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AI Virtual Patient Training for Dental Student History Taking

30 giugno 2026 aggiornato da: Le Van Nhat Thang, Hue University of Medicine and Pharmacy

Artificial Intelligence-Assisted Virtual Patients for History-Taking Training in Dental Students: A Randomized Controlled Trial

This randomized study evaluated whether an artificial intelligence-assisted virtual patient could support third-year dental students in practicing medical and dental history taking. Fifty-six students were assigned to either a Gemini-based virtual-patient training group or a conventional role-play group. Both groups completed four training sessions over 2 weeks using comparable clinical cases, practice time, and feedback criteria. The study compared changes in case-based history-taking competency as well as student satisfaction and perceived usefulness of the training methods.

Panoramica dello studio

Descrizione dettagliata

This single-center, parallel-group randomized educational intervention was conducted among third-year undergraduate dental students at the Faculty of Odonto-Stomatology, University of Medicine and Pharmacy, Hue University, Hue, Vietnam.

Eligible students were third-year dental students who had not previously received history-taking training supported by a large language model. Participants were assigned in a 1:1 ratio to either a Gemini-based virtual-patient group or a conventional role-play group. Each group included 28 students.

The Gemini-based virtual patient was developed as a curriculum-bounded learning tool for common oral and maxillofacial clinical scenarios. Its knowledge base included third-year dental curriculum materials, sample medical and dental records, a clinical assessment rubric, and anonymized case scenarios adapted from patient records. The virtual patient was instructed to act only as the patient, disclose information only in response to relevant questions, remain consistent with the predefined case, avoid providing diagnostic guidance during the interview, and provide rubric-aligned feedback after the student completed the encounter.

Students in the virtual-patient group typed questions to the Gemini-based virtual patient, documented the elicited history, and received automated feedback after each case. Students in the conventional role-play group practiced with trained role-players or faculty members using standardized case scripts and the same feedback criteria. Both groups completed four sessions over 2 weeks, with each session lasting approximately 30 to 45 minutes. The groups received comparable scheduled practice time, clinical topics, number of cases, and feedback criteria.

The primary outcome was the change in case-based clinical history-taking competency score from baseline to postintervention assessment. Competency was assessed using five clinical scenarios representing common conditions in the third-year dental curriculum. The possible score range was 0 to 10 points. Each assessment was independently scored by two faculty assessors who were blinded to group allocation and questionnaire responses.

Secondary outcomes included student satisfaction and perceived effectiveness of the training method. Satisfaction covered ease of use, naturalness of interaction, willingness to recommend the method, and diversity of clinical conditions. Perceived effectiveness included self-directed learning, interest in learning, communication and feedback skills, question phrasing, systematic and logical history taking, and stress during history-taking practice. All questionnaire items used a 5-point Likert scale.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

56

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Hue City
      • Huế, Hue City, Vietnam, 530000
        • Faculty of Odonto-Stomatology, University of Medicine and Pharmacy, Hue University

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto
  • Adulto più anziano

Accetta volontari sani

Descrizione

Inclusion Criteria:

  • Third-year undergraduate dental students enrolled in the dental program at the Faculty of Odonto-Stomatology, University of Medicine and Pharmacy, Hue University.
  • No previous history-taking training supported by a large language model.
  • Willingness to participate and provision of written informed consent.

Exclusion Criteria:

  • Withdrawal from the study.
  • Failure to complete the baseline assessment, scheduled training sessions, or postintervention assessment.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Altro
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Gemini-Based AI Virtual-Patient Training
Participants received Gemini-based artificial intelligence virtual-patient training for dental history taking. They completed four training sessions over 2 weeks using curriculum-bounded clinical cases and automated rubric-aligned feedback.
Students completed four 30- to 45-minute history-taking training sessions over 2 weeks using a Gemini-based artificial intelligence virtual patient. Students typed questions, documented elicited medical and dental history, and received automated rubric-aligned feedback after each simulated patient encounter. The virtual patient used predefined curriculum-based case information and disclosed information only in response to relevant student questions.
Comparatore attivo: Conventional Role-Play Group
Participants received conventional role-play training for dental history taking. They completed four training sessions over 2 weeks using comparable clinical cases, practice time, and rubric-guided feedback.
Students completed four 30- to 45-minute history-taking training sessions over 2 weeks with trained role-players or faculty members using standardized case scripts. Students practiced eliciting medical and dental history and received feedback guided by the same assessment rubric used in the virtual-patient group.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Case-Based Clinical History-Taking Competency Score
Lasso di tempo: Baseline and immediately after completion of the 2-week training intervention
Change from baseline to postintervention in the composite case-based clinical history-taking competency score. Competency was assessed using five clinical scenarios representing common conditions in the third-year dental curriculum. Scores ranged from 0 to 10 points, with higher scores indicating better history-taking-related clinical competency. Each assessment was independently scored by two faculty assessors who were blinded to study-group allocation.
Baseline and immediately after completion of the 2-week training intervention

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Student Satisfaction With the Training Method
Lasso di tempo: Immediately after completion of the 2-week training intervention
Student satisfaction was assessed immediately after training using four individual 5-point Likert-scale items: ease of use, naturalness of interaction, willingness to recommend the training method, and diversity of clinical conditions. Each item was analyzed separately. Scores ranged from 1 (strongly disagree) to 5 (strongly agree), with higher scores indicating greater satisfaction.
Immediately after completion of the 2-week training intervention
Perceived Effectiveness of the Training Method
Lasso di tempo: Immediately after completion of the 2-week training intervention
Perceived effectiveness was assessed immediately after training using six individual 5-point Likert-scale items: self-directed learning after class, interest in learning, communication skills and ability to receive feedback, question phrasing and expression, systematic and logical history taking, and stress during history-taking practice. Each item was analyzed separately. Scores ranged from 1 (strongly disagree) to 5 (strongly agree), with higher scores indicating greater perceived effectiveness.
Immediately after completion of the 2-week training intervention

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Van Nhat Thang Le, DDS PhD, Faculty of Odonto-Stomatology, University of Medicine and Pharmacy, Hue University

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

30 maggio 2026

Completamento primario (Effettivo)

15 giugno 2026

Completamento dello studio (Effettivo)

18 giugno 2026

Date di iscrizione allo studio

Primo inviato

30 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

30 giugno 2026

Primo Inserito (Effettivo)

7 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

7 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

30 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • H2026/548

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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