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Visual Discrimination of Morphological Variations in Corneal Endothelial Graft Markers: A Psychophysical Assessment of Healthcare Staff

Visual Discrimination of Morphological Variations in Corneal Endothelial Graft Markers: A Psychophysical Assessment of Healthcare Staff

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113594
Enrollment
Unknown
Registered
2025-12-01
Start date
2025-12-15
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Visual Discrimination

Interventions

Observation group:None

Sponsors

Chengdu Aidi Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Age between 18 and 60 years old, regardless of gender; 2. Visual acuity or corrected visual acuity >=1.0 (assessed using the international standard visual acuity chart); 3. Normal color vision (evaluated with Ishihara color vision test charts); 4. No prior cognitive experience related to the morphology of corneal endothelial graft markers (screened via a preliminary questionnaire); 5. Voluntary participation in the study and signing of a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. History of neurological diseases (e.g., stroke, Parkinson's disease) or organic ocular diseases (e.g., glaucoma, retinal diseases) that may affect visual cognitive function; 2. Taking drugs that affect attention or reaction ability (e.g., sedative-hypnotic drugs) within 24 hours prior to the test; 3. Confirmed diagnosis of mental or psychological disorders (e.g., anxiety disorder, depressive disorder) in accordance with the diagnostic criteria of the International Classification of Diseases, 11th Revision (ICD-11); 4. Presence of significant memory impairment (assessed using the Mini-Mental State Examination (MMSE)); 5. Experiencing major life events (e.g., the death of a loved one, severe illness) or traumatic stress within 1 month prior to the test; 6. Other conditions deemed unsuitable for study participation as judged by the researchers (e.g., physical discomfort during the test).

Design outcomes

Primary

MeasureTime frame
The average accuracy rate;Average relative response time ;

Secondary

MeasureTime frame
Types and distribution of misjudgments: Direction confusion (e.g., misjudging the upright F-type as the inverted direction), morphological misidentification (e.g., misidentifying the F-type as the S-type), and no clear misjudgment.;

Countries

China

Contacts

Public ContactXaoming Yao

Chengdu Aidi Eye Hospital

xmyeye@163.com+86 139 0297 8492

Outcome results

None listed

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