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NCT06032338Active, not recruiting

Trial of Direct Home Delivery of Colorectal Cancer Screening Kit Without Pre-ordering

EXPérimentation d'Envoi Postal DIrect à Domicile du kiT de dépistage du Cancer Colorectal Sans Commande préalable [Trial of Direct Home Delivery of Colorectal Cancer Screening Kit Without Pre-ordering]

Source: ClinicalTrials.gov · Last updated 18 Mar 2026

Brief summary (registry, in English)

The effect of mailing FIT with the invitation on participation and colonoscopy rates will be evaluated in a randomized controlled trial conducted in the Centre-Val de Loire (CVL) region, involving 64,000 people from the population eligible for colorectal cancer population-based organised screening program (CRC-PBOSP). In the "C" control group, invitations, test delivery and reminders will be carried out in accordance with the CRC-PBOSP rules at the time of the study. Intervention group "B" will evaluate two experimental modes of invitation with direct home mailing of the test: * Method "B1": invitation with test sent to home without prior information letter * Method "B2": information letter followed by invitation with test sent home, designed to optimize participation by first-time subjects (aged 50-51) invited to the CRC-PBOSP for the first time. Ancillary studies will focus 1/ on acceptability of this intervention (qualitative study on a few general practitioners, gastroenterologists and invitees), 2/ on social and geographical inequalities of participation on a subsample of individuals included in EXPEDIT study using ecological indices (EDI, SCALE).

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
64000 (estimated)
First submitted
20 Jul 2023
Start date
14 Sept 2023
Primary completion date
14 Apr 2026
Lead sponsor
University Hospital, Caen
NCT number
NCT06032338

What you commit to

  • Study type: Interventional
  • Planned participants: 64000
  • From 14 Sept 2023 to the primary completion date, 14 Apr 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • CRC screening exclusion criteria notified to CRCDC-CVL in a previous screening round (family or personal history of CRC/adenoma, inflammatory bowel disease)
  • Colonoscopy in the previous 5 years)
    • Subjects refusing data transmission to research team will be excluded from statistical analyses.

Who the study is looking for

  • 50 to 74 years old
  • Resident of Centre Val de Loire French area
  • Eligible for CRC screening invitation within the biennal CRC-PBOSP during the inclusion period
  • Affiliated to the health insurance scheme

Age in the registry: 50 years to 74 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Crcdc-Cvl
Coordinator of this site? Confirm its status
ToursFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.