- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07353242
The Effect of Buteyko Breathing Technique on Asthma Patients (Buteyko Breath)
"THE EFFECT OF BUTEIKO RESPIRATORY TECHNIQUE APPLIED TO ASTHMA PATIENTS ON FATIGUE, EXERCISE CAPACITY, AND ASTHMA CONTROL"
This study was designed as a pre-test-post-test randomized controlled experimental trial to determine the effects of buteyko breathing technique application on fatigue, exercise capacity, and asthma control in asthma patients.The study, planned as a randomized controlled experimental study, included a total of 90 participants.
The sample consisted of asthma patients who applied to the Chest Diseases outpatient clinic of Gaziantep University Application and Research Hospital, had been diagnosed with asthma within the last 6 months, did not have heart failure, did not have communication or perception problems, did not have walking disabilities, and were between 18-59 years old.Following random assignment, participants were divided into two groups of 45 participants each. The groups were: 1) Buteyko 2) Control
Study Overview
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Şehitkamil
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Gaziantep, Şehitkamil, Turkey (Türkiye), 27000
- Gaziantep University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Having been diagnosed with asthma within the last 6 months
- Absence of heart failure
- Absence of communication and perception problems
- Absence of walking impairment Being between 18-59 years of age-
Exclusion Criteria:
- -Child patients
- Those diagnosed with heart failure
- Conditions that impede walking
- Those with communication and perception problems
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Buteyko group
In the Buteyko group, in addition to standard treatment, participants received training and practice in the Buteyko Breathing Technique aimed at reducing hyperventilation.
The intervention was delivered as face-to-face group training by an internationally certified instructor and included a 30-minute theoretical session followed by practical exercises.
These consisted of controlled breath-holding with reduced breathing performed while seated and walking, as well as a relaxation phase focusing on nasal breathing accompanied by calming music.
Mouth taping was used throughout the exercises to promote nasal breathing.
Participants were instructed to perform the exercises at home three times daily, with weekly outpatient follow-up visits, and were monitored for a total of six weeks.
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This intervention is distinguished by its standardized delivery by an internationally certified Buteyko practitioner and its integration of key Buteyko components, including reduced breathing, controlled breath-holding, nasal breathing with mouth taping, and relaxation.
It incorporates both seated and walking-based exercises, uses objective measures such as Control Pause and step counting, and includes a structured home-based practice with weekly follow-up over six weeks.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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The Asthma Control Test (ACT)
Time Frame: 6 weeks
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The Asthma Control Test (ACT) is a practical, patient-completed scale consisting of five questions, scored between 5 and 25 points, that assesses the level of asthma control; higher scores indicate better control.
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6 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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The Chronic Obstructive Pulmonary Disease and Asthma Fatigue Scale (COPD)
Time Frame: 6 weeks
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The Chronic Obstructive Pulmonary Disease and Asthma Fatigue Scale (COPD) is a 12-item, five-point Likert-type scale that assesses fatigue in individuals with asthma and COPD; higher scores indicate higher fatigue levels.
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6 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Adile Neşe, University of Gaziantep
Publications and helpful links
General Publications
- Aluwı, M. F., Azmı, N. A., Zanudın, A., & Ramlı, A. (2025). Effect of Buteyko Breathing Technique and Inspiratory Muscle Training on Acute Exacerbation of Bronchial Asthma in a 55-Year-Old Patient: A Case Report. Buletin SK, 9(1), 55-60
- AbdElmawla Elsaid, R. A., Zahran, W. E. K., & Elsaid Hafez, D. M. (2023). Comparison of the Effects of Buteyko and Diaphragmatic Breathing Technique on Improving Pulmonary Functions and Asthma Control among Patients with Bronchial Asthma. Egyptian Journal of Nursing and Health Sciences, 4(3), 58-76.
- Abd Allah Abd El Hafeez, N., Khalil Hafez, M., Mohamed Ahmed, Z., Metwally El-Sayed, M., Abdelwahab Khedr, M., & Fathy Ahmed Dawood, R. (2025). Evaluating the Effect of Buteyko Breathing Technique in Enhancing Asthma Control and Life Quality Among Asthma Patients: A Nursing-Led Quasi-Experimental Study. Egyptian Journal of Health Care, 16(1), 831-852.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Buteyko Breathing Technique
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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