Menu
Not yet recruiting NCT06943027

Investigation of the Relationship Between Dysfunctional Breathing and Physical Fitness Parameters in Healty Adults

Observational Dysfunctional Breathing

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Dysfunctional Breathing. Basic parameters: 18 years — 35 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Investigation of the Relationship Between Dysfunctional Breathing and Physical Fitness Parameters in Healthy Adults

Overview

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.

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.

Primary outcome measures

  • Nijmegen Questionnaire Score [Time frame: Baseline]
Secondary outcome measures (2)
  • ALPHA-FIT Test Battery Performance [Time frame: Baseline]
  • Maximum Inspiratory Pressure (MIP) and Maximum Expiratory Pressure (MEP) [Time frame: Baseline]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-only

Study locations

Center list to be confirmed — check the primary protocol.

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. PMID 21522210
  • 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

Identifiers

NCT: NCT06943027 · ISTU-DS-2025-ET · 2209-A

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗