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NCT06477367Completed

Changes in Dyspnea, Activity and Sleep in COPD by Video-Based Breathing Exercises

The Effect of Video-Based Breathing Exercises Taught to COPD Patients on Dyspnea Severity, Activity Level, and Sleep Quality

Source: ClinicalTrials.gov · Last updated 18 Mar 2026

Brief summary (registry, in English)

Chronic Obstructive Pulmonary Disease (COPD) is one of the most prevalent and high-mortality chronic diseases worldwide. Symptoms such as dyspnea, cough, sleep disturbances, fatigue, restricted activity levels, anxiety, and depression develop in COPD patients, negatively affecting their quality of life. Dyspnea, associated with various symptoms in COPD patients such as reduced activity levels and sleep disturbances, is a significant issue. Therefore, effective management of dyspnea will contribute to reducing other important problems associated with COPD. One of the non-pharmacological methods used in managing these symptoms associated with COPD is breathing exercises. Particularly, pursed-lip breathing exercises and diaphragmatic breathing exercises are recommended for symptom management in COPD patients in the literature. The aim of this study was to learn the effects of video-based breathing exercises (pursed lips and diaphragmatic breathing) training given to COPD patients over 18 years of age on the severity of dyspnea experienced by the patient, activity level and sleep quality. The main question it aims to answer is: Does the use of video-based breathing exercises for 30 days result in a decrease in dyspnea severity and an increase in activity level and sleep quality in COPD patients over 18 years of age? Patients will receive video-based breathing exercises lasting approximately 5-7 minutes and will perform the breathing exercises regularly for 30 days, keep a diary and receive follow-up messages (sms). Afterwards, dyspnea severity, activity level and sleep quality will be assessed again, both in the group itself and in comparison with the control group that did not receive this education and follow-up.

Status (registry)
Completed
Study type
Interventional
Enrollment
60 (actual)
First submitted
4 Jun 2024
Start date
20 Jun 2024
Primary completion date
20 Dec 2025
Lead sponsor
Bartın Unıversity
Diseases
COPD
NCT number
NCT06477367

What you commit to

  • Study type: Interventional
  • Participants enrolled: 60
  • From 20 Jun 2024 to the primary completion date, 20 Dec 2025
  • 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.

Other illness

  • Having cognitive impairment
  • Failure to perform respiratory exercises regularly
  • Having non-COPD lung diseases such as tuberculosis

Other

  • Not willing to participate in the study

Who the study is looking for

  • Individuals aged 18 and above
  • Diagnosed with COPD for at least six months
  • Modified Borg Dyspnea Scale score of at least 3
  • Unable to complete the 6-minute walk test
  • Not previously participated in a respiratory exercise program

Age in the registry: 18 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
Bartin University
Coordinator of this site? Confirm its status
BartınTurkey (Türkiye)Unknown status

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