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Mobile Vehicle-Based Delivery of Lenacapavir PrEP in Los Angeles County

Mobile Vehicle-Based Delivery of Lenacapavir PrEP in Los Angeles County (MOVE-LA)

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07467018
Acronym
MOVE-LA
Enrollment
100
Registered
2026-03-12
Start date
2026-04-07
Completion date
2027-12-31
Last updated
2026-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Prevention

Keywords

lenacapavir, community-based health delivery, HIV prevention, homelessness

Brief summary

This project evaluates the implementation strategy of the delivery of lenacapavir pre-exposure prophylaxis (LEN PrEP) - a newly available long-acting, injectable medication for HIV prevention - via a mobile health van model for people who are unstably housed in Los Angeles County. People who are unhoused or are facing housing instability experience significant barriers to accessing HIV prevention care in traditional clinic settings. In 2022, approximately 13% of newly diagnosed HIV cases in Los Angeles County were experiencing homelessness, a 36% increase over the prior period. We will work with UCLA Health's Homeless Healthcare Collaborative (HHC), which operates mobile health vans staffed by clinicians, social workers, and community health workers, to bring LEN PrEP directly to community settings, such as shelters, encampments, community centers, and transitional housing facilities. This study has three primary aims: 1. Characterize uptake of LEN PrEP among unstably housed people in Los Angeles County receiving health services via HHC's mobile program. 2. Evaluate how many study participants stay on LEN PrEP through 52 weeks. 3. Understand costs, acceptability, and sustainability of the mobile LEN PrEP delivery model.

Detailed description

Access to HIV prevention services for unstably housed people in LAC has been limited due to barriers in seeking care at health facilities. Unstably housed people face barriers including competing life priorities (such as seeking food, shelter, and employment), low health literacy, particularly around HIV prevention, and comorbidities such as substance use and mental health disorders. A mobile healthcare service that offers LEN PrEP is ideal to help overcome these barriers by providing a low-complexity biomedical PrEP option in locations where unstably housed people congregate (i.e., shelters, encampments, community centers, and transitional housing facilities). The UCLA Health Homeless Healthcare Collaborative (HHC) was founded in January 2022 and currently operates six mobile vans, which deliver urgent care, primary care, behavioral health services, and medication-assisted treatment for substance use disorders. At least one mobile van is in the field offering services every day of the week, including weekends. The van is staffed by clinicians and community health workers, who link clients to social services. HHC recently began providing point-of-care HIV and STI testing and is well-positioned to integrate LEN PrEP into their program. Based on Andersen's behavioral model (3) and using Proctor et al's implementation outcomes (4), we propose the following: Aim 1. Characterize uptake of LEN PrEP among unstably housed people in Los Angeles County receiving health services via HHC's mobile program. People without HIV receiving health services via the HHC mobile unit (n=100) will be offered LEN PrEP. A baseline survey will be performed (sociodemographics, clinical information, HIV risk, PrEP knowledge, self-efficacy for health care, and acceptability of mobile PrEP offer). The primary outcome will be uptake, defined as receiving a first injection of LEN PrEP and both oral doses on days 1 and 2. All participants will have the option to receive an Apple AirTag to enable directly observed therapy (DOT) for the second oral LEN dose and for follow-up LEN PrEP injections. Aim 2. Evaluate LEN PrEP persistence through 52 weeks. Participants who initiate LEN PrEP will receive ongoing visits from the HHC mobile unit for HIV/STI testing every 3 months and HIV testing and LEN injections every 6 months. We will estimate the share of initiators who receive LEN PrEP through week 52 ("persistence" defined as completing the third dose on-time \[+/-14 days\]). Surveys will be performed with all individuals who can be reached at 52 weeks (both persisters and non-persisters), to understand acceptability of mobile LEN PrEP, barriers to this care, and satisfaction with care. Aim 3. Understand costs and sustainability of the mobile LEN PrEP delivery model. Costs will be collected from the health system perspective. We will calculate the cost per person who initiates LEN PrEP, and cost per person persisting over 52 weeks. We will additionally perform in-depth interviews with stakeholders, including HHC leadership and van staff, public health leaders, and community leaders (n=25) to understand acceptability and feasibility of this model, and service- and system-level factors hypothesized to be associated with scalability and sustainability of the program.

Interventions

OTHERCommunity-based healthcare delivery

This study evaluates the implementation strategy of community-based delivery of HIV biomedical prevention with lenacapavir.

Mobile, community-based delivery of lenacapavir

Sponsors

University of California, Los Angeles
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Being reached for mobile health services by a UCLA HHC mobile van * ≥18 years of age * Able to provide informed consent * English or Spanish-speaking * Willing and able to comply with study procedures * HIV unknown or negative status and HIV negative based on rapid 4th generation Ag/Ab test on the day of enrollment * At-risk for HIV, based on clinician assessment (based on CDC guidelines; includes any individual requesting PrEP, regardless of reported risk factors for HIV) * Pregnant and breastfeeding women/people can be offered LEN with counseling about benefits and risks.

Exclusion criteria

* Any clinical or psychosocial condition or prior therapy that, in the opinion of the investigator, would make the participant unsuitable for the study or unable to take LEN PrEP * Known hypersensitivity to the study drug, the metabolites, or formulation excipient * BMI \<35 kg/m2 (77 pounds) * On oral or other long-acting PrEP and unwilling to discontinue * Already taking LEN for HIV prevention * Known HIV diagnosis or positive 4th generation HIV Ab/Ag test (on day of enrollment) or subsequent lab-based confirmatory testing. * Do not have any active insurance, including Medi-Cal (those without insurance will be referred to an enrollment counselor and may be re-screened for the study once insurance is active)

Design outcomes

Primary

MeasureTime frameDescription
Uptake of LEN PrEP3 months after enrollmentThe primary outcome will be defined as receiving a first injection of LEN (along with both oral doses on days 1 and 2).

Secondary

MeasureTime frameDescription
Predictors of uptake3 months after enrollmentSurveys will be performed at baseline to measure sociodemographic factors, HIV risk perception, PrEP knowledge, PrEP self-efficacy, and clinical factors.
Persistence on LEN PrEP at 26 and 52 weeks [+/- 14 days])52 weeksPersistence defined by receiving the injection at each timepoint on-time (+/- 14 days from target due date)
Acceptability52 weeksAcceptability of the mobile delivery of LEN PrEP
Predictors of persistence52 weeksSurveys will be performed at baseline to measure sociodemographic factors, HIV risk perception, PrEP knowledge, PrEP self-efficacy, and clinical factors. These will be used to explore factors associated with persistence on LEN at 26 and 52 weeks.
Costs of mobile delivery of LEN PrEP52 weeksCosts will be collected from the health system perspective. We will calculate the cost per person who initiates LEN and cost per person persisting on LEN PrEP over 52 weeks, in a cost-outcome analysis.

Countries

United States

Contacts

CONTACTRisa Hoffman, MD, MPH
rhoffman@mednet.ucla.edu310-206-6766
CONTACTDaisy Walker, MPH
DaisyWalker@mednet.ucla.edu424-832-6674

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026