Pre-Exposure Prophylaxis (PrEP) Provision for Ugandan Fisherfolk

Sponsor
RAND (Other)
Overall Status
Recruiting
CT.gov ID
NCT05084716
Collaborator
Mildmay Uganda Limited (Other), Makerere University (Other)
100
2
2
18.2
50
2.8

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Enhanced PrEP provision
N/A

Detailed Description

The study will take place at two landing sites at which PrEP is provided to fisherfolk through the national PrEP program. The control site will administer the standard of care for PrEP provision through the national program. 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 can learn basic facts about PrEP and also can be 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 regularly (e.g., 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 them 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
PrEP Provision for Ugandan Fisherfolk
Actual Study Start Date :
Sep 24, 2021
Anticipated Primary Completion Date :
Jun 30, 2022
Anticipated Study Completion Date :
Mar 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

At the intervention site during healthcare facility outreach events, PrEP initiators will be offered guidance on selecting an adherence supporter during PrEP initiation. All outreach event attendees at the events will be offered the opportunity to attend the intervention workshops. Check-in reminder calls will be conducted systematically with PrEP users.

Behavioral: Enhanced PrEP provision
The intervention will train health care providers to facilitate workshops at outreach events where attendees can learn basic facts about PrEP and be taught skills about how to advocate for PrEP in their community. Healthcare facility staff will encourage PrEP initiators to select an adherence supporter. Check-in reminder calls will be conducted systematically with PrEP users.

No Intervention: Control

At the control site, healthcare facility staff will continue to provide PrEP according to the standard of care.

Outcome Measures

Primary Outcome Measures

  1. Length of time on PrEP [Baseline to six months after]

    Number of months (0-6) that a participant is on PrEP

  2. Percent of people who accept PrEP of those offered [6 months]

    Percent of people who accept PrEP of those offered

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Tests HIV-negative at a healthcare outreach/HIV testing event in one of the two selected fishing communities and is PrEP-eligible
Exclusion Criteria:
  • Not meeting the inclusion criteria

Contacts and Locations

Locations

Site City State Country Postal Code
1 Makerere University School of Public Health Kampala Uganda
2 Mildmay Uganda Kampala Uganda

Sponsors and Collaborators

  • RAND
  • Mildmay Uganda Limited
  • Makerere University

Investigators

  • Principal Investigator: Laura M Bogart, PhD, RAND
  • Principal Investigator: Rhoda K Wanyenze, MBChB, PhD, MPH, Makerere University

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
RAND
ClinicalTrials.gov Identifier:
NCT05084716
Other Study ID Numbers:
  • R34MH119924
First Posted:
Oct 20, 2021
Last Update Posted:
Feb 2, 2022
Last Verified:
Jan 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by RAND

Study Results

No Results Posted as of Feb 2, 2022