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Project On Preterm and Small for Gestational Age Infants (POPS)
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Sample details

POPS is a nationwide multicentre birth cohort investigating the long-term health and neurodevelopmental outcomes of very preterm and/or very low birth weight infants born in the Netherlands in 1983. The original POPS cohort comprised 1,338 infants, representing 94% of infants born alive in the Netherlands in 1983 who were very preterm and/or very low birth weight. During the first two years of life, the infants were monitored four times. Further follow-up was conducted at the ages of 5, 9, 10–11, 14, 19, 28, and 35 years, with additional follow-up planned for age 40+.

Study design
Cohort - birth, Cohort

Number of participants at first data collection

1,338 (participants)

Age at first data collection

Birth (participants)

Participant year of birth

1983 (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Children and young people
Preterm infants
Small for Gestational Age (SGA) Infants
Very low birthweight infants (VLBW)
Young adults
Dataset details

Country

Netherlands

Year of first data collection

1983

Primary Institutions

Netherlands Organisation for Applied Scientific Research (Nederlandse Organisatie voor Toegepast Natuurwetenschappelijk Onderzoek, TNO)

Links

tno.nl/pops

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

bronnen.zorggegevens.nl/Bron

Funders

Dutch Kidney Foundation (Nierstichting)

European Union Horizon 2020 Research and Innovation Program

Koninklijke Effatha Guyot Groep (Royal Effatha Guyot group)

Netherlands Organisation for Applied Scientific Research (Nederlandse Organisatie voor Toegepast Natuurwetenschappelijk Onderzoek, TNO)

Phelps Foundation

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – face-to-face
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – online
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Mortality data
Features

Engagement

  • Community engagement
  • Keywords

    Cognitive function
    Disability
    Infant outcomes
    Motor function
    Neurocognitive development
    Neurodevelopment
    Neurological examination
    Physical health
    Premature birth
    Quality of life
    School performance

    Consortia and dataset groups

    Adults Born Preterm International Collaboration (APIC)
    RECAP preterm Project
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