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Longitudinal Preterm Outcome Project (LOLLIPOP)
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Sample details

LOLLIPOP was a community-based study on the growth and development of preterm and full-term children born in the Netherlands in 2002 and 2003. The study recruited children before their regular well-child visit, typically between the ages of three and four years. After every two preterm-born children, one full-term child was included as a control. In total, the cohort included over 1,800 preterm children and 700 full-term children, along with their parents. Data was collected from external sources, such as medical records, and participants were assessed at ages 4, 5, 7 and 13 to 14 years.

Study design
Cohort, Cohort - birth, Cohort - primary caregiver and child

Number of participants at first data collection

1,843 (preterm children)

674 (full-term children)

Age at first data collection

Birth (preterm children)

Birth (full-term children)

Participant year of birth

2002 - 2003 (preterm children)

2002 - 2003 (full-term children)

Participant sex
All

Representative sample at baseline?
No

Sample features

Caregiver and child dyad
Children and young people
Community-based sample
Newborns, infants and babies
Preterm infants
Dataset details

Country

Netherlands

Year of first data collection

2005

Primary Institutions

University Medical Center Groningen (Universitair Medisch Centrum Groningen, UMCG)

Links

doi.org/10.1186/ISRCTN80622320

doi.org/10.1016/j.jpeds.2018.07.083

doi.org/10.1542/peds.2011-2079

Funders

Abbott

Anneke Bulk General Child Health Care Research Fund

Beatrix Children’s Hospital

Cornelia Foundation for the Handicapped Child

Dutch Brain Foundation

Ongoing?
No

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)
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Medical birth registry
Features

Engagement

  • None
  • Keywords

    Behavioural problems
    Birth records
    Birth records and measurement
    Emotion
    Human development
    Lifestyle factors
    Maternal health
    Motherhood
    Neurophysiological testing
    Pregnancy
    Respiratory health and disease
    Sociodemographics
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