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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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Summary Report/Recommendations
This article provides a brief overview of a framework to incorporate data and community engagement into a targeted approach to promote equitable testing and treatment of COVID-19, and to address underlying social determinant of health risks that disproportionately burden racial minority communities.
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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Webinar
This national webinar series convened by the CDC Foundation discussed the future of public health in collaboration with the Association of State and Territorial Health Officials, the National Association of County and City Health Officials, Big Cities Health Coalition, and other public health partners to advance recommendations for a modernized U.S. public health system. The series includes four convenings, with recommendations from the Bipartisan Policy Center’s Public Health Forward.
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.
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.
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Webinar
This webinar series focuses on the Community Information Exchange (CIE) Data Equity Framework, in which the 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. Part one of the series focuses on reviewing the CIE Data Equity Framework and part two focuses on examining the application of the framework across different systems including public health, social, philanthropy, and more.
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.
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.
RELEASE DATE:
Summary Report/Recommendations
The Robert Wood Johnson Foundation established a National Commission to Transform Public Health Data Systems to reimagine how data are collected, shared, and used, and to identify the investments needed to improve health equity. Commissioners examined both the systems and the data needed to ensure public health information works for all. The commission offers recommendations for government at all levels — business, community-based organizations, philanthropy, and others — to take specific action to reimagine and modernize the public health data system. A series of white papers describe the current landscape, emerging innovations, and the opportunities for transforming and transitioning to a new public health data system.