Effects of Online Training Aimed at Increasing Participation in Everyday Life During a Pandemic (SCD Online).
Preventing Cognitive and Functional Decline Among Seniors at Risk-Effects of Online Training Aimed at Increasing Participation in Everyday Life During a Pandemic.
1 other identifier
interventional
32
1 country
1
Brief Summary
This study evaluates the efficacy of Real-World Strategy Training (RWST) compared to a psycho-education workshop for improving everyday life performance in older adults with subjective cognitive decline (SCD). Participants will be randomly assigned to receive one of these approaches. Additionally, this study will provide insight into the benefits of the program while people are not able to meet in person during a pandemic.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2020
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2020
CompletedFirst Submitted
Initial submission to the registry
June 17, 2020
CompletedFirst Posted
Study publicly available on registry
June 19, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 31, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2021
CompletedJuly 21, 2021
July 1, 2021
11 months
June 17, 2020
July 19, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Changes in improved performance (measured as total number of untrained goals improved to criterion) on the Canadian Occupational Performance Measure (COPM) immediately post-intervention.
The COPM is a standardized semi-structure interview in which participants identify everyday life difficulties (defined as things they need to or want to do). These issues are converted to goals with performance rated on a 10-point Likert-type scale. Goals considered improved to criterion are those that have a 2 or more points increase on ratings.
Changes from baseline to post-intervention at 10 weeks
Secondary Outcomes (6)
Improved performance on the Canadian Occupational Performance Measure (COPM) measured at three and six months post-intervention.
Three and six months post-intervention
Improved satisfaction with performance on trained and untrained goals identified using the COPM.
10 weeks after baseline (after intervention), 3 months post-intervention, 6 months post-intervention
Changes on Social Support Survey Instrument (MOS-SSS)
Baseline, 10 weeks, 3 months post-intervention, 6 months post-intervention
Changes on DeJong Gierveld Loneliness Scale
Baseline, 10 weeks, 3 months post-intervention, 6 months post-intervention
Changes on Lubben Social Network Scale
Baseline, 10 weeks, 3 months post-intervention, 6 months post-intervention
- +1 more secondary outcomes
Study Arms (2)
Real World Strategy Training
EXPERIMENTALGroup intervention including education and strategy training to manage everyday functional difficulties.
Psychosocial Education
ACTIVE COMPARATORGroup sessions including education on brain health.
Interventions
The key features of the protocol are: i. Participants are actively engaged in selecting their treatment goals. The research clinician will work with the participants to identify five specific, measurable real-world goals using a standardized semi-structured interview, the Canadian Occupational Performance Measure. Three of these will be training goals, two will not be trained but evaluated post-intervention for evidence of generalization and transfer to non-trained tasks; ii. A global problem solving approach is used (Goal- Plan- Do- Check). Participants are guided by the trainer to apply this strategy to their goals.
The active comparator uses an information-based format and is designed to engage participants without providing any specific training techniques or strategies. During weekly sessions, participants will receive factual information on brain structure and function, age-related cognitive changes, and general brain health issues and will spend time doing non-specific cognitive exercises including crossword and Sodoku puzzles. Homework will consist of reading assignments related to the session topics.
Eligibility Criteria
You may qualify if:
- Have access to high speed internet and a computer or mobile device with a webcam
- Have subjective cognitive complaints
- Be fluent in written and spoken English
- Able to self-identify areas of their everyday lives in which they would like to improve.
You may not qualify if:
- Diagnosis of neurological conditions (e.g. dementia, mild cognitive impairment, Parkinson's)
- Presence of severe depression
- Presence of substance abuse
- History of hospitalization for psychiatric reasons
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Baycrestlead
Study Sites (1)
Baycrest Health Sciences
Toronto, Ontario, M6A 2E1, Canada
Study Officials
- PRINCIPAL INVESTIGATOR
Deirdre Dawson, PhD
Rotman Research Institute, Baycrest Health Sciences
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Rotman Research Institute, Baycrest
Study Record Dates
First Submitted
June 17, 2020
First Posted
June 19, 2020
Study Start
May 1, 2020
Primary Completion
March 31, 2021
Study Completion
March 31, 2021
Last Updated
July 21, 2021
Record last verified: 2021-07