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Clinical Trials/NCT00973570
NCT00973570
Completed
Not Applicable

Evaluation of a Smoking Cessation Program Among ADOlescents in Vocational Training Centers

Institut National de la Santé Et de la Recherche Médicale, France1 site in 1 country2,000 target enrollmentFebruary 2008
ConditionsTobacco Use

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tobacco Use
Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Enrollment
2000
Locations
1
Primary Endpoint
The primary outcome is the rate of smoking abstinence after 12 months, measured on the basis of the statements of the whole sample, not only among volunteers.
Status
Completed
Last Updated
last year

Overview

Brief Summary

Background: Most of the efforts to fight against young people's tobacco addiction have focused on smoking prevention and little on smoking cessation. A smoking cessation program, associating pharmacologic and cognitive-behavioural strategy, on a particularly vulnerable population (vocational trainees), was developed by a team of tobacco addiction specialist physicians. We developed a study to evaluate the efficacy of the program. Its main objective is to compare the efficacy of a smoking cessation program offered to all smokers in a population aged 15 to 20 years in Vocational Training Centers (VTC) with that in a control population. The objective of this paper is to present the TABADO study protocol and the results of the pilot study.

Methods: The study is quasi-experimental, prospective, evaluative and comparative and takes place during the 2 years of vocational training. The final population will be composed of 2000 trainees entering a VTC (in Lorraine, France): The intervention group (1000 trainees) benefited from the TABADO program while no specific intervention took place in the "control" group (1000 trainees) other than the treatment and education services usually available. Our primary outcome will be the tobacco abstinence rate at 12 months.

The pilot study is a descriptive monocentric cross-sectional study conducted among the whole group of students, completed by a longitudinal prospective study of smoker volunteers.

Registry
clinicaltrials.gov
Start Date
February 2008
End Date
January 2010
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

The primary outcome is the rate of smoking abstinence after 12 months, measured on the basis of the statements of the whole sample, not only among volunteers.

Time Frame: 12 months

Secondary Outcomes

  • Overall prevalence of tobacco use in the institutions concerned at 12 months.(12 months)
  • Students' motivation to quit smoking (motivational score) and frequency of attempts to quit within the 12 months after the intervention(12 months)
  • Rate of withdrawal from the program among the volunteers after 12 months.(12 months)

Study Sites (1)

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