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Promising Practices that show evidence of effectiveness in improving public health outcomes in a specific real-life setting, as indicated by achievement of aims consistent with the objectives of the activities, and are suitable for adaptation by other communities.
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Data Collection Tool
The Coronavirus Disease 2019 (COVID-19)-Associated Hospitalization Surveillance Network (COVID-NET) conducts population-based surveillance for laboratory-confirmed COVID-19-associated hospitalizations in children (less than 18 years of age) and adults. The data can be used for data collection and analysis and is available by race, age, and sex. COVID-NET covers nearly 100 counties in the 10 Emerging Infections Program states (CA, CO, CT, GA, MD, MN, NM, NY, OR, TN) and four Influenza Hospitalization Surveillance Project states (IA, MI, OH, and UT).
Promising Practices that show evidence of effectiveness in improving public health outcomes in a specific real-life setting, as indicated by achievement of aims consistent with the objectives of the activities, and are suitable for adaptation by other communities.
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Data Collection Tool
This case surveillance public use dataset can be used for data collection and analysis. The dataset includes 12 elements for all COVID-19 cases shared with the Centers for Disease Prevention and Control and includes demographics, any exposure history, disease severity indicators and outcomes, presence of any underlying medical conditions and risk behaviors, and no geographic data.
Promising Practices that show evidence of effectiveness in improving public health outcomes in a specific real-life setting, as indicated by achievement of aims consistent with the objectives of the activities, and are suitable for adaptation by other communities.
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Data Collection Tool
This dashboard provides national-level demographic COVID-19 vaccination data for data collection and analysis. The data is available by race, sex, and age.
Promising Practices that show evidence of effectiveness in improving public health outcomes in a specific real-life setting, as indicated by achievement of aims consistent with the objectives of the activities, and are suitable for adaptation by other communities.
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Data Collection Tool
The National Healthcare Quality and Disparities Reports (NHQDR) is a resource that provides reports, state snapshots, and national summaries across quality measures to provide a set of data tools to assist in focusing efforts on identifying areas where the healthcare system has distributed services inefficiently and unevenly across populations in the United States.
Promising Practices that show evidence of effectiveness in improving public health outcomes in a specific real-life setting, as indicated by achievement of aims consistent with the objectives of the activities, and are suitable for adaptation by other communities.
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Data Collection Tool
The Mapping Medicare Disparities (MMD) Population View provides a user-friendly way to explore and better understand disparities in chronic diseases, and allows users to: (1) visualize health outcome measures at a national, state, or county level; (2) explore health outcome measures by age, sex, race and ethnicity; (3) compare differences between two geographic locations (e.g., benchmark against the national average); and (4) compare differences between two racial and ethnic groups within the same geographic area.
Promising Practices that show evidence of effectiveness in improving public health outcomes in a specific real-life setting, as indicated by achievement of aims consistent with the objectives of the activities, and are suitable for adaptation by other communities.
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Data Collection Tool
The Neighborhood Atlas website was created in order to freely share measures of neighborhood disadvantage with the public, including educational institutions, health systems, not-for-profit organizations, and government agencies, in order to make these metrics available for use in research, program planning, and policy development. The Area Deprivation Index allows for rankings of neighborhoods by socioeconomic disadvantage in a region of interest (e.g., at the state or national level). It includes factors for the theoretical domains of income, education, employment, and housing quality.
Best Practices that show evidence of effectiveness in improving public health outcomes when implemented in multiple real-life settings, as indicated by achievement of aims consistent with the objectives of the activities.
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Toolkit
The PhenX Social Determinants of Health (SDOH) Assessments Collection, now available in the PhenX Toolkit, contains protocols to help measure upstream factors that shape behaviors and health outcomes. The PhenX Toolkit provides recommended standard data collection protocols for conducting biomedical research. The protocols are selected by working groups of domain experts using a consensus process, which includes the scientific community. The toolkit provides detailed protocols for collecting data and tools to help investigators incorporate these protocols into their studies. Using protocols from the PhenX Toolkit facilitates cross-study analysis, potentially increasing the scientific impact of individual studies.
Emerging Practices that show potential to achieve desirable public health outcomes in a specific real-life setting and produce early results that are consistent with the objectives of the activities and thus indicate effectiveness.
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Toolkit
This data dashboard provides a map that details which states are reporting race and ethnicity in their case, mortality, testing, and vaccination data, and includes a state action chart that provides information on how states plan to focus on equity beyond the COVID-19 pandemic.
Novel Practices that show potential to achieve desirable public health outcomes in a specific real-life setting and are in the process of generating evidence of effectiveness or may not yet be tested.
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Toolkit
The toolkit describes positive and problematic practices for centering racial equity across the six stages of the data life cycle: (1) data collection, (2) data access, (3) use of algorithms and statistical tools, (4) data analysis, and (5) reporting and dissemination.
Novel Practices that show potential to achieve desirable public health outcomes in a specific real-life setting and are in the process of generating evidence of effectiveness or may not yet be tested.
RELEASE DATE:
Toolkit
The Community Information Exchange (CIE) Data Equity Framework’s goal is to build data systems to help institutions, and the communities they serve, approach CIE® planning and systems change work from a place of anti-racism by: (1) naming how data system design reflects understanding of and participation by the intended beneficiaries of current programs and interventions; (2) acknowledging and documenting the effects of a spectrum of data system design types on oppressed populations and communities; (3) identifying strategies needed to eliminate the harm of current processes and practices; (4) highlighting the behavior change needed to rebuild or change the overall data system to better meet community needs across racial and ethnic populations; and (5) adopting practices that promote restorative justice and mitigate harm and exploitation.