Changes of spirometric data in the 6-MWT due to an outpatient PR in COPD patients: a controlled trial

Not Applicable

Recruiting

• Conditions: chronic obstructive pulmonary disease; J44.9; Chronic obstructive pulmonary disease, unspecified

• Registration Number: DRKS00009759
• Lead Sponsor: St. Remigius Krankenhaus

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2015-12-10
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

COPD stage II-IV in a stable condition, maximum 2 weeks to the last exacerbation, written consent, ability to walk

Exclusion Criteria

Oxygen dependency, lost mobility, diagnosis making it impossible to complete the rehab program, no written consent

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
spirmetric mesasured inspiratory capacity, before and three weeks later, after the rehabilitation.

Secondary Outcome Measures

Name	Time	Method
Maximum Minute volumne, breathing frequency, Walking distance in the 6 Minute Walking test, Oxygensaturation measured during the 6-MWT, usability questionere (7 Points lickert scale); before the rehabilitation program and three weeks later, at its end.