- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07398105
Comparison of Virtual Reality and Mixed Reality Head-Mounted Displays for Dental Anxiety Control During Local Anesthesia in Children
A Clinical Study Comparing Virtual Reality and Mixed Reality Head-Mounted Displays for Dental Anxiety and Pain Control During Local Anesthesia in Children
Dental anxiety is a common problem in children and may negatively affect cooperation, pain perception, and treatment success during dental procedures. Distraction techniques are widely used to reduce anxiety during dental treatment. In recent years, virtual reality (VR) and mixed reality (MR) technologies have been introduced as innovative audiovisual distraction methods in pediatric dentistry.
The aim of this randomized clinical study is to compare the effects of virtual reality and mixed reality head-mounted displays on dental anxiety and pain perception in children during local anesthesia administration. A total of 142 systemically healthy children aged 6 to 12 years who required dental treatment under local anesthesia were included. Participants were randomly assigned to either a VR group or an MR group.
Dental anxiety and pain levels were assessed using validated scales before and during local anesthesia administration. Behavioral responses and physiological parameters were also recorded. The results of this study will help determine whether VR or MR provides superior anxiety control during pediatric dental procedures.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Dental anxiety in children is associated with increased pain perception, behavioral problems, and reduced treatment compliance. Managing anxiety during dental procedures is therefore a critical component of pediatric dental care. Conventional behavior guidance techniques may not always be sufficient, particularly during invasive procedures such as local anesthesia administration.
This randomized, parallel-group clinical trial was conducted to compare the effects of virtual reality (VR) and mixed reality (MR) head-mounted displays on dental anxiety and pain perception in pediatric patients. The study included 142 systemically healthy children aged between 6 and 12 years who required dental treatment under local anesthesia. Only children with positive or definitely positive behavior according to the Frankl Behavior Rating Scale were included.
Participants were randomly allocated into two groups: a VR group and an MR group. During local anesthesia administration, children in the VR group were exposed to a fully immersive virtual environment, while children in the MR group interacted with virtual content while maintaining partial awareness of the clinical environment.
Dental anxiety was evaluated using the Children's Fear Survey Schedule-Dental Subscale, and pain perception was assessed using the Wong-Baker FACES Pain Rating Scale. Behavioral pain responses during local anesthesia were scored using the FLACC scale by two independent observers. Heart rate measurements were recorded as a physiological indicator of anxiety. Interobserver reliability for behavioral assessments was also evaluated.
The primary outcome of the study was the change in dental anxiety levels during local anesthesia administration. Secondary outcomes included pain perception, behavioral responses, and physiological changes. The findings of this study aim to provide evidence regarding the effectiveness of VR and MR technologies as distraction tools for anxiety management in pediatric dentistry.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Konya
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Konya, Konya, Turkey (Türkiye), 42150
- Selcuk University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Children aged between 6 and 12 years.
- Systemically healthy children.
- Children requiring dental treatment under local anesthesia.
- Positive or definitely positive behavior according to the Frankl Behavior Rating Scale.
- Written informed consent obtained from parents or legal guardians.
Exclusion Criteria:
- Presence of systemic disease or neurological disorders.
- Visual or auditory impairment that could interfere with the use of head-mounted displays.
- History of epilepsy, vertigo, or motion sickness related to audiovisual stimulation.
- Negative or definitely negative behavior according to the Frankl Behavior Rating Scale.
- Refusal to use virtual reality or mixed reality devices.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Virtual Reality (VR) Group
Children who preferred virtual reality distraction received audiovisual content through a head-mounted display during local anesthesia administration.
The virtual reality mode provided a fully immersive environment intended to reduce dental anxiety and pain perception.
|
Participants received audiovisual distraction through a head-mounted display during local anesthesia administration.
The intervention was delivered in two modes based on participant preference: a virtual reality (VR) mode providing a fully immersive audiovisual environment, and a mixed reality (MR) mode allowing interaction with virtual content while maintaining partial awareness of the clinical environment.
|
|
Other: Mixed Reality (MR) Group
Children who preferred mixed reality distraction received audiovisual content through a head-mounted display during local anesthesia administration.
The mixed reality mode allowed interaction with virtual content while maintaining partial awareness of the clinical environment to support anxiety and pain control.
|
Participants received audiovisual distraction through a head-mounted display during local anesthesia administration.
The intervention was delivered in two modes based on participant preference: a virtual reality (VR) mode providing a fully immersive audiovisual environment, and a mixed reality (MR) mode allowing interaction with virtual content while maintaining partial awareness of the clinical environment.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Dental Anxiety Level During Local Anesthesia
Time Frame: Immediately before and during local anesthesia administration
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Dental anxiety levels were assessed using the Children's Fear Survey Schedule-Dental Subscale (CFSS-DS).
Anxiety scores were recorded before and during local anesthesia administration to evaluate changes associated with virtual reality and mixed reality distraction methods.
|
Immediately before and during local anesthesia administration
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Perception During Local Anesthesia
Time Frame: During local anesthesia administration
|
Pain perception was evaluated using the Wong-Baker FACES Pain Rating Scale during local anesthesia administration.
|
During local anesthesia administration
|
|
Behavioral Pain Response Assessed by FLACC Scale
Time Frame: During local anesthesia administration
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Behavioral pain responses during local anesthesia administration were assessed using the FLACC (Face, Legs, Activity, Cry, Consolability) scale by two independent observers.
|
During local anesthesia administration
|
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Heart Rate Changes During Local Anesthesia
Time Frame: Immediately before, after and during local anesthesia administration
|
Heart rate was measured as a physiological indicator of anxiety before and during local anesthesia administration.
|
Immediately before, after and during local anesthesia administration
|
Collaborators and Investigators
Sponsor
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
Other Study ID Numbers
- SBAE Thesis Project
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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