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Spinal Cord Stimulation and Training
RecruitingHealthy volunteers welcome
Neural Plasticity by Spinal Cord Stimulation and Training in People With Spinal Cord Injury
Who can join
Ages 16 to 65 · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: Healthy Volunteers * Age between 16 and 65 years old * Healthy people with no major comorbidities of any organ system Exclusion Criteria: Healthy Volunteers * Subjects younger than 16 or older than 65 years old * Subjects not providing consent or not able to consent * Subjects with any acute or chronic pain condition * Subjects with any acute or chronic disease of a major organ system * Use of analgesics within 24 hours prior to study period * Use of caffeine with 3 hours of study appointment Inclusion criteria: Participants with spinal cord injury (SCI) * Age between 16-65 years old * Traumatic SCI C4-T9 level, incomplete (ASIA C or D) * at least 1 year post injury * Stable medical condition * difficulty independently performing leg movements in routine activities * able to follow simple commands * able to speak and respond to questions Exclusion criteria: Participants with spinal cord injury (SCI) * Subjects younger than 16 or older than 65 years old * Not willing or able to provide consent * Any acute or chronic pain condition * Any acute or chronic disease of a major organ system * Use of analgesics within 24 hours prior to study appointment * Use of caffeine with 3 hours of study appointment * Presence of tremors, spasms and other significant involuntary movements * Etiology of SCI other than trauma * Concomitant neurologic disease traumatic brain injury (TBI) that will significantly impact the ability to follow through on study directions, multiple sclerosis (MS), stroke or peripheral neuropathy) * History of significant medical illness (cardiovascular disease, uncontrolled diabetes, uncontrolled hypertension, osteoporosis, cancer, chronic obstructive pulmonary disease, severe asthma requiring hospitalization for treatment, renal insufficiency requiring dialysis, autonomic dysreflexia, etc). * Severe joint contractures disabling or restricting lower limb movements. * Unhealed fracture, contracture, pressure sore, urinary tract infection or other uncontrolled infections, other illnesses that might interfere with lower extremity exercises or testing activities * Depression, anxiety, or cognitive impairment * Deficit of visuospatial orientation * Sitting tolerance less than 1 hour * Severe hearing or visual deficiency * Miss more than 3 appointments without notification * Unable to comply with any of the procedures in the protocol * Botulinum toxin injection in lower extremity muscles in the prior six months * Any passive implants (osteosynthesis material, metallic plates or screws) below T9. * Any implanted stimulator in the body (pacemaker, vagus nerve stimulator, etc.) * History of alcoholism or another drug abuse * Pregnancy (or possible pregnancy) * Having an Intrathecal Baclofen Therapy Pump (ITB pump) * History of epilepsy
About the study
This study will help the investigators better understand the changes in short-term excitability and long-term plasticity of corticospinal, reticulospinal and spinal neural circuits and how the changes impact the improvements of spinal cord stimulation (SCS) mediated motor function.
What is being tested
- Electrophysiology assessment - corticospinal tract (other)
- Electrophysiology assessment - reticulospinal tract (other)
- Electrophysiology assessment - spinal motoneuron (other)
- Activity-based training (other)
- Transcutaneous spinal cord stimulation (other)
Sponsor: Washington University School of Medicine · Participants: 120 · Started: Jul 21, 2023
Contact the study team
- Ismael Seanez, PHD · Phone: 314-935-7665
Official record on ClinicalTrials.gov — NCT05472584
Locations in the U.S.
| Missouri | Washington University, St Louis |
Conditions
From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.