Search Results for "Poverty Guidelines, Research"
Displaying 581 - 600 of 9460 results. 20 results shown per page. Page 30 of 473.
Expanding Data Collection for the National Program of Cancer Registries (NPCR) for Comparative Effectiveness Research (CER)
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Enhancing state cancer registries to collect specialized data and expanding electronic health record reporting to central cancer
HHS Roadmap for Behavioral Health Integration
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This brief introduces the HHS Roadmap for Behavioral Health Integration, which advances the President’s Strategy to Address our National Mental Health Crisis. It provides a general overview of the approach HHS is taking to drive toward integrated care within the three pillars of the President’s Strategy and highlights selected programs and policy actions that will get us there.
The Feasibility of Using Electronic Health Data for Research on Small Populations
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ASPE REPORT The Feasibility of Using Electronic Health Data for Research on Small Populations September 2013 By: Kelly Devers, Bradford Gray et. Al. Disclaimer
Incarceration and the Family: A Review of Research and Promising Approaches for Serving Fathers and Families
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Prepared for U.S. Department of Health and Human Services (HHS)Assistant Secretary for Planning and Evaluation (ASPE)Administration for Children and Families/Office of Family Assistance
Peer Support as a Social Capital Strategy for Programs Serving Individuals Reentering from Incarceration and Survivors of Intimate Partner Violence or Human Sex Trafficking
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Many human services programs recognize the power of “social capital,” or the value that arises from relationships. This report offers insight into how programs use peer supports to help build social capital with participants who are reentering the community after incarceration or are survivors of intimate partner violence or sex trafficking.
Research Summit on Dementia Care: Day 3 Recommendations Review Session
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This is the PDF version of the National Research Summit on Care, Services, and Supports for Persons with Dementia and Their Caregivers paper from the Recommendations Review Session. This Session was held on October 18 (Day 3), and was attended by the Summit Co-Chairs and each of the Session Chairs.
Research on Care Coordination for People with Dementia and Family Caregivers
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This is the PDF version of a Session Background Paper prepared for the National Research Summit on Care, Services, and Supports for Persons with Dementia and Their Caregivers (also called the Research Summit on Dementia Care).
Estimates of Uninsured Adults Newly Eligible for Medicaid If Remaining 12 Non-Expansion States Expand Medicaid: 2022 Update
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This Data Point presents updated estimates of potential Medicaid eligibility among uninsured, non-elderly adults in states that have not expanded Medicaid coverage to adults with incomes up to 138% of the federal poverty level as of 2022. This analysis updates a previous Data Point by accounting for Medicaid expansion in two states, Missouri and Oklahoma, in 2021.
Valuing COVID-19 Mortality and Morbidity Risk Reductions in U.S. Department of Health and Human Services Regulatory Impact Analyses
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This report develops an approach for valuing COVID-19 mortality and morbidity risk reductions based on the U.S. Department of Health and Human Services (HHS) Guidelines for Regulatory Impact Analysis. Valuing risk reductions associated with regulations or other policies that address the novel coronavirus disease 2019 (COVID-19) presents major challenges.
Top Six Research Outcomes: Family Caregiver Stakeholder Workgroup
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This is the PDF version of a Stakeholder Group Paper prepared for the National Research Summit on Care, Services, and Supports for Persons with Dementia and Their Caregivers (also called the Research Summit on Dementia Care).
National Center for Marriage Research: Announcement of 2007 Award
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Announcement of Award of Fiscal Year 2007
Public Comments from Advisory Council Meeting, July 2022
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Research on Care Needs and Supportive Approaches for Persons with Dementia
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This is the PDF version of a Session Background Paper prepared for the National Research Summit on Care, Services, and Supports for Persons with Dementia and Their Caregivers (also called the Research Summit on Dementia Care).
Human-Centered Design Study on Federal Data Access and Acquisition Processes of CMS Data
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Human-Centered Design Study on Federal Data Access and Acquisition Processes of CMS Data
¡Cuídate!: Impact Findings from the Teen Pregnancy Prevention Replication Study (Research Brief)
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This research brief highlights findings from the evaluation of ¡Cuídate!, an HIV/AIDS prevention program that uses an approach culturally tailored to Latino youth. The study examined data from three different replications of ¡Cuídate!, pooling the data to examine the overall program impact.
RESEARCH AGENDA: Managed Care
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U.S. Department of Health and Human Services RESEARCH AGENDA: Managed Care Andreas Frank U.S. Department of Health and Human Services January 1995 PDF Version (37 PDF pages)
Welfare Indicators and Risk Factors, 21st Report to Congress
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This report provides welfare dependence indicators through 2019 for most indicators and through 2020 for other indicators, reflecting changes that have taken place since enactment of the Personal Responsibility and Work Opportunity Reconciliation Act (PRWORA) in 1996.
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.
Methods and Emerging Strategies to Engage People with Lived Experience
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This brief identifies methods and emerging strategies to engage people with lived experience in federal research, programming, and policymaking. It draws on lessons learned from federal initiatives across a range of human services areas to identify ways that federal staff can meaningfully and effectively engage people with lived experience.
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Data Capacity for Patient-Centered Outcomes Research through Creation of an Electronic Care Plan for People with Multiple Chronic Conditions
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Building Data Capacity to Conduct Pragmatic, Patient Centered Outcomes Research by Developing an Interoperable Electronic (eCare) Pla