About this trial
The goal of this study is to evaluate the HandMATE device's effectiveness in the rehabilitation of stroke patients and asses if the HandMATE application is received well by stroke survivors.
Participants will use the HandMate device in clinic and in the home. They will also complete clinical upper extremity assessments.
Eligibility criteria
Qualifiers
Age of 21 or older
diagnosis of stroke more than 6 months prior confirmed from MRI or CT
voluntary hand activity (score of 1 or more, finger extension item, Fugl-Meyer Test)
adequate cognitive status
Disqualifiers
hemispatial neglect
severe sensory loss (2 or more on the sensory item, NIH Stroke Scale/Score)
receiving or planning to receive antispasticity medications during enrollment into the study
less than full passive range of motion in finger joints
Trial design
Treatments tested in this trial
- HandMate