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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02696863
Other study ID # 2015-05
Secondary ID
Status Recruiting
Phase N/A
First received February 8, 2016
Last updated September 13, 2017
Start date March 2016
Est. completion date December 2017

Study information

Verified date September 2017
Source Institut de Cancérologie de la Loire
Contact Carole PELISSIER, MD
Email carole.pelissier@chu-st-etienne.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
questionnaire


Locations

Country Name City State
France CHU Saint-Etienne Saint-Etienne
France ICLN St-Priest-en-Jarez

Sponsors (2)

Lead Sponsor Collaborator
Institut de Cancérologie de la Loire Centre Hospitalier Universitaire de Saint Etienne

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Interview Obstacles and elements facilitating the establishment of a work-related bronchopulmonary cancer tracking device during the course of care. These are collected in an interview with a sociologist. It will be analyse with NVivo. 45 minutes