Transcutaneous Spinal Cord Stimulation (tSCS) During Assisted Cycling Training for Incomplete Spinal Cord Injury.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorFundació Sant Joan de Déu

About this trial

The goal of this clinical trial is to learn if transcutaneous spinal cord stimulation works to improve lower limb motor function in adults with incomplete spinal cord injury. It will also learn about the safety of transcutaneous spinal cord stimulation when combined with assisted cycling training.

The main questions it aims to answer are:

Does transcutaneous spinal cord stimulation while training with assisted cycling improve lower limb motor function? Does transcutaneous spinal cord stimulation while training with assisted cycling reduce muscle spasms or improve bladder or bowel function?

Researchers will compare transcutaneous spinal cord stimulation to a sham (a look-alike stimulation that does not deliver therapeutic electrical current) to see if transcutaneous spinal cord stimulation during assisted cycling improves motor function in people with incomplete spinal cord injury.

Participants will:

Participate in the training program with assisted cycling. Receive active stimulation or placebo stimulation during this training. Undergo motor function assessments, and be monitored about muscle spasms, bladder and bowel function and side effects.

The study will include 40 participants with incomplete spinal cord injury with less than 12 months since injury.

Eligibility criteria

Qualifiers

Age at least 18.

Diagnosis of spinal cord injury at levels C2-T11, classified as ASIA Impairment Scale grades B, C, or D.

Less than 1 year since the injury.

Ability to follow instructions and tolerate the intervention.

Disqualifiers

Comorbidities that limit active participation (severe heart disease, serious active infections, pressure ulcers in the area).

Use of devices incompatible with electrical stimulation.

Metallic implant in the T11-T12 area.

History of epilepsy.

Trial design

Treatments tested in this trial

  • Transcutaneous spinal cord stimulation on the dorsal region between T11 and T12
  • Sham transcutaneous spinal cord stimulation on the dorsal region between T11 and T12

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Fundació Sant Joan de Déu

Lead sponsor

Hospital San Juan de Dios, Spain

Collaborator