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WHC+ (Women's Health CoOp PLUS)

Primary Purpose

HIV, Sexual Risk, Sexually Transmitted Diseases

Status
Completed
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
Test, Treat, Retain(TTR) + Women's Health CoOp (WHC)
Test, Treat, Retain(TTR) only
Sponsored by
RTI International
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV focused on measuring Gender-based Violence, HIV, Randomized Controlled Trial, Sexually Transmitted Diseases, Substance Abuse Detection, Test, Treat and Retain

Eligibility Criteria

15 Years - 55 Years (Child, Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Female
  2. Black/African
  3. 15 years or older (if under 18, must be able to sign assent)
  4. Use at least one of the following drugs: alcohol, marijuana (dagga), methamphetamine (tik), Mandrax (methaqualone), cocaine (crack and/or powder), heroin (Thai White), inhalants (glue and benzene) methylenedioxymethamphetamine (MDMA -ecstasy), lysergic acid diethylamide (LSD), or Kat/cat, Nyaope (a mixture of marijuana and heroin) - weekly in the past 90 days
  5. Have had unprotected vaginal sex with a male partner in the last six months
  6. Able to speak English, Sesotho, Tswana, or Zulu
  7. Consent to HIV rapid testing and drug testing
  8. Provide written verbal and assent/consent to participate
  9. Able to provide verifiable locator information for the Tshwane area and plan to stay there in the next 12 months

Exclusion Criteria:

  1. Males
  2. Individuals who do not self-identify as Black/African

Sites / Locations

  • RTI International - Headquarters
  • Wesley Community Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Test, Treat, Retain(TTR) only

Test, Treat, Retain(TTR) + Women's Health CoOp (WHC)

Arm Description

Participants in this group will be screened for HIV. HIV positive women will be given post-test counseling and referrals for prompt medical evaluation.

TTR +WHC: Participants in this group will be screened for HIV. HIV positive women, will be given post-test counseling and referrals for prompt medical evaluation and assessment. Both HIV negative and positive participants in this group will participate in 2 individual behavioral counseling sessions focusing on reducing HIV risk behaviours, alcohol and other drug use, and risk of violent victimization. It also adds case management to increase follow through with referrals and risk reduction plans and activities. This intervention is an adaptation of the evidence-based Women's CoOp(PI: Dr. Wendee M. Wechsberg).

Outcomes

Primary Outcome Measures

Unprotected intercourse among women
Percentages of condom use at last sex
Unprotected intercourse among women
Percentages of condom use at last sex

Secondary Outcome Measures

Medical evaluation initiation amongst HIV-positive
Percentages of HIV-positive women receiving medical evaluations.
Medical evaluation initiation amongst HIV-positive
Percentages of HIV-positive women receiving medical evaluations.
Treatment initiation and retention amongst HIV-positive women
Percentages of HIV-positive women starting and staying in treatment
Treatment initiation and retention amongst HIV-positive women
Percentages of HIV-positive women starting and staying in treatment
HIV viral load among HIV-positive women who meet criteria for antiretroviral treatment (ART) and who produce medical records with HIV viral loads
HIV viral load from medical record
HIV viral load among HIV-positive women who meet criteria for antiretroviral treatment (ART) and who produce medical records with HIV viral loads
HIV viral load from medical record
Alcohol use
Frequency of alcohol use in previous 30 days measured by Revised Risk Behavior Assessment (RRBA) and breath test
Alcohol use
Frequency of alcohol use in previous 30 days measured by Revised Risk Behavior Assessment (RRBA) and breath test
Victimization
Percentages of women who report being beaten, attacked with a weapon, or forced to have sex in the previous 90 days
Victimization
Percentages of women who report being beaten, attacked with a weapon, or forced to have sex in the previous 90 days

Full Information

First Posted
December 1, 2011
Last Updated
September 18, 2017
Sponsor
RTI International
Collaborators
University of North Carolina, Chapel Hill
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1. Study Identification

Unique Protocol Identification Number
NCT01497405
Brief Title
WHC+ (Women's Health CoOp PLUS)
Official Title
Combination Prevention for Vulnerable Women in South Africa
Study Type
Interventional

2. Study Status

Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
May 2012 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
RTI International
Collaborators
University of North Carolina, Chapel Hill

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study compares the effects of standard HIV test, treat and retain (TTR) practices with TTR plus a woman-focused enhanced strategy--Women's Health CoOp (WHC+) intervention) targeting hard-to-reach and vulnerable alcohol and other drug (AOD)-using women to determine if the WHC+ intervention is more efficacious than TTR alone in reducing HIV risk behavior. Additionally, the study will determine whether HIV positive women in the WHC+ arm are more likely to follow through with referrals for further medical evaluation and linkages to HIV treatment and other care than women in the TTR arm.
Detailed Description
There is growing recognition that no single strategy will be sufficient to eliminate transmission. In light of evidence that neither existing biomedical interventions nor any existing behavioral interventions will be sufficient to control the HIV epidemic in South Africa, the proposed study will combine a biomedical intervention with an evidence-based behavioral intervention (i.e., the Women's Health CoOp) to maximize the efficacy of both strategies. If this combination intervention proves efficacious, there is a high likelihood that it can be widely implemented, be sustainable and have a substantial public health impact by reducing the exceedingly high HIV incidence in South Africa. The overarching goal of the proposed research is to determine whether this enhanced combination prevention strategy targeting vulnerable AOD-using women is more efficacious than current standard practices. The specific aims of the proposed study are: Aim 1: To expand the WHC outreach strategies to reach more alcohol and other drug (AOD) - using vulnerable women in Pretoria, South Africa. Aim 2: To test whether adding WHC to standard Treat, Test, and Retain (TTR) practices results in more HIV-positive AOD-using women getting medical evaluations (e.g., cluster of differentiation 4 (CD4), viral load), starting treatment, staying in treatment and in greater reductions in risk behaviors (e.g., AOD use, condom use, victimization) among all women-positive or negative. The study uses a geographical cluster randomized design. Hotspots (i.e. places where sex workers and drug using women congregate) in the city of Pretoria and the surrounding areas were mapped using geographic information system (GIS) software. Fourteen hotspots were identified and geocoded. The entire area was divided into 14 zones, each of which included a hotspot. Seven matched pairs of zones were created based on socio-economic conditions and estimates of the numbers of sex workers and drug-using women residing in them. Zones within pairs were randomized to the TTR arm or the WHC+ arm. Participants are recruited by outreach workers and their intervention condition is based on the zone from which they were recruited. At study enrollment/baseline, eligible participants complete a questionnaire and baseline HIV, drug and pregnancy testing. Follow-up data collection will be conducted at 6-months and 12-months post-baseline.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV, Sexual Risk, Sexually Transmitted Diseases, Substance Abuse, Violence, Victimization
Keywords
Gender-based Violence, HIV, Randomized Controlled Trial, Sexually Transmitted Diseases, Substance Abuse Detection, Test, Treat and Retain

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
641 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Test, Treat, Retain(TTR) only
Arm Type
Active Comparator
Arm Description
Participants in this group will be screened for HIV. HIV positive women will be given post-test counseling and referrals for prompt medical evaluation.
Arm Title
Test, Treat, Retain(TTR) + Women's Health CoOp (WHC)
Arm Type
Experimental
Arm Description
TTR +WHC: Participants in this group will be screened for HIV. HIV positive women, will be given post-test counseling and referrals for prompt medical evaluation and assessment. Both HIV negative and positive participants in this group will participate in 2 individual behavioral counseling sessions focusing on reducing HIV risk behaviours, alcohol and other drug use, and risk of violent victimization. It also adds case management to increase follow through with referrals and risk reduction plans and activities. This intervention is an adaptation of the evidence-based Women's CoOp(PI: Dr. Wendee M. Wechsberg).
Intervention Type
Behavioral
Intervention Name(s)
Test, Treat, Retain(TTR) + Women's Health CoOp (WHC)
Intervention Description
TTR +WHC: Participants in this group will be screened for HIV. HIV positive women, will be given post-test counseling and referrals for prompt medical evaluation and assessment.Both HIV negative and positive participants in this group will participate in 2 individual behavioral counseling sessions focusing on reducing HIV risk behaviours, alcohol and other drug use, and risk of violent victimization. It also adds case management to increase follow through with referrals and risk reduction plans and activities.This will also include case management sessions. This intervention is an adaptation of the evidence-based Women's CoOp (PI: Dr. Wendee M. Wechsberg).
Intervention Type
Biological
Intervention Name(s)
Test, Treat, Retain(TTR) only
Intervention Description
TTR +only: Participants in this group will be screened for HIV. HIV positive women will be given post-test counseling and referrals for prompt medical evaluation.
Primary Outcome Measure Information:
Title
Unprotected intercourse among women
Description
Percentages of condom use at last sex
Time Frame
6 months
Title
Unprotected intercourse among women
Description
Percentages of condom use at last sex
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Medical evaluation initiation amongst HIV-positive
Description
Percentages of HIV-positive women receiving medical evaluations.
Time Frame
6 months
Title
Medical evaluation initiation amongst HIV-positive
Description
Percentages of HIV-positive women receiving medical evaluations.
Time Frame
12 months
Title
Treatment initiation and retention amongst HIV-positive women
Description
Percentages of HIV-positive women starting and staying in treatment
Time Frame
6 months
Title
Treatment initiation and retention amongst HIV-positive women
Description
Percentages of HIV-positive women starting and staying in treatment
Time Frame
12 months
Title
HIV viral load among HIV-positive women who meet criteria for antiretroviral treatment (ART) and who produce medical records with HIV viral loads
Description
HIV viral load from medical record
Time Frame
6 months
Title
HIV viral load among HIV-positive women who meet criteria for antiretroviral treatment (ART) and who produce medical records with HIV viral loads
Description
HIV viral load from medical record
Time Frame
12 months
Title
Alcohol use
Description
Frequency of alcohol use in previous 30 days measured by Revised Risk Behavior Assessment (RRBA) and breath test
Time Frame
6 months post intervention
Title
Alcohol use
Description
Frequency of alcohol use in previous 30 days measured by Revised Risk Behavior Assessment (RRBA) and breath test
Time Frame
12 months post intervention
Title
Victimization
Description
Percentages of women who report being beaten, attacked with a weapon, or forced to have sex in the previous 90 days
Time Frame
6 months post intervention
Title
Victimization
Description
Percentages of women who report being beaten, attacked with a weapon, or forced to have sex in the previous 90 days
Time Frame
12 months post intervention

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Female Black/African 15 years or older (if under 18, must be able to sign assent) Use at least one of the following drugs: alcohol, marijuana (dagga), methamphetamine (tik), Mandrax (methaqualone), cocaine (crack and/or powder), heroin (Thai White), inhalants (glue and benzene) methylenedioxymethamphetamine (MDMA -ecstasy), lysergic acid diethylamide (LSD), or Kat/cat, Nyaope (a mixture of marijuana and heroin) - weekly in the past 90 days Have had unprotected vaginal sex with a male partner in the last six months Able to speak English, Sesotho, Tswana, or Zulu Consent to HIV rapid testing and drug testing Provide written verbal and assent/consent to participate Able to provide verifiable locator information for the Tshwane area and plan to stay there in the next 12 months Exclusion Criteria: Males Individuals who do not self-identify as Black/African
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wendee M Wechsberg, PhD
Organizational Affiliation
RTI International
Official's Role
Principal Investigator
Facility Information:
Facility Name
RTI International - Headquarters
City
Research Triangle Park
State/Province
North Carolina
ZIP/Postal Code
27709
Country
United States
Facility Name
Wesley Community Centre
City
Pretoria
ZIP/Postal Code
0126
Country
South Africa

12. IPD Sharing Statement

Citations:
PubMed Identifier
25978479
Citation
Wechsberg WM, Deren S, Myers B, Kirtadze I, Zule WA, Howard B, El-Bassel N. Gender-Specific HIV Prevention Interventions for Women Who Use Alcohol and Other Drugs: The Evolution of the Science and Future Directions. J Acquir Immune Defic Syndr. 2015 Jun 1;69 Suppl 2(0 1):S128-39. doi: 10.1097/QAI.0000000000000627.
Results Reference
background
PubMed Identifier
28887751
Citation
Wechsberg WM, Peasant C, Kline T, Zule WA, Ndirangu J, Browne FA, Gabel C, van der Horst C. HIV Prevention Among Women Who Use Substances And Report Sex Work: Risk Groups Identified Among South African Women. AIDS Behav. 2017 Nov;21(Suppl 2):155-166. doi: 10.1007/s10461-017-1889-0.
Results Reference
derived
PubMed Identifier
28441975
Citation
Wechsberg WM, van der Horst C, Ndirangu J, Doherty IA, Kline T, Browne FA, Belus JM, Nance R, Zule WA. Seek, test, treat: substance-using women in the HIV treatment cascade in South Africa. Addict Sci Clin Pract. 2017 Apr 26;12(1):12. doi: 10.1186/s13722-017-0077-x.
Results Reference
derived
PubMed Identifier
25318563
Citation
Wechsberg WM, Zule WA, Ndirangu J, Kline TL, Rodman NF, Doherty IA, Novak SP, van der Horst CM. The biobehavioral Women's Health CoOp in Pretoria, South Africa: study protocol for a cluster-randomized design. BMC Public Health. 2014 Oct 15;14:1074. doi: 10.1186/1471-2458-14-1074.
Results Reference
derived

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WHC+ (Women's Health CoOp PLUS)

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