23
Participants
Start Date
August 31, 2012
Primary Completion Date
November 30, 2015
Study Completion Date
November 30, 2015
IpsiHand Device
Once a participant has completed (3) EEG Signal Screens and (2) separate set of baseline measurements, the IpsiHand BCI Device is provided to participants to use a minimum of (5) out of (7) days a week for a total duration of 12 weeks. Participants are seen bi-weekly throughout the duration of the trial to assess affected upper extremity and assess functional impact. At the completion of 12 weeks of device use, the participants complete a set of measurements to assess function of the affected upper extremity.
Washington University School of Medicine, St Louis
Washington University School of Medicine
OTHER