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Clinical Trial Summary

The purpose of this study is to evaluate the feasibility of using a commercial WATD (Wearable Activity Tracker Device) to collect HRV (Heart Rate Variability) data from pancreatic and breast cancer patients.


Clinical Trial Description

This feasibility study is designed to evaluate the collection of longitudinal HRV (Heart Rate Variability) data and assess acceptability of the device among adult cancer patients in the research setting. Over the course of the four-week study, participants will be asked to provide experiential diaries detailing adherence to and acceptability of the WATD (Wearable Activity Tracker Device) and conduct PRO (Patient Reported Outcome) measures at week two and week four (end of study). During the final research visit at week four, subjects will return the WATD and will complete the acceptability survey. Each week of the four-week study, the WATD data and experiential diaries will be downloaded for analysis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06291324
Study type Observational
Source Wake Forest University Health Sciences
Contact Alicia Patrick
Phone 980-292-1746
Email alicia.patrick@atriumhealth.org
Status Not yet recruiting
Phase
Start date May 2024
Completion date December 15, 2025

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