Search Results for "Poverty Guidelines, Research"
Displaying 1 - 20 of 161 results. 20 results shown per page. Page 1 of 9.
Building the Data Capacity for Patient-Centered Outcomes Research: The 2023 Annual Report
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The 2023 Office of the Secretary Patient-Centered Outcomes Research Trust Fund (OS-PCORTF) Annual Report highlights the accomplishments of 36 multi-agency projects that supports the four goals of the strategic plan:
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.
Improving Data on the Workforce Delivering Home and Community-Based Services
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On April 25, 2024, HHS and DoL released recommendations, in the form of an Issue Brief, to improve data infrastructure on the workforce delivering home and community-based services (HCBS) in response to President Biden’s
State All Payer Claims Databases: Identifying Challenges and Opportunities for Conducting Patient-Centered Outcomes Research and Multi-State Studies
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This report is the third in a series of reports commissioned by the Office of the Assistant Secretary for Planning and Evaluation (ASPE) from the RAND Corporation addressing state all payer claims databases (APCDs). APCDs include medical, pharmacy, and dental claims, as well as enrollment and provider files collected from private and public payers by states, usually as part of a State mandate.
Bridging the Patient-Center Outcome Research Infrastructure and Technology
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The goal of this project was to strengthen the coordinated registry network as a real-world data source for high quality, relevant, reliable, timely and actionable evidence to improve patient outcomes of medical devices, specifically for technologies affecting women’s health.
Federal Data for Conducting Patient-Centered Outcomes Research on Economic Outcomes
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Researchers from ASPE, NORC, Washington University in St. Louis, Catholic Physicians’ Guild of San Antonio, and the U.S.
Assessing Outcomes Relevant for Patient-Centered Outcomes Research Among Adults Aged 18–64 with Disabilities and Federal Data Infrastructure Opportunities
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This report and dataset inventory identifies individual-level measures for conducting patient-centered outcomes research (PCOR) relevant to adults with disabilities, aged 18–64 years.
Measuring Income and Poverty in Four Surveys: an Overview
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Measuring Income and Poverty in Four Surveys: An Overview Final Report Prepared by:
Building the Data Capacity for Patient-Centered Outcomes Research: The 2022 Annual Report Report and Infographic
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The 2022 Office of the Secretary Patient-Centered Outcomes Research Trust Fund (OS PCORTF) Annual Report and infographic highlights the accomplishments of 32 multi-agency projects that supports the four goals of the new strategic plan:
Measuring Income and Poverty in Four Surveys: an Overview
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Policy makers use national surveys to paint a picture of the U.S. population along a variety of dimensions. If major surveys are equally successful in capturing income, then, for the same time period, populations and income types, consistently defined income estimates and poverty rates across surveys will be highly similar varying somewhat due to sampling error.
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.
Medicare Data Linkages for Conducting Patient-Centered Outcomes Research on Economic Outcomes
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This report and dataset inventory identifies federally funded data linkages that may facilitate patient-centered outcomes research (PCOR) on economic outcomes for Medicare fee-for-service (FFS) beneficiaries.
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.
Rural Research Needs and Data Sources for Selected Human Services Topics - Research Summary
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Rural Research Needs and Data Sources for Selected Human Services Topics
Leveraging ACF Administrative Data for Evidence and Research
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This brief analyzes information on administrative data resources collected by the Administration for Children and Families (ACF). It explores how the data can be leveraged to improve evidence and research on ACF programs and beneficiaries. Key highlights include:
Improving Data Infrastructure for Patient-Centered Outcomes Research for People with Intellectual and Developmental Disabilities
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This report describes insights gained from key informant interviews and an ASPE-hosted listening session on short-term opportunities for improving patient-centered outcomes research (PCOR) data infrastructure that addresses the needs of individuals with intellectual and developmental disabilities (ID/DD).
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Refugee and Asylee Data on the Utilization of Medicaid
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This brief describes a joint project of the ASPE and the Office of Refugee Resettlement in the Administration for Children and Families to enhance the data infrastructure of agencies managing refugees and Medicaid services. This project is funded by the Patient-Centered Outcomes Research Trust Fund.
Identifying and Classifying Medicaid Home and Community-Based Services Claims in the Transformed Medicaid Statistical Information System, 2016-2020 Issue Brief
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Home and community-based services (HCBS) are a range of medical and non-medical services provided in the home and community that support individuals with functional limitations, enabling them to reside in the community rather than in institutional settings.
Strengthening and Expanding the Community Health Applied Research Network (CHARN) Registry to Conduct Patient-Centered Outcomes Research (PCOR)
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Expanding CHARN data registries and making data available to PCOR investigators outside of the CHARN network.
Rural Research Needs and Data Sources for Selected Human Services Topics
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Contents The Rural Context Review of Existing Research on the Three Focal Topics Data Sources Available to Conduct Research on the Focal Topics Implications of Study Findings Enhancing Rural Hu