The aim of the study is to asses the efficacy of the spirometry and a minimal smoking cessation counselling intervention to quit smoking after a year in patients older than 40 years, smokers of more than 10 packs-year and without a chronic obstructive pulmonary disease (COPD) diagnosis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
335
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.
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.
Basque health service
Vitoria-Gasteiz, Alava 45, Spain
The primary measure of results will be the differences in smoking cessation rates between intervention and control groups
In all patients who report smoking withdrawal, smoking cessation will be confirmed by air carbon monoxide concentration.
Time frame: 12 months after been conducted the intervention
Reduce the number of cigarettes among those who continue smoking
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
Time frame: 12 months after been conducted the intervention
Increase smoking abstinence rates in patients with COPD
Evaluate the differences in smoking cessation rates between patients with COPD and those without.
Time frame: 12 months after been conducted the intervention
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