Search Results for "Poverty Guidelines, Research"
Displaying 1 - 12 of 12 results. 20 results shown per page. Page 1 of 1.
Advancing Research on Intersections of Child Welfare and Medicaid Using Linked Data from the CCOULD Project
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Increasing availability of linked child welfare and Medicaid data can advance research on the intersections of child welfare and Medicaid. The project, Child and Caregiver Outcomes Using Linked Data (CCOULD), developed a research-use dataset combining child welfare records and Medicaid claims for children and families involved in child welfare systems in Florida and Kentucky.
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.
Caregivers and Long-Term Services and Supports
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As the United States population ages, a larger proportion of individuals will likely need and use long-term services and supports (LTSS). Much of this support is provided by informal (i.e., unpaid) caregivers. For those that need paid LTSS, most Americans pay out-of-pocket. Some may do so until their personal resources are exhausted, and then rely on the Medicaid safety net.
Federal Efforts to Address ADRD Disparities
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The National Alzheimer’s Project Act (NAPA) requires “the inclusion of ethnic and racial populations at higher risk for Alzheimer's or least likely to receive care, in clinical, research, and service efforts with the purpose of decreasing health disparities in Alzheimer's”.1 In order to meet this requirement, in 2020 the Advisory Council on Alzheimer’s Research, Care, and Services recommended t
Federal Efforts to Address Racial and Ethnic Disparities in Alzheimer’s Disease and Related Dementias
Publication Date
The National Alzheimer’s Project Act (NAPA) requires “the inclusion of ethnic and racial populations at higher risk for Alzheimer's or least likely to receive care, in clinical, research, and service efforts with the purpose of decreasing health disparities in Alzheimer's”.1 In order to meet this requirement, in 2020 the Advisory Council on Alzheimer’s Research, Care, and Services recommended t
Public Members of the NAPA Advisory Council: 2019 Recommendations
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Printer Friendly Version in PDF Format (15 PDF pages)
Clinical Care Subcommittee
Clinical Care Themes:
Public Members of the NAPA Advisory Council: 2018 Recommendations
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Printer Friendly Version in PDF Format (12 PDF pages)
Clinical Care Subcommittee
Clinical Care Themes:
U.S. Department of Health and Human Services Overdose Prevention Strategy
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From 1999 through 2019, there were more than 840,000 drug overdose deaths in the United States. The crisis has continually evolved and escalated, including during the COVID-19 pandemic, when an estimated 93,000 persons lost their lives to drug overdose in 2020--approximately a 30% increase over the year prior.
A Profile of Older Adults with Dementia and their Caregivers Issue Brief
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September 2018 Printer Friendly Version in PDF Format (7 PDF pages)
Public Members of the NAPA Advisory Council: 2017 Recommendations
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Printer Friendly Version in PDF Format (9 PDF pages)
Caregiving for People with Non-Alzheimer's Dementias Issue Brief
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This is the PDF version of a Reference Paper prepared for the National Research Summit on Care, Services, and Supports for Persons with Dementia and Their Caregivers (also called the Research Summit on Dementia Care).
Public Members of the NAPA Advisory Council: 2016 Recommendations
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Printer Friendly Version in PDF Format (7 PDF pages)
Since 2012, the National Plan and its accompanying recommendations have catalyzed progress in the field of AD/ADRD.