Effectiveness of Spirometry as a Motivational Tool to Quit Smoking (ESPIMOAT)
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|ClinicalTrials.gov Identifier: NCT01821885|
Recruitment Status : Completed
First Posted : April 1, 2013
Last Update Posted : January 27, 2015
|Condition or disease||Intervention/treatment||Phase|
|Smoking Cessation COPD||Behavioral: Spirometry and a brief advice to quit smoking Behavioral: Brief advice to quit smoking||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||335 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Effectiveness of Spirometry and the Report of Spirometric Test Results by a Primary Care Physician on Smoking Cessation Rate in Adult Smokers: a Randomized Controlled Trial.|
|Study Start Date :||April 2012|
|Actual Primary Completion Date :||December 2013|
|Actual Study Completion Date :||January 2015|
Experimental: Spirometry and a brief advice to quit smoking
The intervention consists of completing a questionnaire and undergo spirometry with bronchodilator test by a trained nurse. Later, the patients receives a brief advice to quit smoking and a report of the spirometry results by their family doctor.
Behavioral: Spirometry and a brief advice to quit smoking
During a year, recruitment for active smoker patients was done by doctors in primary care medical offices. In the intervention group, after been randomized, one trained nurse completed the questionnaires and did the spirometry with bronchodilator test and set a date with its family doctor who did a minimal smoking cessation counselling intervention and informed the patients about the spirometry results according to established protocol.
Active Comparator: Brief advice to quit smoking
Patients in the control group complete a questionnaire by a nurse and then receive a brief advice to quit smoking by their family doctor.
Behavioral: Brief advice to quit smoking
During a year, recruitment for active smokers patients occurred through doctors in primary care medical offices. After be randomized, in de control group, a nurse complete the questionnaires. Below, patients go to the family doctor who will do a minimal smoking cessation counselling intervention.
- The primary measure of results will be the differences in smoking cessation rates between intervention and control groups [ Time Frame: 12 months after been conducted the intervention ]In all patients who report smoking withdrawal, smoking cessation will be confirmed by air carbon monoxide concentration.
- Reduce the number of cigarettes among those who continue smoking [ Time Frame: 12 months after been conducted the intervention ]One secondary outcome will be to reduce the number of cigarettes. In all patients who continue smoking will be recorded the number of cigarettes smoked per day currently
- Increase smoking abstinence rates in patients with COPD [ Time Frame: 12 months after been conducted the intervention ]Evaluate the differences in smoking cessation rates between patients with COPD and those without.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01821885
|Basque health service|
|Vitoria-Gasteiz, Alava 45, Spain, 1006|
|Principal Investigator:||Mª Isabel Irizar Aramburu||Osakidetza|