Atlas Logo
Millennium Cohort Study (UK) (MCS)
Millennium Cohort Study (UK) logo
BACK
Sample details

The MCS is a national longitudinal birth cohort study following the lives of around 19,000 young people born across England, Scotland, Wales and Northern Ireland in 2000-2002. The study began with an original sample of 18,818 children from 18,552 families selected from a random sample of electoral wards. The recruitment strategy of the cohort aimed to ensure adequate representation of all four countries of the United Kingdom, deprived areas and areas with high concentrations of Black and Asian families.

Study design
Cohort - birth

Number of participants at first data collection

18,818 (children)

Age at first data collection

9 months (children)

Participant year of birth

2000 - 2002 (children)

Participant sex
All

Representative sample at baseline?
The United Kingdom population born in 2000 - 2001.

Sample features

Adolescents
Adults
Children and young people
Dizygotic and monozygotic twins
Triplets
Dataset details
Loading map...

Countries

England, Guernsey, Isle of Man, Jersey, Northern Ireland

Year of first data collection

2001

Primary Institutions

University College London (UCL)

Links

cls.ucl.ac.uk/cls-studies/millennium-cohort-study/

cataloguementalhealth.ac.uk/

discovery.closer.ac.uk/item/uk.cls.mcs/0d8a7220-c61b-4542-967d-a40cb5aca430

Profile paper DOI

doi.org/10.1093/ije/dyu001

Funders

Department for Education (DfE)

Department for Education and Skills

Department for International Development (DFID) now known as Foreign, Commonwealth & Development Office (FCDO)

Department for Work and Pensions (DWP)

Department of Education (An Roinn Oideachais, DENI)

Ongoing?
Yes

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 – 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
  • Wearable devices
Qualitative data collection
  • Interviews or focus groups
Neuroimaging data collection
  • None
Linked or secondary data
  • Education data
  • Geographic, spatial & environmental data
  • Healthcare data
  • Medical birth registry
  • Mortality data
  • Tax, income & benefit data
Features

Engagement

  • Patients, service users, lived experience involvement
  • Participant or community advisory groups
  • Community engagement
  • Keywords

    Biological samples/biospecimens
    Early-life determinants
    Exposure - outcome associations
    Family environment and factors
    Human development
    Parental influences
    Social inequality

    Consortia and dataset groups

    Centre for Longitudinal Studies (CLS) cohorts
    Contact us

    |

    FAQS

    |

    Privacy

    |

    © 2024 Louise Arseneault

    Platform by Delosis