Actively Recruiting
Memory Support System Feasibility Study
Led by Bruyère Health Research Institute. · Updated on 2026-04-01
40
Participants Needed
1
Research Sites
171 weeks
Total Duration
On this page
Sponsors
B
Bruyère Health Research Institute.
Lead Sponsor
O
Ottawa Hospital Research Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to determining the feasibility of providing the Memory Support System (MSS) to individuals with mild cognitive impairment (MCI) and their partners at a clinic in Ontario, Canada. This will involve a) collecting information from patients referred to the a memory clinic and geriatric day hospital about the patient's interest in and the patient's preferred method to administer the MSS; and b) a cost analysis related to implementation of the MSS. The study will also measure efficacy outcomes of the MSS regarding program adherence as well as to self-reported IADLs, self-efficacy for memory, quality of life, mood, anxiety, and caregiver burden among a sample of individuals with MCI and their care partners
CONDITIONS
Official Title
Memory Support System Feasibility Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of single or multi-domain mild cognitive impairment (MCI)
- Clinical Dementia Rating global (CDR) score of 0.5 or less
- Montreal Cognitive Assessment score of 18 or higher
- Available contact with a care partner at least twice weekly
- Absence or stable intake of nootropic(s) for at least 3 months
You will not qualify if you...
- Visual or hearing impairment or history of reading or writing disability sufficient to interfere with MSS training
- Concurrent participation in another related clinical trial
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Bruyère Health Research Institute
Ottawa, Ontario, Canada, K1H 5C8
Actively Recruiting
Research Team
N
Neil Thomas, MD
CONTACT
F
Fjolla Berbatovci
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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