- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07632547
Video-Enhanced Tell-Show-Do for Managing Dental Anxiety in Children
Reinforcing the Tell-Show-Do Technique With a Simulated Real-mouth Video to Manage Dental Anxiety in Children During Dental Treatment (A Randomized Controlled Trial)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Dental fear and anxiety in children are associated with several visual stimuli, such as the shape of the dental handpiece or saliva ejector, as well as painful procedures like local anaesthesia, which may create a barrier to receiving dental treatment. Many studies have explored various behaviour management techniques to reduce anxiety during treatment; however, few have investigated the effect of using a video simulation of the real oral environment to familiarise children with treatment steps and reinforce the phrases commonly used by the dentist. This study was designed to reassure children by using a video that demonstrates carious lesions and dental instruments, including the mirror, saliva ejector, handpiece, and syringe, and shows how they work inside the mouth in a child-friendly manner.
This research is a randomised controlled clinical trial in which participants were assigned to two groups based on the behaviour management technique used. Anxiety was assessed using three integrated measures: a self-reported anxiety scale, an observer-rated behaviour scale, and physiological indicators including oxygen saturation and heart rate. All measures were recorded before, during, and after treatment to provide a comprehensive evaluation of the intervention's effect on children's anxiety levels.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Rana Soleman
- Phone Number: +963 934 966 599
- Email: drranasoliman66@gmail.com
Study Locations
-
-
-
Damascus, Syria
- Recruiting
- Damascus University
-
Contact:
- Rana Soliman
- Phone Number: +963 934 966 599drranasoliman6
- Email: drranasoliman66@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Children aged 4-6 years, with or without previous dental experience.
- Children with a positive behavior rating according to the Frankl scale.
- Children with primary molars requiring conservative dental treatment.
Exclusion Criteria:
- Children with systemic or mental disorders.
- Children who received sedative or analgesic medications within the 3 hours prior to the dental visit.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Tell-Show-Do behavior management technique
Children in this group will receive restorative treatment with following the traditional TSD technique without any visual aids.
|
This group received treatment guided by the Tell-Show-Do (TSD) method.
Each step was explained through simple analogies-referring to local anesthesia as 'sleepy juice' and the rubber dam as a 'trap' for the 'tooth worm.'
After the explanation and instrument demonstration, restorative treatment was carried out.
The protocol excluded the use of any audiovisual aids.
All procedures involved conservative restoration of the mandibular primary molars
Other Names:
Children in this group were managed using a video-assisted Tell-Show-Do (VATSD) approach incorporating real-oral simulation.
Each procedural step was preceded by a specific segment of a pre-recorded video tailored to the upcoming task.
The video featured a simulated intraoral environment where dental caries was personified by an animated 'tooth worm' to explain decay and its removal.
Consistent with conventional TSD, the video integrated child-friendly analogies: local anesthesia was introduced as 'sleepy juice'-depicting the 'tooth worm' falling asleep-and the rubber dam was shown as a barrier to prevent its escape.
These segments sequentially covered examination, anesthesia, rubber dam placement, and cavity preparation.
Each viewing was followed by a standardized verbal explanation before performing the clinical procedure.
All participants underwent conservative restorative treatment of the mandibular primary molars
Other Names:
|
|
Experimental: Real-Oral Simulation Video-Assisted Tell-Show-Do Technique
Children in this group will receive restorative treatment with following the enhanced Tell-Show-Do technique with a video simulating the real oral environment
|
This group received treatment guided by the Tell-Show-Do (TSD) method.
Each step was explained through simple analogies-referring to local anesthesia as 'sleepy juice' and the rubber dam as a 'trap' for the 'tooth worm.'
After the explanation and instrument demonstration, restorative treatment was carried out.
The protocol excluded the use of any audiovisual aids.
All procedures involved conservative restoration of the mandibular primary molars
Other Names:
Children in this group were managed using a video-assisted Tell-Show-Do (VATSD) approach incorporating real-oral simulation.
Each procedural step was preceded by a specific segment of a pre-recorded video tailored to the upcoming task.
The video featured a simulated intraoral environment where dental caries was personified by an animated 'tooth worm' to explain decay and its removal.
Consistent with conventional TSD, the video integrated child-friendly analogies: local anesthesia was introduced as 'sleepy juice'-depicting the 'tooth worm' falling asleep-and the rubber dam was shown as a barrier to prevent its escape.
These segments sequentially covered examination, anesthesia, rubber dam placement, and cavity preparation.
Each viewing was followed by a standardized verbal explanation before performing the clinical procedure.
All participants underwent conservative restorative treatment of the mandibular primary molars
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart Rate
Time Frame: during a single dental treatment visit at baseline before treatment, after behavior management, during local anesthetic injection, before and during rubber dam placement, before handpiece use, and during restorative treatment.
|
Assessment tool: Pulse oximeter Measurement unit: Beats per minute (bpm) Assessment time points: Heart rate was assessed during a single dental treatment visit at baseline before treatment, after behavior management, during local anesthetic injection, before and during rubber dam placement, before handpiece use, and during restorative treatment. |
during a single dental treatment visit at baseline before treatment, after behavior management, during local anesthetic injection, before and during rubber dam placement, before handpiece use, and during restorative treatment.
|
|
Facial Image Scale (FIS)
Time Frame: The Facial Image Scale was assessed during a single dental treatment visit at baseline (first visit before intervention) and during dental treatment.
|
Assessment tool: Facial Image Scale questionnaire Measurement unit: Ordinal score (1-5) Assessment time points: Facial Image Scale was assessed during a single dental treatment visit at baseline and during treatment. |
The Facial Image Scale was assessed during a single dental treatment visit at baseline (first visit before intervention) and during dental treatment.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Oxygen Saturation (SpO₂)
Time Frame: Baseline; after behavior management; during injection; before rubber dam placement; during rubber dam placement; before handpiece use; during treatment during a single dental treatment visit.
|
Assessment tool: Pulse oximeter Measurement unit: Percentage (%) Assessment time points: Oxygen saturation was measured using a pulse oximeter and recorded during a single dental treatment visit at baseline, after behavior management, during local anesthetic injection, before and during rubber dam placement, before handpiece use, and during dental treatment. |
Baseline; after behavior management; during injection; before rubber dam placement; during rubber dam placement; before handpiece use; during treatment during a single dental treatment visit.
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Chaza Kouchaji, Damascus University
Publications and helpful links
General Publications
- Liu Y, Gu Z, Wang Y, Wu Q, Chen V, Xu X, Zhou X. Effect of audiovisual distraction on the management of dental anxiety in children: A systematic review. Int J Paediatr Dent. 2019 Jan;29(1):14-21. doi: 10.1111/ipd.12430. Epub 2018 Oct 26.
- Abbasi H, Saqib M, Jouhar R, Lal A, Ahmed N, Ahmed MA, Alam MK. The Efficacy of Little Lovely Dentist, Dental Song, and Tell-Show-Do Techniques in Alleviating Dental Anxiety in Paediatric Patients: A Clinical Trial. Biomed Res Int. 2021 May 23;2021:1119710. doi: 10.1155/2021/1119710. eCollection 2021.
- Khandelwal D, Kalra N, Tyagi R, Khatri A, Gupta K. Control of Anxiety in Pediatric Patients using "Tell Show Do" Method and Audiovisual Distraction. J Contemp Dent Pract. 2018 Sep 1;19(9):1058-1064.
- Seligman LD, Hovey JD, Chacon K, Ollendick TH. Dental anxiety: An understudied problem in youth. Clin Psychol Rev. 2017 Jul;55:25-40. doi: 10.1016/j.cpr.2017.04.004. Epub 2017 Apr 19.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- UDDS-Pedo-03-2026
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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