Prospective Memory training

profileKATHERINE BECKS
46525760_researchproposal_2.pdf

Running  head:  RESEARCH  PROPOSAL   1  

 

Research Proposal

Ashleigh Barber

Australian Catholic University

RESEARCH  PROPOSAL   2  

 

Research Proposal

Background

Australia’s Ageing population

At present, Australia’s population is aged, as indicated by the large proportion of older

adult residents, and . This would at least be partially attributable to 100 years of progressively

greater longevities (Howat & Stoneham, 2011). With increasing longevity come several

challenges, for individuals and the health care sector if a number individuals later life is spent in

a state of morbidity. While normal ageing research is not without contention (e.g., about the

underpinning processes in cognitive decline), evidence suggests that the process of normal

ageing appears to involve a decline in such higher order cognitive domains as memory and

information processing REF, which are crucial for living autonomously. While many cognitive

functions are studied in relation to ageing, memory impairment topic of research in older

adulthood, as it comprises multiple cognitive abilities that are each fundamental to in successful

ageing.

The Ageing Process

A normal ageing trajectory human beings represents a latent, time-dependent biological

process (Moody & Sasser, 2014), which albeit it is not pathological, is often characterised by

functional degradation in one or more of physical, sensory, or cognitive abilities (Desjardins,

2012). Many adults experience some age-related cognitive decline (Deary et al., 2009), but the

explicit causal underpinnings of such changes are not robustly understood. The idea of negative

learning was proposed in Mahncke et al.’s (2006) framework, which argues that normal

cognitive changes stem from the combined effect of physical ageing of the cortices and negative

cortical plasticity (i.e., plasticity with negative consequences) (Mahncke, Bronstone, and

Merzenich, 2006).

Briefly outsine the scaffolding idea and negative cortical plasticity

Normal ageing

The maximum upper limit of human lifespan

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The maximum human lifespan is indicated to have a fixed theoretical upper limit of 120 years

(Moody & Sasser, 2014). This upper bound has remained unchanged over time, while the life

expectancy continues to climb.

Promoting optimal development right across the lifespan is a crucial task of developmental psychology

Compression of morbidity hypothesis

Discuss briefly in conjunction: max lifespan, compression of morbidity theory in relation

to health goals and the possibility of human beings, as prevention strategies implemented with

healthy participants fosters the healthy trajectory not the one of morbidity.

“With this concept of limit in mind, compression of morbidity is attractive because

delaying dysfunction would enhance the quality of life, extend life expectancy, and reduce health

care costs (Butler, 1995). A compression-of-morbidity strategy would move life “

Prospective Memory

What is PM (related to RM, what do they encompass?)

Qualitative study: Subjective complaints of particcipants were all PM and some

RM, some really dangerous (community-dwelling older adults, focus group)

Types of PM, cued.

Cortical Plasticity

Evidence of maintaining plasticity throughout lifespan

Negative learning (NCP)

Conclusions of OA misbeliefs (negative learning)

Cognitive training programs

Extant research

Process vs. system designs

Virtual week

Original, P. R.

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Computerised, 2000

VW14, computerised with graded difficulty etc.

Rationale.

Gaps in literature study aims to address

Firstly, relatively few studies include control groups when running studies with cognitive

training (REF), yet it is crucial for being able to make causal inferences about its efficacy.

Secondly, many cognitive training programs are conducted in laboratories, which limits

ecological validity. The design of the study has participants carrying out the tasks in their own

home, without the experimenter there was they play, and the tasks are relevant to functioning

outside of the study. Finally, the adherence of participants to the prescribed training program

and protocol is not a prioritised assessment in training studies.

Current Study

Aims and objectives.

The two primary objectives of this pilot study are to examine both the usability and

assess the preliminary efficacy of 6-weeks of Virtual Week Training 2014 (VWT14) program for

improving prospective memory in healthy Australian older adults. In addition, this study will aim

to analyse changes in subjective reports of memory functioning following 6-weeks of VWT14

program.

VWT14 may represent one way of decelerating normal prospective memory decline in

older adulthood, and as such, it is hypothesised that participants who have completed the training

program will have significant improvement in their prospective memory compared to waitlist

controls, based on Memory for Intentions Screening Test (MIST) (S. Raskin, Buckheit, &

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Sherrod, 2010) performance. It is also hypothesised that when all participants’ posttest data are

pooled, there will significant changes from pre- to posttest performance on the MIST. Finally, it

is hypothesised that subjective reports of memory, based on the Memory Function Questionnaire

Revised (MFQ-R, Gilewski, Zelinski, & Schaie, 1990), will improve from pre- to posttest.

Research Methodology

Participants

A B C D E F

1

Recruitment phase

Prospective participants

2 Make contact (phone/email)

Pre-screen checklist

First assessment

3 Arrange in-person meeting Cog screen; BG

survey; MFQ

4 Participants

assigned to 1/2 conditions

5 Stratified by age, gender,

ACE-III score

6 Pretesting phase

Figure 1: Participant Selection Map (coordinates referred to throughout research methods section)

Study design

This pilot study will be a pre-post-test waitlist control design with both intervention and

comparison groups, so as to pilot the VWT14 program as a means of improving prospective

memory in healthy older adults.

Inclusion/exclusion criteria

Participants will be deemed eligible to partake in the study if they meet all of the criteria

examined during the screening assessment (see Appendix 1).

Measures

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Addenbrooke’s Cognitive Examination III ipad version (ACEmobile) (Newman, Noad,

& Hodges, 2014)

The ACE-III (Mathuranath, Nestor, Berrios, Rakowicz, & Hodges, 2000) is a sensitive

and specific screening tool for general cognitive functioning that takes appropriately 15 minutes

to administer. Nineteen brief subtests comprise the following five dimensions:

attention/orientation, memory, verbal fluency, language, and visuo-spatial, which give five sub-

scores and a total score out of 100. The ACE-III has the capacity to screen for cognitive

impairment and diagnoses, severity and profile of cognitive functioning, and has three Australian

alternate forms for assessing change and comparing scores between groups. ACEmobile, an

electronic version of ACE-III was released for the iPad June 2014, and will be used in this study.

It enhances administration through on-screen instructions, requires no training, reduces error by

scoring automatically, and provides results instantly on-screen and via email to the researcher.

Memory Functioning Questionnaire Revised REF

DESCRIBE TEST

Memory for Intentions Screening Test

The Memory for Intentions Screening Test (MIST) (S. A. Raskin, 2009) is a standardised

tool for measuring prospective memory that takes approximately 30 minutes to administer. The

MIST is reported to have sound psychometric properties (Woods et al., 2008), and be sensitive to

mild impairment (Karantzoulis, Troyer, & Rich, 2009). Participants are provided with an eight-

task set of tests at the outset of a testing session and must remember, throughout the session, to

perform both time-based tasks (‘in exactly x minutes, please alert me that it is break time’) and

event-based tasks (‘when I pass you the blue pen, may you write your name on this sheet of

paper’). Between these PM tasks, participants solve word puzzles, while the researcher observes

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whether the PM tasks are remembered and carried out. Correct and error responses are both

recorded, while variables and error scores can be combined to discern different types of

prospective memory fail

Recruitment

Participants will be sourced from the community (Catholic homes, advertisements in

relevant public locations, word-of-mouth) (A1, 2, 3). Prospective participants will be asked to

contact the researcher via either email or telephone if they are interested in partaking or to find

out more information about the study (B1, B2, 3). The researcher will then screen these

individuals over the phone using a checklist (C2).

Procedure

After eligible participants have been explained the details of the study (C2) and provided

informed consent (D2), they will then be asked to fill in a background information survey, the

Memory Functions Questionnaire (Revised), and be screened on global cognitive ability to

ensure healthy cognitive functioning on the ACE-III (D3). Both the intervention and waitlist

control groups will partake in the VWT14 program, but the immediate intervention group will

commence the 6-week training within the first two weeks of screening (C2), while the waitlist

control will commence their 6-week block around 8 weeks after screening (C2). Given the data

collection and intervention implementation procedures are conducted one participant at a time

rather than altogether in a group, so long as each participant has the appropriate intervals across

screening, pre-test, and post-test for their assigned condition (i.e., immediate intervention or

waitlist control), the waitlist control group does not necessarily have to wait until each

immediate intervention participant has completed the training. Specifically, so long as the

waitlist control has had a 6-week no-contact interval after screening, they can be pre-tested and

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commence training as soon as this 6-week period is over (see Appendix 2 for visual

representation).

The Memory for Intentions Test (MIST) (S. Raskin et al., 2010) will be administered at

two time points for each participant: for the immediate intervention group, first time (pretest)

will be within two weeks following the first meeting between participant and researcher (D2, 3),

and two weeks before the start of the VWT14 program, and second time (posttest) will be within

a week of completing VWT14. For the waitlist control group, their pretest will be 6 weeks after

the first meeting between participant and researcher, and this pretest data will serve as a

comparison point for intervention effects.

Planned Statistical Analyses

The following table outlines how data will be analysed in order to address the aims and

objectives of the study. Due to the nature of a pilot study, the sample size is projected to be

relatively small so until distributions are analysed, it is unknown whether non- or parametric

statistical analyses will be more appropriate, so both are recorded below where necessary.

Table 1

Planned Statistical Analyses

Assessing By: Variables Statistics

Efficacy (a) Of VW at improving PM performance on MIST (control comparison)

Change scores on MIST from pre- to posttest: between groups difference (independent samples)

IV1 group: intervention /control IV2 time point: pretest/ posttest

DV change scores: MIST

Hodges-Lehmann estimate of median differences (estimates the median difference between the groups’ change scores from pre-post test)

Efficacy (b) Of VW at improving PM performance on MIST (pooled comparison)

Scores on MIST, difference from pre- to posttest: within groups difference (paired sample)

IV1 time point: pretest/ posttest

DV scores: MIST

Paired samples t-test or Wilcoxon test (changes in the same participants’ scores across two time points)

Efficacy (c) Of VW at Scores on MFQ IV1 time point: Paired samples t-test or Wilcoxon

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improving subjective perceptions of memory (pooled comparison)

difference from pre- to posttest: within groups difference

pretest/ posttest

DV scores: MFQ test (changes in the same participants’ scores across two time points)

Usability

Of VW training program for older adults

Scores on VWUQ- 14, an adapted version of Lewis’ 1995 questionnaire

DV scores: VWUQ- 14

Descriptive statistics: means, standard deviations, confidence intervals, and % ≥ or ≤ given scoring ranges (i.e., difficulty: easy, med, hard) according to author’s recommended scoring.

Adherence/ compliance

To training program’s prescribed protocol

Rate of sessions completed per week (χ/4) (& total χ/24)

DV rate: of completed sessions out of 4

Descriptive statistics: means, SDs, CIs, n’s and % rates of completed sessions per week, total over program, and % of participants completing all prescribed sessions.

Usability of VWT14

A usability questionnaire (adapted from Lewis, 1995) will be administered via email or

post within one week of each participant’s final VWT14 session (as shown by automated data).

Participants rated how strongly they agreed with each item on a scale of 1(Strongly Disagree) to

7 (Strongly Agree) (see Appendix 3).

Efficacy of VWT14

The primary efficacy outcome measure was performance on the MIST (S. Raskin et al.,

2010) (with control comparison), which aims to objectively measure prospective memory.

The secondary efficacy outcome measures were performance on the MIST (without

control comparison), and responses on the MFQ, a self-report questionnaire that assessed

subjective perceptions of memory functioning.

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Appendix 1: Pre-Screen and Screener Assessments

The following will be asked/assessed during phone calls with prospective participants (pre- screen)

Inclusion Criteria No. Question Y N 1 Are you aged 60 or older 2 Are you retired 3 Do you have a windows computer? 4 Are you comfortable using the computer 5 Are you living independently in the community (i.e. without assistance) 6 Are you comfortable reading and understanding written instructions in English Exclusion Criteria 1 Do you have any neuro/psychiatric disorders or medical conditions that could affect your ability

to play a computer game e.g., epilepsy, blindness

2 Are you involved in another research study at this time The following will be information will be collected during the first face-to-face meeting (Screener)

1. Cognitive functioning using Addenbrooke’s Cognitive Examination V.3 (ACE-III) ipad version

2. Background information using a demographic questionnaire 3. Subjective memory functioning using the MFQ

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Appendix 2:

Data Collection and Intervention Timelines for Two Groups The following two hypothetical timelines are displaying one of two pathways each participant

can take depending on which group they are assigned.

1

2 ! ! 3

4

5

6

7

8

9

10

11

12

13

14

15

16

17

18

19

20

In te

rv en

ti on

w ee

ks o

f as

se ss

m en

t a nd

in te

rv en

ti on

POSTTEST

In te

rv en

ti on

PRETESTPOSTTEST

N o contact

PRETEST

Immediate Intervention

Waitlist Control

SCREENER

PRESCREEN

PARTICIPANT RECRUITMENT

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Appendix 3: Usability Questionnaire

The following questionnaire will be given at the completion of the 6-week training period; it is adapted from Lewis (1995).

Virtual Week 14 Usability Questionnaire (VWUQ-14) For each of the statements below, please circle the rating of your choice.

1 Overall, I am satisfied with the ease of completing the Virtual Week program Strongly AGREE 1 2 3 4 5 6 7

Strongly DISAGREE

2 I am satisfied with the availability of support information (phone calls, messages, instructions/documentation) for completing this task

Strongly AGREE 1 2 3 4 5 6 7

Strongly DISAGREE

3 I am satisfied with how clear/easy to understand instructions/documentation for completing this task was

Strongly AGREE 1 2 3 4 5 6 7

Strongly DISAGREE

4 I enjoyed playing Virtual Week Strongly AGREE 1 2 3 4 5 6 7

Strongly DISAGREE

5 It was easy to learn to play/use Virtual Week Strongly AGREE 1 2 3 4 5 6 7

Strongly DISAGREE

6 I felt comfortable using the Virtual Week program Strongly AGREE 1 2 3 4 5 6 7

Strongly DISAGREE

7 I would recommend Virtual Week to family and friends Strongly AGREE 1 2 3 4 5 6 7

Strongly DISAGREE

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Appendix 4:

Memory Functioning Questionnaire-Revised

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110

Se riousness of Fo rgetting

When you actually forget in these situations, how serious of a problem do you consider the memory to be?

very serious somewhat serious not serious a. names 1 2 3 4 5 6 7 b. faces 1 2 3 4 5 6 7 c. where you put things (e.g., keys) 1 2 3 4 5 6 7 d. directions to places 1 2 3 4 5 6 7 e. beginning to do something and

forgetting what you were doing 1 2 3 4 5 6 7 ______________________________________________________________________________ R et rospective F unctioning

How is your memory compared to the way is was?

much worse same much better a. 1 year ago? 1 2 3 4 5 6 7 b. 5 years ago? 1 2 3 4 5 6 7 c. 10 years ago? 1 2 3 4 5 6 7 d. 20 years ago? 1 2 3 4 5 6 7 e. when you were 18? 1 2 3 4 5 6 7 ______________________________________________________________________________

M nemonics Usage

How often do you use these techniques to remind yourself about things?

always sometimes never a. keep an appointment book 1 2 3 4 5 6 7 b. write yourself reminder notes 1 2 3 4 5 6 7 c. make lists of things to do 1 2 3 4 5 6 7 d. make grocery lists 1 2 3 4 5 6 7 e. plan your daily schedule

in advance 1 2 3 4 5 6 7 f. mental repetition 1 2 3 4 5 6 7 g. associations with other things 1 2 3 4 5 6 7 h. keep things you need to do in a

prominent place where you will notice them 1 2 3 4 5 6 7

______________________________________________________________________________

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References

Deary, I. J., Corley, J., Gow, A. J., Harris, S. E., Houlihan, L. M., Marioni, R. E., . . . Starr, J. M. (2009). Age-associated cognitive decline. British Medical Bulletin, 92(1), 135-152.

Desjardins, R. (2012). Ageing and skills: a review and analysis of skill gain and skill loss over the lifespan and over time.

Gilewski, M. J., Zelinski, E. M., & Schaie, K. W. (1990). The Memory Functioning Questionnaire for assessment of memory complaints in adulthood and old age. Psychology and aging, 5(4), 482.

Howat, P., & Stoneham, M. (2011). Why sustainable population growth is a key to climate change and public health equity. Health Promotion Journal of Australia, 22(4), 34-38.

Karantzoulis, S., Troyer, A. K., & Rich, J. B. (2009). Prospective memory in amnestic mild cognitive impairment. Journal of the International Neuropsychological Society, 15(3), 407-415. doi: 10.1017/S1355617709090596

Lewis, J. R. (1995). IBM computer usability satisfaction questionnaires: Psychometric evaluation and instructions for use. International Journal of Human-Computer Interaction, 7(1), 57- 78.

Mathuranath, P. S., Nestor, P. J., Berrios, G. E., Rakowicz, W., & Hodges, J. R. (2000). A brief cognitive test battery to differentiate Alzheimer's disease and frontotemporal dementia. Neurology, 55(11), 1613-1620.

Moody, H. R., & Sasser, J. R. (2014). Aging: Concepts and Controversies: SAGE Publications. Newman, C., Noad, R., & Hodges, J. (2014). ACEmobile (Version iPad): Neuroscience

Research Australia & Plymouth University. Retrieved from http://www.acemobile.org Raskin, S., Buckheit, C., & Sherrod, C. (2010). Memory for intentions test (MIST). Lutz, FL:

Psychological Assessment Resources. Raskin, S. A. (2009). Memory for intentions screening test: Psychometric properties and clinical

evidence. Brain Impairment, 10(1), 23-33. doi: 10.1375/brim.10.1.23 Woods, S. P., Moran, L. M., Dawson, M. S., Carey, C. L., Grant, I., Atkinson, J. H., . . . Vaida,

F. (2008). Psychometric characteristics of the memory for intentions screening test. Clinical Neuropsychologist, 22(5), 864-878. doi: 10.1080/13854040701595999