Association of a HABIT-ILE Course and a Home Programme on the Bimanual Performance of Children With Cerebral Palsy
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Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 3 and 5 years old?
Source: NCT06963151, who can take part
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- How often do I need to come in, and for how long each time?
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- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- Fondation Ildys
- Trial code
- NCT06963151
- Record updated
- 15 April 2026
- Original description
This non-inferiority, mixed-methods, multicentre randomised controlled trial will compare the effects of functional changes and families' resources at 3 months of the PARTNER programme (35h HABIT-ILE + 15h home programme) with the reference HABIT-ILE programme (50h) on the bimanual performance (Assisting Hand Assessment [AHA]) of 66 children with unilateral CP aged 3 to 5 years.Read full original descriptionShow less
Association of a HABIT-ILE Course and a Home Programme on the Bimanual Performance of Children Aged 3 to 5 Years With Cerebral Palsy: a Multicentre Randomised Controlled Trial of Non-inferiority
This non-inferiority, mixed-methods, multicentre randomised controlled trial will compare the effects of functional changes and families' resources at 3 months of the PARTNER programme (35h HABIT-ILE + 15h home programme) with the reference HABIT-ILE programme (50h) on the bimanual performance (Assisting Hand Assessment [AHA]) of 66 children with unilateral CP aged 3 to 5 years.
Inclusion: Child with unilateral CP confirmed by a physician; Child aged between 3 years and 5 years 11 months (corrected age) at study entry; Ability to grasp a light object and lift it ≥15cm above the table using the affected hand; Ability to understand instructions and complete all assessments; Matched with another child based on age (± 3 months), CP aetiology, and Manual Ability Classification System (MACS) level; Written informed consent obtained from a parent or legal guardian; Commitment to having the same parent or guardian participate throughout the study.
Exclusion: Significant cognitive or behavioural disorder limiting the ability to follow instructions, as reported in discussions with the family, therapists and/or during a prior assessment; Uncontrolled epilepsy; History of botulinum toxin injection or surgery within 6 months of study entry or scheduled within 3 months of the intervention (ie, during the study period); Diagnosis of ataxic CP; Visual or auditory deficits that could interfere with participation in the study.