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Smoking Cessation and Reduction in Schizophrenia (SCARIS) with e-cigarette: study protocol for a randomized control trial

BACKGROUND: It is well established in studies across several countries that tobacco smoking is more prevalent among schizophrenic patients than the general population. Electronic cigarettes are becoming increasingly popular with smokers worldwide. To date there are no large randomized trials of elec...

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Autores principales: Caponnetto, Pasquale, Polosa, Riccardo, Auditore, Roberta, Minutolo, Giuseppe, Signorelli, Maria, Maglia, Marilena, Alamo, Angela, Palermo, Filippo, Aguglia, Eugenio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994421/
https://www.ncbi.nlm.nih.gov/pubmed/24655473
http://dx.doi.org/10.1186/1745-6215-15-88
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author Caponnetto, Pasquale
Polosa, Riccardo
Auditore, Roberta
Minutolo, Giuseppe
Signorelli, Maria
Maglia, Marilena
Alamo, Angela
Palermo, Filippo
Aguglia, Eugenio
author_facet Caponnetto, Pasquale
Polosa, Riccardo
Auditore, Roberta
Minutolo, Giuseppe
Signorelli, Maria
Maglia, Marilena
Alamo, Angela
Palermo, Filippo
Aguglia, Eugenio
author_sort Caponnetto, Pasquale
collection PubMed
description BACKGROUND: It is well established in studies across several countries that tobacco smoking is more prevalent among schizophrenic patients than the general population. Electronic cigarettes are becoming increasingly popular with smokers worldwide. To date there are no large randomized trials of electronic cigarettes in schizophrenic smokers. A well-designed trial is needed to compare efficacy and safety of these products in this special population. METHODS/DESIGN: Intervention: We have designed a randomized controlled trial investigating the efficacy and safety of electronic cigarette. The trial will take the form of a prospective 12-month randomized clinical study to evaluate smoking reduction, smoking abstinence and adverse events in schizophrenic smokers not intending to quit. We will also monitor quality of life, neurocognitive functioning and measure participants’ perception and satisfaction of the product. Outcome measures: A ≥50% reduction in the number of cigarettes/day from baseline, will be calculated at each study visit (“reducers”). Abstinence from smoking will be calculated at each study visit (“quitters”). Smokers who leave the study protocol before its completion and will carry out the Early Termination Visit or who will not satisfy the criteria of “reducers” and “quitters” will be defined “non responders”. Statistical analysis: The differences of continuous variables between the three groups will be evaluated with the Kruskal-Wallis Test, followed by the Dunn multiple comparison test. The differences between the three groups for normally distributed data will be evaluated with ANOVA test one way, followed by the Newman-Keuls multiple comparison test. The normality of the distribution will be evaluated with the Kolmogorov-Smirnov test. Any correlations between the variables under evaluation will be assessed by Spearman r correlation. To compare qualitative data will be used the Chi-square test. DISCUSSION: The main strengths of the SCARIS study are the following: it’s the first large RCT on schizophrenic patient, involving in and outpatient, evaluating the effect of a three-arm study design, and a long term of follow-up (52-weeks). The goal is to propose an effective intervention to reduce the risk of tobacco smoking, as a complementary tool to treat tobacco addiction in schizophrenia. TRIAL REGISTRATION: ClinicalTrials.gov, NCT01979796.
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spelling pubmed-39944212014-04-23 Smoking Cessation and Reduction in Schizophrenia (SCARIS) with e-cigarette: study protocol for a randomized control trial Caponnetto, Pasquale Polosa, Riccardo Auditore, Roberta Minutolo, Giuseppe Signorelli, Maria Maglia, Marilena Alamo, Angela Palermo, Filippo Aguglia, Eugenio Trials Study Protocol BACKGROUND: It is well established in studies across several countries that tobacco smoking is more prevalent among schizophrenic patients than the general population. Electronic cigarettes are becoming increasingly popular with smokers worldwide. To date there are no large randomized trials of electronic cigarettes in schizophrenic smokers. A well-designed trial is needed to compare efficacy and safety of these products in this special population. METHODS/DESIGN: Intervention: We have designed a randomized controlled trial investigating the efficacy and safety of electronic cigarette. The trial will take the form of a prospective 12-month randomized clinical study to evaluate smoking reduction, smoking abstinence and adverse events in schizophrenic smokers not intending to quit. We will also monitor quality of life, neurocognitive functioning and measure participants’ perception and satisfaction of the product. Outcome measures: A ≥50% reduction in the number of cigarettes/day from baseline, will be calculated at each study visit (“reducers”). Abstinence from smoking will be calculated at each study visit (“quitters”). Smokers who leave the study protocol before its completion and will carry out the Early Termination Visit or who will not satisfy the criteria of “reducers” and “quitters” will be defined “non responders”. Statistical analysis: The differences of continuous variables between the three groups will be evaluated with the Kruskal-Wallis Test, followed by the Dunn multiple comparison test. The differences between the three groups for normally distributed data will be evaluated with ANOVA test one way, followed by the Newman-Keuls multiple comparison test. The normality of the distribution will be evaluated with the Kolmogorov-Smirnov test. Any correlations between the variables under evaluation will be assessed by Spearman r correlation. To compare qualitative data will be used the Chi-square test. DISCUSSION: The main strengths of the SCARIS study are the following: it’s the first large RCT on schizophrenic patient, involving in and outpatient, evaluating the effect of a three-arm study design, and a long term of follow-up (52-weeks). The goal is to propose an effective intervention to reduce the risk of tobacco smoking, as a complementary tool to treat tobacco addiction in schizophrenia. TRIAL REGISTRATION: ClinicalTrials.gov, NCT01979796. BioMed Central 2014-03-22 /pmc/articles/PMC3994421/ /pubmed/24655473 http://dx.doi.org/10.1186/1745-6215-15-88 Text en Copyright © 2014 Caponnetto et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Caponnetto, Pasquale
Polosa, Riccardo
Auditore, Roberta
Minutolo, Giuseppe
Signorelli, Maria
Maglia, Marilena
Alamo, Angela
Palermo, Filippo
Aguglia, Eugenio
Smoking Cessation and Reduction in Schizophrenia (SCARIS) with e-cigarette: study protocol for a randomized control trial
title Smoking Cessation and Reduction in Schizophrenia (SCARIS) with e-cigarette: study protocol for a randomized control trial
title_full Smoking Cessation and Reduction in Schizophrenia (SCARIS) with e-cigarette: study protocol for a randomized control trial
title_fullStr Smoking Cessation and Reduction in Schizophrenia (SCARIS) with e-cigarette: study protocol for a randomized control trial
title_full_unstemmed Smoking Cessation and Reduction in Schizophrenia (SCARIS) with e-cigarette: study protocol for a randomized control trial
title_short Smoking Cessation and Reduction in Schizophrenia (SCARIS) with e-cigarette: study protocol for a randomized control trial
title_sort smoking cessation and reduction in schizophrenia (scaris) with e-cigarette: study protocol for a randomized control trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994421/
https://www.ncbi.nlm.nih.gov/pubmed/24655473
http://dx.doi.org/10.1186/1745-6215-15-88
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