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 @ 11:18 PM
Ignite Modification Date:
2025-12-24 @ 11:18 PM
NCT ID:
NCT06533956
Eligibility Criteria:
Inclusion Criteria:
* Patients aged 8 to 18 with bilateral spastic cerebral palsy
* Patient with functional level II or III according to the Gross Motor Function Classification System (GMFCS)
* Patient able to assess pain with NRS-11
* Patient able to walk on a treadmill without body weight support, with or without technical aids
* Patient able to perform the 10-meter walk test
* No skin pathology at the pressure cuff application site (eczema, inflammatory scarring, etc.)
* Patient affiliated to or benefiting from a social security scheme
* Informed consent, dated and signed by parents or guardians (if a minor) or by the patient (if of age), to participate in the study;
Exclusion Criteria:
* Patients who have undergone surgical treatment or intramuscular injections of botulinum toxin in the lower limbs within the last 3 months
* Patients with a history of arterial hypertension, thrombo-embolic events, thrombophilia or cancer.
* Patient with insufficient understanding of the French language;
* Opposition of the patient (child or adolescent);
* Pregnant, breast-feeding or parturient women;
* Persons deprived of their liberty by judicial or administrative decision;
* Persons under compulsory psychiatric care;
* Persons under legal protection
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
8 Years
Maximum Age:
18 Years
Study:
NCT06533956
Study Brief:
Protocol Section:
NCT06533956