Could a simple questionnaire spot colorectal cancer before It's too late?
NCT ID NCT07692555
First seen Jul 09, 2026 · Last updated Jul 24, 2026 · Updated 3 times
Summary
This study aims to develop a diagnostic model that predicts the risk of colorectal cancer and advanced polyps in adults aged 18 to 80 who are already scheduled for a routine colonoscopy in China. Participants fill out a questionnaire about their lifestyle, medical history, and symptoms before the procedure. Researchers will then use that information, along with colonoscopy results, to build and test a risk-prediction tool using statistical and machine-learning methods. The goal is to create a simple, non-invasive way to identify people who need a colonoscopy most urgently.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a simple risk-prediction tool that helps doctors identify who is most likely to have colorectal cancer or advanced polyps, potentially improving screening efficiency.
- What could go wrong
- This is an observational study, not a treatment trial. The model may not perform well in other populations or settings, and it relies on self-reported data which can be inaccurate.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 20,000 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adults aged 18 to 80 years who have already been scheduled for or referred to colonoscopy as part of routine clinical care, physical examination, or screening pathways at participating medical institutions in China will be enrolled. All participants must be willing and able to provide informed consent and complete a standardized risk factor questionnaire before the colonoscopy procedure. This population is selected because the primary study outcome, i.e., the presence of advanced colorectal neoplasia, must be confirmed by colonoscopy and histopathology, which are available through routine clinical care without requiring additional invasive procedures for research purposes.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age between 18 and 80 years at the time of enrollment. * Already scheduled to undergo colonoscopy according to routine clinical care, physical examination, or screening pathways at a participating medical institution. * No prior history of colorectal cancer or advanced colorectal neoplasia. * No contraindications to colonoscopy (as determined by the treating physician). * Able to understand the study information and complete the colorectal cancer risk-factor questionnaire independently or with appropriate assistance. * Willing to provide informed consent for completion of the questionnaire and for collection of routine clinical colonoscopy, pathology, and related medical-record data. Exclusion Criteria: * The baseline colorectal cancer risk-factor questionnaire is not completed, or considered invalid because of substantial missing or inconsistent information. * The scheduled index colonoscopy is cancelled, not performed, or not completed regardless of the underlying reason (e.g., inadequate bowel preparation). * Incomplete or unavailable colonoscopy or pathology data after the procedure. * Refusal or withdrawal of informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Fujian Provincial Hospital
Fuzhou, Fujian, 350001, China
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Peking University Cancer Hospital & Institute
Beijing, Beijing Municipality, 100142, China
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People's Hospital of Ningxia Hui Autonomous Region
Yinchuan, Ningxia, 750001, China
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The First Affiliated Hospital of Xiamen University
Xiamen, Fujian, 361003, China
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