A randomized trial of short psychotherapy versus sustained‐release bupropion for smoking cessation

ABSTRACT Aims  To compare the efficacy and safety of a novel psychological intervention for smoking cessation called psychodynamic model (PDM) training to an active control condition of sustained‐release bupropion. Design  Randomized controlled clinical trial with allocation concealment. Setting  Pr...

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Veröffentlicht in:Addiction (Abingdon, England) England), 2008-12, Vol.103 (12), p.2024-2031
Hauptverfasser: Zernig, Gerald, Wallner, Reinhild, Grohs, Ursula, Kriechbaum, Norbert, Kemmler, Georg, Saria, Alois
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container_end_page 2031
container_issue 12
container_start_page 2024
container_title Addiction (Abingdon, England)
container_volume 103
creator Zernig, Gerald
Wallner, Reinhild
Grohs, Ursula
Kriechbaum, Norbert
Kemmler, Georg
Saria, Alois
description ABSTRACT Aims  To compare the efficacy and safety of a novel psychological intervention for smoking cessation called psychodynamic model (PDM) training to an active control condition of sustained‐release bupropion. Design  Randomized controlled clinical trial with allocation concealment. Setting  Private psychiatric practice. Participants  Seven hundred and seventy‐nine adult smokers recruited by advertising. Interventions  PDM training (n = 366 participants) consisted of a very brief (1.5 days) psychoeducation and a supervised training in autosuggestion techniques (guided imageries) aimed at enhancing self‐management, decidedness, assertiveness, security and competence in relationships, natural functions of organs and awareness of bodily functions. Bupropion SR (n = 413) was increased to 150 mg twice daily over 1 week and given over a 8‐week period. Measurements  Twelve‐month continuous abstinence confirmed by exhaled carbon monoxide (CO) of 9 parts per million (p.p.m.) or less at all interviews conducted at 3, 6 and 12 months. Findings  Intention‐to‐treat analysis revealed Russell standard 12‐month continuous abstinence rates of 39.1% in the psychotherapy group versus 12.3% in the bupropion SR group (P 
doi_str_mv 10.1111/j.1360-0443.2008.02348.x
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Design  Randomized controlled clinical trial with allocation concealment. Setting  Private psychiatric practice. Participants  Seven hundred and seventy‐nine adult smokers recruited by advertising. Interventions  PDM training (n = 366 participants) consisted of a very brief (1.5 days) psychoeducation and a supervised training in autosuggestion techniques (guided imageries) aimed at enhancing self‐management, decidedness, assertiveness, security and competence in relationships, natural functions of organs and awareness of bodily functions. Bupropion SR (n = 413) was increased to 150 mg twice daily over 1 week and given over a 8‐week period. Measurements  Twelve‐month continuous abstinence confirmed by exhaled carbon monoxide (CO) of 9 parts per million (p.p.m.) or less at all interviews conducted at 3, 6 and 12 months. Findings  Intention‐to‐treat analysis revealed Russell standard 12‐month continuous abstinence rates of 39.1% in the psychotherapy group versus 12.3% in the bupropion SR group (P &lt; 0.001) with a relative benefit (RB) of 3.16 (2.38–4.26). Completer analysis revealed 12‐month continuous abstinence rates of 39.9% in the psychotherapy group versus 22.5% in the bupropion group [P &lt; 0.001; RB 1.78 (1.35–2.34)]. Of note, bupropion abstinence rates were comparable to previous medications/placebo‐only comparisons in geographically different samples. Conclusions  The 1.5‐day psychotherapy exceeded bupropion's efficacy, presenting an alternative to pharmacological smoking cessation aids, especially for smokers who reject drugs to treat their substance dependence, at a similar cost (€350) as the bupropion treatment (€355).</description><identifier>ISSN: 0965-2140</identifier><identifier>EISSN: 1360-0443</identifier><identifier>DOI: 10.1111/j.1360-0443.2008.02348.x</identifier><identifier>PMID: 19469746</identifier><identifier>CODEN: ADICE5</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Abstinence ; Addiction ; Adult ; Bupropion ; Bupropion - adverse effects ; Bupropion - therapeutic use ; Cessation ; Clinical outcomes ; Clinical trials ; Drug therapy ; Efficacy ; Female ; Group psychotherapy ; Humans ; Imagery (Psychotherapy) ; Male ; Methodology ; Middle Aged ; Nicotine dependence ; Patient Compliance ; Prescription drugs ; psychodynamic model training ; Psychotherapy ; Psychotherapy, Brief - methods ; Public health ; Random sampling ; randomized controlled trial ; Smoking ; Smoking - therapy ; Smoking cessation ; Smoking Cessation - methods ; Social problems ; sustained‐release bupropion ; Tobacco Use Disorder - therapy ; Treatment Outcome</subject><ispartof>Addiction (Abingdon, England), 2008-12, Vol.103 (12), p.2024-2031</ispartof><rights>2008 The Authors. 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Design  Randomized controlled clinical trial with allocation concealment. Setting  Private psychiatric practice. Participants  Seven hundred and seventy‐nine adult smokers recruited by advertising. Interventions  PDM training (n = 366 participants) consisted of a very brief (1.5 days) psychoeducation and a supervised training in autosuggestion techniques (guided imageries) aimed at enhancing self‐management, decidedness, assertiveness, security and competence in relationships, natural functions of organs and awareness of bodily functions. Bupropion SR (n = 413) was increased to 150 mg twice daily over 1 week and given over a 8‐week period. Measurements  Twelve‐month continuous abstinence confirmed by exhaled carbon monoxide (CO) of 9 parts per million (p.p.m.) or less at all interviews conducted at 3, 6 and 12 months. Findings  Intention‐to‐treat analysis revealed Russell standard 12‐month continuous abstinence rates of 39.1% in the psychotherapy group versus 12.3% in the bupropion SR group (P &lt; 0.001) with a relative benefit (RB) of 3.16 (2.38–4.26). Completer analysis revealed 12‐month continuous abstinence rates of 39.9% in the psychotherapy group versus 22.5% in the bupropion group [P &lt; 0.001; RB 1.78 (1.35–2.34)]. Of note, bupropion abstinence rates were comparable to previous medications/placebo‐only comparisons in geographically different samples. 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Safety Science and Risk</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Applied Social Sciences Index &amp; Abstracts (ASSIA)</collection><jtitle>Addiction (Abingdon, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zernig, Gerald</au><au>Wallner, Reinhild</au><au>Grohs, Ursula</au><au>Kriechbaum, Norbert</au><au>Kemmler, Georg</au><au>Saria, Alois</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A randomized trial of short psychotherapy versus sustained‐release bupropion for smoking cessation</atitle><jtitle>Addiction (Abingdon, England)</jtitle><addtitle>Addiction</addtitle><date>2008-12</date><risdate>2008</risdate><volume>103</volume><issue>12</issue><spage>2024</spage><epage>2031</epage><pages>2024-2031</pages><issn>0965-2140</issn><eissn>1360-0443</eissn><coden>ADICE5</coden><abstract>ABSTRACT Aims  To compare the efficacy and safety of a novel psychological intervention for smoking cessation called psychodynamic model (PDM) training to an active control condition of sustained‐release bupropion. Design  Randomized controlled clinical trial with allocation concealment. Setting  Private psychiatric practice. Participants  Seven hundred and seventy‐nine adult smokers recruited by advertising. Interventions  PDM training (n = 366 participants) consisted of a very brief (1.5 days) psychoeducation and a supervised training in autosuggestion techniques (guided imageries) aimed at enhancing self‐management, decidedness, assertiveness, security and competence in relationships, natural functions of organs and awareness of bodily functions. Bupropion SR (n = 413) was increased to 150 mg twice daily over 1 week and given over a 8‐week period. Measurements  Twelve‐month continuous abstinence confirmed by exhaled carbon monoxide (CO) of 9 parts per million (p.p.m.) or less at all interviews conducted at 3, 6 and 12 months. Findings  Intention‐to‐treat analysis revealed Russell standard 12‐month continuous abstinence rates of 39.1% in the psychotherapy group versus 12.3% in the bupropion SR group (P &lt; 0.001) with a relative benefit (RB) of 3.16 (2.38–4.26). Completer analysis revealed 12‐month continuous abstinence rates of 39.9% in the psychotherapy group versus 22.5% in the bupropion group [P &lt; 0.001; RB 1.78 (1.35–2.34)]. Of note, bupropion abstinence rates were comparable to previous medications/placebo‐only comparisons in geographically different samples. Conclusions  The 1.5‐day psychotherapy exceeded bupropion's efficacy, presenting an alternative to pharmacological smoking cessation aids, especially for smokers who reject drugs to treat their substance dependence, at a similar cost (€350) as the bupropion treatment (€355).</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19469746</pmid><doi>10.1111/j.1360-0443.2008.02348.x</doi><tpages>8</tpages></addata></record>
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source Applied Social Sciences Index & Abstracts (ASSIA); MEDLINE; Wiley Online Library All Journals
subjects Abstinence
Addiction
Adult
Bupropion
Bupropion - adverse effects
Bupropion - therapeutic use
Cessation
Clinical outcomes
Clinical trials
Drug therapy
Efficacy
Female
Group psychotherapy
Humans
Imagery (Psychotherapy)
Male
Methodology
Middle Aged
Nicotine dependence
Patient Compliance
Prescription drugs
psychodynamic model training
Psychotherapy
Psychotherapy, Brief - methods
Public health
Random sampling
randomized controlled trial
Smoking
Smoking - therapy
Smoking cessation
Smoking Cessation - methods
Social problems
sustained‐release bupropion
Tobacco Use Disorder - therapy
Treatment Outcome
title A randomized trial of short psychotherapy versus sustained‐release bupropion for smoking cessation
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