During 1999 and 2000, researchers at the University of Minnesota School of Public Health conducted a study to determine what data was available to states for tracking the status of people without health insurance.
Key Findings and Recommendations
The investigators found the following:
- State-specific data drive state health policy, but states with few resources must rely on national data that do not meet their needs.
- States find privately sponsored surveys useful, but not all states are included in these surveys.
- States would like reliable, timely data that allow them to perform state-level analyses.
- States vary in their need for technical assistance.
- The researchers concluded that high-quality state data should:
- Be based on a good survey design.
- Provide state identifiers for all 50 states.
- Have a sample size large enough for valid and reliable state estimates.
- Provide timely and routine release of data.
- Provide easy access to micro-data or public use tapes for additional analysis.
The Robert Wood Johnson Foundation (RWJF) supported this project through a grant of $49,954.
After the Grant
In September 2000, the investigators established the State Health Access Data Assistance Center at the University of Minnesota.