Combining spinal stimulation with mobility devices to improve movement in children with neurological conditions
Transcutaneous Stimulation and Mobility Device Use for Individuals With Neurologic Conditions
This study is testing whether using spinal stimulation along with mobility devices can help improve movement in children with neurological conditions like cerebral palsy and stroke.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 4 Years to 70 Years |
| Sex | All |
| Sponsor | University of Washington Academic / other |
| Locations | 1 site (Seattle, Washington) |
| Trial ID | NCT05520359 on ClinicalTrials.gov |
What this trial studies
This research combines non-invasive spinal stimulation with mobility devices to assess their individual and combined effects on mobility in children with conditions like cerebral palsy and stroke. The study aims to understand how these interventions can enhance sensory feedback and improve movement mechanics in pediatric patients with neurological impairments. By examining the impact of these innovative techniques, the research seeks to inform future long-term studies and clinical practices for better rehabilitation outcomes.
Who should consider this trial
Good fit: Ideal candidates are children aged 4-70 with stable neurological conditions who can perform simple motor tasks.
Not a fit: Patients with significant medical diseases or conditions that prevent full participation in physical therapy may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance mobility and quality of life for children with neurological conditions.
How similar studies have performed: Previous studies have shown promise in using spinal stimulation for improving motor function, suggesting potential success for this combined approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * have a neurologic condition * are 4-70 years of age * have stable medical condition * can perform simple cued motor tasks and who can follow 2-3 step commands * who are volunteering to be involved in this study * can provide feedback on comfort and experience during lab visits Exclusion Criteria: * have significant medical disease; including uncontrolled systemic hypertension with values above 170/100 mmHg; cardiac or pulmonary disease; uncorrected coagulation abnormalities or need for therapeutic anticoagulation. * have cardiovascular or musculoskeletal disease or injury that would prevent full participation in physical therapy intervention * have a history of uncontrolled seizures * have unhealed fracture or other musculoskeletal impairment that might interfere with lower extremity rehabilitation or testing activities * are dependent on ventilation support * have implanted stimulator (e.g. epidural stimulator, vagus nerve stimulator, pacemaker, cochlear implant, etc) or drug delivery device (e.g. baclofen pump) * have history of orthopedic surgery in lower extremities or neurosurgery that may be a confounding factor for interpretation of the results (such as tendon transfer, tendon or muscle lengthening for spasticity management, injection therapies to lower extremity muscles, etc.) in last 12 months * have established osteoporosis and taking medication for osteoporosis treatment. * have rheumatic diseases (rheumatoid arthritis, systemic lupus erythematosus, etc.) * have active cancer
Where this trial is running
Seattle, Washington
- University of Washington — Seattle, Washington, United States (Recruiting)
Study contacts
- Principal investigator: Katherine Steele, PHD — University of Washington
- Study coordinator: Katherine Steele, PHD
- Email: kmsteele@uw.edu
- Phone: 206-685-2390
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.