The goal of this observational study is to create a computer model to help doctors predict any problems occurring during development of babies after being diagnosed with brain injury. This will help provide better care to future babies. Next to this, the experiences of parents or caregivers surrounding the first two years after birth of a baby at risk of developing cerebral palsy will be researched to develop recommendations to support parents. Parents of participants will: \- Fill in two online questionnaires, one when their child is 3-4 months corrected age. The second when their child is 2 years corrected age. For the child no additional tests are needed. Only tests that are part of standard clinical practice are performed and are also saved in the study database.
Study Type
OBSERVATIONAL
Enrollment
1,000
Assistance Publique Hôpitaux de Paris
Paris, France
RECRUITINGUniversity Hospital Essen
Essen, Germany
RECRUITINGOspedale Pediatrico Meyer Firenze
Florence, Italy
RECRUITINGIstituto Giannina Gaslini
Genova, Italy
NOT_YET_RECRUITINGOspedale Maggiore di Milano
Milan, Italy
RECRUITINGFondazione Stella Maris
Pisa, Italy
RECRUITINGUMC Utrecht
Utrecht, Netherlands
RECRUITINGUniversity Hospital La Paz
Madrid, Spain
RECRUITINGDevelopment of a machine learning based prediction model
To develop and evaluate a new prediction model using machine learning to predict the risk, severity, and long-term outcome of cerebral palsy (CP) at the level of the individual patient. This model will also provide automatic scoring for each clinical modality (MRI, EEG, GM, HINE, infant cry), which is to be compared with the clinician assessments.
Time frame: Neurodevelopmental outcome at 2 years predicted by clinical data from birth to 3-4 months corrected age
Gaining insight into parental mental well-being and family= and social functioning.
To gain insight in parental mental well-being and family- and social functioning, over the first two years after the birth of their child with brain injury, born preterm or full-term, at high risk of developing CP. Including evaluation of parents' experiences around the disclosure of diagnosis, and the impact of these experiences, child-related factors and social support on parental mental well-being. To understand the needs and preferences of parents on the process of disclosure of diagnosis and on information regarding prediction and prognosis, and to identify what information is meaningful to families.
Time frame: Parent experience asked in questionnaires at age 3-4 months and 2 years.
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