Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06823037

Hormonal Contraception Access Through Pharmacist Prescribing Implementation

Led by EMPOWERX INC · Updated on 2025-12-04

150

Participants Needed

1

Research Sites

46 weeks

Total Duration

On this page

Sponsors

E

EMPOWERX INC

Lead Sponsor

P

Purdue University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if use of the HAPPI software can improve pharmacist-provided birth control services. The main questions it aims to answer are: 1. Does the HAPPI software make it easier for pharmacists to provide birth control services in their pharmacy? 2. Does the HAPPI software make it easier for patients to access birth control? Researchers will compare pharmacists' implementation and patients' access when using the HAPPI software and when not using the HAPPI software to see if the software improves implementation and access. Participants will include pharmacists and patients. Pharmacists will be asked to provide birth control services as normal while using the HAPPI software. Patients will be asked to receive birth control services from a pharmacist as normal, while using the HAPPI software.

CONDITIONS

Official Title

Hormonal Contraception Access Through Pharmacist Prescribing Implementation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be 18 years of age or older
  • Provide birth control services in a participating pharmacy
  • Use the HAPPI software to provide birth control services
  • Seek birth control services at a participating pharmacy
  • Use the HAPPI software to receive birth control services at a participating pharmacy
Not Eligible

You will not qualify if you...

  • None

AI-Screening

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Trial Site Locations

Total: 1 location

1

EmpoweRx, Inc

Del Mar, California, United States, 92014

Actively Recruiting

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Research Team

J

Jenny L Newlon, PharmD, PhD

CONTACT

S

Sally Rafie, PharmD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

1

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