RECRUITING

Patient Experiences With Contraceptive Care Provided by Community Pharmacists Using the Pharmacist Resource to Implement Services as Modules Platform

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Hormonal contraceptives are medications that require a prescription, traditionally from a physician or advanced practice provider. Over the past decade, pharmacists have gained the authority to prescribe contraceptives in many states, allowing patients to access these medications directly in pharmacies without first seeing another healthcare provider. The Pharmacist Resource to Implement Services as Modules (PRISM) is an Electronic Health Record platform designed to streamline workflows and provide clinical decision support, making it easier and safer to deliver clinical services in community pharmacies. This pilot study will evaluate patient-reported outcomes for women receiving contraceptive services from pharmacists using the PRISM platform at five community pharmacies across the United States over a 12-week period. The study will assess the quality of care, contraception continuation and failure rates, side effect rates, preventative healthcare utilization, and overall patient experience with pharmacy contraceptive services.

Official Title

Patient-Reported Outcomes of Contraceptive Services Rendered by Community Pharmacists Using the Pharmacist Resource to Implement Services as Modules Platform: The PRISM-CS Study

Quick Facts

Study Start:2025-07-12
Study Completion:2026-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06819787

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 51 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. * Age less than 18 years
  2. * Pregnancy
  3. * Unable to become pregnant
  4. * Not English speaking
  5. * Suspected coercion
  6. * Unable to consent

Contacts and Locations

Study Contact

Mary Kucek
CONTACT
(888) 464-9988
MaryKucek@ovaryit.com
Devin Bustin
CONTACT
(888) 464-9988
Devinbustin@ovaryit.com

Study Locations (Sites)

Calabasas Pharmacy
Calabasas, California, 91302
United States
Desert Pharmacy
El Centro, California, 92243
United States
Local Health Pharmacy
Chicago, Illinois, 60647
United States
Wolves Den Pharmacy
Stanford, Montana, 59479
United States
Gaston Family Pharmacy
Gaston, South Carolina, 29053
United States

Collaborators and Investigators

Sponsor: OvaryIt, LLC

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-07-12
Study Completion Date2026-01

Study Record Updates

Study Start Date2025-07-12
Study Completion Date2026-01

Terms related to this study

Keywords Provided by Researchers

  • Contraception
  • Pregnancy Prevention
  • Digital Health
  • Pharmacist
  • Community Pharmacy Services
  • Patient-reported Outcomes

Additional Relevant MeSH Terms

  • Contraception