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New treatment option for Colorectal Cancer Screening
Official title Impact of Training Patient-centered Approach on Shared Decision in Colorectal Cancer Screening
ClinicalTrials.gov ID: NCT06074536
What this study is testing
- What it's testing
- The purpose of this study is to compare the effect of face-to-face training of general practitioners on the implementation of a shared decision (in the context of colorectal cancer screening), versus current practice (i.e. without training in the patient-centered approach).
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 50 to 74
You may be able to join if
- Patient aged 50 to 74:
- Eligible for organized CRC screening,
- Having declared as attending clinician a general practitioner investigator of the study ✓ Consulting their attending clinician for the duration of...
- AND able and willing to comply with all trial requirements Non \- ✓ Screened for CRC less than 2 years ago
- Not eligible for organized CRC screening:
See the full eligibility criteria
- Patient aged 50 to 74:
- Eligible for organized CRC screening,
- Having declared as attending clinician a general practitioner investigator of the study ✓ Consulting their attending clinician for the duration of the study,
- AND able and willing to comply with all trial requirements Non \- ✓ Screened for CRC less than 2 years ago
- Not eligible for organized CRC screening:
- History of adenomas or CRC: \- Family (1st degree)
- Personal history of IBD:
- Crohn's disease
- Ulcerative colitis)
- Hereditary predispositions:
- Familial adenomatous polyposis
- Hereditary non-polyposis colorectal cancer (Lynch syndrome)
- Patient with symptoms requiring colonoscopy
- Having a level of literacy that does not allow the completion of the self-questionnaire.
- Having an inability to give express consent.
- Being under guardianship, curatorship or having cognitive disorders
The study team makes the final eligibility decision.
Where it's taking place
- Soisy-sous-Montmorency, France
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 50 years to 74 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Soisy-sous-Montmorency, France. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.