Alzheimer's Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
Group 1 – People living with a major brain/memory disorder and their caregivers:
- People aged 65 or older who are currently being assessed for, or have already been diagnosed with, a serious memory or brain disorder (such as dementia)
- People who live in the CISSS CA health region (a specific regional health authority in Quebec)
- People who live at home, in a retirement home, an intermediate residence, or a family-type care setting
- People who are able to give their own consent to participate in research
- People who agree to allow the research team to access relevant medical records
OR
- People who are a caregiver for someone aged 65 or older living with a serious memory or brain disorder (diagnosed or being assessed), where that person lives in the CISSS CA region
- Caregivers who are able to give their own consent to participate in research
- Caregivers who agree to allow the research team to access the medical records of the person they care for
Group 2 – People attending CoMPAS+ program workshops:
- Health professionals working at a CISSS CA health facility or with a community organisation
- Decision-makers or local managers within the CISSS CA
- Representatives of community services (for example, the Alzheimer's Society or L'APPUI)
Group 3 – People involved in implementing the CoMPAS+ program:
- Health professionals, decision-makers, community service representatives, caregivers, users, workshop facilitators, INESSS professionals, certain research team members (as specified by the trial), and representatives of the Quebec Ministry of Health and Social Services (MSSS), where they are actively involved in putting the CoMPAS+ program into practice
Who may not be able to join:
Group 1 – People living with a memory/brain disorder and their caregivers:
- People under 65 years of age living with a serious memory or brain disorder
- People who are already living in a provincial long-term care facility at the time of recruitment
- People aged 65 or older with a serious memory or brain disorder who cannot give their own consent and who have no caregiver, or whose caregiver is also unable to give consent independently
- People who live outside the CISSS CA health region
- People who do not agree to allow the research team to access their medical records
- Caregivers of people who do not live in the CISSS CA region, are under 65, do not live in an eligible setting (home, retirement home, intermediate residence), or who passed away before the study began
- Caregivers who do not agree to allow the research team to access the medical records of the person they care for
Group 2 – Workshop participants:
- Members of the research team
- Workshop facilitators
- INESSS professionals
- People who are users or partner caregivers (in this group specifically)
- Anyone unable to give their own consent
- Anyone who does not agree to participate
Group 3 – People involved in program implementation:
- Anyone unable to give their own consent
- Anyone who does not agree to participate
- Specific named members of the research team responsible for leading or coordinating this part of the study (Laetitia Bert, Alexander Cornea, Martyne Audet, Clémence Dallaire, André Côté, Félix Pageau, and Catherine Paquet)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Patrick M Archambault, MD, MSc, FRCPC, Laval University
Phone: 4189552552
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Perceived quality of care: The variation in the Physician Enabling Skills Questionnaire (PESQ) scores.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.