Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 10:39 PM
Ignite Modification Date:
2025-12-24 @ 10:39 PM
NCT ID:
NCT06808035
Eligibility Criteria:
Inclusion Criteria:
* 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 Criteria:
* 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
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
3 Years
Maximum Age:
8 Years
Study:
NCT06808035
Study Brief:
Protocol Section:
NCT06808035