tSCS in Children With Spina Bifida

Part of paid clinical trials in Pittsburgh, Pennsylvania.

Sponsor
Bailey Petersen
Study ID
NCT07615686
Status
Recruiting

Conditions

  • Myelomeningocele
  • Spina Bifida

Eligibility Criteria

Sex
ALL
Age
4 Years - 17 Years
Healthy Volunteers
Not accepted

Interventions

  • Transcutaneous stimulator — DEVICE
    an off the shelf TENS unit or Digitimer DS8R (using same parameters as TENS unit)

Study Details

A single-center, open-label, investigational pilot trial to explore potential effects of transcutaneous spinal cord stimulation on leg muscle strength and walking in children with myelomeningocele.

Key Dates

Start date
Jun 10, 2026
Status verified
May 2026
Primary completion
Mar 10, 2028
Completion
Mar 10, 2029

Study Design

Enrollment
20 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER

Arms

  • Experimental: Transcutaneous SCS
    All participants will be receiving transcutaneous spinal cord stimulation

Primary Outcome Measure

Muscle Strength [ Time Frame: 4-6 weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of PittsburghPittsburghPennsylvania15213
Sydney Bader, MS

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