- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06856005
"Assessing the Impact of Personalized Music Playlists on Procedural Anxiety and Crown Preparation Performance Among Young Dentists: a Randomized Controlled Trial"
The objective of this study was to evaluate the effectiveness of personalized music playlists in reducing procedural anxiety among young dentists performing crown preparations for porcelain-fused-to-metal (PFM) crowns.
A randomized controlled trial with a parallel-group design was conducted at the Department of Prosthodontics, School of Dentistry, Shaheed Zulfiqar Ali Bhutto Medical University, from April 12th, 2024, to October 11th, 2024. A total of 64 young dentists (20-30 years old) were randomly assigned to two groups: the experimental group (Group A), which listened to personalized music during the procedure, and the control group (Group B), which received no music. Anxiety was measured using the State-Trait Anxiety Inventory (STAI) before and after the procedure. Physiological parameters, including heart rate and respiratory rate, were also monitored. The preparation was evaluated based on a structured scoring rubric, assessing critical parameters. The scoring was conducted by two experienced prosthodontists who were blinded to the participant's group allocation. Statistical analysis was performed using SPSS version 25.0.0, with a p-value of <0.05 considered statistically significant.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Federal
-
Islamabad, Federal, Pakistan
- School of dentistry, SZABMU
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Both male and female
- Young dentists 20-30 years.
- Recently graduated from dental school. (graduated within the last 1-3 years.)
- No hearing impairments or known psychiatric disorders.
Exclusion Criteria:
- Dentists with previous experience in anxiety management techniques.
- Those who have already participated in similar studies.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Group B
|
|
|
Experimental: Group A
which listened to personalized music during the procedure
|
to evaluate the effectiveness of personalized music playlists in reducing procedural anxiety among young dentists performing crown preparations for porcelain-fused-to-metal (PFM) crowns and to compare the crown preparation performance of students who listened to music with those who did not. • Experimental Group: o Participants in the experimental group were asked to use personalized music playlists during the procedure. These playlists were already available on their personal devices (e.g., smartphones) and reflected their individual music preferences. Participants selected music they found relaxing or enjoyable, ensuring the intervention was tailored to their unique tastes. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anxiety Assessment: trait and state anxiety.
Time Frame: 2 minutes after the procedure
|
The State-Trait Anxiety Inventory (STAI) was used to measure it
|
2 minutes after the procedure
|
|
Crown preparation was evaluated based on a structured scoring rubric, assessing critical parameters
Time Frame: 2 minutes after the procedure
|
The preparation was evaluated based on a structured scoring rubric, assessing critical parameters.
The scoring was conducted by two experienced prosthodontists who were blinded to the participant's group allocation
|
2 minutes after the procedure
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart rate was recorded before and after the procedure.
Time Frame: immediately after the procedure
|
Heart rate was recorded before and after the procedure.
|
immediately after the procedure
|
|
Respiratory rate was recorded before and after the procedure.
Time Frame: immediately after the procedure
|
respiratory rate was recorded before and after the procedure.
|
immediately after the procedure
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- SOD/ERB/2025/61
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
product manufactured in and exported from the U.S.
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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