MyHand-SCI: An Active Hand Orthosis for Spinal Cord Injury
Columbia University · with National Institute of Neurological Disorders and Stroke (NINDS) · NCT05553457
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 40
- US sites recruiting
- 1
- Study start
- October 4, 2022
- Record last updated
- October 5, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this study is to develop and test the hardware and software components of the MyHand-SCI device to assist with hand function for individuals with C6-C7 spinal cord injury.
Being studied: Testing of MyHand-SCI Device
Conditions: Spinal Cord Injuries; Tetraplegia
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Individuals with C6-C7 spinal cord injury, at least 6-months post-injury with impaired upper limb function
- Substantially reduced motor control and strength below the level of their SCI with regard to hand and finger function
- Able to provide informed consent
Exclusion Criteria
- Fixed upper limb contractures that limit functional use of the hand and arm or ability to use the device
- Severe spasticity (modified Ashworth >2) at elbow, wrist, or fingers
- Any open wounds or unusual skin fragility
- Persistent severe pain in their upper limb
Recruiting US locations
Columbia University Irving Medical Center
New York, NY 10032
Site contact: Lauren Winterbottom, EdD · 212-305-6722 · lbw2136@cumc.columbia.edu
Study contacts (from the official record)
- Lauren Winterbottom, EdD · 212-305-6722 · lbw2136@cumc.columbia.edu
- Joel Stein, MD · 212-305-4818
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