RecruitingNot ApplicableNCT06272279

Neuromodulation With Spinal Stimulation Methods


Sponsor

University of Manitoba

Enrollment

24 participants

Start Date

Mar 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This is a pilot research study to test the protocols needed for transcutaneous spinal electrical stimulation in persons living with spinal cord injury (SCI). Up to 24 participants will be enrolled. A variety of stimulation parameters and outcome measures will be assessed.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Inclusion Criteria2

  • spinal cord injury C4 to L4
  • ability to understand and follow directions

Exclusion Criteria1

  • history of seizures, head injury, concussion, unexplained loss of consciousness or if they lived with an implanted cochlear stimulator, brain/neurostimulator, cardiac pacemaker, medication infusion device or live with metal implants in their body or if they are pregnant.

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Interventions

DEVICEspinal stimulation-DCS

transcutaneous spinal stimulation by direct current stimulation

OTHERspinal stimulation-sham DCS

sham transcutaneous spinal stimulation by direct current stimulation

OTHERspinal stimulation-EPS

transcutaneous spinal stimulation by electrical pulsed stimulation

OTHERsham spinal stimulation-EPS

sham transcutaneous spinal stimulation by electrical pulsed stimulation


Locations(2)

University of Manitoba

Winnipeg, Manitoba, Canada

University of Manitoba

Winnipeg, Manitoba, Canada

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NCT06272279


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