MedPath

Pre-Exposure Prophylaxis (PrEP) Provision for Ugandan Fisherfolk

Not Applicable
Completed
Conditions
HIV
Interventions
Behavioral: Enhanced PrEP provision
Registration Number
NCT05084716
Lead Sponsor
RAND
Brief Summary

This study is a pilot test of enhancements to the standard of care for providing PrEP in Ugandan fishing communities. The specific aims are to conduct a mixed-methods study assessing enhancements to the standard of care for providing PrEP in fisherfolk communities in Lake Victoria, Uganda.

Detailed Description

The study will take place at two landing sites at which PrEP is provided to fisherfolk through the Ugandan national PrEP program. The comparison site will receive the standard of care for PrEP provision. At the intervention site, the investigators will implement a three-pronged intervention:

1. During healthcare outreach events we will conduct PrEP workshops, in which people who want to know more about PrEP learn basic facts about PrEP and are taught skills about how to advocate for PrEP in their community.

2. Check-in Calls: To support PrEP adherence, healthcare workers will call PrEP users two weeks after initiation, and the week before refill events, to check in about any questions and to remind them of the next date and place to pick up refills. Calls after PrEP initiation will ask about side effects.

3. To support PrEP adherence, healthcare workers will encourage PrEP users to select an adherence supporter, who is a family member or friend to whom they disclose their PrEP use. The adherence supporter agrees to remind the PrEP user to adhere to PrEP and get refills. Healthcare workers will ask the PrEP user for the name and contact information for the adherence supporter, so that the adherence supporter can be contacted to remind them about refills, as well as if the PrEP user does not show up for a refill.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
885
Inclusion Criteria

Not provided

Exclusion Criteria
  • Not meeting the inclusion criteria

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionEnhanced PrEP provisionAt the intervention site during healthcare facility outreach events, all community members will be offered the opportunity to attend intervention workshops where they can learn basic facts about PrEP and be taught skills about how to advocate for PrEP in their community. Check-in reminder calls will be conducted systematically with PrEP users. Healthcare facility staff will encourage PrEP initiators to select an adherence supporter.
Primary Outcome Measures
NameTimeMethod
Number of Participants Who Persisted On PrEP After Initiation6 months

Percentage of PrEP users who are still on PrEP at 6 months post-initiation

Number of Participants With PrEP InitiationBaseline. Individuals are asked if they wish to initiate PrEP after they have been tested and deemed eligible

Individuals who are eligible for PrEP (tested HIV-negative, aged 18 and older, in fisherfolk community) are asked by a healthcare provider whether they want to start taking PrEP

Secondary Outcome Measures
NameTimeMethod
Number of Participants Who Maintained PrEP Prescriptions Over 6 Months6 months

Percentage of PrEP users with a PrEP medication possession ratio of at least 80% coverage by PrEP prescriptions over 6 months. (i.e., 144 of 180 days)

Trial Locations

Locations (2)

Mildmay Uganda

πŸ‡ΊπŸ‡¬

Kampala, Uganda

Makerere University School of Public Health

πŸ‡ΊπŸ‡¬

Kampala, Uganda

Β© Copyright 2025. All Rights Reserved by MedPath