Actively Recruiting

Age: 65Years +
All Genders
ID06496945

Assessing the Impact of Day Programs on Individuals Living with Dementia and Their Family/Friend Caregivers (AIDA-DemCare)

Led by York University · Updated on 2025-01-24

3000

Participants Needed

4

Research Sites

60 weeks

Total Duration

On this page

Sponsors

Y

York University

Lead Sponsor

C

Carswell Family Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of adult day programs on older adults living with dementia and their family or friend caregivers across four Canadian provinces: Alberta, British Columbia, Manitoba, and Ontario. The study aims to understand how day program attendance influences the quality of life and mental health of attendees and caregivers, as well as how different program characteristics and social identities relate to these outcomes. This observational study compares day program users and non-users to explore patterns of care and health outcomes in this population. Participants include older adults aged 65 and above with dementia who either attend an adult day program or receive other community-based continuing care services, along with their primary caregivers. The study gathers comprehensive data through surveys at baseline and follow-ups after one and two years, combined with health administrative records. Day program characteristics such as staffing and programming will be assessed, and participants will be grouped by levels of day program usage. During the study, participants will complete quality of life and mental health surveys at the start and at one- and two-year intervals. Researchers will also track cognitive and physical changes, time to admission into continuing care homes, and healthcare use including emergency visits and hospital stays over up to 2.5 years. This comprehensive approach aims to provide a detailed understanding of how adult day programs support older adults with dementia and their caregivers over time.

CONDITIONS

Brief Title

Assessing the Impact of DAy Programs on Individuals Living with Dementia and Their Family/friend Caregivers

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Older adults aged 65 years or older with a diagnosis of dementia who live in the community
  • Older adults who either attend an adult day program or receive continuing care in the community with an initial assessment completed
  • Primary caregiver who is most involved with and informed about the care of the older adult
Not Eligible

You will not qualify if you...

  • Older adults with or without dementia who do not receive any community-based continuing care service
  • Day program attendees or community care recipients who do not have a diagnosis of dementia
  • Individuals younger than 65 years
  • Secondary caregivers

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Baseline Survey and Assessments

Duration - 3 months (January to March 2025)

Participants complete baseline surveys and assessments including quality of life, mental health, physical and cognitive status for older adults with dementia and their caregivers.

1 baseline visit (in-person or remote)

Long-term Monitoring

Duration - Up to 2 years after baseline

Participants are followed over time through surveys and health data collection to track quality of life, mental health, cognitive and physical decline, healthcare use, and time to admission to continuing care homes.

Surveys at 1 year and 2 years, plus ongoing health data monitoring

Trial Site Locations

Total: 4 locations

1

Edmonton and Calgary Health Zones

Edmonton & Calgary, Alberta, Canada

Not Yet Recruiting

2

Interior Health Region

Multiple, British Columbia, Canada

Not Yet Recruiting

3

Winnipeg Regional Health Authority

Winnipeg, Manitoba, Canada

Not Yet Recruiting

4

York Region

Multiple, Ontario, Canada

Actively Recruiting

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Research Team

M

Matthias Hoben, Dr rer medic

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Frequently Asked Questions

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Published Research Related To This Trial

Assessing the impact of day programs on individuals living with dementia and their family/friend caregivers (AIDA-DemCare): protocol of a prospective cohort study combined with a qualitative evaluation.

Matthias Hoben, Andrea Ubell, Colleen J Maxwell...

https://pubmed.ncbi.nlm.nih.gov/40830776