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CompletedNCT07688668Updated Jul 7, 2026

AI Virtual Patient Training for Dental Student History Taking

An interventional study of Gemini-Based AI Virtual-Patient Training and Conventional Role-Play Training in Dental Education, Artificial Intelligence (AI) and Virtual Patient, sponsored by Hue University of Medicine and Pharmacy. Completed at 1 site in Vietnam. Per ClinicalTrials.gov, last updated 2026-07-07.

Sponsored by Hue University of Medicine and Pharmacy · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
56
Allocation
Randomized
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Dental Education
  • Artificial Intelligence (AI)
  • Virtual Patient
  • History Taking
  • Large Language Model

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03

In context

Language

243 studies on the registry are indexed under Language; 76 are open to participants now.

This study's enrollment of 56 is below the median of 65 across 158 interventional studies indexed under Language.

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Lead sponsor

Hue University of Medicine and Pharmacy is the lead sponsor of 13 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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 .

Exclusion criteria

Exclusion Criteria:

  • Withdrawal from the study.
  • Failure to complete the baseline assessment, scheduled training sessions, or postintervention assessment.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

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05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
56 participants (actual)

Study arms

  • Experimental
    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.

    Behavioral: Gemini-Based AI Virtual-Patient Training

  • Active comparator
    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.

    Behavioral: Conventional Role-Play Training

Interventions

  • BehavioralGemini-Based AI Virtual-Patient Training

    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.

  • BehavioralConventional Role-Play Training

    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.

06

What researchers measure

Primary outcomes

  1. Change in Case-Based Clinical History-Taking Competency Score

    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.

    Time frame: Baseline and immediately after completion of the 2-week training intervention

Secondary outcomes

  1. Student Satisfaction With the Training Method

    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.

    Time frame: Immediately after completion of the 2-week training intervention

  2. Perceived Effectiveness of the Training Method

    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.

    Time frame: Immediately after completion of the 2-week training intervention

07

Study locations

1 site
  • Faculty of Odonto-Stomatology, University of Medicine and Pharmacy, Hue University
    Huế, Hue City 530000, Vietnam
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07688668
Lead sponsor
Hue University of Medicine and Pharmacy
Responsible party
Le Van Nhat Thang (Principal Investigator, Hue University of Medicine and Pharmacy) — Principal investigator
First posted
Jul 7, 2026
Start date
May 30, 2026
Primary completion
Jun 15, 2026
Completion
Jun 18, 2026
Last update
Jul 7, 2026

Study contacts

Van Nhat Thang Le, DDS PhD
principal investigator · Faculty of Odonto-Stomatology, University of Medicine and Pharmacy, Hue University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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