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This document is a reporting form for Ryan White CARE Act grantees to outline service provision and client demographics related to HIV/AIDS support services.
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How to fill out Ryan White CARE Act Data Report

01
Gather necessary client information, including demographics and service data.
02
Access the Ryan White CARE Act Data Report online form or appropriate software.
03
Begin inputting client data in the designated fields, ensuring accuracy.
04
Fill in services received by each client, using the correct codes and descriptions.
05
Complete any required sections regarding client enrollment and eligibility.
06
Review the report for completeness and accuracy before submission.
07
Submit the report within the specified deadline to the appropriate agency.

Who needs Ryan White CARE Act Data Report?

01
Healthcare providers offering services to individuals living with HIV/AIDS.
02
Agencies that receive funding under the Ryan White CARE Act.
03
Researchers and policymakers seeking data on HIV services and outcomes.
04
Advocacy organizations working to improve services for individuals with HIV.
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People Also Ask about

In 2023, the Ryan White HIV/AIDS Program (RWHAP) reached a record-breaking 90.6% viral suppression rate among clients receiving HIV medical care, a significant increase from 69.5% virally suppressed in 2010, demonstrating exceptional progress in HIV treatment effectiveness and care quality.
Ryan White helped to increase public awareness that HIV/AIDS was a significant epidemic. Numerous charities formed around White's death. The Indiana University Dance Marathon, started in 1991, raises money for the Riley Hospital for Children.
Definition: The Universal Standards of Care are the minimum requirements that service providers are expected to meet when providing Ryan White funded HIV/AIDS care and services. The standards of care establish the minimum standards intended to help service providers meet the needs of their clients.
L. 101–381, 104 Stat. 576, enacted August 18, 1990) was an act of the United States Congress and is the largest federally funded program in the United States for people living with HIV/AIDS.
The Ryan White HIV/AIDS Program provided life-saving care, medication, and essential support services to over 576,000 people with HIV in 2023, an increase from 561,000 people with HIV in 2020, representing more than 50% of people with diagnosed HIV in the U.S.
Part G of the 2009 Ryan White HIV/AIDS Treatment Extension Act establishes a process for medical facilities to inform emergency responders that they may have been exposed to certain infectious diseases, so that they can make informed decisions about subsequent diagnosis, prevention, or treatment measures (42 USC §§

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The Ryan White CARE Act Data Report is a comprehensive data collection tool used to gather information on the services provided to individuals living with HIV/AIDS, primarily funded through the Ryan White HIV/AIDS Program.
Entities receiving funding from the Ryan White HIV/AIDS Program, including state and local health departments, community-based organizations, and healthcare providers offering HIV-related services, are required to file the Ryan White CARE Act Data Report.
To fill out the Ryan White CARE Act Data Report, agencies must gather data on demographics, service utilization, and health outcomes for the clients served, utilizing standardized reporting tools and guidelines provided by the Health Resources and Services Administration (HRSA).
The purpose of the Ryan White CARE Act Data Report is to assess the effectiveness of HIV care programs, ensure compliance with funding requirements, and facilitate data-driven decision-making to improve services for individuals living with HIV/AIDS.
The information reported on the Ryan White CARE Act Data Report includes client demographics, types of services received, number of visits, clinical outcomes, and social determinants of health that may impact service delivery for individuals living with HIV.
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