Can a custom AI storybook tame Kids' dental fear?

NCT ID NCT07778134

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
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Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

About 69 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2026

Expected to finish

Nov 2027

An estimate. End dates often move.

Lead sponsor

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

4 to 7 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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

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How to take part

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Contacts and locations

Locations

  • epartment of Pediatric Dentistry, Eskişehir Osmangazi University Faculty of Dentistry

    RECRUITING

    Eskişehir, Turkey (Türkiye)

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