← Back to Search

Behavioral Intervention

Contingency management arm for HIV (Human Immunodeficiency Virus) (CoMBo Trial)

N/A
Waitlist Available
Led By Ayesha Appa, MD
Research Sponsored by University of California, San Francisco
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
* Stimulant use disorder
* Living with HIV or risk for HIV
Timeline
Screening 3 weeks
Treatment Varies
Follow Up interviews performed within 6 months of intervention participation.
Awards & highlights

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 we propose a trial of contingency management (providing incentives for behavioral change) targeting both reduced methamphetamine use and improved adherence to HIV medications. We 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. We will also study hair levels as a quantitative outcome for reduction in methamphetamine use.

Who is the study for?
This trial is for individuals with HIV who also struggle with stimulant use, specifically methamphetamine. Participants should be currently using methamphetamines and have difficulty sticking to their antiretroviral therapy (ART) for HIV. The study excludes details on specific inclusion or exclusion criteria.
What is being tested?
The study tests a strategy called contingency management, which rewards patients for reducing methamphetamine use and improving adherence to HIV medication. It uses real-time urine tests to monitor progress and hair analysis to measure long-term changes in drug use.
What are the potential side effects?
Since the intervention involves behavioral incentives rather than medications, traditional side effects are not applicable. However, participants may experience stress or anxiety related to meeting the requirements for incentives.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~interviews performed within 6 months of intervention participation.
This trial's timeline: 3 weeks for screening, Varies for treatment, and interviews performed within 6 months of intervention participation. for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Acceptability: in-depth interviews with participants, staff
Feasibility: proportion of CM visits attended
Secondary study objectives
Effectiveness (Hair)
Effectiveness (Urine)

Trial Design

1Treatment groups
Experimental Treatment
Group I: Contingency management armExperimental Treatment1 Intervention
Participants are offered once weekly contingency management in clinic to support reduced stimulant use and HIV medication adherence.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Contingency management
2006
Completed Phase 4
~960

Find a Location

Who is running the clinical trial?

University of California, San FranciscoLead Sponsor
2,537 Previous Clinical Trials
15,262,425 Total Patients Enrolled
Ayesha Appa, MDPrincipal InvestigatorUniversity of California, San Francisco
~18 spots leftby Sep 2025