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Perinatal Hepatitis B Prevention Program - Auxiliary Prevention Projects

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The purpose of these activities is to support the goals of the HHS Action Plan for the Prevention, Care, and Treatment of Viral Hepatitis, 2014-2016 by ensuring Hep B-infected pregnant women are identified so that their infants can receive timely post-exposure prophylaxis, improvements in post-vaccination serologic testing to improve efficiencies, and data collection to assess infant outcomes.

Training and Technical Assistance for Health Department Demonstration Projects for Comprehensive Prevention, Care, Behavioral...

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The purpose of this program is to strengthen the capacity of PS15-1509 funded health departments and their collaborative partners  to plan, implement, and sustain (ongoing engagement, assessment, linkage, and retention) comprehensive prevention, care, behavioral health, and social services models for MSM of color at risk for and living with HIV infection.

Methodologies to Enhance Understanding of HIV Associated Social Determinants (R01)

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This Funding Opportunity Announcement (FOA) invites applications that propose to understand social determinants, that is, those social conditions and economic circumstances that influence health. In particular, this FOA solicits research to better characterize social determinants of health as they relate to HIV infection and disease outcomes.

Quality Improvement Capacity & Impact Project

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The purpose of this cooperative agreement is to improve the effectiveness, efficiency, patient-centeredness, safety, accessibility, and equity of HIV clinical services through a variety of approaches including by building the capacity of host country health systems and/or host country government agencies responsible for improving performance.

Positive Health Check Evaluation Trial

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The grantee will conduct CDC's Positive Health Check Evaluation Trial with English-speaking people living with HIV from 3-4 diverse HIV primary care clinics in the U.S. to test if this web-based intervention improves clinical outcomes. The grantee will enroll a min. of 2,320 eligible participants (1,160 per study arm) in the study trial, with a min. of 580 to a max. of 1,160 enrolled per clinic.


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