NCT lookup

Pull any trial record directly from ClinicalTrials.gov.

Simplifying Treatment and Monitoring for HIV (STREAM HIV)

Active Not RecruitingNA

Sponsor: University of Washington

Conditions: HIV/AIDS, HIV-1-infection

Interventions: Point-of-care viral load testing and tenofovir adherence testing

Countries: South Africa

This study seeks to determine the clinical efficacy and cost effectiveness of implementing an integrated model for HIV monitoring using point of care (POC) tenofovir (TFV) adherence testing and POC viral load (VL) monitoring in improving ART adherence, maintaining durable VL suppression, and improving retention in care among HIV-positive individuals initiating first-line tenofovir disoproxil fumarate (TDF)-based ART in South Africa.

Eligibility overview

Sex: ALL

Age: 16 Years to —

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria:

* HIV-positive
* ≥16 years old
* Initiating a TDF-based, first-line ART regimen
* Do not self-report being on an ART regimen in the prior month
* Willing/able to provide written informed consent

Exclusion Criteria:

* Does not plan to continue receiving HIV care at the CDC Clinic
* Per the decision or opinion of the PI (for example, a clinically significant acute or chronic medical condition or circumstances that would make the patient unsuitable for participation or jeopardize the safety or rights of the participant

Locations (1)

Durban, KwaZulu-Natal, South Africa