Effects of Online Training Aimed at Increasing Participation in Everyday Life During a Pandemic (SCD Online).
Primary Purpose
Subjective Cognitive Decline
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Real World Strategy Training
Brain Education
Sponsored by

About this trial
This is an interventional prevention trial for Subjective Cognitive Decline focused on measuring Age-related cognitive changes
Eligibility Criteria
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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
Sites / Locations
- Baycrest Health Sciences
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Real World Strategy Training
Psychosocial Education
Arm Description
Group intervention including education and strategy training to manage everyday functional difficulties.
Group sessions including education on brain health.
Outcomes
Primary Outcome Measures
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.
Secondary Outcome Measures
Improved performance on the Canadian Occupational Performance Measure (COPM) measured at three and six months post-intervention.
Same as outcome 1. Goals considered improved to criterion are those that have a 2 or more points increase on ratings.
Improved satisfaction with performance on trained and untrained goals identified using the COPM.
Satisfaction with performance is measured on a 10-point Likert type scale using the Canadian Occupational Performance Measure. Goals considered improved to criterion are those that have a 2 or more points increase on ratings.
Changes on Social Support Survey Instrument (MOS-SSS)
This 5-point likert type instrument measures participants' perceived availability of social support in various situations. The lowest possible score is 20 and highest possible is 100. Higher scores indicate better outcome.
Changes on DeJong Gierveld Loneliness Scale
This scale measures loneliness and perceived social isolation. It will be administered to evaluate the impact of the intervention on participants' levels of self-isolation and loneliness. Lowest possible score is 0 and highest score is 6. Lower scores indicate better outcome.
Changes on Lubben Social Network Scale
This 5-point likert type scale measures social isolation by measuring frequency, size, and closeness of contacts of the respondent's social network by assessing the perceived level of support they get from friends and families. Lowest possible score is 0 and highest possible score is 30. Higher scores indicate better outcome.
Change in health-related Quality of Life
Health-related quality of life will be measured using the Short From Health Survey (SF-36). This survey includes the following sub scales (higher scores on each sub-scale indicate better outcome):
Physical functioning with lowest possible score being 10 and highest 30; Role functioning with lowest possible score of 4 and highest 8; Bodily pain with lowest possible score of 2 and highest of 12; General health with lowest possible score of 5 and highest of 25; Vitality with lowest possible score of 4 and highest of 24; Social functioning with lowest possible score of 2 and highest of 10; Role-emotional with lowest possible score of 3 and highest of 6; Mental health with lowest possible score of 5 and highest of 30.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04439500
Brief Title
Effects of Online Training Aimed at Increasing Participation in Everyday Life During a Pandemic (SCD Online).
Official Title
Preventing Cognitive and Functional Decline Among Seniors at Risk-Effects of Online Training Aimed at Increasing Participation in Everyday Life During a Pandemic.
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
May 1, 2020 (Actual)
Primary Completion Date
March 31, 2021 (Actual)
Study Completion Date
March 31, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Baycrest
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
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.
Detailed Description
Evidence suggests that 25-50% of community-dwelling older adults report SCD and that these individuals have an elevated risk for developing Mild Cognitive Impairment and/or dementia. Many of these individuals report difficulties with complex activities of daily living.
RWST aims to reduce these difficulties in everyday life by providing a meta-cognitive training approach that compensates for age-related executive changes. The approach is provided within the context of individually identified everyday-life difficulties.
The psycho-education approach is a Brain-Health Workshop supplemented by intellectually stimulating activities such as doing Sudoku and/or word searches. This approach provides information people may use to inform health behaviour changes.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Subjective Cognitive Decline
Keywords
Age-related cognitive changes
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
32 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Real World Strategy Training
Arm Type
Experimental
Arm Description
Group intervention including education and strategy training to manage everyday functional difficulties.
Arm Title
Psychosocial Education
Arm Type
Active Comparator
Arm Description
Group sessions including education on brain health.
Intervention Type
Behavioral
Intervention Name(s)
Real World Strategy Training
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Brain Education
Intervention Description
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.
Primary Outcome Measure Information:
Title
Changes in improved performance (measured as total number of untrained goals improved to criterion) on the Canadian Occupational Performance Measure (COPM) immediately post-intervention.
Description
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.
Time Frame
Changes from baseline to post-intervention at 10 weeks
Secondary Outcome Measure Information:
Title
Improved performance on the Canadian Occupational Performance Measure (COPM) measured at three and six months post-intervention.
Description
Same as outcome 1. Goals considered improved to criterion are those that have a 2 or more points increase on ratings.
Time Frame
Three and six months post-intervention
Title
Improved satisfaction with performance on trained and untrained goals identified using the COPM.
Description
Satisfaction with performance is measured on a 10-point Likert type scale using the Canadian Occupational Performance Measure. Goals considered improved to criterion are those that have a 2 or more points increase on ratings.
Time Frame
10 weeks after baseline (after intervention), 3 months post-intervention, 6 months post-intervention
Title
Changes on Social Support Survey Instrument (MOS-SSS)
Description
This 5-point likert type instrument measures participants' perceived availability of social support in various situations. The lowest possible score is 20 and highest possible is 100. Higher scores indicate better outcome.
Time Frame
Baseline, 10 weeks, 3 months post-intervention, 6 months post-intervention
Title
Changes on DeJong Gierveld Loneliness Scale
Description
This scale measures loneliness and perceived social isolation. It will be administered to evaluate the impact of the intervention on participants' levels of self-isolation and loneliness. Lowest possible score is 0 and highest score is 6. Lower scores indicate better outcome.
Time Frame
Baseline, 10 weeks, 3 months post-intervention, 6 months post-intervention
Title
Changes on Lubben Social Network Scale
Description
This 5-point likert type scale measures social isolation by measuring frequency, size, and closeness of contacts of the respondent's social network by assessing the perceived level of support they get from friends and families. Lowest possible score is 0 and highest possible score is 30. Higher scores indicate better outcome.
Time Frame
Baseline, 10 weeks, 3 months post-intervention, 6 months post-intervention
Title
Change in health-related Quality of Life
Description
Health-related quality of life will be measured using the Short From Health Survey (SF-36). This survey includes the following sub scales (higher scores on each sub-scale indicate better outcome):
Physical functioning with lowest possible score being 10 and highest 30; Role functioning with lowest possible score of 4 and highest 8; Bodily pain with lowest possible score of 2 and highest of 12; General health with lowest possible score of 5 and highest of 25; Vitality with lowest possible score of 4 and highest of 24; Social functioning with lowest possible score of 2 and highest of 10; Role-emotional with lowest possible score of 3 and highest of 6; Mental health with lowest possible score of 5 and highest of 30.
Time Frame
Baseline, 10 weeks, 3 months post-intervention, 6 months post-intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
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.
Exclusion Criteria:
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Deirdre Dawson, PhD
Organizational Affiliation
Rotman Research Institute, Baycrest Health Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Baycrest Health Sciences
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M6A 2E1
Country
Canada
12. IPD Sharing Statement
Learn more about this trial
Effects of Online Training Aimed at Increasing Participation in Everyday Life During a Pandemic (SCD Online).
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