ClinicalTrials.gg
CompletedNCT07903844RCTUpdated Oct 29, 2026

Effects of Different 432 Hz Auditory Stimuli on Physiological Stress Responses and Patient Satisfaction in Adults With Dental Anxiety During Restorative Treatment

An observational study in Dental Anxiety, Musical Therapy and Physiological Stress, sponsored by Dokuz Eylul University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-29.

Sponsored by Dokuz Eylul University · Observational

Updated Oct 29, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
120
Ages
18 Years to 50 Years
Sex
All
01

Study summary

In this four-arm randomized controlled clinical trial, 120 adults aged 18-50 years with baseline Modified Dental Anxiety Scale scores ≥13 were allocated equally to 432 Hz-based instrumental music, water sounds, human-vocal music, or a no-audio control during standardized restorative cavity preparation. Heart rate, systolic and diastolic blood pressure, peripheral oxygen saturation, and body temperature were recorded before and immediately after preparation; patient satisfaction was assessed after restoration. Physiological outcomes were compared using baseline-adjusted analysis of covariance, with Holm-adjusted pairwise comparisons. The null hypothesis was that there would be no significant differences among the four study groups in changes in physiological parameters or post-treatment patient satisfaction. The alternative hypothesis was that at least one auditory intervention condition would differ from the other study conditions in physiological responses and/or patient satisfaction.

02

Conditions studied

  • Dental Anxiety
  • Musical Therapy
  • Physiological Stress

Browse trials for

Keywords

  • dental anxiety
  • 432 Hz
  • auditory intervention
  • music
  • physiological stress response
  • restorative dentistry
  • patient satisfaction
03

In context

Patient Satisfaction

877 studies on the registry are indexed under Patient Satisfaction; 202 are open to participants now.

This study's enrollment of 120 is below the median of 149 across 225 observational studies indexed under Patient Satisfaction.

Browse Patient Satisfaction studies →

Lead sponsor

Dokuz Eylul University is the lead sponsor of 261 studies on the registry; 35 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Participants were selected from adult patients presenting to the Department of Restorative Dentistry for routine restorative dental treatment.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adults aged 18-50 years.
  • Meeting the protocol-defined medical eligibility criteria.
  • Not using regular medication.
  • Modified Dental Anxiety Scale (MDAS) score ≥13.
  • Presence of a Class II carious lesion in a mandibular premolar tooth.
  • Carious lesion extending into dentin but not exceeding one-third of the total dentin thickness.
  • Suitability for cavity preparation without local anesthesia.

Exclusion criteria

Exclusion Criteria:

  • Presence of a serious systemic condition.
  • Use of medication.
  • Smoking or alcohol consumption.
  • Hearing impairment.
  • Cardiac arrhythmia.
  • Presence of a serious psychological disorder that could interfere with participation.
  • Inability or unwillingness to tolerate the headphones used for the auditory intervention.
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
120 participants (actual)
Target follow-up
1 Week
Patient registry
Yes

Groups and cohorts

  • Group 1. 432 Hz Instrumental Music

    Group 1-432 Hz Instrumental Music (n = 30): Participants listened to the standardized instrumental music recording prepared at a nominal tuning frequency of 432 Hz.

    Behavioral: Music Therapy

  • Group 2-Water-Based Auditory Stimulus

    Participants listened to the standardized water-sound recording prepared according to the music specialist's 432 Hz-reference protocol; the exact signal-processing procedure remains to be confirmed.

    Behavioral: Music Therapy

  • Group 3-432 Hz Human-Vocal Music

    Participants listened to the standardized music recording containing human vocals, prepared at a nominal tuning frequency of 432 Hz.

    Behavioral: Music Therapy

  • Group 4-Control

    Participants underwent the same standardized restorative procedure without an auditory intervention.

Interventions

  • BehavioralMusic Therapy

    Three standardized auditory recordings were specifically prepared for the study by a music specialist: instrumental music, music containing human vocals, and water-based natural sounds. The two musical recordings were prepared with reference to a nominal A4 tuning frequency of 432 Hz.

06

What researchers measure

Primary outcomes

  1. Change in Dental Anxiety Status and Patient Satisfaction

    Dental anxiety will be assessed using the Modified Dental Anxiety Scale (MDAS), a five-item questionnaire with a total score ranging from 5 to 25. Higher scores indicate greater dental anxiety. Patient satisfaction will be assessed using a five-point Likert-type scale, ranging from 1 (very dissatisfied) to 5 (very satisfied), with higher scores indicating greater satisfaction.

    Time frame: Baseline (before music therapy) and immediately after the dental procedure

Secondary outcomes

  1. Change in Heart Rate

    Heart rate will be measured in beats per minute (bpm) using a digital pulse oximeter. Measurements will be obtained at baseline, before the auditory intervention, and immediately after completion of the standardized cavity preparation procedure. Changes in heart rate between the two measurement points will be evaluated to assess physiological responses to the dental procedure.

    Time frame: Baseline (immediately before the auditory intervention) and immediately after cavity preparation (approximately 10 minutes after baseline).

  2. Change in Body Temperature

    Body temperature will be measured in degrees Celsius (°C) using a digital thermometer. Measurements will be obtained at baseline, before the auditory intervention, and immediately after completion of the standardized cavity preparation procedure. Changes in body temperature between the two measurement points will be evaluated to assess physiological responses to the dental procedure.

    Time frame: Baseline (immediately before the auditory intervention) and immediately after cavity preparation (approximately 10 minutes after baseline).

  3. Change in Systolic Blood Pressure

    Systolic blood pressure will be measured in millimeters of mercury (mmHg) using a digital blood pressure monitor. Measurements will be obtained at baseline, before the auditory intervention, and immediately after completion of the standardized cavity preparation procedure. Changes in systolic blood pressure will be calculated as the post-procedural value minus the baseline value to assess physiological responses to the dental procedure.

    Time frame: Baseline (immediately before the auditory intervention) and immediately after cavity preparation (approximately 10 minutes after baseline).

  4. Change in Diastolic Blood Pressure

    Diastolic blood pressure will be measured in millimeters of mercury (mmHg) using a digital blood pressure monitor. Measurements will be obtained at baseline, before the auditory intervention, and immediately after completion of the standardized cavity preparation procedure. Changes in diastolic blood pressure will be calculated as the post-procedural value minus the baseline value to assess physiological responses to the dental procedure.

    Time frame: Baseline (immediately before the auditory intervention) and immediately after cavity preparation (approximately 10 minutes after baseline).

  5. Change in Peripheral Oxygen Saturation (SpO₂)

    Peripheral oxygen saturation (SpO₂) will be measured as a percentage (%) using a digital pulse oximeter. Measurements will be obtained at baseline, before the auditory intervention, and immediately after completion of the standardized cavity preparation procedure. Changes in oxygen saturation will be calculated as the post-procedural value minus the baseline value to assess physiological responses to the dental procedure.

    Time frame: Baseline (immediately before the auditory intervention) and immediately after cavity preparation (approximately 10 minutes after baseline).

07

Study locations

1 site
  • DEU Restorative Dentistry, Faculty of Dentistry
    Izmir, 35340, Turkey (Türkiye)
08

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 29, 2026
Show all 1 update
  1. Oct 29, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07903844
Responsible party
Asli Silkü Oflioğlu (Research Assistant, Dokuz Eylul University) — Principal investigator
First posted
Oct 29, 2026
Start date
Aug 10, 2026
Primary completion
Sep 30, 2026
Completion
Oct 2, 2026
Last update
Oct 29, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion