HIV Treatment

4

Review clinical trials related to HIV Treatment. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Building Rapid Inpatient Delivery of ART to Generate Engagement in HIV Care

The study team will pilot rapid antiretroviral therapy (ART) initiation as part of routine inpatient care at the University of Chicago Medicine (UCM), comparing outcomes over a 12-month implementation period. Electronic medical record (EMR) data will be used to evaluate clinical outcomes such as ART initiation within 24-48 hours, linkage to HIV care, retention, and viral suppression, as well as demographic and clinical factors associated with these outcomes. Implementation outcomes will be assessed using Proctor's framework, including acceptability, feasibility, fidelity, and appropriateness.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of ChicagoUpdated: Sep 29, 2026Locations: 1Duration: 12 Months
Eligibility criteria

18 years of age or older [+5]

Less than 18 years of age [+5]

Status: Recruiting

Evaluating the Impact of Using the B-OK Bottles for HIV and ART Literacy in South Africa

Consistent use of antiretroviral therapy (ART) is essential for achieving suppression among people with HIV (PWH). Yet despite improvements in access to ART and improving viral suppression rates, an estimated one-third of PWH globally do not take ART as prescribed, thus allowing the virus to remain detectable and transmissible. This study tests whether a low-cost visual education tool, B-OK bottles, improves understanding of HIV, antiretroviral therapy (ART), and the concept of Undetectable = Untransmittable (U=U) among adults in Gauteng, South Africa using a randomized trial. Participants will be randomly assigned to one of three groups: (1) standard-of-care verbal information based on Department of Health guidelines, (2) information delivered in person using B-OK bottles, or (3) information delivered via a video demonstrating the B-OK bottles. The study will compare the two intervention formats to standard care, and to each other, to assess whether the tool improves knowledge, attitudes, and intentions related to HIV treatment and prevention, and whether the intervention results depend on delivery mode (in-person vs. video). Outcomes will be measured at baseline, immediately after the intervention, and at six-week follow-up.

Participants needed: 600
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of PennsylvaniaUpdated: Aug 27, 2026Locations: 1
Eligibility criteria

Aged 18 years or older [+4]

Unwilling or unable to provide written informed consent for study participation

Status: Recruiting

Implementation Trial to Evaluate a Population Health Combination Intervention to Meet HIV Testing, Linkage, and Viral Suppression Goals in Alabama

The purpose of this study is to adapt and evaluate a combination intervention that includes: (1) a data-driven approach to directed community-based HIV testing to areas with high need, (2) Project Connect to expedite linkage to care at time of diagnosis, (3) and a Rapid ART (antiretroviral therapy)Start program, all in Mobile County Health Department (MCHD) jurisdictions in Alabama.

Participants needed: 80
Trial details
Age: 13+Biological sex: AllType: InterventionalSponsor: University of Alabama at BirminghamUpdated: May 18, 2026Locations: 1
Eligibility criteria

Over the age of 18 years old. [+2]

Exclusion criteria include unwillingness or inability to provide informed consen...

Status: Recruiting

HIV Outpatient Monitoring Evaluation Through Self-collection of Dried Blood Spots

The goal of this observational study is to establish an operational framework for home self-collections of blood samples to be used for antiviral drug concentration measurements. Participants will continue on their prescribed antiviral(s) for HIV treatment or prevention and followed for up to approximately 1 year. The investigators will compare drug concentrations of antivirals and relevant metabolites/anabolites in clinic-collected and self-collected blood samples.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of Colorado, DenverUpdated: Mar 3, 2026Locations: 1
Eligibility criteria

≥18 years old [+3]

Inability to provide informed consent [+3]