The aim of this study is to evaluate the usefulness of the chronic obstructive pulmonary disease-population questionnaire (COPD-PS) and the COPD-6 device in the early detection of chronic obstructive pulmonary disease in smoker patients .
- Study Type: Observational
- Study Design
- Time Perspective: Other
- Study Primary Completion Date: March 15, 2020
- Other: Chronic obstructive pulmonary disease screening
- To verify the tobacco withdrawal, the patients will make a cooximetry. For the detection of a possible obstructive pattern a measurement of the ventilatory capacity will be make using the COPD-6 device and for the confirmation of COPD diagnosis and the assesment of the airflow obstruction severity a spirometry will be make. The patients will also complete the COPD-PS questionnaire.
Arms, Groups and Cohorts
- Tobacco detoxication cohort
- Patients appointed in a tobacco detoxication consultation
Clinical Trial Outcome Measures
- Demonstrate the usefulness of the COPD-PS questionnaire and the COPD-6 device in the COPD early detection.
- Time Frame: Up to 12 months after the first consultation
- Suitability of the COPD-PS questionnaire (simple tool for the detection of chronic airflow obstruction made up of breath shortness and productive cough as COPD clinic items, activity limitation due to respiratory problems as the item related to the disease impact, history as a smoker and participant´s age) and the COPD-6 device (tool that measures the ventilatory capacity using the quotient between the forced exhaled volume at 6 seconds (FEV6) and the forced exhaled volume in the first second of the maneuver (FEV1)) in the early detection of COPD.
Participating in This Clinical Trial
- > 35 years old
- Accumulative tobacco rate > 10 paq-year that go to the tobacco detoxication consultation
- Unable to fulfill the questionnarie
- Unable to adequately perform the COPD-6 or forced spirometry maneuvers included in the study.
- Reject to participate and sign the informed consent.
Gender Eligibility: All
Minimum Age: 35 Years
Maximum Age: N/A
Are Healthy Volunteers Accepted: No
- Lead Sponsor
- Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
- Provider of Information About this Clinical Study
- Overall Official(s)
- Agustín Valido Morales, Principal Investigator, Hospital Universitario Virgen Macarena
- Overall Contact(s)
- Agustín Valido Morales, 955 00 80 00, firstname.lastname@example.org
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