A Self-Monitoring Platform for Tracking Medication Safety and Concerns in Cancer Patients
NCT07291414 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80
Last updated 2026-01-21
Summary
This clinical trial evaluates the usefulness of a self-monitoring platform for tracking medication safety events and concerns in patients with lung, colorectal, breast, and prostate cancer. Patients receiving oral anticancer agents often encounter challenges in managing complex treatment regimens, potentially life-threatening toxicities, and drug-drug and drug-food interactions at home. To achieve the goal of medication safety, they need to become "vigilant partners" in medication and toxicity self-monitoring, including timely reporting of medication events to clinicians when their care transitions back home. In this study, patients use an online self-monitoring platform to track their experiences or concerns about taking their medications, including their experiences with symptoms. This platform may be a useful way for patients to track problems they have when taking their medications at home and may help them take better care of their health.
Conditions
- Breast Carcinoma
- Colorectal Carcinoma
- Lung Carcinoma
- Malignant Solid Neoplasm
- Prostate Carcinoma
Interventions
- OTHER
-
Educational Intervention
Receive educational materials and resources
- OTHER
-
Electronic Health Record Review
Ancillary studies
- PROCEDURE
-
Follow-Up
Receive follow-up contact
- OTHER
-
Internet-Based Intervention
Use self-monitoring platform
- OTHER
-
Interview
Ancillary studies
- OTHER
-
Survey Administration
Ancillary studies
Sponsors & Collaborators
-
Agency for Healthcare Research and Quality (AHRQ)
collaborator FED -
University of Michigan Rogel Cancer Center
lead OTHER
Principal Investigators
-
Yun Jiang · University of Michigan Rogel Cancer Center
-
Yang Gong · UTHealth Houston McWilliam School of Biomedical Informatics
Study Design
- Allocation
- NA
- Purpose
- HEALTH_SERVICES_RESEARCH
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-01-09
- Primary Completion
- 2028-01-01
- Completion
- 2028-01-01
Countries
- United States
Study Locations
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