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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

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Bruyère Health Élisabeth-Bruyère Hospital
Coordinator of this site? Confirm its status
OttawaCanadaUnknown status
Toronto Rehabilitation Institute (UHN)
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
Providence Healthcare (Unity Health Toronto)
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
West Park Healthcare Centre (UHN)
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
Sunnybrook Health Sciences Centre
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
Hennick Bridgepoint Hospital
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.