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

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07291414 on ClinicalTrials.gov