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NCT07125235 · ClinicalTrials.gov registry record · NA

Reactive Driven Support for Treatment, Adherence, Resilience, and Thriving (reSTART) Clinical Trial

A NA study of Behavioral Intervention and ART Adherence, sponsored by University of California, San Francisco.

Recruiting
Registry status
NA
Development phase
270
Enrollment target
1
Study location

NCT07125235: Recruiting NA study of Behavioral Intervention and ART Adherence, sponsored by University of California, San Francisco.

NCT07125235 is a NA study of Behavioral Intervention and ART Adherence that is actively recruiting participants, run by University of California, San Francisco. The registered enrollment target is 270 participants, below the 5,417-participant average among 3 other Behavioral Intervention trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07125235, a NA study of Behavioral Intervention and ART Adherence, is actively recruiting participants, sponsored by University of California, San Francisco.

RECRUITING
Registry status
NA
Development phase
270 participants
Enrollment target
1
Study location

Study Summary

Men who are living with HIV and use stimulants face many challenges and barriers that may interfere with remembering to take their HIV medication. Forgetting to take HIV medication puts men living with HIV at a greater risk of becoming virally unsuppressed. Researchers are doing this study to test if a remote intervention can help participants improve remembering to take their HIV medications and reduce the HIV viral load among men living with HIV who use stimulants.

Primary Outcome

The primary endpoint will be change in viral suppression comparing baseline to post-intervention viral load results measured by HIV-1 RNA, Quantitative, Real-Time PCR. Viral suppression is defined as viral load results that yield less than 50 copies/mL.

Interventions

  • BEHAVIORAL reSTART Objective Adherence Self-Monitoring and Postive Affect mHealth Intervention
  • DEVICE urine tenofovir point-of-care self-test

Study Locations (1)

California

  • University of California, San Francisco - San Francisco

Trial Details

FieldValue
Enrollment Target 270 participants
Start Date 2026-02-09
Est. Completion 2028-07-30
Phase NA

What NCT07125235 shows while recruiting

NCT07125235 is an interventional study that assigns participants to a tested intervention. The registered 270 participants enrollment target is mid-sized for trials with a published cap, below the 5,417-participant average among 3 other Behavioral Intervention trials with a reported enrollment target (95% lower).

The record links to 3 conditions, with Behavioral Intervention appearing as the primary indexed condition, and to 2 interventions - of which reSTART Objective Adherence Self-Monitoring and Postive Affect mHealth Intervention is the first listed.

NCT07125235 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT07125235 about?

NCT07125235 is a clinical study titled "Reactive Driven Support for Treatment, Adherence, Resilience, and Thriving (reSTART) Clinical Trial". Men who are living with HIV and use stimulants face many challenges and barriers that may interfere with remembering to take their HIV medication. Forgetting to take HIV medication puts men living with HIV at a greater risk of becoming virally unsuppressed. Researchers are doing this study to test i...

What is the current status of trial NCT07125235?

This trial is currently recruiting. It is a NA study. The enrollment target is 270 participants. The study started on 2026-02-09. Estimated completion is 2028-07-30.

What conditions does trial NCT07125235 study?

This clinical trial studies the following conditions: Behavioral Intervention, ART Adherence, Viral Suppression of HIV Infection.

What interventions are being tested in trial NCT07125235?

The interventions under investigation include: reSTART Objective Adherence Self-Monitoring and Postive Affect mHealth Intervention (BEHAVIORAL), urine tenofovir point-of-care self-test (DEVICE).

Who is sponsoring clinical trial NCT07125235?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07125235 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT07125235, the US trial registry maintained by the National Library of Medicine. NCT07125235 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.