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
Compensation
$75 per visit
IRB Number:
R-1176-22
Research Coordinator
