A set of person-centered measures that evaluates and monitors physical, mental, and social health in adults and children. It can be used with the general population and with individuals living with chronic conditions.
Activities Completed over Time in 24-hours (ACT24) is a web-based previous-day recall instrument that was designed to estimate daily summary values for physical activity and sedentary behavior, including energy expenditure, time spent sitting and in different types and intensities of physical activity.
These maps use combined data from 2017 through 2020 from the Behavioral Risk Factor Surveillance System. Survey respondents were classified as physically inactive if they reported no physical activity outside their regular job in the last month.
Provides interactive views of the publicly available All of Us Research Program participant data. Currently, participant-provided information, including data from surveys, wearables, physical measurements taken at the time of participant enrollment, and electronic health records (EHR) are available. EHR data are reported by health care providers and are not participant reported. In order to protect participant privacy, the data are de-identified, limited to aggregate counts rounded up to counts of 20, and summary demographic information.
A cloud-based platform where registered researchers can access Registered and Controlled Tier data, perform queries and analysis, organize and collaborate on research projects, build datasets, and create and annotate groups of participant data.
Provides easy access to national and state level CDC data on a range of key indicators of health and well-being for older adults, including caregiving, subjective cognitive decline, screenings and vaccinations, and mental health. These indicators provide a snapshot of currently available surveillance information and can be useful for prioritization and evaluation of public health interventions.
List of tools to help researchers analyze data developed by the National Cancer Institute (NCI) Division of Cancer Epidemiology and Genetics (DCEG).
Enables multiple, automatically coded, self-administered 24-hour recalls. The ASA24 system is freely available for use by researchers, clinicians, and teachers.
The nation’s premier system of health-related telephone surveys that collect state data about U.S. residents regarding their health-related risk behaviors, chronic health conditions, and use of preventive services.
A glossary that captures the distinctions between biomarkers and clinical assessments and describes their distinct roles in biomedical research, clinical practice, and medical product development.
National data trends that examine obesity prevention and reducing the risk of certain types of cancer, and improving cancer outcomes.
Publicly available datasets relevant to childhood obesity research, including obesity-related health behaviors, outcomes, and determinants; and policies and environmental factors.
This index is a customized version of the Centers for Disease Control and Prevention/Agency for Toxic Substances and Disease Registry Social Vulnerability Index (CDC/ATSDR SVI). Minority Health SVI uses data from the United States Census Bureau and other public sources to help identify communities that may need support before, during, and after disasters, with a focus on minority racial, ethnic, and language groups as well as medical vulnerability.
A comprehensive list of national and international surveys on tobacco use, smoking cessation, secondhand smoke exposure, and other tobacco-related topics among youth, adults, and specific populations.
Provides many public health data sets to researchers and the public, including access to preliminary mortality estimates from the National Center for Health Statistics (NCHS). CDC WONDER can be valuable in public health research, decision making, priority setting, program evaluation, and resource allocation. Access statistical research data published by CDC, as well as reference materials, reports and guidelines on health-related topics. Search public-use data sets about deaths, cancer incidence, HIV and AIDS, tuberculosis, vaccinations, births, census data and more.
A repository of data from environmental health academic, industrial, and government laboratories to support study design and data integration for novel meta analysis.
An integrated, curated bibliographic database of global peer-reviewed research and gray literature on the science of climate impacts on human health.
A database that archives and distributes the data and results from studies that have investigated the interaction of genotype and phenotype in humans.
A freely available food frequency questionnaire (FFQ). The most recent version, DHQ III, can be used by researchers, clinicians, or educators to assess food and dietary supplement intakes.
A register of calibration/validation studies and publications which compare dietary intake estimates from two or more dietary assessment methods.