Usability user testing of the Easy-EyeFM AI platform

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500096168

Enrollment

Unknown

Registered

2025-01-20

Start date

2025-01-26

Completion date

Unknown

Last updated

2025-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ocular Diseases

Interventions

Group A:Firstly test Easy-EyeFM, and after completing the Easy-EyeFM test, then test AutoML after an appropriate washout period.

Group B:In reverse order to group A, testing AutoML first, and after completing the test and undergoing a washout period, testing Easy-EyeFM.

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Medical students or doctors 2. Have enough time to participate in this program, about 1 hour continuous assessment 3. Agree to sign the informed consent form

Exclusion criteria

Exclusion criteria: 1. Poor computer and mobile phone use and reading ability 2. Poor language expression or dialect category is not included in the speech recognition function of the platform

Design outcomes

Primary

Measure	Time frame
System Usability Scale;	—

Secondary

Measure	Time frame
Usage Time;Assistance Requests;	—

Countries

China

Contacts

Public ContactWong Tien Yin

Tsinghua University

wongtienyin@tsinghua.edu.cn+86 151 0100 3732

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026