Functional Impact of a Memory Intervention Program

Sponsor
Baycrest (Other)
Overall Status
Completed
CT.gov ID
NCT02087137
Collaborator
(none)
69
1
2
17
4.1

Study Details

Study Description

Brief Summary

Normal aging is associated with decline in some aspects of memory, and this can be a risk factor for reductions in everyday functioning. The Baycrest Memory and Aging Program teaches positive adaptation to age-related memory changes, including strategies for minimizing the everyday impact of normal memory change and positive lifestyle change to maximize brain health. Prior research has shown that the Memory and Aging program is effective in increasing participants' knowledge about memory, use of memory strategies, and confidence in memory function, as well as adoption of healthier lifestyle practices and reduction in intention to use unneeded health care resources.

Although not one of the stated goals of the program, informal feedback from participants suggests that the educational content and skills training in the Memory and Aging Program has led some participants to change behaviours in ways that lead to significant improvements in their everyday functioning. For example, graduating participants often volunteer examples of how they have applied what they have learned to succeed in everyday memory tasks such as learning a new name or keeping track of future plans. Based on this participant feedback, it is hypothesized that the knowledge, skills, and confidence gained by Memory and Aging Program participants may lead to positive behaviour changes that, in turn, lead to improved everyday functioning. The present study will test this hypothesis using a randomized controlled pretest-posttest design.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Memory and Aging Program
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
69 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Functional Impact of a Memory Intervention Program
Study Start Date :
May 1, 2014
Actual Primary Completion Date :
Oct 1, 2015
Actual Study Completion Date :
Oct 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Memory and Aging Program

The Memory and Aging Program intervention consists of five 2-hour sessions conducted over five consecutive weeks. The content of the program includes: (a) the provision of factual information (i.e., about memory, age-related memory changes, lifestyle factors affecting memory, and memory strategies) in an informal lecture format; and (b) memory intervention (i.e., practice and application of several evidence-based memory strategies) in a hands-on interactive format.

Behavioral: Memory and Aging Program

No Intervention: Wait-list Control

Participants randomized to the wait-list control group will receive no intervention following randomization. They will be offered the intervention immediately following completion of the week 14 outcome testing session.

Outcome Measures

Primary Outcome Measures

  1. Change from baseline in healthy lifestyle behaviours as measured by Health Promoting Lifestyle Profile II (Walker, Sechrist, & Pender, 1987) [Baseline, Week 8, week 14]

  2. Change from baseline in memory strategy use as measured by the Memory Strategy Toolbox (modified from Troyer, 2001) [Baseline, Week 8, week 14]

  3. Attainment of individualized goals for (a) lifestyle change, (b) memory strategy use, and (c) functional outcomes of memory strategy use as measured by Goal Attainment Scaling (Gordon, Powell, & Rockwood, 2000; Kiresuk, Smith, & Cardillo, 1994) [Baseline, Week 8, week 14]

Secondary Outcome Measures

  1. Change in positive and negative affect as measured by Positive and Negative Affect Schedule (Watson, Clark, & Tellegen, 1988) [Baseline, Week 8, week 14]

  2. Change in general health status as measured by the RAND 36-Item Short-Form Health Survey (Ware & Sherbourne, 1992). [Baseline, Week 8, week 14]

  3. General Self-Efficacy Scale (Schwarzer & Jerusalem, 1995) [Baseline, Week 8, week 14]

  4. Prospective and Retrospective Memory Questionnaire (Smith, Della Sala, Logie, & Maylor, 2000) [Baseline, Week 8, week 14]

  5. Self-report health status, lifestyle changes, attitudes about aging [Baseline, Week 8, week 14]

Other Outcome Measures

  1. Change in memory knowledge as measured by Memory knowledge quiz (modified from Troyer, 2001). [Baseline, Week 8, week 14]

  2. Change in self-perceived memory as measured by Multifactorial Metamemory Questionnaire (Troyer & Rich, 2002) [Baseline, 8 weeks, 14 weeks]

  3. Change in prospective memory function (Prospective telephone-call task, Troyer, 2001; actual week, Rendell & Craik, 2001) [Baseline, 8 weeks, 14 weeks]

  4. Change in name learning (Name-learning task, based on Troyer, Häfliger, Cadieux, & Craik, 2006) [Baseline, 8 weeks, 14 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age 50-90

  • Available to participate in all testing and intervention sessions (located in Toronto, Canada)

Exclusion Criteria:
  • health conditions with major effects on cognition, including a current or previous history of stroke, brain surgery, or diagnosed neurological disorder

  • dependence in instrumental activities of daily living

  • cognitive impairment, defined as performance below cutoff for cognitive impairment on a standardized cognitive test, the Telephone Interview for Cognitive Status (Brandt, Spencer, & Folstein, 1988).

  • affective impairment, defined as performance below cutoff for depression on standardized depression screen, the Geriatric Depression Scale (Yesavage et al., 1983)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Baycrest Toronto Ontario Canada M6A 2E1

Sponsors and Collaborators

  • Baycrest

Investigators

  • Principal Investigator: Susan Vandermorris, PhD, Baycrest

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Susan Vandermorris, Ph.D., C.Psych., Psychologist, Baycrest
ClinicalTrials.gov Identifier:
NCT02087137
Other Study ID Numbers:
  • 14-21
First Posted:
Mar 14, 2014
Last Update Posted:
Jan 13, 2016
Last Verified:
Jan 1, 2016
Keywords provided by Susan Vandermorris, Ph.D., C.Psych., Psychologist, Baycrest

Study Results

No Results Posted as of Jan 13, 2016