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NCT06564792 · ClinicalTrials.gov registry record · NA

Contingency Management in HIV Care for Both Stimulant Use & ART Adherence

A NA study of HIV and Stimulant Use (Diagnosis), sponsored by University of California, San Francisco.

Completed
Registry status
NA
Development phase
37
Enrollment target
1
Study location

NCT06564792 is a NA study of HIV and Stimulant Use (Diagnosis) that has completed, run by University of California, San Francisco. The registered enrollment target is 37 participants, below the 440-participant average among 303 other HIV trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06564792, a NA study of HIV and Stimulant Use (Diagnosis), has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
NA
Development phase
37 participants
Enrollment target
1
Study location

Study Summary

Methamphetamine use and associated sequelae have been rising, and represent a major barrier to successful control of the HIV epidemic. Methamphetamine use is associated with poor adherence to antiretroviral therapy for HIV, and the investigators propose a trial of contingency management (providing incentives for behavioral change) targeting both reduced methamphetamine use and improved adherence to HIV medications. The investigators will utilize a real-time, point-of-care urine assay for both outcomes, aiming to evaluate feasibility, acceptability and preliminary effectiveness of HIV care-based contingency management. Hair levels will also be studied as a quantitative outcome for reduction in methamphetamine use.

Interventions

  • BEHAVIORAL Contingency management

Study Locations (1)

California

  • UCSF at San Francisco General Hospital - San Francisco

Trial Details

FieldValue
Enrollment Target 37 participants
Start Date 2023-09-15
Est. Completion 2025-10-01
Phase NA

What the Registry Record Tells You About NCT06564792

The ClinicalTrials.gov registry entry for NCT06564792 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 37 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 440-participant average among 303 other HIV trials with a reported enrollment target (92% lower). The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with HIV appearing as the primary indexed condition, and to 1 intervention - of which Contingency management is the first listed.

NCT06564792 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT06564792 about?

NCT06564792 is a clinical study titled "Contingency Management in HIV Care for Both Stimulant Use & ART Adherence". Methamphetamine use and associated sequelae have been rising, and represent a major barrier to successful control of the HIV epidemic. Methamphetamine use is associated with poor adherence to antiretroviral therapy for HIV, and the investigators propose a trial of contingency management (providing i...

What is the current status of trial NCT06564792?

This trial is currently completed. It is a NA study. The enrollment target is 37 participants. The study started on 2023-09-15. Estimated completion is 2025-10-01.

What conditions does trial NCT06564792 study?

This clinical trial studies the following conditions: HIV, Stimulant Use (Diagnosis).

What interventions are being tested in trial NCT06564792?

The interventions under investigation include: Contingency management (BEHAVIORAL).

Who is sponsoring clinical trial NCT06564792?

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

Where is trial NCT06564792 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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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.