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Generation Victoria (GenV)
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Sample details

GenV is a prospective, whole-of-state, cross-generational study in Victoria (population 6.7 million, 18% of whom are 0–14 year-old children), Australia, targeting all the expected 150,000 newborns and their parents over two full years from late 2021. Since GenV targets an entire population, it covers all service sectors, geographies, morbidities, and socioeconomic and demographic groups. Although relatively affluent, the full range of advantage-disadvantage exists; Victoria’s multiple ethnicities speak more than 250 languages, around 1% identify as Aboriginal and/or Torres Strait Islander, and over 70% of parents report that their child has at least 1 ongoing health or developmental problem at every age from 2 to 15 years.

Study design
Cohort - primary caregiver and child, Biobank, Registry, Cohort - intergenerational

Number of participants at first data collection

> 120,000 (participants as of 2024)

Recruitment is ongoing

Age at first data collection

Birth (children)

Varied (mothers)

Participant year of birth

2021 - 2023 (children)

Varied (mothers)

Participant sex
All

Representative sample at baseline?
Metropolitan, regional, and rural communities of Victoria, Australia.

Sample features

Children and young people
Families
Mother and child dyad
Mothers
Dataset details

Country

Australia

Year of first data collection

2011

Primary Institutions

Murdoch Children’s Research Institute (MCRI)

University of Melbourne

Links

genv.org.au/

doi.org/10.1186/s12874-020-01111-x

Funders

Paul Ramsay Foundation

The Royal Children’s Hospital Foundation (RCHF)

Victorian Government

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – unspecified
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Education data
  • Healthcare data
  • Medical birth registry
  • Mortality data
  • Other government data
  • Police & judicial system data
Features

Engagement

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

    Biological samples/biospecimens
    Breastfeeding
    Diet and nutrition
    Health and wellbeing
    Human development
    Maternal health
    Physical health
    Pregnancy outcomes
    Prenatal exposures
    Prenatal risk factors
    Respiratory health and disease
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