search
Back to results

Couples Health CoOp Plus (CHC+)

Primary Purpose

HIV, Substance Use, Stigma, Social

Status
Recruiting
Phase
Not Applicable
Locations
South Africa
Study Type
Interventional
Intervention
Community stigma reduction training
Couples Health CoOp Plus (CHC+)
Sponsored by
RTI International
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for HIV focused on measuring Pre-exposure prophylaxis (PrEP), Antiretroviral therapy (ART), Alcohol and other drugs (AODs), Human Immunodeficiency Virus (HIV), Couples, Substance use, Stigma, Couples Health CoOp (CHC), South Africa, Undetectable=Untransmittable (U=U), Status-neutral

Eligibility Criteria

18 Years - 30 Years (Adult)All SexesAccepts Healthy Volunteers

Selected Inclusion Criteria (for Couples):

  • Is in a relationship with a primary partner
  • Had recent condomless sex with their primary partner
  • Has not taken PrEP or ART in the past 90 days
  • Has drunk alcohol and/or used drugs at least once a week over the past 90 days

Selected Exclusion Criteria (for Couples):

  • Not currently pregnant (for women)
  • Not currently being treated for drug-resistant tuberculosis (TB)

Sites / Locations

  • South African Medical Research CouncilRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

No Intervention

Experimental

Arm Label

Community Stigma Reduction Training and HTS/ART/PrEP Only

Community Stigma Reduction Training and HTS/ART/PrEP with CHC+

No Community Stigma Reduction Training and HTS/ART/PrEP Only

No Community Stigma Reduction Training and HTS/ART/PrEP with CHC+

Arm Description

Participants in the communities/catchment areas randomized to this arm will complete the community stigma assessments and will receive with stigma reduction training through community workshops. Couples will have access to standard HIV testing services (HTS) with antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) but not the Couples Health CoOp Plus (CHC+) intervention.

Participants in the communities/catchment areas randomized to this arm will complete the community stigma assessments with stigma reduction training through community workshops. Couples will have access to the Couples Health CoOp Plus (CHC+) intervention and standard HTS with antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP).

Participants in the communities/catchment areas randomized to this arm will complete the community stigma assessments but will not receive the stigma reduction training workshops. Couples will have access to standard HIV testing services (HTS) with antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) but not the Couples Health CoOp Plus (CHC+) intervention.

Participants in the communities/catchment areas randomized to this arm will complete the community assessments but not the stigma reduction training workshops. Couples will have access to the Couples Health CoOp Plus (CHC+) intervention and standard HIV testing services (HTS) with antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP).

Outcomes

Primary Outcome Measures

Antiretroviral Therapy (ART) Initiation [individual and couple-level]
ART initiation will be measured using initiation information recorded in the participant's clinic medical record.
Antiretroviral Therapy (ART) Initiation [individual and couple-level]
ART initiation will be measured using initiation information recorded in the participant's clinic medical record.
Antiretroviral Therapy (ART) Initiation [individual and couple-level]
ART initiation will be measured using initiation information recorded in the participant's clinic medical record.
Pre-Exposure Prophylaxis (PrEP) Initiation [individual and couple-level]
Pre-exposure prophylaxis (PrEP) initiation will be measured using initiation information recorded in the participant's clinic medical record.
Pre-Exposure Prophylaxis (PrEP) Initiation [individual and couple-level]
Pre-exposure prophylaxis (PrEP) initiation will be measured using initiation information recorded in the participant's clinic medical record.
Pre-Exposure Prophylaxis (PrEP) Initiation [individual and couple-level]
Pre-exposure prophylaxis (PrEP) initiation will be measured using initiation information recorded in the participant's clinic medical record.
Biological: Antiretroviral Therapy (ART) Adherence [individual and couple-level]
ART adherence will be measured using viral load or cluster of differentiation 4 (CD4) count measures recorded in the participant's medical record. Threshold for adherence will be cluster of differentiation 4 (CD4) count (more than 200) and HIV viral load (less than 50 copies per ml).
Biological: Antiretroviral Therapy (ART) Adherence [individual and couple-level]
ART adherence will be measured using viral load or cluster of differentiation 4 (CD4) count measures recorded in the participant's medical record. Threshold for adherence will be cluster of differentiation 4 (CD4) count (more than 200) and HIV viral load (less than 50 copies per ml).
Biological: Antiretroviral Therapy (ART) Adherence [individual and couple-level]
ART adherence will be measured using viral load or cluster of differentiation 4 (CD4) count measures recorded in the participant's medical record. Threshold for adherence will be cluster of differentiation 4 (CD4) count (more than 200) and HIV viral load (less than 50 copies per ml).
Self-Report: Antiretroviral Therapy (ART) Adherence [individual and couple-level]
Self-report past 30-day use, missed doses and patterns of use of antiretroviral therapy (ART) for self-report adherence will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Antiretroviral Therapy (ART) Adherence [individual and couple-level]
Self-report past 30-day use, missed doses and patterns of use of antiretroviral therapy (ART) for self-report adherence will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Antiretroviral Therapy (ART) Adherence [individual and couple-level]
Self-report past 30-day use, missed doses and patterns of use of antiretroviral therapy (ART) for self-report adherence will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Biological: Pre-Exposure Prophylaxis (PrEP) Adherence [individual and couple-level]
Tenofovir Diphosphate (TFV-DP) and FTC Triphosphate (FTC-TP) concentrations in dried blood spots (DBS) with drug concentrations of greater than 700 femtomoles (fmol)/liters(L) will be considered adherent to pre-exposure prophylaxis (PrEP).
Biological: Pre-Exposure Prophylaxis (PrEP) Adherence [individual and couple-level]
Tenofovir Diphosphate (TFV-DP) and FTC Triphosphate (FTC-TP) concentrations in dried blood spots (DBS) with drug concentrations of greater than 700 femtomoles (fmol)/liters(L) will be considered adherent to pre-exposure prophylaxis (PrEP).
Biological: Pre-Exposure Prophylaxis (PrEP) Adherence [individual and couple-level]
Tenofovir Diphosphate (TFV-DP) and FTC Triphosphate (FTC-TP) concentrations in dried blood spots (DBS) with drug concentrations of greater than 700 femtomoles (fmol)/liters(L) will be considered adherent to pre-exposure prophylaxis (PrEP).
Self-Report: Pre-Exposure Prophylaxis (PrEP) Adherence [individual and couple-level]
Self-report past 30-day use, missed doses and patterns of use of pre-exposure prophylaxis (PrEP) for self-report adherence will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Pre-Exposure Prophylaxis (PrEP) Adherence [individual and couple-level]
Self-report past 30-day use, missed doses and patterns of use of pre-exposure prophylaxis (PrEP) for self-report adherence will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Pre-Exposure Prophylaxis (PrEP) Adherence [individual and couple-level]
Self-report past 30-day use, missed doses and patterns of use of pre-exposure prophylaxis (PrEP) for self-report adherence will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Antiretroviral Therapy (ART) Persistence and Discontinuation [individual and couple-level]
Number of antiretroviral therapy (ART) refills since initiation recorded in clinic medical records.
Antiretroviral Therapy (ART) Persistence and Discontinuation [individual and couple-level]
Number of antiretroviral therapy (ART) refills since initiation recorded in clinic medical records.
Antiretroviral Therapy (ART) Persistence and Discontinuation [individual and couple-level]
Number of antiretroviral therapy (ART) refills since initiation recorded in clinic medical records.
Self-Report: Antiretroviral therapy (ART) Persistence and Discontinuation [individual and couple-level]
Self-reported time in months on antiretroviral therapy (ART) since initiation will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Antiretroviral therapy (ART) Persistence and Discontinuation [individual and couple-level]
Self-reported time in months on antiretroviral therapy (ART) since initiation will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Antiretroviral therapy (ART) Persistence and Discontinuation [individual and couple-level]
Self-reported time in months on antiretroviral therapy (ART) since initiation will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Data Extraction: Pre-Exposure Prophylaxis (PrEP) Persistence and Discontinuation [individual and couple-level
Number of pre-exposure prophylaxis (PrEP) refills since initiation as recorded clinic medical records.
Data Extraction: Pre-Exposure Prophylaxis (PrEP) Persistence and Discontinuation [individual and couple-level
Number of pre-exposure prophylaxis (PrEP) refills since initiation as recorded clinic medical records.
Data Extraction: Pre-Exposure Prophylaxis (PrEP) Persistence and Discontinuation [individual and couple-level
Number of pre-exposure prophylaxis (PrEP) refills since initiation as recorded clinic medical records.
Self-Report: Pre-Exposure Prophylaxis (PrEP) Persistence and Discontinuation [individual and couple-level]
Self-reported time in months on pre-exposure prophylaxis (PrEP) since initiation on pre-exposure prophylaxis (PrEP) will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Pre-Exposure Prophylaxis (PrEP) Persistence and Discontinuation [individual and couple-level]
Self-reported time in months on pre-exposure prophylaxis (PrEP) since initiation on pre-exposure prophylaxis (PrEP) will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Pre-Exposure Prophylaxis (PrEP) Persistence and Discontinuation [individual and couple-level]
Self-reported time in months on pre-exposure prophylaxis (PrEP) since initiation on pre-exposure prophylaxis (PrEP) will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Data Extraction: Antiretroviral therapy (ART) Retention
Antiretroviral therapy (ART) retention in care will be measured as attendance to follow-up visits as recorded in clinic medical records.
Data Extraction: Antiretroviral therapy (ART) Retention
Antiretroviral therapy (ART) retention in care will be measured as attendance to follow-up visits as recorded in clinic medical records.
Data Extraction: Antiretroviral therapy (ART) Retention
Antiretroviral therapy (ART) retention in care will be measured as attendance to follow-up visits as recorded in clinic medical records.
Self-Report: Pre-exposure Prophylaxis (PrEP) Retention [individual and couple-level]
Self-report pre-exposure prophylaxis (PrEP) retention in care will be measured as attendance to follow-up visits using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Pre-exposure Prophylaxis (PrEP) Retention [individual and couple-level]
Self-report pre-exposure prophylaxis (PrEP) retention in care will be measured as attendance to follow-up visits using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Pre-exposure Prophylaxis (PrEP) Retention [individual and couple-level]
Self-report pre-exposure prophylaxis (PrEP) retention in care will be measured as attendance to follow-up visits using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).

Secondary Outcome Measures

Community Stigma [structural level]
Surveys will be used to measure stigmatizing attitudes and perceptions towards people who use alcohol and other drugs (AODs), living with HIV and seeking and antiretroviral therapy (ART) or pre-exposure prophylaxis (PrEP) services for prevention. Greater values indicate higher levels of community-level stigma and discrimination.
Community Stigma [structural level]
Surveys will be used to measure stigmatizing attitudes and perceptions towards people who use alcohol and other drugs (AODs), living with HIV and seeking and antiretroviral therapy (ART) or pre-exposure prophylaxis (PrEP) services for prevention. Greater values indicate higher levels of community-level stigma and discrimination.
Community Stigma [structural level]
Surveys will be used to measure stigmatizing attitudes and perceptions towards people who use alcohol and other drugs (AODs), living with HIV and seeking and antiretroviral therapy (ART) or pre-exposure prophylaxis (PrEP) services for prevention. Greater values indicate higher levels of community-level stigma and discrimination.
Biological: Drug use [individual level]
Recent drug use (amphetamine, cocaine, methamphetamine, marijuana [THC], opiates and/or Mandrax) will be measured using a rapid urine-based drug screening test panel.
Biological: Drug use [individual level]
Recent drug use (amphetamine, cocaine, methamphetamine, marijuana [THC], opiates and/or Mandrax) will be measured using a rapid urine-based drug screening test panel.
Biological: Drug use [individual level]
Recent drug use (amphetamine, cocaine, methamphetamine, marijuana [THC], opiates and/or Mandrax) will be measured using a rapid urine-based drug screening test panel.
Biological: Drug use [individual level]
Recent drug use (amphetamine, cocaine, methamphetamine, marijuana [THC], opiates and/or Mandrax) will be measured using a rapid urine-based drug screening test panel.
Biological: Alcohol use [individual level]
Recent alcohol (last 10 days) use will be measured by the presence of ethyl glucuronide (EtG), a breakdown product of ethanol, using an ethyl glucuronide (EtG) urine test.
Biological: Alcohol use [individual level]
Recent alcohol (last 10 days) use will be measured by the presence of ethyl glucuronide (EtG), a breakdown product of ethanol, using an ethyl glucuronide (EtG) urine test.
Biological: Alcohol use [individual level]
Recent alcohol (last 10 days) use will be measured by the presence of ethyl glucuronide (EtG), a breakdown product of ethanol, using an ethyl glucuronide (EtG) urine test.
Biological: Alcohol use [individual level]
Recent alcohol (last 10 days) use will be measured by the presence of ethyl glucuronide (EtG), a breakdown product of ethanol, using an ethyl glucuronide (EtG) urine test.
Self-Report: Gender-Based Violence (GBV) [individual and couple-level]
Self-report emotional, physical, and sexual abuse, recent victimization, and family violence & experience of physical & sexual abuse will be measured using the World Health Organization (WHO) assessment of emotional, physical, & sexual abuse and the Revised Risk Behavior Assessment (RRBA).
Self-Report: Gender-Based Violence (GBV) [individual and couple-level]
Self-report emotional, physical, and sexual abuse, recent victimization, and family violence & experience of physical & sexual abuse will be measured using the World Health Organization (WHO) assessment of emotional, physical, & sexual abuse and the Revised Risk Behavior Assessment (RRBA).
Self-Report: Gender-Based Violence (GBV) [individual and couple-level]
Self-report emotional, physical, and sexual abuse, recent victimization, and family violence & experience of physical & sexual abuse will be measured using the World Health Organization (WHO) assessment of emotional, physical, & sexual abuse and the Revised Risk Behavior Assessment (RRBA).
Self-Report: Gender-Based Violence (GBV) [individual and couple-level]
Self-report emotional, physical, and sexual abuse, recent victimization, and family violence & experience of physical & sexual abuse will be measured using the World Health Organization (WHO) assessment of emotional, physical, & sexual abuse and the Revised Risk Behavior Assessment (RRBA).
Self-Report: Sexual Risk [individual and couple-level]
Self-reported frequency of condom use at last sex over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Sexual Risk [individual and couple-level]
Self-reported frequency of condom use at last sex over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Sexual Risk [individual and couple-level]
Self-reported frequency of condom use at last sex over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Sexual Risk [individual and couple-level]
Self-reported frequency of condom use at last sex over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Sexual Risk [individual and couple-level]
Self-reported frequency of alcohol and other drug (AOD) use prior to sex in the last 3 months as measured by the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Sexual Risk [individual and couple-level]
Self-reported frequency of alcohol and other drug (AOD) use prior to sex in the last 3 months as measured by the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Sexual Risk [individual and couple-level]
Self-reported frequency of alcohol and other drug (AOD) use prior to sex in the last 3 months as measured by the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Sexual Risk [individual and couple-level]
Self-reported frequency of alcohol and other drug (AOD) use prior to sex in the last 3 months as measured by the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Sexual Risk [individual and couple-level]
Self-reported number of sex partners, concurrent sexual partners and sex trading partners over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Sexual Risk [individual and couple-level]
Self-reported number of sex partners, concurrent sexual partners and sex trading partners over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Sexual Risk [individual and couple-level]
Self-reported number of sex partners, concurrent sexual partners and sex trading partners over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Sexual Risk [individual and couple-level]
Self-reported number of sex partners, concurrent sexual partners and sex trading partners over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Sexual Risk [individual and couple-level]
Self-report responses on the single item measured by the Pretoria Risk Behavior Assessment (PRBA+) will be used to assess use of contraception and types of contraception.
Self-Report: Sexual Risk [individual and couple-level]
Self-report responses on the single item measured by the Pretoria Risk Behavior Assessment (PRBA+) will be used to assess use of contraception and types of contraception.
Self-Report: Sexual Risk [individual and couple-level]
Self-report responses on the single item measured by the Pretoria Risk Behavior Assessment (PRBA+) will be used to assess use of contraception and types of contraception.
Self-Report: Sexual Risk [individual and couple-level]
Self-report responses on the single item measured by the Pretoria Risk Behavior Assessment (PRBA+) will be used to assess use of contraception and types of contraception.
Self-Report: Sexual Risk [individual and couple-level]
Self-report responses on single-item questions will be used to assess the extent to which participants perceive themselves as at risk for HIV infection measured by the Pretoria Risk Behavior Assessment (PRBA+). Higher levels indicate greater perceived HIV risk.
Self-Report: Sexual Risk [individual and couple-level]
Self-report responses on single-item questions will be used to assess the extent to which participants perceive themselves as at risk for HIV infection measured by the Pretoria Risk Behavior Assessment (PRBA+). Higher levels indicate greater perceived HIV risk.
Self-Report: Sexual Risk [individual and couple-level]
Self-report responses on single-item questions will be used to assess the extent to which participants perceive themselves as at risk for HIV infection measured by the Pretoria Risk Behavior Assessment (PRBA+). Higher levels indicate greater perceived HIV risk.
Self-Report: Sexual Risk [individual and couple-level]
Self-report responses on single-item questions will be used to assess the extent to which participants perceive themselves as at risk for HIV infection measured by the Pretoria Risk Behavior Assessment (PRBA+). Higher levels indicate greater perceived HIV risk.
Self-Report: Gender Norms [individual and couple-level]
Self-reported attitudes about traditional gender roles, empowerment, and assertiveness will be measured by the Gender ideology Scale (GIS) and the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Gender Norms [individual and couple-level]
Self-reported attitudes about traditional gender roles, empowerment, and assertiveness will be measured by the Gender ideology Scale (GIS) and the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Gender Norms [individual and couple-level]
Self-reported attitudes about traditional gender roles, empowerment, and assertiveness will be measured by the Gender ideology Scale (GIS) and the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Gender Norms [individual and couple-level]
Self-reported attitudes about traditional gender roles, empowerment, and assertiveness will be measured by the Gender ideology Scale (GIS) and the Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Communication [individual and couple-level]
Self-reported communication between partners regarding testing, HIV and sexually transmitted infection (STI) status, other partners, sexual negotiation, and condom use as measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Communication [individual and couple-level]
Self-reported communication between partners regarding testing, HIV and sexually transmitted infection (STI) status, other partners, sexual negotiation, and condom use as measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Communication [individual and couple-level]
Self-reported communication between partners regarding testing, HIV and sexually transmitted infection (STI) status, other partners, sexual negotiation, and condom use as measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Communication [individual and couple-level]
Self-reported communication between partners regarding testing, HIV and sexually transmitted infection (STI) status, other partners, sexual negotiation, and condom use as measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Observed or Knowledge of Stigma [individual and couple-level]
Observations or knowledge of stigma perpetrated by others in the community will be measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Observed or Knowledge of Stigma [individual and couple-level]
Observations or knowledge of stigma perpetrated by others in the community will be measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Observed or Knowledge of Stigma [individual and couple-level]
Observations or knowledge of stigma perpetrated by others in the community will be measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Self-Report: Observed or Knowledge of Stigma [individual and couple-level]
Observations or knowledge of stigma perpetrated by others in the community will be measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).

Full Information

First Posted
February 21, 2022
Last Updated
May 23, 2023
Sponsor
RTI International
Collaborators
Medical Research Council, South Africa
search

1. Study Identification

Unique Protocol Identification Number
NCT05310773
Brief Title
Couples Health CoOp Plus
Acronym
CHC+
Official Title
Multilevel Strategies & Tailored HIV Prevention and Care for Young Couples Who Use Alcohol and Other Drugs Across Cape Town: Couples Health CoOp Plus
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 6, 2022 (Actual)
Primary Completion Date
May 31, 2025 (Anticipated)
Study Completion Date
May 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
RTI International
Collaborators
Medical Research Council, South Africa

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study addresses HIV prevention and treatment for young couples living in Cape Town, South Africa, through a comprehensive biobehavioral multilevel approach-the Couples Health CoOp Plus (CHC+). Through a cluster randomized trial with a modified factorial design, 24 Cape Town communities consisting of catchment areas for clinics that provide antiretroviral therapy (ART) and pre-exposure prophylaxis (PrEP), will receive either stigma-reduction training or no training with repeated measures. Within clinic catchment areas, 480 couples (young women and their primary male sex partners both aged 18 to 30) will be recruited. These couples will receive HIV testing services (HTS) and/or the Couples Health CoOp Plus (CHC+), depending on their intervention arm. The overarching aim of these interventions is to prevent new cases of HIV. It is hypothesized that communities that are assigned to the stigma reduction training will demonstrate higher levels of social acceptance and fewer cases of enacted/experienced stigma at the community level. Additionally, it is expected couples assigned to the Couples Health CoOp Plus (CHC+) intervention will have greater antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) initiation and adherence, lower alcohol and other drug (AOD) use, less sexual risk, less gender-based violence (GBV), and more positive gender norms and communication. Specifically, the study aims to: Aim 1: Modify the Couples Health CoOp (CHC) intervention to include antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) in a formative phase and with review from the Community Collaborative Board (CCB) and Peer Advisory Board (PAB). Aim 2: Evaluate the impact of a stigma reduction training and education on community members attitudes and behaviors toward young women and their primary male partners seeking HIV testing services (HTS)/antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) and other sexual and reproductive health services in their local clinics at 4- and 8-month follow-up. Aim 3: Test the efficacy of the Couples Health CoOp Plus (CHC+) to increase both partners' antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) initiation and adherence (primary outcome) and reduce alcohol and other drug (AOD) use, sexual risk and gender-based violence (GBV), and enhance positive gender norms and communication relative to HIV testing services (HTS) (secondary outcomes). Aim 4: Examine through mixed methods the interaction of the stigma-reduction training and the Couples Health CoOp Plus (CHC+) on increased antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) and initiation, retention, and adherence among young women and their primary partners.
Detailed Description
The Couples Health CoOp Plus (CHC+) was adapted from the Couples Health CoOp (CHC)-an empowerment-based intervention developed for South African couples that addresses the syndemic of alcohol and other drug (AOD) use, gender-based violence (GBV), and HIV risk. It is grounded in Social Cognitive Theory and promoted prevention strategies that addressed the relational context of equality in which sexual risk takes place. The Couples Health CoOp (CHC) has demonstrated efficacy in increasing condom use, improving gender norms, decreasing heavy alcohol use among men, and decreasing HIV incidence among women. Long-term benefits of the Couples Health CoOp (CHC) have been explored including women reporting less fighting with their partner and men reporting being more faithful and loving. As part of this current study (Aim 1), the behavioral Couples Health CoOp (CHC) was adapted to include biomedical HIV strategies antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) and updated materials. Formative qualitative work with a Community Collaborative Board (CCB) and a Peer Advisory Board (PAB) has guided the adaptation and updating of the Couples Health CoOp Plus (CHC+) intervention. The Couples Health CoOp Plus (CHC+) is a 2-module workshop delivered over two days and contains didactic and experiential lessons on alcohol and other drug (AOD) use, a status-neutral approach to the prevention and management of HIV, sexual and reproductive health (SRH), gender norms, gender-based violence (GBV), and tools to improve communication. Formative findings regarding clinic-level stigma and discrimination showed that stigma reduction training provided in communities surrounding healthcare clinics may reduce stigmatizing behaviors and attitudes that are enacted by family, friends, and other community members toward those seeking healthcare. The stigma reduction survey and training has been developed and adapted as part of Aim 1 formative activities. The study will enroll 20 couples in 24 communities in and around Cape Town, South Africa. Communities surrounding healthcare clinics will be paired according to community demographic and socioeconomic factors and randomized to one of four arms: stigma reduction training (community) and HIV testing services (HTS)/antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) (couple); stigma reduction training (community), and HIV testing services (HTS)/antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) with Couples Health CoOp Plus (CHC+) (couple); no stigma reduction training (community) and HIV testing services (HTS)/antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) (couple); no stigma reduction training (community), and HIV testing services (HTS)/antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) with Couples Health CoOp Plus (CHC+) (couple). As noted, couples in communities that do not receive the CHC+ intervention will receive HIV testing services (HTS), including provision of antiretroviral therapy (ART) and pre-exposure prophylaxis (PrEP) as part of standard of care. HIV, alcohol and other drug (AOD), and pregnancy testing will be conducted at baseline and at 3-, 6-, and 9-month follow-up. Assessment of community stigma occurs at baseline with all 24 communities and the stigma reduction training will occur in only those randomized to it. The follow-up occurs within all communities at 4- and 8-months post-baseline.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV, Substance Use, Stigma, Social
Keywords
Pre-exposure prophylaxis (PrEP), Antiretroviral therapy (ART), Alcohol and other drugs (AODs), Human Immunodeficiency Virus (HIV), Couples, Substance use, Stigma, Couples Health CoOp (CHC), South Africa, Undetectable=Untransmittable (U=U), Status-neutral

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
24 communities in clinic catchment areas (clinics selected and approved by City Health) that provide antiretroviral therapy (ART) and pre-exposure prophylaxis (PrEP) will be randomly assigned to the four arms of the study (6 communities per arm). Arm 1 will receive the community stigma reduction training and HIV testing services (HTS)/pre-exposure prophylaxis (PrEP)/anti-retroviral therapy (ART) but no Couples Health CoOp Plus (CHC+); Arm 2 will receive community stigma reduction training with HTS/PrEP/ART and CHC+; Arm 3 will receive neither the community stigma reduction training nor CHC+ but will receive HTS/PrEP/ART; and Arm 4 will receive HTS/PrEP/ART and CHC+ but not the community stigma reduction training. All communities will receive the community stigma assessments at baseline, 4 months, and 8 months follow-up.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
7944 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Community Stigma Reduction Training and HTS/ART/PrEP Only
Arm Type
Experimental
Arm Description
Participants in the communities/catchment areas randomized to this arm will complete the community stigma assessments and will receive with stigma reduction training through community workshops. Couples will have access to standard HIV testing services (HTS) with antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) but not the Couples Health CoOp Plus (CHC+) intervention.
Arm Title
Community Stigma Reduction Training and HTS/ART/PrEP with CHC+
Arm Type
Experimental
Arm Description
Participants in the communities/catchment areas randomized to this arm will complete the community stigma assessments with stigma reduction training through community workshops. Couples will have access to the Couples Health CoOp Plus (CHC+) intervention and standard HTS with antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP).
Arm Title
No Community Stigma Reduction Training and HTS/ART/PrEP Only
Arm Type
No Intervention
Arm Description
Participants in the communities/catchment areas randomized to this arm will complete the community stigma assessments but will not receive the stigma reduction training workshops. Couples will have access to standard HIV testing services (HTS) with antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) but not the Couples Health CoOp Plus (CHC+) intervention.
Arm Title
No Community Stigma Reduction Training and HTS/ART/PrEP with CHC+
Arm Type
Experimental
Arm Description
Participants in the communities/catchment areas randomized to this arm will complete the community assessments but not the stigma reduction training workshops. Couples will have access to the Couples Health CoOp Plus (CHC+) intervention and standard HIV testing services (HTS) with antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP).
Intervention Type
Behavioral
Intervention Name(s)
Community stigma reduction training
Intervention Description
Key aspects of the training include community stigma awareness training of people living with HIV, use of antiretroviral therapy (ART), pre-exposure prophylaxis (PrEP) for prevention of HIV and attitudes towards people who use alcohol and drugs. Selected modules will be modified from the existing clinic-based training to fit community stigma awareness and attitudes, as needed, to focus on aspects of stigma specific only to young women and men who engage in syndemic-related behaviours who live in their communities. This intervention has been adapted from implementation in clinics in Pretoria for use in a community setting in Cape Town. The stigma reduction training workshops will be delivered in communities randomized to receive this training (N=12 communities; estimated N=1164 participants).
Intervention Type
Behavioral
Intervention Name(s)
Couples Health CoOp Plus (CHC+)
Intervention Description
The Couples Health CoOp Plus (CHC+) was adapted from the initial Couples Health CoOp (CHC)-an empowerment-based intervention developed for South African couples that addresses the syndemic of alcohol and other drug (AOD) use, gender-based violence (GBV), and HIV risk. It is grounded in Social Cognitive Theory and promotes prevention strategies that address the relational context of equality in which sexual risk takes place. The adapted Couples Health CoOp Plus (CHC+) incorporates antiretroviral therapy (ART)/pre-exposure prophylaxis (PrEP) for a biobehavioral approach with an emphasis on uptake and good adherence (N=12 communities; estimated N=240 couples).
Primary Outcome Measure Information:
Title
Antiretroviral Therapy (ART) Initiation [individual and couple-level]
Description
ART initiation will be measured using initiation information recorded in the participant's clinic medical record.
Time Frame
3-month follow-up
Title
Antiretroviral Therapy (ART) Initiation [individual and couple-level]
Description
ART initiation will be measured using initiation information recorded in the participant's clinic medical record.
Time Frame
6-month follow-up
Title
Antiretroviral Therapy (ART) Initiation [individual and couple-level]
Description
ART initiation will be measured using initiation information recorded in the participant's clinic medical record.
Time Frame
9-month follow-up
Title
Pre-Exposure Prophylaxis (PrEP) Initiation [individual and couple-level]
Description
Pre-exposure prophylaxis (PrEP) initiation will be measured using initiation information recorded in the participant's clinic medical record.
Time Frame
3-month follow-up
Title
Pre-Exposure Prophylaxis (PrEP) Initiation [individual and couple-level]
Description
Pre-exposure prophylaxis (PrEP) initiation will be measured using initiation information recorded in the participant's clinic medical record.
Time Frame
6-month follow-up
Title
Pre-Exposure Prophylaxis (PrEP) Initiation [individual and couple-level]
Description
Pre-exposure prophylaxis (PrEP) initiation will be measured using initiation information recorded in the participant's clinic medical record.
Time Frame
9-month follow-up
Title
Biological: Antiretroviral Therapy (ART) Adherence [individual and couple-level]
Description
ART adherence will be measured using viral load or cluster of differentiation 4 (CD4) count measures recorded in the participant's medical record. Threshold for adherence will be cluster of differentiation 4 (CD4) count (more than 200) and HIV viral load (less than 50 copies per ml).
Time Frame
3-month follow-up
Title
Biological: Antiretroviral Therapy (ART) Adherence [individual and couple-level]
Description
ART adherence will be measured using viral load or cluster of differentiation 4 (CD4) count measures recorded in the participant's medical record. Threshold for adherence will be cluster of differentiation 4 (CD4) count (more than 200) and HIV viral load (less than 50 copies per ml).
Time Frame
6-month follow-up
Title
Biological: Antiretroviral Therapy (ART) Adherence [individual and couple-level]
Description
ART adherence will be measured using viral load or cluster of differentiation 4 (CD4) count measures recorded in the participant's medical record. Threshold for adherence will be cluster of differentiation 4 (CD4) count (more than 200) and HIV viral load (less than 50 copies per ml).
Time Frame
9-month follow-up
Title
Self-Report: Antiretroviral Therapy (ART) Adherence [individual and couple-level]
Description
Self-report past 30-day use, missed doses and patterns of use of antiretroviral therapy (ART) for self-report adherence will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
3-month follow-up
Title
Self-Report: Antiretroviral Therapy (ART) Adherence [individual and couple-level]
Description
Self-report past 30-day use, missed doses and patterns of use of antiretroviral therapy (ART) for self-report adherence will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
6-month follow-up
Title
Self-Report: Antiretroviral Therapy (ART) Adherence [individual and couple-level]
Description
Self-report past 30-day use, missed doses and patterns of use of antiretroviral therapy (ART) for self-report adherence will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
9-month follow-up
Title
Biological: Pre-Exposure Prophylaxis (PrEP) Adherence [individual and couple-level]
Description
Tenofovir Diphosphate (TFV-DP) and FTC Triphosphate (FTC-TP) concentrations in dried blood spots (DBS) with drug concentrations of greater than 700 femtomoles (fmol)/liters(L) will be considered adherent to pre-exposure prophylaxis (PrEP).
Time Frame
3-month follow-up
Title
Biological: Pre-Exposure Prophylaxis (PrEP) Adherence [individual and couple-level]
Description
Tenofovir Diphosphate (TFV-DP) and FTC Triphosphate (FTC-TP) concentrations in dried blood spots (DBS) with drug concentrations of greater than 700 femtomoles (fmol)/liters(L) will be considered adherent to pre-exposure prophylaxis (PrEP).
Time Frame
6-month follow-up
Title
Biological: Pre-Exposure Prophylaxis (PrEP) Adherence [individual and couple-level]
Description
Tenofovir Diphosphate (TFV-DP) and FTC Triphosphate (FTC-TP) concentrations in dried blood spots (DBS) with drug concentrations of greater than 700 femtomoles (fmol)/liters(L) will be considered adherent to pre-exposure prophylaxis (PrEP).
Time Frame
9-month follow-up
Title
Self-Report: Pre-Exposure Prophylaxis (PrEP) Adherence [individual and couple-level]
Description
Self-report past 30-day use, missed doses and patterns of use of pre-exposure prophylaxis (PrEP) for self-report adherence will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
3-month follow-up
Title
Self-Report: Pre-Exposure Prophylaxis (PrEP) Adherence [individual and couple-level]
Description
Self-report past 30-day use, missed doses and patterns of use of pre-exposure prophylaxis (PrEP) for self-report adherence will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
6-month follow-up
Title
Self-Report: Pre-Exposure Prophylaxis (PrEP) Adherence [individual and couple-level]
Description
Self-report past 30-day use, missed doses and patterns of use of pre-exposure prophylaxis (PrEP) for self-report adherence will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
9-month follow-up
Title
Antiretroviral Therapy (ART) Persistence and Discontinuation [individual and couple-level]
Description
Number of antiretroviral therapy (ART) refills since initiation recorded in clinic medical records.
Time Frame
3-month follow-up
Title
Antiretroviral Therapy (ART) Persistence and Discontinuation [individual and couple-level]
Description
Number of antiretroviral therapy (ART) refills since initiation recorded in clinic medical records.
Time Frame
6-month follow-up
Title
Antiretroviral Therapy (ART) Persistence and Discontinuation [individual and couple-level]
Description
Number of antiretroviral therapy (ART) refills since initiation recorded in clinic medical records.
Time Frame
9-month follow-up
Title
Self-Report: Antiretroviral therapy (ART) Persistence and Discontinuation [individual and couple-level]
Description
Self-reported time in months on antiretroviral therapy (ART) since initiation will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
3-month follow-up
Title
Self-Report: Antiretroviral therapy (ART) Persistence and Discontinuation [individual and couple-level]
Description
Self-reported time in months on antiretroviral therapy (ART) since initiation will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
6-month follow-up
Title
Self-Report: Antiretroviral therapy (ART) Persistence and Discontinuation [individual and couple-level]
Description
Self-reported time in months on antiretroviral therapy (ART) since initiation will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
9-month follow-up
Title
Data Extraction: Pre-Exposure Prophylaxis (PrEP) Persistence and Discontinuation [individual and couple-level
Description
Number of pre-exposure prophylaxis (PrEP) refills since initiation as recorded clinic medical records.
Time Frame
3-month follow-up
Title
Data Extraction: Pre-Exposure Prophylaxis (PrEP) Persistence and Discontinuation [individual and couple-level
Description
Number of pre-exposure prophylaxis (PrEP) refills since initiation as recorded clinic medical records.
Time Frame
6-month follow-up
Title
Data Extraction: Pre-Exposure Prophylaxis (PrEP) Persistence and Discontinuation [individual and couple-level
Description
Number of pre-exposure prophylaxis (PrEP) refills since initiation as recorded clinic medical records.
Time Frame
9-month follow-up
Title
Self-Report: Pre-Exposure Prophylaxis (PrEP) Persistence and Discontinuation [individual and couple-level]
Description
Self-reported time in months on pre-exposure prophylaxis (PrEP) since initiation on pre-exposure prophylaxis (PrEP) will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
3-month follow-up
Title
Self-Report: Pre-Exposure Prophylaxis (PrEP) Persistence and Discontinuation [individual and couple-level]
Description
Self-reported time in months on pre-exposure prophylaxis (PrEP) since initiation on pre-exposure prophylaxis (PrEP) will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
6-month follow-up
Title
Self-Report: Pre-Exposure Prophylaxis (PrEP) Persistence and Discontinuation [individual and couple-level]
Description
Self-reported time in months on pre-exposure prophylaxis (PrEP) since initiation on pre-exposure prophylaxis (PrEP) will be measured using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
9-month follow-up
Title
Data Extraction: Antiretroviral therapy (ART) Retention
Description
Antiretroviral therapy (ART) retention in care will be measured as attendance to follow-up visits as recorded in clinic medical records.
Time Frame
3-month follow-up
Title
Data Extraction: Antiretroviral therapy (ART) Retention
Description
Antiretroviral therapy (ART) retention in care will be measured as attendance to follow-up visits as recorded in clinic medical records.
Time Frame
6-month follow-up
Title
Data Extraction: Antiretroviral therapy (ART) Retention
Description
Antiretroviral therapy (ART) retention in care will be measured as attendance to follow-up visits as recorded in clinic medical records.
Time Frame
9-month follow-up
Title
Self-Report: Pre-exposure Prophylaxis (PrEP) Retention [individual and couple-level]
Description
Self-report pre-exposure prophylaxis (PrEP) retention in care will be measured as attendance to follow-up visits using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
3-month follow-up
Title
Self-Report: Pre-exposure Prophylaxis (PrEP) Retention [individual and couple-level]
Description
Self-report pre-exposure prophylaxis (PrEP) retention in care will be measured as attendance to follow-up visits using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
6-month follow-up
Title
Self-Report: Pre-exposure Prophylaxis (PrEP) Retention [individual and couple-level]
Description
Self-report pre-exposure prophylaxis (PrEP) retention in care will be measured as attendance to follow-up visits using the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
9-month follow-up
Secondary Outcome Measure Information:
Title
Community Stigma [structural level]
Description
Surveys will be used to measure stigmatizing attitudes and perceptions towards people who use alcohol and other drugs (AODs), living with HIV and seeking and antiretroviral therapy (ART) or pre-exposure prophylaxis (PrEP) services for prevention. Greater values indicate higher levels of community-level stigma and discrimination.
Time Frame
Baseline
Title
Community Stigma [structural level]
Description
Surveys will be used to measure stigmatizing attitudes and perceptions towards people who use alcohol and other drugs (AODs), living with HIV and seeking and antiretroviral therapy (ART) or pre-exposure prophylaxis (PrEP) services for prevention. Greater values indicate higher levels of community-level stigma and discrimination.
Time Frame
4-month follow-up
Title
Community Stigma [structural level]
Description
Surveys will be used to measure stigmatizing attitudes and perceptions towards people who use alcohol and other drugs (AODs), living with HIV and seeking and antiretroviral therapy (ART) or pre-exposure prophylaxis (PrEP) services for prevention. Greater values indicate higher levels of community-level stigma and discrimination.
Time Frame
8-month follow-up
Title
Biological: Drug use [individual level]
Description
Recent drug use (amphetamine, cocaine, methamphetamine, marijuana [THC], opiates and/or Mandrax) will be measured using a rapid urine-based drug screening test panel.
Time Frame
Baseline
Title
Biological: Drug use [individual level]
Description
Recent drug use (amphetamine, cocaine, methamphetamine, marijuana [THC], opiates and/or Mandrax) will be measured using a rapid urine-based drug screening test panel.
Time Frame
3-month follow-up
Title
Biological: Drug use [individual level]
Description
Recent drug use (amphetamine, cocaine, methamphetamine, marijuana [THC], opiates and/or Mandrax) will be measured using a rapid urine-based drug screening test panel.
Time Frame
6-month follow-up
Title
Biological: Drug use [individual level]
Description
Recent drug use (amphetamine, cocaine, methamphetamine, marijuana [THC], opiates and/or Mandrax) will be measured using a rapid urine-based drug screening test panel.
Time Frame
9-month follow-up
Title
Biological: Alcohol use [individual level]
Description
Recent alcohol (last 10 days) use will be measured by the presence of ethyl glucuronide (EtG), a breakdown product of ethanol, using an ethyl glucuronide (EtG) urine test.
Time Frame
Baseline
Title
Biological: Alcohol use [individual level]
Description
Recent alcohol (last 10 days) use will be measured by the presence of ethyl glucuronide (EtG), a breakdown product of ethanol, using an ethyl glucuronide (EtG) urine test.
Time Frame
3-month follow-up
Title
Biological: Alcohol use [individual level]
Description
Recent alcohol (last 10 days) use will be measured by the presence of ethyl glucuronide (EtG), a breakdown product of ethanol, using an ethyl glucuronide (EtG) urine test.
Time Frame
6-month follow-up
Title
Biological: Alcohol use [individual level]
Description
Recent alcohol (last 10 days) use will be measured by the presence of ethyl glucuronide (EtG), a breakdown product of ethanol, using an ethyl glucuronide (EtG) urine test.
Time Frame
9-month follow-up
Title
Self-Report: Gender-Based Violence (GBV) [individual and couple-level]
Description
Self-report emotional, physical, and sexual abuse, recent victimization, and family violence & experience of physical & sexual abuse will be measured using the World Health Organization (WHO) assessment of emotional, physical, & sexual abuse and the Revised Risk Behavior Assessment (RRBA).
Time Frame
Baseline
Title
Self-Report: Gender-Based Violence (GBV) [individual and couple-level]
Description
Self-report emotional, physical, and sexual abuse, recent victimization, and family violence & experience of physical & sexual abuse will be measured using the World Health Organization (WHO) assessment of emotional, physical, & sexual abuse and the Revised Risk Behavior Assessment (RRBA).
Time Frame
3-month follow-up
Title
Self-Report: Gender-Based Violence (GBV) [individual and couple-level]
Description
Self-report emotional, physical, and sexual abuse, recent victimization, and family violence & experience of physical & sexual abuse will be measured using the World Health Organization (WHO) assessment of emotional, physical, & sexual abuse and the Revised Risk Behavior Assessment (RRBA).
Time Frame
6-month follow-up
Title
Self-Report: Gender-Based Violence (GBV) [individual and couple-level]
Description
Self-report emotional, physical, and sexual abuse, recent victimization, and family violence & experience of physical & sexual abuse will be measured using the World Health Organization (WHO) assessment of emotional, physical, & sexual abuse and the Revised Risk Behavior Assessment (RRBA).
Time Frame
9-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-reported frequency of condom use at last sex over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
Baseline
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-reported frequency of condom use at last sex over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
3-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-reported frequency of condom use at last sex over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
6-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-reported frequency of condom use at last sex over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
9-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-reported frequency of alcohol and other drug (AOD) use prior to sex in the last 3 months as measured by the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
Baseline
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-reported frequency of alcohol and other drug (AOD) use prior to sex in the last 3 months as measured by the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
3-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-reported frequency of alcohol and other drug (AOD) use prior to sex in the last 3 months as measured by the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
6-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-reported frequency of alcohol and other drug (AOD) use prior to sex in the last 3 months as measured by the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
9-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-reported number of sex partners, concurrent sexual partners and sex trading partners over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
Baseline
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-reported number of sex partners, concurrent sexual partners and sex trading partners over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
3-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-reported number of sex partners, concurrent sexual partners and sex trading partners over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
6-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-reported number of sex partners, concurrent sexual partners and sex trading partners over the past 3 months measured by the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
9-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-report responses on the single item measured by the Pretoria Risk Behavior Assessment (PRBA+) will be used to assess use of contraception and types of contraception.
Time Frame
Baseline
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-report responses on the single item measured by the Pretoria Risk Behavior Assessment (PRBA+) will be used to assess use of contraception and types of contraception.
Time Frame
3-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-report responses on the single item measured by the Pretoria Risk Behavior Assessment (PRBA+) will be used to assess use of contraception and types of contraception.
Time Frame
6-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-report responses on the single item measured by the Pretoria Risk Behavior Assessment (PRBA+) will be used to assess use of contraception and types of contraception.
Time Frame
9-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-report responses on single-item questions will be used to assess the extent to which participants perceive themselves as at risk for HIV infection measured by the Pretoria Risk Behavior Assessment (PRBA+). Higher levels indicate greater perceived HIV risk.
Time Frame
Baseline
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-report responses on single-item questions will be used to assess the extent to which participants perceive themselves as at risk for HIV infection measured by the Pretoria Risk Behavior Assessment (PRBA+). Higher levels indicate greater perceived HIV risk.
Time Frame
3-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-report responses on single-item questions will be used to assess the extent to which participants perceive themselves as at risk for HIV infection measured by the Pretoria Risk Behavior Assessment (PRBA+). Higher levels indicate greater perceived HIV risk.
Time Frame
6-month follow-up
Title
Self-Report: Sexual Risk [individual and couple-level]
Description
Self-report responses on single-item questions will be used to assess the extent to which participants perceive themselves as at risk for HIV infection measured by the Pretoria Risk Behavior Assessment (PRBA+). Higher levels indicate greater perceived HIV risk.
Time Frame
9-month follow-up
Title
Self-Report: Gender Norms [individual and couple-level]
Description
Self-reported attitudes about traditional gender roles, empowerment, and assertiveness will be measured by the Gender ideology Scale (GIS) and the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
Baseline
Title
Self-Report: Gender Norms [individual and couple-level]
Description
Self-reported attitudes about traditional gender roles, empowerment, and assertiveness will be measured by the Gender ideology Scale (GIS) and the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
3-month follow-up
Title
Self-Report: Gender Norms [individual and couple-level]
Description
Self-reported attitudes about traditional gender roles, empowerment, and assertiveness will be measured by the Gender ideology Scale (GIS) and the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
6-month follow-up
Title
Self-Report: Gender Norms [individual and couple-level]
Description
Self-reported attitudes about traditional gender roles, empowerment, and assertiveness will be measured by the Gender ideology Scale (GIS) and the Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
9-month follow-up
Title
Self-Report: Communication [individual and couple-level]
Description
Self-reported communication between partners regarding testing, HIV and sexually transmitted infection (STI) status, other partners, sexual negotiation, and condom use as measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
Baseline
Title
Self-Report: Communication [individual and couple-level]
Description
Self-reported communication between partners regarding testing, HIV and sexually transmitted infection (STI) status, other partners, sexual negotiation, and condom use as measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
3-month follow-up
Title
Self-Report: Communication [individual and couple-level]
Description
Self-reported communication between partners regarding testing, HIV and sexually transmitted infection (STI) status, other partners, sexual negotiation, and condom use as measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
6-month follow-up
Title
Self-Report: Communication [individual and couple-level]
Description
Self-reported communication between partners regarding testing, HIV and sexually transmitted infection (STI) status, other partners, sexual negotiation, and condom use as measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
9-month follow-up
Title
Self-Report: Observed or Knowledge of Stigma [individual and couple-level]
Description
Observations or knowledge of stigma perpetrated by others in the community will be measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
Baseline
Title
Self-Report: Observed or Knowledge of Stigma [individual and couple-level]
Description
Observations or knowledge of stigma perpetrated by others in the community will be measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
3-month follow-up
Title
Self-Report: Observed or Knowledge of Stigma [individual and couple-level]
Description
Observations or knowledge of stigma perpetrated by others in the community will be measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
6-month follow-up
Title
Self-Report: Observed or Knowledge of Stigma [individual and couple-level]
Description
Observations or knowledge of stigma perpetrated by others in the community will be measured by the Revised Risk Behavior Assessment (RRBA)/Pretoria Risk Behavior Assessment (PRBA+).
Time Frame
9-month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Selected Inclusion Criteria (for Couples): Is in a relationship with a primary partner Had recent condomless sex with their primary partner Has not taken PrEP or ART in the past 90 days Has drunk alcohol and/or used drugs at least once a week over the past 90 days Selected Exclusion Criteria (for Couples): Not currently pregnant (for women) Not currently being treated for drug-resistant tuberculosis (TB)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wendee Wechsberg, PhD
Phone
919-541-6422
Email
wmw@rti.org
First Name & Middle Initial & Last Name or Official Title & Degree
Tara Carney, PhD
Phone
+27 21 9380326
Email
tara.carney@mrc.ac.za
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wendee Wechsberg, PhD
Organizational Affiliation
RTI International
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Felicia Browne, ScD, MPH
Organizational Affiliation
RTI International
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Tara Carney, PhD
Organizational Affiliation
Medical Research Council, South Africa
Official's Role
Principal Investigator
Facility Information:
Facility Name
South African Medical Research Council
City
Cape Town
State/Province
Western Cape
ZIP/Postal Code
7500
Country
South Africa
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tara Carney, PhD
Phone
+27 21 9380326
Email
tara.carney@mrc.ac.za

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Couples Health CoOp Plus

We'll reach out to this number within 24 hrs