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Clinical Trials/NCT02626286
NCT02626286
Completed
N/A

Prevention of HIV Infection in Men Who Have Sex With Men in Sub-Saharan Africa: Feasibility and Interest of a Quarterly Preventive Global Care (CohMSM)

ANRS, Emerging Infectious Diseases6 sites in 5 countries885 target enrollmentJune 1, 2015

Overview

Phase
N/A
Intervention
HIV quarterly global care
Conditions
HIV Infection
Sponsor
ANRS, Emerging Infectious Diseases
Enrollment
885
Locations
6
Primary Endpoint
Percentage of performed tests/scheduled tests
Status
Completed
Last Updated
17 days ago

Overview

Brief Summary

The objective of the study is to evaluate the feasibility and interest of a HIV quarterly preventive global care for men who have sex with men (MSM) in sub-Saharan Africa to help reducing HIV incidence in this key population, their female partners, and the general population. This interventional, open label, multicenter, multidisciplinary cohort study will be conducted in Burkina Faso, Ivory Coast, Mali and Togo.

All participants will receive a HIV quarterly preventive global care including:

i) data collection on health status, symptoms of sexually transmitted infections (STI) and sexual behavior, ii) a clinical examination, iii) STI diagnosis and treatment, iv) counselling adapted for MSM, and v) the provision of condoms and lubricants.

Detailed Description

The objective of the study is to evaluate the feasibility and interest of a HIV quarterly preventive global care for men who have sex with men (MSM) in sub-Saharan Africa to help reducing HIV incidence in this key population, their female partners, and the general population. Regarding HIV-negative MSM, the specific objectives are to assess: 1. the acceptability of the preventive global care including quarterly monitoring and HIV screening as well as the associated medical, behavioral and social factors, and 2. changes in sexual behavior among MSM during the project as well as the associated medical, behavioral and social factors. Regarding HIV-positive MSM, the specific objectives are to assess: 1. the acceptability of the preventive global care including antiretroviral therapy initiation whatever the CD4 T cell count and the clinical stage, as well as the associated medical, behavioral and social factors, 2. adherence and response to antiretroviral therapy as well as the associated medical, behavioral and social factors, 3. changes in sexual behavior among MSM during the project as well as the associated medical, behavioral and social factors, 4. risk of HIV transmission as well as the associated medical, behavioral and social factors, and 5. describe the virologic characteristics (subtypes / circulating recombinant forms, co-infection with multiple variants and transmitted and acquired resistance profiles). Regarding healthcare professionals, the specific objective is to evaluate the perception of the preventive global care. This interventional, open label, multicenter, multidisciplinary cohort study will be conducted in Burkina Faso, Ivory Coast, Mali and Togo. All participants will receive a HIV quarterly preventive global care including: i) data collection on health status, symptoms of sexually transmitted infections (STI) and sexual behavior, ii) a clinical examination, iii) STI diagnosis and treatment, iv) counselling adapted for MSM, and v) the provision of condoms and lubricants. In addition, vaccination against hepatitis B virus and annual tests for syphilis will be offered. HIV-negative MSM will also be offered an HIV screening test at each quarterly visit. HIV-positive MSM will be offered immediate support of HIV infection including antiretroviral therapy. A total of 700 MSM over 18 years (500 HIV-negative and 200 HIV-positive) reporting at least one anal sex (passive or active) with another man within the last three months will be recruited and followed for 24 to 36 months. MSM lost to follow-up, transferred, died or having seroconverted for HIV during follow-up will be replaced in their respective group (seronegative or seropositive) by other MSM. The study will last 3 years.

Registry
clinicaltrials.gov
Start Date
June 1, 2015
End Date
January 5, 2021
Last Updated
17 days ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Man over 18 years
  • Reporting at least one anal sex (passive or active) with another man within the last three months
  • Able to reach the local site of the study
  • Agreeing to participate in the study and signing the informed consent form

Exclusion Criteria

  • History of antiretroviral therapy (except for pre- or post-exposure prophylaxis)
  • Participation in another biomedical or behavioral research on HIV or sexually transmitted infections
  • Impairment of the person making his participation in the study, or information understanding, difficult or impossible
  • Predictable protocol violation (geographical distance or other reasons)

Arms & Interventions

HIV quarterly global care

HIV quarterly global care including i) data collection on health status, symptoms of sexually transmitted infections (STI) and sexual behavior, ii) a clinical examination, iii) STI diagnosis and treatment, iv) prevention counselling adapted for MSM, v) the provision of condoms and lubricants, and vi) HIV screening test at each quarterly visit for HIV-negative MSM or immediate support of HIV infection including antiretroviral therapy for HIV-positive MSM.

Intervention: HIV quarterly global care

Outcomes

Primary Outcomes

Percentage of performed tests/scheduled tests

Time Frame: 3 years

Number of people followed after 3 years compared to the number of persons included (retention in the program)

Time Frame: 3 years

Incidence of sexually transmitted infections

Time Frame: 3 years

Antiretroviral therapy initiation probability in HIV-positive MSM

Time Frame: 3 years

Antiretroviral therapy maintenance probability in HIV-positive MSM

Time Frame: 3 years

Percentage of HIV-positive MSM died under antiretroviral therapy

Time Frame: 3 years

Number of unprotected anal sex

Time Frame: 3 years

Percentage of antiretroviral therapy observance in HIV-positive MSM

Time Frame: 3 years

Percentage of HIV-positive MSM with viral load>1000 copies/mL

Time Frame: 3 years

Percentage of HIV-positive MSM with CD4≤reference (or CD4<100/mm3)

Time Frame: 3 years

Percentage of performed visits/scheduled visits

Time Frame: 3 years

Number of transmitted and acquired resistance mutations

Time Frame: 3 years

Percentage of HIV-positive MSM with new or recurrent AIDS-defining events (clinical stage 4)

Time Frame: 3 years

Number of HIV subtypes / circulating recombinant forms

Time Frame: 3 years

Number of co-infections with several viral variants

Time Frame: 3 years

Percentage of HIV-positive MSM with detectable viral load and inconsistent condom use with a partner seronegative or with unknown HIV status

Time Frame: 3 years

Number of male sex partners

Time Frame: 3 years

Study Sites (6)

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