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NCT06274957Completed

The Effect of Airway and Chest Wall Oscillation on Respiratory Functions in COPD Patients in Acute Exacerbation

The Effect of Airway Oscillation and Chest Wall Oscillation on Respiratory Functions and Sleep Quality in COPD Patients in Acute Exacerbation Period and Technical Inspection of Devices

Source: ClinicalTrials.gov · Last updated 29 Apr 2026

Brief summary (registry, in English)

Chronic obstructive pulmonary disease (COPD); It is a common, treatable and preventable disease characterized by progressive and irreversible airflow limitation and has systemic effects with respiratory system involvement. Increased respiratory workload, decreased work .

Status (registry)
Completed
Study type
Interventional
Enrollment
33 (actual)
First submitted
2 Feb 2024
Start date
1 May 2024
Primary completion date
10 Jun 2024
Lead sponsor
Saglik Bilimleri Universitesi
Diseases
COPD
NCT number
NCT06274957

What you commit to

  • Study type: Interventional
  • Participants enrolled: 33
  • From 1 May 2024 to the primary completion date, 10 Jun 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Having undergone surgery on the upper extremities, lower extremities, neck, and back.

Other illness

  • Systemic fungal infections.
  • Having cognitive impairment affecting the decision to participate in the study, such as confusion, orientation disorder, or dementia.
  • Patients with lung cancer or metastasis in the lungs.
  • Diagnosis of conditions provoking shortness of breath other than COPD exacerbation, such as pneumonia, pneumothorax, heart failure, and pulmonary embolism.
  • Presence of a new-onset rhythm disorder or ischemic changes requiring intervention on the EKG, excluding sinus tachycardia and multifocal atrial tachycardia.
  • Chronic kidney failure requiring hemodialysis.
  • Patients with conditions causing weakness in the lower extremities, such as arthritis, neurological disease, deep vein thrombosis, peripheral artery disease, muscle weakness, fractures, osteoarthritis, etc.

Other

  • Having a hospital admission with a diagnosis of asthma attack in the last 5 years.
  • Monitoring suspicious focal points for pneumonia on lung radiology.
  • Hospitalization due to reasons other than exacerbation despite having a diagnosis of COPD.
  • Presence of pulmonary fibrosis or suspicious findings of fibrosis on radiology.
  • Having ankylosing spondylitis with a Cobb angle of 10 degrees or more in the radiographic evaluation of the vertebral column.

Who the study is looking for

  • Being classified as GOLD stage 3 or 4 based on spirometric evaluation in the medical history.
  • Having a hospital admission within the specified time frame, evaluated by a pulmonary specialist, and admitted to the pulmonary diseases service with a diagnosis of COPD exacerbation.
  • Being 40 years of age or older.
  • Voluntarily agreeing to participate in the study.

Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Health Sciences
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.