Can a custom AI storybook tame Kids' dental fear?
NCT ID NCT07778134
First seen Aug 21, 2026 · Last updated Aug 21, 2026
Summary
This trial tests whether a storybook personalized by artificial intelligence can help children feel calmer and cooperate better during dental treatment. Children aged 3-12 with mild to moderate dental anxiety will be randomly assigned to hear either an AI-generated story tailored to their interests, a standard dental storybook, or usual behavior guidance. Researchers will measure anxiety and cooperation using validated scales and physiological signs like pulse and oxygen levels.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- AI-generated personalized dental storybook (behavioral intervention)
- What this could lead to
- If effective, this could offer a simple, non-drug way to reduce dental anxiety and improve cooperation in children, potentially reducing the need for sedation or restraint.
- What could go wrong
- This is a small, early-stage trial, so results may not be conclusive. The benefit might be modest or not differ from standard storybooks, and individual responses can vary.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 69 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2026
- Expected to finish
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Nov 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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4 to 7 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Participants classified as Frankl II (Negative) or Frankl III (Positive) according to the Frankl Behavior Rating Scale. * Systemically healthy participants classified as American Society of Anesthesiologists (ASA) Physical Status I. * Participants with at least two primary molars requiring Class I occlusal restorations for superficial carious lesions that do not require local anesthesia. * Parents or legal guardians who voluntarily provide written informed consent for participation in the study. Exclusion Criteria: * Participants younger than 4 years or older than 7 years of age. * Participants with systemic diseases or developmental delay. * Participants with a current psychiatric disorder or who have been under psychiatric follow-up within the previous 6 months. * Participants receiving psychotropic medication. * Participants diagnosed with neurodevelopmental disorders (e.g., autism spectrum disorder or moderate-to-severe attention-deficit/hyperactivity disorder). * Participants with communication or developmental impairments that may interfere with the reliable administration of the study assessment scales. * Children with special health care needs. * Participants with general or dental developmental anomalies (e.g., amelogenesis imperfecta, cleft lip and/or palate, osteogenesis imperfecta). * Participants classified as Frankl I (Definitely Negative) or Frankl IV (Definitely Positive) according to the Frankl Behavior Rating Scale. * Participants with a history of spontaneous dental pain or symptomatic teeth requiring emergency treatment. * Participants whose parent or legal guardian does not provide written informed consent.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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epartment of Pediatric Dentistry, Eskişehir Osmangazi University Faculty of Dentistry
RECRUITINGEskişehir, Turkey (Türkiye)
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