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Not yet recruiting NCT07034833

Assessment of a Ventriloquist Puppet for Reducing Dental Anxiety in Children

No phase Interventional Dental Anxiety

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Ventriloquist Puppet Interaction.
Who it may be relevant to
Registry conditions: Dental Anxiety. Basic parameters: 5 years — 10 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

thhe goal of this clinical trial is to assess the effect of ventriloquist puppets to reduce the strees accompined by the dental visit in cgilren . The main questions it aims to answer are: * Does the ventriloquist puppet can reduce the stress accompanied by the dental visit for the children ? * What medical problems do participants have when taking drug ABC? Researchers will compare ventriloquist puppet to a control group (conventional behavior management techniques ) to see if ventriloquist puppet can lower the anxiety or not.

Interventions

  • Behavioral Ventriloquist Puppet Interaction
    children allocated to the Ventriloquist Puppet group were introduced to a Ventriloquist Puppet inside the clinic and were allowed to play, talk, and interact with the puppet for 5-10 minutes.

Primary outcome measures

  • Dental anxiety [Time frame: From immediately before to immediately after the dental procedure]
  • Heart rate [Time frame: From immediately before to immediately after the dental procedure]

Eligibility criteria

Inclusion criteria

  • healthy children with no systemic diseases.
  • children require dental intervention

Exclusion criteria

  • children with bad dental experience
  • children require invasive surgical intervention

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07034833 · 1200/384

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗