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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01173328
Other study ID # CEP/HUCFF/UFRJ 187/07
Secondary ID
Status Completed
Phase N/A
First received July 19, 2010
Last updated July 30, 2010
Start date March 2007
Est. completion date October 2009

Study information

Verified date August 2008
Source Universidade Federal do Rio de Janeiro
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

Pursed-lip breathing (PLB) has been advocated to reduce respiratory rate and improve oxygen saturation in patients with chronic obstructive pulmonary disease (COPD) at rest. Although PLB is a strategy that potentially reduces expiratory flow limitation, there are only few studies addressing its effects on exercise.

This study aimed to assess the ability of PLB to change the breathing pattern, degree of dynamic hyperinflation (DH) and arterial oxygenation in COPD patients during exercise. Exercise tolerance was evaluated by endurance time and respiratory mechanics was evaluated by forced oscillation technique.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date October 2009
Est. primary completion date October 2009
Accepts healthy volunteers No
Gender Both
Age group 40 Years and older
Eligibility Inclusion Criteria:

- Clinical diagnosis of chronic obstructive pulmonary disease (COPD)

- Regular treatment at Clementino Fraga Filho University Hospital (UFRJ)

Exclusion Criteria:

- Exacerbation in the preceding 4 weeks

- SpO2<85% at peak exercise

- Other diseases that may contribute to dyspnea and exercise intolerance

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Pursed-lip breathing
Pursed-lip breathing involves a nasal inspiration followed by expiratory blowing against partially closed lips, avoiding forceful exhalation.
Normal Breathing


Locations

Country Name City State
Brazil Clementino Fraga Filho University Hospital Rio de Janeiro

Sponsors (1)

Lead Sponsor Collaborator
Universidade Federal do Rio de Janeiro

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Endurance time within the first 01 hour No
Secondary inspiratory capacity within the first 01 hour No
Secondary oxygen saturation within the first 01 hour No
Secondary dyspnea within the first 01 hour No
Secondary forced oscillation variables within the first 01 hour No
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