About this trial
The goal of this study is to identify the effect of different types of noninvasive spinal stimulation on spasticity (involuntary muscle activity), muscle strength, and pain in people with spinal cord injury. The spinal stimulation consists of electrical stimulation applied through one electrode over the skin of the lower back and two electrodes over the stomach. Testing will include participating in measurements before the intervention, during intervention, and immediately after the intervention. This study requires participants to come into Shepherd Center 4 consecutive days a week for 2-3 hours per day across 2-3 weeks.
Eligibility criteria
Qualifiers
Participants must agree to allow use of health information.
Participants should be 16 years old or older.
Participants must have had a spinal cord injury (SCI) of any severity (AIS A, B, C, or D) that happened at least 3 months ago.
Objectively measurable spasticity in your legs.
Disqualifiers
People with spinal issues that are getting worse, such as degenerative or progressive vascular disorders.
People neurological problems other than SCI.
People with an injury level is below T12.
People with un-treated or uncontrolled heart problems that the lead investigator believes could be affected by stimulation or affected by an increase in blood pressure.
Trial design
Treatments tested in this trial
- Transcutaneous Spinal Stimulation
Treatment groups
Sponsors and collaborators
Shepherd Center, Atlanta GA
Lead sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborator