NCT07844044

Brief 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. Participants will be randomly assigned to receive or not receive 3M-6D education before using ChatGPT for medical consultation.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
396

participants targeted

Target at P75+ for not_applicable

Timeline
1mo left

Started Sep 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

4 active sites

Status
recruiting

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

Study Progress12%
Sep 2026Oct 2026

First Submitted

Initial submission to the registry

September 22, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 28, 2026

Completed
2 days until next milestone

Study Start

First participant enrolled

September 30, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 31, 2026

Last Updated

October 2, 2026

Status Verified

September 1, 2026

Enrollment Period

1 month

First QC Date

September 22, 2026

Last Update Submit

September 29, 2026

Conditions

Keywords

3M-6D educationLarge Language ModelsCognitive Load Theoryneurology outpatientscondition category concordance

Outcome Measures

Primary Outcomes (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.

    30 days

Secondary Outcomes (5)

  • Preparation for Decision Making Scale

    Within 1 hour

  • Consultation duration

    Within 1 hour

  • Patient satisfaction with this consultation

    Within 1 hour after the outpatient visit

  • Red-flag identification

    Within 1 hour after the outpatient visit

  • NASA-TLX score

    Within 1 hour

Study Arms (2)

3M-6D education GPT Group

EXPERIMENTAL

Participants will first be trained in 3M-6D education, then use ChatGPT to complete a consultation task in unrestricted natural language.

Behavioral: three minutes six dimensions educationOther: ChatGPT

GPT Group

ACTIVE COMPARATOR

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

Other: ChatGPT

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).

Also known as: 3M-6D education
3M-6D education GPT Group
ChatGPTOTHER

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

3M-6D education GPT GroupGPT Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (4)

Aerospace Center Hospital

Beijing, Beijing Municipality, China

RECRUITING

Huimin Hospital

Beijing, Beijing Municipality, China

RECRUITING

Mentougou District Hospital

Beijing, Beijing Municipality, China

RECRUITING

Xuanwu Hospita

Beijing, China

RECRUITING

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
Model Details: Participants will be randomly assigned in a 1:1 ratio to the 3M-6D education GPT group or the GPT group.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 22, 2026

First Posted

September 28, 2026

Study Start

September 30, 2026

Primary Completion (Estimated)

October 31, 2026

Study Completion (Estimated)

October 31, 2026

Last Updated

October 2, 2026

Record last verified: 2026-09

Locations