Collaborative Research: Multiscale Modeling and Intervention for Improving Long-Term Medication

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age21-70
SponsorSan Diego State University

About this trial

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.

Eligibility criteria

Qualifiers

are English-speaking and reading;

are between ages 21 and 70 years;

are diagnosed with stage 0-3 breast cancer in the past 5 years;

have completed all surgery, radiation, and chemotherapy, except endocrine therapy;

Disqualifiers

None

Trial design

Treatments tested in this trial

  • integrated medication monitoring (MM) system

Treatment groups

15 Participants
are divided into 1 treatment group

Sponsors and collaborators

San Diego State University

Lead sponsor

University of Virginia

Collaborator

National Cancer Institute (NCI)

Collaborator