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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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Systematic Review/Meta-Analysis
This review of state data collection and reporting practices during the COVID-19 pandemic found inconsistencies and gaps in data collected by race and ethnicity. Improved standardization across the U.S.–which may come in the form of a federally-operated centralized database–would address some of the concerns in data representation of all Americans.
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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Commentary
This article outlines a framework for partnering with Indigenous nations in research and data collection and calls for the need for equitable data use agreements. The framework guidelines include (1) incorporating respect and collaboration early in negotiations; (2) recognition that specificity of terms is key to trust-building; (3) remembering that good data stewardship entails safeguarding; and (4) building sustainable relationships.