Walking and tSCS in Non-ambulatory Stroke Survivors (NCT07226518) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Walking and tSCS in Non-ambulatory Stroke Survivors
United States20 participantsStarted 2026-01-01
Plain-language summary
Rehabilitation interventions commonly used for stroke survivors include task-specific training, balance and strength exercises, and the use of assistive devices to enhance mobility and independence. Advanced technologies, such as body-weight-supported treadmill systems and robotic devices, may be employed when appropriate. Current rehabilitation therapies for stroke survivors are moderately effective with a limited effect size, especially in stroke survivors with severe impairment. Novel therapies, such as transcutaneous spinal cord stimulation (tSCS), may further improve outcomes in the target population. This pilot study will allow us to examine the feasibility and gather pilot data on a combined intervention of assistive gait training and tSCS in non-ambulatory stroke survivors.
Who can participate
Age range18 Years – 80 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
✓. Age 18-80 years at time of consent
✓. All genders included.
✓. Chronic ischemic or hemorrhagic stroke \>=6 months, with limited within-home comfortable walking speed \<= 0.49 m/s and unable to walk independently in community (FAC \<= 3)
✓. Able to communicate with investigators, follow 2-step command, and correctly answer consent comprehension questions in English.
✓. Currently not participating in treadmill walking exercises or exercises involving weight-bearing activities.
✓. Have physicians' approval for exercise and be in a stable medical condition
Exclusion criteria
✕. Hospitalization for cardiac or pulmonary disease within the past 3 months
✕. Have musculoskeletal disorders that prevent the participant from participating in the exercise
✕. Blood pressure higher than 200/110 mm Hg
What they're measuring
1
Cardiac Output (Measured by Impedance Cardiography - BIOPAC MP160 System)
Timeframe: Before and after 24 training sessions (8 weeks)