Intensive Rehabilitation Program for Upper Limb in Children and Adolescents With Cerebral Palsy
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Intensive Rehabilitation.
- Who it may be relevant to
- Registry conditions: Cerebral Palsy (CP). Basic parameters: 3 years — 17 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Effect of an Intensive Rehabilitation Protocol Combining Constraint-Induced Movement Therapy and Bimanual Training on Upper Limb Use and Gross Motor Function in Children and Adolescents With Cerebral Palsy
Overview
Cerebral palsy is the most common motor disability in children. Individuals with CP often experience significant difficulties in the use of their upper limbs, which affects their autonomy and quality of life. Conventional rehabilitation, although essential, is often insufficient to compensate for these deficits in a meaningful way. The French National Authority for Health has issued recommendations for intensifying rehabilitation in order to maximize functional gains in children with CP. Among the intensive approaches that have been studied, two techniques have demonstrated efficacy: Constraint-Induced Movement Therapy (CIMT) and Bimanual Intensive Therapy (BIT). CIMT focuses on restricting the use of the unaffected limb to encourage the use of the affected limb, thereby promoting neuroplasticity and functional improvement. In contrast, BIT emphasizes intensive training of both hands simultaneously to enhance coordination and overall upper limb functionality. At the Ellen Poidatz Foundation, an intensive rehabilitation program has been developed that combines these two complementary approaches. This program, which is already in place, is based on the principles of neuromotor rehabilitation and motor learning. It integrates several methods recommended by the HAS, including Bimanual Intensive Therapy (BIT) such as HABIT (Grade A) or HABIT-ILE (Grade B), Modified Constraint-Induced Movement Therapy (mCIMT) (Grade B), and Adapted Physical Activity (APA) (Grade A). The aim of this intensive program is to enhance the functional use of the upper limb by improving bimanual coordination, grasping, manipulation, and overall motor function. The program lasts 10 days over a 2-week period and is tailored to the child's age and care setting. It includes approximately 60 hours of rehabilitation for children aged 3 to 8 years and 80 hours for those aged 9 to 17 years, in line with current international recommendations. The aim of this study is to evaluate the effectiveness of this existing intensive rehabilitation program in improving manual abilities in children with CP. Specifically, the study seeks to objectively assess the benefits of the Habil'Hand+ program and to contribute to the optimization of rehabilitation protocols for this population.
Interventions
- Other Intensive Rehabilitation
Children aged 3 to 8 years : 2 weeks program over 10 days including two individual sessions and three group sessions per participant per day combining CIMT and BIT. Adolescents aged 9 to 17 years in day-hospital care/ in inpatient care: 2 weeks program over 10 days including two individual sessions and three group sessions per participant per day combining CIMT and BIT. Daily routines, and activities involve functional and playful motor tasks of progressively increasing difficulty.
Primary outcome measures
- Assisting Hand Assessment (AHA) /Both Hands Assessment(BoHA) [Time frame: 3 months]
Secondary outcome measures (7)
- Melbourne Assessment 2 [Time frame: 3 months]
- Canadian Occupational Performance Measure (COPM) [Time frame: 3 months]
- Goal Attainment Scaling (GAS) [Time frame: 3 months]
- Children's Hand Experience Questionnaire (CHEQ) [Time frame: 3 months]
- Box and Blocks test [Time frame: 3 months]
- Gross Motor Function Measure (GMFM) [Time frame: 3 months]
- 6 minutes walking test [Time frame: 3 months]
Eligibility criteria
Inclusion criteria
- A clinical diagnosis of CP mentioned in the medical record
- Aged between 3 and 17 years inclusive (<18 years)
- Global Motor Function Classification System (GMFCS) and Manual Ability Classification System (MACS) levels I to IV
- Ability to cooperate, understand and follow simple instructions
- Patient affiliated to the French social security system
- Voluntary patient whose parents have given their consent for their child to participate in the study.
Exclusion criteria
- Presence of injuries incompatible with participation in the program, or pain rated >3 on the Visual Analogue Scale (VAS)
- Presence of behavioral disorders
- History of botulinum toxin injections or surgical intervention within six months prior to study enrollment.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
France · 1 center
- Fondation Ellen Poidatz — Saint-Fargeau-Ponthierry
Identifiers
NCT: NCT07285837 · Habil'Hand+