NCT07590076Not yet recruiting
Volunteer Facilitated Discharge Assistance and Supports at Home (DASH) for People With Stroke
Volunteer Facilitated Discharge Assistance and Supports at Home (DASH) for People With Stroke: An Effectiveness-implementation Hybrid Trial.
Source: ClinicalTrials.gov · Last updated 18 May 2026
Brief summary (registry, in English)
The goal of this clinical trial is to learn if a home visit by a trained volunteer can improve stroke recovery after a stroke survivor is discharged home from the hospital. The main questions it aims to answer are: 1. After 3 months of being discharged from the hospital, does this additional volunteer support at home improve coping skills for stroke survivors? 2. Does the effects of the volunteer support last over 3 to 6 months after being discharged home? Researchers will compare between a group who will receive the volunteer support and a group who will not to see if the additional support can improve stroke recovery. Participants will: * Either receive volunteer support over an 8-week time period OR receive no additional volunteer support * Continue with their usual care plan and receive educational resources from the research team during the study * Complete online surveys during study enrollment, at 3 months, and at 6 months after hospital discharge
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 840 (estimated)
- First submitted
- 11 May 2026
- Start date
- Jun 2026
- Primary completion date
- Jan 2028
- Lead sponsor
- Bruyère Health Research Institute.
- Diseases
- Stroke
- NCT number
- NCT07590076
What you commit to
- Study type: Interventional
- Planned participants: 840
- From Jun 2026 to the primary completion date, Jan 2028
- 6 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Discharged to additional hospital inpatient care, nursing home, or other long-term care
- Inability to communicate in English
- Inability to provide informed consent due to cognitive deficits
Who the study is looking for
- Confirmed diagnosis of stroke
- Either undergoing or recently completed in-patient rehabilitation within the last 3 weeks
- Lived at home pre-stroke
- Discharged directly home (to own residence or that of a family member)
- Live in one of the program implementation areas (i.e., Toronto, Ottawa)
Sex: All · Does not accept healthy volunteers
Sites (6)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Bruyère Health Élisabeth-Bruyère Hospital Coordinator of this site? Confirm its status | Ottawa | Canada | Unknown status |
| Toronto Rehabilitation Institute (UHN) Coordinator of this site? Confirm its status | Toronto | Canada | Unknown status |
| Providence Healthcare (Unity Health Toronto) Coordinator of this site? Confirm its status | Toronto | Canada | Unknown status |
| West Park Healthcare Centre (UHN) Coordinator of this site? Confirm its status | Toronto | Canada | Unknown status |
| Sunnybrook Health Sciences Centre Coordinator of this site? Confirm its status | Toronto | Canada | Unknown status |
| Hennick Bridgepoint Hospital Coordinator of this site? Confirm its status | Toronto | Canada | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.