Actively Recruiting
Wellness, Intervention Strategies and HIV Care
Led by University of California, San Francisco · Updated on 2026-01-27
50
Participants Needed
2
Research Sites
30 weeks
Total Duration
On this page
Sponsors
U
University of California, San Francisco
Lead Sponsor
N
National Institute on Drug Abuse (NIDA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This is a pilot trial designed to assess the feasibility and acceptability of an intervention aimed at improving adherence to antiretroviral therapy (ART), viral suppression, and engagement in HIV care. The intervention will address behavioral coping strategies, HIV care engagement behaviors, and substance use management.
CONDITIONS
Official Title
Wellness, Intervention Strategies and HIV Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be at least 18 years of age
- Self-report biological characteristics consistent with the population under study
- Be HIV-positive
- Report use of at least one of the following substances in the last 90 days: cannabis, methamphetamine, cocaine/crack, cocaine, heroin, non-prescribed opioids (e.g., fentanyl, morphine), ecstasy, phencyclidine (PCP), psychedelics (e.g., LSD, mescaline, ketamine), poppers (alkyl nitrites), non-prescribed benzodiazepines (e.g., Valium, Xanax, Klonopin, Librium), or barbiturates
- Be English-speaking
- Be able and willing to provide informed consent
You will not qualify if you...
- Evidence of severe cognitive impairment or active psychosis that may impede ability to provide fully informed consent, determined by research staff
- Inability to meaningfully participate or provide consent due to mental illness or impairment as identified by trained research staff
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
Oakland MWCCS Site Office
Oakland, California, United States, 94612
Actively Recruiting
2
SF MWCCS Site Office
San Francisco, California, United States, 94115
Actively Recruiting
Research Team
H
Heather Freasier Project Director, MS
CONTACT
J
Julian Paredes-Gotamco Clinical Research Coordinator
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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