Pancreatic Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults aged 18 years or older
- People who have been identified as having an increased risk of certain cancers, as defined by the Interception program
- People whose baseline WCRF (World Cancer Research Fund) lifestyle score was 5 or lower when they entered the Interception program (confirm with trial site)
- People who have agreed to take part and have signed a written consent form
- People who agree to complete questionnaires on a dedicated online platform for the full duration of the study
- People who own and are willing to use a smartphone
- People who can understand and communicate in spoken and written French
Who may not be able to join:
- People with psychiatric conditions or cognitive difficulties that would prevent them from taking part
- People who are under legal guardianship, have had their liberty restricted by a court or administrative decision, or are unable to give their own consent
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Bruno Raynard, MD, Gustave Roussy, Villejuif, France
Phone: +33 (0) 1 42 11 42 11
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Proportion (%) of participants with at least 1-point improvement in the WCRF score
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.