Actively Recruiting
Unintentional Weight Loss and Cancer: A Prospective Trial of Patient-centered Weight Tracking Combin
Led by Case Comprehensive Cancer Center · Updated on 2026-02-19
1000
Participants Needed
1
Research Sites
191 weeks
Total Duration
On this page
Sponsors
C
Case Comprehensive Cancer Center
Lead Sponsor
U
University Hospitals Seidman Cancer Center
Collaborating Sponsor
AI-Summary
What this Trial Is About
Unintentional weight loss (UWL) is commonly associated with a wide variety of diseases and there is still no valid diagnostic pathway for evaluating UWL. When detecting UWL coupled with GRAIL Galleri testing, (an investigational pan-cancer early detection test), it is thought that there is a greater positive predictive value in detecting malignancies. This study aims to test the potential synergistic effects of UWL detection and GRAIL usage to detect malignancy at an even earlier rate. UWL will be measured using weekly weight tracking.
CONDITIONS
Official Title
Unintentional Weight Loss and Cancer: A Prospective Trial of Patient-centered Weight Tracking Combin
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 40 and 80 years
- Access to a device compatible with the Fitbit Aria Air smart scale
- Willingness to follow all study procedures and be available for the entire study duration
- Mentally competent, able to understand and willing to sign informed consent
- Able to speak English to understand the trial rationale and procedures
You will not qualify if you...
- Current cancer diagnosis, undergoing cancer treatment, or completed treatment within the past 3 years
- Actively trying to lose weight using medications or bariatric surgery
- Pregnant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center
Cleveland, Ohio, United States, 44106
Actively Recruiting
Research Team
J
Jordan M Winter, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SCREENING
Number of Arms
1
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