- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06247475
Generating Fast and Slow for Entree Level Medical Knowledge
February 14, 2024 updated by: National Taiwan University Hospital
The generative artificial intelligence tool, ChatGPT, has garnered widespread interest since its launch.
This innovative multimedia platform has the potential to enhance medical communication and health education, thereby improving medical accessibility and reducing the burden on healthcare professionals.
Some studies have indicated that ChatGPT achieves higher levels of satisfaction in counseling compared to human healthcare professionals.
Additionally, research has shown that ChatGPT's performance in answering objective structured clinical examination questions is comparable to that of typical medical students.
However, in both scenarios, it still requires editing by professionals before being used.
Moreover, a recent meta-analysis evaluating ChatGPT's ability in various types of medical exams revealed inconsistent results.
Before its application and actual integration into clinical practice, the investigators need to comprehend the advantages, disadvantages, and relevant limitations of ChatGPT in the field of medical communication.
This study aims to simulate virtual consultations between ChatGPT, acting as a health professional, and study participants, serving as patients.
It will evaluate the participants' satisfaction with the virtual consultation questions, categorized by different levels of cognition through Bloom's Taxonomy.
This study plans to recruit medical professionals, healthcare-related professionals, medical students from National Taiwan University Hospital, and the general public.
Two researchers will select 20 questions from the USMLE step 3 practice tests and the second stage of the Taiwan Medical Licensing Examination.
These questions will be categorized into different levels of cognition based on knowledge, comprehension, application, analysis, synthesis, or evaluation.
ChatGPT 3.5 and 4.0 will answer these 20 questions without specifying the question's level of cognition.
Each participant will review the answers to these 20 questions and assign a satisfaction score based on the appropriateness of each answer.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
120
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Taipei, Taiwan, 100
- National Taiwan University
-
Contact:
- Kuanju Huang, MS
- Phone Number: 63413 +886-5-5323911
- Email: Y06058@ms1.ylh.gov.tw
-
Contact:
- Kuanju Huang
- Phone Number: +886-972655731
- Email: restroomer@icloud.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
The medical professionals, healthcare-related professionals, and medical students refer to attending physician, medical radiation technologist from National Taiwan University Hospital, and medical students from National Taiwan University College of Medicine, respectively.
The general public refer to volunteers from Taiwan Emergency Medical Technician Association.
Description
Inclusion Criteria:
National Taiwan University Hospital
- Medical professionals
- Healthcare-related professionals
- Medical students
Taiwan Emergency Medical Technician Association.
- Volunteers
Exclusion Criteria:
- N/A.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Medical professionals
Attending physicians of National Taiwan University Hospital
|
Participants will assign a satisfaction score based on the appropriateness of each answer.
|
Healthcare-related professionals
Medical Radiation Technologist of National Taiwan University Hospital
|
Participants will assign a satisfaction score based on the appropriateness of each answer.
|
Medical students
Medical students of National Taiwan University College of Medicine who have passed the first stage of Taiwan Medical Licencing Exam.
|
Participants will assign a satisfaction score based on the appropriateness of each answer.
|
General public
Volunteers from Taiwan Emergency Medical Technician Association
|
Participants will assign a satisfaction score based on the appropriateness of each answer.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Correlation between satisfaction and Bloom's taxonomy
Time Frame: baseline (at completion of study questionnaire)
|
Divided by the four participant groups
|
baseline (at completion of study questionnaire)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Correctness of answers
Time Frame: baseline (at completion of study questionnaire)
|
Answers from ChatGPT 3.5/4.0
and the answers provided by Medical Licencing Exam institutions
|
baseline (at completion of study questionnaire)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
February 1, 2024
Primary Completion (Estimated)
June 1, 2024
Study Completion (Estimated)
June 1, 2024
Study Registration Dates
First Submitted
January 29, 2024
First Submitted That Met QC Criteria
February 6, 2024
First Posted (Actual)
February 8, 2024
Study Record Updates
Last Update Posted (Actual)
February 16, 2024
Last Update Submitted That Met QC Criteria
February 14, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 202308059RINB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Data would be shared by request.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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