An active hand device to help stroke patients regain hand function

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 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.

Why it matters

Who can join: the full rules

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 it's running

• 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

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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.