grant

Innovative strategies to promote biomedical HIV prevention uptake and retention among high-risk adults at drinking venues in Kenya and Uganda

Organization UNIVERSITY OF CALIFORNIA, SAN FRANCISCOLocation SAN FRANCISCO, UNITED STATESPosted 1 Sept 2022Deadline 30 Jun 2027
NIHUS FederalResearch GrantFY202521+ years oldAIDS VirusAIDS preventionAIDS testAIDS/HIV testAcquired Immune Deficiency Syndrome VirusAcquired Immunodeficiency Syndrome VirusAddressAdherenceAdultAdult HumanAfrica South of the SaharaAlcohol Chemical ClassAlcohol DrinkingAlcohol consumptionAlcoholsAnti-HIV PositivityAnti-Retroviral AgentsAwarenessCaringCommunitiesConsumptionCounselingCountryDataDiseaseDisorderEffectiveness of InterventionsEtOH drinkingEtOH useFaceHIVHIV PositiveHIV PositivityHIV PreventionHIV SeroconversionHIV SeropositivityHIV antibody positiveHIV riskHIV testHIV therapyHIV-1 testHIV-2 testHIV/AIDS preventionHTLV-III SeroconversionHTLV-III SeropositivityHealthHeavy DrinkingHigh-Risk SexHot SpotHuman Immunodeficiency VirusesHuman immunodeficiency virus testIncidenceInjectableInterventionInterviewKenyaLAV-HTLV-IIILymphadenopathy-Associated VirusOralParticipantPerceptionPersonsPlayPrEPPrevalencePreventionProphylactic treatmentProphylaxisRandomization trialResearchRiskRisk FactorsRoleRuralSamplingSexual PartnersSiteSub-Saharan AfricaSubsaharan AfricaTestingTimeTransmissionUgandaUnprotected SexUnsafe SexViralVirus-HIVWomanadulthoodalcohol ingestionalcohol initiationalcohol intakealcohol product usealcohol usealcohol use initiationalcoholic beverage consumptionalcoholic drink intakeanti-retroviralantiretroviral therapyantiretroviral treatmentarmassessing cost effectivenessbarrier to testingcommunity settingcompare effectivenesscondomless intercoursecondomless sexcost effectivenesscost estimatecost estimationcost-effectiveness evaluationdetermine cost effectivenessdetermine efficacydrink heavilydrinkingdrinking initiationeffectiveness measureeffectiveness trialefficacy analysisefficacy assessmentefficacy determinationefficacy evaluationefficacy examinationethanol consumptionethanol drinkingethanol ingestionethanol intakeethanol product useethanol useevaluate cost-effectivenessevaluate efficacyexamine cost effectivenessexamine efficacyexcessive alcohol consumptionexcessive alcohol ingestionexcessive alcohol intakeexcessive drinkingexcessive ethanol ingestionextreme drinkingfacesfacialheavy alcohol usehigh riskhurdle to testinginnovateinnovationinnovativeinsightmenobstacle to testingphosphatidylethanolpre-exposure prophylaxisprevention serviceprimary outcomerandomized trialrecruitreduced alcohol userisk perceptionscreeningscreeningssecondary outcomesex partnersocial rolesocial stigmastandard carestandard treatmentstigmatesting barriertesting hurdletesting obstacletesting uptaketherapy adherencetherapy compliancetransactional sextransmission processunprotected intercourseuptake
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Full Description

Project Summary
HIV incidence remains unacceptably high in sub-Saharan Africa (SSA) due in part to inadequate access,

uptake, and retention in biomedical HIV prevention services, including pre- and post-exposure prophylaxis

(PrEP/PEP), among persons at increased HIV risk. Alcohol use is a common risk factor for both HIV

acquisition and poor HIV prevention uptake and retention in SSA. Interventions that promote biomedical HIV

prevention among persons with heavy alcohol use and their sexual partners are urgently needed.

Alcohol-serving drinking venues play an important role as sites of HIV transmission in SSA and are ideal sites

to engage women and men at increased risk of HIV in biomedical prevention services. However, despite long-

standing awareness of drinking venues as transmission “hot spots”, few interventions exist to reach and

engage persons in PrEP and PEP from drinking venues in SSA. Major barriers to reaching and engaging

persons at high risk of HIV from community settings such as drinking venues in HIV testing – a critical first step

to accessing biomedical HIV prevention – include HIV-associated stigma and poor perceptions of risk. To

address these barriers, we have developed a mobilization strategy of integrating HIV testing within multi-

disease screening to recruit >2,000 people from drinking venues in Kenya and Uganda, reaching >75% of

adults recruited for HIV testing. We now need to determine whether multi-disease mobilization can promote

uptake of HIV prevention for adults at drinking venues in the context of new biomedical prevention options.

Following uptake of biomedical HIV prevention, persons with heavy alcohol use face challenges with retention

in care and adherence to PrEP/PEP. We have adapted a brief alcohol counseling intervention (Health Living)

to reduce alcohol use and promote antiretroviral therapy (ART) adherence and HIV viral suppression among

persons with HIV in Kenya and Uganda. We now need to determine whether this intervention can promote

retention in biomedical prevention and PrEP/PEP adherence among adults with heavy alcohol use.

The project will rigorously test innovative interventions in Kenya and Uganda to increase uptake and use of

biomedical HIV prevention, and assess facilitators, barriers, and cost-effectiveness of these approaches.

The project will have the following aims: Aim 1: Compare the effectiveness of two mobilization strategies to

increase uptake of biomedical HIV prevention among adults at drinking venues. Aim 2: Determine the efficacy

of the Healthy Living Intervention (HLI) to reduce heavy alcohol use vs. standard care (control) on retention in

biomedical HIV prevention in a randomized trial among adults with heavy alcohol use. Aim 3: Determine the

cost-effectiveness of interventions that increase biomedical HIV prevention uptake (Aim 1) and retention (Aim

2) among adults at high-risk for HIV who attend drinking venues.

The proposed research will address the critical intersection of alcohol use and HIV risk in SSA, by promoting

reach, uptake and retention in biomedical HIV prevention and exploring associated facilitators and barriers.

Grant Number: 3R01AA030464-04S1
NIH Institute/Center: NIH

Principal Investigator: Gabriel Chamie

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