Danish Cerebral Palsy Follow-up Program (CPOP)
CPOP aims to monitor and track the quality of healthcare follow-up and interventions for children and young people with cerebral palsy or who are being evaluated for cerebral palsy. Participants include over 1,600 children aged 0 to 15 years who were born in Denmark after 2003 and have been evaluated for cerebral palsy. The cohort was established in 2010 and recruitment is ongoing. The study links participants' census and healthcare records and includes clinical assessment follow-ups until the participant is 15 years old.
Study design
Registry
Number of participants at first data collection
1,686 (participants as of 2024)
Recruitment is ongoing
Age at first data collection
0 - 15 years (participants)
Participant year of birth
Varied (participants)
Participant sex
All
Representative sample at baseline?
No
Sample features
Country
Year of first data collection
2010
Primary Institutions
Danish Regions
Profile paper DOI
Funders
Danish Clinical Registries (RKKP)
Lundbeck Foundation
Novo Nordisk Foundation
Ongoing?
Yes
Data types collected
- Secondary data
- None
- Magnetic Resonance Imaging (MRI)
- Census data
- Healthcare data
- Medical birth registry
Engagement
Keywords
