Skip to content

Generation Victoria Cohort 2020s: A Statewide Longitudinal Cohort Study of Victorian Children and Their Parents

Generation Victoria Cohort 2020s. A Statewide Longitudinal Cohort of Victorian Children and Their Parents

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05394363
Acronym
GenV
Enrollment
150000
Registered
2022-05-27
Start date
2021-10-04
Completion date
2033-10-01
Last updated
2026-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Allergy and Immunology, Child Development, Child Health, Child Wellbeing, Cognition, Communicable Diseases, Congenital Abnormalities, Diet, Disability, Environmental Exposure, Genetics, Health Equity, Healthy Aging, Infant Health, Inflammation, Injuries, Intergenerational Relations, Learning, Mental Health, Noncommunicable Diseases, Obesity, Physical Fitness, Quality of Life, Reproductive Health, Social Determinants of Health

Keywords

Generation Victoria, GenV, Cohort Studies, Data Collection, Data Linkage, Child Health, Midlife Health, Children, Infants, Family, Parents, Mothers, Fathers, Life course perspective, Population Health, Longitudinal Studies, Genetics, population, Demography, Epidemiology, Health Disparity, Minority Health, Vulnerable Populations, Health Equity, Clinical Trial, Randomized Controlled Trial, Pragmatic Clinical Trial, Health Services Research, Economic Models, Value of Life, Geographic Information Systems, Social Determinants of Health, Climate Change, Built Environment

Brief summary

Generation Victoria (GenV) is a longitudinal, population-based study of Victorian children and their parents that will bring together data on a wide range of conditions ,exposures and outcomes. GenV blends study-collected, study-enhanced and linked data. It will be multi-purpose, supporting observational, interventional, health services and policy research within the same cohort. It is designed to address physical, mental and social issues experienced during childhood, as well as the antecedents of a wide range of diseases of ageing. It seeks to generate translatable evidence (prediction, prevention, treatments, services) to improve future wellbeing and reduce the future disease burden of children and adults. The GenV Cohort 2020s is open to all children born over a two-year period, and their parents, residing in the state of Victoria Australia. The GenV Cohort 2020s is preceded by an Advance Cohort of children born between 5 Dec 2020 and 3 October 2021, and their parents. This comprises all families recruited at GenV's Vanguard hospital (Joan Kirner Women's and Children's) and at birthing hospitals throughout Victoria as GenV scaled up to commence recruiting for the GenV Cohort 2020s. The Advance Cohort have ongoing and full participation in GenV for their lifetime unless they withdraw but may have less complete data and biosamples.

Detailed description

GenV aims to create large, parallel whole-of-state birth and parent cohorts for discovery and interventional research. The four cornerstones of GenV's first decade are: * Consented Cohort - Targeting all Victorian children born in a 2-year period and their parents, with the first major recruitment period targeting newborns and infants * Biosamples - Curation of residual universal biosamples and collection of new biosamples * Accessing existing data - Continuously-updated linkage to or ingestion of extensive administrative, service, geospatial and clinical datasets, including prospectively-collected datasets from before the child's birth * Early School Wave - GenV-led phenomic assessment during the child's early school years. Additional foundations activities are: * GenV-collected survey data * Integrated studies - Collaborative observational or interventional research studies embedded within or alongside GenV, with ethically-supported agreements that include arrangements for data sharing. * IT and data platforms - to support all GenV activities including user research data access. GenV focuses on 10 big issues: COVID, healthy pregnancy, healthy newborns, equity, climate & environment, mental health, healthy development, allergy & immunity, infection, and obesity & diabetes, with a cross cutting commitment of population genomics. These focus areas drive current planning for data collection but are not intended to be exhaustive and may change over the life of the project. GenV partnered with all birthing hospitals across Victoria (i.e. 58 hospital sites). In-hospital face-to-face recruitment took place during the newborn period (December 2020 - November 2023). Recruitment visits were completed by trained study staff with clinical and/or research backgrounds, including initial GenV-collected data and biosamples. GenV remains open to eligible families through phone and/or self-guided recruitment. Participant-provided data are collected digitally (e.g. via website or smart phone app) about four times per year from age 3 months to 1 year, then 6-12 monthly until 5 years, taking 3-20 minutes per session. A face-to-face visit is planned for when the index child is around 6-years of age, completed by trained study staff with clinical and/or research backgrounds. The project duration is expected to be at least 10 years and potentially lifelong for its participants, dependent on study funding and willingness to continue. GenV estimated that the sampling frame for the main Cohort 2020s would comprise 150,000 children,150,000 birthing parents, and 130,000 (i.e. for 90 percent of children) second parents. GenV's recruitment rate is around 30% of all Victorian families with an eligible child. With a current sample size of 50,000 children, calculations show that this can detect odds ratios of around 1.3 for an outcome with 1.5% prevalence and an exposure with 20% prevalence.

Interventions

None listed

Sponsors

Murdoch Childrens Research Institute
Lead SponsorOTHER
The Paul Ramsay Foundation
CollaboratorUNKNOWN
Royal Children's Hospital
CollaboratorOTHER
Victoria State Government
CollaboratorUNKNOWN
Royal Children's Hospital Foundation
CollaboratorUNKNOWN
University of Melbourne
CollaboratorOTHER
National Health and Medical Research Council, Australia
CollaboratorOTHER
Medical Research Future Fund
CollaboratorOTHER
Angliss Health Service
CollaboratorUNKNOWN
Bairnsdale Regional Health Service
CollaboratorUNKNOWN
Grampians Health - Ballarat Base Hospital
CollaboratorUNKNOWN
Bass Coast Regional Health
CollaboratorUNKNOWN
The Bays Private Hospital
CollaboratorUNKNOWN
Benalla & District Memorial Hospital
CollaboratorUNKNOWN
Bendigo Hospital
CollaboratorUNKNOWN
Box Hill Hospital
CollaboratorUNKNOWN
Cabrini Private Hospital
CollaboratorUNKNOWN
Casey Hospital
CollaboratorUNKNOWN
Castlemaine Hospital
CollaboratorUNKNOWN
Central Gippsland Health Service
CollaboratorUNKNOWN
Colac Area Health
CollaboratorUNKNOWN
Dandenong Hospital
CollaboratorUNKNOWN
Bacchus Marsh - Western Health (formerly Djerriwarrh Health Service)
CollaboratorUNKNOWN
East Grampians Health Service
CollaboratorUNKNOWN
Echuca Regional Health
CollaboratorUNKNOWN
Epworth Freemason's Private Hospital
CollaboratorUNKNOWN
Frances Perry Private Hospital
CollaboratorUNKNOWN
Peninsula Health
CollaboratorOTHER_GOV
Epworth Geelong
CollaboratorUNKNOWN
Geelong University Hospital
CollaboratorUNKNOWN
Goulburn Valley Health
CollaboratorUNKNOWN
Hamilton Base Hospital
CollaboratorUNKNOWN
Jessie McPherson Private Hospital
CollaboratorUNKNOWN
Joan Kirner Women's and Children's Hospital
CollaboratorUNKNOWN
The Kilmore & District Hospital
CollaboratorUNKNOWN
Latrobe Regional Hospital
CollaboratorUNKNOWN
Leongatha Memorial Hospital
CollaboratorUNKNOWN
Mansfield District Hospital
CollaboratorUNKNOWN
Maryborough District Health Service
CollaboratorUNKNOWN
Mercy Hospital for Women
CollaboratorUNKNOWN
Mercy Werribee Public Hospital
CollaboratorUNKNOWN
Mildura Base Hospital
CollaboratorUNKNOWN
Mitcham Private Hospital
CollaboratorUNKNOWN
Monash Medical Centre
CollaboratorOTHER
Northeast Health Wangaratta
CollaboratorUNKNOWN
The Northern Hospital
CollaboratorUNKNOWN
Northpark Private Hospital
CollaboratorUNKNOWN
Peninsula Private Hospital
CollaboratorUNKNOWN
Royal Women's Hospital
CollaboratorUNKNOWN
Sandringham & District Memorial Hospital
CollaboratorUNKNOWN
South Gippsland Hospital
CollaboratorUNKNOWN
South West Healthcare Camperdown
CollaboratorUNKNOWN
South West Healthcare Warnambool
CollaboratorUNKNOWN
St John of God Hospital Ballarat
CollaboratorUNKNOWN
St John of God Hospital Bendigo
CollaboratorUNKNOWN
St John of God Hospital Berwick
CollaboratorUNKNOWN
St John of God Hospital Geelong
CollaboratorUNKNOWN
St Vincents Private Hospital
CollaboratorUNKNOWN
Swan Hill District Hospital
CollaboratorUNKNOWN
Waverley Private Hospital
CollaboratorUNKNOWN
West Gippsland Healthcare Group
CollaboratorUNKNOWN
Grampians Health - Horsham (formerly Wimmera Health Care Group)
CollaboratorUNKNOWN
Albury Wodonga Health
CollaboratorUNKNOWN
Yarrawonga District Health Service
CollaboratorUNKNOWN
Portland District Health
CollaboratorUNKNOWN

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Days to No maximum
Healthy volunteers
Yes

Inclusion criteria

(Children): * Birth date between 4th October 2021 and 3rd October 2023 * Live at the time of recruitment * Residing in Victoria at the time of recruitment * Has a legally acceptable representative capable of understanding the informed consent document and providing consent on the child's behalf, who provides a signed and dated informed consent form (e.g. a parent/guardian) Inclusion Criteria (Adults): * Be a parent or guardian of a child who meets the eligibility criteria above * Provide a signed and dated informed consent form or have a legally acceptable representative capable of understanding the informed consent document and providing consent on the participant's behalf.

Exclusion criteria

* Children who are deceased at the time of recruitment (i.e. still born or died after birth) and their parents/guardians * Families unable to provide informed consent in any of the languages available

Design outcomes

Primary

MeasureTime frameDescription
Number of parents and children enrolled in the GenV Cohort 2020sPoint of consent until study completion (up to 10 years)Assessed by analysis of records in the study-specific Participant Relationship Management System (PRMS)
Number of participants with complete data collection at each wavePoint of consent until study completion (up to 10 years)Assessed by analysis of records in the study-specific Participant Relationship Management System (PRMS), e-Consent platform and GenV data repository
Number of participants with successful data linkage at each wavePoint of consent until study completion (up to 10 years)Assessed by analysis of records in the study-specific Participant Relationship Management System (PRMS), e-Consent platform and GenV data repository
Number of participants with the targeted biosamples received at each wavePoint of consent until study completion (up to 10 years)Assessed by analysis of records in the study-specific Participant Relationship Management System (PRMS), e-Consent platform and GenV Laboratory Information Management System (LIMS)

Secondary

MeasureTime frameDescription
Number of applications to access and analyse GenV end-user datasetsPoint of consent until study completion (up to 10 years)Assessed by analysis of the GenV data access registry
Number of collaborative observational research studies supportedPoint of consent until study completion (up to 10 years)Assessed by analysis of GenV Integrated Studies Register
Number of collaborative interventional research studies supportedPoint of consent until study completion (up to 10 years)Assessed by analysis of GenV Integrated Studies Register
Number of participants involved in concurrent observational research studies embedded within or alongside GenVPoint of consent until study completion (up to 10 years)Assessed by analysis of shared study participant relationship management system data
Number of participants involved in concurrent interventional research studies embedded within or alongside GenVPoint of consent until study completion (up to 10 years)Assessed by analysis of shared study participant relationship management system data

Countries

Australia

Contacts

CONTACTGenV Cohort Coordinator
genv@mcri.edu.au+61 1800 436 888
CONTACTGenV Cohort Design Lead
libby.hughes@mcri.edu.au+61 3 9345 4738
PRINCIPAL_INVESTIGATORMelissa Wake, MBChB, FRACP, FAHMS, MD

Murdoch Childrens Research Institute

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026