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Recruiting NCT06633224

Fatigue and Molecular Mechanisms in Cancer Patients Receiving CCRT

Trial Parameters

Condition Cancer
Sponsor University of California, San Francisco
Study Type OBSERVATIONAL
Phase N/A
Enrollment 125
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-12-27
Completion 2026-09-01
Interventions
Blood Specimen CollectionStool Specimen CollectionQuality of Life (QOL) Questionnaires

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * Participants have not received any prior treatment (i.e., cancer systemic therapies or radiation therapy) in the month except surgery or inductive Chemotherapy (CTX). * Participants receiving \>= 15 fractions. * Participants is male or female and is \>18 years of age on the day of signing the informed consent. * Ability to understand a written informed consent document. * Able and willing to complete all of the study questionnaires and provide blood and stool samples prior to, midway, and following the completion of treatment. * Willing to have medical records reviewed for clinical information. * Able to read, write and understand English or Spanish. Exclusion Criteria: * Contraindication to phlebotomy for removal of approximately 50 mL of peripheral blood within 6 week period (Institutional Review Board (IRB) limit).

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