Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Cerebral Palsy
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: AllocationMasking: Double (Care Provider, Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Younger than 818 years
Gender
Both males and females

Description

Using a randomized controlled trial design, the possible changes in neuroimaging, motor function and everyday life activities of infants and toddlers at risk of or with a diagnosis of cerebral palsy after participating of the intensive treatment programme "Hand-arm Bimanual Intensive Therapy Includi...

Using a randomized controlled trial design, the possible changes in neuroimaging, motor function and everyday life activities of infants and toddlers at risk of or with a diagnosis of cerebral palsy after participating of the intensive treatment programme "Hand-arm Bimanual Intensive Therapy Including Lower Extremities (HABIT-ILE)" will be studied . Changes, scored by parents in case of questionnaires and by experts in the case of tests, will be observed comparing infants/toddlers after their regular care and after receiving HABIT-ILE. Motor function and daily life activities will be correlated with neuroplastic changes. Moreover, possible therapy onset outcomes differences will be observed.

Tracking Information

NCT #
NCT04698395
Collaborators
University Hospital of Mont-Godinne
Investigators
Principal Investigator: Yannick Bleyenheuft, PhD MSL-IN Lab, Institute of Neuroscience, UCLouvain Principal Investigator: Yves Vandermeeren, MD, PhD Institute of Neuroscience, UCLouvain; CHU-UCL Namur, Neurology Department, UCLouvain