The goal of this study is to learn about the impact of an integrated medication monitoring system in breast cancer survivors aged 21-70 who are prescribed endocrine therapy. The main question it aims to address is: Does the integrated medication monitoring system improve medication adherence among breast cancer survivors when used over a six-month period? Fifteen English-speaking breast cancer survivors who meet the inclusion criteria will use a combination of smartphone-based ecological momentary assessments, a medication event monitoring system (Wisepill), and a wearable sensor (Fitbit). After 2 months, participants will be provided personalized content to facilitate medication adherence through an app (Digital Trails) and through WisePill. Participants will complete online surveys at baseline, 3 months, and 6 months to assess their experiences and adherence.
Age range
21 Years – 70 Years
Sex
FEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Wisepill MEMS Sensor data collection
Timeframe: From enrollment to the end of study at 6 months
Intervention component - Introduction
Timeframe: 6 months after enrollment into study
Intervention component - Instructions
Timeframe: 6 months after enrollment into the study
Intervention component - calendar
Timeframe: 6 months after enrollment into the study
Intervention component - resources
Timeframe: 6 months after enrollment into the study
Intervention component - relaxation audio files
Timeframe: 6 months after enrollment into the study
Intervention component - social support
Timeframe: 6 months after enrollment into the study
Intervention component - tamoxifen
Timeframe: 6 months after enrollment into the study
Intervention component - aromatase inhibitors
Timeframe: 6 months after enrollment into the study
Intervention component - routine
Timeframe: 6 months after enrollment into the study
Intervention component - reminders
Timeframe: 6 months after enrollment into the study
Intervention component - joint pain
Timeframe: 6 months after enrollment into the study
Intervention component - hot flashes
Timeframe: 6 months after enrollment into the study
Intervention component - pacing
Timeframe: 6 months after enrollment into the study
Intervention component - relaxation
Timeframe: 6 months after enrollment into the study
Intervention component - needs
Timeframe: 6 months after enrollment into the study
Intervention component - travel
Timeframe: 6 months after enrollment into the study
Intervention component - thoughts
Timeframe: 6 months after enrollment into the study
Intervention component - most useful
Timeframe: 6 months after enrollment into the study
Intervention component - least useful
Timeframe: 6 months after enrollment into the study
Intervention component - most attractive
Timeframe: 6 months after enrollment into the study
Intervention component - least attractive
Timeframe: 6 months after enrollment into the study
Intervention component - problems
Timeframe: 6 months after enrollment into the study
Intervention component - changes
Timeframe: 6 months after enrollment into the study
Intervention component - additional information
Timeframe: 6 months after enrollment into the study
Intervention component - future use
Timeframe: 6 months after enrollment into the study