Data

The RAINE Study

RAINE Study

Dataset description

The Raine Study: A multi-generational life-course study utilising rich genetic, phenotypic (cardiometabolic, respiratory, immunological, musculoskeletal, psychological, hormonal, reproductive, vision, hearing), behavioural (sleep, activity, diet, risky behaviour), environmental (chemical, spatial, social) and education and work data to improve human health and well-being.

Date Information

Issued from 2026-02-03
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Source Study

Trial acronym

Not available

Trial ID

ACTRN12617001599369

Funding

Government body, National Health and Medical Research Council of Australia

Scientific enquiries

Ms Blagica Penova-Veselinovic

Brief Summary

In 1989 Professor John Newnham and colleagues invited more than 3000 pregnant women to join a National Health and Medical Research Council funded research study at King Edward Memorial Hospital to examine the possible beneficial effects of repeated fetal ultrasound imaging studies. Women were allocated at random into one of two groups – Regular Care or Intensive Care. Those in the Regular Care group had a single ultrasound imaging study at 18 weeks gestation, with further scans only if clinicall .... Read more

Key Inclusion Criteria

Generation 1 - 18 weeks pregnant and attending King Edward Memorial Hospital in Perth, Western Australia or surrounding clinics during 1989-1991; anticipating giving birth in Perth; sufficiently understands English and gives consent. Generation 2 - live born child of Generation 1 pregnancy listed above Generation 3 - all biological children of Generation 2 participants Generation 2B - other biological parent of the Generation 3 participant Generation 0 - grandparents of Generation 2

Key Exclusion Criteria

Generation 1: Pregnancy did not result in live birth. Generation 2: none. Generation 3: none. Generation 2B: none

Can healthy volunteers participate?

Yes

Population

Sample Size    5000

Min. age    No limit

Max. age    No limit

Sex    Both males and females

Condition category    genetic conditions , cardiometabolic conditions , respiratory conditions , immunological and inflammatory conditions , hormonal and reproduction conditions , musculoskeletal conditions , psychological conditions , vision conditions , hearing conditions

Condition code    Human Genetics and Inherited Disorders , Cardiovascular , Metabolic and Endocrine , Respiratory , Inflammatory and Immune System , Reproductive Health and Childbirth , Musculoskeletal , Mental Health , Eye , Public Health

Intervention

Intervention code Not applicable

Four Generations are currently involved in the Raine Study: Generation 1 - women (and their partners) presenting to King Edward Memorial Hospital and surrounding private clinics in Perth, Western Australia who were between 16 and 20 weeks pregnant. 2,900 women were recruited between May 1989 and November 1991. In 2017 average age was 56 years (range 40-80). Assessments may continue every 3-5 years until death. Enrolment for Generation 1 participants is closed; they can choose to participate in a ....
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Comparison

Control group Uncontrolled

No control group

Outcomes

Outcome: Physical health status for example: Height was measured by neonatometer for infants and stadiometer for children and adults.
Timepoint: Generation 1 - across adulthood from pregnancy onwards. For example height was assessed at 5, 8, 14, 17 and 26 year follow-ups. Generation 2 - from 18 weeks gestation onwards across the life-course. For example height was assessed at follow-ups 1, 2, 3, 5, 8, 10, 14, 17, 20, 22, 27 years. Generation 3 - across the life-course. For ....

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Outcome: Mental health status for example: Child mental health was measured by parent-reported Child Behaviour Checklist
Timepoint: Generation 1 - across adulthood from pregnancy onwards. Generation 2 - from 18 weeks gestation onwards across the life-course. For example Child Behaviour Checklist was assessed at follow-ups 3, 5, 8, 10, 14 years. Generation 3 - across the life-course. Generation 0 - at current collection

Outcome: Behaviour outcomes For example: self reported physical activity was assessed by International Physical Activity Questionnaire
Timepoint: Generation 1 - across adulthood from pregnancy onwards. Generation 2 - from 18 weeks gestation onwards across the life-course. For example International Physical Activity Questionnaire at 14, 17, 20, 22, 27 year follow-ups. Generation 3 - across the life-course.

Will the study consider sharing individual participant data?

Yes

Who can request access to individual participant data?

Data is available to investigators on approved projects, conditional on investigators agreeing to a code of conduct

Are there any conditions for requesting access to individual participant data?

-

What individual participant data might be shared?

Individual participant data not covered above

All Raine Study data is available for use in projects approved by the Raine Study through its Raine Online Submission System

What types of analyses could be done with individual participant data?

no specific limitations on types of analyses that could be performed.

Are there extra considerations when requesting access to individual participant data?

No

When can requests for individual data be made (start and end dates)?

From: Data is available in 2019 and planned to be available forever

To: -

Source study information is derived from the Australian New Zealand Clinical Trials Registry (ANZCTR). For more information on the ANZCTR, please see anzctr.org.au

How is Heath Data Australia supporting health research?

To assist secondary data users in understanding the real-world impact of health and medical research data sharing, the Australian Research Data Commons (ARDC) has created an online guide that outlines a theoretical framework for four key data reuse scenarios. This practical guide was extracted from research papers, and consultation with stakeholders and the research community.

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How to access data via Health Data Australia

With Health Data Australia, researchers can explore descriptions of data from our publishing partners, identify relevant datasets, and request access. These requests will then be forwarded to the data owner for review.

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