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- Klinische proef NCT00973570
Smoking Cessation Program Among Adolescents in Vocational Training Centers (TABADO)
Evaluation of a Smoking Cessation Program Among ADOlescents in Vocational Training Centers
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.
Studie Overzicht
Studietype
Inschrijving (Verwacht)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
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Lorraine
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Nancy, Lorraine, Frankrijk, 54000
- Werving
- Chu Nancy
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Contact:
- Laetitia MINARY, MSc
- E-mail: l.minary@chu-nancy.fr
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Hoofdonderzoeker:
- François ALLA, MD/ PhD
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Hoofdonderzoeker:
- Denis Zmirou-Navier, MD/ PhD
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Onderonderzoeker:
- Yves MARTINET, MD/ PhD
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Contact:
- François ALLA, MD/PhD
- E-mail: f.alla@chu-nancy.fr
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion criteria:
- All students, males and females, registered in the VTC for at least a 2-year training period
- Aged from 15 to 20 years
Exclusion criteria:
- Subjects with current serious psychiatric disorders or who may be susceptible to decompensation upon quitting smoking (major depression)
- Smokers who are involved in an ongoing attempt to quit, with medical monitoring.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Preventie
- Toewijzing: Niet-gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: "Intervention" group
The "intervention" group benefits from the TABADO program
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The intervention takes place in 3 stages: (i) a general information session on tobacco consumption is delivered to all teenagers, both smokers and nonsmokers.
(ii) For smokers wishing to join the program, this session is followed by individualized consultations with a team of tobacco addiction physicians.
(iii) The volunteers then benefit from a small group approach, consisting of discussion sessions to share experiences, strengthen motivation, and prevent relapse.
There will be 4 sessions in total, comprising individual counseling and work in groups spread over 3 months (taking into account the availability of the trainees because of their alternate-week training schedule).
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Geen tussenkomst: "Control" group
The "control" group not benefit from any specific intervention other than the treatment and education usually available
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
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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.
Tijdsspanne: 12 months
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12 months
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Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
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Overall prevalence of tobacco use in the institutions concerned at 12 months.
Tijdsspanne: 12 months
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12 months
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Students' motivation to quit smoking (motivational score) and frequency of attempts to quit within the 12 months after the intervention
Tijdsspanne: 12 months
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12 months
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Rate of withdrawal from the program among the volunteers after 12 months.
Tijdsspanne: 12 months
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12 months
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Medewerkers en onderzoekers
Onderzoekers
- Hoofdonderzoeker: François ALLA, MD/ PhD, Institut National de la Santé Et de la Recherche Médicale, France
Publicaties en nuttige links
Studie record data
Bestudeer belangrijke data
Studie start
Primaire voltooiing (Verwacht)
Studie voltooiing (Verwacht)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Schatting)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Andere studie-ID-nummers
- C07-43
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .
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Medical University of South CarolinaNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)VoltooidObesitas | Cardiovasculaire risicofactor | Diabetes Mellitus-risico
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Cefaly TechnologyVoltooid