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Prescribe to Prevent HIV: A Hybrid Trial Helping Addiction Clinics Prevent HIV & Infections Through Safer Drug Use Support

Prescribe to Prevent HIV (P2PH): Enhancing Clinic-based Prescribing of Harm Reduction: A Clinical Trial to Prevent HIV and Severe Injection-related Infections Among PWID

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07073924
Acronym
P2PH
Enrollment
536
Registered
2025-07-20
Start date
2026-08-01
Completion date
2028-06-01
Last updated
2026-06-09

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

Conditions

People Who Use Opioids/People With Opioid Use Disorder (OUD)

Keywords

people who use drugs, HIV, PrEP, Opioid-Related Disorders, implementation, Substance-Related Disorders

Brief summary

In the U.S., an estimated 3.6 million people who inject drugs (PWID) face a growing yet preventable health crisis, with rising cases of serious injection-related infections (SIRI), including HIV, due to limited access to two high-priority interventions: sterile injection equipment and daily oral HIV pre-exposure prophylaxis (PrEP). Outpatient clinics represent an opportune venue to implement these interventions. Yet most clinical providers in these settings do not currently provide them, contributing to a wide gap between evidence and routine practice. The Prescribe to Prevent HIV (P2PH) trial is a participatory study designed to co-develop and pilot test a set of implementation strategies to support outpatients clinics in offering sterile injection equipment and PrEP with the goal of reducing the risk of HIV and SIRI among PWID. This study is supported by the HEAL Initiative (https://heal.nih.gov/).

Detailed description

In the U.S., 3.6 million people who inject drugs (PWID) face a syndemic of overdose and severe injection related infections (SIRI). Current efforts addressing this crisis remain inadequate as evidence-informed interventions (EIIs) to prevent or reduce SIRI from injection opioid use are not widely implemented and typically limited to syringe service programs. SIRI, which includes bacterial infections (e.g., cellulitis, osteomyelitis, endocarditis), hepatitis C virus, and HIV, significantly increase morbidity, mortality, and costs. HIV, in particular, can be prevented through access to two EIIs: sterile injection equipment and pre-exposure prophylaxis (PrEP). However, PWID in many jurisdictions lack access to these interventions due to shortages of syringe servie programs and clinicians willing to prescribe them. As a result, PWID nationwide have seen rising HIV incidence, threatening the goal of ending the HIV epidemic by 2030. For example, in Pennsylvania, where 90% of PWID lack access to SSPs, acute HIV infections rose by 150% between 2016 and 2019, and SIRI-related hospitalizations increased by 250% since 2010. This wide evidence-to-implementation gap underscores the urgent need for participatory implementation research to integrate these two high-priority EIIs into routine medical practice. Outpatient clinics represent a missed opportunity to implement these two EIIs. Outpatient clinics, including primary care and Federally Qualified Health Centers, are more accessible and face fewer restrictions than SSPs. While integrating these EIIs in outpatient clinics aligns with federal priorities, prescribing remains uncommon even in addiction treatment contexts. Modeling shows that when outpatient clinics prescribe injection equipment, SIRI-related hospitalizations are reduced by 30%, and when PrEP is prescribed, it increases uptake among PWID. However, gaps remain in how to effectively implement the prescribing of injection equipment and PrEP in these settings. Prescribe to Prevent HIV, is a participatory study designed to co-create and pilot a tailored implementation strategy bundle for prescribing injection equipment and PrEP in four Pennsylvania Centers of Excellence in Opioid Use Disorders (COEs). The approach combines implementation science with human-centered design, engaging a collaborative of individuals with lived experience, clinicians, and organizations serving PWID throughout all study phases to ensure relevance and sustainability. Development of the strategy bundle will begin by identifying implementation barriers and facilitators through 24 semi-structured interviews with COE patients, administrators, clinicians, and staff, guided by the Consolidated Framework for Implementation Research and informed by input from a community collaborative of individuals with lived experience. Then, using a human-centered design process, a tailored, practical, and adaptable strategy bundle will be co-created based on findings from the semi-structured interviews, insights from the community collaborative, and input gathered through four focus groups-one each with COE patients, clinicians, staff, and administrators-for implementation across the four COE sites. A cluster randomized, waitlist-controlled hybrid type 3 implementation-effectiveness pilot trial will then be conducted at the 4 COEs. The trial will assess implementation of the strategy bundle for prescribing injection equipment and PrEP in outpatient clinics. Primary implementation outcomes will include site-level adoption and maintenance, measured by the proportion of clinicians prescribing injection equipment and/or PrEP at the end of the 6-month implementation period (adoption), and at 12 months (maintenance). Secondary outcomes will include patient-level SIRI-related hospitalizations and negative HIV test results.

Interventions

The anticipated strategy bundle will include integrated patient-, provider-, and system-level interventions to support sustainable implementation. At the patient level, this may involve education, peer support, and navigation services; at the provider level, training, decision-support tools, and workflow enhancements; and at the system level, policy changes, electronic health record integration, and organizational alignment to promote and maintain prescribing of PrEP and injection equipment.

Sponsors

University of Pittsburgh
Lead SponsorOTHER
National Institute on Drug Abuse (NIDA)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Cluster randomized, waitlist-controlled hybrid type 3 implementation-effectiveness pilot trial

Eligibility

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

Inclusion criteria

Patients: Pre-implementation interviews (N=12), pre-implementation focus groups (N=8), and post-implementation interviews (N=10) Inclusion Criteria: -Adult patients with history of active injection drug use in the past 1 year from the 4 COEs

Exclusion criteria

* Ages \<18 * If history of injection drug use \>1 year * Non-English speaking * Pending or legal action that could prohibit or interfere with participation (Ie. incarceration) * Residence or discharge to a treatment facility that bans the possession of drug checking supplies * Acute, severe psychiatric condition in need of immediate treatment. Clinical Partners: Pre-implementation interviews (N=12), pre-implementation focus groups (N = 24), post-implementation surveys (N = 80), and post-implementation interviews (N=10) Inclusion Criteria: -Prescribing clinicians (e.g., physicians, advanced practice providers such as nurse practitioners and physician assistants), administrators, medical assistants, and nurses from the 4 COEs

Design outcomes

Primary

MeasureTime frameDescription
Implementation Outcomes: Site Level Adoption6 months post implementationThis is defined as the proportion of clinicians who prescribed injection equipment and/or PrEP per site, assessed at 6 months post-implementation, respectively using electronic health record data.
Implementation Outcomes: Site-level maintenance12 months post implementationThis is defined as the proportion of clinicians who prescribed injection equipment and/or PrEP per site, assessed at 12 months post-implementation respectively using electronic health record data.
Implementation Outcomes: Acceptability of the strategy bundle6 months post implementationAcceptability of the implementation strategy bundle will be assessed via post-implementation surveys of participating clinical partners (N=60-80) using a reliable 4-item survey from Weiner et al., where scores ≥16 indicate "acceptable" if 80% of participants agree.

Secondary

MeasureTime frameDescription
Clinical Outcome: Rate of SIRI-related hospitalizations6 months pre-implementation and 6 months post-implementationWe will assess the rate of SIRI-related hospitalizations by extracting electronic health record data from participating sites using an established search algorithm that identifies relevant cases through ICD-10 codes associated with injection drug use infections.
Clinical Outcome: Rate of negative HIV tests6 months pre-implementation and 6 months post-implementationWe will assess the rate of negative HIV screening tests by extracting electronic health record data from participating sites using which will be collected as part of routine clinical care.

Countries

United States

Contacts

CONTACTRaagini Jawa, MD, MPH
rjawa@pitt.edu(412) 232-6275
PRINCIPAL_INVESTIGATORRaagini Jawa, MD, MPH

University of Pittsburgh

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 10, 2026