People & Place: Impacts on Substance Use and HIV Outcomes in Los Angeles

NCT ID: NCT07200973

Last Updated: 2025-10-06

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 250 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2026-05-31
• Study Completion Date: 2028-10-31

Brief Summary

This study will implement an adapted peer navigation intervention to improve linkage to and retention in HIV care for people living with HIV who experience substance use within Los Angeles County.

Detailed Description

People living with HIV often experience additional challenges when substance use is also part of their lives. Staying in consistent HIV care is essential for maintaining health, but this can be complicated when services are difficult to access or require navigating multiple systems. In a large, urban county like Los Angeles, where clinics and treatment centers are widely dispersed, people may need to travel long distances, rely on limited transportation, or attend separate locations for HIV care and substance use treatment. These factors can create real barriers to staying engaged in care, even when services are technically available. The "People & Place" study is designed to better understand how individuals living with HIV move through Los Angeles to obtain their care, and how the organization of healthcare services and policies influence those experiences. The study examines the role and impact of peer case managers-individuals with relevant, compatible experiences who can guide and support participants as they navigate the healthcare system. Peer case managers may be able to reduce barriers by helping patients find care within their nearby communities, strengthening connections with providers, and encouraging continuity of treatment.

The project represents a collaboration between researchers at University of California, Los Angeles (UCLA), the University of California, Santa Barbara (UCSB), and a local HIV clinic, bringing together expertise in medicine, public health, and community-based care. By combining academic research with input from patients and healthcare providers, this research aims to create practical and effective strategies for reducing barriers such as distance, transportation, and fragmented services, ultimately improving the accessibility, coordination and patient-centeredness of healthcare delivery for people living with HIV who also use substances.

Specific Aims include:

Aim 1. Connect existing policies and conditions (e.g., heat exposure, policing, and economic distribution) with geospatial patterns of health outcomes among people living with HIV via compilation of secondary data with new data collected among people living with HIV through an innovative "activity space" survey. These harmonized data will document spatial associations between local, state, and federal policies and contemporary contextual determinants of health at the neighborhood level and identify how perceptions of territorial reputations, and local spaces influence preferences for HIV care and SU harm reduction services.

Aim 2. Qualitatively assess the HIV and substance use care experience among people living with HIV (n=30) as well as staff members at a large HIV care clinic in LA (n=15) via qualitative interviews (N=45 total) to examine how experiences and perceptions of space influence service use and movement through HIV and substance use hotspots, in other words: the geography of care.

Aim 3. Adapt and pilot the evidenced based intervention, LINK LA (NCT01406626), to examine the role of a compatible peer case management intervention on HIV and substance use outcomes. Activities of this aim include: (a) undertaking a process of intervention adaptation utilizing results from qualitative interviews in Aim 2 with clinic staff and people living with HIV, and conduct theatre testing of the intervention, (b) piloting the adapted intervention among N=250 people living with HIV to assess acceptability and feasibility and assess the preliminary impacts of the adapted intervention on HIV and substance use outcomes, and (c) examining the relationship between the distance of where participants live and their choice of an enhanced HIV and substance use care experience based on an adapted intervention. Results will identify patterns in HIV and substance use care choices and outcomes across LAC's geographically broad neighborhoods and determine if an intervention can modify such choices and outcomes. The intervention is hypothesized to result in greater linkage to care, increased self-reported ART adherence, and decreased levels of HIV RNA viral load in comparison to pre-intervention periods.

Conditions

HIV

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Adapted LINK-LA Peer Case Management

LINK-LA Peer Case Management Intervention, adapted for people living with HIV who use substances

Group Type: EXPERIMENTAL

Adapted LINK LA Peer Navigator

Intervention Type: BEHAVIORAL

Our study will adapt the LINK LA peer navigation intervention (NCT01406626) for the current context (e.g., HIV care provision, substance use risk environments, etc.) and measure its effects on participants' HIV and substance care engagement.

Interventions

Adapted LINK LA Peer Navigator

Our study will adapt the LINK LA peer navigation intervention (NCT01406626) for the current context (e.g., HIV care provision, substance use risk environments, etc.) and measure its effects on participants' HIV and substance care engagement.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Living with HIV
• Assigned male sex at birth
• Willing to return for follow-up study visits every six months as long as the study is ongoing and be available to return for all study visits, barring unforeseen circumstances
• Willing and able to provide written informed consent to take part in the study
• Willing and able to provide adequate information for locator purposes
• Willing to undergo repeat HIV viral load testing at select study visits
• Willing to undergo substance use testing at each study visit

Exclusion Criteria

• Born biologically female
• Unwilling or unable to provide reliable contact information
• Unwilling to provide urine or blood
• Any other condition or prior therapy that, in the opinion of the research staff would preclude informed consent, make study participation unsafe, make the individual unsuitable for the study or unable to comply with the study requirements. Such conditions may include, but are not limited to, renal, hepatic, hematological, gastrointestinal, endocrine, pulmonary, neurological, or cerebral disease, among others

• Minimum Eligible Age: 18 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

University of California, Los Angeles

OTHER

Sponsor Role: lead

Responsible Party

Pamina Mae Gorbach

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

5R01DA061345

Identifier Type: NIH

Identifier Source: org_study_id

View Link