- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07688668
AI Virtual Patient Training for Dental Student History Taking
Artificial Intelligence-Assisted Virtual Patients for History-Taking Training in Dental Students: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
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.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Hue City
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Huế, Hue City, Vietnam, 530000
- Faculty of Odonto-Stomatology, University of Medicine and Pharmacy, Hue University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
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.
|
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.
|
|
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.
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Case-Based Clinical History-Taking Competency Score
Time Frame: 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
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Student Satisfaction With the Training Method
Time Frame: 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
Time Frame: 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
|
Collaborators and Investigators
Investigators
- Principal Investigator: Van Nhat Thang Le, DDS PhD, Faculty of Odonto-Stomatology, University of Medicine and Pharmacy, Hue University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- H2026/548
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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