Effects of HABIT-ILE in Adults with Bilateral Cerebral Palsy
Not yet recruitingNot applicableNCT06767930
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
This randomized controlled trial (RCT) aims to evaluate the effects of intensive Hand and Arm Bimanual Intensive Therapy Including Lower Extremities (HABIT-ILE) in improving body structure, function, daily activities, and participation outcomes among adults with cerebral palsy.
Study details
- Official title
- Effects of Hand-Arm Bimanual Intensive Therapy Including Lower Extremities (HABIT-ILE) in Adults with Bilateral Cerebral Palsy
- Conditions
- Cerebral Palsy
- Bilateral Cerebral Palsy
- Interventions
- Behavioral: Hand and Arm Bimanual Intensive Therapy Including Lower Extremities
- Behavioral: Conventional intervention
- Sponsor
- Université Catholique de Louvain
- Collaborators
- Paris 12 Val de Marne University
- Start date
- 2025-01-06
- Primary completion
- 2026-12-31
- Sex
- All
- Age range
- from 18 Years to 50 Years
- Healthy volunteers
- true
- Results posted
- No results posted in this snapshot
- Countries
- Belgium
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Diagnosed bilateral cerebral palsy, * Adults aged 18 to 50 years old, * Level of manual ability : level I to V of MACS * Level of gross motor function : level I to IV of GMFCS * Ability to follow instructions and complete testing, * Ability to walk 10 meters independently without human assistance (technical aids such as orthoses or walking aids are permitted). Exclusion Criteria: * Unstable seizure * Programmed botulinum toxin or orthopedic surgery in the 6 months before the intervention, during intervention period or 6 months after the intervention time * Alcohol/drug abuse * Pregnancy * Severe visual or cognitive (severe aphasia, psychiatric conditions) impairments likely to interfere with intervention or testing session completion * Uncontrolled health issues (cardiac, metabolic...)
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06767930