- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07228910
Respiratory and Anxiety Status of Music Students
Relationship Between Dysfunctional Breathing, Respiratory Patterns, and Performance Anxiety in Music Students
Study Overview
Status
Conditions
Detailed Description
Dysfunctional breathing (DB) represents a spectrum of maladaptive respiratory patterns that cannot be explained by an underlying medical condition. It may involve biomechanical, biochemical, or psychophysiological components, including abnormal breathing mechanics, altered carbon dioxide regulation, and stress-related breathing irregularities. Previous research has suggested that DB can exacerbate symptoms in conditions such as asthma, migraine, orofacial pain, and temporomandibular disorders.
Music performance anxiety (MPA), a common issue among music students and professional musicians, manifests through both psychological and physiological symptoms. Among these, respiratory complaints such as dyspnea, breath-holding, or hyperventilation are frequently reported. Despite this, the potential overlap between DB and MPA has not been adequately investigated.
This cross-sectional study will assess 233 music students using validated self-report questionnaires to evaluate dysfunctional breathing patterns and levels of music performance anxiety. The study seeks to identify the prevalence of DB in this population and to explore possible associations between breathing dysfunction and anxiety related to musical performance. Findings may contribute to a better understanding of respiratory-related mechanisms underlying performance anxiety and inform preventive or therapeutic strategies for musicians.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Erhan KIZMAZ, PhD
- Phone Number: +90 541 896 66 76
- Email: erhankizmaz@hotmail.com
Study Contact Backup
- Name: Ayşenur YILMAZ, PhD
- Phone Number: +90 543 283 38 19
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Being a student of music department
- Playing an instrument for at least 1 year
- Volunteer
Exclusion Criteria:
- Having any respiratory disease (Asthma , COPD etc.)
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dysfunctional breathing
Time Frame: 15 minutes drom enrollment
|
An umbrella term used to describe a harmful adaptation in breathing that cannot be explained by a medical diagnosis such as asthma.
The Self Evaluation of Breathing Questionnaire (SEBQ) will be used to assess dysfunctional breathing.
The SEBQ is a scale developed to identify the nature of unexplained symptoms commonly reported by individuals with dysfunctional breathing.
It was designed to capture all domains of respiratory symptoms, regardless of whether the individual has hyperventilation syndrome.
The questionnaire consists of 25 items rated on a 4-point Likert scale ranging from 0 to 3 (0 = never / not true at all, 1 = occasionally / somewhat true, 2 = often / mostly true, 3 = very often / very true).
Higher scores indicate a greater degree of breathing dysfunction
|
15 minutes drom enrollment
|
|
Breathing pattern
Time Frame: 15-30 minutes from enrollment
|
The Breathing Pattern Assessment Tool (BPAT) will be used to assess breathing pattern.
The BPAT is a clinician-administered assessment developed to evaluate breathing pattern disorders.
Its validity has been confirmed for screening breathing pattern dysfunction in patients with asthma or unexplained dyspnea.
During the assessment, the participant is seated in a chair with back support while the clinician evaluates seven components of the breathing pattern: abdominal and chest wall movements, inspiratory and expiratory sounds, sighing or other signs of air hunger, nasal and oral breathing, breathing rate, and rhythmicity of the pattern.
Each item is scored from 0 to 2, yielding a total score ranging from 0 to 14. Higher scores indicate a greater likelihood of breathing pattern disorder.
A total score of ≥4 is considered a positive screen, with a sensitivity of 92% and specificity of 75%.
|
15-30 minutes from enrollment
|
|
Music performance anxiety
Time Frame: 30-45 minutes from enrollment
|
The Kenny Music Performance Anxiety Inventory (K-MPAI) will be used to assess the level and underlying causes of music performance anxiety.
T. The inventory consists of 25 items grouped under five subscales: (1) Negative Performance Perception (items 5, 6, 10, 11, 13, 14, 15, 16, 18, 19, 22, 23, 24, 25), (2) Psychological Vulnerability (items 1, 2, 3, 7, 8, 9, 12, 21), (3) Somatic Anxiety (item 4), (4) Personal Control (item 17), and (5) Physiological Vulnerability (item 20).
Each item is rated on a 7-point Likert scale ranging from 0 (strongly disagree) to 6 (strongly agree), yielding a total score between 0 and 150.
Scores of 105 and above indicate high music performance anxiety, whereas scores of 45 and below indicate low anxiety levels.
|
30-45 minutes from enrollment
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Erhan KIZMAZ, PhD, University of Gaziantep
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Music
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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