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Preparing for International Prevention Trials Involving HIV-Infected Individuals in Care Settings

Preparing for International Prevention Trials Involving HIV-Infected Individuals in Care Settings

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01264185
Acronym
HPTN063
Enrollment
751
Registered
2010-12-21
Start date
2010-04-30
Completion date
2014-08-31
Last updated
2022-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV

Brief summary

The purpose of this study is to conduct preparatory research needed to design a behavioral intervention to decrease sexual transmission risk behaviors in HIV-infected individuals in care and to determine whether a similar intervention structure can be used across various sexual risk groups and cultural settings.

Interventions

None listed

Sponsors

HIV Prevention Trials Network
Lead SponsorNETWORK

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Men and women at least 18 years of age (Note: Pregnant and breast feeding women are allowed to enroll into the study) * Documented evidence of HIV infection (HIV diagnosis performed outside of the trial is acceptable so long as local/country guidelines were followed in the testing) * Receiving HIV/AIDS care (defined as at least two visits within 9 months of enrollment) in a formal health care setting (clinic or hospital) * Reported history of sexual risk behavior in the previous 12 months, including: acquisition of a sexually transmitted infection, vaginal or anal intercourse without a condom, difficulty negotiating condom use, or non-disclosure of HIV status to an HIV-uninfected partner or partner of unknown HIV serostatus. * NOTE: For the MSM population, we will enroll men who have sex with men, regardless of whether or not they also have sex with women

Exclusion criteria

* Anyone currently enrolled in another study that involves protocolized HIV risk reduction counseling (e.g. ACTG 5175 or HPTN 052) or any other prevention study * Anyone having unprotected (i.e. without a condom) sex for the expressed purpose of conceiving * Planning to relocate out of the area in the next year * Any condition that, in the opinion of the Investigator of Record or designee, would make participation in the study unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives

Design outcomes

Primary

MeasureTime frameDescription
Establish baseline rates of sexual HIV transmission risk1 yearTo establish baseline rates of sexual HIV transmission risk behavior in high risk HIV-infected individuals, and to observe the rates and patterns of behavior change over time
Structure and content of a behavioral intervention for individuals with HIV1 yearTo gather formative data on the potential structure and content of a behavioral intervention for individuals with HIV in care in international settings and to determine the best, culturally appropriate model for the intervention that will link prevention to care for HIV-infected individuals.
Identify psychosocial and sociodemographic correlates of sexual risk-taking1 yearTo examine potential psychosocial and sociodemographic correlates of sexual risk-taking in these individuals in order to help shape the content of an individualized behavioral intervention

Secondary

MeasureTime frameDescription
Determine sexually transmitted infection(STI)prevalence and incidence1 yearEvaluate STI prevalence and incidence and investigate whether these biomarkers may be used to corroborate self-reported sexual behavior associated with potential transmission risks

Countries

Brazil, Thailand, Zambia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026