NCT01554423

Brief Summary

This study is a Randomized Controlled Trial (RCT) of Integrated and Cognitive Behavioral Therapy for HIV Prevention in Pretoria, South Africa. The RCT will evaluate the efficacy of a brief motivational interview (BMI) and a cognitive-behavioral couples' (IFCBT) intervention alone and in combination against a comparison condition to reduce new cases of HIV and sexually transmitted infections and increase condom use and decrease sexual risk behavior, drug use, and intimate partner violence among young female drug users in Pretoria, South Africa and their primary intimate partners. In the RCT, 384 couples comprised of young female drug users who do (N = 192) and do not (N = 192) trade sex and their primary intimate heterosexual partners will be randomly assigned to one-of-four conditions: (1) testing and counseling; (2) brief motivational interview (BMI); (3) cognitive-behavioral couples' intervention (IFCBT); or (4) BMI and IFCBT combined. Eligibility criteria for couples include an HIV-negative drug using female aged 18 to 40 and their primary intimate partner or spouse who is also HIV negative. Each partner of each couple will be administered assessments with a rapid test for HIV and urine tests for Chlamydia, gonorrhea, trichomoniasis, and drug use at baseline and 3-month, 6-month, and 12-month follow-up.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
464

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jul 2010

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2010

Completed
1.6 years until next milestone

First Submitted

Initial submission to the registry

February 7, 2012

Completed
1 month until next milestone

First Posted

Study publicly available on registry

March 15, 2012

Completed
4.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 31, 2017

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2017

Completed
Last Updated

July 19, 2017

Status Verified

July 1, 2017

Enrollment Period

6.6 years

First QC Date

February 7, 2012

Last Update Submit

July 18, 2017

Conditions

Keywords

HIV Prevention Intervention

Outcome Measures

Primary Outcomes (4)

  • Biologically confirmed infectious disease status

    Biologically confirmed infectious disease (HIV, Chlamydia, gonorrhea, and trichomoniasis)

    Outcome measure will be assessed up to 18 months after enrollment.

  • Condom use and sexual risk behavior

    Condom use during last sexual intercourse, proportion of unprotected sex episodes; number of partners.

    Outcome measure will be assessed up to 18 months after enrollment.

  • Drug taking risk behavior

    Hazardous alcohol use, and positive urinalysis for marijuana, cocaine, heroin.

    Outcome measure will be assessed up to 18 months after enrollment.

  • Intimate partner violence

    Psychological, physical, and sexual violence.

    Outcome measure will be assessed up to 18 months after enrollment.

Study Arms (4)

Testing and Counseling

ACTIVE COMPARATOR

One of the four RCT arms will be comprised of couples randomly assigned to testing and counseling on HIV and associated STI co-infections based on revised procedures developed by the CDC. Couples will receive information on the transmission and prevention of HIV and STIs, the meaning of test results, and health consequences. Randomized trial studies of behavioral interventions have incorporated testing and counseling as a comparison condition and studies in the US and SSA countries have shown that testing and counseling on its own can help to reduce HIV/STI risk behaviors.

Other: Testing and Counseling

Brief Motivational Interview (BMI)

EXPERIMENTAL

The brief motivational interview (BMI) to be tested in the RCT in Pretoria is a one-session, 45 minute intervention that will coordinate three, 15-minute modules with one module each to (1) reduce hazardous drinking; (2) reduce illicit drug use; and (3) promote condom use. Each module is delivered by the clinician using a two-sided laminated card that includes scripted questions and visual aids. Consistent with brief intervention models, the BMI intervention is delivered during one 45 minute session with advice giving as a primary characteristic. Motivational interviewing is also incorporated within the BMI intervention by using a client-centered method of communication to foster behavior change through five techniques of expressing empathy, developing discrepancy, avoiding argumentation, supporting self-efficacy, and motivational rules.

Behavioral: Brief Motivational Interview (BMI)

Integrated Family and Cognitive Behavioral Therapy

EXPERIMENTAL

The IFCBT model is 6 sessions in length and coordinates the delivery of 4 cognitive-behavioral group couples' sessions with 2 individual couples' sessions to prevent HIV and STI co-infections among adult drug users. IFCBT targets HIV risk and protective factors that operate across multiple ecological systems. The four group couples' sessions coordinate Rational Emotive Therapy and Problem Solving Therapy strategies to reduce HIV risk behavior and promote protective behaviors. The two individual couples' sessions utilize structural and strategic approaches to promote adaptive communication and shared responsibility for condom use and gender equality and to directly address and reduce any form of abuse between partners when present. The six IFCBT sessions are delivered during a 2-week period with two group couples' sessions and one individual couples' session each week.

Behavioral: Integrated Family and Cognitive Behavioral Therapy

BMI + IFCBT

EXPERIMENTAL

Participants assigned to this experimental arm will receive Brief Motivational Interviewing combined with Integrated Family and Cognitive Behavioral Therapy.

Behavioral: Brief Motivational Interview (BMI)Behavioral: Integrated Family and Cognitive Behavioral Therapy

Interventions

Couples will receive information on the transmission and prevention of HIV and STIs, the meaning of test results, and health consequences.

Testing and Counseling

The brief motivational interview (BMI) to be tested in the RCT in Pretoria is a one-session, 45 minute intervention that will coordinate three, 15-minute modules with one module each to (1) reduce hazardous drinking; (2) reduce illicit drug use; and (3) promote condom use.

BMI + IFCBTBrief Motivational Interview (BMI)

The IFCBT model is 6 sessions in length and coordinates the delivery of 4 cognitive-behavioral group couples' sessions with 2 individual couples' sessions to prevent HIV and STI co-infections among adult drug users. IFCBT targets HIV risk and protective factors that operate across multiple ecological systems. The four group couples' sessions coordinate Rational Emotive Therapy and Problem Solving Therapy strategies to reduce HIV risk behavior and promote protective behaviors. The two individual couples' sessions utilize structural and strategic approaches to promote adaptive communication and shared responsibility for condom use and gender equality and to directly address and reduce any form of abuse between partners when present.

BMI + IFCBTIntegrated Family and Cognitive Behavioral Therapy

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Live in the Pretoria, South Africa region
  • Years of Age
  • In a steady, intimate relationship for 6 months or longer
  • Used illicit drugs in the past 6 months

You may not qualify if:

  • Acute suicidality/homicidality

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Louis Pasteur Medical Centre

Pretoria, Gauteng, 0002, South Africa

Location

MeSH Terms

Interventions

CounselingCognitive Behavioral Therapy

Intervention Hierarchy (Ancestors)

Mental Health ServicesBehavioral Disciplines and ActivitiesCommunity Health ServicesHealth ServicesHealth Care Facilities Workforce and ServicesBehavior TherapyPsychotherapy

Study Officials

  • William W Latimer, Ph.D.

    University of Florida

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor and Dean

Study Record Dates

First Submitted

February 7, 2012

First Posted

March 15, 2012

Study Start

July 1, 2010

Primary Completion

January 31, 2017

Study Completion

June 30, 2017

Last Updated

July 19, 2017

Record last verified: 2017-07

Locations