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Forced oscillation as lung function test in pulmonary rehabilitation

The forced oscillation technique in patients with lung diseases subjected to pulmonary rehabilitation.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN31987937
Enrollment
240
Registered
2020-07-23
Start date
2018-10-01
Completion date
Unknown
Last updated
2023-08-28

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

Conditions

Lung diseases (idiopathic interstitial pneumonia, chronic obstructive pulmonary disease and patients after thoracic surgery) Respiratory

Interventions

Lung function tests include: forced oscillation technique, spirometry and bodyplethysmography. All lung function tests will be evaluated before and after completing 3 weeks of pulmonary rehabilitation

Sponsors

Medical University of Silesia
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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) 2. Changes in distance in 6MWT- at baseline and after 3-week rehabilitation (study group)

Secondary

MeasureTime frame
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) 2. Changes in spirometry results (FEV1, FVC, FEV1/FVC, measured by spirometer LungTest 1000)- at beseline and after 3-week rehabilitation (study group) 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)

Countries

Poland

Contacts

Public ContactSabina Kostorz-Nosal
kostorz.sabina@gmail.com+48 662197798

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026