- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07527780
Prevalence of Misophonia and Hyperacusis Among Teachers
Could Hyperacusis and Misophonia Be Causes of Occupational Stress Among Teachers?
Study Overview
Status
Conditions
Detailed Description
Misophonia is characterized by reduced tolerance to specific everyday sounds, such as chewing, breathing, or tapping, and may also be triggered by environmental noises from engines, animals, or mechanical sources. Hyperacusis, similarly, involves an increased sensitivity to ordinary sounds and discomfort in response to noises that are typically well tolerated by individuals with normal hearing.
Teachers represent a population potentially at higher risk for these conditions due to daily exposure to varying classroom sounds and occupational noise. Understanding how common these auditory sensitivities may be in this group will help clarify their potential impact on teachers' well-being and occupational functioning. Therefore this study will investigate the prevalence of misophonia and hyperacusis among actively working teachers.
The study will include teachers aged 22-45 without diagnosed hearing loss, chronic illness, or psychological disorders. Participants will complete a sociodemographic form assessing health and work-related characteristics, followed by validated measures: the Khalfa Hyperacusis Scale for hyperacusis and the AMISOS-R for misophonia. Data obtained from these assessments are expected to contribute to a clearer understanding of sensory challenges in educational environments and support future strategies to improve teachers' occupational health.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Handan Turan Dizdar, PhD
- Phone Number: +905055970627
- Email: handan.dizdar@omu.edu.tr
Study Contact Backup
- Name: Buket Sena Çelik
- Phone Number: +905551919801
- Email: bukettscelik@gmail.com
Study Locations
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Samsun, Turkey (Türkiye), 55000
- Recruiting
- Ondokuz May Highschool
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Contact:
- Handan Turan Dizdar, Teacher
- Phone Number: +9005055970627
- Email: handan.dizdar@omu.edu.tr
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Çorum, Turkey (Türkiye), 19000
- Recruiting
- Atatürk Anatolia Highschool
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Contact:
- Buket Sena Çelik, Student
- Phone Number: +9005551919801
- Email: bukettscelik@gmail.com
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Teachers actively working in preschool, elementary, middle, or high schools.
- Age between 22 and 45 years.
- Willingness to participate and provide informed consent.
- No diagnosed hearing loss.
- No chronic illnesses.
- No diagnosed psychological or psychiatric disorders.
Exclusion Criteria:
- Individuals with hearing loss.
- Individuals with chronic illnesses.
- Individuals with serious psychological or psychiatric diagnoses.
- Individuals who are not actively teaching.
- Participants unwilling to provide informed consent.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevalence of Misophonia Among Teachers
Time Frame: Baseline (single assessment)
|
The proportion of teachers identified as having misophonia based on predefined classification criteria using the Amsterdam Misophonia Scale-Revised (AMISOS-R).
The AMISOS-R total score ranges from 0 to 40, with higher scores indicating greater misophonia severity.
Misophonia severity is classified as none, mild, moderate, or severe according to established cutoff values.
|
Baseline (single assessment)
|
|
Prevalence of Hyperacusis Among Teachers
Time Frame: Baseline (single assessment)
|
The proportion of teachers identified as having hyperacusis based on predefined classification criteria using the Khalfa Hyperacusis Scale.
The scale consists of 14 items scored on a 4-point Likert scale, with a total possible score of 0-42.
Participants are classified as having "no hyperacusis" (≤15), "suspected hyperacusis" (16-28), or "hyperacusis" (≥29).
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Baseline (single assessment)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Severity Levels of Misophonia Symptoms
Time Frame: Baseline (single assessment)
|
Distribution of teachers according to misophonia severity levels (none, mild, moderate, severe) based on the AMISOS-R.
The AMISOS-R total score ranges from 0 to 40, with higher scores indicating more severe misophonia symptoms.
|
Baseline (single assessment)
|
|
Severity Levels of Hyperacusis Symptoms
Time Frame: Baseline (single assessment)
|
Distribution of teachers according to hyperacusis severity levels ("no hyperacusis," "suspected hyperacusis," "hyperacusis") based on the Khalfa Hyperacusis Scale.
The scale has a total score range of 0-42, with higher scores indicating more severe hyperacusis symptoms.
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Baseline (single assessment)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Association of Misophonia and Hyperacusis with Occupational Stress
Time Frame: Baseline (single assessment)
|
Distribution of misophonia (AMISOS-R) and hyperacusis (Khalfa Hyperacusis Scale) severity levels according to teachers' self-reported occupational stress.
Misophonia and hyperacusis severity will be classified using the same criteria as above.
This outcome will examine the potential relationship between auditory sensitivity and work-related stress.
|
Baseline (single assessment)
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Handan Turan Dizdar, PhD, Ondokuz Mayıs University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- 2024/580
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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