Wearable Technology for Cancer
(WISE Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
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.
Who Is on the Research Team?
Gabrielle Rocque, MD
Principal Investigator
University of Alabama at Birmingham
Are You a Good Fit for This Trial?
Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants use a wearable device to track physiological health metrics while receiving cancer treatment
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Wearable
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Patients are given a wearable to use which tracks physiological health metrics (e.g., sleep, activity, heart rate variability)
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Alabama at Birmingham
Lead Sponsor
Breast Cancer Research Foundation of Alabama
Collaborator
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