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.
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.
Study Type
OBSERVATIONAL
Enrollment
150,000
Murdoch Children's Research Institute
Parkville, Victoria, Australia
RECRUITINGNumber of parents and children enrolled in the GenV Cohort 2020s
Assessed by analysis of records in the study-specific Participant Relationship Management System (PRMS)
Time frame: Point of consent until study completion (up to 10 years)
Number of participants with complete data collection at each wave
Assessed by analysis of records in the study-specific Participant Relationship Management System (PRMS), e-Consent platform and GenV data repository
Time frame: Point of consent until study completion (up to 10 years)
Number of participants with successful data linkage at each wave
Assessed by analysis of records in the study-specific Participant Relationship Management System (PRMS), e-Consent platform and GenV data repository
Time frame: Point of consent until study completion (up to 10 years)
Number of participants with the targeted biosamples received at each wave
Assessed by analysis of records in the study-specific Participant Relationship Management System (PRMS), e-Consent platform and GenV Laboratory Information Management System (LIMS)
Time frame: Point of consent until study completion (up to 10 years)
Number of applications to access and analyse GenV end-user datasets
Assessed by analysis of the GenV data access registry
Time frame: Point of consent until study completion (up to 10 years)
Number of collaborative observational research studies supported
Assessed by analysis of GenV Integrated Studies Register
Time frame: Point of consent until study completion (up to 10 years)
Number of collaborative interventional research studies supported
Assessed by analysis of GenV Integrated Studies Register
Time frame: Point of consent until study completion (up to 10 years)
Number of participants involved in concurrent observational research studies embedded within or alongside GenV
Assessed by analysis of shared study participant relationship management system data
Time frame: Point of consent until study completion (up to 10 years)
Number of participants involved in concurrent interventional research studies embedded within or alongside GenV
Assessed by analysis of shared study participant relationship management system data
Time frame: Point of consent until study completion (up to 10 years)
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