Muhimbili University of Health and Allied Programs
Dar Es Salaam, Coast Region, Tanzania
NCT Number: NCT03098693
This is a prospective observational study of couples in Kisarawe, Tanzania who will be provided an intervention that offers: (1) HIV self-testing kits and pre-test counseling provided at the household, (2) linkage to a counseling and referral center for those who test positive, (3) facilitated enrollment to care and treatment for couples with confirmed HIV infection; and (4) access to pre-exposure prophylaxis for the negative partner in a HIV sero-discordant couple. We will identify HIV sero-discordant couples through the HIV self-testing component, and through identifying discordant couples at the local HIV clinic. HIV sero-discordant couples (N=64 couples) will be administered a baseline, 6- ,12-, and 18-month survey, and the investigators will collect ongoing clinical data from each clinic visit. Biometric data (fingerprint) will be collected at enrollment, and all encounters with the counseling and referral center, and HIV treatment center, to allow linking of utilization of services with survey data.
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Notify Me18 year–55 year
All sexes
Observational
Dar Es Salaam, Coast Region, Tanzania
The investigators propose to conduct a prospective observational study of cohabitating couples aged 18 years and above in Kisarawe, Tanzania who will be provided: (1) distribution of HIV self-testing kits to cohabitating couples; (2) linkage to confirmatory HIV-testing & counseling for those who test HIV-positive; (3) facilitated enrollment to care and treatment for those couples with confirmed HIV infection; and (4) for HIV serodiscordant couples, access to PrEP for the HIV-negative partner. A baseline survey, and a follow-up survey approximately 2 weeks later and HIV test, will be administered to all couples involved in the self-testing phase of the study. A cohort of 60 to 70 HIV serodiscordant couples will receive a survey at baseline 6-, 12-, and 18-month survey, and the investigators will collect ongoing clinical data from each clinic visit. Biometric data (fingerprint) will be collected at study and intervention encounters to link utilization of services with survey data. The investigators will also enroll serodiscordant couples from patients already receiving care from the Kisarawe Care and Treatment Center (CTC).
The specific AIMS evaluate 4 key strategic goals, including:
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
To be eligible for participation in the self-testing cohort, each individual has to be:
To be eligible for the prevention and care portion of the study, couples must be:
Exclusion criteria
Couples will not be eligible for enrolled in the sero-discordant sub-cohort if:
Access to home-based HIV self-testing kits for stable couples.
Immediate access to ART for HIV infected couple members (per current Tanzanian standard of care).
Access to PrEP for HIV uninfected couple members.
Time frame: 2 weeks
The proportion of eligible individuals who received an HIV self-test kit who successfully used the kit within two weeks of receiving the test kit.
Time frame: 18 months
The self-reported proportion of study participants who told their primary partner the results of the HIV test generated by the self-test kit.
Time frame: 18 months
Proportion of HIV Sero-discordant Couples who Engage in HIV Care Together
Time frame: 18 months
Self-reported proportion of doses of ART medication successfully taken on recommended schedule.
Time frame: 18 months
Having ≥2 outpatient visits at least 3 months apart per year
Time frame: 18 months
Proportion of eligible HIV-uninfected cohort members who opt to take PrEP
Time frame: 18 months
Proportion of eligible HIV-infected cohort members who opt to take ART
Time frame: 18-Months
Proportion of ART prescriptions successfully filled based on pharmacy records among HIV-infected members of sero-discordant couples.
Time frame: 18-months
Copies per mL of HIV detected in blood sample.
Time frame: 18 months
Self-reported number of sexual partners.
Time frame: 18-Months
Any self-reported sex with non-primary sexual partner.
Time frame: 18-months
Self-reported number of vaginal and anal sex acts.
Time frame: 18-months
Self-reported proportion of vaginal and anal sex acts in which a condom was used.
Time frame: 18 months
Program cost per client served
Medical University of South Carolina
Other
Acronym: DDCP
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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