Forced oscillation as lung function test in pulmonary rehabilitatio

Not Applicable

Completed

• Conditions: ung diseases (idiopathic interstitial pneumonia, chronic obstructive pulmonary disease and patients after thoracic surgery); Respiratory

• Registration Number: ISRCTN31987937
• Lead Sponsor: Medical University of Silesia

Brief Summary

2022 Results article in https://doi.org/10.3390/jcm11133657 (added 18/08/2023) 2022 Results article in https://doi.org/10.3390/medicina58111551 (added 18/08/2023)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-07-23
• Study Completion: 2021-12-30
• Last Update Posted: 28 August 2023

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 240

Inclusion Criteria

1. Patients with different lung diseases admitted to pulmonary rehabilitation ward
2. Informed consent provided
3. Stable period of illness without infection/exacerbation during the last 4 weeks

Exclusion Criteria

1. Unstable angina
2. Respiratory failure
3. Anemia HgB <10g/dl
4. Bone or central nervous system metastasis
5. Low level of physical activity
6. Severe complications of operative treatment

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Changes in FOT results (R5, R11, R19, X5, X11, X19, delta X, Fres, measured by oscillometer Resmon Pro Full device) - at baseline and after 3-week rehabilitation (study group)/3-week interval (control group)<br>2. Changes in distance in 6MWT- at baseline and after 3-week rehabilitation (study group)

Secondary Outcome Measures

Name	Time	Method
1. Changes in lung plethysmography results (Raw, RV, TLC, measured by MedGraphic Plethysmograph)- at baseline and after 3-week rehabilitation (study group)/ 3-week interval (control group)<br>2. Changes in spirometry results (FEV1, FVC, FEV1/FVC, measured by spirometer LungTest 1000)- at beseline and after 3-week rehabilitation (study group)<br>3. Changes in grip strength measured with a Meden-Inmed Baseline hydraulic hand dynamometer of left and right hand- at baseline and after 3-week rehabilitation (study group)/ 3-week interval (control group)