Regulatory impact analyses (RIAs) apply a well-established and widely-used framework for collecting, organizing, and evaluating data on the anticipated consequences of alternative policies. They help ensure that regulatory actions are justified and necessary to achieve social goals, and that these actions are implemented in the most efficient, lea
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This research brief presents findings from a survey administered to state health and human services officials asking about their efforts to strengthen connections between health and human services programs for low-income populations through increased data interoperability and systems integration.
This PDF was submitted as an attachment to a Public Comment sent to the Advisory Council on Alzheimer's Research, Care, and Services and/or the National Alzheimer's Project Act website. The opinions and views expressed in this PDF are those of the authors and the person who submitted it. They do not necessarily reflect the views of any federal a
Report to Congress: Social Risk Factors and Performance Under Medicare's Value-Based Purchasing Programs
This report, mandated by the Improving Medicare Post-Acute Care Transformation Act of 2014 or the IMPACT Act (P.L. 113-185), requires the Secretary, acting through the Assistant Secretary for Planning and Evaluation (ASPE), to conduct research on issues related to socioeconomic status (SES) in Medicare’s value-based payment programs. The term so
NCVHS Membership of the WORKGROUP on the NATIONAL HEALTH INFORMATION INFRASTRUCTURE
This report summarizes findings from an ASPE study of the first year of the White House Rural Council/HHS Rural IMPACT demonstration, which aims to reduce poverty through coordinated services for both children and parents.
This is the PDF version of the Racial and Ethnic Disparities in Dementia Panel Bios handout for the October 2016 meeting of the Advisory Council on Alzheimer's Research, Care, and Services.
This is the PDF version of the meeting summary for the October 2016 meeting of the Advisory Council on Alzheimer's Research, Care, and Services.
RACIAL AND ETHNIC DISPARITIES IN DEMENTIA Panel Bios Monday, October 31, 2016 Printer Friendly Version in PDF Format (4 PDF pages)
ADVISORY COUNCIL ON ALZHEIMER'S RESEARCH, CARE, AND SERVICES Public Comments on Advisory Council Meeting, October 2016 List of Comments M. Ellenbogen | 10-06-2016 M. Hogan | 10-25-2016 M. Janicki | 10-25-2016 I. Kremer | 10-25-2016
ADVISORY COUNCIL ON ALZHEIMER'S RESEARCH, CARE, AND SERVICES October 31, 2016 Washington, DC Printer Friendly Version in PDF Format (20 PDF pages) WELCOME Ronald Petersen opened the meeting at 9:07 AM, thanked everyone for coming, and invited Council members to introduce themselves.
Report to the Congress Presenting HHS's Response to the Recommendations of the Commission to Eliminate Child Abuse and Neglect Fatalities
This statutorily mandated report to Congress responds for the U.S. Department of Health and Human Services to the many recommendations contained in the March 2016 final report of the Commission to Eliminate Child Abuse and Neglect Fatalities. Overall, HHS heartily embraces the Commission's vision for a robust response to families in crisis: one th
This report summarizes findings from an environmental scan about practices and programs addressing trauma and related behavioral health needs among American Indian and Alaska Native (AI/AN) youth. The report includes descriptions of trauma-informed and trauma-specific interventions, common elements of behavioral health programs targeted to help AI