NCT07467395

Brief Summary

The aim of this study is to evaluate the impact of using virtual reality glasses compared to augmented reality glasses as distraction methods to reduce the dental anxiety and pain in children during extraction of primary molars.

Trial Health

65
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
1mo left

Started Apr 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress58%
Apr 2026Jul 2026

First Submitted

Initial submission to the registry

March 9, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 12, 2026

Completed
20 days until next milestone

Study Start

First participant enrolled

April 1, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2026

Last Updated

March 12, 2026

Status Verified

March 1, 2026

Enrollment Period

3 months

First QC Date

March 9, 2026

Last Update Submit

March 9, 2026

Conditions

Outcome Measures

Primary Outcomes (5)

  • Heart rate (HR) assessment

    Heart rate (HR) will be employed as an anxiety indicator, as stress or anxiety can increase it. It will be measured using a pulse oximeter. A brief demonstration using the pulse oximeter will be done, and the patient will be instructed to stay still and not to move his hands a lot in order to obtain accurate readings. The pulse oximeter will be placed on the patient's index finger.

    Baseline to immediately after the procedure (within the same treatment visit).

  • Anxiety assessment using the Facial Image Scale (FIS)

    The FIS comprises one item with a response set of five faces (ranging from a very sad to a very smiley face). Children will be asked to indicate which of the faces they feel most like at that moment, it is a 'state' measure of anxiety that provides an immediate reflection of how the child is feeling.

    Baseline to immediately after the procedure (within the same treatment visit).

  • Anxiety assessment using Venham's clinical anxiety scale

    The Venham's clinical anxiety rating scale will be used to assess the child's dental anxiety at baseline, during and after anesthesia injection and extraction procedure. The assessment will take place by the operator and the independent outcome assessor using the recorded video tapes. This objective measure scores the child's level of anxiety with a correlating behavior description It consists of 6 categories (range from 0 to 5) where 0= relaxed, 1=uneasy, 2= tense, 3= reluctant, 4= interference, 5= out of contact.

    Baseline to immediately after the procedure (within the same treatment visit).

  • Pain assessment using Wong-Baker FACES pain rating scale

    The Wong-Baker FACES Pain Rating Scale will be used to quantify the child's pain experience. This scale ranges from a neutral face, assigned a score of "0," indicating no pain, to a frowning face with a score of "10," representing the highest level of discomfort. The scale will be explained to the child, who will be asked to choose the face that represents how much pain he or she will feel during anesthesia injection and extraction from one of the graphic rating scales by pointing his finger at one of the six faces shown on the chart will be given to him.

    Baseline to immediately after the procedure (within the same treatment visit).

  • Pain assessment using Face, legs, activity, cry, consolability (FLACC) scale

    FLACC behavioral pain assessment scale will be used to assess the child's dental pain during the procedure. This objective measure scores the child's level of pain with a correlating behavior description. It consists of 5 categories (F) face, (L) leg, (A) activity, (C) cry, (C) consolability each is scored from 0 to 2, which results in a total score between zero and ten. The assessment will take place by the operator and the independent outcome assessor, the assessors will assign a score to each category based on the child's response during anesthesia injection and extraction by analysis of the recorded videotapes.

    Baseline to immediately after the procedure (within the same treatment visit).

Study Arms (2)

Augmented Reality

EXPERIMENTAL
Device: Augmented reality glasses

Virtual Reality

ACTIVE COMPARATOR
Device: VR glasses

Interventions

Augmented reality glasses will be introduced to the child and he will be allowed to choose his favourite cartoon movie from this list: Rapunzel, Stitch, Ratatouille, Frozen, Minions, Zootopia, and The lion king during the first dental visit to get familiar with the AR glasses. The augmented reality is an eye goggle that will be connected to the laptop through a wire, then after playing the cartoon that will be selected by the child on the laptop the child will enjoy watching the cartoon movie through the eye goggle.

Augmented Reality

Children allocated to this group will be managed by Virtual reality glasses, which will be introduced to the child and he will be allowed to choose his favourite cartoon from the same list during the first dental visit to get familiar with the VR glasses. The virtual reality is a head-mounted display, the child will be asked to select his favourite cartoon on a mobile, then the mobile will be inserted in that head-mounted display

Virtual Reality

Eligibility Criteria

Age6 Years - 8 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Medically free children without visual or auditory impairment (ASA I).
  • Children aged 6-8 years.
  • Children with Frankl behaviour rating score 3 or 4.
  • Children requiring extraction in one of their primary molars.
  • Parents who will accept to give their consent and participate in the study

You may not qualify if:

  • Children require emergency dental treatment.
  • Children with a history of epilepsy and anxiety disorder.
  • Children with previous bad dental experience.
  • Allergy to local anaesthetic drugs.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
MSc. researcher of pediatric dentistry

Study Record Dates

First Submitted

March 9, 2026

First Posted

March 12, 2026

Study Start

April 1, 2026

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

July 1, 2026

Last Updated

March 12, 2026

Record last verified: 2026-03