Search Results for "Human Trafficking"
Displaying 1 - 20 of 114 results. 20 results shown per page. Page 1 of 6.
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
Directory of Health and Human Services Data Resources
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INTRODUCTION to Directory of Data Resources
Health and Human Services (HHS) Data Council
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The HHS Data Council is the principal internal advisory body to the Secretary on health and human services data policy. The Council coordinates data policy activities in HHS, including the development and implementation of an HHS data strategy. The Council consists of senior level officials and staff designated by their operating and staff division leadership.
Status of State Efforts to Integrate Health and Human Services Systems and Data: 2016
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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.
HHS Directory of Health and Human Services Data Resources - Introduction
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Overview The HHS Directory of Health and Human Services Data Resources is a compilation of information about virtually all major data collection systems sponsored by the U.S. Department of Health and Human Services (HHS).
Rural Research Needs and Data Sources for Selected Human Services Topics
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Prepared by: Mathematica Policy Research, Inc. Contents Research Summary (in PDF format)
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
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.
Medicare Part B Drugs: Trends in Spending and Utilization, 2008-2021
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The U.S. Department of Health and Human Services (HHS), Office of the Assistant Secretary for Planning and Evaluation (ASPE) released new research on spending and utilization trends of Medicare Part B drugs, drugs administered in physicians' office or hospital outpatient departments rather than being purchased at the pharmacy counter or by mail order.
Glossary of Common Data-Related Terms
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The Department of Health and Human Services (HHS) has several different policy groups such as the HHS Data Council, Data Governance Board, Evidence and Evaluation Policy Council, and the HHS AI Council that frequently use many terms related to data, but likely with inconsistent understanding of their definitions and how these terms should be used.
Severe Maternal Morbidity and Mortality-Electronic Health Record (EHR) Data Infrastructure
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Severe Maternal Morbidity and Mortality-Electronic Health Record (EHR) Data Infrastructure
A Compendium of Administrative and Survey Data Resources in the Administration for Children and Families
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This compendium is an effort to understand and document the data collected by ACF that is or could be used for evidence-building purposes. It includes summaries of twelve major ACF administrative data sources and seven surveys.
Public Listing Status of Data-Waivered Providers: Data Brief
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A large proportion of DATA-waivered providers choose not to be publicly listed on the SAMHSA website. Greater proportions of physician assistants and nurse practitioners, compared to physicians, opt to be listed on the SAMHSA website.
Aligning Federal Performance Indicators Across Programs Promoting Self-Sufficiency: Local Perspectives
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Individuals and families frequently qualify for multiple human services and employment programs that are funded, regulated, and administered by different federal agencies—each with their own eligibility criteria, program requirements, and performance indicators.
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.
Beta Testing the Multi-Payer Claims Database (MPCD)
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Consolidating data and evaluating the utility of the Multi-Payer Claims Database.
Collection of Patient-Provided Information through a Mobile Device Application for Use in Comparative Effectiveness and Drug Safety Research
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Creating infrastructure for collecting data from patients through a mobile device application and enhancing data linkages.
Office of Science and Data Policy Issues
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The Office of Science Policy guides and coordinates the development of science policy in areas such as genetic testing, environmental health, xenotransplantation and asthma. The office works closely with all of the agencies and institutes within the Department and with external scientific and research communities.