Non-invasive therapies to improve arm and hand function in spinal cord injury
Official title: Comparative Evaluation of Non-Invasive Neuromodulation Therapies to Restore Upper Extremity Function in Chronic Cervical Spinal Cord Injury
Run by University of Alberta · NCT06903416 · Data updated 2026-11-12
This study is testing two new therapies to see if they can help people with spinal cord injuries improve their arm and hand function.
Quick facts
| Phase | Phase2; Phase3 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 10 (estimated) |
| Sponsor | University of Alberta Academic / other |
| Locations | 1 site (Edmonton, Alberta) |
| Status | Recruiting |
| Started | May 7, 2025 |
| Main results expected | March 30, 2030 |
| Study ends | March 31, 2030 |
| Registry record updated | May 29, 2026 |
| Trial ID | NCT06903416 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals with cervical spinal cord injuries who are more than nine months post-injury and have stable doses of anti-spasmodics.
✕Probably not a fit
Patients with injuries to the nervous system other than the spinal cord or those who are pregnant may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates two non-invasive therapies aimed at restoring arm and hand function in individuals with chronic cervical spinal cord injury. Participants will undergo a crossover design, receiving transcutaneous spinal cord stimulation and paired corticospinal-motoneuronal stimulation, each combined with rehabilitation, for two months with a one-month washout period in between. The study will assess safety, effectiveness, and patient-reported outcomes related to daily living and quality of life, alongside neurophysiological changes. The goal is to tailor treatments to individual needs, enhancing personalized care and outcomes.
Why it matters
Potential benefit: If successful, this study could significantly improve upper extremity function and quality of life for patients with spinal cord injuries.
How similar studies have gone: Other studies have shown promise with similar non-invasive neuromodulation approaches, indicating potential for success in this area.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Cervical (C2-C8) level SCI * \> 9 months post-injury * Traumatic SCI * AIS A-D * Stable dose of anti-spasmodics Exclusion Criteria: * individuals with injury to the nervous system other than to the spinal cord * pregnant
Where it's running
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Glenrose Rehabilitation Hospital
Edmonton, Alberta, Canada Recruiting
Study contacts
- Principal investigator: Jessica M D'Amico, PhD — University of Alberta
- Study coordinator: Jessica M D'Amico, PhD
- Email: damico1@ualberta.ca
- Phone: 7802039478
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Electrical stimulation for arm function after cervical spinal cord injury in veterans
In veterans with a recent cervical spinal cord injury, researchers are testing whether transcutaneous spinal stimulation (TSS) can improve arm and hand function more than the standard functional electrical stimulation (FES) during inpatient rehab.
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Wireless implant for brain-computer interface in people with tetraplegia from spinal cord injury
This trial tests a wireless brain-computer interface implanted in adults with tetraplegia to see if it is safe and if it can help restore some function.
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Epidural spinal cord stimulation to help breathing after cervical spinal cord injury
This trial tests whether adding epidural spinal cord stimulation to standard care can improve breathing in adults with cervical spinal cord injury and respiratory failure.
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Optimizing sensory feedback to maximize hand and arm function after tetraplegia
This project tests different patterns of brain and nerve electrical stimulation to restore touch and pressure sensations in people with cervical spinal cord injuries who already have ReHAB implants.
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Non-invasive breathing therapies to improve respiratory function after chronic spinal cord injury
We will try combining non-invasive spinal electrical stimulation and brief high-carbon-dioxide breathing with respiratory resistance exercises to see if they improve breathing in adults with chronic incomplete spinal cord injury.
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Using brain-computer interface technology to improve walking in spinal cord injury patients
This study is testing a new brain-computer interface system to see if it can help people with spinal cord injuries walk better and improve their quality of life.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.