ADVISORY COUNCIL ON ALZHEIMER'S RESEARCH, CARE, AND SERVICES Friday, February 3, 2017 Printer Friendly Version in PDF Format (5 PDF pages) Clinical Studies Recruitment Strategy: Update from NIA Laurie Ryan, Ph.D. Chief, Dementias of Aging Branch Division of Neuroscience, NIA/NIH
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CLINICAL TRIALS IN ALZHEIMER'S DISEASE AND RELATED DEMENTIAS: RECRUITMENT CHALLENGES Panelist Bios Friday, February 3, 2017 Printer Friendly Version in PDF Format (3 PDF pages)
ADVISORY COUNCIL ON ALZHEIMER'S RESEARCH, CARE, AND SERVICES February 3, 2017 Washington, DC Printer Friendly Version in PDF Format (30 PDF pages)
Final Report Volume I: Background Paper, Declining Response Rates in Federal Surveys: Trends and Implications
Over the last decade, survey response rates have been steadily declining, and this decline has raised concerns across the federal government regarding the quality and utility of national survey data. Response rates are commonly considered the most important indicator of the representativeness of a survey sample and overall data quality, and low re
In April 2016 the Office of the Assistant Secretary for Planning and Evaluation (ASPE) contracted with the Center for Policy Research and the National Resource Center on Domestic Violence to host a two day roundtable convening of experts to discuss opportunities to build the evidence base for domestic violence (DV) services. This framing paper p
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
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.