CClinicalTrials.gg
RecruitingNCT07683117PEPPIUpdated Jul 7, 2026

PEP/PrEP Via Pharmacist-Prescribing Implementation (PEPPI)

An interventional study of PEPPI Pharmacies in HIV Prevention, HIV Pre-exposure Prophylaxis and Access and Linkage to Healthcare, sponsored by EMPOWERX INC. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-07.

Sponsored by EMPOWERX INC · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
195
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this clinical trial is to learn if use of the PEPPI software can improve pharmacist-provided HIV prevention (PEP/PrEP) services. The main questions it aims to answer are:

  1. Does the PEPPI software make it easier for pharmacists to provide PEP/PrEP services in their pharmacy?
  2. Does the PEPPI software make it easier for patients to access PEP/PrEP?

Researchers will compare pharmacists' implementation and patients' access when using the PEPPI software and when not using the PEPPI software to see if the software improves implementation and access.

Participants will include pharmacists and patients. Pharmacists will be asked to provide PEP/PrEP services as normal while using the PEPPI software. Patients will be asked to receive PEP/PrEP services from a pharmacist as normal, while using the PEPPI software.

02

Conditions studied

  • HIV Prevention
  • HIV Pre-exposure Prophylaxis
  • Access and Linkage to Healthcare
  • Technology Use

Keywords

  • community pharmacy
  • access to care
  • pharmacist services
  • HIV prevention
  • PEP/PrEP
  • scope of practice
  • health technology
  • pharmacist prescribing
03

In context

Lead sponsor

EMPOWERX INC is the lead sponsor of 2 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

PHARMACIST Participants

Inclusion Criteria:

  • 18 years of age or older
  • Provide, or willing to provide, PEP/PrEP services in a participating pharmacy
  • Use the PEPPI software to provide birth control services

Exclusion Criteria:

  • None

PATIENT Participants

Inclusion Criteria:

  • 18 years of age or older
  • Seek PEP or PrEP services at a participating pharmacy
  • Use the PEPPI software to receive PEP/PrEP services at a participating pharmacy

Exclusion Criteria:

  • NONE
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
195 participants (estimated)

Study arms

  • Other
    PEPPI Pharmacies

    This is a single-arm trial, so all pharmacies will serve as their own control. We will enroll 10 community pharmacies. These 10 pharmacies will continue to provide PEP/PrEP services as normal for several months (control). Then, we will introduce the first phase of the intervention: the minimally viable product (MVP) version of the PEPPI software. The second phase of the intervention will be the enhanced version of the PEPPI software. The pharmacies will continue to provide PEP/PrEP services while using the PEPPI software in place of any paper or electronic processes that they were previously using. The results will then be compared between the control and the intervention periods.

    Other: PEPPI Pharmacies

Interventions

  • OtherPEPPI Pharmacies

    We will enroll 10 community pharmacies. These 10 pharmacies will continue to provide PEP/PrEP services as normal for several months (control). Then, we will introduce the first phase of the intervention: the minimally viable product (MVP) version of the PEPPI software. The second phase of the intervention will use the enhanced version of the PEPPI software. The pharmacies will continue to provide PEP/PrEP services while using the PEPPI software in place of any paper or electronic processes that they were previously using. The results will then be compared between the control and the intervention periods.

06

What researchers measure

Primary outcomes

  1. Implementation - Service Characteristics Number of Pharmacists

    Implementation outcomes will focus on how the service (pharmacist-prescribed PEP/PrEP services) is implemented. Name of the Measurement: Implementation - Service Characteristics Measurement Tool: Pharmacy Service Characteristics Questionnaire Unit of Measure: -Number of pharmacists involved in providing birth control services

    Time frame: up to 12 months

  2. Implementation - Service Characteristics Number of Pharmacy Staff

    Implementation outcomes will focus on how the service (pharmacist-prescribed PEP/PrEP services) is implemented. Name of the Measurement: Implementation - Service Characteristics Measurement Tool: Pharmacy Service Characteristics Questionnaire Unit of Measure: -Number of pharmacy staff (non-pharmacists) involved in providing PEP/PrEP services

    Time frame: up to 12 months

  3. Implementation - Service Characteristics Cash Pay

    Implementation outcomes will focus on how the service (pharmacist-prescribed PEP/PrEP services) is implemented. Name of the Measurement: Implementation - Service Characteristics Measurement Tool: Pharmacy Service Characteristics Questionnaire Unit of Measure: -Total amount of money coming in (revenue) from the service via cash pay

    Time frame: up to 12 months

  4. Implementation - Service Characteristics Insurance Billing

    Implementation outcomes will focus on how the service (pharmacist-prescribed PEP/PrEP services) is implemented. Name of the Measurement: Implementation - Service Characteristics Measurement Tool: Pharmacy Service Characteristics Questionnaire Unit of Measure: -Total amount of money coming in (revenue) from the service via insurance billing

    Time frame: up to 12 months

  5. Implementation - Proctor Implementation Outcomes

    Implementation outcomes will be measured using Proctor et al.'s (2011) implementation framework. The domains in this framework include appropriateness, acceptability, adoption, feasibility, and fidelity. Survey items will map to each of these domains. Name of the measurement: Implementation - Proctor Implementation Outcomes Measurement tool: Implementation Outcomes Scale Unit of Measure: 5-point Likert-type scale (1= strongly disagree, 2 = disagree, 3 = neither agree nor disagree, 4 = agree, 5 = strongly agree). This same scale is used for all implementation domains (appropriateness, acceptability, adoption, feasibility, and fidelity).

    Time frame: up to 12 months

Secondary outcomes

  1. Access to Care

    Access to Care outcomes will be assessed using an adapted version of the previously developed scale of Access to Contraceptive Care (Newlon 2021) that assesses patients' access in terms of approachability, acceptability, availability and accommodation, affordability, appropriateness, and privacy. Unite of measure: 5-point Likert-type scale (1= strongly disagree, 2 = disagree, 3 = neither agree nor disagree, 4 = agree, 5 = strongly agree). This same scale is used for all implementation domains (approachability, acceptability, availability and accommodation, affordability, appropriateness, and privacy).

    Time frame: up to 12 months

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07683117
Lead sponsor
EMPOWERX INC
Collaborators
National Institute of Mental Health (NIMH)
Responsible party
Jenny Newlon (Research Director, EMPOWERX INC) — Principal investigator
First posted
Jul 6, 2026
Start date
Aug 2026 (estimated)
Primary completion
Aug 2028 (estimated)
Completion
Sep 2028 (estimated)
Last update
Jul 7, 2026

Study contacts

Jenny L Newlon, PharmD, PhD
Contact
jenny@birthcontrolpharmacist.com
8584120984
Sally Rafie, PharmD
Contact
Sally@birthcontrolpharmacist.com

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion