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1970 British Cohort Study (BCS70)
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Sample details

BCS70 follows the development and life experiences of a group born in a single week in 1970 in England, Scotland, and Wales. Those born in Northern Ireland were included in the birth sweep but were not followed up in subsequent sweeps. The initial cohort comprised of around 17,000 participants with data collection at birth being conducted by midwives. Participants have been followed 10 times over 50 years, with the most recent sweep in 2021, when participants were aged 51 to 52 years. During the age 34 sweep, the children of BCS70 participants took part, making the study intergenerational.

Study design
Cohort - birth, Cohort, Cohort - intergenerational

Number of participants at first data collection

16,589 (participants)

Age at first data collection

Birth (participants)

Participant year of birth

1970 (participants)

Participant sex
All

Representative sample at baseline?
Children born in 1970 in England, Scotland and Wales.

Sample features

Dizygotic and monozygotic twins
Intergenerational
Nationally representative
Newborns, infants and babies
Dataset details
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Countries

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

Year of first data collection

1970

Primary Institutions

Centre for Longitudinal Studies (CLS)

University College London (UCL)

Links

cls.ucl.ac.uk/cls-studies/1970-british-cohort-study/

cataloguementalhealth.ac.uk/

bcs70.info/

Profile paper DOI

doi.org/10.1093/ije/dyac148

Funders

Economic and Social Research Council (ESRC)

Ongoing?
Yes

Data types collected

mentalHealthData
qualitativeData
dataLinkage
Quantitative data collection
  • Activity log (e.g. food, sleep, exercise)
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – face-to-face
  • Interview – online
  • Interview – phone
  • 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
  • Qualitative survey
Neuroimaging data collection
  • None
Linked or secondary data
  • Geographic, spatial & environmental data
  • Healthcare data
  • Mortality data
  • Tax, income & benefit data
Features

Engagement

  • Community engagement
  • Participant or community advisory groups
  • Keywords

    Biological samples/biospecimens
    Cognition
    Education
    Health and wellbeing
    Housing
    Income and expenses
    Lifecourse
    Mental health
    Parenting and family
    Physical development
    Social mobility
    Work and employment

    Consortia and dataset groups

    Catalogue of Mental Health Measures
    Centre for Longitudinal Studies (CLS) cohorts
    Social Science Genetic Association Consortium
    The Lifecourse GWAS consortium
    UCL Human Genomics centre
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