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Australian Aboriginal Birth Cohort (ABC)
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Sample details

The Australian ABC is a birth cohort of Indigenous Australians. Babies were eligible for enrolment if they were a singleton born between January 1987 and March 1990 to a mother self-identified as either Aboriginal or Torres State Islander, referred collectively as Indigenous. As of February 2024, cohort members have been followed up four times since baseline.

Study design
Cohort - birth

Number of participants at first data collection

686 (participants)

Age at first data collection

Birth (children)

Varied (mothers)

Participant year of birth

1987 - 1990 (children)

Varied (mothers)

Participant sex
All

Representative sample at baseline?
No

Sample features

Adolescents
Children and young people
Racial and ethnic minorities
Dataset details

Country

Australia

Year of first data collection

1987

Primary Institutions

Charles Darwin University

Links

lifecoursemenzies.net.au/studies/aboriginal-birth-cohort

web.archive.org/web/20250312023906/https://lifecourse.org.au/cohorts/abc/

bmcinthealthhumrights.biomedcentral.com/articles/10.1186/1472-698X-9-23

Profile paper DOI

doi.org/10.1093/ije/dyw291

Funders

National Health and Medical Research Council (NHMRC)

Channel 7 Children's Research Foundation of South Australia

Colonial Foundation

Diabetes Australia

National Heart Foundation of Australia

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)
  • Self-report questionnaire – online
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Education data
  • Other government data
  • Police & judicial system data
  • Social care data
Features

Engagement

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

    Biological samples/biospecimens
    Chronic illness
    Minority groups
    Noncommunicable diseases
    Pregnancy outcomes

    Consortia and dataset groups

    Life Course Program
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