Usability User Testing of the Easy-EyeFM AI Platform

NCT06834906 | Recruiting

• 1 other identifier: Easy-EyeFM
• Study Type: interventional
• Target: 84
• Locations: 1 country
• Sites: 1

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.

Conditions

Ocular Diseases

Outcome Measures

Primary Outcomes (1)

• System Usability Scale

  Minimum Value: 0 Maximum Value: 100 Higher scores indicate a better outcome, meaning higher system usability.

  1 day

Secondary Outcomes (2)

• Usage Time

  1 day

• Users Assistance Requests Times

  1 day

Study Arms (2)

group A

EXPERIMENTAL

Diagnostic Test: EasyEyeFM-AutoML-AI-platform test

group B

EXPERIMENTAL

Diagnostic Test: AutoML-EasyEyeFM-AI-platform test

Interventions

EasyEyeFM-AutoML-AI-platform test DIAGNOSTIC_TEST

AI platforms using

group A

AutoML-EasyEyeFM-AI-platform test DIAGNOSTIC_TEST

AI-platform using

group B

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

• 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

Sponsors & Collaborators

• Tsinghua University: lead
• First Hospital of Tsinghua University: collaborator
• Beijing Tsinghua Changgeng Hospital: collaborator
• Augenarzt-Praxisgemeinschaft Gutblick AG: collaborator
• Sankara Nethralaya: collaborator
• Department of Medical Services Ministry of Public Health of Thailand: collaborator
• Moorfields Eye Hospital NHS Foundation Trust: collaborator
• Pomeranian Hospitals: collaborator
• Shanghai Health and Medical Center: collaborator
• Hong Kong Eye Hospital: collaborator
• Royal Victoria Eye and Ear Hospital: collaborator
• Hanyang University Guri Hospitall: collaborator
• Alshifa Trust Eye Hospital: collaborator
• Korle-Bu Teaching Hospital, Accra, Ghana: collaborator
• Nippon Medical School Tama Nagayama Hospital: collaborator

Study Sites (1)

Tsinghua University

Beijing, China

RECRUITING

Study Officials

• Tien Yin Wong

  Tsinghua University

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Jinyuan Wang

CONTACT

086-15801191316; jinyuanwang@tsinghua.edu.cn

Hongqiu Wang

CONTACT

hwang007@connect.hkust-gz.edu.cn

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: OTHER
• Intervention Model: CROSSOVER
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: February 9, 2025
• First Posted: February 19, 2025
• Study Start: January 26, 2025
• Primary Completion: September 1, 2025
• Study Completion: September 1, 2025
• Last Updated: August 15, 2025

Record last verified: 2025-01

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)