Usability User Testing of the Easy-EyeFM AI Platform

Not Applicable

Recruiting

• Conditions: Ocular Diseases

• Registration Number: NCT06834906
• Lead Sponsor: Tsinghua University

Brief Summary

Easy-EyeFM is a code-free artificial intelligence platform designed for ophthalmologists to provide diagnostic and treatment recommendations and help doctors develop customized diagnostic models.

This project aims to evaluate the usability and user-friendliness of the Easy-EyeFM platform for physicians. The study will gather feedback from medical professionals to evaluate the intuitiveness and effectiveness of the platform in supporting model customization and medical image analysis tasks.

Subjects will participate in the trial of the Easy-EyeFM platform and the comparison with the existing commercial platform (AutoML) at the appointed time. The researchers will inform subjects of relevant precautions and assist them to read the user manual before the test. Subjects will complete model customization and picture diagnosis within the prescribed test time, and according to the test results, Score the human-computer interaction experience of the AI platform, fill in the questionnaire, and finally complete the evaluation content.

Detailed Description

Not available

Study Timeline

• Status Verified: 2025-01
• Study Start: 2025-01-26
• Study First Submitted: 2025-02-09
• Study First Submitted QC: 2025-02-13
• Study First Posted: 2025-02-19
• Last Update Submitted: 2025-03-14
• Last Update Posted: 2025-03-19
• Primary Completion: 2025-07
• Study Completion: 2026-07

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 72

Inclusion Criteria

• Medical students or doctors
• Have enough time to participate in this program, about 1 hour continuous assessment
• Agree to sign the informed consent form

Exclusion Criteria

• Poor computer and mobile phone use and reading ability
• Poor language expression or dialect category is not included in the speech recognition function of the platform

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Primary Outcome Measures

Name	Time	Method
System Usability Scale	1 day	Minimum Value: 0 Maximum Value: 100 Higher scores indicate a better outcome, meaning higher system usability.

Secondary Outcome Measures

Name	Time	Method
Usage Time	1 day
Users Assistance Requests Times	1 day

Trial Locations

Locations (1)

Tsinghua University; 🇨🇳 Beijing, China