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Clinical trial on the efficacy of exhaled carbon monoxide measurement in smoking cessation in primary health care
BACKGROUND: Smoking cessation is beneficial for our health at any point in life, both in healthy people and in people already suffering from a smoking-related disease. Any help to quit smoking can produce considerable benefits for Public Health. The purpose of the present study is to evaluate the ef...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3390274/ https://www.ncbi.nlm.nih.gov/pubmed/22551017 http://dx.doi.org/10.1186/1471-2458-12-322 |
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author | Ripoll, Joana Girauta, Helena Ramos, Maria Medina-Bombardó, David Pastor, Agnès Alvarez-Ossorio, Cristina Gorreto, Lucía Esteva, Maria García, Elena Uréndez, Ana Buades, Ana Torres, Elena |
author_facet | Ripoll, Joana Girauta, Helena Ramos, Maria Medina-Bombardó, David Pastor, Agnès Alvarez-Ossorio, Cristina Gorreto, Lucía Esteva, Maria García, Elena Uréndez, Ana Buades, Ana Torres, Elena |
author_sort | Ripoll, Joana |
collection | PubMed |
description | BACKGROUND: Smoking cessation is beneficial for our health at any point in life, both in healthy people and in people already suffering from a smoking-related disease. Any help to quit smoking can produce considerable benefits for Public Health. The purpose of the present study is to evaluate the efficacy of the CO-oximetry technique together with brief advice in smoking cessation, in terms of reduction of the number of cigarettes or in the variation of the motivation to quit smoking at month 12 compared with brief advice alone. METHODS/DESIGN: Randomised, parallel, single-blind clinical trial in a primary health care setting in Majorca (Spain). Smokers in contemplation or pre-contemplation phase will be included in the study. Exclusion criteria: Smokers in preparation phase, subjects with a terminal illness or whose health status does not allow them to understand the study or complete the informed consent, and pregnant or breastfeeding women. The subjects will be randomly assigned to the control group (CG) or the intervention group (IG). The CG will receive brief advice, and the IG will receive brief advice together with a measurement of exhaled CO. There will be follow-up evaluations at 6 and 12 months after inclusion. 471 subjects will be needed per group in order to detect a difference between groups ≥ 5%. Primary outcome: sustained smoking cessation (at 6 and 12 months) confirmed by urine cotinine test. Secondary outcomes: point smoking cessation at 6 and 12 months both confirmed by urine cotinine analysis and self-reported, reduction in cigarette consumption, and variation in phase of smoking cessation. DISCUSSION: CO-oximetry is an inexpensive, non-invasive, fast technique that requires little technical training; making it a technique for risk assessment in smokers that can be easily applied in primary care and, if proven effective, could serve as a reinforcement aid in smoking cessation intervention activities. TRIAL REGISTRATION: Current Controlled Trials ISRCTN67499921 |
format | Online Article Text |
id | pubmed-3390274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33902742012-07-06 Clinical trial on the efficacy of exhaled carbon monoxide measurement in smoking cessation in primary health care Ripoll, Joana Girauta, Helena Ramos, Maria Medina-Bombardó, David Pastor, Agnès Alvarez-Ossorio, Cristina Gorreto, Lucía Esteva, Maria García, Elena Uréndez, Ana Buades, Ana Torres, Elena BMC Public Health Study Protocol BACKGROUND: Smoking cessation is beneficial for our health at any point in life, both in healthy people and in people already suffering from a smoking-related disease. Any help to quit smoking can produce considerable benefits for Public Health. The purpose of the present study is to evaluate the efficacy of the CO-oximetry technique together with brief advice in smoking cessation, in terms of reduction of the number of cigarettes or in the variation of the motivation to quit smoking at month 12 compared with brief advice alone. METHODS/DESIGN: Randomised, parallel, single-blind clinical trial in a primary health care setting in Majorca (Spain). Smokers in contemplation or pre-contemplation phase will be included in the study. Exclusion criteria: Smokers in preparation phase, subjects with a terminal illness or whose health status does not allow them to understand the study or complete the informed consent, and pregnant or breastfeeding women. The subjects will be randomly assigned to the control group (CG) or the intervention group (IG). The CG will receive brief advice, and the IG will receive brief advice together with a measurement of exhaled CO. There will be follow-up evaluations at 6 and 12 months after inclusion. 471 subjects will be needed per group in order to detect a difference between groups ≥ 5%. Primary outcome: sustained smoking cessation (at 6 and 12 months) confirmed by urine cotinine test. Secondary outcomes: point smoking cessation at 6 and 12 months both confirmed by urine cotinine analysis and self-reported, reduction in cigarette consumption, and variation in phase of smoking cessation. DISCUSSION: CO-oximetry is an inexpensive, non-invasive, fast technique that requires little technical training; making it a technique for risk assessment in smokers that can be easily applied in primary care and, if proven effective, could serve as a reinforcement aid in smoking cessation intervention activities. TRIAL REGISTRATION: Current Controlled Trials ISRCTN67499921 BioMed Central 2012-07-04 /pmc/articles/PMC3390274/ /pubmed/22551017 http://dx.doi.org/10.1186/1471-2458-12-322 Text en Copyright ©2012 Ripoll 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 cited. |
spellingShingle | Study Protocol Ripoll, Joana Girauta, Helena Ramos, Maria Medina-Bombardó, David Pastor, Agnès Alvarez-Ossorio, Cristina Gorreto, Lucía Esteva, Maria García, Elena Uréndez, Ana Buades, Ana Torres, Elena Clinical trial on the efficacy of exhaled carbon monoxide measurement in smoking cessation in primary health care |
title | Clinical trial on the efficacy of exhaled carbon monoxide measurement in smoking cessation in primary health care |
title_full | Clinical trial on the efficacy of exhaled carbon monoxide measurement in smoking cessation in primary health care |
title_fullStr | Clinical trial on the efficacy of exhaled carbon monoxide measurement in smoking cessation in primary health care |
title_full_unstemmed | Clinical trial on the efficacy of exhaled carbon monoxide measurement in smoking cessation in primary health care |
title_short | Clinical trial on the efficacy of exhaled carbon monoxide measurement in smoking cessation in primary health care |
title_sort | clinical trial on the efficacy of exhaled carbon monoxide measurement in smoking cessation in primary health care |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3390274/ https://www.ncbi.nlm.nih.gov/pubmed/22551017 http://dx.doi.org/10.1186/1471-2458-12-322 |
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