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Completed

NCT Number: NCT06819787

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

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.

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Key information

Conditions

Age range

18 year–51 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Calabasas Pharmacy, Calabasas, California, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women presenting for hormonal contraceptives

Exclusion criteria

  • Age less than 18 years
  • Pregnancy
  • Unable to become pregnant
  • Not English speaking
  • Suspected coercion
  • Unable to consent

Treatment and study plan

Electronic Heath Record Platform to Support Pharmacists in Delivering Contraceptive Services

Other

An electronic health record (EHR) platform specifically designed to support community pharmacists in delivering contraceptive services. The platform streamlines clinical workflows, provides clinical decision support, and promotes adherence to the US Medical Eligibility Criteria (USMEC) guidelines and state regulatory requirements.

Primary outcomes

  1. Person-Centered Contraceptive Counseling (PCCC) Measure

    Time frame: Within 7 days post-intervention

    The percentage of patients who report that the pharmacist provided overall patient-centered care, as defined by achieving the highest rating on all four items of the PCCC survey.

Secondary outcomes

  1. Three-month Contraceptive Continuation Rate

    Time frame: Within 97 days post-intervention

    The percentage of patients who report continuous use of their selected contraceptive method three months after the pharmacist encounter. Continuous use is defined as using the method at the time of the survey with no gaps in use of one month or longer.

Other outcomes

  1. Contraceptive Failure Rate

    Time frame: Within 97 days post-intervention

    The percentage of patients who have experienced unintended pregnancy while using the contraceptive method prescribed during the encounter.

  2. Contraceptive Side Effect Rate

    Time frame: Within 97 days post-intervention

    The percentage of patients who report one or more side effects from the contraceptive method prescribed during the encounter.

  3. Patient Contraceptive Satisfaction

    Time frame: Within 97 days post-intervention

    7-point Likert scale rating of patient satisfaction with the contraceptive method prescribed during the encounter.

  4. Patient Perception, Attitudes, and Satisfaction Regarding Pharmacist Contraceptive Services

    Time frame: Within 97 days post-intervention

    A series of Likert scale, Yes/No, and open-ended questions to discover patient perceptions, attitudes, and satisfaction regarding pharmacist contraceptive services.

  5. Preventative Health Services Utilization

    Time frame: Within 97 post-intervention

    A series of Yes/No and multiple-choice questions to discover patient utilization of preventative health services including primary care and medical screening exams.

Sponsors and collaborators

Lead sponsor

OvaryIt, LLC

Industry

Collaborators

  • National Institutes of Health (NIH)
  • University of Utah

Registry information

Official study 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

Acronym: PRISM-CS

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Feb 11, 2025
Registry last updated
Feb 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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