Actively Recruiting

Phase 2
Phase 3
Age: 18Years - 75Years
All Genders
NCT06903416

Non-Invasive Neuromodulation for Upper Extremity Function in Spinal Cord Injury: A Crossover Trial

Led by University of Alberta · Updated on 2025-05-22

10

Participants Needed

1

Research Sites

255 weeks

Total Duration

On this page

Sponsors

U

University of Alberta

Lead Sponsor

P

Praxis Spinal Cord Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study explores two promising therapies for restoring arm and hand function in people with chronic cervical spinal cord injury (SCI), a condition that affects independence and quality of life. It will compare transcutaneous spinal cord stimulation and paired corticospinal-motoneuronal stimulation, both combined with rehabilitation. Using a crossover design, participants will receive each therapy for two months, with a one-month washout period in between. Safety, effectiveness, and patient-reported outcomes like daily living ability and quality of life will be assessed, alongside changes in neural excitability. The results of this study may enable us to tailor treatments to individual needs, promoting personalized care and improved outcomes.

CONDITIONS

Official Title

Non-Invasive Neuromodulation for Upper Extremity Function in Spinal Cord Injury: A Crossover Trial

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Cervical (C2-C8) level spinal cord injury
  • More than 9 months since injury
  • Traumatic spinal cord injury
  • AIS grade A to D
  • Stable dose of anti-spasmodic medications
Not Eligible

You will not qualify if you...

  • Injury to the nervous system other than the spinal cord
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Glenrose Rehabilitation Hospital

Edmonton, Alberta, Canada, T5G0B7

Actively Recruiting

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Research Team

J

Jessica M D'Amico, PhD

CONTACT

C

Caitlin Hurd, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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