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EyeCU Mobile Application for Glaucoma
N/A
Waitlist Available
Research Sponsored by Bronx-Lebanon Hospital Center Health Care System
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
- Patients with a clinical diagnosis of glaucoma on medical therapy for at least 4 months
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up before and 6 months after intervention
Awards & highlights
Study Summary
This trial is testing an augmented reality mobile phone application, EyeCU, to see if it can help people with glaucoma better understand the disease and its progression. The app is available in English and Spanish on Android and Apple app store.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ before and 6 months after intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~before and 6 months after intervention
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Follow Up Adherence
Change in Medication Adherence
Change in Questionnaire Scores
Trial Design
1Treatment groups
Experimental Treatment
Group I: EyeCU AppExperimental Treatment1 Intervention
Augmented reality mobile application called "EyeCU" which simulates glaucoma progression and enhances understanding about the disease and its course. It is a bilingual (English/Spanish) application that is free-to-download on the Android and Apple app store. It will be delivered on a hospital owned tablet device and patients will be instructed to complete two sections, taking approximately 10 minutes.
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Who is running the clinical trial?
Bronx-Lebanon Hospital Center Health Care SystemLead Sponsor
7 Previous Clinical Trials
1,515 Total Patients Enrolled
EyeCU GroupUNKNOWN
VISREUNKNOWN
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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