- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06943027
Investigation of the Relationship Between Dysfunctional Breathing and Physical Fitness Parameters in Healty Adults (DISFIT)
April 17, 2025 updated by: Elif Tunç
Investigation of the Relationship Between Dysfunctional Breathing and Physical Fitness Parameters in Healthy Adults
This observational study aims to investigate the relationship between dysfunctional breathing and physical fitness parameters in healthy adults aged 18-35.
Participants will be evaluated using the Nijmegen Questionnaire to assess dysfunctional breathing symptoms, and their physical fitness will be measured using the ALPHA-FIT Test Battery.
Respiratory muscle strength and pulmonary function will also be assessed.
The findings may help healthcare professionals better understand dysfunctional breathing and develop targeted treatment programs.
Study Overview
Status
Not yet recruiting
Conditions
Detailed Description
Dysfunctional breathing (DB) is characterized by chronic alterations in the respiratory cycle, often leading to symptoms such as dyspnea, chest tightness, and hyperventilation.
Despite its prevalence, DB is frequently underdiagnosed and mismanaged due to limited awareness among healthcare professionals.
This cross-sectional study aims to evaluate the relationship between DB symptoms and physical fitness in healthy young adults.
A total of 38 participants diagnosed with DB will be assessed at Istinye University using the Nijmegen Questionnaire, ALPHA-FIT Test Battery, spirometry, and measurements of maximum inspiratory (MIP) and expiratory (MEP) mouth pressures.
Data on sociodemographic characteristics will also be collected.
The results of this study are expected to support clinicians in the accurate identification of DB and provide insight for the development of personalized rehabilitation strategies that improve physical fitness and respiratory health.
Study Type
Observational
Enrollment (Estimated)
38
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Elif Tunç, MSc, PhD(c)
- Phone Number: +90 535 076 31 39
- Email: fzteliftunc@gmail.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
The study population will consist of healthy adults aged 18-35 years with no known systemic, neurological, or musculoskeletal conditions.
Participants will be screened using the Nijmegen Questionnaire to identify symptoms of dysfunctional breathing.
Description
Inclusion Criteria:
- Aged between 18-35 years
- Healthy individuals with no known systemic, neurological, or musculoskeletal disorders
- Nijmegen Questionnaire score >23 (indicative of dysfunctional breathing)
- Voluntary participation with informed consent
Exclusion Criteria:
- Diagnosed with respiratory, cardiovascular, or metabolic disease
- Currently receiving physiotherapy or pulmonary rehabilitation
- Regular use of medication affecting breathing or exercise capacity
- Pregnancy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Nijmegen Questionnaire Score
Time Frame: Baseline
|
Assessment of dysfunctional breathing symptoms using the Nijmegen Questionnaire.
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
ALPHA-FIT Test Battery Performance
Time Frame: Baseline
|
Evaluation of physical fitness components such as strength, flexibility, balance, and endurance in participants.
|
Baseline
|
|
Maximum Inspiratory Pressure (MIP) and Maximum Expiratory Pressure (MEP)
Time Frame: Baseline
|
Measurement of respiratory muscle strength using a mouth pressure device to evaluate inspiratory and expiratory capacities.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Kiesel K, Plisky PJ, Voight ML. Can Serious Injury in Professional Football be Predicted by a Preseason Functional Movement Screen? N Am J Sports Phys Ther. 2007 Aug;2(3):147-58.
- Courtney R. The functions of breathing and its dysfunctions and their relationship to breathing therapy. Int J Osteopath Med. 2009;12(3):78-85. doi:10.1016/j.ijosm.2009.04.002
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
May 15, 2025
Primary Completion (Estimated)
June 15, 2025
Study Completion (Estimated)
July 15, 2025
Study Registration Dates
First Submitted
April 17, 2025
First Submitted That Met QC Criteria
April 17, 2025
First Posted (Actual)
April 24, 2025
Study Record Updates
Last Update Posted (Actual)
April 24, 2025
Last Update Submitted That Met QC Criteria
April 17, 2025
Last Verified
April 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ISTU-DS-2025-ET
- 2209-A (Other Grant/Funding Number: The Scientific and Technological Research Council of Turkey (TUBITAK))
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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