What this study is
This study is designed to further develop and test the hardware and software components of the MyHand device based on user feedback and results from our pilot study. The goal is to refine the device so that is more effective and easier for stroke patients to use to increase their hand function.
What's being tested
- MyHand Device
Intervention · DEVICE
These subjects may be asked to attend 1-40 sessions (approximately 90 mins) to trial a variety of device controls and/or components.
Study details
- Sponsor
- Columbia University
- Conditions
- Stroke · Hemiparesis
- Enrolling
- 25 people
- Starts
- 2020-03-06
- Est. completion
- 2028-01
- Design
- Open-label, single group
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- 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
You can't join if
- Other neurological conditions besides stroke
- Other orthopedic conditions to affected upper extremity
- Significant spasticity in affected upper extremity that impairs device fit
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
Loading treatment details…
Study locations (1)
1 openColumbia University Irving Medical Center
New York, New York, United States
- Lauren Winterbottom, MS · Contact212-305-6722lbw2136@cumc.columbia.edu
Recruiting
Study team
Sponsor
Columbia University
Study ID AAAS8104
Principal investigator
Joel Stein
Columbia University
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.