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Caregiver-Assisted Strategy Training for Adults Recovering From Stroke

Tests a caregiver-assisted training program for adults after stroke who have trouble with daily activities.

Plain-language title generated from the registry record
Registry title: Feasibility Study of Caregiver-Assist Strategy Training

Key facts

Where
New Taipei City and Taipei, TaiwanSee the 3 sites

Where in Taiwan

  • Taipei Medical University - Shuang Ho Hospital, Ministry of Health and WelfareNew Taipei City, TaiwanTaking people
  • Taipei Medical University HospitalTaipei, TaiwanTaking people
  • Taipei Municipal Wanfang HospitalTaipei, TaiwanTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Taipei Medical University
Trial code
NCT06741475
Record updated
17 February 2025
Original description
The goal of this study is to examine the feasibility of delivering an innovative intervention, caregiver-assisted strategy training (CaST), targeting enhancing activity functions in community-dwelling adults after stroke. The main questions it aims to answer are:Read full original descriptionShow less

Optimizing Activity Performance of Stroke Patients Through Caregiver-Assisted Rehabilitation With Strategy Training: A Feasibility Study

The goal of this study is to examine the feasibility of delivering an innovative intervention, caregiver-assisted strategy training (CaST), targeting enhancing activity functions in community-dwelling adults after stroke. The main questions it aims to answer are:

* Is CaST acceptable to stroke survivors with functional limitations? * Does CaST show positive effects on functional outcomes?

Researchers will compare the CaST program to a control education program to investigate the interventional effect size for the selected stroke participants.

Participants will:

* Receive CAST or an education program 1 to 2 sessions per week until finishing 10 sessions. * Be assessed clinical outcomes at 4 times: pre-intervention, post-intervention, 3-month, and 6-month follow-up. * Be interviewed once after finishing their intervention.

Inclusion: Being willing to provide informed consent; Diagnosis with ischemic and/or hemorrhagic stroke; Modified Rankin Scale (mRS) ranges from 2 to 4; Rehabilitation frequency less than 3 days per week; Having a healthy caregiver.

Exclusion: Major diseases or severe conditions influencing study participation, such as global aphasia, dementia, multiple organ failure, immobilization due to fracture, etc Moderate post-stroke cognitive impairment, with Montreal Cognitive Assessment score <22; Pre-stroke mRS > 1; Undergoing palliative care; Participating in other interventional study concurrently.

ClinicalTrials.gov NCT06741475