Using a motor-driven system to help stroke patients recover wrist and forearm movement
Pilot Study of Motor-cable-driven System for Stroke Wrist and Forearm Rehabilitation
This study is testing a new motor-driven system to see if it can help stroke patients regain movement in their wrist and forearm.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 18 Years to 85 Years |
| Sex | All |
| Sponsor | Chinese University of Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Trial ID | NCT06062121 on ClinicalTrials.gov |
What this trial studies
This pilot study investigates the feasibility of a motor-cable-driven system designed to assist in the rehabilitation of wrist and forearm movements in hemiplegic stroke patients. The system generates assistive force through cables connected to pulleys and electrical motors, potentially utilizing EMG signals to control movements. The study aims to evaluate how effectively this technology can aid in recovery for patients who have experienced a stroke, focusing on both sub-acute and chronic cases.
Who should consider this trial
Good fit: Ideal candidates for this study are sub-acute and chronic stroke patients who have sufficient cognitive ability to follow instructions.
Not a fit: Patients with severe dysphasia or other medical conditions that hinder their ability to comply with the study protocol may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance rehabilitation outcomes for stroke patients, improving their ability to regain movement in their affected limbs.
How similar studies have performed: While this approach is innovative, similar studies using robotic systems for rehabilitation have shown promising results, indicating potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Sub-acute and chronic stroke patients (ischemic or hemorrhagic). * Sufficient cognition to follow simple instructions as well as understand the content and purpose of the study. Exclusion criteria: 1. Patients with severe dysphasia (either expressive or comprehensive) with inadequate communication. 2. Any additional medical or psychological condition affecting their ability to comply with the study protocol.
Where this trial is running
Hong Kong
- Department of Biomedical Engineering, The Chinese University of Hong Kong — Hong Kong, Hong Kong (Recruiting)
Study contacts
- Principal investigator: Raymond Kai-yu Tong — Department of Biomedical Engineering, The Chinese University of Hong Kong
- Study coordinator: Raymond Kai-yu Tong
- Email: kytong@cuhk.edu.hk
- Phone: +85239438454
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.