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临床试验/NCT06045390
NCT06045390已完成不适用

Assessing the Effects of an In-office, Language-concordant App on Eye Drop Recall in Patients With Multi-drop Regimens

University of California, San Francisco2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2024年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
2
主要终点
Percentage accuracy of drop regimen recall

研究概览

简要总结

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.

详细描述

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:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients with a diagnosis of glaucoma (any type)
  • drop regimen of at least 2 pressure-lowering drops
  • languages supported at this time: English, Spanish, Cantonese

排除标准

  • concurrent eye conditions necessitating additional eye drops
  • inability to self-administer eye drops
  • inability to engage with app (either visual or other barrier)

结局指标

主要结局

Percentage accuracy of drop regimen recall

时间窗: 1 month follow up from time of intervention

This will be assessed through questions querying which drops the patients are taking, the number of times they are taking each drop, and the laterality of each drop. Each answer/drop will be individual recorded, and then total number of correct answers will be divided by the total number of questions.

次要结局

  • Overall medication adherence, assessed through the modified Morisky Adherence Scale, a widely published scale for general medication adherence(1 month follow up from time of intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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