An active hand device to help stroke patients regain hand function
MyHand 2: An Active Hand Orthosis for Stroke Patients
NA · Columbia University · NCT04436042
This study is testing a new hand device to see if it can help stroke patients regain better hand function and make everyday tasks easier.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Columbia University (other) |
| Locations | 1 site (New York, New York) |
| Trial ID | NCT04436042 on ClinicalTrials.gov |
What this trial studies
This study focuses on refining the MyHand device, an active hand orthosis designed for stroke patients with hemiparesis. Based on user feedback and pilot study results, the researchers aim to enhance the device's hardware and software components to improve its usability and effectiveness. The goal is to enable patients to grasp a wider variety of objects and perform daily activities more easily. The study will assess the device's impact on functional tasks and overall hand function in stroke survivors.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 who have experienced a stroke at least six months prior and have upper extremity weakness affecting daily activities.
Not a fit: Patients with other neurological or orthopedic conditions affecting the upper extremity or significant spasticity may not benefit from this study.
Why it matters
Potential benefit: If successful, this device could significantly improve hand function and independence for stroke patients.
How similar studies have performed: Previous studies with similar robotic rehabilitation devices have shown promise in improving hand function for stroke patients.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults over 18 years old * History of stroke(s) with most recent stroke at least six months ago * Upper extremity weakness with impaired ability to complete daily activities with affected hand * Full passive range of motion in all digits * Intact cognition to follow directions * Gross control of proximal upper extremity musculature Exclusion Criteria: * Other neurological conditions besides stroke * Other orthopedic conditions to affected upper extremity * Significant spasticity in affected upper extremity that impairs device fit
Where this trial is running
New York, New York
- Columbia University Irving Medical Center — New York, New York, United States (RECRUITING)
Study contacts
- Principal investigator: Joel Stein, MD — Columbia University
- Study coordinator: Carley Teachout, MS
- Email: ct3351@cumc.columbia.edu
- Phone: 212-305-6722
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.
Conditions: Stroke, Hemiparesis, Rehabilitation, Robotics