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Simunye: A Couples-focused Intervention for HIV Prevention and Care in South Africa

Primary Purpose

Human Immunodeficiency Virus

Status
Recruiting
Phase
Not Applicable
Locations
South Africa
Study Type
Interventional
Intervention
A couples-focused intervention for HIV prevention and care in South Africa
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Human Immunodeficiency Virus focused on measuring HIV, Couples

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Human Sciences Research CouncilRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intervention

Attention Matched Control

Arm Description

For couples who are prevalent sero-discordant, this will be a CHTC session. For couples who are prevalent concordant HIV-positive, the first visit will be the first Partner Steps session. For couples in which one or both do not know their sero-status or have not tested for HIV in the past 12 months, the first session will be a CHTC session.

Participants in the control group will receive an intervention, with the same number of sessions as couples of the same sero-status in the intervention condition, delivered via one-on-one couples counseling sessions (i.e., one couple with one counselor).

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

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

Full Information

First Posted
January 28, 2022
Last Updated
September 29, 2023
Sponsor
University of Michigan
Collaborators
University of California, San Francisco, Human Sciences Research Council
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1. Study Identification

Unique Protocol Identification Number
NCT05231707
Brief Title
Simunye: A Couples-focused Intervention for HIV Prevention and Care in South Africa
Official Title
A Couples-focused Intervention for HIV Prevention and Care in South Africa
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 29, 2022 (Actual)
Primary Completion Date
July 1, 2024 (Anticipated)
Study Completion Date
July 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
University of California, San Francisco, Human Sciences Research Council

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
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.
Detailed Description
South Africa remains one of the countries mostly heavily impacted by the HIV epidemic, with an overall estimated adult HIV prevalence of 18% to 30% among female antenatal clinic attendees. There is now substantial evidence that more than 80% of new infections occur within primary male-female partnerships. The high rates of new infections among primary partnerships are attributed to a combination of low levels of HIV testing and a high prevalence of outside sex partners. Recent work by Darbes (MPI), in KwaZulu-Natal (KZN) - the site of the proposed new research - found that among a sample of 330 heterosexual couples, 49% of men and 41% of women had no previous HIV testing history. In 20% of couples, neither partner had ever tested for HIV, despite living in a region with one of the highest adult HIV prevalence globally. Beyond the low levels of HIV testing, recent work also demonstrates significant deficits across the continuum of care in South Africa: recent work by Haber in KZN shows that only 45% of HIV-positive individuals are linked to care, 35% initiate ART, and 33% reach viral suppression. There is increasing evidence of efficacy for couples' focused HIV prevention interventions. Couples HIV Testing and Counseling (CHTC) is a proven strategy to reduce the risk of HIV transmission between partners. However, CHTC focuses only on the first stage of the cascade of HIV care - testing - are there are no interventions that allow couples to pass through the cascade of care together. Using a randomized controlled trial design with 272 couples, we aim to address this gap in HIV prevention and care literature by comparing a package of dyadic focused HIV testing and counseling interventions, against an attention matched control. The proposed RCT will test the efficacy of the dyadic intervention for achieving gains in viral suppression and engagement in HIV care. Heterosexual couples represent a significant yet over- looked risk group in South Africa, and innovative solutions are urgently needed to improve progression across the continuum of HIV care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Human Immunodeficiency Virus
Keywords
HIV, Couples

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
544 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
For couples who are prevalent sero-discordant, this will be a CHTC session. For couples who are prevalent concordant HIV-positive, the first visit will be the first Partner Steps session. For couples in which one or both do not know their sero-status or have not tested for HIV in the past 12 months, the first session will be a CHTC session.
Arm Title
Attention Matched Control
Arm Type
Active Comparator
Arm Description
Participants in the control group will receive an intervention, with the same number of sessions as couples of the same sero-status in the intervention condition, delivered via one-on-one couples counseling sessions (i.e., one couple with one counselor).
Intervention Type
Behavioral
Intervention Name(s)
A couples-focused intervention for HIV prevention and care in South Africa
Intervention Description
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.
Primary Outcome Measure Information:
Title
Virologic suppression change
Description
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.
Time Frame
Baseline and every 6 months for 24 months
Secondary Outcome Measure Information:
Title
Behavioral indicators of engagement in HIV care
Description
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
Time Frame
Baseline and every 6 months for 24 months

10. Eligibility

Sex
All
Gender Based
Yes
Gender Eligibility Description
Cisgender only
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: both aged between 18-50 report being a cis-gender male and a cis-gender female report being in a relationship with each other for at least 6 months 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: have never initiated ART not currently on ART (but can have been on it before) if already on ART, that they have missed 3 doses of medication in the past 30 days Exclusion Criteria: Couples in which one or both members report experiencing or perpetrating severe IPV in the prior 6 months Below age 18 or above age 50 Report being transgender Report not being a relationship at all or for <6 months Are in a polyamorous marriage Are not sexual active with participating partner
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lynae Darbes, Ph.D.
Phone
5104594164
Email
lynaed@umich.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lynae Darbes, Ph.D.
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
Human Sciences Research Council
City
Sweetwaters
State/Province
KwaZulu Natal
ZIP/Postal Code
3201
Country
South Africa
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alastair van Heerden, PhD
Email
avanheerden@hsrc.ac.za
First Name & Middle Initial & Last Name & Degree
Sphamandla Mpisane
Phone
+27 76 580 9526
Email
SPMpisane@hsrc.ac.za

12. IPD Sharing Statement

Plan to Share IPD
No

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Simunye: A Couples-focused Intervention for HIV Prevention and Care in South Africa

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