Validation of the Accuracy of an AI-Based System for Diagnosing Anxiety Disorders
Accuracy of an Artificial Intelligence-Based System for Diagnosing Anxiety Disorders: A Paired Comparison With Psychiatrist Clinical Diagnoses
1 other identifier
observational
100
1 country
1
Brief Summary
The trial aimed to evaluate the efficacy of an artificial intelligence-based system for diagnosing anxiety disorders. Specifically, it sought to determine whether the system's assessment validity is non-inferior to that of psychiatric specialists.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Feb 2026
Shorter than P25 for all trials
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
November 17, 2025
CompletedFirst Posted
Study publicly available on registry
December 31, 2025
CompletedStudy Start
First participant enrolled
February 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 15, 2026
CompletedDecember 31, 2025
August 1, 2025
1 month
November 17, 2025
December 29, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Diagnostic Accuracy (Sensitivity, Specificity, and Area Under the Curve) of the AI-Based Screening System for Anxiety Disorders
In this study, the evaluation results of the subjects were taken as the gold standard based on the diagnostic conclusions of psychiatrists. The screening results of the aided-diagnostic system were compared with the diagnostic conclusions of the psychiatrists to verify the screening effectiveness of this system. Sensitivity : Calculated as \[True Positives / (True Positives + False Negatives)\], evaluating the AI system's ability to correctly identify patients with anxiety. Specificity : Calculated as \[True Negatives / (True Negatives + False Positives)\], evaluating the AI system's ability to correctly exclude non-anxious individuals.Area Under the Receiver Operating Characteristic Curve (AUC), which comprehensively evaluates the diagnostic discriminative power of the system by plotting sensitivity versus 1-specificity across different decision thresholds and calculating the AUC value .
through study completion, an average of 1 week
Eligibility Criteria
The study includes the subjects with anxiety disorders and healthy control into the experiment. Anxious individuals for the study will be recruited from actual outpatient patients at the Shanghai Mental Health Center. The healthy control will be recruited through public advertisements, both online and offline. Psychiatrists will be recruited through public advertisements by the Shanghai Mental Health Center.
You may qualify if:
- In accordance with ICD-11 for Anxiety Disorders;
- Between the ages of 18-60;
- Ability to use computers or smartphone;
- Native Chinese speaker;
- Signing informed consent.
You may not qualify if:
- With severe psychiatric symptoms requiring hospitalization, or unable to complete the required assessment and treatment;
- With a high risk of suicide or self-injury;
- With severe physical diseases, central nervous system diseases, or substance abuse;
- With intellectual, visual, or auditory impairments that affect their ability to interact with aided-diagnostic systems.
- Health Control
- Not meet ICD-11 criteria for Mental Disorders;
- Between the ages of 18-60;
- Ability to use computers or smartphone;
- Native Chinese speaker;
- Signing informed consent.
- With mental illness, or unable to complete the required assessment and treatment;
- With severe physical diseases, central nervous system diseases, or substance abuse;
- With intellectual, visual, or auditory impairments that affect their ability to interact with aided-diagnostic systems.
- Psychiatrist
- Over 18 years old;
- +4 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Shanghai Mental Health Center
Shanghai, Shanghai Municipality, 200030, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 17, 2025
First Posted
December 31, 2025
Study Start
February 1, 2026
Primary Completion
March 15, 2026
Study Completion
March 15, 2026
Last Updated
December 31, 2025
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share