Impact of Training Patient-centered Approach on Shared Decision in Colorectal Cancer Screening

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50-74
SponsorCNGE Conseil

About this trial

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).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Eligible for organized CRC screening,

Having declared as attending clinician a general practitioner investigator of the study

AND able and willing to comply with all trial requirements

Crohn's disease

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • patient-centered approach training

    Procedure/Surgery

    face to face training of general practitioner of interventional arm

Treatment groups

400 Participants
are divided into 2 treatment groups
Group A: Interventional armExperimental treatment 1 intervention
Group B: Control armNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

The Measurement of the achievement oh the shared decision shared decision making in CRC screening using the patient shared a self-decision-making questionnaire (SDM-Q9), validated in French

comparison of the mean of the SDM-Q9 between each arm of the study from 0 (weak shared decision) to 100 (strong shared decision). We will compare the average of the SDM-Q9 between each arm of the study

Time frame
6 to 8 months after after patient nclusion (carrying out the screening test)

Secondary outcomes

1

Evaluate the effect of training on the CRC screening rate

participation rate in organized CRC screening at individual level. Measurements taken 6 months after the last patient was included in the trial,

Time frame
Measurements taken 6 months after the last patient was included in the trial, i.e. no later than 18 months after the start of the trial
2

Confronting the shared decision made by the patient regarding the completion of CRC screening

Participation rate (IC95%) in CRC screening according to the patient's decision at the end of the initial consultation: wish to be screened, neutral, wish not to be screened.

Time frame
Measurements taken 6 months after the last patient was included in the trial, i.e. no later than 18 months after the start of the trial
3

Explore understanding of the shared decision process among general practitioners and patients

Proportion (IC95%) of included patients with a SURE test result of less than 4

Time frame
Data collected immediately after the inclusion visit

Other outcomes

Sponsors and contacts

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