Improving the Reliability of LLMs as Medical Assistants for the General Public
LAMP-1
1 other identifier
interventional
525
1 country
1
Brief Summary
This study will evaluate whether three-minute six-dimensions education(3M-6D education) can improve the reliability of large language models as medical assistants for the general public. Participants will be randomly assigned to receive or not receive 3M-6D education and then use ChatGPT, Gemini, or non-AI information resources. The study will assess relevant condition identification, disposition concordance, red-flag identification, and NASA-TLX score.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jul 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 11, 2026
CompletedFirst Posted
Study publicly available on registry
June 16, 2026
CompletedStudy Start
First participant enrolled
July 3, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 20, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
July 20, 2026
CompletedJuly 7, 2026
July 1, 2026
17 days
June 11, 2026
July 3, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Relevant conditions identification of the 3M-6D education GPT group compared with the GPT group
Relevant conditions identification is defined as the proportion of participants whose final response includes the expert-defined final diagnosis or a relevant differential diagnosis.
1 hour.
Disposition concordance of the 3M-6D education GPT group compared with the GPT group
Disposition concordance is defined as the proportion of participants whose final care recommendation matches the expert-defined level. The five levels are self-care, routine outpatient care, urgent outpatient care, emergency department visit, and emergency medical services.
1 hour.
Relevant conditions identification of the 3M-6D education Gemini group compared with the Gemini group
1 hour.
Disposition concordance of the 3M-6D education Gemini group compared with the Gemini group
1 hour.
Secondary Outcomes (16)
Relevant conditions identification of the 3M-6D education GPT group compared with the control group
1 hour.
Relevant conditions identification of the 3M-6D education Gemini group compared with the control group
1 hour.
Disposition concordance of the 3M-6D education GPT group compared with the control group
1 hour.
Disposition concordance of the 3M-6D education Gemini group compared with the control group
1 hour.
Red-flag identification in the 3M-6D education GPT group compared with the GPT group
1 hour.
- +11 more secondary outcomes
Other Outcomes (8)
Failure to identify red flags in the 3M-6D education GPT group compared with the GPT group
1 hour.
Failure to identify red flags in the 3M-6D education GPT group compared with the control group
1 hour.
Failure to identify red flags in the 3M-6D education Gemini group compared with the Gemini group
1 hour.
- +5 more other outcomes
Study Arms (5)
3M-6D education GPT Group
EXPERIMENTALParticipants will first be trained in 3M-6D education, then use ChatGPT to complete a consultation task in unrestricted natural language in approximately 10 minutes.
3M-6D education Gemini Group
EXPERIMENTALParticipants will first be trained in 3M-6D education, then use Gemini to complete a consultation task in unrestricted natural language in approximately 10 minutes.
GPT Group
ACTIVE COMPARATORParticipants will use ChatGPT to complete a consultation task in unrestricted natural language in approximately 10 minutes.
Gemini Group
ACTIVE COMPARATORParticipants will use Gemini to complete a consultation task in unrestricted natural language in approximately 10 minutes.
Control group
NO INTERVENTIONParticipants will use non-AI tools such as internet searches and medical websites to complete a consultation task in unrestricted natural language in approximately 10 minutes.
Interventions
3M-6D education is designed based on Cognitive Load Theory to reduce the cognitive burden on patients during medical interactions with AI and to improve the clarity and completeness of symptom reporting. Guided by cognitive load theory and the natural process physicians use to take medical histories, the investigators identified candidate information dimensions and developed a structured expression framework with six dimensions for public health queries through a Delphi expert consensus process. Participants were instructed to use the framework to describe their symptoms across these six dimensions; this process can typically be completed within three minutes, so the investigators call this approach three minutes six dimensions education (3M-6D education).
Participants use ChatGPT to complete a standardized simulated clinical scenarios in unrestricted natural language.
Participants use Gemini to complete a standardized simulated clinical scenarios in unrestricted natural language.
Eligibility Criteria
You may qualify if:
- Age 18 years or greater, male or female;
- Completed primary school or higher education;
- Able to use a smartphone or computer to complete online interaction;
- No history of acute ischemic stroke, systemic lupus erythematosus, gastric ulcer, pneumonia, acute cardiac infarction, urinary tract infection, uterine fibroids, diabetes, osteoarthritis, or migraine.
- Able to understand and comply with study procedures and to provide written informed consent.
You may not qualify if:
- Currently or previously employed as a healthcare worker;
- Previously received systematic medical training;
- Currently involved in concurrent research that may interfere with the results of the present trial;
- The investigator considered that the participant had other conditions that might affect compliance or preclude participation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Capital Medical Universitylead
- Xuanwu Hospital, Beijingcollaborator
Study Sites (1)
Beijing Ctiy
Beijing, Beijing Municipality, China
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Outcome assessors will be blinded to group assignment when evaluating participants' outcomes. Group information will be removed from the outcomes before assessment.
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
June 11, 2026
First Posted
June 16, 2026
Study Start
July 3, 2026
Primary Completion
July 20, 2026
Study Completion
July 20, 2026
Last Updated
July 7, 2026
Record last verified: 2026-07