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Condition Category ConcordanceLAMP-2NCT07844044

3M-6D Educational Intervention to Improve LLM-Assisted Medical Consultation in Neurology Outpatients

A study testing three minutes six dimensions education and ChatGPT in people with Condition Category Concordance, run by Capital Medical University at 4 sites in China.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This study will evaluate whether three-minute six-dimension education (3M-6D education) can improve the reliability of large language models (LLMs) as medical assistants in neurology outpatients. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Condition Category Concordance
What is being tested?
three minutes six dimensions education and ChatGPT
Could I receive a placebo?
No, everyone receives an active treatment
How many people
396 participants
Where
4 sitesChina
Study dates
30 Sep 2026to 31 Oct 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Aged ≥ 18 years
  • Completed primary school or higher education;
  • Able to use a smartphone or computer to complete online interactions;
  • Presenting to the hospital for neurological symptoms;
  • This visit is the first consultation for the current symptoms;
  • Has not used AI tools or online resources to assess the current condition prior to this visit;
  • Able to understand and comply with study procedures and to provide written informed consent.

Who cannot join

  • Currently or previously employed as a healthcare worker;
  • Previously received systematic medical training;
  • Condition requires emergency care;
  • Participating in another clinical trial that may affect this study's outcomes;
  • Any other condition the investigators consider unsuitable for enrollment or likely to interfere with trial results.

Trial locations and contacts

4 sites in 1 country. Contact the study team or a site near you to ask about taking part.

China4 sites, 4 recruiting
  • Aerospace Center Hospital

    Beijing, Beijing Municipality

    Hui Lu, 86+18844815888, gyibngc1@163.com

    Recruiting
  • Huimin Hospital

    Beijing, Beijing Municipality

    Peng Yu, 86+13500129973, luojiaqi1008@126.com

    Recruiting
  • Mentougou District Hospital

    Beijing, Beijing Municipality

    Yanbo Zhao, 86+15097941106, a15097941106@163.com

    Recruiting
  • Xuanwu Hospita

    Beijing

    Chuanjie Wu, MD, 01083199439, wuchuanjie@ccmu.edu.cn

    Xunming Ji, PhD/MD, 01083198962, jixm@ccmu.edu.cn

    Recruiting

Other trials in China

About this study

Official title: Improving the Reliability of LLM-Assisted Medical Consultation in Neurology Outpatients Through a 3M-6D Structured Educational Intervention: a Randomized Controlled Trial

This study will evaluate whether three-minute six-dimension education (3M-6D education) can improve the reliability of large language models (LLMs) as medical assistants in neurology outpatients. Participants will be randomly assigned to receive or not receive 3M-6D education before using ChatGPT for medical consultation.

Read the detailed description

This randomized, controlled clinical trial will evaluate whether three-minute six-dimension education (3M-6D education) can improve the reliability of large language models (LLMs) as medical assistants in neurology outpatients.

Eligible participants will be randomly assigned in a 1:1 ratio to the 3M-6D education GPT group or the GPT group. Participants in the 3M-6D education GPT group will first receive approximately three minutes of structured education and then use ChatGPT for medical consultation. Participants in the GPT group will directly use ChatGPT for medical consultation without receiving 3M-6D education. All participants will communicate with ChatGPT using unrestricted natural language.

The 3M-6D education is a structured framework designed to help patients describe their symptoms and provide more complete medical information during LLM-assisted medical consultation. It guides patients to describe six key dimensions.

Being tested
three minutes six dimensions education, ChatGPT
Keywords
3M-6D education, Large Language Models, Cognitive Load Theory, neurology outpatients, condition category concordance

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • three minutes six dimensions educationBehavioural

    Also called 3M-6D education

    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).

  • ChatGPTOther

    Participants use ChatGPT to complete a consultation task in unrestricted natural language.

Study groups in NCT07844044
Study groupRoleWhat they receive
3M-6D education GPT GroupExperimentalParticipants will first be trained in 3M-6D education, then use ChatGPT to complete a consultation task in unrestricted natural language.
Receives: Behavioral: three minutes six dimensions education; Other: ChatGPT
GPT GroupActive comparatorParticipants will use ChatGPT to complete a consultation task in unrestricted natural language.
Receives: Other: ChatGPT

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Condition category concordance

    The primary outcome of the LAMP-2 trial was condition category concordance, defined as at least one condition listed in a participant's response falling within the same prespecified neurological disease category as the final reference diagnosis.

    Measured: 30 days

Secondary outcomes (5)
  1. Preparation for Decision Making Scale

    Preparation for Decision Making Scale (PrepDM) is a self-reported scale used to assess participants' readiness for medical decision-making after medical consultation. The scale includes 10 items. Each item is scored from 1 to 5 using a 5-point Likert scale. The total score is the mean of the 10 items. Higher scores indicate greater preparation for decision-making.

    Measured: Within 1 hour

  2. Consultation duration

    Consultation duration is defined as the time from the patient's arrival at the outpatient clinic to the completion of the outpatient visit.

    Measured: Within 1 hour

  3. Patient satisfaction with this consultation

    Patient satisfaction is a self-reported measure used to assess participants' satisfaction with the outpatient visit. Higher scores indicate greater satisfaction.

    Measured: Within 1 hour after the outpatient visit

  4. Red-flag identification

    Red-flag identification is defined as the proportion of participants whose final response includes the key warning signs predefined by experts for the participant's presenting symptoms.

    Measured: Within 1 hour after the outpatient visit

  5. NASA-TLX score

    NASA-TLX score is a self-reported task-load score measured immediately after the LLM-assisted medical consultation with ChatGPT. It includes six domains: mental demand, physical demand, temporal demand, effort, frustration, and performance. Each domain is scored from 0 to 100. The total score is the mean of the six domains. Higher scores indicate greater perceived task load.

    Measured: Within 1 hour

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Sep 2026
  2. Study start30 Sep 2026
  3. Primary completion31 Oct 2026 (estimated)
  4. Study completion31 Oct 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Model description
Participants will be randomly assigned in a 1:1 ratio to the 3M-6D education GPT group or the GPT group.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
396 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07844044
Sponsor's protocol ID
LAMP-2
Acronym
LAMP-2
Status last verified
Sep 2026
First submitted
22 Sep 2026
Last updated
2 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing three minutes six dimensions education and ChatGPT in people with Condition Category Concordance, run by Capital Medical University at 4 sites in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 2 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 4 sites in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Xunming Ji (01083198962, jixm@ccmu.edu.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Condition category concordance (time frame: 30 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Oct 2026.

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