- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06229379
The Effects of a Large Language Model on Clinical Questioning Skills
A Randomized Controlled Trial of the Effects of a Large Language Model on Medical Students' Clinical Questioning Skills
The researchers have used the ophthalmology textbook, clinical guideline consensus, the Internet conversation data and knowledge base of Zhongshan Ophthalmology Center in the early stage, combined with artificial feedback reinforcement learning and other techniques to fine-tune and train the LLM, and developed "Digital Twin Patient", a localized large language model that has the ability to answer ophthalmology-related medical questions, and also constructed a combination of automated model evaluation and manual evaluation by medical experts. The evaluation system combining automated model evaluation and manual evaluation by medical experts was constructed at the same time.
This project intends to integrate "Digital Twin Patient" into undergraduate ophthalmology apprenticeship, simulate the consultation process of real patients through the online interaction between students and "Digital Twin Patient", explore the effect of "Digital Twin Patient" consultation teaching, provide emerging technology tools for guiding medical students to actively learn a variety of ophthalmology cases, cultivate clinical thinking, and provide the possibility of creating a new mode of intelligent teaching.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
At present, the main form of clinical questioning skills teaching is to let undergraduates who participate in the apprenticeship first learn the characteristics and diagnostic points of cases, and then practice questioning on real patients in the wards. However, due to the large number of trainee students, it is difficult to meet the teaching demand in terms of the number of cases available for questioning and the richness of disease types under the current teaching mode. Therefore, it is necessary to utilize new intelligent technologies and create a new model of questioning skills teaching to improve teaching efficiency and enhance students' clinical thinking.
Large-scale language modeling (LLM) is a deep learning technology that can learn knowledge from a large amount of text, and AI chatbots such as ChatGPT are a typical example of its application. AI chatbots are characterized by anthropomorphic comprehension and diversified natural language generation abilities in different contexts, and have been initially applied in the medical field, such as passing the U.S. Medical Licensing Examination, assisting in ophthalmic history documentation and answering ophthalmic questions. However, it has been found that although LLM has fair modeling performance in general medical knowledge, it still needs to be improved in the area of specialty diseases. Based on this, the researcher's team has used the ophthalmology textbook, clinical guideline consensus, the Internet conversation data and knowledge base of Zhongshan Ophthalmology Center in the early stage, combined with artificial feedback reinforcement learning and other techniques to fine-tune and train the LLM, and developed "Digital Twin Patient", a localized large language model that has the ability to answer ophthalmology-related medical questions, and also constructed a combination of automated model evaluation and manual evaluation by medical experts. The evaluation system combining automated model evaluation and manual evaluation by medical experts was constructed at the same time.
This project intends to integrate "Digital Twin Patient" into undergraduate ophthalmology apprenticeship, simulate the consultation process of real patients through the online interaction between students and "Digital Twin Patient", explore the effect of "Digital Twin Patient" consultation teaching, provide emerging technology tools for guiding medical students to actively learn a variety of ophthalmology cases, cultivate clinical thinking, and provide the possibility of creating a new mode of intelligent teaching.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Guangdong
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Guangzhou, Guangdong, China, 510060
- Zhongshan Ophthalmic Center, Sun Yat-sen Univerisity
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- All undergraduate students from Sun Yat-sen University who participate in the ophthalmological internship.
Exclusion Criteria:
- Students who refuse to sign informed consent.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: "Digital twin patient"
The students in the "Digital twin patient" group were trained in history taking using a "digital twin patient" on the first day of a training program, and then took a 15-minute clinical questioning exam using the "digital twin patient" on the second day.
|
"Digital twin patient" can serve as patients with specific diseases for medical students to acquire disease history and thus practice clinical questioning skills.
|
|
Other: Real patient
The students in the Real patient group were trained in history taking using a real patient on the first day of a training program, and then took a 15-minute clinical questioning exam using the "digital twin patient" on the second day.
|
"Digital twin patient" can serve as patients with specific diseases for medical students to acquire disease history and thus practice clinical questioning skills.
As in traditional medical education, medical students need to interact with real patients to practice history collection skills.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Students' scores in the medical history acquisition exam
Time Frame: Weekly during this study (up to 10 months)
|
Weekly during this study (up to 10 months)
|
Collaborators and Investigators
Sponsor
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 (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023KYPJ283
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
product manufactured in and exported from the U.S.
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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