Actively Recruiting
Fatigue and Molecular Mechanisms in Cancer Patients Receiving CCRT
Led by University of California, San Francisco · Updated on 2025-09-16
125
Participants Needed
1
Research Sites
139 weeks
Total Duration
On this page
Sponsors
U
University of California, San Francisco
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Cancer-related fatigue (CRF) is a significant problem for cancer patients. This prospective, basic science, observational study will evaluate for changes in CRF associated with molecular characteristics prior to, during, and at the completion of non-investigational, standard-of-care, combined chemotherapy and radiation therapy (CCRT) and to develop and assess predictive models for CRF severity.
CONDITIONS
Official Title
Fatigue and Molecular Mechanisms in Cancer Patients Receiving CCRT
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants have not received any cancer systemic therapies or radiation therapy in the past month, except surgery or inductive chemotherapy.
- Participants are planned to receive 15 or more fractions of combined chemotherapy and radiation therapy.
- Participants are male or female and 18 years of age or older at the time of signing informed consent.
- Ability to understand and sign a written informed consent document.
- Willing and able to complete all study questionnaires and provide blood and stool samples before, midway, and after treatment.
- Willing to allow medical record review for clinical information.
- Able to read, write, and understand English or Spanish.
You will not qualify if you...
- Contraindication to phlebotomy for removal of approximately 50 mL of peripheral blood within a 6-week period (per Institutional Review Board limit).
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of California, San Francisco
San Francisco, California, United States, 94143
Actively Recruiting
Research Team
J
Jamese Johnson
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
1
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