- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07469033
Prevalence of Misophonia in Turkish High School Students
Prevalence of Misophonia in Turkish High School Students: A Sample From Kayseri and Samsun
Study Overview
Status
Conditions
Detailed Description
Misophonia is a condition characterized by decreased tolerance and heightened sensitivity to specific sounds. It is more closely related to the character of the sound than to its intensity and is often reported to begin during childhood or early adolescence. Misophonia may negatively affect students' social interactions and academic performance, particularly in school environments where exposure to auditory stimuli is unavoidable.
This cross-sectional descriptive prevalence study aims to determine the prevalence and severity of misophonia among high school students in Kayseri and Samsun, Turkey. The study population will include students in grades 9 through 12 attending selected high schools. Students with hearing loss, chronic illness, severe psychological disorders, intellectual disabilities, or those outside the defined age range will be excluded.
Data will be collected using a sociodemographic data form and the 10-item Amsterdam Misophonia Scale-Revised (AMISOS-R), a validated self-report instrument assessing the presence and severity of misophonia symptoms. Statistical analyses will be conducted to evaluate the distribution of misophonia symptoms and their associations with demographic variables. The study will be conducted in accordance with ethical principles.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Handan Turan Dizdar, PhD
- Phone Number: +905055970627
- Email: handan.dizdar@omu.edu.tr
Study Locations
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Kayseri, Turkey (Türkiye)
- Recruiting
- Selected High Schools in Kayseri
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Samsun, Turkey (Türkiye)
- Recruiting
- Selected High Schools in Samsun
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Students enrolled in grades 9 through 12
- Students without diagnosed hearing loss
- Students without chronic illness
- Students without severe psychological disorders
Exclusion Criteria:
- Students with diagnosed hearing loss
- Students with any chronic illness
- Students with severe psychological disorders
- Students outside the defined age range
- Students who are illiterate
- Students with intellectual disabilities
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 in high school students
Time Frame: Baseline (single assessment)
|
The proportion of high school students 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 classification is determined according to established cutoff values.
|
Baseline (single assessment)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Severity levels of misophonia symptoms
Time Frame: Baseline (single assessment)
|
Distribution of students according to misophonia severity levels (normal, mild, moderate, and severe) based on the Amsterdam Misophonia Scale-Revised (AMISOS-R).
The AMISOS-R total score ranges from 0 to 40, with higher scores indicating more severe misophonia symptoms.
|
Baseline (single assessment)
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Asya Sıla Alacahan, 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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024/581
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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