Danish Schizophrenia Registry
The Danish National Schizophrenia Database, established in 2003, is a nationwide clinical quality database which monitors and develops the quality of treatment and care for children, young people, and adults in Denmark with a diagnosis of schizophrenia. The database records approximately 15,000 patient procedures annually. Data is reported via the patient administrative systems to the National Patient Register and coordinated with data from the CPR register, the Laboratory Register, and the Prescription Database.
Study design
Registry
Number of participants at first data collection
14,324 (participants in 2014)
Recruitment is ongoing
Age at first data collection
Varied (participants)
Participant year of birth
Varied (participants)
Participant sex
All
Representative sample at baseline?
No
Sample features
Country
Year of first data collection
2003
Primary Institutions
Regionernes Kliniske Kvalitetsudviklingsprogram (RKKP)
Profile paper DOI
Funders
Danish Clinical Registries (RKKP)
Ongoing?
Yes
Data types collected
- Secondary data
- None
- None
- Healthcare data
Engagement
Keywords
