NCT07301892

Brief Summary

Generative AI (GenAI) based on large language models (LLMs) is expected to improve the diagnosis and treatment of autoimmune diseases. We are studying how GenAI may affect the diagnosis of various complications of rheumatoid arthritis (RA). In a retrospective study using RA patients' EHR records, we will quantify physician adoption of GenAI predictions for RA complications and co-existing diseases. In a prospective observational study, we will assess the feasibility of using GenAI predictions as additional clinical information to help physicians make more complete diagnoses of RA complications and co-existing diseases, including complex, uncommon, or rare conditions.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
1mo left

Started Oct 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

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 Progress90%
Oct 2025Jun 2026

First Submitted

Initial submission to the registry

September 28, 2025

Completed
3 days until next milestone

Study Start

First participant enrolled

October 1, 2025

Completed
3 months until next milestone

First Posted

Study publicly available on registry

December 24, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2026

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Expected
Last Updated

December 24, 2025

Status Verified

December 1, 2025

Enrollment Period

4 months

First QC Date

September 28, 2025

Last Update Submit

December 22, 2025

Conditions

Keywords

Rheumatoid Arthritisgenerative AIlarge language modelRheumatoid arthritis complications

Outcome Measures

Primary Outcomes (1)

  • Will physicians adopt GenAI predictions in diagnosing RA complications?

    In the routine care workflow, large language models (LLMs) are used to predict potential RA complications for each de-identified patient case and generate an AI report listing possible complications and co-existing diseases. Additional diagnostic tests are suggested to verify the predicted conditions. After reviewing the AI report, physicians immediately evaluate each disease prediction using a 5-point Likert scale (1 = complete disagreement; 2 = disagreement; 3 = neutral; 4 = agreement; 5 = complete agreement). The mean score is calculated as a measure of perceived prediction accuracy. Physicians also indicate whether each specific disease prediction could potentially be adopted or used to assist differential diagnosis (binary: 0 or 1). The percentage of positive adoption responses is calculated as a measure of potential adoption rate, or adoptability.

    Immediately after reviewing patient AI report on the day of admission.

Secondary Outcomes (1)

  • To what extent are RA complication diagnoses actually affected by GenAI predictions?

    Immediately after making the final diagnosis at discharge.

Study Arms (1)

RA patient group using generative AI prediction reports

Inpatients newly diagnosed with rheumatoid arthritis in our rheumatology department between October 1, 2025, and June 2026 will be recruited for the study. Physicians will use GenAI predictions of potential RA complications and co-existing diseases, together with confirmatory diagnostic tests, as additional inputs in the differential diagnosis process.

Other: Generative AI prediction report for RA complications

Interventions

Generative AI based on multiple large language models (LLMs) is used to predict potential complications and co-existing diseases in patients with rheumatoid arthritis using EHR data available at admission. Physicians use these AI predictions as additional information to adjust their diagnostic plans during differential diagnosis. The impact of this intervention on the final diagnoses at discharge will be measured. Before the prospective study, the adoptability of the generative AI prediction reports will be validated using EHR records from retrospective RA patients.

RA patient group using generative AI prediction reports

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult male and female RA inpatients admitted to our Rheumatology Department who fulfill the 2010 American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) classification and diagnostic criteria for rheumatoid arthritis.

You may qualify if:

  • Patients with an initial diagnosis of rheumatoid arthritis (RA).
  • All real-world RA inpatients admitted to our department.
  • Admission occurring within the real-world data study period.

You may not qualify if:

  • Patients subsequently confirmed not to have RA during the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

Beijing, Beijing Municipality, 100053, China

RECRUITING

Related Links

MeSH Terms

Conditions

Arthritis, RheumatoidOsteoporosisOsteoarthritisLung Diseases, InterstitialThyroid DiseasesCardiovascular DiseasesSjogren's SyndromeDigestive System DiseasesVasculitisAmyloidosisPeripheral Nervous System DiseasesThrombosis

Condition Hierarchy (Ancestors)

ArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic DiseasesConnective Tissue DiseasesSkin and Connective Tissue DiseasesAutoimmune DiseasesImmune System DiseasesBone Diseases, MetabolicBone DiseasesMetabolic DiseasesNutritional and Metabolic DiseasesLung DiseasesRespiratory Tract DiseasesEndocrine System DiseasesXerostomiaSalivary Gland DiseasesMouth DiseasesStomatognathic DiseasesDry Eye SyndromesLacrimal Apparatus DiseasesEye DiseasesVascular DiseasesProteostasis DeficienciesNeuromuscular DiseasesNervous System DiseasesEmbolism and Thrombosis

Central Study Contacts

Quan Jiang Guang'anmen Hospital, China Academy of Chinese Medical Science

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Director of the Rheumatology Department

Study Record Dates

First Submitted

September 28, 2025

First Posted

December 24, 2025

Study Start

October 1, 2025

Primary Completion

February 1, 2026

Study Completion (Estimated)

June 1, 2026

Last Updated

December 24, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Locations