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Victorian Infant Collaborative Study 1997 cohort (VICS 1997 cohort)
Victorian Infant Collaborative Study 1997 cohort logo
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Sample details

The VICS aims to better understand the long-term health outcomes of extremely preterm (EP; before 28 weeks of pregnancy) or extremely low birth weight (ELBW; <1000 g) babies born in Victoria, Australia. VICS includes several cohorts recruited in distinct birth eras (from 1979-80 to the most recent 2023 cohort). The VICS 1997 cohort includes approximately 200 EP/ELBW infants born in Victoria in 1997, and 200 term-born infants. birth. Perinatal data were collected, and participants were followed up at ages 2, 8 and 18 years.

Study design
Cohort, Cohort - birth

Number of participants at first data collection

201 (EP/ELBW participants)

199 (term-born control participants)

Age at first data collection

Birth (EP/ELBW participants)

Birth (term-born control participants)

Participant year of birth

1997 (EP/ELBW participants)

1997 (term-born control participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Control participants
Low birthweight infants
Newborns, infants and babies
Preterm infants
Dataset details

Country

Australia

Year of first data collection

1997

Primary Institutions

Joan Kirner Women’s and Children’s Hospital

Mercy Hospital for Women

Monash Medical Centre

Royal Children's Hospital (RCH)

Royal Women’s Hospital

Links

vicsinfant-study.org.au/

medicine.unimelb.edu.au/research-groups/obstetrics-and-gynaecology-research/victorian-infant-collaborative-study

doi.org/10.1542/peds.2012-2311

Profile paper DOI

doi.org/10.1002/ppul.22619

Funders

National Health and Medical Research Council (NHMRC)

Royal Women's Hospital

Ongoing?
No

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – online
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
Features

Engagement

  • Community engagement
  • Keywords

    Birth records and measurement
    Cardiovascular health and disease
    Human development
    Lung health
    Mental health
    Neurodevelopment
    Parental wellbeing
    Respiratory health and disease
    Sociodemographics

    Consortia and dataset groups

    Adults Born Preterm International Collaboration (APIC)
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