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The Outreach and Prevention at ALcohol Venues in East Africa Study (OPAL-East Africa- Aim 1)

Not Applicable
Completed
Conditions
HIV/AIDS
Interventions
Behavioral: HIV-focused mobilization
Behavioral: Multi-disease-focused mobilization
Registration Number
NCT05862857
Lead Sponsor
University of California, San Francisco
Brief Summary

This study will test innovative interventions to increase uptake and use of biomedical HIV prevention options by engaging women and men at drinking venues in rural Kenya and Uganda in care, while gaining insights into the facilitators, barriers, and cost-effectiveness of these approaches.

Detailed Description

\[BACKGROUND\] Alcohol use is a common risk factor for both HIV prevention uptake and retention in sub-Saharan Africa (SSA). Interventions that promote biomedical HIV prevention (PrEP and PEP) 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.

\[OVERVIEW\] The investigators 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. The investigators 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.

The project will rigorously test innovative interventions in Kenya and Uganda to increase uptake of biomedical HIV prevention, and assess facilitators, barriers, and cost-effectiveness of these approaches.

Specific Aims:

* Compare the effectiveness of two mobilization strategies to increase uptake of biomedical HIV prevention among adults at drinking venues.

* Determine the cost-effectiveness of interventions that increase biomedical HIV prevention uptake 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 and uptake of biomedical HIV prevention and exploring associated facilitators and barriers.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
7727
Inclusion Criteria
  • adult (≥18 years)
  • patron or worker at a drinking venue within the study community
Exclusion Criteria
  • age <18 years
  • previous participation in the study (may only participate once)
  • inability to consent (including gross inebriation)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Aim 1: HIV-focused mobilizationHIV-focused mobilizationPatrons and workers at drinking venues will be given a recruitment card for free HIV testing at the local clinic.
Aim 1: Multi-disease-focused mobilizationMulti-disease-focused mobilizationPatrons and workers at drinking venues will be given a recruitment card for free multi-disease testing at the local clinic, including: diabetes, hypertension, HIV, malaria, TB, pregnancy.
Primary Outcome Measures
NameTimeMethod
Biomedical HIV prevention uptake at 4 weeksMeasured 4 weeks after clinic screening visit

The proportion of HIV-negative adults, receiving an Aim 1 recruitment card, who initiate PrEP or PEP after mobilization. This outcome will be measured by pill dispensing records and Ministry of Health (MoH) PrEP and PEP registry records.

Secondary Outcome Measures
NameTimeMethod
Yield of adults with heavy alcohol useMeasured at clinic screening visit

Heavy alcohol use is defined as self-reported AUDIT-C score (a standardized, three question survey) of greater than or equal to 4 for men and greater than or equal to 3 for women. These outcomes will be recorded on study CRFs.

Biomedical HIV prevention uptake at 12 weeksMeasured 12 weeks after clinic screening visit

The proportion of HIV-negative adults, receiving an Aim 1 recruitment card, who initiate PrEP or PEP after mobilization. This outcome will be measured by pill dispensing records and Ministry of Health (MoH) PrEP and PEP registry records.

Adults with untreated HIV who initiate ARTMeasured within one week of presenting for clinic-based screening with a recruitment card

The proportion of adults with untreated HIV that initiate ART. Current and prior ART use will be self-reported and recoded on study CRFs. New ART prescriptions will be measured through pill dispensing data and MoH registries.

Biomedical HIV prevention uptake at 8 weeksMeasured 8 weeks after clinic screening visit

The proportion of HIV-negative adults, receiving an Aim 1 recruitment card, who initiate PrEP or PEP after mobilization. This outcome will be measured by pill dispensing records and Ministry of Health (MoH) PrEP and PEP registry records.

HIV testing uptakeMeasured at clinic screening visit

The proportion of HIV-negative adults, receiving an Aim 1 recruitment card, who accept clinic-based HIV testing at the clinic screening visit. HIV testing will be done in accordance with Kenyan and Ugandan national testing algorithms. Uptake will be recorded on study CRFs.

Yield of adults with untreated HIVMeasured at clinic screening visit

The proportion of persons accepting HIV testing who are identified with newly diagnosed HIV or those who are self-reported to have known HIV infection but out of care and off of ART. HIV testing will be done in accordance with Kenyan and Ugandan national testing algorithms. Uptake, test results, HIV status, and current ART use will be recorded on study CRFs.

Trial Locations

Locations (2)

Infectious Diseases Research Collaboration (IDRC)

🇺🇬

Mbarara, Uganda

Kenya Medical Research Institute (KEMRI)

🇰🇪

Mbita, Kenya

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