Back to search results
NCT06808035

Understanding Perinatal Spinal Cord Injury

Enrolling by Invitation
NAAges 3–8InterventionalTreatment
University of Louisville
~6 participants
Updated 2025-02-05 on ClinicalTrials.gov
What's tested:Activity-Based Recovery TrainingTranscutaneous Spinal Cord Stimulation

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Participant Specific Outcome Measures
Measured over At study enrollment, following 20 sessions (approximately 1 month), and following 40 sessions (approximately 2 months)

Conditions

Perinatal Spinal Cord Injury

Explore related trials

Pediatric Spinal Cord InjuryPerinatal Spinal Cord InjurySpinal Cord Injury

Where it's being run

1 sites across 1 states
Kentucky1

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

diagnosed with a perinatal (injured in utero or at birth), upper motor neuron spinal cord injury involving cervical spinal levels
discharged from inpatient hospitalization/inpatient rehabilitation

Exclusion

Botox use within the past 3 months
Current oral baclofen or baclofen pump use
Musculoskeletal impairment limiting range of motion (e.g. severe scoliosis), unhealed fracture, or other medical impairment limiting study participation
History of allodynia (heightened skin sensitivity typically at the level of the lesion site)
History of scoliosis surgery
Ventilator-dependence
Unwillingness to wean from daytime use of thoroco/lumbosacral orthosis and ankle/foot orthosis during the intervention period

What this trial measures

  • Participant Specific Outcome MeasuresAt study enrollment, following 20 sessions (approximately 1 month), and following 40 sessions (approximately 2 months)

    Participant specific outcomes measures will be identified at study initiation via parent interview. Parents will identify daily, functional tasks that the participant has difficulty or challenges performing at a practical, successful level. Functional tasks performed by the participant will be video recorded at study initiation, post-20 sessions, and post-40 intervention sessions. Metrics of task performance include success or failure of the task.