Can a standardized care framework improve life for colorectal cancer patients?
NCT ID NCT03965325
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether using a standardized set of measurements, including patient-reported outcomes, can improve care for people with colorectal cancer. Researchers followed 133 patients over time, collecting data on their health and quality of life. The goal was to see if this approach helps doctors and patients make better decisions together.
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 approach could help standardize care and improve quality of life monitoring for colorectal cancer patients.
- What could go wrong
- This is an observational study, not a treatment trial, so it cannot directly improve outcomes. Results may not apply to all patients or settings.
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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133 people
The number who actually took part.
- Started
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Jun 2019
- Finished
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Feb 2024
- 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
Subjects diagnosed with a CRC who had a surgical consultation, and who meet the inclusion/exclusion criteria are intended to participate in this study. Subject enrollment will continue for the whole study duration. The eligibility criteria are kept comprehensive to all CRC types to reflect centers routine clinical practice ("all-comer" or "real world" subjects). To avoid subject selection bias, consecutive screening and enrollment will be requested.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: 1. Confirmed CRC diagnosis not older than 8 years from the first treatment; 2. Age ≥18 years or minimum age as required by local regulations; 3. Ability and willingness to give written consent form ("Patient informed consent Form" or "Patient Data Release Authorization Form"); 4. Ability and willingness to comply with the clinical investigational plan. Exclusion Criteria: 1. Pregnant or breastfeeding woman; 2. Psychiatric and cognitive impairment; 3. Patient under juristic protection or under guardianship
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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.
Contacts and locations
Locations
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Service de Chirurgie Digestive et Endocrinienne, NHC
Strasbourg, 67 091, France
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