Research and data is one of NC Child’s core strategies to support kids and families. We provide advocates and decision-makers with reliable data to better understand child well-being.
The KIDS COUNT Data Center is an easy-to-use, powerful, online database that allows anyone to generate custom reports. You can find reports for one geographic area (Profiles), or compare different geographic areas across a specific topic (Ranking, Maps, or Line Graphs).
The database includes information on education, employment and income, health, access to health insurance, population, family characteristics, poverty, and youth risk factors.
KIDS COUNT is a national and state-by-state project of the Annie E. Casey Foundation to track the well-being of children in the United States. NC Child is the North Carolina KIDS COUNT partner. NC Child maintains and records more than 100 measures of child well-being at the state and local levels.
For 20 years, the North Carolina Child Health Report Card has served as the go-to source for top-level analysis on the health and safety of children and youth in North Carolina. The Report Card compiles 40 indicators into one easy-to-read document. It is used by policymakers, practitioners, advocates, and local communities to monitor changes in child-health outcomes, uncover emerging data trends, and support strategic planning for future investments. NC Child partners with the North Carolina Institute of Medicine to produce this report every other year.
In partnership with the NC Division of Public Health, NC Child has developed a tool to help fight persistent racial disparities in health outcomes. The North Carolina Health Equity Impact Assessment helps decision-makers focus their efforts, and align their strategies, to get the best possible outcomes for families of all races and ethnic backgrounds.