Clinical trial Recruiting at 1 site Interventional Ages 4 to 7

AI-powered personalized storybook to help kids stay cooperative during dental visits

Official title: The Effectiveness of an Artificial Intelligence-Generated, Patient-Specific Storybook for Behaviour Guidance: A Randomized Controlled Trial

Run by Eskisehir Osmangazi University · NCT07778134 · Data updated 2026-11-12

This trial tests whether an AI-generated, personalized storybook before dental treatment helps children be less anxious and more cooperative compared with a standard storybook or standard behavior guidance.

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Quick facts

Study typeInterventional
Ages4 Years to 7 Years
SexAll
Enrollment69 (estimated)
SponsorEskisehir Osmangazi University
Academic / other
Locations1 site (Eskişehir)
StatusRecruiting
StartedJune 8, 2026
Main results expectedNovember 12, 2027
Study endsNovember 12, 2027
Registry record updatedAugust 21, 2026
Trial IDNCT07778134 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are healthy children aged 4–7 with Frankl scores of II or III and two primary molars needing superficial restorations, whose guardians consent to participation.

Probably not a fit

Children outside the age range, with systemic disease or developmental delays, psychiatric conditions, or those on psychotropic meds may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized trial compares three behavior guidance approaches for pediatric dental care: an AI-generated personalized digital storybook tailored to each child, a standard non-personalized storybook, and standard behavior guidance alone. Participants are children aged 4 to 7 with dental anxiety or challenging behavior undergoing preventive or restorative care, and they are randomized to one of the three arms. The AI storybook is created using demographic and interest data, reviewed clinically before use, and presented on a tablet prior to procedures. Outcomes will measure changes in dental anxiety and cooperation during treatment. The study aims to determine if personalized storytelling can enhance non-pharmacologic behavior management in pediatric dentistry.

Why it matters

Potential benefit: If successful, personalized AI storytelling could reduce dental anxiety and improve cooperation, potentially lowering the need for pharmacological behavior management.

How similar studies have gone: Prior storytelling approaches have shown benefit in pediatric dental settings; this study tests a novel AI-personalization strategy.

Who can join: the full rules

Show full inclusion / exclusion criteria
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.

Where it's running

  • epartment of Pediatric Dentistry, Eskişehir Osmangazi University Faculty of Dentistry
    Eskişehir, Turkey (Türkiye)
    Recruiting

Study contacts

  • Principal investigator: İrem Bağ Baytar — Eskişehir Osmangazi University Faculty of Dentistry
  • Study coordinator: Associate Professor
  • Email: irem.bag@ogu.edu.tr
  • Phone: +905064379883

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.