Augmented Reality Mobile Application for Glaucoma Education in the South Bronx

Summary

Participation Requirements

Description

Experimental design: Pilot cohort study Sample size: Initial test population will be confined to 54 patients Proposed study time period: January 2020-July 2021 Data collection: Patient characteristics such as age, sex, ethnicity, preferred language, zip code, employment status, highest educational a...

Experimental design: Pilot cohort study Sample size: Initial test population will be confined to 54 patients Proposed study time period: January 2020-July 2021 Data collection: Patient characteristics such as age, sex, ethnicity, preferred language, zip code, employment status, highest educational attainment, current topical eye medications, Past Ocular History, Past Medical History Recruitment for participation in the study will be performed via leaflet by clinic coordinator during glaucoma clinic registration. Consent will be conducted by clinic coordinator or another member of the research team who is not directly involved in the participant's clinical care. Pre-intervention glaucoma knowledge questionnaire (NEHEP glaucoma knowledge questionnaire) will be given to participants, to be completed on dedicated clinic tablet device. Post-intervention glaucoma knowledge questionnaire (NEHEP glaucoma knowledge questionnaire) will be given to participants, to be completed on dedicated clinic tablet device. Rate of missed glaucoma follow-up appointments before and 6 months after application use will be collected from the electronic medical record. Rate of medication adherence before and 6 months after application use will be collected from the electronic medical record.

Tracking Information