Robotic Training for Stroke Neurorehabilitation
Stroke
About this trial
This is an interventional treatment trial for Stroke focused on measuring Robotics, upper extremity, neurorehabilitation, movement therapy
Eligibility Criteria
Inclusion Criteria:
- Age 21 or older
- Ischemic or hemorrhagic stroke (with confirmatory neuroimaging) that occurred more than 6 months before entering the study
- Presence of voluntary hand activity indicated by a score of at least 1 on the finger mass extension/grasp release item of the Fugl-Meyer Test of Motor Function
- Adequate cognitive status, as determined by clinical evaluation
- No upper extremity injury or conditions that limited use prior to the stroke
Exclusion Criteria:
- Cannot give informed consent
- Have clinically significant fluctuations in mental status within a month of enrollment
- Were not independent prior to the stroke as measured by scores <95 on the Barthel Index or >1 on the Modified Rankin Scale
- Have hemispatial neglect as determined by >3 errors on the Star Cancellation Test
- Have severe sensory loss as determined by a score of 2 on the sensory item of the NIHSS
- Receiving oral or injected antispasticity medications during study treatment
- Pain that interferes with daily activities
- History of prior stroke
Sites / Locations
- Washington DC VA Medical Center, Washington, DC
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Robotic
Conventional
The experimental group will receive 1-hour robotic training sessions, 3 times per week for a total of 12 sessions supervised by a research assistant. Immediately following this robot training, these subjects will receive the same dosage and schedule (1-hour sessions, 3 times/week, 12 total sessions) of conventional one-on-one therapy from an occupational therapist.
Subjects will receive 24 hours of one-on-one treatment from an occupational therapist. The treatment schedule will parallel that given to the experimental group (1-hour sessions, 3 times/week).