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Clinical Trial Summary

The goal of this interventional study is to assess whether an in-office, language-concordant instructional app improves drop regimen recall in a population of glaucoma patients who are on multi-drop regimens. Participants will be divided into two groups -- those who use the app and those who do not. The app will have narrated information regarding the drop regimen, a quiz to test understanding of the regimen, and will enable a graphical printout of the eye drops and schedule. At one month, both groups will be assessed on their eye drop regimen recall.


Clinical Trial Description

Specific Aim: To investigate whether a language-concordant instructional application improves drop regimen recall in population of glaucoma patients at a 1-month follow-up period. App features 1. Pictorial representation of drops (color-coded) and schedule. 2. Quiz to assess understanding of the regimen. 3. Narrated instructions (language-concordant) on how and when (frequency and eye laterality) to take each drop. 4. Graphical print-out of the regimen. Study design 1. Study design: Randomized study, two groups: (1) patients that use the app, and (2) patients that do not use the app. 2. Study population: Inclusion criteria: patients with primary open-angle glaucoma on at least 2 eye drops Exclusion criteria: patients taking additional prescribed eye drops for other eye conditions; patients diagnosed within the last 3 months; patients unable to self-administer eye drops 3. Intervention: Use of an in-office app that has both graphical and verbal (language-concordant) instruction for how to use drops. 4. Main outcome measure: Ability to correctly identify drops/regimen ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06045390
Study type Interventional
Source University of California, San Francisco
Contact Sachin Patel, MD, PhD
Phone 415-353-2800
Email sachin.patel@ucsf.edu
Status Not yet recruiting
Phase N/A
Start date July 1, 2024
Completion date September 1, 2024

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