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


Sponsor

Wake Forest University Health Sciences

Enrollment

46 participants

Start Date

Oct 4, 2024

Study Type

OBSERVATIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is investigating whether a wearable activity-tracking device (WATD) — which monitors movement and activity — can help measure and manage cancer-related fatigue in people undergoing cancer treatment. Fatigue is one of the most common and disruptive side effects of cancer therapy. **You may be eligible if...** - You have pancreatic cancer or invasive breast cancer - You are currently receiving or planning to start anti-cancer treatment - You have any level of self-reported fatigue - You are 18 or older - You can read and understand English **You may NOT be eligible if...** - You have a medical condition that the investigator believes would interfere with using the wearable device or completing questionnaires - You are not planning to receive anti-cancer treatment Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

Levine Cancer Institute

Charlotte, North Carolina, United States

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NCT06291324


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