Maintaining Independence in Everyday Life Among Seniors With Subjective Cognitive Complaints

Sponsor
Baycrest (Other)
Overall Status
Completed
CT.gov ID
NCT02655497
Collaborator
Canadian Institutes of Health Research (CIHR) (Other)
16
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2
12
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Study Details

Study Description

Brief Summary

The purpose of this study is to determine the effectiveness of cognitive strategies in improving participation in daily activities within older adults who report subjective cognitive decline.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Cognitive training
  • Behavioral: Psychosocial education
N/A

Detailed Description

The planned project explores the effects of several interventions designed to promote independence in everyday life, with older adults who identify cognitive complaints. Evidence suggests that 25-50% of community dwelling older adults report cognitive difficulties, such as reduced memory or concentration, in the absence of any diagnosed condition. Cognitive skills are crucial to living independently. The investigators plan to examine two approaches in a randomized controlled trial. Based on our successful pilot study, the investigators hypothesize that this training which combines education on healthy lifestyles and problem solving training to address everyday life difficulties, will be effective in maximizing and maintaining independence of older adults.

Study Design

Study Type:
Interventional
Actual Enrollment :
16 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Maintaining Independence in Everyday Life Among Seniors With Subjective Cognitive Complaints
Study Start Date :
Sep 1, 2015
Actual Primary Completion Date :
Aug 1, 2016
Actual Study Completion Date :
Sep 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Cognitive Training

Cognitive training intervention. The intervention includes seven 2-hour group sessions interspersed with four individual 45-minute sessions for a total of 17 hours of intervention over an 8-week period. The experimental group will receive real-world strategy training, a cognitive strategy based approach that trains people to improve their level of independence on meaningful activities of daily life with which they are having difficulty.

Behavioral: Cognitive training

Active Comparator: Psychosocial education

The intervention includes seven 2-hour group sessions interspersed with four individual 45-minute sessions for a total of 17 hours of intervention over an 8-week period. The control group will receive brain-health education.

Behavioral: Psychosocial education

Outcome Measures

Primary Outcome Measures

  1. Change in the Canadian Occupational Performance Measure (COPM) scores [8 weeks after pretest and 3 months after intervention finished]

    The Canadian Occupational Performance Measure (COPM) is the primary outcome measure. All participants will identify five everyday life activities that they need to or want to do using the COPM. The primary outcome will be (a) the number of goals improved by two points.

Eligibility Criteria

Criteria

Ages Eligible for Study:
60 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Community-dwelling older adults aged 60+

  • Fluent in written and spoken English

  • Have subjective cognitive complaints (SCC)

  • Performance within normal limits on a neuropsychological assessment battery

  • Participants must also be able to self-identify specific areas of difficulty in their everyday life that they would like to improve

Exclusion Criteria:
  • Significant neurological or psychiatric history (e.g., multiple sclerosis, psychiatric illness requiring hospitalization)

  • Concurrent depression

  • Anaesthesia in previous 6 months; and substance abuse

Contacts and Locations

Locations

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

Sponsors and Collaborators

  • Baycrest
  • Canadian Institutes of Health Research (CIHR)

Investigators

  • Principal Investigator: Deirdre Dawson, PhD, Baycrest Health Sciences

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. Deirdre Dawson, Senior Scientist, Baycrest
ClinicalTrials.gov Identifier:
NCT02655497
Other Study ID Numbers:
  • REB#15-29
First Posted:
Jan 14, 2016
Last Update Posted:
Nov 18, 2016
Last Verified:
Nov 1, 2016

Study Results

No Results Posted as of Nov 18, 2016