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Effective Perinatal Intensive Care in Europe cohort (EPICE)
Effective Perinatal Intensive Care in Europe cohort logo
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Sample details

The EPICE cohort is an area‑based, multinational study of over 9,500 still‑ and live‑born very preterm infants (22 + 0 to 31 + 6 weeks’ gestation) recruited between April 2011 and September 2012 across 19 regions in 11 European countries. Infants were identified using obstetric and neonatal medical records, and the study also collected qualitative and quantitative data from parents and healthcare professionals on topics such as decision‑making in neonatal intensive care and the uptake of follow‑up care. The cohort has been followed longitudinally, with major follow‑ups conducted at 2 years’ corrected age and again at 5 years of age. The 5‑year follow‑up was conducted through the Screening to Improve Health in Very Preterm Infants (SHIPS) project, the dedicated long‑term follow‑up arm of EPICE, which provides extended data on children’s health, development, and healthcare utilisation. Through SHIPS, the EPICE cohort was reassessed between June 2016 and February 2017.

Study design
Cohort - birth, Cohort

Number of participants at first data collection

9,514 (participants)

Age at first data collection

Birth (participants)

Participant year of birth

2011 - 2012 (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Newborns, infants and babies
Population-based sample
Dataset details
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Countries

Belgium, Denmark, England, Estonia, France

Year of first data collection

2011

Primary Institutions

National Institute of Health and Medical Research (Institut National de la Santé et de la Recherche Médicale, INSERM) (Research, France)

Links

epiceproject.eu/en/

platform.recap-preterm.eu/pub/study/epice

Profile paper DOI

doi.org/10.1093/ije/dyz270

Funders

European Union (EU) (Government, Europe)

Ongoing?
No

Data types collected

mentalHealthData
qualitativeData
dataLinkage
Quantitative data collection
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – unspecified
  • Secondary data
  • Self-completed questionnaire – unspecified
Qualitative data collection
  • Interviews or focus groups
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Medical birth registry
Features

Engagement

  • Participant or community advisory groups
  • Community engagement
  • Keywords

    Childcare
    Family-based
    Healthcare access and use
    Intensive care
    Multi-site
    Neurodevelopment
    Perinatal health
    Population-based
    Premature birth

    Consortia and dataset groups

    RECAP preterm Project
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