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Pittsburgh Girls Study (PGS)
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Sample details

The PGS is a longitudinal, community–based study of 2,451 girls who were initially recruited when they were between the ages of 5 and 8 years. Participants were recruited in 1999–2000 via random household sampling, with over-sampling of households in low resourced neighborhoods. The study consisted of yearly assessments that began early in development (ages 5–8 years) and extended into late adolescence/early adulthood (ages 17–20 years). In 2016, PGS researchers began a large-scale sub-study called PGS-ECHO, where any PGS participant who become pregnant or recently had a baby were invited to participate.

Study design
Cohort

Number of participants at first data collection

2,451 (participants)

Age at first data collection

5 - 8 years (participants)

Participant year of birth

1991 - 1994 (participants)

Participant sex
Female

Representative sample at baseline?
No

Sample features

Children and young people
Economically disadvantaged people
Young women
Dataset details

Country

United States of America

Year of first data collection

1999

Primary Institutions

University of Pittsburgh (Academic, United States of America)

Links

intergenstudies.pitt.edu/about-pgs

pghgirlsstudy.wixsite.com/my-site-1/people

Funders

Foreign Intelligence Surveillance Act of 1978 (FISA) (Government, United States of America)

National Heart, Lung, and Blood Institute (NHLBI) (Government, United States of America)

National Institute on Drug Abuse (NIDA) (Government, United States of America)

National Institutes of Health (NIH) (Government, United States of America)

Office of Juvenile Justice and Delinquency Prevention (Government, United States of America)

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Self-completed questionnaire – online
  • Self-completed questionnaire – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Medical birth registry
Features

Engagement

  • Community engagement
  • Keywords

    Epidemiology
    Ethnic minorities
    Human development
    Low income
    Mental health
    Poverty
    Sexual development
    Substance use
    Trauma

    Consortia and dataset groups

    Environmental influences on Child Health Outcomes (ECHO)
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