The purpose of this research study is to assess the effects of receiving transcutaneous spinal stimulation while performing walking exercises compared to completing walking exercises without spinal stimulation for individuals with hemiplegic TBI.
Age range
18 Years – 65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
10MWT (Aim 1)
Timeframe: Change from Baseline 10MWT at 6 weeks and 3 months
6MWT (Aim 1)
Timeframe: Change from Baseline 6MWT at 6 weeks and 3 months
TUG (Aim 1)
Timeframe: Change from Baseline 6MWT at 6 weeks and 3 months
DGI (Aim 1)
Timeframe: Change from Baseline DGI at 6 weeks and 3 months
Berg Balance Scale (Aim 1)
Timeframe: Change from Baseline Berg at 6 weeks and 3 months
Temporospatial Loading (Aim 1)
Timeframe: Change from Baseline at 6 weeks and 3 months
Joint Range of Motion (kinematics) (Aim 2)
Timeframe: Change from Baseline at 6 weeks and 3 months
Transcranial magnetic stimulation (TMS) (Aim 2)
Timeframe: Change from Baseline at 6 weeks and 3 months
Participation Objective Participation Subjective (Aim 3)
Timeframe: Change from Baseline at 6 weeks and 3 months
Community Integration Questionnaire (Aim 3)
Timeframe: Change from Baseline at 6 weeks and 3 months
Patient Competency Rating Scale (Aim 3)
Timeframe: Change from Baseline at 6 weeks and 3 months
Perceived Control Scale for Brain Injury (Aim 3)
Timeframe: Change from Baseline at 6 weeks and 3 months
SF-36 (Aim 3)
Timeframe: Change from Baseline at 6 weeks and 3 months