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Western Australian Aboriginal Child Health Survey Linked Data Study (WAACHS Linked Data Study)
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Sample details

This study aims to provide evidence-based information to Aboriginal communities across Western Australia, governments, and non-government agencies on the heterogeneous life trajectories of Aboriginal children and families. The linkage of child and carer cohorts from a historical cross-sectional survey (the WAACHS) with longitudinal health-service and social-service administrative data has created a unique and powerful data resource. There are three cohorts within the WAACHS linked data study, representing 10,489 unique individuals with any linked data (noting some cross-membership across Cohorts 1, 2, and 3). While Cohort 1 (the WAACHS children) is the primary focus, Cohort 2 (all WAACHS carers) is critical for understanding the developmental circumstances of the children (data on children and carers are linked). Cohort 3 (all other members of the household) serves to provide further contextual information. There are also two control groups: control group 1 is a random sample of non-Aboriginal children from the statutory WA Midwives Notification System matched to Cohort 1 on gender and age at a ratio of 10:1, and control group 2 were participants in the 1993 WA Child Health Survey (WA-CHS), including 2,736 4 to 16 year-old children (born 1976 to 1990) and their carers in 1,462 households.

Study design
Household panel, Cohort, Cohort - intergenerational

Number of participants at first data collection

5,289 (cohort 1 - WAACHS children)

3,690 (cohort 2 - primary carers)

1,549 (cohort 3 - other household members)

52,890 (control group 1)

2,736 (control group 2)

Age at first data collection

0 - 17 years (cohort 1 - WAACHS children)

Varied (cohort 2 - primary carers)

Varied (cohort 3 - other household members)

Varied (control group 1)

Varied (control group 2)

Participant year of birth

1982 - 2001 (cohort 1 - WAACHS children)

Varied (cohort 2 - primary carers)

Varied (cohort 3 - other household members)

Varied (control group 1)

Varied (control group 2)

Participant sex
All

Representative sample at baseline?
Cohort 1 represents Aboriginal children and adolescents, aged 0 to 17 years, living in Australia in 2000.

Sample features

Racial and ethnic minorities
Dataset details

Country

Australia

Year of first data collection

2000 (WAACHS cohorts)

1945 (linked records)

Primary Institutions

The Kids Research Institute Australia

Links

thekids.org.au/our-research/Indigenous-health/waachs/

Funders

Australian Research Council (ARC)

BHP Group Limited

National Health and Medical Research Council (NHMRC)

The Kids Research Institute Australia

Western Australia Department of Health

Ongoing?
Yes

Data types collected

mentalHealthData
qualitativeData
dataLinkage
Quantitative data collection
  • Interview – face-to-face
  • Secondary data
Qualitative data collection
  • Interviews or focus groups
Neuroimaging data collection
  • None
Linked or secondary data
  • Education data
  • Existing research data
  • Healthcare data
  • Medical birth registry
  • Mortality data
  • Police & judicial system data
  • Social care data
Features

Engagement

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

    Child protection
    Community
    Culture
    Education
    Health and wellbeing
    Human development
    Justice system
    Minority groups
    Physical health
    Trajectory
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