CClinicalTrials.gg
Status unknownNCT02696863RECAP 2Updated Sep 14, 2017

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

An observational study in Broncho Pulmonary Cancer, sponsored by Institut de Cancérologie de la Loire. Status unknown at 2 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-09-14.

Sponsored by Institut de Cancérologie de la Loire · Observational

The sponsor has not verified this record recently (last verified Sep 2017), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
20
Ages
18 Years and older
Sex
All
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Study 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

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Conditions studied

  • Broncho Pulmonary Cancer

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03

In context

Lung Neoplasms

7,243 studies on the registry are indexed under Lung Neoplasms; 1,557 are open to participants now.

This study's planned enrollment of 20 is below the median of 189 across 1,514 observational studies indexed under Lung Neoplasms.

Browse Lung Neoplasms studies →

Lead sponsor

Institut de Cancérologie de la Loire is the lead sponsor of 28 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

primitive CBP Patients

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

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.
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Study design

Observational model
Other
Time perspective
Prospective
Enrollment
20 participants (estimated)
Patient registry
No

Groups and cohorts

  • 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

    Behavioral: questionnaire

Interventions

  • Behavioralquestionnaire
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What researchers measure

Primary outcomes

  1. 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.

    Time frame: 45 minutes

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Study locations

2 of 2 sites recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 14, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02696863
Lead sponsor
Institut de Cancérologie de la Loire
Collaborators
Centre Hospitalier Universitaire de Saint Etienne
Responsible party
Sponsor
First posted
Mar 2, 2016
Start date
Mar 2016
Primary completion
Dec 2017 (estimated)
Completion
Dec 2017 (estimated)
Last update
Sep 14, 2017

Study contacts

Carole PELISSIER, MD
Contact
carole.pelissier@chu-st-etienne.fr
Vanessa DUTERTRE
Contact
vanessa.dutertre@icloire.fr
04 77 91 74 49

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2017. You cannot join it, but the record below documents what was studied.

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