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Evaluation of the cognitive behavioral smoking reduction program "Smoke_less": a randomized controlled trial.
Rüther, Tobias; Kiss, Alexa; Eberhardt, Kerstin; Linhardt, Andrea; Kröger, Christoph; Pogarell, Oliver.
Afiliación
  • Rüther T; Department of Psychiatry and Psychotherapy, Medical Center of the University of Munich, Nussbaumstrasse 7, 80336, Munich, Germany. tobias.ruether@med.uni-muenchen.de.
  • Kiss A; Department of Psychiatry and Psychotherapy, Medical Center of the University of Munich, Nussbaumstrasse 7, 80336, Munich, Germany.
  • Eberhardt K; Department of Psychiatry and Psychotherapy, Medical Center of the University of Munich, Nussbaumstrasse 7, 80336, Munich, Germany.
  • Linhardt A; Department of Psychiatry and Psychotherapy, Medical Center of the University of Munich, Nussbaumstrasse 7, 80336, Munich, Germany.
  • Kröger C; IFT Gesundheitsförderung Gesellschaft mbH, Montsalvatstrasse 14, 80804, Munich, Germany.
  • Pogarell O; Department of Psychiatry and Psychotherapy, Medical Center of the University of Munich, Nussbaumstrasse 7, 80336, Munich, Germany.
Eur Arch Psychiatry Clin Neurosci ; 268(3): 269-277, 2018 Apr.
Article en En | MEDLINE | ID: mdl-28616772
The vast majority of smokers are unable or unwilling to quit, but many are open to reducing smoking. No treatment options exist for these smokers besides medication-based therapies. Thus, this study investigated the efficacy of a cognitive behavioral therapy (CBT) smoking reduction program, Smoke_less. A sample of 155 outpatient smokers aged 18-70 years was recruited at the Tobacco Dependence Outpatient Clinic of the Medical Center of the University of Munich, Germany, and randomly assigned to the experimental group (Smoke_less: four weekly CBT group sessions and two telephone calls over 5 weeks, n = 51), active comparator group (one 15-minute counseling session, n = 49), or waiting control group (no intervention during the study, n = 55). The primary endpoint was a ≥50% smoking reduction in the intention-to-treat group 1 week and 6 months after the intervention. We evaluated also abstinence rates at follow-up. Significantly more participants in the Smoke_less group had reduced smoking ≥50% compared to the waiting group at 1 week [OR 7.59 (2.59-22.19)] and 6 months [OR 5.00 (1.68-14.84)] and compared to the active comparison group at 1 week [OR 8.58 (2.67-27.31)] but not at 6 months [OR 1.73 (0.71-4.20)]. We found no significant effects on abstinence rates. The CBT smoking reduction program Smoke_less is effective for smoking reduction but is superior to brief counseling only in the short term. Further research is required to improve its efficacy in long-term smoking reduction to provide a valid, non-medication-based alternative to smokers unable or unwilling to quit. TRIAL REGISTRATION: Clinicaltrials.gov Identifier: NCT02337400.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Tabaquismo / Fumar / Trastornos del Conocimiento / Reducción del Consumo de Tabaco Tipo de estudio: Evaluation_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur Arch Psychiatry Clin Neurosci Asunto de la revista: NEUROLOGIA / PSIQUIATRIA Año: 2018 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Tabaquismo / Fumar / Trastornos del Conocimiento / Reducción del Consumo de Tabaco Tipo de estudio: Evaluation_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur Arch Psychiatry Clin Neurosci Asunto de la revista: NEUROLOGIA / PSIQUIATRIA Año: 2018 Tipo del documento: Article País de afiliación: Alemania