Plan for Systematic Identification of Lung Cancers of Occupational Origin: Implementation Study

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-03-31

Study Completion Date

2017-12-31

Brief Summary

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The main objective is to identify obstacles and elements facilitating the implementation of a tracking device Broncho Pulmonary Cancer during the course of care.

The secondary objective is to assess patient knowledge and information received on their previous occupational exposure during their professional activity.

This is a prospective multicenter study of qualitative methodology through in-depth interviews conducted with patients treated at ICLN and CHU Saint-Etienne

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Detailed Description

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Conditions

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Broncho Pulmonary Cancer

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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filling a questionnaire and interview

The questionnaire is tracking occupational carcinogens. It consists of 30 questions , fills an average of 3 minutes and includes three response categories: "yes", "no" and "do not know". A questionnaire will be added social and professional issues.

Interviews will be conducted with the patient to identify obstacles and facilitating elements

questionnaire

Intervention Type BEHAVIORAL

Interventions

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questionnaire

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* primitive CBP Patients;
* Patients employees or have been employees of the general scheme and / or the agricultural social security system;
* Patients understand French.

Exclusion Criteria

* Patients recognized occupational disease for CBP;
* recognized disability in patients for CBP by the social security system;
* Patients who have never been employees of the General or the agricultural social security system plan
* Patients already included in phase 1 of the study;
* Refusal of participation, signed consent major patients protected under guardianship;
* Patients unable to understand the course of the study.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No