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RECRUITING
NCT05999929
NA

Memory Support System Feasibility Study

Sponsor: Bruyère Health Research Institute.

View on ClinicalTrials.gov

Summary

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

Official title: Implementation of the Memory Support System: A Feasibility Study

Key Details

Gender

All

Age Range

50 Years - Any

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2023-12-17

Completion Date

2027-03-31

Last Updated

2026-04-01

Healthy Volunteers

No

Interventions

BEHAVIORAL

Memory Support System

The MSS is a two-page-per-day, pocket-sized calendar/note-taking system with three sections: (a) events; (b) to do's; and (c) journaling for logging important things to be remembered (e.g., news about family/friends). MSS training consists of ten 1-hour sessions delivered over two or six weeks, starting 7-10 days after baseline assessment.

Locations (1)

Bruyère Health Research Institute

Ottawa, Ontario, Canada