Search Results for "Poverty Guidelines, Research"
Displaying 1 - 20 of 82 results. 20 results shown per page. Page 1 of 5.
Improving Access to Affordable and Equitable Health Coverage: A Review from 2010 to 2024
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Recent legislative and administrative policy initiatives have built on the Affordable Care Act’s (ACA) expansion of health insurance coverage and improvements in access to and utilization of health care services.
Linking State Medicaid Data and Birth Certificates For Maternal Health Research
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This report presents the set of guiding principles for linking state Medicaid data with birth certificates that was developed by state and national experts and leaders. These guiding principles can be implemented to create a multistate linked database that researchers would be able to access and use for research on maternal health, including patient-centered outcomes research (PCOR).
Childhood Obesity Data Initiative (CODI): Integrated Data for Patient-Centered Outcomes Research Project
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Expand Availability of Data for Childhood Obesity Outcomes Research
Source Data Capture from Electronic Health Records: Using Standardized Clinical Research Data
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A working example to showcase the Food and Drug Administration’s guidance on electronic source data in clinical investigations.
Innovations in Effective Compassion: Compendium of Research Papers. Presented at the Faith-Based and Community Initiatives Conference on Research, Outcomes, and Evaluation
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Prepared for:U.S. Department of Health and Human ServicesOffice of the Assistant Secretary for Planning and EvaluationThe Center for Faith-Based and Community Initiatives
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.
Trends in Ownership Structures of U.S. Nursing Homes and the Relationship with Facility Traits and Quality of Care (2013-2022)
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Stakeholders, researchers, and policymakers have identified varying nursing home ownership structures and ownership transactions as potentially influencing the quality of care delivered to vulnerable residents.
Enhancing Data Resources for Researching Patterns of Mortality in Patient Centered Outcomes Research
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Linking the National Death Index to other sources to increase the availability of information on the cause of death.
Enhancing Patient-Centered Outcomes Research (PCOR): Creating a National Small-Area Social Determinants of Health Data Platform
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Develop a Consolidated Set of National Standardized Databases on Valid and Reliable Social Determinants of Health Factors at the
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.
Comparative Effectiveness Research (CER) Inventory
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Evaluating the performance of Comparative Effectiveness Research Inventory against other databases.
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.
A Synthetic Health Data Generation Engine to Accelerate Patient-Centered Outcomes Research
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Providing PCOR Researchers with a Low Risk, Readily Available Synthetic Data Source
Training Data for Machine Learning to Enhance Patient-Centered Outcomes Research (PCOR) Data Infrastructure
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Creating a Foundation to Advance the use of Artificial Intelligence for Patient Centered Outcomes Research and Clinical Practice
Strengthening the Data Infrastructure for Outcomes Research on Mortality Associated with Opioid Poisonings
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Modernizing the Infrastructure for Capturing Drug Death Data and Enhancing Research on Opioid Poisoning Using Death Certificates
SHIELD - Standardization of Lab Data to Enhance Patient-Centered Outcomes Research and Value-Based Care
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Improving the Quality, Interoperability and Portability of Laboratory Data within and Between Institutions
Maintenance and Support of the Chronic Conditions Warehouse (CCW) for Comparative Effectiveness Research (CER)
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Supporting expanded data infrastructure enhancements to the Chronic Conditions Data Warehouse to facilitate patient-centered outc
Making Electronic Health Record (EHR) Data More Available for Research and Public Health
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Developing an Application and Reference Architecture Using Industry Standards and Technology to Improve the Availability of Clini
Development of Data Infrastructure for Use of Electronic Health Records (EHRs) in Comparative Effectiveness Research (CER)
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Establishing an infrastructure for the use of electronic health records in clinical comparative effectiveness research.
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