 384, 393 Westenberg, H. G., 6, 135 Westerhof, G. J., 230
Westling, B. E., 26 Westra, H. A., 17, 233 Wetzel, R. D., 259, 262 Wetzler, S., 15 Weyers, P., 221 Whalley, L. J., 259 Wheeler, J. G., 742, 749 Whisman, M. A., 185, 268, 276, 743 Whisman, M. S., 742 Whitaker, C., 494 Whitaker, C. A., 417 White, K. S., 16, 23, 31 White, M. A., 707 Whitfield, K., 76 Whitford, H. S., 265 Whitford, T. J., 464 Whittal, M., 7 Whittal, M. L., 144 Wicklow, A., 641, 654 Wickwire, K., 11 Widerlöv, B., 523 Wiech, K., 675 Wiedemann, G., 9 Wilbourne, P. L., 558, 580, 619 Wilcox, C., 577 Wild, K. V., 259 Wilding, H., 445 Wilens, T. E., 483 Wilfley, D. E., 318, 706, 711 Wilhelm, F. H., 25 Wilhelm, S., 136 Wilkins, K. C., 563 Wilkinson, D. J., 2 Willcox, C. H., 389 Williams, A., 673 Williams, A. C. de C., 673 Williams, C., 23 Williams, J., 343 Williams, J. B., 226, 452, 495, 681 Williams, J. B. W., 70, 225, 343, 382, 453,
568 Williams, J. M., 186 Williams, J. M. G., 207, 210, 262, 265,
306, 353 Williams, K. E., 13, 15, 191 Williams, R., 77, 110 Williams, S. L., 10, 27 Willoughby, T., 449 Wills, R. M., 743 Wilner Tirpak, J., 222 Wilson, A. C., 673 Wilson, G. T., 318, 707, 711, 717 Wilson, K. G., 10, 30, 112, 118, 186, 188,
192, 234, 342 Wilson, N., 620
Author Index 797
Wilson, P. H., 275 Wiltsey Stirman, S. W., 258 Wimberly, J. D., 760 Winfield, I., 382 Winograd, G., 382 Winters, R., 483, 486 Wiprovnick, A. E., 619 Wirtz, P. W., 562 Wirz-Justice, A., 664 Wiser, S., 268 Wish, E. D., 622 Wislar, J. S., 622 Wisniewski, S. R., 496 Witkiewitz, K., 559, 562, 580, 584, 585,
588 Wittchen, H., 7, 184 Wittchen, H. U., 2, 4, 5, 109 Witthöft, M., 275 Wittkowski, A., 531 Wittmann, L., 675 Wohlgemuth, W. K., 662 Wolf, M., 389 Wolff, J., 260 Wolff, J. C., 448 Wolitzky-Taylor, K. B., 1, 4, 7, 15, 187, 463 Wolpe, J., 260 Wong, W., 530 Wood, J. M., 652 Wood, P. K., 381 Woodcock, E. A., 343 Woods, D. W., 142 Woods, S. E., 448 Woods, S. W., 2, 16, 224 Woodward, J. J., 562 Woody, S., 14 Woody, S. R., 138, 144 Woolaway-Bickel, K., 464 Wooten, V., 644 Worhunsky, P., 153 World Health Organization, 382, 444, 742 Wright, J. H., 259, 275 Wright, K., 275, 487 Wright, K. D., 675 Wright, N., 621 Wu, J. Q., 640
Wuellhorst, V., 342 Wunderlich, U., 109 Wurm, M., 470 Wyatt, J. K., 653 Wykes, T., 523, 525, 530, 531, 532
X
Xie, L., 639 Xu, Y., 109
Y
Yadin, E., 138 Yamamoto, T., 342 Yan, L. J., 487 Yang, Y., 619 Yang, Z., 268 Yap, K., 756 Yaryura-Tobias, J. A., 134 Yates, J., 259 Yatham, L. N., 484, 494 Ybanez, A., 342 Yeomans, F. E., 445 Yeterian, J. D., 562 Yeung, W. F., 662 Yi, J., 760, 761 Ying, J., 448 Yorke, L., 673 You, J., 448 Young, J. E., 234, 257, 258, 266, 267, 269,
270, 272, 273, 274, 296, 297, 306, 386, 387, 445, 654
Young, M. A., 448, 464 Young, M. E., 491 Youngstrom, E., 482 Yusupoff, L., 531
Z
Zahner, G. E., 136 Zaleski, E. H., 355
Zalta, A. K., 67, 77 Zanarini, M. C., 382, 385, 386, 445, 446 Zane, G., 10 Zane, N. W. S., 190 Zargar, F., 187 Zaslavsky, A. M., 4, 184 Zatzick, D. F., 355 Zbozinek, T., 139 Zebb, B. J., 28 Zee, P. C., 639 Zeelenberg, M., 126 Zeiss, A., 217 Zeiss, A. M., 342 Zeiss, A. S., 340 Zerubavel, N., 381, 730 Zerubavel , N., 218 Zettle, R., 266 Zettle, R. D., 342 Zhang, H., 220 Zhao, Y., 276 Ziedonis, D., 621 Zilcha-Mano, S., 120 Zimering, R. T., 66 Zimmerman, A., 555 Zimmerman, J., 355 Zimmerman, M., 381, 446 Zimmermann, G., 523 Zinbarg, R. E., 6, 7, 23 Zinzow, H. M., 526 Zipfel, S., 711 Zipple, A. M., 515 Zittel, C. C., 393 Zizza, M., 260 Zoellner, L. A., 8, 146, 384 Zohar, J., 145 Zohar-Kadouch, R., 145 Zopf, R., 464 Zorick, F., 639 Zucker, B. G., 14, 31, 220 Zupancic, J., 318 Zvolensky, M. J., 7 Zweben, A., 590 Zweben, J., 619 Zysk, E., 29 Zywiak, W. H., 562, 569
799
A-B-C Worksheets, 82–84, 83f, 683, 690–691, 691f
Abrupt exposures, 141. See also Exposure techniques
Abstinence goals, 579–581, 582f, 602–604 Abstinence violation effect (AVE), 562,
589, 592 Abuse. See also Physical abuse; Sexual abuse
alcohol use disorder treatment model and, 586
assessment of traumatic events and, 70 biosocial theory of BPD and, 394 depression and, 266 early maladaptive schemas and, 270f panic disorder and agoraphobia and,
7–8 Acceptance
cognitive-behavioral therapy for insomnia and, 655
generalized anxiety disorder and, 186–187, 189
integrative behavioral couple therapy and, 745–746, 754–758, 764–767, 768
panic disorder and agoraphobia and, 30–31, 48
PBT of social anxiety and, 118 role of during exposures, 30–31, 41, 43
Acceptance and commitment therapy (ACT)
behavioral activation and, 342 exposure and ritual prevention and, 175 generalized anxiety disorder and,
186–187, 192 panic disorder and agoraphobia and, 31 social anxiety disorder and, 109
Acceptance-based behavioral model of GAD, 187–189
Acceptance-based behavioral therapy (ABBT). See also Treatment approaches in general
case studies, 196–211, 207t, 208f, 210f client characteristics, 190 context for, 189 generalized anxiety disorder and, 186,
189–196 goals of, 189 overview, 211 pharmacological treatment and,
190–191 therapist characteristics, 189–190 treatment elements of, 191–196
ACTION acronym, 352–353 Action stage of change, 560 Actions, values-based. See Values-based
actions Actissist intervention, 528 Activation, behavioral. See Behavioral
activation (BA) for depression Active avoidance, 147. See also Avoidance Active passivity, 395–396, 395f Activity levels, 536 Activity pacing, 683–684, 694–696 Activity Records in behavioral activation,
348–350, 349f, 360–363, 361f, 366, 372–373, 372f. See also Behavioral activation (BA) for depression
Activity scheduling behavioral activation and, 350–352 cognitive therapy for depression and,
279–280, 280f
cognitive-behavioral therapy for chronic pain and, 684
UP for emotional disorders and SITBs and, 464–465
Acute pain, 671. See also Chronic pain Adaptive behaviors, 325, 340 Adaptive nature of emotion, 456–457 Addiction, 572–574, 613t. See also Alcohol
use disorder (AUD); Alcohol use disorder (AUD) treatment model; Opioid use disorder treatment; Substance use disorders (SUDs)
Addiction Severity Index (ASI), 568, 616 Adolescents. See also Children
behavioral activation and, 355 bipolar disorder and, 482, 495 CBT for depression and, 260–261 cognitive-behavioral therapy for
insomnia and, 644, 661 dialectical behavior therapy for BPD
and, 388, 389–390 obsessive–compulsive disorder and, 135 panic disorder and agoraphobia and, 4 social anxiety disorder and, 109
Affective expression, 67, 320, 547 Age of onset, 4, 134–135, 266 Agenda setting, 276–277, 278–279, 346 Agoraphobia
assessment and, 19–24, 20f, 22f case studies, 18–24, 20f, 22f, 32–48 CBT treatment protocol for, 24–31,
32–48 efficacy of CBT for, 31–32 etiological and maintaining factors for,
5–10
Subject Index
Note. f, t, or n following a page number indicates a figure, a table, or a note.
800 Subject Index
Agoraphobia (cont.) history of psychological treatment for, 5 interpersonal context variables in the
treatment of, 12–13 nature of, 1–4 overview, 1, 3, 48–49 patient variables in the treatment of,
14–16 pharmacological treatment and, 16–18 presenting features of, 4–5 relationship of with panic, 3–4 therapist variables in the treatment of,
13–14 treatment format, 11–12 treatment setting and, 10–11
Agoraphobia Cognitions Questionnaire, 23 Albany Panic and Phobia Questionnaire,
23 Alcohol use disorder (AUD). See also
Alcohol use disorder (AUD) treatment model; Alcohol use/abuse; Alcoholics Anonymous model; Substance use disorders (SUDs)
case studies, 466–470, 468t cognitive-behavioral therapy for
insomnia and, 644 cognitive-behavioral therapy for
psychosis and, 549–550 detoxification and, 572–574 diagnosis and definitions, 556–558 overview, 555–556 treatment planning model, 558–563,
558t–559t Alcohol use disorder (AUD) treatment
model. See also Alcohol use disorder (AUD); Treatment approaches in general
assessment and, 568–571, 569t, 570f, 571f
case identification and entry into treatment, 563–568, 565t
case studies, 564, 566–568, 577, 579, 580–583, 582f, 586, 589, 592–605, 597f, 598f, 599f, 601f
client variables in, 591–592 complicating conditions, 589–590 coping strategies, 585–587 functional analysis and, 581 initiating abstinence or reduced
drinking, 580–581, 582f involvement of others in treatment,
587–588 long-term maintenance, 588–589 motivation to change and, 577–579,
578f
mutual-help groups and, 590 overview, 563, 563t, 606 predictors of treatment success and,
605–606 reduction or sobriety strategies, 581,
583–585 relapse prevention and, 588–589 selection of drinking goals, 579–581 therapist variables in, 590–591 treatment modality selection, 575–577 treatment planning model, 558–563,
558t–559t treatment setting and level of care and,
571–575, 573t Alcohol Use Disorders Identification Test
(AUDIT), 564, 565t Alcohol use/abuse. See also Alcohol use
disorder (AUD) cognitive-behavioral therapy for
psychosis and, 549–550 family-focused treatment for bipolar
disorder and, 493, 494 panic disorder and agoraphobia and, 15
Alcoholics Anonymous model, 562, 575–576, 588, 590. See also 12-step model; Alcohol use disorder (AUD)
All-or-nothing thinking, 269, 562 Alternative action, 246–247, 584–585 Ambition, 486 American Society of Addiction Medicine
(ASAM) criteria, 572, 573t Analog mental representation system, 69 Analogy, 410 Ancillary care, 407 Anger, 174, 236f, 272f. See also Anger
management skills Anger management skills, 390–391, 586,
684, 697–698. See also Anger; Skills training
Anorexia nervosa (AN). See also Eating disorders; Enhanced cognitive- behavioral therapy (CBT-E); Transdiagnostic CBT treatment protocol for eating disorders
CBT-E for underweight patients and, 733–737, 734f, 735f, 736t
clinical features of, 706–707 diagnosis and classification of, 706 dialectical behavior therapy for BPD
and, 389 overview, 705–706, 737n–738n transdiagnostic perspective and,
708–711, 709f, 710f Antecedent and Coping Interview (ACI),
534
Antecedent–behavior–consequence (ABC) analysis. See Functional analysis
Anticonvulsants, 484, 577. See also Pharmacological treatment
Antidepressants. See also Pharmacological treatment
acceptance-based behavioral therapy for GAD, 190–191
acute phase of CT treatment for depression and, 259–261
behavioral activation and, 342 borderline personality disorder and,
386 depression and, 152, 259–261 obsessive–compulsive disorder and,
145–146, 152–153 relapse prevention and, 262–264 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 224
Antipsychotics, 386, 484. See also Pharmacological treatment
Antiseizure medications, 577. See also Pharmacological treatment
Anxiety. See also Anxiety disorders acceptance-based behavioral therapy for
GAD, 199 alcohol use disorder treatment model
and, 586, 590 behavioral activation and, 355 cognitive-behavioral therapy for chronic
pain and, 675 cognitive-behavioral therapy for
insomnia and, 644 dialectical behavior therapy for BPD
and, 388–389 eating disorders and, 707 emotional behaviors and, 236f opposite action skill and, 403 substance use disorders and, 615
Anxiety and Related Disorders Interview Schedule for DSM-5 (ADIS-5), 225–226
Anxiety Control Questionnaire, 23 Anxiety disorders. See also Anxiety;
Generalized anxiety disorder (GAD); Panic disorder; Unified Protocol for transdiagnostic treatment
bipolar disorder and, 483–484 case studies, 466–470, 468t cognitive-behavioral therapy for chronic
pain and, 675 dialectical behavior therapy for BPD
and, 388 differential diagnosis and, 136–137
Subject Index 801
obsessive–compulsive disorder and, 135–137
self-injurious thoughts and behaviors and, 446–447
UP for emotional disorders and SITBs and, 449–450
Anxiety Disorders Interview Schedule (ADIS-IV; ADIS-5)
acceptance-based behavioral therapy for GAD, 191
panic disorder and agoraphobia and, 19–21, 20f
self-injurious thoughts and behaviors and, 453
social anxiety disorder and, 119 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 222
Anxiety management training, 140 Anxiety sensitivity, 6–7, 8–10, 21, 23,
187–188 Anxiety Sensitivity Index, 7, 21, 23 Apparent competence, 395–396, 395f Applied relaxation, 26. See also Relaxation
techniques Appraisals
cognitive reappraisal and, 26–27, 114–116
cognitive-behavioral therapy for psychosis and, 537
panic disorder and agoraphobia and, 9 posttraumatic stress disorder and,
67–68 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 234, 242–245
Arbitrary inference, 269 ARC (antecedent, response, consequence)
acronym, 226, 227f, 233, 240–241 Areas of Change Questionnaire (ACQ),
571 Arguments, 174. See also Conflict, family Arousal
cognitive-behavioral therapy for psychosis and, 527
generalized anxiety disorder and, 185 panic disorder and agoraphobia and,
2, 8 Assessment. See also Diagnosis; Medical
evaluations acceptance-based behavioral therapy for
GAD, 191–192, 196–197 alcohol use disorder treatment model
and, 568–571, 569t, 570f, 571f, 586, 592–594
behavioral activation and, 343, 347–350, 349f, 356–357
borderline personality disorder, 382–383
chronic pain and, 671–672 cognitive therapy for depression and,
287–288, 305–306 cognitive-behavioral therapy for chronic
pain and, 678–682 cognitive-behavioral therapy for
insomnia and, 644–645, 646f, 660, 663
cognitive-behavioral therapy for psychosis and, 527, 534
enhanced cognitive-behavioral therapy for eating disorders and, 712–715, 718
family-focused treatment for bipolar disorder and, 495–497, 496f
integrative behavioral couple therapy and, 748–753, 749t, 763–764
intensive EX/RP program for OCD and, 153–156
interpersonal psychotherapy and, 319, 323–324
obsessive–compulsive disorder and, 146–147
panic disorder and agoraphobia and, 19–24, 20f, 22f
PBT of social anxiety and, 113, 114, 115f
posttraumatic stress disorder and, 69–72 schema therapy and, 297 self-injurious thoughts and behaviors
and, 453–454 social anxiety disorder and, 119 substance use disorders and, 613–618 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 224–232, 227f, 228f, 231f, 238–239, 452–454
Associative mental representation system, 69
Assumptions, 44, 306n Attachment disorders, 385 Attendance, 714 Attention bias modification, 109 Attention narrowing, 535 Attention strategies, 657–658 Attention switching, 535 Attention-deficit/hyperactivity disorder
(ADHD), 136, 390–391, 482 Atypical antipsychotics, 484. See also
Antipsychotics; Pharmacological treatment
Auditory hallucinations. See Hallucinations Automatic appraisals, 9, 243–245. See also
Appraisals; Cognitive errors; Core beliefs
Automatic thoughts. See also Cognitive errors; Core beliefs; Distorted thinking; Thoughts
cognitive flexibility and, 461 cognitive therapy for depression and,
279–280, 281–283, 282f, 288–289, 291–295
cognitive-behavioral therapy for chronic pain and, 690–693, 691f, 692f
cognitive-behavioral therapy for insomnia and, 654–655, 656t
questioning and, 284 testing, 282–283 underlying assumptions and, 306n
Aversion therapy agents, 577, 620. See also Pharmacological treatment
Avoidance acceptance-based behavioral therapy for
GAD, 188–189, 191–192, 195–196, 204
agoraphobia and, 3 behavioral activation and, 342, 346,
352–353 cognitive-behavioral therapy for
psychosis and, 527, 536 dialectical behavior therapy for BPD
and, 403 early maladaptive schemas and, 272 emotional behaviors and, 235 emotional disorders and, 221 enhanced cognitive-behavioral therapy
for eating disorders and, 727–728, 729–730
exposure and ritual prevention and, 147, 150–151, 173
fear–avoidance model of pain and, 672–673
functional model of emotional disorders and, 447
generalized anxiety disorder and, 185, 186 intensive EX/RP program for OCD
and, 156–157 obsessive–compulsive disorder and, 137 opposite action skill and, 403 panic disorder and agoraphobia and,
10, 43 social anxiety disorder and, 112 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 245–247, 462
Avoidant personality disorder, 5, 14–15, 335
802 Subject Index
Awareness cognitive-behavioral therapy for
psychosis and, 535–536 relapse prevention and, 265 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 233–234, 241–242, 449
B
Beck Anxiety Inventory (BAI), 615 Beck Depression Inventory–II (BDI-II)
behavioral activation and, 343 IPT model of depression and, 319 opioid use disorder treatment and, 615 overview, 225 schema therapy and, 297 social anxiety disorder and, 119
Behavior. See also Emotional behaviors cognitive-behavioral therapy for
psychosis and, 537 dialectical behavior therapy for BPD
and, 392 enhanced cognitive-behavioral therapy
for eating disorders and, 724–729, 725f, 726f, 730
Unified Protocol for transdiagnostic treatment of emotional disorders and, 234–237, 236f, 245–247, 449, 462–463
Behavior dyscontrol, 390–391, 398–400 Behavior modification, 537 Behavioral activation, 586 Behavioral activation (BA) for depression.
See also Depression assessment and, 343 behavioral models of depression and,
340–341 case studies, 355–375, 361f, 372f course of treatment, 344–355, 344f,
345t, 349f empirical context, 341–343 overview, 339, 375
Behavioral Activation for Depression Scale (BADS), 343
Behavioral analysis, 414–415, 416–417, 426–431
Behavioral avoidance, 188–189. See also Avoidance
Behavioral experiments. See also Exposure techniques
cognitive-behavioral therapy for insomnia and, 655, 656t, 660–661
cognitive-behavioral therapy for psychosis and, 537
PBT of social anxiety and, 113, 116–117 social anxiety disorder and, 123–125,
124f UP for emotional disorders and SITBs
and, 464–465 Behavioral formulation, 594–595 Behavioral models, 137–139, 557, 576,
641 Behavioral rituals, 134, 139. See also
Compulsions Behavioral tests, 23–24. See also
Assessment Behavioral treatment approaches. See also
Integrative behavioral couple therapy (IBCT)
cognitive therapy for depression and, 279–281, 280f
dialectical behavior therapy for BPD and, 387
obsessive–compulsive disorder and, 176
sleep disorders and, 651–654 substance use disorders and, 618,
619–624, 621f, 623f Beliefs, 536–537, 583–584, 658–659,
661–662. See also Core beliefs Benevolent demanding, 408 Benzodiazepines, 17, 31, 190–191, 577. See
also Pharmacological treatment Between-session practices, 654–655. See
also Out-of-session practices Bibliotherapy, 342 Binge eating, 709–710, 709f, 710f. See
also Binge-eating disorder (BED); Bulimia nervosa (BN); Eating disorders
Binge-eating disorder (BED). See also Eating disorders; Enhanced cognitive-behavioral therapy (CBT- E); Transdiagnostic CBT treatment protocol for eating disorders
clinical features of, 706–708 diagnosis and classification of, 706 dialectical behavior therapy for BPD
and, 389, 390–391 overview, 705–706 transdiagnostic perspective and,
708–711, 709f, 710f Biochemical monitoring, 614. See also
Assessment Biological processes. See also
Neurobiological processes; Vulnerability–stress model
alcohol use disorder and, 556–557, 561 bipolar disorder and, 485
cognitive model of depression and, 268 dialectical behavior therapy for BPD
and, 392 posttraumatic stress disorder and, 71 psychoeducation regarding, 498–499 validation in DBT and, 412
Biopsychosocial models, 1, 494 Biosocial theory of borderline personality
disorder, 392, 393–397, 395f, 414– 415. See also Borderline personality disorder (BPD)
Bipolar disorders. See also Depression; Family-focused treatment (FFT) for bipolar disorder
assessment and, 495–497, 496f case studies, 505–514 cognitive therapy for depression and,
275–276 diagnosis and, 480–484 dialectical behavior therapy for BPD
and, 390–391 future directions and research and, 515 medication nonadherence and, 485 overview, 480 pharmacological treatment and,
275–276, 484–485, 514–515 sleep disorders and, 662–663 treatment approaches, 487–491 vulnerability–stress model and,
485–487 Bodily sensations. See Physical sensations Body checking, 727–728 Body dysmorphic disorder (BDD), 137 Body Sensations Questionnaire, 23 Body shape dissatisfaction, 706–707,
724–729, 725f, 726f. See also Eating disorders
Bond facet of therapeutic alliance, 120. See also Therapeutic relationship/alliance
Booster sessions, 30, 48–49, 263, 325 Borderline personality disorder (BPD).
See also Dialectical behavior therapy (DBT) for BPD
biosocial theory of, 392, 393–397, 395f, 414–415
bipolar disorder and, 482 case studies, 418–434 overview, 381–384 self-injurious thoughts and behaviors
and, 444, 446 treatment approaches, 384–387
Borderline personality organization (BPO), 384–385
Borderline Symptom List (BSL), 382 Borderline symptoms, 355
Subject Index 803
Breathing retraining. See also Relaxation techniques
alcohol use disorder treatment model and, 586
cognitive-behavioral therapy for chronic pain and, 683, 687, 687f
panic disorder and agoraphobia and, 25–26, 35–42, 43–46
Brief Pain Inventory—Short Form (BPI), 615, 680–681
Brief Symptom Inventory–II (BSI-II), 615
Brief Trauma Questionnaire (BTQ), 70 Brief treatment, 11–12, 189 Bulimia nervosa (BN). See also Eating
disorders; Enhanced cognitive- behavioral therapy (CBT-E); Transdiagnostic CBT treatment protocol for eating disorders
case studies, 714–715 clinical features of, 706–707 diagnosis and classification of, 706 dialectical behavior therapy for BPD
and, 389, 390–391 overview, 705–706 transdiagnostic perspective and,
708–711, 709f, 710f Buprenorphine. See Aversion therapy
agents; Interim buprenorphine treatment (IBT)
Buprenorphine agreement form, 617f Burning. See Self-injurious thoughts and
behaviors (SITBs)
C
CAGE (cut down, annoyed, guilty, eye- opener) interview, 564, 565t
Calm Tools for Living (CALM), 14, 15 Camberwell Family Interview, 486,
496–497 Capnometry-assisted respiratory training
(CART), 25–26, 36. See also Breathing retraining
Case formulation/conceptualization. See also Treatment goals
alcohol use disorder and, 560–561, 592–594
behavioral activation and, 347–350, 349f
cognitive-behavioral therapy for chronic pain and, 682
cognitive-behavioral therapy for insomnia and, 647–650, 648f, 663
cognitive-behavioral therapy for psychosis and, 527
dialectical behavior therapy for BPD and, 392
enhanced cognitive-behavioral therapy for eating disorders and, 718, 723, 735–736
integrative behavioral couple therapy and, 747–748, 752–753
Case identification, 563–564, 565t Case management, 407 Catastrophic cognitions. See also Cognitive
errors cognitive-behavioral therapy for chronic
pain and, 683 fear–avoidance model of pain and, 673 feared consequences and, 149–150 panic disorder and agoraphobia and,
9, 37 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 234, 243–245
Chain analysis, 414–415, 416–417, 426–427. See also Behavioral analysis
Challenging Beliefs Worksheet, 92–96, 93f, 95f, 97, 98f, 99, 100
Challenging Questions Worksheet, 87, 88–90, 89f, 99–100
Change, 560, 746, 757–760 Checking behavior, 727–728 Cheerleading strategies, 413, 426, 431–432 Child modes, 272–273, 273f Childhood experiences. See also Abuse;
Children; Early maladaptive schemas (EMS)
assessment of traumatic events and, 70 biosocial theory of BPD and, 393–394 depression and, 266 interpersonal psychotherapy and,
320–321 panic disorder and agoraphobia and,
7–8 schema therapy and, 296
Children. See also Adolescents; Childhood experiences
bipolar disorder and, 482, 483–484, 491, 495
CBT for depression and, 260–261 depression and, 266 obsessive–compulsive disorder and,
135, 136 panic disorder and agoraphobia and, 4
Choice, 206 Chronic depression, 265–268, 296–305.
See also Depression
Chronic pain. See also Cognitive- behavioral therapy for chronic pain
assessment and, 678–682 case studies, 676–682, 684–700, 685f,
686f, 687f, 688f, 691f, 692f, 695f, 696f, 700t
cognitive-behavioral therapy for insomnia and, 664
fear–avoidance model of pain and, 672–673
overview, 670–671, 701 prevalence and cost of, 672
Client variables. See Patient/client variables Client-centered therapy (CCT), 388 Clinical Impairment Assessment (CIA),
713 Clinical Institute Withdrawal Assessment
(CIWA), 572–573 Clinical interviews. See Assessment;
Interviews in assessment; Structured clinical interviews
Clinician-Administered PTSD Scale for DSM-5 (CAPS-5), 70
Cognition modification, 537–538, 583–584
Cognitive avoidance, 235. See also Avoidance
Cognitive errors. See also Automatic thoughts; Core beliefs; Distorted thinking; Thoughts
alcohol use disorder and, 562 cognitive model of depression and,
268–269 cognitive-behavioral therapy for chronic
pain and, 683, 690–693, 691f, 692f dialectical behavior therapy for BPD
and, 416 panic disorder and agoraphobia and,
36–38 posttraumatic stress disorder and,
90–94, 91f, 93f Unified Protocol for transdiagnostic
treatment of emotional disorders and, 234, 242–245, 459–461
Cognitive flexibility. See also Flexibility in thinking
dialectics and, 391–392 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 234, 242–245, 449, 459–461, 469
Cognitive functioning, 557, 574 Cognitive interventions, 176 Cognitive models, 67–68, 137–139,
268–269, 641 Cognitive modification, 416
804 Subject Index
Cognitive processes, 111–112 Cognitive processing therapy (CPT), 73,
76–77, 400 Cognitive reappraisal, 114–116 Cognitive reframing, 586 Cognitive rehearsal, 280 Cognitive restructuring
alcohol use disorder and, 561 cognitive-behavioral therapy for chronic
pain and, 691–693, 692f dialectical behavior therapy for BPD
and, 416 panic disorder and agoraphobia and, 5,
26–27, 36–42, 44–46, 47 PBT of social anxiety and, 113 posttraumatic stress disorder and, 73 social anxiety disorder and, 121–123, 122f
Cognitive techniques, 281–283, 282f Cognitive therapy (CT). See also Cognitive
therapy for depression; Cognitive- behavioral therapy (CBT); Treatment approaches in general
behavioral activation and, 341–342 borderline personality disorder and,
386–387 generalized anxiety disorder and, 185–186 obsessive–compulsive disorder and,
144–145 overview, 259 posttraumatic stress disorder and, 72, 73 self-injurious thoughts and behaviors
and, 445 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 234
Cognitive therapy for depression. See also Cognitive therapy (CT); Depression
acute phase of, 259–261 behavioral techniques, 279–281, 280f case studies, 287–296 characteristics of, 275–276 cognitive techniques, 281–283, 282f collaboration and, 276 homework assignments and, 284–285 overview, 257–259, 305–306 process and structure of, 277–279 questioning, 283–284 relapse prevention and, 261–265 research on chronic depression and,
265–268 special problems, 285–287 symptom reduction and, 279–287, 280f,
282f Cognitive-behavioral analysis system of
psychotherapy (CBASP), 266, 267
Cognitive-behavioral conjoint therapy (CBCT), 72
Cognitive-behavioral interpersonal theory (C-BIT), 69
Cognitive-behavioral models, 138–139, 641 Cognitive-behavioral therapy (CBT). See
also Cognitive-behavioral therapy for chronic pain; Cognitive-behavioral therapy for insomnia (CBT-I); Cognitive-behavioral therapy for psychosis (CBTp); Enhanced cognitive-behavioral therapy (CBT- E); Process-based therapy (PBT); Treatment approaches in general; Unified Protocol for transdiagnostic treatment of emotional disorders
acute phase of CT treatment for depression and, 259–261
alcohol use disorder and, 560, 561 behavioral activation and, 341–342 bipolar disorder and, 487–488 borderline personality disorder and,
386–387 compared to interpersonal
psychotherapy, 320–321, 334–335 depression and, 258–259 dialectical behavior therapy for BPD
and, 389 efficacy of for panic disorder and
agoraphobia, 31–32 generalized anxiety disorder and, 185–187 motivational interviewing and, 233 obsessive–compulsive disorder and, 136,
140, 143–144, 175–176 panic disorder and agoraphobia and, 1,
10–18, 24–48 pharmacological treatment and, 224,
259–261 relapse prevention and, 261–265 research on chronic depression and,
265–268 schema theory and, 274 schizophrenia and, 523 self-injurious thoughts and behaviors
and, 445–446 social anxiety disorder and, 109–110 substance use disorders and, 618,
619–624, 621f, 623f Cognitive-behavioral therapy (CBT) for
suicide prevention (CBT-SP), 445 Cognitive-behavioral therapy for bulimia
nervosa (CBT-BN), 708–711, 709f. See also Bulimia nervosa (BN); Transdiagnostic CBT treatment protocol for eating disorders
Cognitive-behavioral therapy for chronic pain. See also Chronic pain; Cognitive-behavioral therapy (CBT)
assessment and, 678–682 case studies, 676–682, 684–700, 685f,
686f, 687f, 688f, 691f, 692f, 695f, 696f, 700t
components of, 682–684 engaging the patient in treatment and,
677–678 overview, 670–671, 673–676, 701 process of, 684–700, 685f, 686f, 687f,
688f, 691f, 692f, 695f, 696f, 700t Cognitive-behavioral therapy for eating
disorders (CBT-ED), 711. See also Transdiagnostic CBT treatment protocol for eating disorders
Cognitive-behavioral therapy for insomnia (CBT-I). See also Cognitive- behavioral therapy (CBT); Insomnia; Sleep problems/disorders
assessment and, 644–645, 646f behavioral components of, 651–654 chronic pain and, 684 cognitive components of, 654–661, 656t comorbidity and, 640 context of, 642–644, 643f evidence for, 642 future directions and research and,
662–664 models of insomnia and, 641 overview, 639, 662–664 problems that may arise during, 661–662 process of, 645, 647–651, 648f relapse prevention and, 661 termination and, 661
Cognitive-behavioral therapy for psychosis (CBTp). See also Cognitive-behavioral therapy (CBT); Psychotic disorders; Schizophrenia; Treatment approaches in general
assessment and, 534 associated features of schizophrenia and,
528–530, 529t case studies, 538–545 clinical principles, 527–528 clinical problems and difficulties,
548–550 context of, 530–532 overview, 523, 528–530, 529t, 550 process of, 532–538, 533f, 534f relapse prevention and, 547–548 research support for, 523–526 self-esteem and, 545–547, 546f theoretical models, 526–527
Subject Index 805
Collaboration. See also Therapeutic relationship/alliance
behavioral activation and, 346, 352 cognitive therapy for depression and,
276, 277, 291 cognitive-behavioral therapy for
insomnia and, 644 dialectical behavior therapy for BPD
and, 398–399 Collaborative Assessment and Management
of Suicidality (CAMS), 445 Collaborative empiricism, 116, 277, 289.
See also Behavioral experiments Collaborative set, 750–751 Collaborative weighing intervention,
720–721, 736 Columbia Suicide Severity Rating Scale
(C-SSRS), 452 Columbo technique, 527 Commitment to treatment, 397–398, 424 Communication analysis, 324–325,
331–332 Communication enhancement training
(CET), 492t, 497, 501–503, 509–513 Communication skills
alcohol use disorder treatment model and, 585
dialectical behavior therapy for BPD and, 417–418, 426–428, 431–432
integrative behavioral couple therapy and, 759–760
panic disorder and agoraphobia and, 43 Community reinforcement and family
training (CRAFT), 564, 566, 619 Community reinforcement approach
(CRA), 587–588, 619–624, 621f. See also Opioid use disorder treatment
Community treatment by nonbehavioral experts (CTBE), 388
Comorbidity acceptance-based behavioral therapy for
GAD, 190 acute phase of CT treatment for
depression and, 260 alcohol use disorder and, 557, 574 behavioral activation and, 355 bipolar disorder and, 481–482,
483–484 borderline personality disorder, 383,
397 chronic pain and, 671 cognitive-behavioral therapy for chronic
pain and, 675–676 cognitive-behavioral therapy for
insomnia and, 644
cognitive-behavioral therapy for psychosis and, 531–532, 549–550
depression and, 266 dialectical behavior therapy for BPD
and, 399 differential diagnosis and, 19, 136–137 enhanced cognitive-behavioral therapy
for eating disorders and, 714 generalized anxiety disorder and,
184–185 integrative behavioral couple therapy
and, 761 obsessive–compulsive disorder and,
135–137 panic disorder and agoraphobia and,
4–5, 14–15, 19 posttraumatic stress disorder and, 76,
77, 675–676 psychotic disorders and, 522–523 schema therapy and, 296 sleep disorders and, 640, 662–663 substance use disorders and, 76 UP for emotional disorders and SITBs
and, 452–453, 471 Compassionate flexibility, 408 Competence, apparent, 395–396, 395f Complex PTSD, 383. See also
Posttraumatic stress disorder (PTSD)
Compulsions, 133–134, 151. See also Obsessive–compulsive disorder (OCD); Rituals
Computer-assisted cognitive therapy, 275. See also Internet-based treatment delivery; Technology
Conditioned stimulus–unconditioned stimulus (CS-US) association, 139
Conditioning, 8–9, 66, 618, 619 Conduct disorder, 482 Conflict, family, 174, 486–487, 503, 571.
See also Couple therapy; Family factors; Family-based interventions; Integrative behavioral couple therapy (IBCT)
Consequences. See also Reinforcement alcohol use disorder and, 561 behavioral activation and, 347–348 depression and, 267, 340–341 dialectical behavior therapy for BPD
and, 415–416 substance use disorders and, 619
Consolidation, 353 Consultation teams, 404–407, 405t, 406t Consultation-to-the-client strategy, 407 Contemplation stage of change, 560
Contextual factors, 113–114, 413, 558t, 574–575, 589–590, 591–592
Contextual idiographic assessment, 113, 114, 115f. See also Assessment
Contingency management (CM), 351, 415–416, 431–432, 619
Contingency procedures, 267, 415–416, 427, 431–432
Contingency-shaped behavior, 745 Continuation-phase cognitive therapy (C-
CT), 264–265 Continuing care, 589 Control, 99–100, 206, 271f Coping Questionnaire, 571 Coping skills. See also Skills training
acceptance and, 30–31 alcohol use disorder and, 562,
585–587 cognitive-behavioral therapy for
psychosis and, 527–528, 534–537 dialectical behavior therapy for BPD
and, 390–391 panic disorder and agoraphobia and,
30–31, 35–42, 44–46 questioning and, 284 self-injurious thoughts and behaviors
and, 444–445 stress inoculation training and, 74–75
Coping with Depression Course for adolescents, 355
Coping–recovery clinical model, 532–534, 533f
Core automatic appraisals, 243. See also Appraisals; Cognitive errors
Core beliefs. See also Automatic thoughts; Beliefs; Cognitive errors; Distorted thinking; Early maladaptive schemas (EMS)
alcohol use disorder treatment model and, 583–584
cognitive-behavioral therapy for psychosis and, 536–537
schema theory and, 269–275, 270f–272f, 273f, 274f
underlying assumptions and, 306n Cotherapy model, 494 Countering Emotional Behaviors Form,
226, 228f Couple adaptation to stress (CATS) model,
69 Couple distress, 742–743, 746–747,
762–768. See also Couple therapy; Integrative behavioral couple therapy (IBCT); Marital factors
Couple Questionnaire, 749–750, 749t
806 Subject Index
Couple therapy. See also Couple distress; Family-based interventions; Integrative behavioral couple therapy (IBCT)
alcohol use disorder treatment model and, 576, 588
case studies, 762–768 change strategies from, 759–760 cognitive therapy for depression and,
275 overview, 743–744
Couples Satisfaction Index, 749, 749t Court-ordered treatment, 408 Crises
dialectical behavior therapy for BPD and, 388, 401, 402
dialectical dilemmas and, 395f, 396–397
enhanced cognitive-behavioral therapy for eating disorders and, 716–717
telephone consultation and, 404 Criticism, 187–188, 272f Cultural factors
acceptance-based behavioral therapy for GAD, 189, 192–193, 196, 197–198
depression and, 257 posttraumatic stress disorder and, 65 social anxiety disorder and, 109
Curiosity, 391–392 Cutting. See Self-injurious thoughts and
behaviors (SITBs) Cycle of pain, 685, 685f Cyclothymic disorder, 483
D
Daily Mood Chart in FFT, 495–496, 496f Daily Mood Record, 21, 22f Daily Record of Dysfunctional Thoughts,
281–282, 282f, 284, 295 Decatastrophizing, 39–40, 245. See also
Catastrophic cognitions Decentering, 194. See also Mindfulness
training Decision analysis, 325 Decisional Balance exercise, 455, 470, 569,
570f DEEP analysis, 747–748, 750–751,
754–755 Default mode network (DMN), 382 Deliberate self-harm. See Self-injurious
thoughts and behaviors (SITBs) Delusional disorder, 137. See also Psychotic
disorders
Delusions. See also Psychotic disorders; Schizophrenia
compared to obsessions, 137 coping–recovery clinical model and,
532–534, 533f overview, 522–523 symptom management and recovery
and, 524–525 Dependence, 12–13 Dependent personality disorder, 5, 14–15 Depression. See also Behavioral activation
(BA) for depression; Bipolar disorders; Cognitive therapy for depression; Interpersonal psychotherapy (IPT) for depression; Unified Protocol for transdiagnostic treatment
acute phase of CT treatment for, 259–261 alcohol use disorder treatment model
and, 586 behavioral models of, 339–341 borderline personality disorder and, 397 case studies, 287–305, 325–333,
355–375, 361f, 372f cognitive model of, 268–269 cognitive-behavioral therapy for chronic
pain and, 675 cognitive-behavioral therapy for
insomnia and, 644 comparing obsessions to ruminations
and, 136 diagnosis and, 136, 323, 483 dialectical behavior therapy for BPD
and, 388–389, 390–391 eating disorders and, 707 enhanced cognitive-behavioral therapy
for eating disorders and, 714 exposure and ritual prevention and, 174 intensive EX/RP program for OCD
and, 153–154 obsessive–compulsive disorder and,
135–136, 152 overview, 257–259 panic disorder and agoraphobia and,
5, 14 relapse prevention and, 261–265 research on chronic depression,
265–268 schema theory and, 269–275,
270f–272f, 273f, 274f, 296–305 self-injurious thoughts and behaviors
and, 446–447 sleep disorders and, 662–663 substance use disorders and, 615 UP for emotional disorders and SITBs
and, 449–450
Depression relapse active monitoring (DRAM), 266–267
Detachment, unified, 755–756, 764–767 Determination stage of change, 560 Detoxification, 572–574, 573t Developmental processes, 639–640, 673 Devil’s advocate technique, 410, 424–425 Diagnosis. See also Assessment
alcohol problems, 556–558, 605 behavioral activation and, 343 bipolar disorder, 480–484 bipolar disorder and evaluation, 495 bipolar disorder and family assessments,
496 bipolar disorder and mood charts, 495–496 borderline personality disorder,
381–383, 397 couple distress and, 742 eating disorders and, 705, 706, 712 generalized anxiety disorder and, 185 interpersonal psychotherapy and, 320,
323, 327 major depressive disorder and, 318 obsessive–compulsive disorder and,
133–134, 136–137, 146–147 panic disorder and agoraphobia and,
1–2, 4–5, 19–24, 22f posttraumatic stress disorder and,
69–70, 71–72 resistance to, 500–501 self-injurious thoughts and behaviors
and, 444 sleep disorders and, 640–641, 644–645 substance use disorders and, 613 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 222
Diagnostic and Statistical Manual of Mental Disorders (DSM-IV), 185, 222
Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR), 444, 640
Diagnostic and Statistical Manual of Mental Disorders (DSM-5)
alcohol use disorder and, 556 bipolar disorder and, 480–481 couple distress and, 742 eating disorders and, 705–706 panic attacks and, 1–3 posttraumatic stress disorder and, 69–70 self-injurious thoughts and behaviors
and, 444 substance use disorders and, 613 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 222
Subject Index 807
Dialectical behavior therapy (DBT), 186, 266, 444–445. See also Dialectical behavior therapy (DBT) for BPD
Dialectical behavior therapy (DBT) for BPD. See also Borderline personality disorder (BPD); Dialectical behavior therapy (DBT)
biosocial theory of BPD and, 393–394 case studies, 418–434 dialectical dilemmas and, 394–397, 395f evidence for, 387–391 failure of, 432–434 functions and modes of treatment,
400–408, 405t, 406t overview, 383–384, 391–392 stages of and treatment goals for, 397–400 treatment strategies in, 408–418
Dialectical behavior therapy/prolonged exposure (DBT/PE), 72, 76
Dialectical dilemmas, 394–397, 395f Dialectical philosophy, 387, 391–392,
444–445 Dialectical strategies, 408–411, 426 Dialogues, 304, 391–392 Diaphragmatic breathing. See also
Breathing retraining cognitive-behavioral therapy for chronic
pain and, 683, 687, 687f, 689 panic disorder and agoraphobia and,
35–36, 38–39, 40 Diathesis–stress model, 274–275, 392, 641 Dietary restraint, 729–730. See also Eating
disorders Differential diagnosis, 19, 136–137,
482–483. See also Diagnosis Direct therapeutic exposure (DTE), 72. See
also Exposure techniques Disruptive mood dysregulation disorder,
481–482. See also Bipolar disorders Distorted thinking. See also Automatic
thoughts; Cognitive errors; Cognitive restructuring; Core beliefs; Thoughts
alcohol use disorder and, 562, 585 cognitive model of depression and,
268–269 cognitive reappraisal and, 114–116 dialectical behavior therapy for BPD
and, 416 panic disorder and agoraphobia and,
26–27, 36–38 PBT of social anxiety and, 114–116 posttraumatic stress disorder and,
90–94, 91f, 93f strength of belief and, 150
Distraction techniques, 281, 584
Distress, 187–188, 266, 465. See also Subjective Units of Discomfort Scale (SUDS)
Diversity, 562–563 Domestic violence, 390–391, 749–750 Downward arrow technique, 36–37, 45–
46. See also Cognitive restructuring Drink refusal skills, 585 Drinker Inventory of Consequences
(DrInC), 568 Drinking Patterns Questionnaire (DPQ),
569–570 Dual diagnosis, 549–550. See also Alcohol
use disorder (AUD); Diagnosis; Substance use disorders (SUDs)
Dual-representation theory, 68–69 Duke Structured Interview for Sleep
Disorders, 645 Dyadic Adjustment Scale (DAS), 571 Dysfunctional Parent modes, 273, 274f.
See also Mode Dysthymia, 5, 266, 296, 333–334
E
Early experiences. See Childhood experiences
Early intervention, 525–526 Early maladaptive schemas (EMS). See also
Automatic thoughts; Core beliefs; Schema theory
borderline personality disorder and, 387 cognitive therapy for depression and,
291–295 overview, 269–272, 270f–272f, 306n questioning and, 284 research regarding, 274–275 schema therapy and, 297–305
Eating disorders. See also Anorexia nervosa (AN); Binge-eating disorder (BED); Bulimia nervosa (BN); Enhanced cognitive-behavioral therapy (CBT- E); Transdiagnostic CBT treatment protocol for eating disorders
assessment and, 712–715 case studies, 714–715, 722–724, 731–732 clinical features of, 706–708 diagnosis and classification of, 706 dialectical behavior therapy for BPD
and, 389, 390–391 overview, 705–706, 737n–738n transdiagnostic perspective and,
708–711, 709f, 710f treatment approaches, 711–712
Eating Disorders Examination Questionnaire (EDE-Q), 713
Education stage of treatment. See also Cognitive-behavioral therapy (CBT); Psychoeducation
panic disorder and agoraphobia and, 24–25, 32–34, 35–36
posttraumatic stress disorder and, 78–79 stress inoculation training and, 74
Ego state, 272–273 Emotion awareness, 449, 456–459, 461,
469 Emotion differentiation, 112, 113, 117–118 Emotion exposures, 237, 248–250, 464–
466. See also Exposure techniques Emotion expression, 320 Emotion Log, 117–118 Emotion reactivity, 448. See also Reactivity Emotion regulation. See also Emotional
processing alcohol use disorder treatment model
and, 586 anxiety disorders and, 112, 113,
117–118, 185 borderline personality disorder and,
383–384, 390–391, 392, 393, 403, 431–432
self-injurious thoughts and behaviors and, 445
Emotion regulation group therapy (ERGT), 445
Emotion regulation therapy (ERT), 186 Emotional acceptance, 118, 754–758. See
also Acceptance Emotional behaviors, 234–237, 236f,
245–247, 462–463, 469. See also Behavior; Emotion-driven behaviors (EDBs)
Emotional disorders. See also Anxiety disorders; Bipolar disorders; Depression; Generalized anxiety disorder (GAD); Mood disorders; Obsessive–compulsive disorder (OCD); Social anxiety disorder (SAD); Unified Protocol for transdiagnostic treatment
assessment and, 224–232, 227f, 228f, 231f
case studies, 224–225 cognitive-behavioral therapy for chronic
pain and, 675 components of UP with, 232–238, 236f,
454–466 functional model of, 447–449 overview, 217–218, 471
808 Subject Index
Emotional disorders (cont.) self-injurious thoughts and behaviors
and, 446–449 sleep disorders and, 662–663
Emotional processing. See also Emotion regulation
anxiety disorders and, 112, 117–118, 125–128, 185
emotional disorders and, 221 exposure and ritual prevention and, 174 habituation and, 28–29 obsessive–compulsive disorder and,
141–142 posttraumatic stress disorder and, 68–69,
80–83, 84–85, 88, 92–94, 93f self-focused attention and, 111–112
Emotional reasoning, 91f. See also Cognitive errors
Emotional vulnerability, 394–395, 395f Emotion-driven behaviors (EDBs),
234–237, 236f, 245–247, 449, 469. See also Emotional behaviors
Empathic joining, 754–755, 764–767 Empathy, 390–391 Empirical thinking, 282–283 Employment, 158, 258, 484–485, 557. See
also Social–occupational functioning Engagement
acceptance-based behavioral therapy for GAD, 195–196, 197–198, 206
alcohol use disorder treatment model and, 564
behavioral activation and, 350–351, 353 cognitive-behavioral therapy for chronic
pain and, 677–678 cognitive-behavioral therapy for
psychosis and, 527, 532 enhanced cognitive-behavioral therapy
for eating disorders and, 717, 718 Enhanced cognitive-behavioral therapy
(CBT-E). See also Cognitive- behavioral therapy (CBT); Eating disorders; Transdiagnostic CBT treatment protocol for eating disorders
assessment and, 712–715 case studies, 714–715, 722–724,
731–732, 733 context of, 712 contraindications to starting, 713–714 overview, 710–711, 715–717, 716f, 737, 738n research support for, 711–712, 738n treatment protocol for, 717–733, 719t,
720f, 725f, 726f for underweight patients, 733–737,
734f, 735f, 736t
Entering the paradox technique, 409–410 Environmental factors
alcohol use disorder treatment model and, 587–588
behavioral analysis in DBT and, 414 behavioral models of depression and,
340–341 borderline personality disorder and,
392, 393–394, 407 cognitive-behavioral therapy for
psychosis and, 527 early maladaptive schemas and, 269,
272 intensive EX/RP program for OCD
and, 157–158 opioid use disorder treatment and, 618 panic disorder and agoraphobia and,
15–16 Environmental Reward Observation Scale
(EROS), 343 Epworth Sleepiness Scale, 645 Escape behavior, 346. See also Avoidance Etiological factors, 5–10, 492t Evidence for and against a thought. See
Examining the evidence technique Evidence-based treatment. See also
Treatment approaches in general acceptance-based behavioral therapy for
GAD, 190 behavioral activation and, 341–343 depression and, 258 interpersonal psychotherapy and,
319–320, 334–335 posttraumatic stress disorder and,
75–77 schema theory and, 274 self-injurious thoughts and behaviors
and, 444–446 Exaggeration, 91f. See also Cognitive errors Examining the evidence technique, 37–38,
283 Expectations
alcohol use disorder and, 559–560 alcohol use disorder treatment model
and, 583–584, 592 cognitive therapy for depression and,
286 cognitive-behavioral therapy for
insomnia and, 661–662 Experience–belief–action–confirmation
(EBAC) cycle, 533–534, 534f Experiential avoidance, 10, 112, 188,
191–192. See also Avoidance Experiments, behavioral. See Behavioral
experiments
Exposure and ritual prevention (EX/RP). See also Exposure techniques
case studies, 160–172 comorbidity and, 135–136 compared to pharmacotherapy and,
145–146 complications during, 172–175 initial interview and sessions for,
147–153 intensive EX/RP program for OCD
and, 153–159 obsessive–compulsive disorder and,
139–145 overview, 133, 175–176 strength of belief and, 150 thought disorder symptoms and, 137 tic disorders and, 137
Exposure techniques. See also Behavioral experiments; Dialectical behavior therapy/prolonged exposure (DBT/ PE); Exposure and ritual prevention (EX/RP); In vivo exposure; Prolonged exposure (PE); Treatment approaches in general
acceptance and, 30–31 arguments regarding exposures and,
174 borderline personality disorder,
383–384 cognitive restructuring and, 26–27 dialectical behavior therapy for BPD
and, 416–417 hierarchy development and, 35 obsessive–compulsive disorder and, 139 optimizing learning during, 28–30 panic disorder and agoraphobia and,
10–11, 13, 27–31, 35, 40–48 PBT of social anxiety and, 113,
116–117 posttraumatic stress disorder and, 72–73 social anxiety disorder and, 109,
123–125, 124f Unified Protocol for transdiagnostic
treatment of emotional disorders and, 237, 248–250, 463–466, 469
Expressed emotion (EE), 486–487, 496–497
Extended evolutionary meta-model (EEMM), 114, 115f
Extending technique, 410–411 Extinction, 28–30, 139, 245 Eye movement desensitization and
reprocessing (EMDR), 72, 73–76. See also Treatment approaches in general
Subject Index 809
F
Family assessment, 486, 496–497, 506. See also Assessment
Family factors. See also Couple distress; Family involvement in treatment; Marital factors
alcohol use disorder and, 561, 570–571, 571f, 586–587
bipolar disorder and, 486–487 cognitive-behavioral therapy for
insomnia and, 643 depression and, 266 exposure and ritual prevention and,
175 panic disorder and agoraphobia and,
7–8 schema therapy and, 296 short-fuse families, 503
Family involvement in treatment. See also Family-based interventions
alcohol use disorder treatment model and, 587–588
behavioral activation and, 354 cognitive therapy for depression and,
275 enhanced cognitive-behavioral therapy
for eating disorders and, 722 exposure and ritual prevention and,
143–144 Family psychoeducation, 490–491. See also
Psychoeducation Family-based interventions. See also
Couple therapy; Family involvement in treatment; Family-focused treatment (FFT) for bipolar disorder; Integrative behavioral couple therapy (IBCT)
alcohol use disorder treatment model and, 576–577, 588
cognitive-behavioral therapy for psychosis and, 530–531
eating disorders and, 711 exposure and ritual prevention and,
143–144 Family-focused treatment (FFT) for
bipolar disorder. See also Bipolar disorders; Treatment approaches in general
case studies, 505–514 communication enhancement training
and, 501–503, 509–513 context of, 491–494, 492t future directions and research and, 515 overview, 480, 487, 488–491, 514–515
pretreatment assessments, 495–497, 496f
problem-solving skills training and, 503–505, 513–514
process of, 497–505 psychoeducation and, 497–501,
506–509 research support for, 488–491 termination and, 505, 513–514
Fear acceptance-based behavioral therapy for
GAD, 199 development of new fears, 174–175 extinction and, 30 fear conditioning, 139, 155 fear cues, 147–149 fear–avoidance model of pain and,
672–673 obsessive–compulsive disorder and,
138–139, 174–175 reactivity and, 7 strength of belief and, 150
Fear of fear, 6–7, 8–10, 21, 23, 187–188 Fear–avoidance model of pain, 672–673 Feared consequences, 149–150, 155 Feedback, 277, 752–753, 763–764 Feeding disorders, 706. See also Eating
disorders Fidelity, treatment, 77 Fight–flight reactivity, 2, 237 Flexibility in thinking, 234, 242–245,
459–461. See also Cognitive flexibility
Flooding, 72. See also Exposure techniques Following Your ARC Form, 226, 227f Food avoidance, 729–730 Frequency and Acceptability of Partner
Behavior Inventory, 749, 749t Form 90 interview for drinking history,
568 Functional analysis. See also Assessment
alcohol use disorder and, 561, 581, 582f behavioral activation and, 343,
347–350, 349f cognitive-behavioral therapy for
insomnia and, 647, 649–650, 663 integrative behavioral couple therapy
and, 745 panic disorder and agoraphobia and,
19–24, 20f, 22f substance use disorders and, 618, 619,
628f, 629 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 230–232, 231f, 238–239
Functional disengagement, 536 Functional model of emotional disorders,
447–449. See also Emotional disorders
Functional validation, 413. See also Validation
Functioning. See also Social–occupational functioning
alcohol use disorder and, 557, 559 behavioral activation and, 343 borderline personality disorder and, 397 cognitive-behavioral therapy for chronic
pain and, 682 cognitive-behavioral therapy for
insomnia and, 660–661 depression and, 266 exposure and ritual prevention and, 175 pharmacological treatment and bipolar
disorder and, 484–485 sleep disorders and, 638–639 validation in DBT and, 413
Fusion, 187–188
G
Gate control theory, 687 Gender, 64–65, 109 Generalized anxiety disorder (GAD).
See also Anxiety disorders; Unified Protocol for transdiagnostic treatment
acceptance-based behavioral therapy for, 187–196
borderline personality disorder and, 384
case studies, 196–211, 207t, 208f, 210f exposures and, 142 obsessive–compulsive disorder and, 136 overview, 184–185, 211 panic disorder and agoraphobia and, 5 self-injurious thoughts and behaviors
and, 447 treatment options for, 185–187
Generalized Anxiety Disorder Severity Scale (GADSS), 230
Generalizing results, 304–305 Genetic factors. See also Vulnerability–
stress model biosocial theory of BPD and, 393 bipolar disorder and, 485 dialectical behavior therapy for BPD
and, 392 emotional disorders and, 221 panic disorder and agoraphobia and, 6
810 Subject Index
Genetic factors (cont.) psychoeducation regarding, 498–499 substance use disorders and, 618
Genuineness, 413 Goal setting. See also Treatment goals
alcohol use disorder treatment model and, 579–581
behavioral activation and, 346 bipolar disorder and, 486 cognitive therapy for depression and,
276–277, 278 cognitive-behavioral therapy for chronic
pain and, 682, 685–687, 686f, 688f cognitive-behavioral therapy for
insomnia and, 650–651 interpersonal psychotherapy and, 324 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 233, 239, 449, 455–456, 466
Goals facet of therapeutic alliance, 120. See also Therapeutic relationship/alliance
Graded task assignment, 351–352, 370– 371. See also Activity scheduling; Out-of-session practices
Gradual exposures, 141. See also Exposure techniques
Grandiosity, 271f Grief, 321–322, 325–333, 395f, 396–397.
See also Loss Group treatment format. See also
Treatment format acceptance-based behavioral therapy for
GAD, 189 acute phase of CT treatment for
depression and, 261, 265 alcohol use disorder treatment model
and, 575–576 behavioral activation and, 354 bipolar disorder and, 488 borderline personality disorder and, 387 cognitive-behavioral therapy for
psychosis and, 530 dialectical behavior therapy for BPD
and, 388–390, 402–404, 408 exposure and ritual prevention and,
142–143 group CBT, 261, 264 group schema-focused therapy, 267–268 panic disorder and agoraphobia and,
11–12 posttraumatic stress disorder and, 77 self-injurious thoughts and behaviors
and, 445 social anxiety disorder and, 109
Guided activation, 341 Guided discovery, 527
Guided imagery, 198–199. See also Imaginal exposures
Guilt, 236f, 564
H
Habituation emotional behaviors and, 245 exposure and ritual prevention and,
155, 173 exposures and, 28–29 obsessive–compulsive disorder and, 140,
141–142 posttraumatic stress disorder and, 67
Hallucinations, 522–523, 524–525, 532–534, 533f. See also Psychotic disorders; Schizophrenia
Hamilton Anxiety Rating Scale (HARS), 226
Hamilton Depression Rating Scale (HDRS), 226, 319, 343
Happiness, 236f Health. See also Medical conditions
alcohol use disorder and, 557 depression and, 258 detoxification and, 573–574 sleep problems and, 638–639, 640
Healthy Adult mode, 273. See also Mode Helplessness, 325 Hepatitis education, 622 Hierarchy development. See also Subjective
Units of Discomfort Scale (SUDS) dialectical behavior therapy for BPD
and, 401, 404 panic disorder and agoraphobia and,
35–38, 41 posttraumatic stress disorder and,
72–73 UP for emotional disorders and SITBs
and, 464–465 High estimated social cost, 111 Histrionic personality disorder, 14–15 Hitting oneself. See Self-injurious thoughts
and behaviors (SITBs) HIV education, 622 HIV/AIDS Knowledge Test, 622 Home visits, 157–158 Homework between sessions. See Out-of-
session practices Homework goals, 682. See also Treatment
goals Hopelessness
behavioral activation and, 347–348 borderline personality disorder and,
386–387
cognitive therapy for depression and, 286, 289–290
dialectical behavior therapy for BPD and, 388
interpersonal psychotherapy and, 333–334
IPT model of depression and, 319 Hospitalization. See also Inpatient
treatment setting; Treatment setting alcohol use disorder treatment model
and, 574 cognitive-behavioral therapy for
psychosis and, 525 detoxification and, 573 dialectical behavior therapy for BPD
and, 388 interpersonal psychotherapy and, 334
Humor, 418 Hypercriticalness, 272f Hypersomnolence, 663. See also Sleep
problems/disorders Hyperventalization, 35–36 Hypomanic symptoms, 481–482. See also
Bipolar disorders; Mania Hypothesis testing, 283
I
Idiographic data collection, 391–392 Ignoring important parts, 91f. See also
Cognitive errors Imagery work
alcohol use disorder treatment model and, 583
cognitive-behavioral therapy for chronic pain and, 683, 689–690
cognitive-behavioral therapy for insomnia and, 661
schema therapy and, 297 Imaginal exposures. See also Exposure
techniques acceptance-based behavioral therapy for
GAD, 198–199 depression and, 174 feared consequences and, 149–150 intensive EX/RP program for OCD
and, 156–157, 169 obsessive–compulsive disorder and,
140, 141 posttraumatic stress disorder and,
72–73 UP for emotional disorders and SITBs
and, 465–466 Impact Statement, 80–81, 102–103 Impulsive responding, 486
Subject Index 811
In vivo exposure. See also Exposure techniques
acceptance and, 30–31 applied relaxation and, 26 breathing retraining and, 25 hierarchy development and, 35 intensive EX/RP program for OCD
and, 157, 169 obsessive–compulsive disorder and,
139, 140 panic disorder and agoraphobia and,
10–11, 13, 27, 35, 40–48 Individual treatment format. See also
Treatment format alcohol use disorder treatment model
and, 576 behavioral activation and, 353–354 bipolar disorder and, 487–488 borderline personality disorder and, 387 cognitive-behavioral therapy for
insomnia and, 643 dialectical behavior therapy for BPD
and, 388, 401–402 exposure and ritual prevention and,
142–143 panic disorder and agoraphobia and,
11–12 Information gathering, 153–156. See also
Assessment Information processing, 66–67, 139,
268–269 Inhibited grieving, 395f, 396–397 Inhibition, 29, 272f Initiative on Methods, Measurement, and
Pain Assessment in Clinical Trials (IMMACT), 680–681
Inpatient treatment setting. See also Hospitalization; Treatment setting
alcohol use disorder treatment model and, 574
behavioral activation and, 355 borderline personality disorder and, 385 detoxification and, 573 dialectical behavior therapy for BPD
and, 388–389 enhanced cognitive-behavioral therapy
for eating disorders and, 713 interpersonal psychotherapy and, 334 panic disorder and agoraphobia and, 11 social anxiety disorder and, 109–110
Insight, 134, 137, 150, 284, 424 Insomnia. See also Cognitive-behavioral
therapy for insomnia (CBT-I); Sleep problems/disorders
assessment and, 644–645 chronic pain and, 684
diagnosis and, 640–641 future directions and research and,
662–664 overview, 638–640 overview of sleep in general, 639–640
Insomnia Severity Indexing, 645 Intake assessment, 613–618. See also
Assessment Integrative behavioral couple therapy
(IBCT). See also Couple distress; Couple therapy; Family-based interventions
assessment and, 748–753, 749t, 763–764
case studies, 762–768 dissemination and implementation of,
761–762 feedback session, 752–753, 763–764 overview, 742–743, 744–746, 747–760,
749t, 768 research support for, 760–762 resources regarding, 768–769 termination and, 760, 767–768 therapist and patient variables and,
760 treatment phase of, 753–760, 764–767
Interaction, pattern of, 748, 759 Interactive model, 392 Interactive voice response (IVR) systems,
622 Interim buprenorphine treatment (IBT),
620–624, 621f, 623f, 625–633, 628f, 630f, 633t. See also Opioid use disorder treatment
Internal experiences, 148–149, 187–188, 191, 535
International Classification of Diseases (ICD-11), 133–134, 382, 742
International Personality Disorder Examination (IPDE), 382
Internet-based cognitive-behavioral therapy (ICBT), 11, 261. See also Computer- assisted cognitive therapy; Internet- based treatment delivery; Technology
Internet-based treatment delivery, 189, 318, 470–471, 528. See also Internet-based cognitive-behavioral therapy (ICBT); Remote treatment; Technology
Interoceptive exposure. See also Exposure techniques
acceptance and, 30–31 panic disorder and agoraphobia and,
27–28, 42, 43–48 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 237, 463–464, 469
Interpersonal and social rhythm therapy (IPSRT), 486, 488, 489, 490, 491, 515
Interpersonal factors, 12–13, 69, 322, 324, 328–332, 561–562. See also Relationship factors; Support from others
Interpersonal inventory, 323–324, 327–328
Interpersonal psychotherapy (IPT). See also Interpersonal psychotherapy (IPT) for depression
acute phase of CT treatment for depression and, 260
development of, 318–319 overview, 317–318 posttraumatic stress disorder and, 72 schema theory and, 274 social anxiety disorder and, 109–110
Interpersonal psychotherapy (IPT) for depression. See also Depression; Interpersonal psychotherapy (IPT)
case studies, 325–333 characteristics of, 319–320 compared with other psychotherapies,
320–321 development of, 318–319 four problem areas focused on,
321–322 overview, 317–318, 335 predictors of response to, 334–335 principles of, 319 problems that may arise during,
333–334 process of, 322–325 therapist and patient variables and, 321
Interpersonal violence, 390–391, 749–750. See also Violence
Interpretation training, 109 Interviews in assessment. See also
Assessment; Structured clinical interviews
acceptance-based behavioral therapy for GAD, 191
alcohol use disorder treatment model and, 568–569, 569t
bipolar disorder and, 495 cognitive-behavioral therapy for chronic
pain and, 678–680 cognitive-behavioral therapy for
psychosis and, 534 obsessive–compulsive disorder and, 146 opioid use disorder treatment and,
616–618 panic disorder and agoraphobia and,
19–21, 20f
812 Subject Index
Interviews in assessment (cont.) posttraumatic stress disorder and, 70–71 sleep disorders and, 645 social anxiety disorder and, 119 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 225–226
Invalidating environments, 393–394. See also Environmental factors
Inventories, standardized. See Standardized inventories
Inventory of Drinking Situations, 569–570
Involving others in treatment, 354, 587–588, 722. See also Family involvement in treatment
Irreverent communication, 418, 426–427, 431–432
Irritability, 483–484, 707 Isolation, 270f, 325
J
Joint mindfulness, 756. See also Mindfulness training
Joint review of progress, 723. See also Progress in treatment
Judgment, 187–188 Jumping to conclusions, 91f. See also
Cognitive errors Just-in-time adaptive intervention (JITAI),
470–471
K
KSADS Depression and Mania Rating Scales, 495
L
Lability of mood, 707 Laxative misuse, 709–710, 709f, 710f. See
also Bulimia nervosa (BN); Eating disorders
Learning, 28–30, 66–67, 138, 412 Legal system, 557, 589–590 Level of care, 571–575, 573t Leyton Obsessional Inventory, 146–147 Liebowitz Social Anxiety Scale (LSAS),
230 Liebowitz Social Anxiety Scale—Self-
Report (LSAS-SR), 119
Life events. See also Childhood experiences; Vulnerability–stress model
bipolar disorder and, 485–487 enhanced cognitive-behavioral therapy
for eating disorders and, 714, 730 interpersonal psychotherapy and, 320,
335 IPT model of depression and, 319, 320,
325 psychoeducation regarding, 498–499
Life Events Checklist, 70 Lifespan, 639–640, 673 Lifestyle balance, 586–587, 694, 695f Life-threatening behaviors, 398, 401. See
also Nonsuicidal self-injury (NSSI); Suicidality
Limit setting, 416 Linehan Risk Assessment and Management
Protocol (LRAMP), 452 Listening, 412 Loss, 266, 325–333. See also Grief Loss of interest, 325 Low perceived emotional control, 111–112
M
Magnification, 269 Maintaining factors
alcohol use disorder and, 560–561 enhanced cognitive-behavioral therapy
for eating disorders and, 724–733 panic disorder and agoraphobia and,
8–10, 12–13 social anxiety disorder and, 110, 111f
Maintenance of treatment gains acceptance-based behavioral therapy for
GAD, 210–211 alcohol use disorder treatment model
and, 562, 588–589 behavioral activation and, 353 integrative behavioral couple therapy
and, 760–761 panic disorder and agoraphobia and,
30–31 Maintenance stage of change, 560, 562 Major depressive disorder (MDD). See also
Depression bipolar disorder and, 481, 483 case studies, 287–296, 325–333 cognitive therapy for depression and,
275 diagnosis and, 323 dialectical behavior therapy for BPD
and, 388
interpersonal psychotherapy and, 318 obsessive–compulsive disorder and,
135–136 overview, 258 panic disorder and agoraphobia and, 5 self-injurious thoughts and behaviors
and, 444, 447 Making lemonade out of lemons technique,
411, 428–429 Maladaptive Coping modes, 273, 273f. See
also Mode Maladaptive thinking, 115–116. See also
Distorted thinking Maltreatment of children, 7–8. See also
Abuse; Childhood experiences Mania, 485–487, 662–663 Manic symptoms, 480–482. See also
Bipolar disorders Manual-assisted cognitive treatment
(MACT), 387, 446. See also Unified Protocol for transdiagnostic treatment of emotional disorders
Marital factors, 12–13, 749, 749t. See also Couple distress; Couple therapy; Family factors; Integrative behavioral couple therapy (IBCT); Relationship factors
Marital Status Inventory, 749, 749t Maudsley model AN treatment for
adults (MANTRA), 711. See also Transdiagnostic CBT treatment protocol for eating disorders
McGill Pain Questionnaire (MPQ), 681 Medical conditions. See also Health
alcohol use disorder and, 557 behavioral activation and, 355 cognitive-behavioral therapy for
insomnia and, 644 detoxification and, 573 history of, 7–8 panic disorder and agoraphobia and, 15 sleep problems and, 638–639, 640
Medical evaluations, 21, 226, 681–682. See also Assessment
Medical model, 325, 328–329, 333–334, 335
Medical Outcomes Study 36-Item Short Form Health Survey, 343
Medication-assisted treatment (MAT), 624
Medications. See Pharmacological treatment
Meditation exercises, 241, 586. See also Mindfulness training; Relaxation techniques
Subject Index 813
Med-O-Wheel. See also Interim buprenorphine treatment (IBT)
case studies, 624, 625–633, 628f, 630f, 633t
interactive voice response systems and, 622 overview, 621, 621f
Memory, 30, 557 Mental Health Continuum—Short Form
(MHC-SF), 230 Mental representation systems, 69 Mentalization-based therapy (MBT), 385 Metacognitive therapy (MCT), 186, 266 Metaphor, 410 Methadone. See Aversion therapy agents Michigan Alcoholism Screening Test
(MAST), 615 Mind reading, 91f. See also Cognitive errors Mindful emotion awareness, 233–234,
241–242 Mindfulness training
acceptance-based behavioral therapy for GAD, 189, 194–195, 199, 200–204, 206–210, 207t, 208f, 210f
alcohol use disorder treatment model and, 586
consultation teams and, 406 dialectical behavior therapy for BPD
and, 402–403 integrative behavioral couple therapy
and, 756, 768 PBT of social anxiety and, 118 social anxiety disorder and, 109 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 233–234, 241–242, 457–459, 469
Mindfulness-based cognitive therapy (MBCT), 186, 194, 265, 266–267
Mindfulness-based stress reduction (MBSR), 110
Mindsets, 730–731 Minimization, 91f. See also Cognitive errors Minnesota model, 575 Misappraisals. See Appraisals Mixed hypomania, 481. See also Bipolar
disorders; Hypomanic symptoms Mobile health technology, 622. See also
Remote treatment; Smartphone technology; Technology
Mode, 272–274, 273f, 274f, 297–305 Modeling, 74–75 Moderating variables, 76–77 Moderation goals, 579–581, 582f,
595–600, 597f, 598f, 599f Monitoring strategies, 657–658, 718–720,
719t, 720f. See also Self-monitoring
Mood disorders. See Anxiety disorders; Bipolar disorders; Depression; Emotional disorders
Mood stabilizers, 386, 484, 485, 488. See also Pharmacological treatment
Mood state automatic thoughts and, 281 enhanced cognitive-behavioral therapy
for eating disorders and, 730 interpersonal psychotherapy and, 320,
335 mood intolerance, 730 obsessive–compulsive disorder and, 152
Moral injury, 76–77 Motivation
alcohol use disorder and, 560, 564–569, 577–579, 578f, 595
CBT-E for underweight patients and, 735–736, 736t
enhanced cognitive-behavioral therapy for eating disorders and, 714, 717
homework assignments and, 284–285 IPT model of depression and, 334 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 233, 239, 449, 455–456
Motivational enhancement therapy (MET), 560, 619
Motivational interviewing (MI) alcohol use disorder and, 560, 564,
566 cognitive-behavioral therapy for
insomnia and, 651 cognitive-behavioral therapy for
psychosis and, 549–550 substance use disorders and, 619 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 233, 239, 455–456
Motivational-based interventions, 619 Multidisciplinary approaches, 674 Multielement treatments, 619–624, 621f Multimodal Life History Inventory, 297 Mutual trap, 748 Mutual-help groups, 575–576, 588, 590 Myths, 410
N
Naltrexone. See Aversion therapy agents National Vietnam Veterans Longitudinal
Study (NVVLS), 65 National Vietnam Veterans Readjustment
Study (NVVRS), 65
Natural environment treatment setting, 10–11
Naturalistic interoceptive exposure, 46– 48. See also Interoceptive exposure
Negative affectivity, 6, 585–586 Negative automatic thoughts (NATs),
654–655, 656t. See also Automatic thoughts
Negative reinforcement, 267, 347–348, 415–416. See also Reinforcement
Negative schemas, 545–547, 546f Negative self-perception, 111 Negative symptoms, 522–523, 524–525,
531. See also Psychotic disorders; Schizophrenia
Negative thinking, 683. See also Cognitive errors; Thoughts
Neglect, 266. See also Abuse Neurobiological processes. See also
Biological processes alcohol use disorder and, 556–557, 561 borderline personality disorder, 382 cognitive model of depression and,
268 emotional disorders and, 221 fear extinction and, 30
Neuropathic pain, 671–672. See also Chronic pain
NIMH Treatment of Depression Collaborative Research Program (TDCRP), 259–260
Nociceptive pain, 671–672. See also Chronic pain
Nonadherence, medication, 485. See also Pharmacological treatment
Noncompliance, 172–173 Nonsuicidal self-injury (NSSI). See also
Self-injurious thoughts and behaviors (SITBs)
borderline personality disorder, 382, 384, 387
case studies, 418–434, 466–470, 468t cognitive-behavioral therapy for
psychosis and, 548–549 dialectical behavior therapy for BPD
and, 388–390, 398, 401, 404 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 222
O
Obesity. See Eating disorders Observing, 412
814 Subject Index
Obsessions, 133–134, 136, 137, 707. See also Obsessive–compulsive disorder (OCD)
Obsessive–compulsive disorder (OCD). See also Unified Protocol for transdiagnostic treatment
assessment and, 146–147 case studies, 160–172 comorbidity and, 135–136 complications during behavioral
treatment and, 172–175 diagnosis and, 136–137 exposure and ritual prevention and,
139–145 feared consequences and, 149–150 initial interview and sessions for,
147–153 intensive EX/RP program for OCD
and, 153–159 overview, 133–134, 175–176 prevalence and course of, 134–135 serotonergic medications and, 145–146 UP for emotional disorders and SITBs
and, 449–450 Obsessive–Compulsive Inventory—
Revised (OCI-R), 146 Obstructive sleep apnea/hypopnea, 638.
See also Sleep problems/disorders Office-based opioid treatment (OBOT),
620, 624, 629–633. See also Opioid use disorder treatment
Onset of disorder, 4, 134–135, 266 Operant conditioning, 66, 618 Opioid use disorder treatment. See also
Community reinforcement approach (CRA); Interim buprenorphine treatment (IBT); Substance use disorders (SUDs)
assessment and, 613–618 buprenorphine agreement form and,
617f case studies, 624, 625–633, 628f, 630f,
633t multielement treatments, 619–624,
621f, 623f overview, 633 providing a description of the treatment
program to clients, 615–616 treatment approaches, 618, 619–624,
621f, 623f Opposite action skill, 403, 655 Oppositional defiant disorder, 482 Organismic variables, 561 Orientation to treatment, 397–398,
750–751
“Other eating disorders” (OEDs) classification, 706, 708. See also Eating disorders; Enhanced cognitive-behavioral therapy (CBT- E); Transdiagnostic CBT treatment protocol for eating disorders
Others involved in treatment, 354, 587–588, 722. See also Family involvement in treatment
OurRelationship program, 762 Out-of-session practices. See also Self-
monitoring acceptance-based behavioral therapy for
GAD, 194, 195, 197, 198, 203–204, 210–211
alcohol use disorder and, 560, 577–579, 578f, 605
behavioral activation and, 345–346, 345t, 348–352, 349f
cognitive therapy for depression and, 278, 284–285, 293
cognitive-behavioral therapy for chronic pain and, 682
cognitive-behavioral therapy for insomnia and, 643
cognitive-behavioral therapy for psychosis and, 546
integrative behavioral couple therapy and, 750, 753
intensive EX/RP program for OCD and, 156
obsessive–compulsive disorder and, 140 posttraumatic stress disorder and,
80–81, 82–84, 83f, 88–92, 89f, 91f, 94–96, 97, 101–102
UP for emotional disorders and SITBs and, 455, 470
Outpatient treatment setting. See also Treatment setting
alcohol use disorder treatment model and, 574–575, 589
behavioral activation and, 353–354 cognitive-behavioral therapy for
insomnia and, 643 dialectical behavior therapy for BPD
and, 401–402 eating disorders and, 712 enhanced cognitive-behavioral therapy
for eating disorders and, 713 family-focused treatment for bipolar
disorder and, 493 panic disorder and agoraphobia and, 10
Overall Anxiety Severity and Impairment Scale (OASIS), 225, 229, 250, 453–454
Overall Depression Severity and Impairment Scale (ODSIS), 225, 229, 250, 453–454
Overall treatment goals, 682. See also Treatment goals
Overestimations, 37, 234, 243–245. See also Cognitive errors
Overgeneralization, 269 Oversimplification, 91f. See also Cognitive
errors Overt avoidance, 235. See also Avoidance Overvaluation of shape and weight,
706–707, 724–729, 725f, 726f. See also Eating disorders
P
Pain, chronic. See Chronic pain Pain Catastrophizing Scale (PCS), 681 Pain management, 674, 701. See also
Chronic pain; Cognitive-behavioral therapy for chronic pain
Panic Attack Record, 21, 22f, 34 Panic attacks. See also Panic disorder
assessment and, 19–24, 20f, 22f case studies, 18–24, 20f, 22f, 32–48 CBT treatment protocol for, 32–48 efficacy of CBT for, 31–32 first panic attacks, 8 overview, 1–3 relationship of with agoraphobia, 3–4
Panic disorder. See also Anxiety disorders; Panic attacks
assessment and, 19–24, 20f, 22f borderline personality disorder and, 397 case studies, 18–24, 20f, 22f, 32–48 CBT treatment protocol for, 32–48 components of CBT for, 24–31 efficacy of CBT for, 31–32 etiological and maintaining factors for,
5–10 history of psychological treatment for, 5 interpersonal context variables in the
treatment of, 12–13 nature of, 1–4 overview, 1, 48–49 patient variables in the treatment of, 14–16 pharmacological treatment and, 16–18 presenting features of, 4–5 relationship of with agoraphobia, 3–4 therapist variables in the treatment of,
13–14 treatment format, 11–12 treatment setting and, 10–11
Subject Index 815
Panic Disorder Severity Scale (PDSS), 230 Parable in ACT therapy, 410 Paranoid delusions. See Delusions Parasuicide. See Self-injurious thoughts
and behaviors (SITBs) Partial hospitalization programs, 573,
574–575, 713. See also Inpatient treatment setting
Passive avoidance, 147, 173. See also Avoidance
Passivity, active, 395–396, 395f Patient Health Questionnaire–9 (PHQ-9),
343, 452, 681 Patient/client variables
acceptance-based behavioral therapy for GAD, 190
alcohol use disorder and, 559–560, 559t, 562–563, 575, 591–592
arguments regarding exposures and, 174 behavioral activation and, 355 cognitive therapy for depression and, 276 cognitive-behavioral therapy for chronic
pain and, 675–676 cognitive-behavioral therapy for
insomnia and, 644, 661–662 cognitive-behavioral therapy for
psychosis and, 531 dialectical behavior therapy for BPD
and, 398–399, 407–408 enhanced cognitive-behavioral therapy
for eating disorders and, 712, 714 family-focused treatment for bipolar
disorder and, 493 integrative behavioral couple therapy
and, 760 intensive EX/RP program for OCD
and, 159 interpersonal psychotherapy and, 321 panic disorder and agoraphobia and,
14–16 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 223, 452–453
Pattern of interaction, 748, 759 Patterns of Problematic Thinking
Worksheet, 90–92, 91f, 94–96 Pediatric autoimmune neuropsychiatric
disorders associated with strepto- coccal infection (PANDAS), 135
Pediatric autoimmune neuropsychiatric syndrome (PANS), 135
Penn State Worry Questionnaire (PSWQ), 225
Perpetuating factors, 641. See also Diathesis–stress model
Personality disorders bipolar disorder and, 482 cognitive therapy for depression and,
275 interpersonal psychotherapy and, 335 obsessive–compulsive disorder and, 143 panic disorder and agoraphobia and, 5,
14–15 schema therapy and, 296
Personality traits, 5, 335 Pharmacological treatment
alcohol use disorder treatment model and, 577, 586
behavioral activation and, 342 bipolar disorder and, 484–485,
493–494, 514–515 borderline personality disorder and,
385–386, 388, 389 chronic pain and, 676 cognitive-behavioral treatments and,
259–261 depression and, 152, 259–261, 262–264,
265–266, 268, 275–276 emotional disorders and, 223–224 generalized anxiety disorder (GAD)
and, 190–191 interpersonal psychotherapy and,
334–335 obsessive–compulsive disorder and,
145–146, 152–153, 175–176 panic disorder and agoraphobia and, 5,
12, 16–18, 30, 31 psychosis and, 531 relapse prevention and, 262–264 schizophrenia and, 531 sleep disorders and, 642, 644, 645 substance use disorders and, 620 suicidality and, 334
Phobias, 5, 137–139. See also Anxiety disorders; Specific phobias
Phone coaching, 10–11, 389, 404, 470. See also Remote treatment; Telehealth delivery
Physical abuse, 7–8, 70, 266, 586. See also Abuse
Physical Sensation Test, 247–248 Physical sensations
panic attacks and, 9–10 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 237, 247–248, 456–457, 463–464, 469
Physiological measures, 24, 71. See also Assessment
Pittsburgh Sleep Quality Index, 645
Pleasant activity scheduling, 684, 696– 697. See also Pleasurable events
Pleasant Events Schedule, 343 Pleasurable events, 343, 586. See also
Pleasant activity scheduling Polysomnography (PSG), 645 Positive activities, 586–587 Positive and Negative Affect Schedule—
Trait version (PANAS), 229–230 Positive emotional response, 545–547, 546f Positive reinforcement, 340–341,
347–348, 415–416, 584–585. See also Reinforcement
Postevent processing, 113 Posttraumatic Stress Diagnostic Scale
(PDS), 70 Posttraumatic stress disorder (PTSD)
assessment and, 69–72 behavioral activation and, 355 borderline personality disorder,
383–384 case studies, 77–103, 83f, 89f, 91f, 92f,
95f, 98f cognitive-behavioral therapy for chronic
pain and, 675–676 dialectical behavior therapy for BPD
and, 389, 399 integrative behavioral couple therapy
and, 762 obsessive–compulsive disorder and, 136 overview, 64 prevalence, 64–66 self-injurious thoughts and behaviors
and, 446, 447 substance use disorders and, 76 theoretical models, 66–69 treatment and, 72–77
Posttreatment review appointment, 733 Potential Stressful Events Interview, 70 Power, 99–100 Practical concerns regarding treatment,
574–575 Practice between sessions. See Out-of-
session practices Precipitating factors, 641. See also
Diathesis–stress model Precontemplation stage of change, 560 Predisposing factors, 641. See also
Diathesis–stress model Preparation stage of change, 560 Present-focused approach, 75–76,
233–234, 241–242, 320 Prevalence rates
borderline personality disorder, 381–382 chronic pain and, 672
816 Subject Index
Prevalence rates (cont.) depression and, 257–258 generalized anxiety disorder and,
184–185, 189 obsessive–compulsive disorder and,
134–135 panic disorder and agoraphobia and, 4–5 sleep disorders and, 640 social anxiety disorder and, 109
Primary Care Evaluation of Mental Disorders (PRIME-MD), 681
Primary Care PTSD Screen for DSM-5 (PC-PTSD-5), 71
Primary care setting, 564 Proactive problem solving, 730. See also
Problem solving Probability overestimation, 234, 243–245.
See also Overestimations Problem Areas Questionnaire, 749, 749t Problem solving
behavioral activation and, 352–353, 375 dialectical behavior therapy for BPD
and, 411, 413, 414–417, 426–428, 431–432
enhanced cognitive-behavioral therapy for eating disorders and, 730
family-focused treatment for bipolar disorder and, 499–500
problem-solving skills training and, 492t, 497, 503–505, 513–514
solution analysis in DBT and, 415 Problem-oriented stance, 278 Process factors, 76–77 Process-based therapy (PBT). See also
Cognitive-behavioral therapy (CBT); Treatment approaches in general
case studies, 118–128, 122f, 124f overview, 108, 113, 128 predictors of treatment success and, 128 social anxiety disorder and, 113–118, 115f
Processing and feedback, 113 Progress in treatment
cognitive therapy for depression and, 286–287
enhanced cognitive-behavioral therapy for eating disorders and, 723, 732–733
integrative behavioral couple therapy and, 760–761
lack of, 286–287 UP for emotional disorders and SITBs
and, 466 Progressive muscle relaxation (PMR),
26, 28, 683, 689–690. See also Relaxation techniques
Prolonged exposure (PE). See also Dialectical behavior therapy/ prolonged exposure (DBT/PE); Exposure techniques
borderline personality disorder, 383–384, 399, 400
obsessive–compulsive disorder and, 141–142
posttraumatic stress disorder and, 72 Protective factors, 498–499, 574, 751 Psychodynamic therapy, 109, 320–321,
384–385, 391–392 Psychoeducation. See also Education stage
of treatment acceptance-based behavioral therapy for
GAD, 189, 193–194, 200–201 behavioral activation and, 344–346,
344f, 345t, 357–359 bipolar disorder and, 488, 490–491 cognitive therapy for depression and,
278 cognitive-behavioral therapy for chronic
pain and, 684–687, 685f, 686f, 689, 698
cognitive-behavioral therapy for insomnia and, 642, 645, 647, 651, 654, 663
dialectical behavior therapy for BPD and, 402–404
enhanced cognitive-behavioral therapy for eating disorders and, 714, 721, 724–726, 725f, 726f, 735–736
family psychoeducation, 490–491 family-focused treatment for bipolar
disorder and, 490–491, 492, 492t, 497–501, 506–509, 514–515
intensive EX/RP program for OCD and, 154
interpersonal psychotherapy and, 323, 325, 327
opioid use disorder treatment and, 622–624
PBT of social anxiety and, 117–118 social anxiety disorder and, 113, 126 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 233, 239–241, 449, 450, 456–457, 459–461
Psychological model, 110–113, 111f, 574, 761
Psychosocial approaches, 484, 485, 487– 491. See also Behavioral activation (BA) for depression
Psychosocial assessment, 679. See also Assessment
Psychotic disorders. See also Cognitive- behavioral therapy for psychosis (CBTp); Delusional disorder; Psychotic symptoms; Schizophrenia
assessment and, 534 bipolar disorder and, 483 case studies, 538–545 obsessive–compulsive disorder and,
137 overview, 522–523 relapse prevention and, 547–548 research support for CBTp and,
523–526 Psychotic Symptom Rating Scales
(PSYRATS), 534 Psychotic symptoms. See also Psychotic
disorders assessment and, 534 bipolar disorder and, 483 cognitive-behavioral therapy for
psychosis and, 548 coping–recovery clinical model and,
532–534, 533f phases of schizophrenia and, 528, 529t relapse prevention and, 547–548
PTSD Checklist–5 (PCL-5), 71 PTSD Symptom Scale (PSS), 230 PTSD Symptom Scale—Interview for
DSM-5 (PSS-I-5), 71 Public health factors, 638–639, 672 Punishment, 415–416, 619 Purging, 709–710, 709f, 710f. See also
Bulimia nervosa (BN); Eating disorders
Q
Quality of Life and Enjoyment Satisfaction Questionnaire (QLESQ), 230
Quality-of-life-interfering behaviors, 399, 401
Questioning, 281, 283–284, 295, 527 Questionnaires. See also Self-report
inventories; Standardized inventories behavioral activation and, 343 cognitive-behavioral therapy for chronic
pain and, 680–681 eating disorders and, 713 opioid use disorder treatment and,
614–615 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 229–230
Quiet desperation, 399–400
Subject Index 817
R
Racism, 189 Radical genuineness, 413 Rapid cycling, 482. See also Bipolar
disorders Rapport, 276 Reactivity
acceptance-based behavioral model of GAD and, 187–188
borderline personality disorder and, 383–384
functional model of emotional disorders and, 447, 448
posttraumatic stress disorder and, 71 Readiness Rulers, 569 Readiness to Change Questionnaire, 569 Reality testing, 537 Reappraisals, 537. See also Appraisals Reattribution, 283, 535 Reciprocal communication, 417–418,
431–432 Recognition seeking, 271f Reconsolidation process, 30 Recurrences, 484. See also Relapse
prevention Reflection, 412 Refusal skills, 585, 628t, 629 Regular eating intervention, 721–722,
736 Reinforcement. See also Consequences
alcohol use disorder treatment model and, 587–588, 602
behavioral activation and, 347–348 depression and, 267, 340–341 dialectical behavior therapy for BPD
and, 415–416, 417, 428–429 panic disorder and agoraphobia and,
12–13 substance use disorders and, 619
Relapse. See also Relapse prevention alcohol use disorder and, 560, 562 cognitive therapy for depression and,
306n depression and, 258 panic disorder and agoraphobia and, 30,
48–49 substance use disorders and, 615
Relapse prevention. See also Maintenance of treatment gains; Relapse
acceptance-based behavioral therapy for GAD, 196
alcohol use disorder and, 562, 588–589 behavioral activation and, 353,
374–375
chronic pain and, 699–700, 700t cognitive therapy for depression and,
261–265 cognitive-behavioral therapy for
insomnia and, 661 cognitive-behavioral therapy for
psychosis and, 525, 547–548 enhanced cognitive-behavioral therapy
for eating disorders and, 732–733 family-focused treatment for bipolar
disorder and, 499–500 interpersonal psychotherapy and, 325 obsessive–compulsive disorder and,
144–145 posttraumatic stress disorder and,
102–103 substance use disorders and, 618, 619 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 250
UP for emotional disorders and SITBs and, 466, 469–470
Relapse signature, 548 Relationship factors. See also Couple
distress; Couple therapy; Family- based interventions; Integrative behavioral couple therapy (IBCT); Support from others
alcohol use disorder and, 557, 561–562, 570–571, 571f, 587–588
cognitive therapy for depression and, 275
cognitive-behavioral therapy for psychosis and, 536
dialectical behavior therapy for BPD and, 431–432
dialectics and, 391–392 obsessive–compulsive disorder and,
152 panic disorder and agoraphobia and,
12–13 posttraumatic stress disorder and, 69
Relaxation techniques. See also Applied relaxation; Breathing retraining; Progressive muscle relaxation (PMR)
alcohol use disorder treatment model and, 586
cognitive-behavioral therapy for chronic pain and, 683, 687–690, 687f
generalized anxiety disorder and, 185–186
obsessive–compulsive disorder and, 140 panic disorder and agoraphobia and,
5, 26 Remissions, 48–49
Remote treatment, 318, 342–343, 470– 471. See also Internet-based treatment delivery; Smartphone technology; Technology; Telehealth delivery; Video-based treatment
Residential treatment settings. See Inpatient treatment setting
Resistance cognitive therapy for depression and,
284–285 cognitive-behavioral therapy for
insomnia and, 661–662 family-focused treatment for bipolar
disorder and, 500–501, 504–505, 515 medication nonadherence and, 485
Respondent conditioning, 618 Response prevention, 157, 172–173 Response-contingent positive
reinforcement, 340–341. See also Reinforcement
Responsiveness, 417–418 Restriction of eating, 729–730 Revised Conflict Tactics Scales (CTS2),
571, 749–750, 749t Reward Probability Index (RPI), 343 Reward sensitivity, 486 Risk factors, 6–8, 446–447, 548–549.
See also Vulnerability factors; Vulnerability–stress model
Ritual prevention, 140–141. See also Exposure and ritual prevention (EX/ RP)
Rituals. See also Compulsions development of new rituals, 174–175 exposure and ritual prevention and,
151–152 intensive EX/RP program for OCD
and, 154–156 noncompliance with response
prevention and, 172–173 obsessive–compulsive disorder and,
134, 139 Rogerian supportive therapy (RST),
386–387 Role disputes, 322 Role playing
cognitive therapy for depression and, 281
family-focused treatment for bipolar disorder and, 501–503
interpersonal psychotherapy and, 325, 331
stress inoculation training and, 74–75 Role reversal, 281 Role transitions, 322
818 Subject Index
Routine, 346, 653–654 Rule-governed strategies, 745 Ruminations, 136, 353, 368, 370–371
S
Sadness, 236f Safety, 73, 96, 134. See also Safety signals
and behaviors Safety signals and behaviors. See also Safety
breathing retraining and, 40 cognitive-behavioral therapy for
insomnia and, 659–660 cognitive-behavioral therapy for
psychosis and, 536–537 emotional behaviors and, 235 example of a treatment protocol for
panic disorder and agoraphobia, 43 exposure therapy and, 29 panic disorder and agoraphobia and,
17, 47 social anxiety disorder and, 112
Savoring strategy, 655 Schedule for Affective Disorders and
Schizophrenia for School-Age Children—Present and Lifetime Version (KSADS-PL), 495
Schema domain, 306n. See also Early maladaptive schemas (EMS)
Schema Mode Questionnaire, 297–298 Schema theory, 269–275, 270f–272f, 273f,
274f. See also Early maladaptive schemas (EMS)
Schema therapy (ST), 267–268, 296–306 Schema-focused therapy (SFT), 266, 387 Schemas, self, 545–547, 546f. See also Early
maladaptive schemas (EMS) Schematic, propositional, analogue, and
associative representational system (SPAARS), 69
Schematic mental representation system, 69
Schizoaffective disorder, 483 Schizophrenia. See also Cognitive-
behavioral therapy for psychosis (CBTp); Psychotic disorders
assessment and, 534 associated features of, 529–530, 529t behavioral activation and, 355 bipolar disorder and, 483 case studies, 538–545 cognitive-behavioral therapy for, 523 coping–recovery clinical model and,
532–534, 533f
expressed emotion and, 486–487 obsessive–compulsive disorder and,
137 overview, 522–523 phases of, 528, 529t relapse prevention and, 547–548 research support for CBTp and,
523–526 Screening, 563–564, 565t, 749t. See also
Assessment Second-generation antipsychotics, 484. See
also Antipsychotics; Pharmacological treatment
Selective abstraction, 269 Selective serotonin reuptake inhibitors
(SSRIs), 145–146, 190–191, 224. See also Pharmacological treatment
Self-control, 271f Self-directed exposures, 10–11, 142, 176.
See also Exposure techniques Self-discipline, 271f Self-disclosure, 417–418 Self-esteem
cognitive-behavioral therapy for psychosis and, 528
dialectical behavior therapy for BPD and, 389
early maladaptive schemas and, 271f interpersonal psychotherapy and, 325 posttraumatic stress disorder and,
100–101 schizophrenia and, 545–547, 546f
Self-evaluation, 724–729, 725f, 726f Self-focused attention, 110–112, 111f Self-harm. See Nonsuicidal self-injury
(NSSI); Self-injurious thoughts and behaviors (SITBs); Suicidality
Self-help therapy, 30, 284–285 Self-induced vomiting, 709–710, 709f,
710f. See also Bulimia nervosa (BN); Eating disorders
Self-Injurious Thoughts and Behaviors Interview (SITBI), 452, 453, 467
Self-injurious thoughts and behaviors (SITBs). See also Nonsuicidal self- injury (NSSI); Suicidality
case studies, 466–470, 468t cognitive-behavioral therapy for
psychosis and, 548–549 emotional disorders and, 446–449 overview, 443–444, 471 treatment options for, 444–446 UP for emotional disorders and,
449–453, 454–466, 470–471 Self-invalidation, 394–395, 395f
Self-Management and Recovery Training (SMART Recovery), 576, 588, 590
Self-management skills, 404, 492t, 601–602, 601f
Self-monitoring. See also Assessment; Cognitive-behavioral therapy (CBT); Out-of-session practices
acceptance-based behavioral therapy for GAD, 191, 194, 198, 203–204, 206
alcohol use disorder treatment model and, 569–570, 570f, 571f, 577–579, 578f
behavioral activation and, 348–352, 349f
cognitive-behavioral therapy for insomnia and, 645, 646f, 647, 657–658, 660, 663
cognitive-behavioral therapy for psychosis and, 548
dialectical behavior therapy for BPD and, 401–402
enhanced cognitive-behavioral therapy for eating disorders and, 718–720, 719t, 720f
family-focused treatment for bipolar disorder and, 495–496, 496f
panic disorder and agoraphobia and, 21, 25, 34–35, 41–42, 48
relapse prevention and, 548 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 226–229, 227f, 228f, 233, 244–245
Self-reliance training, 280–281 Self-report inventories. See also Assessment;
Standardized inventories acceptance-based behavioral therapy for
GAD, 191 alcohol use disorder treatment model
and, 568, 569–570 behavioral activation and, 343 cognitive-behavioral therapy for chronic
pain and, 680–681 eating disorders and, 713 obsessive–compulsive disorder and,
146–147 opioid use disorder treatment and,
614–615 posttraumatic stress disorder and, 71 social anxiety disorder and, 119
Self-schemas, 545–547, 546f. See also Early maladaptive schemas (EMS)
Self-statements, 37, 75, 80, 535. See also Distorted thinking
Self-worth, 528, 545–547, 546f
Subject Index 819
Semistructured clinical interviews. See also Assessment; Interviews in assessment
acceptance-based behavioral therapy for GAD, 191
alcohol use disorder treatment model and, 569, 569t
bipolar disorder and, 495 cognitive-behavioral therapy for chronic
pain and, 678–680 cognitive-behavioral therapy for
psychosis and, 534 opioid use disorder treatment and, 616–618 sleep disorders and, 645 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 225–226
Serotonergic medications, 145–146, 152–153. See also Pharmacological treatment
Serotonin and norepinephrine reuptake inhibitors (SNRIs), 190–191, 224. See also Pharmacological treatment
Session agenda. See Agenda setting Setbacks, 730–731, 732. See also Relapse Sexual abuse. See also Abuse
alcohol use disorder treatment model and, 586
assessment of traumatic events and, 70 biosocial theory of BPD and, 394 depression and, 266 panic disorder and agoraphobia and, 7–8
Sexual behavior, 707 Sexual violence, 70. See also Sexual abuse Shame, 270f, 417, 564 Sheehan Disability Scale (SDS), 119 Short Inventory of Problems (SIP), 568 Short-fuse families, 503. See also Family
factors “Sick role,” 323, 328–329 Skills training. See also Anger management
skills; Coping skills; Treatment approaches in general
cognitive-behavioral therapy for psychosis and, 534–537
depression and, 266 dialectical behavior therapy for BPD
and, 388–389, 390–391, 398–400, 402–404, 415, 426, 428–429
family-focused treatment for bipolar disorder and, 492t, 497
opioid use disorder treatment and, 628t, 629
posttraumatic stress disorder and, 72 social skills training, 109, 619 substance use disorders and, 618, 619
Skills training in affective and interpersonal regulation (STAIR), 72
Sleep efficiency, 651–652 Sleep hygiene, 652–653, 684, 698–699 Sleep problems/disorders. See also
Cognitive-behavioral therapy for insomnia (CBT-I); Insomnia
assessment and, 644–645 bipolar disorder and, 486 chronic pain and, 684, 698–699 future directions and research and,
662–664 interpersonal psychotherapy and, 335 nocturnal panic, 2 overview, 638–640 overview of sleep in general, 639–640
Sleep restriction technique, 651–652 Slips, 732. See also Relapse SMART Recovery. See Self-Management
and Recovery Training (SMART Recovery)
Smartphone technology alcohol use disorder treatment model
and, 570 cognitive-behavioral therapy for chronic
pain and, 674 cognitive-behavioral therapy for
psychosis and, 528, 548 opioid use disorder treatment and,
622–624 Sobriety/Save Ourselves (SOS), 576 Social Adjustment Scale, 343 Social anxiety disorder (SAD)
case studies, 118–128, 122f, 124f overview, 108–109, 128 PBT and, 113–118, 115f predictors of treatment success and, 128 prevalence, 109 psychological model of, 109–113, 111f
Social Anxiety Questionnaire (SAQ), 119 Social context, 569, 587–588, 643 Social engagement and disengagement, 536 Social functioning, 111–112, 152. See also
Social skills training Social interactions, 536 Social learning theory, 74, 392, 618, 619 Social phobia, 5, 19–21, 20f, 590 Social Phobia Inventory (SPIN), 119 Social Rhythm Metric, 495–496 Social skills training, 109, 619. See also
Skills training; Social functioning Social support, 562, 574. See also Support
from others Social Thoughts and Beliefs Scale
(STABS), 119
Social-cognitive theories, 67, 68–69 Social–occupational functioning,
484–485, 557. See also Employment; Functioning
Socioeconomic status, 15–16 Socratic dialogue, 73, 85–87, 527, 655 Solution analysis, 415, 428–431 Somatic pain, 671–672. See also Chronic
pain Specialist supportive clinical
management (SSCM), 711. See also Transdiagnostic CBT treatment protocol for eating disorders
Specific phobias, 5, 137. See also Anxiety disorders
Spielman model. See Diathesis–stress model
Stages of change, 560, 717 Standardized inventories, 21, 23. See also
Assessment; Self-report inventories STEPPS treatment, 387 Stimulus control, 652 Storytelling, 410 Strengths, 498–499, 574, 751 Stress inoculation training (SIT), 67, 74–76 Stress management, 693–694, 695f Stressful life events, 319, 320, 335. See also
Life events Structured Clinical Interview for DSM-5
(SCID-5) alcohol use disorder treatment model
and, 568 bipolar disorder and, 495 borderline personality disorder, 382 posttraumatic stress disorder and, 70–71 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 225, 467
Structured Clinical Interview for DSM-5—Clinician Version (SCID- 5-CV), 453
Structured Clinical Interview for DSM-IV Axis I Disorders (SCID-I), 343
Structured Clinical Interview for DSM-IV Axis II Personality Disorders (SCID- II), 343
Structured clinical interviews. See also Assessment; Interviews in assessment
acceptance-based behavioral therapy for GAD, 191
alcohol use disorder treatment model and, 568–569, 569t
bipolar disorder and, 495 cognitive-behavioral therapy for chronic
pain and, 678–680
820 Subject Index
Structured clinical interviews (cont.) cognitive-behavioral therapy for
psychosis and, 534 obsessive–compulsive disorder and, 146 posttraumatic stress disorder and, 70–71 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 225–226
Structured clinical management (SCM) approach, 385
Structured Interview Guide for the Hamilton Anxiety Rating Scale (SIGH-A), 226
Structured Interview Guide for the Hamilton Depression Rating Scale (SIGH-D), 226
Stuck Points, 73, 79, 81–84, 83f, 85–90, 89f, 92–96, 93f, 95f, 97, 98f, 102–103
Study of Cognitive Reality Alignment Therapy in Early Schizophrenia (SoCRATES), 524
Stylistic strategies, 417–418, 431–432 Subjective Units of Discomfort Scale (SUDS),
147–148, 156, 157, 170–171. See also Distress; Hierarchy development
Substance use disorders (SUDs). See also Alcohol use disorder (AUD); Interim buprenorphine treatment (IBT); Opioid use disorder treatment; Substance use/abuse
assessment and, 613–618 behavioral activation and, 355 bipolar disorder and, 483–484 case studies, 624, 625–633, 628f, 630f,
633t cognitive-behavioral therapy for
insomnia and, 644 cognitive-behavioral therapy for
psychosis and, 549–550 dialectical behavior therapy for BPD
and, 388 multielement treatments and, 619–624,
621f overview, 555–556, 612–613, 613t panic disorder and agoraphobia and, 15 posttraumatic stress disorder and, 76 treatment approaches, 618, 619–624,
621f, 623f Substance use/abuse. See also Alcohol
use disorder (AUD); Substance use disorders (SUDs)
cognitive-behavioral therapy for chronic pain and, 676, 679
dialectical behavior therapy for BPD and, 399
enhanced cognitive-behavioral therapy for eating disorders and, 714
family-focused treatment for bipolar disorder and, 493, 494
panic disorder and agoraphobia and, 5 Subtle behavioral avoidance, 235. See also
Avoidance Suicidality. See also Self-injurious thoughts
and behaviors (SITBs) behavioral activation and, 355 borderline personality disorder and,
382, 383, 384, 388–390, 397, 398, 401, 404
case studies, 418–434, 466–470, 468t CBT for depression and, 261 cognitive therapy for depression and,
289–290 cognitive-behavioral therapy for
psychosis and, 548–549 failure of treatment and, 432–434 interpersonal psychotherapy and, 334
Support from others alcohol use disorder treatment model
and, 570–571, 571f, 583 early maladaptive schemas and,
270f–272f intensive EX/RP program for OCD
and, 155–156 Suppression strategies, 655 Symptom management, 524 Symptom onset, 134–135 Symptom recovery, 524–525 Symptom relief as a goal, 278, 279–287,
280f, 282f Systematic desensitization (SD), 72 Systematic Treatment Enhancement
Program for Bipolar Disorder (STEP- BD), 489, 490, 494
T
Tasks facet of therapeutic alliance, 120. See also Therapeutic relationship/ alliance
Technology. See also Internet-based treatment delivery; Remote treatment; Smartphone technology
alcohol use disorder treatment model and, 570
cognitive-behavioral therapy for chronic pain and, 674
cognitive-behavioral therapy for psychosis and, 528, 548
opioid use disorder treatment and, 622
Telehealth delivery, 77, 342–343, 674. See also Phone coaching; Remote treatment; Telephone-guided treatment
Telephone-guided treatment, 10–11, 389, 404, 470. See also Remote treatment; Telehealth delivery
Termination acceptance-based behavioral therapy for
GAD, 210–211 alcohol use disorder treatment model
and, 604–605 behavioral activation and, 353, 374–375 case studies, 513–514 chronic pain and, 699–700, 700t cognitive-behavioral therapy for
insomnia and, 661 enhanced cognitive-behavioral therapy
for eating disorders and, 732–733 family-focused treatment for bipolar
disorder and, 492t, 505, 513–514 integrative behavioral couple therapy
and, 760, 767–768 interpersonal psychotherapy and, 325, 333 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 250–251
Theme, in couple therapy, 747 Therapeutic reactance, 286 Therapeutic relationship/alliance. See also
Collaboration acceptance-based behavioral therapy for
GAD, 192–193, 197–198 alcohol use disorder and, 560, 590–591 cognitive therapy for depression and,
276, 278, 286 cognitive-behavioral therapy for
insomnia and, 644 cognitive-behavioral therapy for
psychosis and, 527 dialectical behavior therapy for BPD
and, 398–399, 409, 426 difficulties in, 286 panic disorder and agoraphobia and, 13 posttraumatic stress disorder and, 80 social anxiety disorder and, 119–121
Therapist variables acceptance-based behavioral therapy for
GAD, 189–190 alcohol use disorder and, 558t, 590–591,
605 arguments regarding exposures and, 174 behavioral activation and, 354–355 cognitive therapy for depression and,
276, 286
Subject Index 821
cognitive-behavioral therapy for insomnia and, 644
cognitive-behavioral therapy for psychosis and, 531–532
consultation teams and, 404–407, 405t, 406t
dialectical behavior therapy for BPD and, 398–399, 400–401, 408
enhanced cognitive-behavioral therapy for eating disorders and, 712, 714
family-focused treatment for bipolar disorder and, 494
integrative behavioral couple therapy and, 760
intensive EX/RP program for OCD and, 158–159
interpersonal psychotherapy and, 321 panic disorder and agoraphobia and,
13–14 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 223, 451–452
Therapist-directed exposures, 10–11, 142, 176. See also Exposure techniques
Therapy-interfering behaviors, 398–399, 401, 402
Thinking traps, 243–245, 459–461. See also Cognitive errors; Cognitive flexibility; Distorted thinking
36-item Short Form Health Survey (SF- 36), 573–574
Thought disorder symptoms, 137. See also Psychotic disorders
Thought disorders, 548 Thought–action fusion (TAF), 138, 149 Thoughts. See also Automatic thoughts;
Cognitive errors; Cognitive flexibility; Distorted thinking
cognitive-behavioral therapy for chronic pain and, 683, 690–693, 691f, 692f, 694, 695f
cognitive-behavioral therapy for psychosis and, 537–538
UP for emotional disorders and SITBs and, 456–457
Thoughts, automatic. See Automatic thoughts
Thoughts, distorted. See Distorted thinking
Threat perception, 138–139, 147 Three-P/three factor model. See Diathesis–
stress model Tic disorders, 136, 137 Time-based activity pacing, 683–684,
694–696, 696f
Timeline Follow-Back Interview (TLFB), 568, 616
Tolerance building, 756–757, 764–767 Tourette syndrome, 136, 137 TRAC acronym, 373–374 Traditional behavioral couple therapy
(TBCT), 743–744, 759–760. See also Couple therapy
Training, therapist, 13–14, 494, 737. See also Therapist variables
Transactional model, 392, 394 Transdiagnostic approach, 638, 663–664 Transdiagnostic CBT treatment protocol
for eating disorders, 705–706, 708– 712, 709f, 710f. See also Cognitive- behavioral therapy for bulimia nervosa (CBT-BN); Eating disorders; Enhanced cognitive-behavioral therapy (CBT-E)
Transdiagnostic sleep and circadian interventions (TranS-C), 664
Transdiagnostic treatment of emotional disorders. See Treatment approaches in general; Unified Protocol for transdiagnostic treatment
Transference-focused psychotherapy (TFP), 384–385, 387
TRAP acronym, 353, 373–374 Trauma exposure, 64–65, 70, 449–450.
See also Posttraumatic stress disorder (PTSD)
Trauma History Questionnaire (THQ), 70 Trauma memories, 72–73, 79–80 Trauma-focused cognitive-behavioral
therapies, 75–76 Trauma-focused cognitive-behavioral
therapy for psychosis (TF-CBTp), 527. See also Cognitive-behavioral therapy for psychosis (CBTp)
Treatment approaches in general. See also Pharmacological treatment; individual treatment approaches
alcohol use disorder and, 558–563, 558t–559t, 575–577
bipolar disorder and, 487–491 borderline personality disorder and,
384–387 generalized anxiety disorder and,
185–187 intensive EX/RP program for OCD
and, 156 obsessive–compulsive disorder and,
152–153 panic disorder and agoraphobia and, 5 posttraumatic stress disorder and, 71–77
research on chronic depression and, 265–268
social anxiety disorder and, 109–110 Treatment contract, 324 Treatment for Adolescents with Depression
Study (TADS), 259–260 Treatment for self-injurious behavior
(T-SIB), 446 Treatment format. See also Group
treatment format; Individual treatment format
alcohol use disorder and, 558t behavioral activation and, 353–354 cognitive-behavioral therapy for chronic
pain and, 674 panic disorder and agoraphobia and,
11–12 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 222–223, 451
Treatment goals. See also Goal setting; Treatment planning
alcohol use disorder treatment model and, 579–581
behavioral activation and, 346, 347–350, 349f
cognitive therapy for depression and, 276–277, 278
cognitive-behavioral therapy for chronic pain and, 682
cognitive-behavioral therapy for insomnia and, 650–651
dialectical behavior therapy for BPD and, 397–400
integrative behavioral couple therapy and, 753–754
interpersonal psychotherapy and, 324 opioid use disorder treatment and, 615–616 social anxiety disorder and, 119–121 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 233, 239
Treatment planning. See also Treatment goals
alcohol use disorder and, 558–563, 558t–559t
cognitive therapy for depression and, 276–277
enhanced cognitive-behavioral therapy for eating disorders and, 713
exposure and ritual prevention and, 147 intensive EX/RP program for OCD
and, 153–156, 166–167 posttraumatic stress disorder and, 71–72 social anxiety disorder and, 119–121
822 Subject Index
Treatment setting. See also Inpatient treatment setting; Outpatient treatment setting
alcohol use disorder and, 558t, 571–575, 573t
behavioral activation and, 353–354 cognitive-behavioral therapy for chronic
pain and, 673–674 cognitive-behavioral therapy for
insomnia and, 643 enhanced cognitive-behavioral therapy
for eating disorders and, 713 family-focused treatment for bipolar
disorder and, 493 intensive EX/RP program for OCD
and, 157–158 panic disorder and agoraphobia and, 10–11 Unified Protocol for transdiagnostic
treatment of emotional disorders and, 222, 451
Treatment strategies in DBT, 408–418. See also Dialectical behavior therapy (DBT) for BPD
Tricyclic antidepressants, 145–146, 264. See also Antidepressants; Pharmacological treatment
Trust, 97, 99, 270f Trust Star Worksheet, 97 12-step model, 562, 575–576, 588. See also
Alcoholics Anonymous model Two-process model of sleep, 639. See also
Sleep problems/disorders Two-stage theory, 137–139
U
Ultrarapid cycling, 482. See also Bipolar disorders
Underlying assumptions, 306n. See also Assumptions
Unhelpful beliefs, 658–659. See also Beliefs Unified detachment, 755–756, 764–767 Unified Protocol for transdiagnostic
treatment of emotional disorders. See also Treatment approaches in general;
assessment and, 224–232, 227f, 228f, 231f, 442–444
case studies, 224–225, 232, 238–251, 466–470, 468t
components of, 232–238, 236f, 454–466
efficacy of, 221–222 overview, 217–218, 471 predictors of success and, 471 problems that may arise during,
470–471 rationale for, 218–221 self-injurious thoughts and behaviors
and, 449–453 treatment failure and, 471 treatment variables, 222–224
University of Rhode Island Change Assessment Scale, 569
Unrelenting crises, 395f, 396–397. See also Crises
UP Case Conceptualization Worksheet, 230, 231f
UP Skills Action Plan, 250 Urges, 462–463, 583. See also Emotional
behaviors Using metaphor technique, 410
V
Validation, 411–413, 417–418, 426, 431–432
Valued Activity Log, 206, 208, 208f Valued Living Questionnaire, 192, 198 Values, 189, 205–206 Values-based actions, 189, 192, 195–196,
206–210, 207t, 208f, 210f Verbal abuse, 266. See also Abuse Video-based treatment, 318, 342–343 Violence, 7–8, 70, 390–391, 749–750 Virtual reality exposure therapy (VRET),
72, 109. See also Exposure techniques
Visceral pain, 671–672. See also Chronic pain
Visual hallucinations. See Hallucinations Visual imagery, 683, 689–690. See also
Imagery work Vulnerability factors, 6–8, 394–395, 395f.
See also Risk factors Vulnerability–stress model, 485–487,
492t, 498–499. See also Biological processes; Genetic factors; Life events; Risk factors
W
Wake-up routines, 653 Weekly Activity Schedule, 280, 280f, 284 Weekly behavioral goals, 682. See also
Treatment goals Weekly Diary Cards, 401–402 Weekly Questionnaire, 749t, 752,
753–754, 755, 758 Weighing, collaborative, 720–721, 736 Weight concerns. See also Eating
disorders CBT-E for underweight patients and,
733–737, 734f, 735f, 736t enhanced cognitive-behavioral therapy
for eating disorders and, 721, 724–729, 725f, 726f
transdiagnostic perspective and, 709–710, 709f, 710f
Weight regain, 736 Willingness, 204–206 Wind-down routines, 653 Withdrawal, 325, 346, 536 Withdrawal symptoms, 572–574, 573t Women for Sobriety, 576 Work and Social Adjustment Scale
(WSAS), 230 Worry
acceptance-based behavioral therapy for GAD, 185, 187–189, 199
cognitive-behavioral therapy for insomnia and, 654–655, 656t
Writing activities in treatment, 80–81, 102–103
Written exposure therapy (WET), 72
Y
Yale–Brown Obsessive–Compulsive Scale (Y-BOCS), 146, 230
Young Schema Questionnaire (YSQ), 274, 297
Z
Zanarini’s Rating Scale for BPD (ZAN- BPD), 382
Zen practice, 387
- Cover
- Half Title Page
- Also from David H. Barlow
- Title Page
- Copyright
- About the Editor
- Contributors
- Preface
- Contents
- 1. Panic Disorder and Agoraphobia
- 2. Posttraumatic Stress Disorder
- 3. Social Anxiety: A Process‑Based Treatment Approach
- 4. Obsessive–Compulsive Disorder
- 5. Generalized Anxiety Disorder: An Acceptance‑Based Behavioral Therapy
- 6. Emotional Disorders: A Unified Protocol for Transdiagnostic Treatment
- 7. Cognitive Therapy for Depression
- 8. Interpersonal Psychotherapy for Depression
- 9. Behavioral Activation for Depression
- 10. Borderline Personality Disorder
- 11. Addressing Self-Injurious Thoughts and Behaviors within the Context of Transdiagnostic Treatment for Emotional Disorders
- 12. Bipolar Disorder
- 13. Schizophrenia and Other Psychotic Disorders
- 14. Alcohol Use Disorders
- 15. Substance Use Disorders
- 16. Treatment of Sleep Disturbance
- 17. Cognitive‑B ehavioral Therapy for Chronic Pain
- 18. Eating Disorders: A Transdiagnostic Protocol
- 19. Couple Distress
- Author Index
- Subject Index