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People Who Use Opioids/People With Opioid Use Disorder (OUD)P2PHNCT07073924

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

A study testing Implementation strategy bundle in people with People Who Use Opioids/People With Opioid Use Disorder (OUD), run by University of Pittsburgh at 4 sites in United States.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial 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… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Implementation strategy bundle
Could I receive a placebo?
No, everyone receives an active treatment
How many people
536 participants
Where
4 sitesUnited States
Study dates
Jan 2027to Jun 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • -Adult patients with history of active injection drug use in the past 1 year from the 4 COEs
  • -Prescribing clinicians (e.g., physicians, advanced practice providers such as nurse practitioners and physician assistants), administrators, medical assistants, and nurses from the 4 COEs

Who cannot join

  • 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.
Show all 12Show fewer
  • Clinical Partners:
  • Pre-implementation interviews (N=12), pre-implementation focus groups (N = 24), post-implementation surveys (N = 80), and post-implementation interviews (N=10)
  • Individuals not affiliated with the 4 COEs.
  • Staff outside the specified roles (i.e., not prescribing clinicians, administrators, medical assistants, or nurses).
  • Students, trainees, or individuals not credentialed in the eligible roles.
  • Those on extended leave or not actively working during the study period.

Trial locations and contacts

4 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Raagini Jawa, MD, MPH contact

(412) 232-6275

rjawa@pitt.edu

United States4 sites
  • Latterman Family Health Center

    Pittsburgh, Pennsylvania, 15132

    Hannah Scears, (412) 673-5504, scearshe@upmc.edu

  • Center for Psychiatric And Chemical Dependency Services

    Pittsburgh, Pennsylvania, 15213

    Megan Ganung, (412) 246-5910, ganungm2@upmc.edu

  • Internal Medicine Recovery Engagement Program

    Pittsburgh, Pennsylvania, 15213

    Ariana Freund, (412) 232-6275, freundam2@upmc.edu

  • UPMC Magee-Womens Hospital

    Pittsburgh, Pennsylvania, 15213

    Ilana Hull, MD, 412-530-6154, hulli@upmc.edu

Other trials in United States

About this study

Official title: 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

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/).

Read the 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.

Being tested
Implementation strategy bundle
Keywords
people who use drugs, HIV, PrEP, Opioid-Related Disorders, implementation, Substance-Related Disorders
Medical subject headings
Opioid-Related Disorders, Substance-Related Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Implementation strategy bundleBehavioural

    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.

Study groups in NCT07073924
Study groupRoleWhat they receive
Intervention ArmOtherImmediately gets the intervention of the implementation strategy bundle.
Receives: Behavioral: Implementation strategy bundle
Waitlist Control ArmOtherWaits for 6 months with no intervention, then gets the intervention of the implementation strategy bundle.
Receives: Behavioral: Implementation strategy bundle

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Implementation Outcomes: Site Level Adoption

    This 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.

    Measured: 6 months post implementation

  2. Implementation Outcomes: Site-level maintenance

    This 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.

    Measured: 12 months post implementation

  3. Implementation Outcomes: Acceptability of the strategy bundle

    Acceptability 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.

    Measured: 6 months post implementation

Secondary outcomes (2)
  1. Clinical Outcome: Rate of SIRI-related hospitalizations

    We 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.

    Measured: 6 months pre-implementation and 6 months post-implementation

  2. Clinical Outcome: Rate of negative HIV tests

    We 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.

    Measured: 6 months pre-implementation and 6 months post-implementation

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Jul 2025
  2. Study startJan 2027 (estimated)
  3. Primary completionDec 2027 (estimated)
  4. Study completionJun 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Sequential
Model description
Cluster randomized, waitlist-controlled hybrid type 3 implementation-effectiveness pilot trial
Masking
None (open label)
Enrolment
536 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07073924
Sponsor's protocol ID
STUDY25050118
Other IDs
K23DA063654
Acronym
P2PH
Status last verified
Mar 2026
First submitted
16 Jul 2025
Last updated
6 Nov 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Study protocol and statistical analysis plan for the primary outcomes will be published in a manuscript. Analytic code and participant-level data can be requested from Principal Investigators. Analysis files will be constructed from the stored electronic data and will be stripped of identifying information. Specifically, participants will be identified with a numeric identifier that is not related to any element of their personal identifying information.

Questions about this trial

What is this clinical trial studying?

A study testing Implementation strategy bundle in people with People Who Use Opioids/People With Opioid Use Disorder (OUD), run by University of Pittsburgh at 4 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 6 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 4 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Raagini Jawa, MD, MPH ((412) 232-6275, rjawa@pitt.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Implementation Outcomes: Site Level Adoption (time frame: 6 months post implementation). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Nov 2026.

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