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National Children's Study Vanguard (Pilot) Study (NCS Vanguard Study)
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Sample details

The NCS Vanguard Study was a pilot for a planned cohort study of environmental influences on child health and development. From 2009 to 2013, the study enrolled families from 43 counties across 31 states in the United States of America, including approximately 8,000 women recruited during preconception and pregnancy, 5,600 children born to these women, and 1,000 fathers of the children. Participants were followed up until 2014, and it was decided that the planned main study should not be launched. Participants from this cohort are being followed up in the Utah Children’s Project as part of Environmental influences on Child Health Outcomes (ECHO).

Study design
Cohort

Number of participants at first data collection

7,921 (women)

1,009 (fathers)

5,608 (children)

Age at first data collection

Varied (women)

Varied (fathers)

Birth (children)

Participant year of birth

Varied (women)

Varied (fathers)

Varied (children)

Participant sex
All

Representative sample at baseline?
No

Sample features

Families
Fathers
Mother-father-baby triad
Mothers
Newborns, infants and babies
Dataset details

Country

United States of America

Year of first data collection

2009

Primary Institutions

Centers for Disease Control and Prevention (CDC)

Environmental Protection Agency (EPA)

National Institute of Child Health and Human Development (NICHD)

National Institute of Environmental Health Sciences (NIEHS)

Links

nichd.nih.gov/research/supported/NCS

Funders

National Institute of Child Health & Human Development (NICHD)

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 – face-to-face
  • Interview – phone
  • Physical environment assessment (e.g. pollution, mould)
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
Features

Engagement

  • None
  • Keywords

    Anthropometry
    Behaviour
    Biological samples/biospecimens
    Chemical exposures
    Cognition
    Environmental exposures
    Family environment and factors
    Human development
    Mental health
    Neuropsychological testing
    Physical health
    Social conditions and environment

    Consortia and dataset groups

    International Childhood Cancer Cohort Consortium (I4C)
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