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Volunteer Facilitated Discharge Assistance and Supports at Home (DASH) for People With Stroke

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Bruyère Health Research Institute.

Status

Begins enrollment this month

Conditions

Stroke
Stroke Rehabilitation
Transitional Care

Treatments

Behavioral: Discharge Assistance and Supports at Home (DASH)

Study type

Interventional

Funder types

Other

Identifiers

NCT07590076
191308
5161

Details and patient eligibility

About

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

Full description

Acute stroke often leads to adult disability in Canada, and about 108,707 Canadians experience a stroke each year. While most people survive stroke (80 percent) and return home, some survivors are left with ongoing challenges that require them to seek help in the community. These challenges can lead to stress for the individual and their caregiver. Research on volunteer-supported home-to-hospital programs has shown positive outcomes. However, despite the growing evidence that supports volunteer engagement in care transitions, we have yet to determine the impact of a complex psychosocial volunteer-delivered care transition intervention for stroke survivors. This study will assess whether a volunteer-delivered transitional care intervention, designed by Bruyère Health Research Institute in partnership with March of Dimes Canada (MODC), for adults discharged home from a stroke rehabilitation unit following an acute stroke can improve coping compared to usual care. MODC will implement the volunteer-support transition program across two Ontario regions for stroke rehabilitation sites. Those allocated to the intervention group will receive an initial visit from the Volunteer Coordinator and then weekly one-on-one visits by a trained volunteer for eight weeks. The volunteer may assist the study participant with instrumental daily living activities and psychosocial and informational support. Those not receiving the intervention will receive educational material at 4- and 8-week time points in addition to their usual care. All study participants will complete validated patient-reported outcome measures at 3- and 6-months post-hospital discharge.

Enrollment

840 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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)

Exclusion criteria

  • 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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

840 participants in 2 patient groups

Group A: DASH group
Experimental group
Description:
Participants will receive the DASH intervention + Usual Care + Educational Resources
Treatment:
Behavioral: Discharge Assistance and Supports at Home (DASH)
Group B: Usual care group
No Intervention group
Description:
Participants will receive the Usual Care + Educational Resources

Trial documents
1

Trial contacts and locations

6

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Central trial contact

Research Coordinator; Michelle LA Nelson, MA, PhD, FAHA, FWSO

Data sourced from clinicaltrials.gov

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