3 pages writing
E M P I R I C A L R E S E A R C H
Multi-method Assessments of Sleep over the Transition to College and the Associations with Depression and Anxiety Symptoms
Leah D. Doane • Jenna L. Gress-Smith •
Reagan S. Breitenstein
Received: 30 April 2014 / Accepted: 27 June 2014 / Published online: 18 July 2014
� Springer Science+Business Media New York 2014
Abstract A growing body of research has demonstrated
links between sleep problems and symptoms of depression
and anxiety in community and clinical samples of adoles-
cents and young adults. Scant longitudinal research, how-
ever, has examined reciprocal associations over socio-
contextual shifts such as the transition to college. Using
multiple methods of assessment (e.g., actigraphy, sub-
jective report), the current study assessed whether sleep
quantity, quality or variability changed over the transition
to college and investigated the potential cross-lagged
relationships between adolescents’ sleep and symptoms of
anxiety and depression. The participants (N = 82; 24 %
male) were studied at three time points over approximately
1 year: spring of their senior year of high school (T1), fall
of their first year of college (T2), and spring of their first
year of college (T3). Sleep minutes, sleep efficiency, wake
time variability and anxiety increased over the transition to
college. Subjective reports of sleep problems decreased.
Cross-lagged panel models indicated significant relation-
ships between subjective sleep quality and anxiety symp-
toms over time where subjective sleep problems at T1 were
associated with anxiety at T2, and anxiety at T2 was
associated with subjective sleep problems at T3. In con-
trast, greater depressive symptoms at T1 preceded increa-
ses in subjective sleep problems, sleep latency and sleep
start time variability at T2. Importantly, there were con-
current associations between symptoms of anxiety or
depression at T2 and sleep efficiency, sleep start time
variability, and subjective sleep problems. These findings
suggest that, overall, sleep quantity and quality improved
over the transition to college, although the overall amounts
of sleep were still below developmental recommendations.
However, for some youth, the first semester of college may
be a sensitive period for both sleep problems and symp-
toms of anxiety. In contrast, depressive symptoms were
stable across time but were associated with worsening
sleep problems in the first semester of college. Implications
for future prevention and intervention programs should
include strategies to help youth cope effectively with
adjustment like increased sleep variability and symptoms
of anxiety associated with the transition to college.
Keywords Sleep � Actigraphy � Anxiety symptoms � Depressive symptoms � Adolescence � Transition to college
Introduction
An accumulation of research has documented that sleep
during the adolescent years is shortened, often leading to
daytime dysfunction and health problems such as anxiety,
depressive and somatic symptoms (National Sleep Foun-
dation 2006; Oginska and Pokorski 2006; Roberts et al.
2001). Both biological and psychosocial factors are asso-
ciated with changes in sleep patterns during adolescence
(Carskadon 2011). For example, researchers have identified
changes in adolescents’ circadian rhythm and sleep archi-
tecture, as well as environmental changes such as earlier
school start times, extracurricular activities, and after
school jobs (Carskadon et al. 1998; Dahl and Lewin 2002).
Sleep problems may continue or even become worse for
youth who enter the college environment. Across several
studies, at least 60 % of college students were character-
ized as poor quality sleepers, reported restricted sleep on
weeknights, and frequent ‘‘all-nighters’’ (Lund et al. 2010;
L. D. Doane (&) � J. L. Gress-Smith � R. S. Breitenstein Department of Psychology, Arizona State University,
P.O. Box 871104, Tempe, AZ 85287-1104, USA
e-mail: [email protected]
123
J Youth Adolescence (2015) 44:389–404
DOI 10.1007/s10964-014-0150-7
Pilcher et al. 1997). Social schedules and expectations may
also interact with college students’ biological clocks,
leading to sleep disturbances; this interaction has been
termed ‘‘social jetlag’’ (Wittmann et al. 2006). Further,
first-year college students are more likely to report poor
sleep than second-year students (Suen et al. 2008). Lon-
gitudinal studies indicate that poor sleep quality, quantity
and variability have direct and indirect associations with
college students’ academic performance (Lau et al. 2013;
Orzech et al. 2011), psychosocial functioning (Tavernier
and Willoughby 2014) and alcohol use (Phinney and Haas
2003).
From a developmental perspective, the transition from
high school to college is particularly important to examine
given that most youth experience a socio-contextual shift.
This shift to a new context is often coupled with increased
perceptions of stress, changes in family and peer relation-
ships, greater academic demands and increased responsi-
bilities for their own health and decision-making (Kerr
et al. 2004; Larose and Boivin 1998). Developmental
transitions can also be periods of heightened vulnerability
to stress (Compas et al. 1986). Indeed, first-year college
students report high levels of depression and anxiety (Furr
et al. 2001; Pryor et al. 2010), and poor mental health has
been associated with elevated risk of dropping out of col-
lege (Hartley 2012). Studies of college students have found
significant covariation between affective, stressful and
social experiences and self-reported sleep quality (e.g.,
Galambos et al. 2010). Further, during years of increased
stress, college students demonstrated shorter self-reported
sleep durations, more sleep disturbances, and later waking
times (Galambos et al. 2013). Fewer constraints in college
and variable schedules may lead to significant sleep vari-
ability (e.g., Moore et al. 2009) and reduced sleep quality.
These reductions in quality may be correlated with or
predict a range of developmental outcomes, specifically
those related to emotional health and well-being.
In addition, researchers have identified links (sometimes
reciprocal) between subjective sleep problems and inter-
nalizing problems in community samples of adolescents
and young adults (e.g., Jean Louis et al. 1998; Moo-Estrella
et al. 2005). Longitudinal studies examining associations
between sleep and internalizing problems have shown that
the magnitude of the associations changes over time and
increases from childhood into adolescence (Gregory and
O’Connor 2002; Johnson et al. 2000; Kelly and El-Sheikh
2014). Much prior research has been limited by the reliance
on single subjective or self-report measures of sleep, and
many researchers have solely examined depression or
anxiety, which are highly comorbid in adolescents who
attend college (Eisenberg et al. 2007; Nyer et al. 2013).
Further, little is known about the direction of effects
between sleep and anxiety/depression during adolescence,
particularly across a substantial socio-cultural shift like the
transition to college. In an attempt to address these limi-
tations, the current study examined changes in sleep across
the transition to college and the reciprocal relationships
between adolescent’s sleep and their depressive and anxi-
ety symptoms in a three wave cross-lag design using both
subjective and objective actigraphy-based measures of
sleep quality, quantity and variability.
Sleep, Anxiety, and Depression in Adolescence
and Young Adulthood
Within community and large epidemiological samples of
children and adolescents, research using subjective indi-
cators suggests that there are concurrent associations
between sleep problems, anxiety and depression (e.g.,
Coulombe et al. 2010). However, these associations may
vary by age. Alfano et al. (2009) found that anxiety
symptoms were associated with sleep problems in both
childhood and adolescence, whereas depressive symptoms
were only associated with sleep problems in adolescence.
Evidence from daily diary studies also suggests these
associations interact reciprocally over time. In a diverse
sample of adolescents, Fuligni and Hardway (2006)
showed that stress during the day was associated with
shorter sleep duration, which in turn was associated with
greater anxious and depressive mood the next day.
Studies using subjective reports from college students
typically examine depressive symptoms rather than anxi-
ety; however, the findings are similar to those seen in
adolescent populations. Gress-Smith et al. (2013) reported
high rates of insomnia (i.e., 69.5 % reported at least mild
insomnia severity) and depressive symptoms (i.e., 33.5 %
reported at least mild depressive symptoms) in a large
college student sample. Moo-Estrella et al. (2005) found
that individuals who reported greater sleepiness during the
day reported more depressive symptomatology. Finally, a
recent study demonstrated that female college students who
reported either significant sleepiness during the day or
sleep deprivation (at least 2 h less than recommended
levels) were at greater risk of melancholic symptoms
(Regenstein et al. 2010). In terms of anxiety, one recent
large study of college students found a significant corre-
lation between concurrent self-reported sleep problems and
anxiety symptoms (Orsal et al. 2012). In sum, there is
consistent evidence for concurrent relationships between
self-reported sleep problems, ranging from insomnia to
daytime sleepiness, and symptoms of anxiety and depres-
sion in college students.
Recently, researchers have tested some of the potential
reciprocal relationships between sleep and symptoms of
anxiety and depression (e.g., Kelly and El-Sheikh 2014).
However, most of these studies have been conducted with
390 J Youth Adolescence (2015) 44:389–404
123
children or adults, rather than adolescents. Thus, the
associations among adolescents as they transition to col-
lege remain unclear, and it is possible that these reciprocal
relationships differ for depressive and anxiety symptoms.
Studies using subjective indicators of sleep and sleep
problems are mixed regarding whether poor sleep consis-
tently occurs before anxiety or depressive symptoms, or the
reverse. For example, insomnia preceded impaired psy-
chological functioning during adolescence over the course
of 1 year (Roberts et al. 2002), self-reported sleep prob-
lems at age four predicted depressive and anxiety symp-
toms at age 15 (Gregory and O’Connor 2002), and sleep
problems in childhood predicted depression in pre-adoles-
cence (Gregory et al. 2009). In contrast, a few other studies
have shown the reverse, wherein anxiety or depression
problems predict subsequent insomnia or other sleep
problems (e.g., Johnson et al. 2006). Finally, researchers
have identified bidirectional relationships between sleep
problems, anxiety and depression (e.g., Jansson-Frogmark
and Lindbloom 2008). The most recent study to test the
reciprocal relationships between sleep and anxiety and
depressive symptoms using cross-lag models utilized both
subjective and objective indicators of sleep in a community
sample of children (Kelly and El-Sheikh 2014). The find-
ings suggested differential and complex reciprocal paths
among sleep quality and quantity and anxiety and depres-
sive symptoms from ages 8 to 13. We examined similar
relationships between subjective and objective sleep
quantity, quality and variability later in development as
adolescents navigate the transition to college.
Multi-Method Approach to Measuring Sleep
Recent reviews have suggested that studies of sleep and
associations with adjustment and socioemotional develop-
ment should follow new recommendations to better inform
research and practice (Gregory and Sadeh 2012; Shochat
et al. 2014). The majority of studies have used one type of
assessment (e.g., subjective report, ambulatory assessment
or objective indicators) rather than multiple assessments,
which makes it difficult to understand mechanisms under-
lying associations between sleep and depression and anx-
iety. Researchers have also suggested that subjective sleep
measures may predict different facets of sleep and well-
being than objective sleep measures (Tremaine et al. 2010).
Further, Shochat et al. (2014) argued that developmental
observational studies must be conducted in participants’
naturalistic settings. Following these recommendations, we
examined multiple indicators of sleep in youth’s natural-
istic environments at three measurement periods over
approximately 1 year, using validated subjective reports
and objective indicators of sleep duration, quality and
variability via actigraphy. Thus, we sought to highlight
differential relationships between various indicators of
sleep and anxiety and depressive symptoms over time that
may be important targets for preventive intervention efforts
aimed at improving adjustment for adolescents who tran-
sition to the college environment.
Present Study and Hypotheses
The current study examined cross-lagged relationships
between adolescents’ sleep and symptoms of anxiety and
depression across the transition to college. The first aim of
this study was to identify whether symptoms of anxiety and
depression, sleep quantity, quality or variability changed
over the transition to college. We hypothesized, over the
transition to college (T1–T2), sleep quality (e.g., lower sleep
efficiency, greater sleep latency) would decrease and sleep
variability would increase given less consistent environ-
mental constraints on sleep timing (e.g., school start times,
parental curfew or bedtime). The second aim of this study
was to examine reciprocal relationships between sleep and
symptoms of depression and anxiety separately using cross-
lagged panel models to uncover whether there were differ-
ential associations between sleep and anxiety or depressive
symptoms over a large socio-cultural shift in adolescents’
lives. Based on prior studies (e.g., Gress-Smith et al. 2013;
Kelly and El-Sheikh 2014), we hypothesized that we would
find significant cross-lagged relationships between sub-
jective and objective sleep quality and symptoms of
depression and anxiety. We did not make specific hypotheses
about sleep variability given the lack of prior research on this
construct as it relates to anxiety and depressive symptoms.
Method
Participants
The longitudinal study is comprised of 82 adolescent par-
ticipants from a large Southwestern university. Researchers
recruited participants during the spring of senior year in
high school through college orientation sessions and email.
Inclusion criteria required participants to be accepted to the
university, be seniors in high school, and live within 35
miles of the campus. Assessments occurred at three dif-
ferent time points: Spring of senior year of high school
(T1), fall of their first year of college (T2), and spring of
their first year of college (T3).
Eighty-two adolescents participated in the study at T1
(Mage = 18.05, SD = .41; 24 % male), 76 participated at T2
(93 % retention; 24 % male), and 71 at T3 (87 % retention
from T1; 23 % males). At T2, 17 adolescents (22 %) reported
they were living at home and 59 adolescents (78 %) reported
J Youth Adolescence (2015) 44:389–404 391
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they were living somewhere other than home (e.g., dormitory,
apartment). Participants were racially and ethnically diverse:
54 % European American, 23 % Latino/Hispanic descent,
13 % multiracial, 5 % African American and 5 % Asian
American/Pacific Islander. Youth also came from varying
socioeconomic backgrounds as measured by their parents’
level of education: 11 % reported that their parents completed
some high school, 26.8 % of parents had a high school
diploma, 22 % had some college, 12.2 % received an asso-
ciate’s degree, 18.3 % received a bachelor’s degree and 9.8 %
received a graduate degree. We examined if significant mean
differences on study and demographic variables (e.g., parental
education, race/ethnicity, living at home) were present as a
result of attrition from T1 to T3 using t tests. Adolescents lost
to attrition were more likely to have parents with more edu-
cation, t(80) = -2.58, p \ .05, M = 1.23, SE = .48, and have greater sleep start time variability at T1, t(78) = 2.45,
p \ .05, M = .77, SE = .31.
Procedure
The university Institutional Review Board approved all pro-
cedures and longitudinal sampling of participants. At T1,
participants completed consent forms in the home, and
researchers collected parental consent for participants who
were under age 18. Participants completed a packet of self-
report questionnaires, including measures of subjective sleep
problems, anxiety and depressive symptoms, and wore the
actigraph watch for four weeknights and three weekdays
during a typical week (most commonly Sunday night through
Thursday morning with some variability of weeknights given
participants’ schedules). Study personnel instructed partici-
pants to press a button on the actigraph watch upon waking in
the morning and when they got into bed at night, which served
as secondary indicators of wake times and bedtimes in addi-
tion to accelerometer-based actigraphy data. Participants
received $40 for protocol completion, as well as feedback
regarding their objective sleep throughout the study (gathered
from the actigraph watches). At T2 and T3, study personnel
delivered all protocol materials to the participants’ dorm
rooms at the university or homes (if not living on campus).
Study protocol did not change from T1. The average time
between T1 and T2 assessments was 5.2 months (SD = .96),
and the average time between T2 and T3 was 4.1 months
(SD = .84). Participants received $50 upon protocol com-
pletion at T2 and $70 at T3.
Measures
Objective Sleep
Participants wore an Actiwatch Score (Phillips Respiron-
ics, Inc.) wrist-watch on their non-dominant wrist for all 4
nights and 3 days of the study. The Actiwatch Score con-
tains an accelerometer, which captures movement
throughout the waking day and during sleep periods. Par-
ticipants pressed a button on the watch upon waking in the
morning and when they got into bed at night. Study staff
cross-checked actigraph sleep periods with self-reported
bedtime and wake time as an additional sleep-period
compliance measure. Researchers scored sleep data using
the Phillips Actiware 6 program, which includes a vali-
dated algorithm to measure sleep (Oakley 1997). Activity
counts within each epoch were calculated based on activity
levels during the adjacent 2 min period. 1
The threshold was
set to 40, with a range of 20–80. Utilizing 1-minute epochs
and based on significant movement after at least 10 min of
inactivity, this algorithm calculates a variety of sleep
parameters. Four sleep variables were emphasized in the
current study: total sleep minutes, sleep onset latency, sleep
efficiency and sleep start time variability. Sleep minutes
was the total amount of sleep measured in minutes
(excluding wake periods during the night). Sleep latency
was the amount of time an individual is in bed before
falling asleep. Sleep efficiency represented the proportion
of time an individual is actually asleep when he or she is in
bed. Time in bed was measured by the actiwatch, and
objective time in bed was cross-checked by staff with diary
self- reports of bedtime. Sleep start time and wake time
variability were within-person standard deviation estimates
across the 4 days of assessment. Actigraphy sleep mea-
surement has been validated against concurrent polysom-
nography (Sadeh et al. 1995).
Objective indicators of sleep were validated with diary
self-reports of bed and wake times to identify significant
outliers and equipment malfunction. Days when there was
equipment malfunction or days in which there was signif-
icant discordance between self-reports and objective mea-
surement were not included in analyses (T1: 9 days; T2:
8 days; T3: 20 days). In total at T1, 95.1 % of adolescents
had valid actigraphy data for all 4 nights, 3.7 % had data
for only 3 nights, and 2.4 % had data for 2 or fewer nights
of sleep. For T2, 93.4 % of participants had actigraphy data
for all 4 nights, 5.2 % had data for only 3 nights of sleep,
and 1.4 % had 2 or fewer nights of sleep. At T3, 85.9 % of
adolescents had actigraphy data for all 4 nights, 11.3 % had
data for only 3 nights, and 5.6 % of participants had data
for 2 or fewer nights of sleep. If data consist of fewer than
3 nights of actigraphy, they provide a poor estimation of
regular sleep (Acebo et al. 1999); thus, such data were
excluded for two participants from T1, one participant from
1 The following algorithm was used where A denotes activity counts
and E denotes epoch: A = E - 2(1/25) ? E - 1(1/5) ? E ? E ?
1(1/5) ? E ? 2(1/25).
392 J Youth Adolescence (2015) 44:389–404
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T2, and four participants from T3 who had 2 or fewer
nights of valid data.
Subjective Sleep
Participants completed the Pittsburgh Sleep Quality Index
(PSQI) as a measure of subjective sleep problems (Buysse
et al. 1989). The PSQI is a 19-item self-report measure of
sleep quality and sleep disturbance in the past month. The
PSQI includes seven scales: sleep duration, sleep onset
latency, sleep disturbance, daytime dysfunction, sleep
efficiency, sleep quality, and use of sleep medication
(Buysse et al. 1989). Participants answered open-ended
questions such as, ‘‘During the past month, what time have
you usually gone to bed at night?’’ Participants also
answered four-point Likert scale questions such as, ‘‘Dur-
ing the past month, how often have you had trouble
sleeping because you wake up in the middle of the night or
early morning?’’ Responses were coded from 0 (not during
the past month) to 3 (three or more times in a week). Scores
from scales were summed for an overall global sleep dis-
turbance score. Higher total scores indicate poorer sleep
quality and more sleep disturbance. Scores greater than 5
indicate clinically significant sleep problems (Buysse et al.
1989).
Anxiety Symptoms
Participants completed the 14-item Depression, Anxiety
and Stress Scale- Anxiety Subscale (DASS), which asses-
sed anxiety symptoms in the past week (Lovibond and
Lovibond 1995). An example item includes, ‘‘I was wor-
ried about situations in which I might panic and make a
fool of myself’’ (Lovibond and Lovibond 1995). Partici-
pants responded to items using a four-point Likert scale,
from 0 (Did not apply to me at all) to 3 (Applied to me very
much, or most of the time). Item scores were summed to
create an anxiety score for each participant, with higher
scores reflecting more anxious symptomatology. Cron-
bach’s alphas in this sample were acceptable (T1: .75, T2:
.87, T3: .85). Clinical cut-off scores were also determined
for anxiety (DASS Anxiety subscale) at each time point to
show the proportion of the sample falling in the normal
(scores 0–7), mild (scores 8–9), moderate (scores 10–14),
severe (scores 15–19) and extremely severe anxiety ranges
(scores 20?; Lovibond and Lovibond 1995). In total at T1,
68.3 % of adolescents met the criteria for normal, 9.8 %
for mild, 13.4 % for moderate, 4.9 % for severe, and 2.4 %
for extremely severe depressive symptoms. At T2, 51.2 %
of adolescents met the criteria for normal, 12.2 % for mild,
15.9 % for moderate, 8.5 % for severe, and 4.9 % for
extremely severe depressive symptoms. At T3, 50 % of
adolescents met the criteria for normal, 4.9 % for mild,
20.7 % for moderate, 9.8 % for severe, and 3.7 % for
extremely severe anxiety symptoms.
Depressive Symptoms
Participants completed the 20-item Center for Epidemiol-
ogic Studies Depression Scale (CES-D), which assessed
depressive symptoms over the past week (Radloff 1977).
Participants responded to items using a four-point Likert
scale, from 0 (Rarely or none of the time/Less than once a
week to 3 (Most or all of the time/5–7 days). Positively
phrased items (e.g., ‘‘I felt hopeful about the future’’) were
reverse coded. Items were summed to create a total CES-D
score for each participant (0–60), with higher scores
reflecting more depressive symptoms. Cronbach’s alphas in
this sample were acceptable (T1: .86, T2: .86, T3: .91).
Clinical cut-off scores were determined for subjective
depressive symptoms (CES-D) at each time point to show
the proportion of the sample falling in the normal (scores
0–16), mild (scores 16–22) and moderate to severe symp-
tom ranges (scores 23?; Roberts et al. 1990). In total at T1,
58.5 % of adolescents met criteria for normal, 22 % for
mild, and 17.1 % for moderate to severe depressive
symptoms. At T2, 48.8 % of adolescents met the criteria
for normal, 22 % for mild, and 22 % for moderate to
severe depressive symptoms. At T3, 45.1 % of adolescents
met the criteria for normal, 22 % for mild, and 18.3 % for
moderate to severe depressive symptoms.
Covariates
A number of covariates were included given prior research
demonstrating significant relationships with sleep and/or
symptoms of depression or anxiety: sex (Sadeh et al. 2000),
race/ethnicity (Mezick et al. 2008), parental education
(Buckhalt et al. 2007), and whether the participant was
living at home at the time of the assessment.
Data Analytic Plan
Zero-order correlations among all of the objective sleep
parameters, subjective ratings of sleep, depressive symp-
toms, and anxiety symptoms were examined and tested for
normality (e.g., skewness and kurtosis). Next, we examined
whether sleep changed across the transition to college.
Repeated measures analyses of variance were conducted to
test whether or not there statistically significant changes in
the sleep measures and symptoms of anxiety and depres-
sion across the three time points, and to understand whether
the changes were linear or nonlinear by examining Bon-
feronni-adjusted pairwise comparisons and differences in
means. If there were significant differences, effect sizes
were also noted using Cohen’s d (Cohen 1988) with .2, .5,
J Youth Adolescence (2015) 44:389–404 393
123
and .8 used as benchmarks of a small, medium, and large
effect sizes respectively.
Two-tiered autoregressive path models were tested to
examine the cross-lagged or reciprocal effects of anxiety or
depressive symptoms and the domains of sleep (e.g., sleep
latency, subjective sleep) that demonstrated significant
associations with depressive or anxiety symptoms in cor-
relational analyses. Depressive and anxiety symptoms were
run in separate models and as observable scale scores as
opposed to latent variables, due to sample size limitations
(e.g., n \ 100; Loehlin 2004). These models were tested within a structural equation model (SEM) framework to
investigate the directional influence of psychological
symptoms with later sleep disruption, controlling for prior
sleep behavior, or vice versa during the transition to col-
lege. Cross-lagged models allow for construct variability to
be examined over time, as each time point is regressed on
an earlier time point (e.g., depressive symptoms T2 is
regressed on depressive symptoms T1, etc.). Additionally,
significant paths in cross-lagged models also control for
within-construct stability or the autoregressive effect (Cole
and Maxwell 2003).
These models were analyzed in a four step sequence as
outlined by Jonge et al. (2001) to help determine the mech-
anisms of directional influence. The first step in this sequence
used a baseline model that included only stability paths for
comparison for the subsequent steps and more complex
models. The second step involved comparing the baseline
model to models that included depressive or anxiety symp-
toms at T1 analyzed as predictors of sleep variables at T2,
and then sleep variables at T2 predicted affective symptoms
at T3. The third step compared the baseline model to a model
that included paths examining sleep variables at T1 as pre-
dictors of depressive or anxiety symptoms at T2. Depressive
or anxiety symptoms at T2 were then regressed on sleep
parameters at T3. Finally, the baseline model was compared
to a full model including both sets of cross-lagged effects. All
model comparisons were conducted using v2 tests. Final models were determined to be the best fit to the data based on
Chi-squared model comparison tests, and if there was an
improvement in model fit, as determined by v2, standardized root mean square residual (SRMR), root mean square error of
approximation (RMSEA), and comparative fit index (CFI;
Hu and Bentler 1999). The residual variances among the
exogenous variables were allowed to correlate in these
models. Paths to examine the concurrent associations
between depressive or anxiety symptoms and sleep measures
at each time point were also specified (see Fig. 1 as an
example). Models were analyzed in MPlus 6.0 (Muthén and
Muthén 2012) and accounted for missing data with full
information maximum likelihood (FIML), which is consid-
ered superior compared to pairwise deletion, listwise
deletion, and similar response pattern imputation in SEM
(Enders and Bandalos 2001).
Results
Comparison of Means Across the Transition to College
and Descriptive Results
Repeated measures analyses of variance indicated several
significant changes over time for anxiety symptoms, self-
reported sleep problems, sleep efficiency, sleep minutes
and wake time variability (see Table 1). Additional pair-
wise comparisons of means indicated significant differ-
ences in means from T1 (spring of senior year of high
school) to T2 (fall first year of college; and/or T3, spring of
first year of college), but no significant differences in
means from T2 to T3. Specifically, anxiety symptoms
increased from T1 to T2. Wake time variability increased
from T1 to T3. In contrast, many of the sleep indicators
improved from T1 to T2. Subjective sleep problems
decreased from T1 to T2. Sleep efficiency and sleep min-
utes significantly increased from T1 to T2. All effect sizes
were within the small to medium range. Importantly, while
there were significant differences in means across time
points, there were no significant linear trends. Preliminary
analyses also indicated many of the sleep parameters were
positively related to depressive or anxiety symptoms, both
concurrently and prospectively, with the exception of sleep
efficiency (Table 2).
Based on the significant correlations with depressive
and/or anxiety symptoms, subjective sleep problems, sleep
latency, sleep start variability, and sleep efficiency were
selected as exogenous variables in the cross-lag models (r’s
ranging from .27 to .78; all p’s \ .05). Covariates were included on paths that had a significant effect, which were
then included in v2 model comparisons to ensure the inclusion of covariates enhanced model fit. In general, very
few covariates were indicated based on the zero-order
correlations, with the exception of the subjective sleep
problems model. This process resulted in different covar-
iates in each set of models models, accounting for the
varying degrees of freedom reported below.
Cross-Lagged Analyses of Longitudinal Relationships
Sleep Latency
The first model tested the reciprocal effects of sleep latency
and anxiety symptoms across the transition to college (see
Fig. 1). The baseline model with the stability paths of
394 J Youth Adolescence (2015) 44:389–404
123
Table 1 Repeated measures ANOVA and comparison of means across time
Variable Time 1 Time 2 Time 3 F T1–T2 Effect
size (d)
T1–T3 Effect
size (d) Mean SD Mean SD Mean SD
Depressive symptoms 14.53 8.63 15.78 9.12 16.03 10.70 1.12
Anxiety symptoms 5.87a,b 4.66 7.48a 6.86 8.17b 7.69 5.63** .27 .36
Subjective sleep problems 7.85a,b 3.20 5.86a 2.95 5.93b 3.45 20.12*** .65 .58
Sleep start variability .84 .99 .97 1.01 1.00 .93 .68
Sleep latency 11.60 9.68 9.53 7.84 8.71 6.82 1.99
Sleep efficiency 78.95a, b 12.96 83.90a 10.64 83.40b 10.80 11.21*** .42 .37
Sleep minutes (h) 5.95a,b 1.40 6.27a 1.27 6.38b 1.21 4.33* .24 .33
Wake time variability 0.75a 0.61 1.03 1.20 1.14a 0.70 7.35*** .59
T1 time 1, spring of senior year of high school, T2 time 2, fall of first year of college, T3 time 3, spring of first year of college. Means in a row
sharing a subscript are significantly different from each other. There were only significant differences from T1 to T2 and from T1 to T3 so effect
sizes are only presented for those comparisons
* p \ .05; ** p \ .01; *** p B .001
Table 2 Correlations among study variables
Variables 1 2 3 4 5 6 7 8 9 10 11 12
1. Depressive symptoms
T1
–
2. Anxiety symptoms T1 .62** –
3. Sleep problems T1 .35** .11 –
4. Sleep start variability
T1
.16 .07 .27* –
5. Sleep latency T1 -.01 -.01 .06 -.22 –
6. Sleep efficiency T1 -.03 -.13 -.06 .10 -.15 –
7. Sleep duration T1 -.07 .03 -.16 .05 -.01 .57** –
8. Wake time variability
T1
-.01 -.02 -.16 .37** -.14 .01 .02 –
9. Depressive symptoms
T2
.63** .60** .22 -.13 -.03 -.20 -.04 .007 –
10. Anxiety symptoms T2 .56** .63** .27* -.09 .14 -.10 -.05 -.01 .75** –
11. Sleep problems T2 .33** .15 .48* -.03 .03 -.04 -.08 .09 .42** .40** –
12. Sleep start variability
T2
.22 .18 .19 .12 -.10 -.08 -.03 .18 .33** .37** .07 –
13. Sleep latency T2 .21 .02 .46** .03 .30* .08 .07 -.17 .02 .14 .23* -.03
14. Sleep efficiency T2 -.18 -.18 -.06 .04 -.17 .38** .23 .10 -.11 -.16 .20 .05
15. Sleep duration T2 -.05 .09 -.15 -.22 .29* -.04 .26* -.26* .07 -.09 -.03 -.11
16. Wake time variability
T2
.13 -.03 .31** -.02 -.11 -.09 -.16 -.01 .08 .15 -.01 .57**
17. Depressive symptoms
T3
.39** .43** .29* -.17 .17 -.02 .12 -.02 .53** .54** .33** .19
18. Anxiety symptoms T3 .49** .51** .28* -.18 .23 -.02 .10 -.12 .55** .78** .35** .27*
19. Sleep problems T3 .28* .04 .46* .16 -.02 .03 .07 .25* .36** .43** .63** .18
20. Sleep start variability
T3
-.06 -.17 -.03 .05 -.06 -.04 .03 .02 .03 -.13 -.11 -.08
21. Sleep latency T3 .15 .13 .28* .32** .08 .25** .24 .01 -.11 .11 .16 -.01
22. Sleep efficiency T3 -.01 -.03 -.29* -.22 -.18 .41** .33** -.12 -.13 -.27* -.07 .05
23. Sleep duration T3 .09 .09 -.35** -.10 .24 .09 .25* .02 -.10 .002 -.24 -.17
24. Wake time variability
T3
-.01 -.08 -.02 -.16 -.04 .04 .05 -.08 -.003 .12 -.06 .05
J Youth Adolescence (2015) 44:389–404 395
123
anxiety symptoms and sleep latency was the only good
fit to the data v2 (8) = 7.32, p [ .05; CFI = 1.00; RMSEA = .00; SRMR = .06. All other models with
cross-lagged paths did not provide a superior fit to the data.
Within the stability model, only the autoregressive paths
across anxiety and sleep latency were significant (see
Fig. 1).
Upon examining sleep latency and depressive symp-
toms, the depressive symptoms led model was the best fit to
the data v2 (6) = 7.35, p [ .05; CFI = .99; RMSEA = .05; SRMR = .04. The constructs accounted for 14–44 %
of the variance, with depressive symptoms accounting for
more variance than sleep latency at all of the time points.
The direct paths examining depressive symptoms and sleep
latency were significant across time. There was only one
significant prospective effect, with depressive symptoms at
T1 predicting increased sleep latency at T2 (b = .24, p \ .05). The concurrent, and positive, association between
depressive symptoms and latency at T3 was also significant
(b = .26, p \ .05), but no other concurrent correlations were significant.
Sleep Start Variability
The second set of models included anxiety symptoms and
sleep start variability. The anxiety led model was also the
best fit to the data v2 (6) = 3.48, p [ .05; CFI = 1.00; RMSEA = .00; SRMR = .05. The constructs accounted
for 1 to 73 % of the variance, with anxiety accounting for
more than sleep start variability. Anxiety symptoms were
significantly stable and predictive over time; however,
sleep start variability was not. The two cross-over paths
were marginally significant. The path between anxiety at
T1 and start variability at T2 was marginally significant
(b = .22, p = .06). In turn, sleep start variability at T2 and increased anxiety symptoms at T3 was also marginally
Table 2 continued
Variables 13 14 15 16 17 18 19 20 21 22 23
1. Depressive symptoms T1
2. Anxiety symptoms T1
3. Sleep problems T1
4. Sleep start variability T1
5. Sleep latency T1
6. Sleep efficiency T1
7. Sleep duration T1
8. Wake time variability T1
9. Depressive symptoms T2
10. Anxiety symptoms T2
11. Sleep problems T2
12. Sleep start variability T2
13. Sleep latency T2 –
14. Sleep efficiency T2 -.08 –
15. Sleep duration T2 -.01 .29* –
16. Wake time variability T2 -.01 -.15 -.18 –
17. Depressive symptoms T3 .15 -.19 -.02 -.11 –
18. Anxiety symptoms T3 .32** -.22 -.04 -.06 .67** –
19. Sleep problems T3 .22 .01 -.25* -.12 .45** .42** –
20. Sleep start variability T3 -.17 -.05 -.07 .06 -.02 -.07 .16 –
21. Sleep latency T3 .45** .05 -.14 -.01 .14 .15 .26* .05 –
22. Sleep efficiency T3 -.06 .53** .28* -.01 -.15 -.17 -.27* -.18 -.15 –
23. Sleep duration T3 .03 .08 .48** -.11 -.10 -.02 .20 -.40 .04 .16
24. Wake time variability T3 -.003 -.13 -.04 .18 -.07 .17 .09 .03 -.04 -.18 .08
T1 time 1, spring of senior year of high school, T2 time 2, fall first year of college, T3 time 3, spring first year of college
* p \ .05; ** p \ .01
396 J Youth Adolescence (2015) 44:389–404
123
Anxiety Symptoms T2Anxiety Symptoms T1 Anxiety Symptoms T3
Sleep Start Variability T1
Sleep Start Variability T2
Sleep Start Variability T3
.68*** (.06)
.14 + (.08)
.79*** (.05)
.34***(.10).22 + (.12)
Depressive Symptoms T2
Depressive Symptoms T1
Depressive Symptoms T3
Sleep Start Variability T1
Sleep Start Variability T2
Sleep Start Variability T3
.66*** (.07) .57*** (.09)
.28**(.11)
.25*(.11)
Fig. 2 Sleep start variability cross-lag model with depressive symp- toms and anxiety symptoms. Standardized coefficients are provided.
For readability, non-significant paths are dashed grey, marginally
significant paths are dashed black, significant paths are solid black.
T1, spring of senior year of high school; T2, fall of first year of
college; T3, spring of first year of college. ?
p [ .05 and \ .10; *p \ .05; **p B 01; ***p B .001
Anxiety Symptoms T2Anxiety Symptoms T1 Anxiety Symptoms T3
Sleep Onset Latency T1 Sleep Onset Latency T2 Sleep Onset Latency T3
.68*** (.06) .83*** (.04)
.29**(.10) .45**(.11)
Depressive Symptoms T2Depressive Symptoms T1 Depressive Symptoms T3
Sleep Onset Latency T1 Sleep Onset Latency T2 Sleep Onset Latency T3
.66*** (.07) .61*** (.08)
.28**(.11)
.24* (.11)
.45***(.10)
.26 *(.12)
Fig. 1 Sleep onset latency cross-lag model with depressive symp- toms and anxiety symptoms. Standardized coefficients are provided.
For readability, non-significant paths are dashed grey, marginally
significant paths are dashed black, significant paths are solid black.
T1, spring of senior year of high school; T2, fall of first year of
college; T3, spring of first year of college. *p \ .05; **p \ .01; *** p B .001
J Youth Adolescence (2015) 44:389–404 397
123
significant (b = .14, p = .07). There was also a significant concurrent association between anxiety symptoms and
sleep start variability at T2 (b = .34, p = .001), such that increased anxiety was associated with increased sleep start
variability.
In regards to depressive symptoms and sleep start vari-
ability, the depressive symptoms led model was the best
fit to the data v2 (6) = 3.98, p [ .05; CFI = 1.00; RMSEA = .00; SRMR = .04 (see Fig. 2). The amount of
variance accounted for by the constructs ranged from 1 to
44 %, with depressive symptoms accounting for more vari-
ance than sleep start time variability. Only depressive
symptoms showed significant stability across time. One
crossover effect was significant with depressive symptoms at
T1 predicting increased sleep start variability at T2 (b = .25, p \ .05). The concurrent relationship at T2 was significant (b = .28, p = .01), with higher depressive symptoms being significantly associated with increased sleep start variability.
Sleep Efficiency
The third, and final set of models with objective sleep data,
examined the cross-lagged effects between sleep efficiency
and symptoms of anxiety and depression. In both cases, the
stability models including anxiety or depressive symptoms
and sleep efficiency were the best fits of the data v2 (8) = 11.77, p [ .05; CFI = .99; RMSEA = .08; SRMR = .03, and v2 (8) = 11.11, p [ .05; CFI = .99; RMSEA = .07; SRMR = .05, respectively. Thus, no specific cross-lagged
effects were interpreted. The autoregressive effects across all
time points of sleep efficiency, anxiety symptoms, and
depressive symptoms were significant. There was one con-
current, positive, correlation between depressive symptoms
and sleep efficiency at T2 (b = .24, p \ .05).
Subjective Sleep Problems
The final set of models tested the reciprocal effects of
subjective sleep problems, anxiety, and depressive symp-
toms (see Fig. 3). For anxiety symptoms, the full model
with both cross-lagged effects was the best fit to the data v2
(9) = 12.29, p [ .05; CFI = .98; RMSEA = .07; SRMR = .05. The variance accounted for by the constructs
ranged from 39 to 71 % of the variance, with anxiety
accounting for more variance than subjective sleep prob-
lems. Anxiety symptoms and subjective sleep problems
were significant and stable across all three time points.
There were two cross-lagged effects. Subjective sleep
problems at T1 predicted increased anxiety symptoms at
T2 (b = .29, p = .001). There was also a significant path
Anxiety Symptoms T2Anxiety Symptoms T1 Anxiety Symptoms T3
Subjective Sleep Problems T1
Subjective Sleep Problems T2
Subjective Sleep Problems T3
.65*** (.06) .82*** (.05)
.30**(.11)
.29***(.08)
.58*** (.08)
.24*(.29)
Depressive Symptoms T2Depressive Symptoms T1 Depressive Symptoms T3
Subjective Sleep Problems T1
Subjective Sleep Problems T2
Subjective Sleep Problems T3
.66*** (.07) .49*** (.10)
.28*(.11)
.48*** (.10)
.26** (.09)
.67*** (.07)
.38*** (.10)
.32 **(.11)
.57*** (.09)
Fig. 3 Subjective sleep problems cross-lag model with depressive symptoms and anxiety symptoms. Standardized coefficients are
provided. For readability, non-significant paths are dashed grey,
marginally significant paths are dashed black, significant paths are
solid black. T1, spring of senior year of high school; T2, fall of first
year of college; T3, spring of first year of college. *p \ .05; **p \ .01; ***p B .001
398 J Youth Adolescence (2015) 44:389–404
123
from anxiety at T2 predicting increased subjective sleep
problems at T3 (b = .24, p \ .05). Last, there was one significant concurrent relationship between increased anx-
iety and subjective sleep problems at T2 (b = .30, p \ .01).
When examining depressive symptoms and subjective
sleep problems, the depressive symptoms led model was the
best fit to the data and had adequate fit indices v2 (6) = 9.03, p [ .05; CFI = .98; RMSEA = .08; SRMR = .08. The constructs accounted for 35–45 % of the variance, with
depressive symptoms and subjective sleep problems
accounting for similar amounts of variance. Depressive
symptoms and subjective sleep problems were significant
and stable across all three time points. There was one pre-
dictive effect, such that depressive symptoms at T1 predicted
increased subject sleep complaints at T2 (b = .26, p \ .01). There were also positive and significant concurrent associ-
ation between depressive symptoms and subjective sleep
problems at all three time points (all p’s B .01, see Fig. 3).
Discussion
Researchers have accumulated a wealth of evidence sug-
gesting sleep is reduced in adolescence (National Sleep
Foundation 2006; Roberts et al. 2001), and that sleep
problems may continue for youth who enter college (e.g.,
Lund et al. 2010). These sleep problems have been linked
with a variety of negative physical and mental health
outcomes, including obesity, risk for suicide, anxiety, and
depression (Alfano et al. 2009; Gupta et al. 2002; Liu
2004). Specifically, studies have demonstrated longitudinal
associations (sometimes reciprocal) between sleep prob-
lems and symptoms of depression and anxiety in commu-
nity samples of adolescents and young adults (e.g., Johnson
et al. 2006; Roberts et al. 2002). Most prior research,
though, has been limited by subjective self-report mea-
surements of sleep and little is known about the direction of
effects between sleep and anxiety/depression during ado-
lescence, particularly across a substantial socio-cultural
shift like the transition to college. We utilized a multi-
method approach for assessing sleep quantity and quality in
order to establish a better understanding of which indica-
tors of sleep quantity or quality might change over this
developmental transition, and whether those changes were
associated concurrently or longitudinally with changes in
anxiety and depressive symptoms. We also used rigorous
statistical modeling to best understand if reciprocal rela-
tionships existed over time. Several objective and sub-
jective indicators of sleep improved over the transition to
college, while symptoms of anxiety increased. Further, we
found differential associations between sleep and symp-
toms of depression and anxiety over time. Specifically, we
identified longitudinal relationships between subjective
sleep quality and anxiety symptoms over time. In contrast,
higher depressive symptoms before the transition to college
(T1) preceded increases in subjective sleep problems, sleep
latency and start time variability in the first semester of
college (T2). These findings build on research in child and
adolescent populations (e.g., Kelly and El-Sheikh 2014),
and suggest some important targets in the prevention of
stress-related symptoms and disorders over the transition to
college.
Our findings revealed significant improvements in sev-
eral sleep patterns across the transition to college. Across
the whole sample, we found increases in sleep efficiency,
sleep minutes, and subjective sleep quality from pre- to
post-transition but no changes after the transition (from T2
to T3). Although these results were contrary to our
hypotheses, they reflect recent findings from a national
dataset indicating that sleep duration improves from ado-
lescence into young adulthood (Maslowsky and Ozer
2014). It is important to note that the sleep minutes expe-
rienced by our sample at all three measurement occasions
were significantly lower than recommended levels of 9 h a
night for adolescents and 7–8 h a night for adults (National
Sleep Foundation 2011). Further, our study findings
regarding increases in sleep efficiency and decreases in
sleep latency may reflect compensatory sleep mechanisms:
when either sleep duration or sleep quality decreases,
individuals typically adapt by experiencing improvements
in other components of sleep (Sadeh et al. 2003). In the
current sample, adolescents perceived their sleep to be of
higher quality as they transitioned into college, and even
though sleep duration improved across the transition, val-
ues were still below recommended levels for this age
group.
Wake time variability increased from pre- to post-tran-
sition, likely due to varying external demands like class
times or work schedules or increased autonomy and deci-
sion-making about sleep timing. Our findings partially
support recent studies by researchers who demonstrated
that particular subgroups of youth had high sleep vari-
ability during the first semester of college (Ari and Shul-
man 2012). Although we did not collect objective
indicators of weekend sleep, it is possible that many youth
in our study were experiencing ‘‘catch up’’ sleep on
weekends. This could have resulted in an overall percep-
tion that their sleep was more positive, even when their
weekday durations were shorter than recommended levels.
The variability in timing and overall low level of duration
indicates that many youth were experiencing what has been
termed ‘‘social jetlag’’ (Wittmann et al. 2006), which has
been linked with poor academic performance (Haraszti
et al. 2014) and poor physical and psychological well-being
in morning chronotype college students (Lau et al. 2013).
J Youth Adolescence (2015) 44:389–404 399
123
Importantly, our study was able to examine sleep patterns
both pre- and post-transition to identify whether poor
sleeping habits were established prior to college entry and
whether they continued to improve over time or only
improved in the first semester of college. Our descriptive
findings about sleep specifically indicate that efforts aimed
at improving length of sleep duration or quality are likely
best aimed at adolescents before they enter the college
environment, whereas wake time variability may be a
problem established during the first year of college.
Studies examining reciprocal relationships among
depression and sleep have typically been conducted using
subjective indicators of sleep and have found support for
sleep problems preceding depression in childhood and ado-
lescence (e.g., Gregory et al. 2009). Although some studies
have found support for bidirectional relationships (Cousins
et al. 2011; Kelly and El-Sheikh 2014), none to our knowl-
edge have been conducted over a substantial socio-cultural
shift such as the transition to college. Interestingly, we
consistently found that pre-transition depressive symptoms
were associated with subsequent post-transition subjective
and objective sleep problems (but not the reverse), and post-
transition depressive symptoms were concurrently associ-
ated with greater sleep problems (increased variability and
latency, decreased subjective quality). Our findings com-
plement available research on the existence of concurrent
self-reported sleep problems and depressive symptoms in
adolescents and college students (e.g., Gress-Smith et al.
2013, Orzech et al. 2011; Regenstein et al. 2010). It is also
notable that there were not significant increases in depressive
symptoms across the transition to college. Indeed, results
indicated that depressive symptoms before the transition
may be a risk factor for poor sleep quality in college. Their
co-occurrence may be a result of worsening symptoms of
depression over a stressful transition.
Given other research suggesting the bidirectional inter-
play between daily experiences of stress, anxiety symp-
toms, depressive symptoms and sleep (e.g., Doane and
Thurston 2014, Fuligni and Hardway 2006; Galambos et al.
2010), it is possible that students who were depressed were
less likely to utilize adaptive coping strategies and thus
may have experienced reduced sleep quality (e.g., greater
latency) or greater sleep start time variability. Coping or
emotional regulation strategies were not examined in the
present study; however, other studies have shown the
mediating role of emotion regulation between social ties
and sleep problems in college students (Tavernier and
Willoughby 2014), suggesting that these skills may be
integral when adapting to stressful environments. Although
these hypotheses should be tested in larger samples, it
seems that both depressive symptoms and poor sleep
hygiene are likely responsive targets to prevention efforts
for college student adjustment.
Our results also illustrated that anxiety symptoms
increased over the transition to college and were concur-
rently related to both subjective and objective post-transition
sleep problems (e.g., subjective sleep problems, sleep start
time variability). Although some prior research in children
and adolescents has found that sleep problems typically
precede anxiety symptoms and disorders (e.g., Gregory et al.
2005), we did not find this to be the case over the transition to
college. However, poor subjective sleep quality in high
school (T1) was associated with subsequent anxiety in the
first semester of college (T2). Further, post-transition anxiety
symptoms (T2) were associated with concurrent and pro-
spective subjective sleep problems. The nature of these paths
is similar to those identified in children (Kelly and El-Sheikh
2014) and implicate mechanisms that are common across
sleep disturbance and anxiety symptoms.
We did not identify associations among sleep minutes
and symptoms of depression and anxiety, which was
inconsistent with our hypotheses and some previous
research (e.g., Perlman et al. 2006). Some theorists have
argued that sleep quality is a better predictor of adjustment
than quantity (Krystal and Edinger 2008), but most studies
have only examined these differential associations using
subjective reports. A recent study in a nationally repre-
sentative sample found that sleep duration increased from
adolescence into young adulthood (Maslowsky and Ozer
2014), which was hypothesized to reflect fewer early
morning environmental demands (i.e., early high school
start times). Similarly in this sample, youth likely have
more freedom to set their bed and wake times in college
such that sleep duration most likely reflects choices or
preferences (e.g., eveningness) rather than impairments due
to increases in symptoms.
Researchers have hypothesized potential mechanisms
underlying associations among poor sleep and symptoms of
depression and anxiety. Theories involving emotional reg-
ulation (Dahl 1996) and evidence from neuroimaging studies
suggest that the prefrontal cortex (PFC) and amygdala may
play critical roles. For example, greater activation of the PFC
occurred in response to negative emotion and affect fol-
lowing poor sleep (Ochsner et al. 2004; Urry et al. 2006),
suggesting links with emotion regulation (Wang and Sau-
dino 2011). Sleep deprivation studies have illustrated overall
declines in PFC function after insufficient sleep (Drummond
and Brown 2001; Thomas et al. 2000). Further, researchers
have found that amygdala reactivity to fearful stimuli was
associated with greater depressive symptoms in poor sleep-
ers, but not good sleepers, suggesting that sleep modulates
associations between amygdala reactivity and emotion reg-
ulation (Prather et al. 2013). Finally, ruminating thought
processes and emotional distress are correlates of poor sleep
(for review, see Kahn et al. 2013) and symptoms of anxiety
and depression (McLaughlin and Nolen-Hoeksema 2011),
400 J Youth Adolescence (2015) 44:389–404
123
suggesting that they may serve as mediating factors under-
lying longitudinal relationships over the transition to college.
Despite contributions, several limitations should be
considered. These measurements occurred in a small
sample of youth who were planning to attend a 4-year
university close to home and who were disproportionately
female. Further, our sample was unusual in that higher SES
youth were more likely to be lost to attrition. Given the
characteristics of our sample, our findings may not gener-
alize to adolescents who are transitioning to work or
community college. In addition, given the size of our
sample, we were unable to test the associations between
sleep and anxiety symptoms and sleep and depressive
symptoms simultaneously, and were likely underpowered
to detect significant paths with smaller effect sizes. For
example, we identified two marginally significant cross-
lagged paths between anxiety and sleep start variability.
With a larger sample size we may have had the power to
detect paths with small-medium effect sizes like these at a
statistically significant level. Future work should examine
pathways among sleep parameters (e.g., sleep variability),
depressive symptoms and anxiety symptoms concurrently
over a greater number of days in a larger sample of youth.
We examined a specific transition period that is common
for many adolescents. It is possible that other patterns
might emerge over other periods of development, a longer
study period, or during a time of more stability. Finally, we
did not examine other adverse sleep hygiene behaviors
(e.g., alcohol use) that might contribute to sleep problems
and adjustment. Future research should also include indi-
cators of stress-related coping behaviors to understand
potential mechanisms underlying associations between
sleep and symptoms of depression and anxiety.
Conclusion
Collectively, our findings contribute to the literature
examining developmental trajectories of sleep and symp-
toms of depression and anxiety. We highlighted the lon-
gitudinal and reciprocal relationships among these
indicators of adjustment over a period of time typically
characterized by change and uncertainty for many adoles-
cents. Further, our results underscore the importance of
utilizing multiple methods of assessment (e.g., subjective,
actigraphic) to capture dimensions of sleep duration,
quality and variability within participants’ naturalistic
environments. Our findings have direct relevance for high
school and university administrators seeking to promote
well-being in their student populations and by identifying
potential targets to help promote successful adjustment
during the transition to college. Our research may have
implications for future prevention and intervention
programs in both high school and college that include
strategies to help youth cope effectively with adjustment
problems like sleep variability and symptoms of depression
and anxiety.
Acknowledgments The authors thank Michael R. Sladek and Scott Van Lenten for comments on earlier drafts of this manuscript. This
research was conducted with the support of the Institute for Social
Science Research at Arizona State University (LD, Principal
Investigator).
Author contributions LD conceived of the study, participated in its design, led coordination and data collection and drafted the manu-
script; JGS participated in the design of the study, helped draft the
manuscript and performed the statistical analysis; RS participated in
the design and helped draft the manuscript. All authors read and
approved the final manuscript.
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Leah D. Doane Ph.D is an Assistant Professor of Psychology at Arizona State University. She received her doctorate in Human
Development and Social Policy from Northwestern University’s
School of Education and Social Policy. Her major research interests
include adolescent and emerging adult development, particularly with
regard to identifying and understanding psychophysiological mech-
anisms underlying adolescent and young adult everyday stress
experiences in naturalistic settings.
Jenna L. Gress-Smith Ph.D received her doctorate in Clinical Psychology (Health Psychology emphasis) and Master of Arts in
J Youth Adolescence (2015) 44:389–404 403
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Psychology at Arizona State University. Her major research interests
include the physiological processes associated with mental health
outcomes during major life transitions, such as pregnancy, postpartum
adjustment, and emerging adulthood. She is also interested in
resilience theory and how physiological and biological processes,
such as cortisol and sleep, are associated with stress, affect, and well-
being in populations facing health disparities.
Reagan S. Breitenstein is a candidate for Master of Arts in Develop- mental Psychology at Arizona State University. Her major research
interests include understanding relations between adolescent sleep and
mental and physical health outcomes. She is also focused on identifying
genetic and environmental contributions to associations between inter-
personal relationships and middle childhood sleep and physiology.
404 J Youth Adolescence (2015) 44:389–404
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- Multi-method Assessments of Sleep over the Transition to College and the Associations with Depression and Anxiety Symptoms
- Abstract
- Introduction
- Sleep, Anxiety, and Depression in Adolescence and Young Adulthood
- Multi-Method Approach to Measuring Sleep
- Present Study and Hypotheses
- Method
- Participants
- Procedure
- Measures
- Objective Sleep
- Subjective Sleep
- Anxiety Symptoms
- Depressive Symptoms
- Covariates
- Data Analytic Plan
- Results
- Comparison of Means Across the Transition to College and Descriptive Results
- Cross-Lagged Analyses of Longitudinal Relationships
- Sleep Latency
- Sleep Start Variability
- Sleep Efficiency
- Subjective Sleep Problems
- Discussion
- Conclusion
- Acknowledgments
- References