Stopped: No funding or personnel for project. We are unable to meet the recruitment goals for this pilot study.
The purpose of this study is to test the efficacy of mild breathing bouts of low oxygen (intermittent hypoxia) combined with transcutaneous electrical spinal cord stimulation on restoring hand function in persons with chronic incomplete spinal cord injury.
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.
Change in Upper Extremity Function
Timeframe: Once each intervention week (days 5, 10, and 15), and once at follow-up (week 8)
Change in Upper Extremity Strength - Cylindrical Grip - Less Impaired Hand
Timeframe: Once each intervention week (days 5, 10, and 15), and once at followup (week 8)
Change in Upper Extremity Strength - Cylindrical Grip - More Impaired Hand
Timeframe: Once each intervention week (days 5, 10, and 15), and once at followup (week 8)