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Fragile Families and Child Wellbeing Study

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The Fragile Families and Child Wellbeing Study (FFCWS) is a longitudinal birth cohort study of American children in urban areas, run by Princeton University and Columbia University. It uses a stratified random sample technique and an oversample of non-marital births.[1] Baseline data collection ran from 1998–2000, with interviews with both biological parents shortly after the child’s birth. Follow-up interviews were conducted when the child was one, three, five, and nine years old. In addition to parents, the last three waves have included in-home assessments, child care or teacher assessments, and interviews with the child. Core aims of the study are to learn about capabilities and relationships of unmarried parents as well as how families and children fare on various health and social measures over time.

Sampling Edit

Children in the FFCWS were born in hospitals in 20 large cities across the United States. These cities were selected for diversity in child support enforcement, labor market conditions, and welfare generosity. Within each city, hospitals were sampled and births were sampled in each hospital. The study design called for an over-sample of births to unmarried couples. Thus, although non-marital births accounted for only a third of U.S. births at the time the study began, they make up around three-quarters of the Fragile Families sample. The FFCWS public data files include two sets of weights for each wave of data collection that can be used to make the sample representative of urban births nationwide.

Research Questions and Topics Edit

The Fragile Families and Child Wellbeing Study was designed primarily to address four questions of great interest to researchers and policy makers: (1) What are the conditions and capabilities of unmarried parents, especially fathers?; (2) What is the nature of the relationships between unmarried parents?; (3) How do children born into these families fare?; and (4) How do policies and environmental conditions affect families and children?

Some of the major topic areas covered are as follows:
Household Characteristics: household roster and demographics, child’s living arrangements, employment and income, housing and neighborhoods
Incarceration: current status and history of parents and new partners
Family Relationships: bio-parents relationship, new partnerships, social support, church attendance, civic participation
Parental Health and Cognitive Ability: physical health, mental health, cognitive ability
Parenting: nurturance and discipline, cognitive stimulation, relationship with child, Child Protective Services involvement
Child Health and Development: child’s use of medical care, health of child, child’s health at birth, child’s nutrition, daily routines, cognitive development, child behavior, child relationships
Child Care/Kindergarten: child care use, child care/kindergarten characteristics at 3 and 5
Elementary School (age 9, teacher and caregiver reports): school, classroom, and teacher characteristics; child’s behavior; special education services; comparative academic performance; parental involvement
Genetic Analysis: mother and child, genetic predisposition and gene-environment interaction
Program participation: TANF, food stamps, Medicaid, EITC, child support, housing

Survey Components Edit

Baseline data collection consisted of an in-person interview with the biological mother and biological fathers, usually at the hospital shortly after the child’s birth. Medical records for the mother and infant were also collected when possible.

At the one-year survey wave, the parents were each interviewed by telephone.

When the child was three, the parents were interviewed again by telephone. There was also a visit to where the child lives and an in-person interview with the child’s primary caregiver, usually the mother. The child and mother completed cognitive assessments and their heights and weights were collected. The interviewer also gathered observational data on the home environment, appearance and behaviors of the family, and the neighborhood. In 10 of the 20 cities, the child care setting was also observed and the non-parental caretaker completed a survey.

The five-year interview contained the same components as the three-year, except with the observation and survey conducted in Kindergarten classes instead of child care settings for the 10 city subsample.

Around the child’s ninth birthday, both parents were interviewed by phone. Again a home visit included a primary caregiver interview and physical and cognitive assessments of the child. The primary caregiver also filled out a paper survey. This wave also included an in-person interview with the child and the collection of saliva samples by the mother and child for DNA analysis. All families with home visits were then asked for contact information for the child’s teacher, who was mailed a survey.

This survey differs from many others in its diligence tracking non-custodial parents, generally fathers living outside the household.

Funding and Management Edit

FFCWS is a joint project of Princeton University and Columbia Universities. It is actively managed through the Center for Research on Child Wellbeing at Princeton, in the Office of Population Research (OPR), in collaboration with the Center for Health and Wellbeing at Princeton and the Columbia Population Research Center and the National Center for Children and Families (NCCF) at Columbia University. The principal investigators of the project are Sara McLanahan and Christina Paxson at Princeton and Irwin Garfinkel, Jeanne Brooks-Gunn, and Ron Mincy at Columbia.


The FFCWS is funded by the Eunice Kennedy Shriver National Institute of Child Health and Human Development and a consortium of private foundations and other government agencies.[2]

Data collection for the nine-year wave of FFCWS was administered by Westat. The previous four waves of data collection were conducted by Mathematica Policy Research and National Opinion Research Center (NORC).

Data Access Edit

Public data for the FFCWS is available for free. It is hosted in the OPR data archive, and directions for access through a quick registration process can be obtained from the Fragile Families website.

More sensitive information, such as certain geographic identifiers and contextual census data, may also be obtained on a contract basis.

Hundreds of peer-reviewed articles, books and book chapters, and dissertations or theses have been written using the data.[3]

See alsoEdit

References Edit

  1. Reichman, Nancy et al. Fragile Families: Sample and Design, Children and Youth Services Review 23(4): 303-326.
  2. Understanding Fragile Families, National Institute of Child Health & Human Development, 3 December 2010.
  3. Fragile Families Publications Archive

External links Edit

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