Wearable Integration in Symptom Evaluation for Cancer Survivors

The objective of this work is the production of actionable insights that can be leveraged to improve remote symptom monitoring (RSM) in varied practice settings, which in turn, is expected to improve timely, efficient, and high-quality comprehensive care in oncology. Aim 1: To assess the feasibility of incorporating a wearable into an RSM program for patients receiving cancer treatment. Aim 2: To assess the relationship between the wearable and ePRO-reported physical symptoms and functional status. Aim 3: To characterize barriers and facilitators of using the wearable in the RSM program and suggest approaches to incorporating relevant evidence-based interventions.

NCT Number	NCT07463547
Lead Sponsor	University of Alabama at Birmingham Collaborators: Breast Cancer Research Foundation of Alabama
Conditions	Cancer
Enrollment	20 participants
Start Date	2026-04-17
Primary Completion	2027-02 (estimated)
Study Completion	2027-02 (estimated)
Updated on ClinicalTrials.gov	2026-04-23