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National Youth in Transition Database (NYTD)
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Sample details

NYTD is designed to follow the outcomes of youth exiting the foster care system as they become adults. The study recruits youths from across the United States of America in the foster system who turn 17 years old in the baseline year and surveys them three times: at age 17, at age 19, and finally, at age 21. The study begins with a new cohort every three years. As of 2024, NYTD has cohorts beginning in 2011, 2014, 2017, and 2020. Participants were from all fifty states, including Puerto Rico and the District of Columbia. Participants self-identified as various ethnicities, including American Indian, Asian, black or African American, white, Pacific Islander, and native Hawaiian. Participants of the four cohorts were born in 1994, 1997, 2000, and 2003.

Study design
Cohort - accelerated

Number of participants at first data collection

15,596 (FY2011 cohort)

16,480 (FY2014 cohort)

16,276 (FY2017 cohort)

14,796 (FY2020 cohort)

Age at first data collection

17 years (participants)

Participant year of birth

1994 (FY2011 cohort)

1997 (FY2014 cohort)

2000 (FY2017 cohort)

2003 (FY2020 cohort)

Participant sex
All

Representative sample at baseline?
No

Sample features

Ethnically diverse populations
Multi-site
Young adults
Dataset details

Country

United States of America

Year of first data collection

2011 (FY2011 cohort)

2014 (FY2014 cohort)

2017 (FY2017 cohort)

2020 (FY2020 cohort)

Primary Institutions

Cornell University

Department of Health & Human Services (HHS)

Links

acf.hhs.gov/cb/research-data-technology/reporting-systems/nytd

ndacan.acf.hhs.gov/datasets/datasets-list-nytd.cfm

ndacan.acf.hhs.gov/datasets/pdfs_user_guides/dataset284-nytd-services-users-guide.pdf

Profile paper DOI
Not available

Funders

United States Children's Bureau

Administration for Children and Families (ACF)

Administration for Children and Families (ACF)

Department of Health and Human Services (HHS)

Ongoing?
Yes

Data types collected

dataLinkage
Quantitative data collection
  • Secondary data
  • Self-report questionnaire – unspecified
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Social care data
Features

Engagement

  • None
  • Keywords

    Education
    Finances
    Foster care
    Human development
    Life outcomes
    Service use
    Social welfare
    Work and employment
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