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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02186340
Other study ID # S52852-2
Secondary ID
Status Completed
Phase N/A
First received July 3, 2014
Last updated August 28, 2015
Start date January 2013
Est. completion date July 2015

Study information

Verified date August 2015
Source Katholieke Universiteit Leuven
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The improvement in inspiratory muscle function might result in beneficial changes in breathing pattern during whole body exercise. The hypothesis is the effect of inspiratory muscle training as an adjunct to a pulmonary rehabilitation program improves the breathing pattern during an incremental cycle exercise.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date July 2015
Est. primary completion date July 2015
Accepts healthy volunteers No
Gender Both
Age group 40 Years to 90 Years
Eligibility Inclusion Criteria:

- Clinically stable COPD patients

- maximal inspiratory pressure <100% of the predicted normal value

Exclusion Criteria:

- Major comorbidities preventing successful participation in an 8 week exercise training intervention

Study Design

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


Intervention

Procedure:
Inspiratory muscle training


Locations

Country Name City State
Belgium University Hospital Leuven Leuven

Sponsors (1)

Lead Sponsor Collaborator
Katholieke Universiteit Leuven

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in breathing pattern during an incremental cycle exercise test At comparable levels of ventilation breathing frequency, inspiratory time (Ti), expiratory time (Te), total time of the respiratory cycle (Ttot), inspiratory duty cycle (Ti/Ttot), and inspiratory flow rates will be compared. Baseline and 8 weeks follow-up No
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