Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06291324

WATD and Cancer-Related Fatigue: A Study For Patients Undergoing Anti-Cancer Treatment

Wearable Activity Tracker Devices and Cancer-Related Fatigue: A Clinical Utility Pilot Study For Patients Undergoing Anti-Cancer Treatment

Status
Recruiting
Phase
Study type
Observational
Enrollment
46 (estimated)
Sponsor
Wake Forest University Health Sciences · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Timeline

Start date
2024-10-04
Primary completion
2027-06-30
Completion
2027-06-30
First posted
2024-03-04
Last updated
2026-01-07

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06291324. Inclusion in this directory is not an endorsement.