Wellness, Intervention Strategies and HIV Care

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

∙ • Participants must:

• 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., Lysergic acid diethylamide, mescaline, ketamine)

⁃ Poppers (alkyl nitrites)

⁃ Non-prescribed benzodiazepines (e.g., Valium, Xanax, Klonopin, Librium)

⁃ Barbiturates

• Be English-speaking

• Be able and willing to provide informed consent

Locations
United States
California
Oakland MWCCS Site Office
RECRUITING
Oakland
SF MWCCS Site Office
RECRUITING
San Francisco
Contact Information
Primary
Heather Freasier Project Director, MS
heather.freasier@ucsf.edu
415-502-8800
Backup
Julian Paredes-Gotamco Clinical Research Coordinator
Julian.Paredes-Gotamco@ucsf.edu
415-502-3507
Time Frame
Start Date: 2025-09-03
Estimated Completion Date: 2026-03-30
Participants
Target number of participants: 50
Treatments
Experimental: Intervention Arm
Participants in this arm will attend a structured, group-based behavioral support program consisting of five weekly sessions. The intervention is designed for individuals living with HIV who use substances. It focuses on strategies for managing stress, reducing barriers to care, and improving engagement in HIV-related health services and overall wellness.
Placebo_comparator: Control Arm
Participants in this arm will attend five weekly group-based sessions where non-intervention-related movies are shown. This condition is intended to control for time and group exposure without delivering active behavioral content related to the study outcomes.
Related Therapeutic Areas
Sponsors
Leads: University of California, San Francisco
Collaborators: National Institute on Drug Abuse (NIDA)

This content was sourced from clinicaltrials.gov