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Raine Study
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Sample details

The aim of the Raine Study was to develop a large cohort of Western Australian children studied from 18 weeks’ gestation to ascertain the relative contributions of familial risk factors, fetal growth, placental development, and environmental insults to outcome in infancy and to the precursors of adult morbidity. Between 1989 and 1991, 2,900 pregnant women volunteered to be part of the study at King Edward Hospital in Western Australia, looking at prenatal ultrasound scans when they were 18 weeks pregnant. During this time, information was collected on both the mother and the father. Some of the mothers were followed up at 24, 28, and 38 weeks gestation and the families then continued with follow-up assessments of their babies. A total of 2,868 babies remained with the study and were examined on the first or second day after birth. Since then, the babies born into the study (Gen2) have been followed up at 1, 2, 3, 5, 8, 10, 14, 17, 18, 20, 22, 25, 27, and now 28 years of age. Likewise, data has been collected on their parents (Gen1), their grandparents (Gen0) and now also their own children (Gen3).

Study design
Cohort - intergenerational, Cohort - birth

Number of participants at first data collection

2,868 (children)

2,900 (mothers)

Age at first data collection

Birth (children)

Varied (mothers)

Participant year of birth

1989 - 1991 (children)

Varied (mothers)

Participant sex
All

Representative sample at baseline?
The Western Australian population at the age and times data collection occurred.

Sample features

Children and young people
Pregnant people
Dataset details

Country

Australia

Year of first data collection

1989

Primary Institutions

Flinders University

University of Newcastle

University of Western Australia (UWA)

Links

rainestudy.org.au/

web.archive.org/web/20250312024412/https://lifecourse.org.au/cohorts/raine/

doi.org/10.1186/s12889-015-1944-6

Profile paper DOI

doi.org/10.1093/ije/dyw308

Funders

ADA Bartholomew Medical Research Trust

Asthma Foundation

Australian Arthritis Foundation

Australian Research Council (ARC)

Australian Rotary Health (ARH)

Ongoing?
Yes

Data types collected

neuroImagingData
mentalHealthData
qualitativeData
dataLinkage
Quantitative data collection
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
Qualitative data collection
  • Interviews or focus groups
Neuroimaging data collection
  • Magnetic Resonance Imaging (MRI)
Linked or secondary data
  • Education data
  • Healthcare data
Features

Engagement

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

    Biological samples/biospecimens
    Diet and nutrition
    Education
    Environment
    Genetics
    Hormones
    Human development
    Physical health
    Pregnancy outcomes
    Risky behaviours
    Work and employment
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