Search Results for "Human Trafficking"
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Advancing Equity for Fathers in Human Services Programs
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This practice guide is a resource for a broad range of human services programs aiming to be more inclusive of and responsive to fathers. Building on literature from the field and interviews with human services providers that engage fathers in services, this guide outlines strategies for advancing equity in human services programs:
Measuring Success in Advancing Equity
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Health and human services policies and programs have wide-ranging effects on individuals and communities which can facilitate optimal health and well-being or impose harm, particularly for historically underserved communities.
Leading Practices to Advance Equity and Support of Underserved Communities throughout Health and Human Services Programs
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HHS Call to Action: Addressing Health-Related Social Needs in Communities Across the Nation
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The U.S. Department of Health and Human Services (HHS) envisions a future in which everyone, regardless of their social circumstances, has access to aligned health and social care systems that achieve equitable outcomes through high-quality, affordable, person-centered care. This Call to Action complements the companion U.S.
Strategies to Equitably Identify People with Lived Experience
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This tool highlights concrete strategies that health and human services staff can use to help equitably identify people with lived experience to engage.
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Recruiting Individuals with Lived Experience
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This guide highlights questions for health and human services staff to consider and discuss as a team before recruiting individuals with lived experience, as well as key content to consider including in outreach materials.
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What Does it Look Like to Equitably Engage People with Lived Experience?
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This tool contrasts components of ideal, equitable engagements with components of inequitable engagements, which health and human services staff can use to identify opportunities to strengthen efforts to engage people with lived experience.
Glossary of Common Data-Related Terms
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The Department of Health and Human Services (HHS) has several different policy groups such as the HHS Data Council, Data Governance Board, Evidence and Evaluation Policy Council, and the HHS AI Council that frequently use many terms related to data, but likely with inconsistent understanding of their definitions and how these terms should be used.
Severe Maternal Morbidity and Mortality-Electronic Health Record (EHR) Data Infrastructure
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Severe Maternal Morbidity and Mortality-Electronic Health Record (EHR) Data Infrastructure
Training Data for Machine Learning to Enhance Patient-Centered Outcomes Research (PCOR) Data Infrastructure
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Creating a Foundation to Advance the use of Artificial Intelligence for Patient Centered Outcomes Research and Clinical Practice
Linking State Medicaid and Child Welfare Data for Outcomes Research on Treatment for Opioid Use Disorder and Other Behavioral Health Issues
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Enhance Data Infrastructure and Increase Data Availability for Research on Parents with Substance Use Disorders
Enhancing Patient-Centered Outcomes Research (PCOR): Creating a National Small-Area Social Determinants of Health Data Platform
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Develop a Consolidated Set of National Standardized Databases on Valid and Reliable Social Determinants of Health Factors at the
SHIELD - Standardization of Lab Data to Enhance Patient-Centered Outcomes Research and Value-Based Care
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Improving the Quality, Interoperability and Portability of Laboratory Data within and Between Institutions
Improving Beneficiary Access to Health Information: A Plan to Enhance “Blue Button”
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Empowering patients by re-designing the Centers for Medicare & Medicaid Services Blue Button to enable it as a ‘Data-as-a-Ser
Assessing and Predicting Medical Needs in a Disaster
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Develop a Data Platform to Conduct Patient Centered Outcomes Research Related to Medically Related Disaster Response and Recovery
Beta Testing the Multi-Payer Claims Database (MPCD)
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Consolidating data and evaluating the utility of the Multi-Payer Claims Database.
Development of Data Infrastructure for Use of Electronic Health Records (EHRs) in Comparative Effectiveness Research (CER)
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Establishing an infrastructure for the use of electronic health records in clinical comparative effectiveness research.
Comparative Effectiveness Research (CER) Inventory
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Evaluating the performance of Comparative Effectiveness Research Inventory against other databases.
Collection of Patient-Provided Information through a Mobile Device Application for Use in Comparative Effectiveness and Drug Safety Research
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Creating infrastructure for collecting data from patients through a mobile device application and enhancing data linkages.
Harmonization of Various Common Data Models and Open Standards for Evidence Generation
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Building data infrastructure for conducting patient centered outcomes research using observational data derived from the delivery