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Locomotor Function Following Transcutaneous Electrical Spinal Cord Stimulation in Individuals With Hemiplegic Stroke

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated March 17, 2026 (before its estimated July 31, 2026 completion). Its status may not reflect the trial's current state.

Record History

See every version on ClinicalTrials.gov ↗

  1. Primary completion date: Aug 25, 2026 to Jul 31, 2026
    • Study completion date: Aug 25, 2027 to Jul 31, 2027
    v7
  2. Re-verified, no change to tracked fieldsv6
  3. Interventions: Conventional gait training (Device), Exploratory Phase - Optimization of Gait Training and Spinal Stimulation (Other), Noninvasive spinal… to Conventional gait training (Device), Exploratory Phase - Optimization of Gait Training and Spinal Stimulation (Other), Noninvasive spinal…
    • Study arms: 6 to 4
    v5
  4. Re-verified, no change to tracked fieldsv4
  5. Interventions: Conventional gait training (Device), Noninvasive spinal stimulation (Device), Noninvasive spinal stimulation with gait training (Device)… to Conventional gait training (Device), Exploratory Phase - Optimization of Gait Training and Spinal Stimulation (Other), Noninvasive spinal…
    • Eligibility criteria expanded, about 28 words
    • Secondary endpoints: details revised at 2 of 2 entries
    • Study description expanded, about 4 words
    v3
  6. Trial status: Not Yet Recruiting to Recruitingv2 Show 5 more changesShow less
    • Enrollment target: 75 to 115
    • Start date changed from estimate of Feb 1, 2022 to Mar 1, 2022
    • Study description expanded, about 25 words
    • Site details revised
    • Study arms: 4 to 6
  7. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Shirley Ryan AbilityLab
89 trials monitored
See 1 trial at risk
Stroke
3,531 trials monitored
See 153 trials at risk
This study has two interventional components, the first is a cross-over design and the second is a randomized control trial. Both will evaluate the effectiveness of transcutaneous (non-invasive) spinal cord stimulation on gait and balance function for individuals with hemiplegia due to stroke.
Trial Details
NCT Number NCT05167786
Lead Sponsor Shirley Ryan AbilityLab
Collaborators: University of California, Los Angeles
Conditions
(from sponsor)		 Stroke
Related terms Stroke
Enrollment 115 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov