- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07602075
Effect of Regular Piano Playing on Dental Anxiety and Stress
May 15, 2026 updated by: DİLARA NİL GÜNAÇAR, Recep Tayyip Erdogan University Training and Research Hospital
Evaluation of the Effects of Regular Piano Training on Dental Anxiety and Stress Levels in Children During Preventive Dental Treatment
This study aims to evaluate dental anxiety and stress levels in children receiving regular piano training compared with children without piano training during preventive dental treatment.
A total of 80 children aged 7-11 years, including 40 children receiving piano education and 40 controls, were included in the study.
All participants underwent fissure sealant application using the Tell-Show-Do behavioral guidance technique.
Dental anxiety was assessed before and after treatment using the Modified Child Dental Anxiety Scale-Faces Version (MCDASf), Facial Image Scale (FIS), and physiological parameters including pulse rate, blood pressure, oxygen saturation, and body temperature.
Stress levels were evaluated using the PeSSKi scale.
The study investigates whether regular piano education contributes to reduced dental anxiety and stress responses in pediatric dental patients.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
80
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Rize Province
-
Merkez, Rize Province, Turkey (Türkiye), 53020
- Recep Tayyip Erdogan University
-
-
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
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Children aged between 7 and 11 years
- Patients attending the Department of Pediatric Dentistry, Faculty of Dentistry,
- Recep Tayyip Erdoğan University, and participants invited from two different art schools
- Voluntary participation in the study
- Presence of fissure sealant indication in the mandibular permanent first molars
- Systemically healthy children (ASA I) with no known history of allergy
- No hearing impairment
- Cognitive ability sufficient to understand and answer questionnaire items
- Cooperative behavior classified as "Positive" or "Definitely Positive" according to the Frankl Behavior Rating Scale
Exclusion Criteria:
- Presence of any systemic disease or history of allergy
- Children classified as "Negative" or "Definitely Negative" according to the Frankl Behavior Rating Scale
- Active psychological and/or psychiatric treatment
- Physical or mental disability preventing communication or questionnaire completion
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
- Primary Purpose: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Regular Piano Training Group
Children aged 7-11 years who received regular piano training and underwent fissure sealant application.
|
Regular piano education received by children prior to preventive dental treatment.
Children in this group had ongoing piano training and were evaluated for dental anxiety, stress levels, and physiological responses during fissure sealant application using the Tell-Show-Do technique.
|
|
Other: Control Group
Children aged 7-11 years without regular piano training who underwent fissure sealant application.
|
Children without regular piano training who underwent preventive dental treatment and fissure sealant application using the Tell-Show-Do technique.
Dental anxiety, stress levels, and physiological parameters were evaluated before and after treatment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dental Anxiety Level Measured by the Modified Child Dental Anxiety Scale-Faces Version
Time Frame: Before and immediately after fissure sealant application
|
Dental anxiety levels during preventive dental treatment will be assessed using the Modified Child Dental Anxiety Scale-Faces Version (MCDASf).
The MCDASf score ranges from 8 to 40 points, with higher scores indicating greater dental anxiety.
|
Before and immediately after fissure sealant application
|
|
Dental Anxiety Level Measured by the Facial Image Scale
Time Frame: Before and immediately after fissure sealant application
|
Dental anxiety levels during preventive dental treatment will be assessed using the Facial Image Scale (FIS).
The FIS score ranges from 1 to 5 points, with higher scores indicating greater dental anxiety.
|
Before and immediately after fissure sealant application
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stress Level Measured by the Pediatric Emotional Stress Scale in Kindergarten Intervention (PeSSKI)
Time Frame: Before and immediately after fissure sealant application
|
Stress levels will be assessed using the Pediatric Emotional Stress Scale in Kindergarten Intervention (PeSSKI) during preventive dental treatment. The PeSSKi total score ranges from 10 to 50 points, with higher scores indicating higher perceived stress levels in children. |
Before and immediately after fissure sealant application
|
|
Pulse Rate During Preventive Dental Treatment
Time Frame: Before and immediately after fissure sealant application
|
Pulse rate will be measured in beats per minute (bpm) before and immediately after fissure sealant application during preventive dental treatment.
Higher values indicate increased physiological arousal/anxiety.
|
Before and immediately after fissure sealant application
|
|
Systolic Blood Pressure
Time Frame: Before and immediately after fissure sealant application.
|
Systolic blood pressure will be measured in millimeters of mercury (mmHg) before and immediately after fissure sealant application during preventive dental treatment.
Higher values indicate increased physiological stress response.
|
Before and immediately after fissure sealant application.
|
|
Diastolic Blood Pressure
Time Frame: Before and immediately after fissure sealant application
|
Diastolic blood pressure will be measured in millimeters of mercury (mmHg) before and immediately after fissure sealant application during preventive dental treatment.
Higher values indicate increased physiological stress response.
|
Before and immediately after fissure sealant application
|
|
Oxygen Saturation
Time Frame: Before and immediately after fissure sealant application
|
Peripheral oxygen saturation (SpO₂) will be measured as percentage (%) before and immediately after fissure sealant application during preventive dental treatment.
Higher values indicate better oxygenation status.
|
Before and immediately after fissure sealant application
|
|
Body Temperature
Time Frame: Before and immediately after fissure sealant application
|
Body temperature will be measured in degrees Celsius (°C) before and immediately after fissure sealant application during preventive dental treatment.
|
Before and immediately after fissure sealant application
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Actual)
August 1, 2025
Primary Completion (Actual)
March 25, 2026
Study Completion (Actual)
April 1, 2026
Study Registration Dates
First Submitted
May 10, 2026
First Submitted That Met QC Criteria
May 15, 2026
First Posted (Actual)
May 22, 2026
Study Record Updates
Last Update Posted (Actual)
May 22, 2026
Last Update Submitted That Met QC Criteria
May 15, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 2025/348
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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