SLO-guided eye movements training in the presence of a central scotoma

Not Applicable

• Conditions: Healthy volunteers; H53.4; Visual field defects

• Registration Number: DRKS00021645
• Lead Sponsor: Centro Lions di Riabilitazione Visiva e Microperimetria (CRIM), Marzana, Verona, Italy

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2018-07-16
• Study Start: 2020-05-14
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

presence of a bilateral dense central scotoma within 2 degrees of the fovea
- consent to study participation
- ages 18 - 99 years

Exclusion Criteria

- major cognitive impairments that could impede participation in the study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The outcome measures are the percentage of targets found and target detection rate (TDR) in the three phase task

Secondary Outcome Measures

Name	Time	Method
- Visual acuity of the subjects<br>- Fixation stability<br>