This study aims to expand the knowledge and capacity for neuromodulation to improve the debilitating effects of severe spasticity (spasms, tonic muscle activity and/or clonus) in persons with spinal cord injury.
Actively Recruiting
Yes
Duration
Participation lasts approximately 8-10 months
Inclusion Criteria
- At least 18 years of age
- Have a non-progressive spinal cord injury as determined by the study physician and/or Lead Investigator
- Have met the clinical criteria for an intrathecal baclofen pump
- In stable medical condition
MRI Study
No
Compensation
$75 per visit
IRB Number
R-1176-22
Research Center
Contact Person
Phone
973.324.3557
Email
Location
1199 Pleasant Valley Way, West Orange, NJ
