跳至主要内容
临床试验/NCT07590076
NCT07590076尚未招募不适用

Volunteer Facilitated Discharge Assistance and Supports at Home (DASH) for People With Stroke: An Effectiveness-implementation Hybrid Trial.

Bruyère Health Research Institute.6 个研究点 分布在 1 个国家目标入组 840 人开始时间: 2026年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
840
试验地点
6
主要终点
Coping at Time 1 as assessed by Post-Discharge Coping Difficulty Scale (PDCDS)

研究概览

简要总结

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

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • 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)

排除标准

  • 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

研究组 & 干预措施

Group B: Usual care group

No Intervention

Participants will receive the Usual Care + Educational Resources

Group A: DASH group

Experimental

Participants will receive the DASH intervention + Usual Care + Educational Resources

干预措施: Discharge Assistance and Supports at Home (DASH) (Behavioral)

结局指标

主要结局

Coping at Time 1 as assessed by Post-Discharge Coping Difficulty Scale (PDCDS)

时间窗: Measured at 3 months post-hospital discharge

Coping will be assessed using the Post-Discharge Coping Difficulty Scale (PDCDS), a 10-item patient-reported outcome measure evaluating perceived difficulty coping following hospital discharge. Each item is scored on a scale from 0 to 10. Item scores are summed to yield a total score ranging from 0 to 100, with higher scores indicating greater difficulty coping.

次要结局

  • Change in coping as assessed by Post-Discharge Coping Difficulty Scale (PDCDS)(Measured at 3 months and 6 months post-hospital discharge)
  • Change in quality of life as assessed by Stroke-Specific Quality of Life (SS-QOL)(Measured at 3 months and 6 months post-hospital discharge)
  • Change in symptoms of depression as assessed by Patient Health Questionnaire-9 (PHQ-9)(Measured at 3 months and 6 months post-hospital discharge)
  • Change in social isolation and loneliness indicators as assessed by UCLA Loneliness Scale (Version 3)(Measured at 3 months and 6 months post-hospital discharge)

研究者

发起方
Bruyère Health Research Institute.
申办方类型
Other
责任方
Sponsor

研究点 (6)

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