A measure of diet quality, independent of quantity, that can be used to assess compliance with the U.S. Dietary Guidelines for Americans and monitor changes in dietary patterns. The HEI can also be used to evaluate nutrition interventions and consumer nutrition education programs.
Weekly reports, prepared by the Center for Disease Control and Prevention (CDC), on public health information and recommendations on HIV.
CDC’S National HIV Surveillance System is the primary source for monitoring HIV trends in the United States. This interactive tool provides an effective way to disseminate data, while allowing users to observe trends and patterns by creating detailed reports, maps, and other graphics.
HIV/AIDS surveillance database maintained by the U.S. Census Bureau, which includes prevalence, incidence, and reported cases and can be filtered by population, sex, age, geographic area, and data quality.
Provides researchers access to high-quality, exposure-assessment services including, state of the art laboratory analysis of biological and environmental samples, statistical analysis, and expert consultation on exposure analysis, study design, and data analysis and interpretation. There is no cost to the investigator.
A collection of tools and resources compiled by the National Cancer Institute Implementation Science team to advance the science and improve the practice of implementation. Find research tools, practice tools, and examples of research-practice partnerships to help with everything from planning for and conducting rigorous studies to implementing evidence-based practices, programs, and interventions.
Eight common measures that can collect data to implement plans that connect park and trail infrastructure to public health goals.
A biomarker validation study of internet-based and conventional self-reports for assessing diet and physical activity.
A cooperative international effort to coordinate and leverage clinical research activities on traumatic brain injury research.
Health-related measures from Medicare claims by sex, age, dual eligibility for Medicare and Medicaid, race and ethnicity, and state/territory and county. Provides users with a quick and easy way to identify areas with large numbers of vulnerable populations and to target interventions to address racial and ethnic disparities.
A searchable database of diet and physical activity measures relevant to childhood obesity research.
These modules are designed to complement the Measures Registry and Measures Registry User Guides and assist researchers and practitioners with choosing the best measures across the four domains of the Measures Registry: individual diet, food environment, individual physical activity and physical activity environment.
User guides to help researchers select measures for studies in obesity among youth, including an overview of measurement, principles of measurement selection, case studies and resources.
MEPS is the most complete source of data on the cost and use of health care and health insurance coverage. The MEPS Household Component survey collects demographic characteristics of families and individuals in selected communities across the United States. Health care disparities can be examined for any topics within the MEPS Household Component survey.
Resources, data, statistics, and programs about violence and injury research, including prevention and applying science and real-world solutions to keep people safe, healthy, and productive.
Resources on abuse in older adults, including statistics, data, research reviews, policy, reports, and related materials.
A centralized database of death record information on file in state vital statistics offices.
A national survey on alcohol and drug use and disorders, related risk factors, and associated physical and mental disabilities.
Collects and analyzes data on a broad range of health topics to monitor trends in illness and disability and to track progress toward achieving national health objectives. A major strength of the survey lies in the ability to display these health characteristics by many demographic and socioeconomic characteristics.
The National Institute of Mental Health Data Archive (NDA) makes available human subjects data collected from hundreds of research projects across many scientific domains. NDA provides infrastructure for sharing research data, tools, methods, and analyses enabling collaborative science and discovery. De-identified human subjects data, harmonized to a common standard, are available to qualified researchers. Summary data are available to all.