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

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

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

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

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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