Zambia One Love Aim 3 Trial

A Randomized Control Study to Evaluate Novel Interventions to Reduce Risk Factors Associated With HIV, Neglected Tropical and Non-communicable Diseases Among Couples in Zambia

The aim of this study is to determine whether a Strengthening our Vows (SOV) intervention will reduce HIV exposures from concurrent partnership (CP) when compared to the control Good Health Package Plus (GHPP), in addition to couples' voluntary HIV counseling and testing (CVCT), among concordant HIV-negative couples living in Zambia.

Study Overview

• Status: Completed
• Conditions: Sexually Transmitted Diseases; HIV; Neglected Diseases; Non-communicable Diseases
• Intervention / Treatment: Behavioral: Strengthening Our Vows (SOV); Behavioral: Good Health Package Plus (GHPP)

Detailed Description

This is a randomized control study to evaluate novel interventions to reduce risk factors associated with HIV, neglected tropical and non-communicable diseases among couples in Zambia.

The aim of this study is to determine whether a Strengthening our Vows (SOV) intervention will reduce HIV exposures from concurrent partnership (CP) when compared to the control Good Health Package Plus (GHPP), in addition to couples' voluntary HIV counseling and testing (CVCT), among concordant HIV-negative couples.

Investigators seeks to compare the impact of the SOV intervention and the GHPP intervention on reduction in a composite of risk factors associated with HIV acquisition from concurrent partners, compare the impact of GHPP and SOV on knowledge and use of hygiene and sanitation measures and hypertension and diabetes screening and management, and compare self-reported couples' testing (CVCT) with outside partners in the SOV and GHPP arms.

Couples will receive SOV or GHPP based on the pre-randomization of the clinic which they attend for standard of care HIV counseling and testing. The Strengthening our Vows (SOV) intervention will seek to establish a dialogue or norm where couples will be able to protect each other from HIV infection from outside partners. The Good Health Package Plus (GHPP) intervention focuses on strategies to improve household health related to diarrheal diseases, helminths, schistosomiasis, diabetes, and hypertension.

• Study Type: Interventional
• Enrollment (Actual): 3450
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Zambia
  • Lusaka, Zambia
    • Lusaka Research Site
  • Copperbelt
    • Ndola, Copperbelt, Zambia
      • Ndola Research Site

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 65 years (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

Heterosexual Zambian couples who have undergone CVCT as standard of care in government health clinics in Lusaka and Ndola. Couples must be women 18-45 cohabiting with men 18-65 years old, have cohabited 3 months or greater, are both HIV-negative and are able to attend the scheduled follow-up visits.

• Heterosexual HIV-concordant negative
• Cohabiting at least 3 months
• Both partners at least 18 years of age (women aged 18-45, men aged 18-65)
• Not on antiretroviral therapy including Post Exposure Prophylaxis (PEP) or Pre Exposure Prophylaxis (PrEP)
• Interested in participating
• Able and willing to provide informed consent (literacy is not required)
• Willing to complete interviewer-administered questionnaires on risk factors
• Available for follow-up for the duration of the study
• Willing and able to be contacted via phone or home visit
• Able and willing to provide adequate locator/contact information for retention purposes, and willing to be contacted by the study staff

Exclusion Criteria:

• Presence of any condition that, in the opinion of the investigator or designee, would preclude provision of informed consent, or otherwise interfere with achieving the study objectives
• Either partner HIV-positive or with indeterminate HIV rapid test results
• Attendance to a clinic involved in the opposite arm of the study (i.e., test with partner at a clinic indicated as SOV but attends a clinic indicated as GHPP or vice versa)

Study Plan

How is the study designed?

Design Details

• Primary Purpose: HEALTH_SERVICES_RESEARCH
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: NONE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: Strengthening our Vows (SOV) Group; Participants in the SOV arm will participate in the "Together HIV Free" and "Protecting My Spouse" plans.	Behavioral: Strengthening Our Vows (SOV); Participants, led by a counselor, will discuss options to keep HIV from entering their relationship including both sex partners remaining monogamous, using condoms every time they have sex with outside partners, and being tested together with outside partners to ensure they are HIV negative (Together HIV Free Plan). Participants will discuss options in the event of an outside exposure to HIV including abstaining from having sex with their spouse or by using condoms every time they have sex with their spouse until they can be retested for HIV after 30 days (Protecting my Spouse Plan). Participants will be screened for hypertension, diabetes, schistosomiasis, HIV, syphilis, and trichomonas vaginalis and the presence of sperm (women only). Health problems will be treated or referred. Couples will be administered questionnaires that record self-report of sexually transmitted infections, number of outside partners, and reports of sex without a condom with outside partners.
PLACEBO_COMPARATOR: Good Health Package Plus (GHPP) Group; Participants in the GHPP arm will receive education on the prevention of helminths, schistosomiasis, hypertension, diabetes, and diarrheal diseases through participatory and interactive group sessions.	Behavioral: Good Health Package Plus (GHPP); Participants, led by a counselor, will discuss how to prevent, screen, and treat neglected tropical diseases (helminths and schistosomiasis), non-communicable diseases (hypertension and diabetes) and diarrheal diseases through basic hygiene and sanitation. The facilitator will demonstrate proper handwashing techniques and chlorination of water and discuss diet and lifestyle changes. Participants will be screened for hypertension, diabetes, schistosomiasis, HIV, syphilis, and trichomonas vaginalis and the presence of sperm (women only). Health problems will be treated or referred. Couples will also be administered questionnaires that record self-report of sexually transmitted infections, number of outside partners, and reports of sex without a condom with outside partners.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
HIV Incidence Rate	The number of new laboratory confirmed HIV diagnosis.	Duration of Study (Up to six months)
Syphilis Incidence Rate	The number of new laboratory confirmed syphilis diagnosis.	Duration of Study (Up to six months)
Vaginal Trichomoniasis Incidence Rate	The number of new laboratory confirmed vaginal trichomoniasis diagnosis.	Duration of Study (Up to six months)
Number of Self-Reported Sexually Transmitted Infections (STIs)	The number of self-reported STIs via questionnaire.	Duration of Study (Up to six months)
Number of Reports of Sex without a Condom with Outside Partners	The number of reports of sex without using a condom reported via a study specific questionnaire.	Duration of Study (Up to six months)
Number of Reported Outside Partners	The self-reported number of sexual partners outside of marriage.	Duration of Study (Up to six months)
Knowledge and use of hygiene and sanitation measures	Number of participants who show increased knowledge of hygiene and sanitation measures via a study specific questionnaire.	Duration of Study (Up to six months)
Knowledge of hypertension and diabetes screening and management	Number of participants who show increased knowledge of hypertension and diabetes screening and management via a study specific questionnaire.	Duration of Study (Up to six months)
Number of self-reports of accessing couples' testing (CVCT) with outside partners	Number of participants who report accessing CVCT services with their outside partners reported via a study specific questionnaire.	Duration of Study (Up to six months)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Perceived Efficacy of Chlorine Use	The number of participants who report a perceived effect of chlorine use via a study specific questionnaire.	Duration of Study (Up to six months)
Perceived Efficacy of Handwashing	The number of participants who report a perceived effect of handwashing via a study specific questionnaire.	Duration of Study (Up to six months)
Perceived Efficacy of Deworming	The number of participants who report a perceived effect of deworming via a study specific questionnaire.	Duration of Study (Up to six months)
Perceived Efficacy of Management of Diabetes	The number of participants who report a perceived effect of management of diabetes via a study specific questionnaire.	Duration of Study (Up to six months)
Perceived Efficacy of Management of Hypertension	The number of participants who report a perceived effect of management of hypertension via a study specific questionnaire.	Duration of Study (Up to six months)
Change in Communication between Husband and Wife	Change in communication between husband and wife dyads regarding exposure to HIV through extramarital sexual behaviors will be measured using a study specific questionnaire.	Duration of Study (Up to six months)

Collaborators and Investigators

• Sponsor: Emory University
• Investigators: Principal Investigator: Susan Allen, MD, MPH, Emory University

Study record dates

Study Major Dates

• Study Start: January 1, 2016
• Primary Completion (ACTUAL): December 1, 2016
• Study Completion (ACTUAL): December 1, 2016

Study Registration Dates

• First Submitted: April 15, 2016
• First Submitted That Met QC Criteria: April 15, 2016
• First Posted (ESTIMATE): April 20, 2016

Study Record Updates

• Last Update Posted (ACTUAL): February 1, 2018
• Last Update Submitted That Met QC Criteria: January 30, 2018
• Last Verified: January 1, 2018

More Information

Terms related to this study

• Keywords: Non-communicable diseases; Sexually transmitted infections; Neglected tropical diseases
• Additional Relevant MeSH Terms: Pathologic Processes; Infections; Communicable Diseases; Disease Attributes; Sexually Transmitted Diseases; Noncommunicable Diseases; Neglected Diseases
• Other Study ID Numbers: IRB00083001

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO