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Effectiveness of Two Methods for Quality Control in Primary Care Spirometry

Effectiveness of Two Methods for Quality Control in Primary Care Spirometry

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02005952
Enrollment
3000
Registered
2013-12-09
Start date
2010-02-28
Completion date
2012-06-30
Last updated
2013-12-09

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

Conditions

Spirometry

Brief summary

Still not well resolved access, execution and interpretation of spirometry in primary care medicine. This seriously affects the quality of care of chronic respiratory diseases. OBJECTIVE: To compare the effectiveness of two methods for quality control in performing spirometry in primary care teams (EAP) participating in the Healthcare Process Chronic Obstructive Pulmonary Disease (COPD ) (multidisciplinary program between primary care medicine and hospital for improved care COPD). METHODS: Randomized controlled trial of clusters of EAP participants ( n = 17 ). The quality control of spirometry in each EAP randomize into three branches: 1. Supervision from the pulmonary function laboratory of the Hospital ; computer. 2. Program incorporated into automated spirometer. 3. Spirometric usual practice (control group without any support on the quality ). Spirometry EAP participants include year follow-up study . All sites use the same model spirometer and have received the same previous training . In a 2nd phase results implementing the most effective method shown in the 1st phase was studied. EXPECTED RESULTS : The method for quality control more effective to obtain and maintain the quality spirometry. POTENTIAL IMPACT EXPECTED : performing spirometry quality in the EAP , improve early detection (secondary prevention ) , the diagnosis of the severity and developmental control of COPD.

Interventions

None listed

Sponsors

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients seen in the participating primary care, requiring spirometry for both the diagnosis and control of any disease will be included.

Exclusion criteria

* Patients under 15 years

Design outcomes

Primary

MeasureTime frame
Effectiveness of two methods for quality control in primary care spirometryBasal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026