Home-based rehabilitation program for stroke recovery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the effects of a home-based Graded Repetitive Arm Supplementary Program (GRASP) designed for stroke patients with upper limb impairments. The program is self-administered and focuses on facilitating motor function and recovery while preventing learned nonuse of the affected limb. Participants will engage in group interventions to enhance their rehabilitation experience. The study aims to fill the gap in research regarding the application of GRASP in Taiwan, following its incorporation into Canadian Stroke Best Practice Recommendations.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Age is above 20 years old.
2. Onset of first stroke complicated with hemiplegia or hemiparesis.
3. The affected upper limb remains partially voluntary movements including lifting to chest level and holding for five seconds; slight flexion and extension of wrist and hand.
4. Understanding and complying with two-steps commands.
5. Understanding the content of trial and willing to sign informed consent.

Exclusion Criteria:

1. Complicating with other neurological disease.
2. Having Orthopedic diseases affecting the movements of upper limbs.
3. Having symptoms of pain to affect the movements of upper limbs.
4. Unstable vital sign or medical condition.
5. Participating another rehabilitative or drug research meanwhile.
6. Receiving botulinum toxin injection within three months.

Where it's running

• National Taiwan University Hospital Hsin-Chu Branch
  Hsinchu, Taiwan Recruiting

Study contacts

• Study coordinator: Chia-Yi Lin
• Email: G04812@hch.gov.tw
• Phone: +886-3-5326151#523509

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Deep phenotyping to explore recovery in young adults after stroke

  This project will test whether a detailed health and sample-collection approach (deep phenotyping) is practical and acceptable for people aged 18–55 who have had a stroke.

  Recruiting The Florey Institute of Neuroscience and Mental Health · Heidelberg, Victoria and 1 other locations · NCT07019493

• Stem cell therapy for chronic stroke recovery

  This study is testing whether using a patient's own stem cells can help people with long-term stroke recovery feel better and improve their daily functioning.

  Recruiting Phase 2 Hokkaido University Hospital · Sapporo, Hokkaido · NCT06752720

• AI-based tools to help diagnose, treat and predict stroke outcomes across multiple hospitals

  This study tests AI-powered tools on real-world stroke patients to see if they can improve pre-hospital triage, diagnosis, and outcome prediction while data stay securely within each hospital.

  Recruiting at 2 sites Hospital Universitari Vall d'Hebron Research Institute · Leuven and 6 other locations · NCT07924371

• Web-based therapy using action observation and mirror therapy for arm weakness after stroke

  This trial tests whether a mobile telerehabilitation app delivering action observation therapy (AOT) alone or combined AOT with mirror therapy (AOT-MT) can improve upper limb function in people with subacute stroke.

  Recruiting Chang Gung Memorial Hospital · Taoyuan · NCT07921108

• Remote Ischaemic Conditioning for Fatigue After Stroke 2

  Aat least 12 weeks after stroke, adults with post-stroke fatigue will try a simple hand-arm cuff treatment at home to see if it helps reduce fatigue.

  Recruiting Phase 2 Sheffield Teaching Hospitals NHS Foundation Trust · Sheffield, South Yorkshire · NCT07914647

• Dual-task balance training plus computer-based cognitive training after stroke

  In adults who recently had a stroke, the study tests whether adding computerized cognitive exercises to balance training improves balance and other recovery outcomes.

  Recruiting Matia Foundation · San Sebastián, GUIPUZCOA · NCT07913620

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.