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 @ 10:14 PM
Ignite Modification Date:
2025-12-24 @ 10:14 PM
NCT ID:
NCT06899035
Eligibility Criteria:
Inclusion Criteria:
* Diagnosed with Cerebral Palsy by a specialist physician
* Aged between 4-18 years
* Cooperative with physiotherapy applications
* Gross Motor Function Classification System (GMFCS) levels 1-4
* Willing to participate in the study and undergo assessments
Exclusion Criteria:
* Mental retardation or insufficient cognitive function to comply with study assessments
* GMFCS level 5
* Presence of an intrathecal baclofen pump for spasticity treatment or history of soft tissue and/or bone surgery
* Active infection or localized skin infection at the injection site
* History of active seizures
* Presence of contractures
* Serious systemic disease that may prevent exercise participation
* Injury and/or surgery within the last 6 months
* Botulinum toxin injection within the last 6 months
* Contraindications to hydrotherapy, including severe fear of water, behavioral problems, shortness of breath at rest, infection, incontinence, known chlorine allergy, open wounds, acute systemic illness, epilepsy, tracheostomy, permanent drains, immunodeficiency.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
4 Years
Maximum Age:
18 Years
Study:
NCT06899035
Study Brief:
Protocol Section:
NCT06899035