Actively Recruiting

Phase Not Applicable
Age: 50Years +
All Genders
NCT05999929

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

Age: 50Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Bruyère Health Research Institute

Ottawa, Ontario, Canada, K1H 5C8

Actively Recruiting

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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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