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ENROLLING BY INVITATION
NCT06765707
NA

Symptom Monitoring Using Patient-Report to Improve Medication Use

Sponsor: Medical College of Wisconsin

View on ClinicalTrials.gov

Summary

This is an intervention targeting patients at risk for non-adherence to endocrine therapy after primary treatments for hormone-positive breast cancer. In a randomized study, the study team will collect patient-reported symptoms monthly from participants through surveys. Pharmacists who specialize in cancer at the patients' hospital will give patients recommendations to help improve their symptoms and address other barriers so they can continue daily endocrine therapy medications.

Official title: Symptom Monitoring Using Patient-Reported Outcomes to Optimize Medication Use

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

225

Start Date

2025-06-23

Completion Date

2029-08

Last Updated

2025-07-24

Healthy Volunteers

No

Interventions

BEHAVIORAL

Pharmacist delivered symptom monitoring and management

Patients in the intervention phase will receive PRO-based symptom monitoring once a month and pharmacist-led management for problematic symptoms based on routine clinical care recommendations.

Locations (3)

University of Illinois Chicago

Chicago, Illinois, United States

Mayo Clinic

Rochester, Minnesota, United States

Medical College of Wisconsin

Milwaukee, Wisconsin, United States