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EXploring Patterns of Use and Effects of Adult Day Programs to Improve Trajectories of Continuing CarE

Study acronym: EXPEDITE
StatusNot Yet Recruiting
PhaseNot specified
Started
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Record status
This record was last updated January 24, 2025 (before its estimated June 30, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Notable Start date: Aug 1, 2024 to Mar 1, 2025v2
  2. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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This study seeks to understand the impact of Canada's adult day program on attendees and non-attendees, especially those with dementia and other co-morbidities. A retrospective cohort study will be conducted, including older adults in the community who do or do not attend adult day programs in Alberta, British Columbia, and Manitoba, Canada. The objectives are to (1) compare patterns of day program use (including non-use) by Canadian province (Alberta, British Columbia, Manitoba), and time, (2) compare characteristics of older adults by day program use pattern (including non-use), province, and time, and (3) to examine whether those who are exposed to day programs, compared to a propensity-score matched comparison group of non-exposed older adults in the community, enter long-term care homes at later times (primary outcome), are less likely to have depressive symptoms, physical and cognitive change, and have lower use of primary, acute, and emergency care (secondary outcomes).
Trial Details
NCT Number NCT06440447
Lead Sponsor York University
Collaborators: Carswell Family Foundation, Alzheimer Society of York Region
Conditions
(from sponsor)
Adult Day Programs, Continuing Care, Old Age; Dementia, Family/friend Caregivers
Related terms Alzheimer Disease
Enrollment 500,000 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov