Cerebral Palsy Clinical Trial
Official title:
A Multi-country, Multi-centre, Observational, Cross-sectional Study to Evaluate Individualized Treatment and Management in Children and Adolescents With Cerebral Palsy
HCPs will complete questionnaires about their patients with Cerebral Palsy (CP) and invite parents/caregivers of these patients to fill in questionnaires as well. Questionnaires include questions on individualized treatment, nutritional profile and management, and patient characteristics.
Coordinating health care professionals (HCPs; e.g. paediatric neurologists, physiotherapists)
in different centres across different countries will be asked to participate in this
cross-sectional study.
A) for the HCP to fill out a questionnaire about their CP child, related to general subject
characteristics, motor function, co-morbidities, type of therapies, anthropometry, feeding
mode and nutritional status; and B) for parents (/legal representatives) to receive and fill
out questionnaires about their CP child and themselves, related to general subject
characteristics, motor function, co-morbidities, type of therapies, anthropometry, feeding
mode and nutritional status, participation and (their own) quality of life.
If parents (/legal representatives) agree to "A)", but not "B)" then a subject will still
enter the study, but without the parental assessment.
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