Symptom Monitoring Using Patient-Report to Improve Medication Use
Launched by MEDICAL COLLEGE OF WISCONSIN · Jan 3, 2025
Trial Information
Current as of July 09, 2025
Enrolling by invitation
Keywords
ClinConnect Summary
This clinical trial is focused on helping women with early-stage hormone-positive breast cancer stay on their medication, known as endocrine therapy, after their initial treatments. The study aims to understand how tracking symptoms through monthly surveys can help improve medication use. Participants will receive recommendations from specialized cancer pharmacists based on the symptoms they report, which can help make it easier for them to continue taking their medications daily.
To be eligible for this study, participants need to be women aged 18 or older who have been diagnosed with stage 1-3 hormone receptor-positive breast cancer. They should also be recommended to continue their endocrine therapy for at least two more years and have had some difficulties in sticking to their medication plan in the past. Participants will be asked to communicate in either English or Spanish and should be able to understand and sign a consent form. This study is not yet recruiting, but it aims to provide support and improve medication adherence for those at risk of not taking their prescribed treatments.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • Cisgender women assigned female at birth
- • Age 18 years or older
- • Stage 1-3 hormone receptor-positive breast cancer
- • 1. Premenopausal patients being treated with GNRH agonist/antagonist to induce menopause are eligible
- • 2. Patients who received treatment with CDK 4/6 inhibitors are eligible
- • Recommended to continue AET for ≥2 additional years after enrollment
- • Low adherence defined as prescription fills with a proportion of days covered (PDC) of \<80%, examined over all fills during the 2 years prior to date of eligibility review since the first AET prescription/data of AET start OR unable to calculate adherence
- • Verbal fluency in English or Spanish
- • Ability to understand informed consent and the willingness to sign it
- Exclusion Criteria:
- • Unable to verbalize comprehension of study or impaired decision-making
- • Known distant metastatic disease
- • Not receiving breast cancer care or AET prescription from provider at participating site
- • Evidence that an oncology provider discontinued their AET
- • Pregnant or trying to get pregnant
- • Facility-administered medications (i.e., nursing home, home healthcare agency)
About Medical College Of Wisconsin
The Medical College of Wisconsin (MCW) is a leading academic institution dedicated to advancing healthcare through innovative research, education, and clinical practice. As a prominent clinical trial sponsor, MCW is committed to conducting high-quality, ethically-guided research that aims to improve patient outcomes and address critical health challenges. Leveraging a multidisciplinary approach, MCW collaborates with a diverse network of healthcare professionals, researchers, and community partners to facilitate groundbreaking clinical trials across various medical fields, ensuring the translation of scientific discoveries into effective treatments and practices.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Rochester, Minnesota, United States
Chicago, Illinois, United States
Milwaukee, Wisconsin, United States
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported