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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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Peer Review Study
This study used machine learning to analyze electronic health records from an urban academic medical center and to investigate whether providers’ use of negative patient descriptors varied by patient race or ethnicity.
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.
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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Blog
This blog highlights how states have analyzed and used race and ethnicity data to respond to COVID-19 disparities. The blog also includes a tracker of states’ public reporting of COVID-19 by race and ethnicity.
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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Blog
This blog highlights examples of how states are using data to inform their health equity approaches.
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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Blog
This blog highlights the approaches taken and experiences of state officials in Minnesota and North Carolina in developing COVID-19 immunization data systems, including data challenges, successes, and implications for ensuring an equitable vaccine rollout now and in the future.
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.
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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.
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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White Paper/Brief
The brief summarizes state-level strategies to increase equity in vaccination rates using four primary approaches. The second approach addresses using race and ethnicity data to allocate COVID-19 vaccines according to need. Four strategies are explained under this approach.