Clinical trial on the efficacy of exhaled carbon monoxide measurement in smoking cessation in primary health care

<p>Abstract</p> <p>Background</p> <p>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....

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Main Authors: 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
Format: Article
Language:English
Published: BMC 2012-07-01
Series:BMC Public Health
Online Access:http://www.biomedcentral.com/1471-2458/12/322
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spelling doaj-8793e54702344079b5a378ef186362082020-11-24T21:25:48ZengBMCBMC Public Health1471-24582012-07-0112132210.1186/1471-2458-12-322Clinical trial on the efficacy of exhaled carbon monoxide measurement in smoking cessation in primary health careRipoll JoanaGirauta HelenaRamos MariaMedina-Bombardó DavidPastor AgnèsAlvarez-Ossorio CristinaGorreto LucíaEsteva MariaGarcía ElenaUréndez AnaBuades AnaTorres Elena<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Methods/Design</p> <p>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.</p> <p>Discussion</p> <p>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.</p> <p>Trial Registration</p> <p>Current Controlled Trials ISRCTN67499921</p> http://www.biomedcentral.com/1471-2458/12/322
collection DOAJ
language English
format Article
sources DOAJ
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
spellingShingle 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
BMC Public Health
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
title 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_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_sort clinical trial on the efficacy of exhaled carbon monoxide measurement in smoking cessation in primary health care
publisher BMC
series BMC Public Health
issn 1471-2458
publishDate 2012-07-01
description <p>Abstract</p> <p>Background</p> <p>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.</p> <p>Methods/Design</p> <p>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.</p> <p>Discussion</p> <p>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.</p> <p>Trial Registration</p> <p>Current Controlled Trials ISRCTN67499921</p>
url http://www.biomedcentral.com/1471-2458/12/322
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