Actively Recruiting
WATD and Cancer-Related Fatigue: A Study For Patients Undergoing Anti-Cancer Treatment
Led by Wake Forest University Health Sciences · Updated on 2026-01-07
46
Participants Needed
1
Research Sites
142 weeks
Total Duration
On this page
Sponsors
W
Wake Forest University Health Sciences
Lead Sponsor
A
Atrium Health Levine Cancer Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
WATD and Cancer-Related Fatigue: A Study For Patients Undergoing Anti-Cancer Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Provide written informed consent and authorization for release of personal health information
- Diagnosed with pancreatic or invasive breast cancer and planning or currently undergoing anti-cancer treatment
- Have any severity of self-reported fatigue
- Be at least 18 years old at consent
- Able to read and understand English
- Able to understand and comply with study procedures including completing questionnaires and returning the device
You will not qualify if you...
- Have any clinically significant heart-related abnormality that could affect study results
- Have any other condition that could interfere with participation or study assessments as decided by the investigator
- Lack internet, Wi-Fi access, or an email account
- Lack access to a smartphone or mobile device
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Levine Cancer Institute
Charlotte, North Carolina, United States, 28204
Actively Recruiting
Research Team
M
Maggie Dzhanumova
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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