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Transcutaneous Spinal Cord Stimulation to Promote Walking Recovery After Spinal Cord Injury

StatusActive, Not Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated February 5, 2026 (before its estimated February 27, 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Minor Trial status: Recruiting to Active, Not Recruiting
    • Primary completion date: Dec 15, 2025 to Feb 27, 2026
    • Study completion date: Dec 15, 2025 to Mar 31, 2026
    • Site details revised
    v6
  2. Notable Primary completion date: Apr 15, 2025 to Dec 15, 2025
    • Study completion date: May 15, 2025 to Dec 15, 2025
    • Site contact updated
    v5
  3. Notable Primary completion date: Sep 15, 2024 to Apr 15, 2025
    • Study completion date: Sep 15, 2024 to May 15, 2025
    • Site contact updated
    v4
  4. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    v3
  5. Notable Start date: Sep 15, 2023 to Nov 15, 2023
    • Eligibility criteria shortened, about 3 words
    v2
  6. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this clinical trial is to investigate the effects of transcutaneous spinal cord stimulation (TSCS) combined with exoskeleton training, as compared to exoskeleton training alone to improve motor function in individuals with incomplete spinal cord injury who are 12 months or less post-injury. Participants will be randomly assigned to a treatment group (exoskeleton training with TSCS, or exoskeleton training without TSCS). Participants in both groups will undergo a baseline evaluation, then take part in 24, 1-hour training sessions at Craig Hospital. After the 24 sessions have concluded, participants will undergo a post-treatment evaluation as well as a follow-up evaluation four weeks after training is completed. Researchers will compare the two groups by evaluating the following areas: * walking ability and speed * lower extremity strength, activation, and spasticity * trunk control * bowel and bladder function
Trial Details
NCT Number NCT05982171
Lead Sponsor Craig Hospital
Conditions
(from sponsor)
Spinal Cord Injuries
Related terms Spinal Cord Injuries
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov