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Copenhagen Child Cohort Study (CCC2000)
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Sample details

CCC2000 comprises all children born in 2000 by women residing in one of 16 municipalities in the former Copenhagen County, Denmark. The cohort covers nearly 10% of all children born in Denmark in that year, while the catchment area consists of urban and semirural suburbs surrounding Copenhagen, with a mixture of high-, moderate-, and low-income households. All eligible cohort children and their parents were contacted and asked to participate in questionnaires, interviews, and assessments at key ages of development: 0-10 months and 1.5, 5-7, 11-12, and 16-17 years. In parallel, data from the Danish national registries have been drawn regularly.

Study design
Cohort - birth

Number of participants at first data collection

6,090 (participants)

Age at first data collection

Birth (participants)

Participant year of birth

2000 (participants)

Participant sex
All

Representative sample at baseline?
The Danish child population in terms of perinatal and sociodemographic characteristics at baseline, except for a higher proportion of immigrant families (16% versus the national average 8%) and a slightly higher household income (corresponding to the metropolitan area).

Sample features

Children and young people
Families
Dataset details

Country

Denmark

Year of first data collection

2000

Primary Institutions

Community Health Nurse Services

Copenhagen University Hospital (Rigshospitalet)

Research Centre for Prevention and Health (Forskningscenter for Forebyggelse og Sundhed)

Links

regionh.dk/CCC2000/English/Sider/About-CCC2000-in-short.aspx

Profile paper DOI

doi.org/10.1093/ije/dyz256

Funders

Augustinus Foundation (Augustinus Fonden)

Bagenkop-Nielsen Myopia Fund

Copenhagen County Research Foundation

County of Aarhus

Dagmar Marshalls Fond

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • 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
  • Census data
  • Education data
  • Employer data
  • Healthcare data
  • Medical birth registry
  • Other government data
  • Tax, income & benefit data
Features

Engagement

  • None
  • Keywords

    Attachment
    Behaviour
    Cognition
    Cognitive function
    Eye health
    Family environment and factors
    Feeding behaviour
    Human development
    Relationships
    Risk factors
    Stressful life events
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