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Effectiveness of Spirometry as a Motivational Tool to Quit Smoking

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.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01821885
Acronym
ESPIMOAT
Enrollment
335
Registered
2013-04-01
Start date
2012-04-30
Completion date
2015-01-31
Last updated
2015-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COPD, Smoking Cessation

Keywords

Spirometry, screening, smoking cessation, tobacco, COPD

Brief summary

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.

Interventions

BEHAVIORALSpirometry 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.

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.

Sponsors

Basque Health Service
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

\- Active smokers over 40 years and more than 10 pack-years

Exclusion criteria

* Previous diagnosis of respiratory disease (asthma, COPD, interstitial lung disease) that cause alteration of spirometric pattern. * Patients with limitations in performing spirometry * Age greater than 80 years * Institutionalized patients * Patients with a life expectancy less than 1 year * Spirometry in the past 2 years

Design outcomes

Primary

MeasureTime frameDescription
The primary measure of results will be the differences in smoking cessation rates between intervention and control groups12 months after been conducted the interventionIn all patients who report smoking withdrawal, smoking cessation will be confirmed by air carbon monoxide concentration.

Secondary

MeasureTime frameDescription
Reduce the number of cigarettes among those who continue smoking12 months after been conducted the interventionOne 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 COPD12 months after been conducted the interventionEvaluate the differences in smoking cessation rates between patients with COPD and those without.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 22, 2026