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Implementation Research for Vulnerable Women in South Africa

Primary Purpose

HIV, Substance Abuse

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Women's Health CoOp (WHC)
Sponsored by
RTI International
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for HIV focused on measuring Implementation Science, HIV, Sexual Risk, Sexually Transmitted Diseases, Substance Abuse, Violence and Victimization, Linkage to care, Gender-based Violence, Antiretroviral Therapy (ART)

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Clinic Inclusion Criteria:

  • HIV/antenatal clinic or substance abuse treatment clinic
  • Located in townships surrounding Cape Town
  • Willing to take part in study

Patient Inclusion Criteria:

  • Female;
  • 18 to 45 years of age;
  • Reports use of at least one drug, including alcohol, at least weekly during the previous 3 months;
  • Reports unprotected sex with a male partner in the past 6 months;
  • Has a positive HIV test result from either the participating health clinic or rehab clinic, or a clinic issued ARV card or ARV medication as proof of positive status;
  • Reports the intention to remain in the area for at least the next 6 months;
  • Provides informed consent to participate.

Patient Exclusion Criteria:

  • Not HIV Positive
  • Not willing to do alcohol and drug screening

Sites / Locations

  • RTI International
  • Kheth'Impilo

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Women's Health CoOp (WHC)

Arm Description

This is an adapted behavioral intervention for women in South Africa, who use alcohol and other drugs and are living with HIV or at risk of acquiring HIV.

Outcomes

Primary Outcome Measures

Implementation and Service Outcomes: Readiness for appropriate change (appropriateness)
Explore perceived appropriateness of implementing the intervention through qualitative focus groups with clinic staff and patients
Implementation and Service Outcomes: Readiness for appropriate change (appropriateness)
Explore perceived appropriateness of implementing the intervention through qualitative focus groups with clinic staff and patients
Implementation and Service Outcomes: Readiness for appropriate change (appropriateness)
Explore perceived appropriateness of implementing the intervention through clinic staff survey
Implementation and Service Outcomes: Acceptability of the Women's Health CoOp (WHC) intervention
Assess perceived acceptability through qualitative focus groups with clinic staff and patients
Implementation and Service Outcomes: Acceptability of the Women's Health CoOp (WHC) intervention
Assess perceived acceptability through qualitative focus groups with clinic staff and patients
Implementation and Service Outcomes: Acceptability of the Women's Health CoOp (WHC) intervention
Assess perceived acceptability through patient interviews
Implementation and Service Outcomes: Acceptability of the Women's Health CoOp (WHC) intervention
Assess perceived acceptability through patient interviews
Implementation and Service Outcomes: Acceptability of the Women's Health CoOp (WHC) intervention
Assess perceived acceptability through clinic staff survey
Implementation and Service Outcome: Adoption of the Women's Health CoOp (WHC) intervention
Assess adoption of the intervention through qualitative focus groups with clinic staff.
Implementation and Service Outcome: Adoption of the WHC intervention
Assess adoption of the intervention through qualitative focus groups with clinic staff.
Implementation and Service Outcome: Cost
Assess start up and ongoing implementation costs
Implementation and Service Outcome: Cost
Assess start up and ongoing implementation costs
Implementation and Service Outcome: Feasibility
Exposure as measured by the ratio of the number of intervention workshops delivered to participants (a total of two across the intervention window) (compared to the total expected intervention visits. Acceptable retention measured at ≥85% of patients who complete both workshops within the intervention window.
Implementation and Service Outcome: Fidelity
Observation: fidelity item scores where a 90% or above fidelity rating will indicate acceptable fidelity
Implementation and Service Outcomes: Sustainability
Examine sustainability through qualitative focus groups with clinic staff
Implementation and Service Outcomes: Sustainability
Examine sustainability with clinic staff using an adapted TCU Workshop Assessment Follow-up Scale

Secondary Outcome Measures

Antiretroviral Therapy (ART) Initiation and Adherence
Number of participants that received clinical staging, were prescribed and initiated on antiretroviral therapy (ART) and were adhering to ART.
Antiretroviral Therapy (ART) Initiation and Adherence
Number of participants that received clinical staging, were prescribed and initiated on antiretroviral therapy (ART) and were adhering to ART.
Alcohol Use - self-reported frequency and amount
Participants' self-reported frequency and amount of alcohol use will be used to assess recent alcohol use.
Alcohol Use - self-reported frequency and amount
Participants' self-reported frequency and amount of alcohol use will be used to assess recent alcohol use.
Alcohol Use
Breathalyzer test results will be used to assess recent alcohol use.
Alcohol Use
Breathalyzer test results will be used to assess recent alcohol use.
Substance Use
Participants' frequency of benzodiazepines, cocaine, methamphetamine, MDMA, marijuana, and/or mandrax use will be used to assess recent substance use.
Substance Use
Participants' frequency of benzodiazepines, cocaine, methamphetamine, MDMA, marijuana, and/or mandrax use will be used to assess recent substance use.
Substance use
Urine drug screen test results will be used to assess recent use of drugs (benzodiazepines, cocaine, methamphetamine, MDMA, marijuana, and/or mandrax).
Substance use
Urine drug screen test results will be used to assess recent use of drugs (benzodiazepines, cocaine, methamphetamine, MDMA, marijuana, and/or mandrax).
Sexual Risk
Participants' self-reported frequency of condom use.
Sexual Risk
Participants' self-reported frequency of condom use.
Sexual Risk
Participants' self-reported number of sex partners.
Sexual Risk
Participants' self-reported number of sex partners.
Violence/Victimization
Percentages of participants who report being beaten, attacked with a weapon, or forced to have sex.
Violence/Victimization
Percentages of participants who report being beaten, attacked with a weapon, or forced to have sex.
Sexual Communication
The extent to which women have the skills to discuss sexual topics with their partners
Sexual Communication
The extent to which women have the skills to discuss sexual topics with their partners
Relationship Power
The extent to which women and their partners can equitably make decisions together as measured by the Relationship Power Scale (RPS)
Relationship Power
The extent to which women and their partners can equitably make decisions together as measured by the Relationship Power Scale (RPS)

Full Information

First Posted
January 21, 2016
Last Updated
August 25, 2021
Sponsor
RTI International
Collaborators
Kheth'Impilo
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1. Study Identification

Unique Protocol Identification Number
NCT02733003
Brief Title
Implementation Research for Vulnerable Women in South Africa
Official Title
Implementation Research for Vulnerable Women in South Africa
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Completed
Study Start Date
September 2015 (Actual)
Primary Completion Date
December 4, 2018 (Actual)
Study Completion Date
December 4, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
RTI International
Collaborators
Kheth'Impilo

4. Oversight

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

5. Study Description

Brief Summary
This study sought to implement the Women's Health CoOp (Cooperative) (WHC) intervention into healthcare, antenatal, and substance treatment clinics in South Africa and translated this evidence-based intervention into real-world settings. Implementation, service, and patient outcomes will be evaluated through an iterative stepped wedge design.
Detailed Description
This five-year implementation science study used a cluster-randomized stepped-wedge design to evaluate the implementation, service, and patient outcomes associated with the WHC for alcohol and other drug (AOD)-using HIV positive women in usual care settings. A list of four substance use treatment clinics and four healthcare clinics, identified and approved by the City of Cape Town, South Africa were randomized to begin the intervention during one of the four cycles. Each healthcare clinic was paired with a substance use treatment clinic based on geographic proximity, and each pair was randomized by computer into four succeeding 6-month implementation cycles where implementation of the WHC took place simultaneously at the paired sites. Approximately 120 HIV positive participants were recruited in each cycle (approximately 60 from each clinic) for the patient level outcomes. Both qualitative and quantitative data were collected to assess the appropriateness of marketing plans developed through formative methods, as well as the acceptability, adoption, feasibility, fidelity, and sustainability of the WHC intervention implementation as well as service outcomes (comprehensive services and timely service linkages) during each implementation cycle. Each implementation cycle included a pre-implementation period, implementation period (6-months), and post-implementation period. In the pre-implementation period, focus groups and questionnaires surveys were conducted with clinic staff to assess the readiness of each site to implement the WHC. During the implementation period, employees at each site were trained to facilitate the WHC and the WHC was integrated into site operations. Subsequently, in the post-implementation period the researchers collected data related to challenges, benefits, and sustainability from each site. The process was repeated for each cycle and these formative periods between cycles were used to inform backward- and forward- implementation strategies, make modifications to the WHC, and leave time for site-specific training for the next cycle. Consequently, the sites randomized to the first cycle had the longest post-intervention observation period whose implementation sustainability was checked through fidelity forms and sustainability questionnaires, and sites in the fourth cycle benefited the most because of lessons learned and information shared from previous cycles. The intervention was implemented in a group, however there were instances when only one participant was available and therefore the intervention was implemented one-on-one. The WHC has previously been tested in group and one-on-one formats and both have demonstrated consistent significant intervention effects. Research staff trained clinic staff members to deliver the intervention. The intervention was delivered by clinic staff and was not part of the research. The research questions were related to the feasibility of implementing the intervention in clinics and its acceptability to clinic staff and patients. The researchers collected information on patient-level outcomes to determine if the intervention was effective when it was delivered by clinic staff to patients in the clinic. Also, to assess acceptability of the intervention workshops among patients, the researchers conducted post-implementation focus groups with a randomly selected sub-sample of participants who participated in the intervention and completed their final 6-month appointment in each implementation cycle. Implementation of the WHC in usual care settings has the potential to reach more vulnerable women and could have a high public health impact if implementation is shown to be effective and sustainable in these real-world settings.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV, Substance Abuse
Keywords
Implementation Science, HIV, Sexual Risk, Sexually Transmitted Diseases, Substance Abuse, Violence and Victimization, Linkage to care, Gender-based Violence, Antiretroviral Therapy (ART)

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
564 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Women's Health CoOp (WHC)
Arm Type
Experimental
Arm Description
This is an adapted behavioral intervention for women in South Africa, who use alcohol and other drugs and are living with HIV or at risk of acquiring HIV.
Intervention Type
Behavioral
Intervention Name(s)
Women's Health CoOp (WHC)
Intervention Description
Participants in this group will participate in two workshops of the woman-focused intervention about HIV/STIs, sexual behaviors, alcohol and other drug use, violence, communication skills, and other issues.
Primary Outcome Measure Information:
Title
Implementation and Service Outcomes: Readiness for appropriate change (appropriateness)
Description
Explore perceived appropriateness of implementing the intervention through qualitative focus groups with clinic staff and patients
Time Frame
Baseline
Title
Implementation and Service Outcomes: Readiness for appropriate change (appropriateness)
Description
Explore perceived appropriateness of implementing the intervention through qualitative focus groups with clinic staff and patients
Time Frame
6-months post-enrollment
Title
Implementation and Service Outcomes: Readiness for appropriate change (appropriateness)
Description
Explore perceived appropriateness of implementing the intervention through clinic staff survey
Time Frame
Baseline
Title
Implementation and Service Outcomes: Acceptability of the Women's Health CoOp (WHC) intervention
Description
Assess perceived acceptability through qualitative focus groups with clinic staff and patients
Time Frame
Baseline
Title
Implementation and Service Outcomes: Acceptability of the Women's Health CoOp (WHC) intervention
Description
Assess perceived acceptability through qualitative focus groups with clinic staff and patients
Time Frame
6-months post-enrollment
Title
Implementation and Service Outcomes: Acceptability of the Women's Health CoOp (WHC) intervention
Description
Assess perceived acceptability through patient interviews
Time Frame
Baseline
Title
Implementation and Service Outcomes: Acceptability of the Women's Health CoOp (WHC) intervention
Description
Assess perceived acceptability through patient interviews
Time Frame
6-months post-enrollment
Title
Implementation and Service Outcomes: Acceptability of the Women's Health CoOp (WHC) intervention
Description
Assess perceived acceptability through clinic staff survey
Time Frame
Baseline
Title
Implementation and Service Outcome: Adoption of the Women's Health CoOp (WHC) intervention
Description
Assess adoption of the intervention through qualitative focus groups with clinic staff.
Time Frame
Baseline
Title
Implementation and Service Outcome: Adoption of the WHC intervention
Description
Assess adoption of the intervention through qualitative focus groups with clinic staff.
Time Frame
6-months post-enrollment
Title
Implementation and Service Outcome: Cost
Description
Assess start up and ongoing implementation costs
Time Frame
Baseline
Title
Implementation and Service Outcome: Cost
Description
Assess start up and ongoing implementation costs
Time Frame
6-months post-enrollment
Title
Implementation and Service Outcome: Feasibility
Description
Exposure as measured by the ratio of the number of intervention workshops delivered to participants (a total of two across the intervention window) (compared to the total expected intervention visits. Acceptable retention measured at ≥85% of patients who complete both workshops within the intervention window.
Time Frame
Throughout the period of the study, up to a maximum of one year
Title
Implementation and Service Outcome: Fidelity
Description
Observation: fidelity item scores where a 90% or above fidelity rating will indicate acceptable fidelity
Time Frame
Throughout the study at bimonthly intervals for up to one year
Title
Implementation and Service Outcomes: Sustainability
Description
Examine sustainability through qualitative focus groups with clinic staff
Time Frame
Throughout the period of the study, up to a maximum of one year
Title
Implementation and Service Outcomes: Sustainability
Description
Examine sustainability with clinic staff using an adapted TCU Workshop Assessment Follow-up Scale
Time Frame
6 months post-intervention
Secondary Outcome Measure Information:
Title
Antiretroviral Therapy (ART) Initiation and Adherence
Description
Number of participants that received clinical staging, were prescribed and initiated on antiretroviral therapy (ART) and were adhering to ART.
Time Frame
Baseline
Title
Antiretroviral Therapy (ART) Initiation and Adherence
Description
Number of participants that received clinical staging, were prescribed and initiated on antiretroviral therapy (ART) and were adhering to ART.
Time Frame
6 months post-enrollment
Title
Alcohol Use - self-reported frequency and amount
Description
Participants' self-reported frequency and amount of alcohol use will be used to assess recent alcohol use.
Time Frame
Baseline
Title
Alcohol Use - self-reported frequency and amount
Description
Participants' self-reported frequency and amount of alcohol use will be used to assess recent alcohol use.
Time Frame
6 months post-enrollment
Title
Alcohol Use
Description
Breathalyzer test results will be used to assess recent alcohol use.
Time Frame
Baseline
Title
Alcohol Use
Description
Breathalyzer test results will be used to assess recent alcohol use.
Time Frame
6 months post-enrollment
Title
Substance Use
Description
Participants' frequency of benzodiazepines, cocaine, methamphetamine, MDMA, marijuana, and/or mandrax use will be used to assess recent substance use.
Time Frame
Baseline
Title
Substance Use
Description
Participants' frequency of benzodiazepines, cocaine, methamphetamine, MDMA, marijuana, and/or mandrax use will be used to assess recent substance use.
Time Frame
6-months post-enrollment
Title
Substance use
Description
Urine drug screen test results will be used to assess recent use of drugs (benzodiazepines, cocaine, methamphetamine, MDMA, marijuana, and/or mandrax).
Time Frame
Baseline
Title
Substance use
Description
Urine drug screen test results will be used to assess recent use of drugs (benzodiazepines, cocaine, methamphetamine, MDMA, marijuana, and/or mandrax).
Time Frame
6-months post-enrollment
Title
Sexual Risk
Description
Participants' self-reported frequency of condom use.
Time Frame
Baseline
Title
Sexual Risk
Description
Participants' self-reported frequency of condom use.
Time Frame
6-months post-enrollment
Title
Sexual Risk
Description
Participants' self-reported number of sex partners.
Time Frame
Baseline
Title
Sexual Risk
Description
Participants' self-reported number of sex partners.
Time Frame
6-months post-enrollment
Title
Violence/Victimization
Description
Percentages of participants who report being beaten, attacked with a weapon, or forced to have sex.
Time Frame
Baseline
Title
Violence/Victimization
Description
Percentages of participants who report being beaten, attacked with a weapon, or forced to have sex.
Time Frame
6-months post-enrollment
Title
Sexual Communication
Description
The extent to which women have the skills to discuss sexual topics with their partners
Time Frame
Baseline
Title
Sexual Communication
Description
The extent to which women have the skills to discuss sexual topics with their partners
Time Frame
6-months post-enrollment
Title
Relationship Power
Description
The extent to which women and their partners can equitably make decisions together as measured by the Relationship Power Scale (RPS)
Time Frame
Baseline
Title
Relationship Power
Description
The extent to which women and their partners can equitably make decisions together as measured by the Relationship Power Scale (RPS)
Time Frame
6-months post-enrollment

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Clinic Inclusion Criteria: HIV/antenatal clinic or substance abuse treatment clinic Located in townships surrounding Cape Town Willing to take part in study Patient Inclusion Criteria: Female; 18 to 45 years of age; Reports use of at least one drug, including alcohol, at least weekly during the previous 3 months; Reports unprotected sex with a male partner in the past 6 months; Has a positive HIV test result from either the participating health clinic or rehab clinic, or a clinic issued ARV card or ARV medication as proof of positive status; Reports the intention to remain in the area for at least the next 6 months; Provides informed consent to participate. Patient Exclusion Criteria: Not HIV Positive Not willing to do alcohol and drug screening
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wendee M Wechsberg, PhD
Organizational Affiliation
Principal Researcher and Director of Substance Use, Gender, and Applied Research (SUGAR Program, Director of RTI Global Gender Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
RTI International
City
Research Triangle Park
State/Province
North Carolina
ZIP/Postal Code
27709
Country
United States
Facility Name
Kheth'Impilo
City
Cape Town
ZIP/Postal Code
8001
Country
South Africa

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
28923034
Citation
Wechsberg WM, Ndirangu JW, Speizer IS, Zule WA, Gumula W, Peasant C, Browne FA, Dunlap L. An implementation science protocol of the Women's Health CoOp in healthcare settings in Cape Town, South Africa: A stepped-wedge design. BMC Womens Health. 2017 Sep 18;17(1):85. doi: 10.1186/s12905-017-0433-8.
Results Reference
background
PubMed Identifier
29157230
Citation
Howard BN, Van Dorn R, Myers BJ, Zule WA, Browne FA, Carney T, Wechsberg WM. Barriers and facilitators to implementing an evidence-based woman-focused intervention in South African health services. BMC Health Serv Res. 2017 Nov 21;17(1):746. doi: 10.1186/s12913-017-2669-2.
Results Reference
background
PubMed Identifier
33891233
Citation
Wechsberg WM, Browne FA, Ndirangu J, Bonner CP, Kline TL, Gichane M, Zule WA. Outcomes of Implementing in the Real World the Women's Health CoOp Intervention in Cape Town, South Africa. AIDS Behav. 2021 Dec;25(Suppl 3):276-289. doi: 10.1007/s10461-021-03251-7. Epub 2021 Apr 23.
Results Reference
result
PubMed Identifier
32771909
Citation
Gichane MW, Wechsberg WM, Ndirangu J, Browne FA, Bonner CP, Grimwood A, Shaikh N, Howard B, Zule WA. Implementation science outcomes of a gender-focused HIV and alcohol risk-reduction intervention in usual-care settings in South Africa. Drug Alcohol Depend. 2020 Oct 1;215:108206. doi: 10.1016/j.drugalcdep.2020.108206. Epub 2020 Aug 1.
Results Reference
result

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Implementation Research for Vulnerable Women in South Africa

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