MyHand 2: An Active Hand Orthosis for Stroke Patients
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorColumbia University
About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
Other neurological conditions besides stroke
Other orthopedic conditions to affected upper extremity
Significant spasticity in affected upper extremity that impairs device fit
Trial design
Treatments tested in this trial
- MyHand Device
Treatment groups
60 Participants
are divided into 1 treatment groupSponsors and collaborators
Columbia University
Lead sponsor
National Institute of Neurological Disorders and Stroke (NINDS)
Collaborator
Source ClinicalTrials.gov