RecruitingNot ApplicableNCT06823037

Hormonal Contraception Access Through Pharmacist Prescribing Implementation

HAPPI (Hormonal Contraception Access Through Pharmacist Prescribing Implementation): Phase 2 (Aim 1)

Sponsor

EMPOWERX INC

Enrollment

150 participants

Start Date

Oct 9, 2025

Study Type

INTERVENTIONAL

Conditions

Contraception Technology Use Pharmaceutical Services Access and Linkage to Healthcare

Summary

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.

Eligibility

Min Age: 18 Years

Inclusion Criteria7

PHARMACIST Participants
years of age or older
Provide birth control services in a participating pharmacy
Use the HAPPI software to provide birth control services
years of age or older
Seek birth control services at a participating pharmacy
Use the HAPPI software to receive birth control services at a participating pharmacy

Exclusion Criteria3

None
PATIENT Participants
NONE

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Interventions

OTHERHAPPI software

We will enroll 15 community pharmacies. These 15 pharmacies will continue to provide birth control services as normal for several months (control). Then, we will introduce the intervention: the HAPPI software. The pharmacies will continue to provide birth control services while using the HAPPI 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 period.