- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07489833
Metabolomic Pathways and Traditional Chinese Medicine Body Constitution in Cancer-related Fatigue
March 24, 2026 updated by: Chang Gung Memorial Hospital
The Exploration of the Relationship Between Metabolomic Pathways and Traditional Chinese Medicine Body Constitution in Cancer-related Fatigue in Patients With Colorectal Cancer
The aim of this study is to integrate insights from metabolomics and TCMBC to identify biomarkers and physiological pathways associated with CRF.
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
80
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Yun-Jen Chou, PhD
- Phone Number: 3512 886-3-2118800
- Email: yjchou@mail.cgu.edu.tw
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Newly diagnosed with stage I to III CRC and scheduled for surgical treatment
Description
Inclusion Criteria:
- Patients aged 18 years or older
- Diagnosed with stage I to III CRC and scheduled for surgical treatment
- Cognitively intact and able to communicate in either Mandarin or Taiwanese
- Willing to participate in the study and provide written informed consent.
Exclusion Criteria:
- Patients diagnosed with stage IV colorectal cancer
- Patients with recurrent colorectal cancer or other concurrent cancers.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-report Questionnaire
Time Frame: Change from baseline to 3 months after surgery.
|
The study utilizes two instruments.
First, the Fatigue Symptom Inventory (FSI) is used to assess fatigue; total scores range from 0 to 127, with higher scores indicating greater fatigue severity.
Second, the Body Constitution Questionnaire (BCQ) comprises 16 items, with total scores ranging from 16 to 80.
|
Change from baseline to 3 months after surgery.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
April 20, 2026
Primary Completion (Estimated)
December 31, 2028
Study Completion (Estimated)
February 28, 2029
Study Registration Dates
First Submitted
March 18, 2026
First Submitted That Met QC Criteria
March 18, 2026
First Posted (Actual)
March 24, 2026
Study Record Updates
Last Update Posted (Actual)
March 27, 2026
Last Update Submitted That Met QC Criteria
March 24, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202402033B0
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.