Human Immunodeficiency Virus Clinical Trial
Official title:
A Couples-focused Intervention for HIV Prevention and Care in South Africa
From a sample of 272 male-female couples (544 individuals, 272 men and 272 women) recruited from rural KaZulu-Natal, South Africa, couples will be randomized to receive either individual a package of dyadic counseling and testing (intervention arm) or an attention matched control. The research examines the impact of a package of dyadic counseling and testing on viral suppression and engagement in HIV care among sero-discordant and concordant positive male-female couples in KwaZulu-Natal, South Africa.
Status | Recruiting |
Enrollment | 544 |
Est. completion date | July 1, 2024 |
Est. primary completion date | July 1, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 50 Years |
Eligibility | Inclusion Criteria: 1. both aged between 18-50 2. report being a cis-gender male and a cis-gender female 3. report being in a relationship with each other for at least 6 months 4. are not in a polygamous marriage and 5) report being sexually active with their partner. Serostatus Inclusion Criteria: For those individuals who already know that they are HIV-positive, the inclusion criteria will be that they report one of the following conditions: 1. have never initiated ART 2. not currently on ART (but can have been on it before) 3. if already on ART, that they have missed 3 doses of medication in the past 30 days Exclusion Criteria: 1. Couples in which one or both members report experiencing or perpetrating severe IPV in the prior 6 months 2. Below age 18 or above age 50 3. Report being transgender 4. Report not being a relationship at all or for <6 months 5. Are in a polyamorous marriage 6. Are not sexual active with participating partner |
Country | Name | City | State |
---|---|---|---|
South Africa | Human Sciences Research Council | Sweetwaters | KwaZulu Natal |
Lead Sponsor | Collaborator |
---|---|
University of Michigan | Human Sciences Research Council, University of California, San Francisco |
South Africa,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Virologic suppression change | A blood draw will be conducted to provide a measure of viral load at each visit to look for changes between visits. The outcome will be a binary outcome of detectable versus undetectable viral load. | Baseline and every 6 months for 24 months | |
Secondary | Behavioral indicators of engagement in HIV care | Engagement in care is conceptualized as including linkage to care and retention in HIV care. For HIV-positive partners who report no engagement in HIV care at baseline, linkage to care is defined as attending at least one clinical care appointment, having at least one CD4 test performed, and having at least one viral load test performed within 6 months of the baseline visit | Baseline and every 6 months for 24 months |
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