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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT01364454
Date of registration: 31/05/2011
Primary sponsor: Paris 12 Val de Marne University
Public title: General Practitioners (GP) Involvement in Colorectal Cancer (CRC) Screening
Scientific title: Effect of Eligible Patients Paper-based Reminder for General Practitioners on Colorectal Cancer Screening Participation
Date of first enrolment: June 2010
Target sample size: 8140
Recruitment status: Active, not recruiting
URL:  http://clinicaltrials.gov/show/NCT01364454
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Screening  
Countries of recruitment
France
Contacts
Name:   Julien Le Breton, MD, MPH
Address: 
Telephone:
Email:
Affiliation:  DUERMG
Key inclusion & exclusion criteria

Inclusion Criteria:

1. General Practitioner (GP)

- exercising in the Val de Marne (French department of the suburb of Paris)

- volunteered to participate at the study

2. Patient

- living in the Val de Marne (French department of the suburb of Paris)

- having declared a 'preferred GP' exercising in the Val de Marne to the main
statutory health insurance scheme ("régime général")

- being eligible for colorectal cancer screening (aged 50 to 74 years, not
excluded and having not proceed yet to the screening)

- having consulted his 'preferred GP', whatever the reason, during the study
period

Exclusion Criteria:



Age minimum: 50 Years
Age maximum: 74 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Colorectal Cancer
Intervention(s)
Other: Eligible patients' paper-based reminder
Primary Outcome(s)
Patient's participation to colorectal cancer screening program [Time Frame: 1 year]
Secondary Outcome(s)
Secondary ID(s)
DUERMG
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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