Search Results for "Poverty Guidelines, Research"
Displaying 221 - 240 of 9452 results. 20 results shown per page. Page 12 of 473.
Poverty Estimates, Trends, and Analysis
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The topic of poverty is widely considered a cause for national action because poor families often encounter material hardships and reduced well-being and because children who grow up in poor households are less likely to thrive as adults.
Strengthening the Data Infrastructure for Outcomes Research on Mortality Associated with Opioid Poisonings: Final Report
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Below is a summary of the problems addressed, the solution, and the accomplishments and products.
Problems Addressed:
Researchers and public health officials frequently rely on the cause of death information made available from the coding and processing of death certificate data for critical programmatic, policy, and research needs.
State Efforts to Coordinate Provider Directory Accuracy
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Provider directories are lists of in-network providers produced by health care plans. They are an important tool for individuals seeking health care providers, and for regulators who monitor the adequacy of health plans’ provider networks.
Inflation Reduction Act Research Series: Medicare Part D Enrollee Out-of-Pocket Spending: Recent Trends and Projected Impacts of the Inflation Reduction Act
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The Inflation Reduction Act (IRA) will make key changes to improve drug affordability for people who have Medicare.
Information on Research Supplemental Poverty Measure. A Summary of 2012 Current Population Survey Data
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The Census Bureau recently released data on the research supplemental poverty measure (SPM) indicating that 16.1 percent of the U.S. population in 2011 was poor, representing 49.7 million individuals. This compares to 15.1 percent of the U.S.
Information on Research Supplemental Poverty Measure. A Summary of 2012 Current Population Survey Data
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This ASPE Issue Brief provides information on the research Supplemental Poverty Measure (SPM) calculated by the Census Bureau. In 2011, 16.1 percent of the U.S. population was poor using the SPM, representing 49.7 million individuals. This compares to 15.1 percent of the U.S. population, or 46.6 million individuals, under the official measure.
NAPA Advisory Council 2023 Meeting Material
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This page provides the material available for the Advisory Council meetings held in 2023.
Public Comments from Advisory Council Meeting, October 2023
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List of CommentsJ. Copeland | 11-2-23S. Eissler | 10-30-23M. Rafii | 10-30-23H.
Claims and Provider Payment Data Gaps for Responding to COVID-19
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This report and accompanying discussion by ASPE and NORC highlights the claims data limitations identified during the COVID-19 Public Health Emergency Health (PHE) and provides considerations to address these limitations. The report identifies that limitations related to claims data were existing issues, exacerbated by, but not unique to, the COVID-19 PHE.
Reconnecting Youth: A Compendium of Programs and Evidence Gap Map Exploring Programs and Practices Serving Opportunity Youth and the Evidence Behind Them
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In 2019, approximately 4.1 million young people between the ages of 16 and 24 were neither employed nor in school.
Health Information Technology Adoption and Utilization in Long-Term and Post-Acute Care Settings
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This paper provides an overview of Health Information Technology (HIT) adoption and utilization in long-term and post-acute care (LTPAC) settings. This study found that LTPAC have adopted electronic health records (EHRs) to support clinical and business needs. Interoperable exchange of health information however is not routine or widely used.
Final Report: Training Data for Machine Learning (ML) to Enhance Patient-Centered Outcomes Research (PCOR) Data Infrastructure (ONC)
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Executive Summary
Introduction and Background
The Training Data for Machine Learning to Enhance PCOR Data Infrastructure project (hereafter termed the Project) led by the Office of the National Coordinator for Health Information Technology (ONC) conducted foundational work to support future applications of artificial intelligence (AI), specifically focused on machine learnin
Guide on Advancing Equity by Incorporating Intersectionality in Research and Analysis
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This guide explores intersectionality and why it is essential for advancing equity. It explores strategies for planning and conducting research with an intersectional lens, describes quantitative measures and methods to examine differences across groups of people with intersecting identities, and provides key considerations for using qualitative data to better understand intersectionality.
Information Quality Guidelines
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This site presents the HHS Information Quality Guidelines, the supporting administrative mechanisms to request correction of information covered under the guidelines, and the HHS Peer Review Agenda. The HHS Guidelines were developed in accordance with the provisions of P.L.
Training Data for Machine Learning to Enhance Patient-Centered Outcomes Research (PCOR) Data Infrastructure — A Case Study in Tuberculosis Drug Resistance
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Executive summary
This report describes the research plan and results of a PCOR project that followed a statement of work defined in an intra-agency agreement (IAA) between the Office of the Assistant Secretary for Planning and Evaluation (ASPE) and the National Library of Medicine (NLM). ASPE coordinates efforts to build data capacity for patient-centered outcomes research (PCOR).
Synthetic Health Data Generation to Accelerate Patient-Centered Outcomes Research (PCOR): Final Report
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The Synthetic Health Data Generation to Accelerate PCOR project was launched in 2019 by the Office of the National Coordinator for Health Information Technology (ONC).
Guidelines For Regulatory Impact Analysis
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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.
Project Update: Child Welfare and Health Infrastructure for Linking and Data Analysis of Resources, Effectiveness, and Needs (CHILDREN) Initiative
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This brief describes progress in the Child Welfare and Health Infrastructure for Linking and Data Analysis of Resources, Effectiveness, and Needs (CHILDREN) Initiative, which is entering its second year. At this time, four jurisdictions have been selected for participation in the CHILDREN Initiative and are engaging in feasibility studies to determine readiness for linking data.
Guidelines for Regulatory Impact Analysis Supplement: Addressing International Effects
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This report extends the brief discussion of addressing international effects contained in the Department of Health and Human Service Guidelines for Regulatory Impact Analysis (2016). The purpose of this supplement is to expand that discussion and provide more detailed information on conducting such assessments.
Related Products:
Inflation Reduction Act Research Series: Medicare Part D Enrollee Savings from Elimination of Vaccine Cost-Sharing
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Effective January 1, 2023, the Inflation Reduction Act (IRA) eliminated enrollee cost-sharing for recommended vaccines covered under Medicare Part D. In 2021, 3.4 million people received vaccines under Part D, and annual out-of-pocket costs were $234 million.