Evaluation of the Online Memory & Aging Program and Online Goal Management Training
Aging, Cognitive Decline

About this trial
This is an interventional prevention trial for Aging focused on measuring Healthy aging, executive functions, memory, cognitive training, cognitive intervention, subjective cognitive impairment
Eligibility Criteria
Inclusion Criteria:
- Available to participate in all testing and intervention sessions and access to a computer
- Computer familiarity
- Cognitive complaint/concern/frustration
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 screening measure, the modified Telephone Interview for Cognitive Status (Welsh et al., 1993)
- Affective impairment, defined as performance below cutoff for depression on standardized depression screen, the PHQ 2/9 (Yesavage et al., 1983)
Sites / Locations
- Baycrest Health Sciences
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Experimental
Placebo Comparator
No Intervention
Goal Management Training
Memory & Aging Program
Cambridge Brain Sciences Training
Waitlist
The online version of GMT with a therapist on the back-end monitoring progress and giving feedback throughout the program. Online GMT takes 5-9 weeks (self-paced) to complete 9 modules involving instructional video with interactive content, practice of cognitive strategies through games, and between-module exercises.
The online version of MAP with a therapist moderator on the course discussion pages. MAP takes 5-9 weeks (self-paced) to complete 8 modules involving instructional video with interactive content and practice of memory strategies through various exercises.
This is a commercial and research brain training platform, composed of 7 games that are online adaptations of the standard measures of cognition including working memory and spacial planning.
Participants randomized to this arm will receive no additional information or access to intervention programs until after the follow up testing measures are collected, at which point they will be given access to the intervention of their choosing.