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临床试验/NCT01027312
NCT01027312已完成不适用

Reproducibility and Clinical Usefulness of AARV (Assessment of Ability Related to Vision)

Wills Eye0 个研究点目标入组 121 人开始时间: 2008年2月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
121
主要终点
the reproducibility of AARV, and its relationship to standard clinical tests

研究概览

简要总结

To determine the clinical usefulness of a refined third-generation instrument - The Assessment of Ability Related to Vision (AARV) in establishing the amount of disability, charting the detrimental effects of progressive disease and establishing the beneficial effects of treatment

详细描述

This research study is designed to test the usefulness and repeatability of testing how much disability is caused by vision loss due to glaucoma. We are recruiting 100 patients with glaucoma and 20 healthy (have no eye disease) individuals to be enrolled in this study. The healthy study participants will be enrolled in order to describe how a healthy individual will perform on the test designed to assess one's performance when completing ten activities of daily living.

Clinical testing will be conducted by binocular and monocular visual fields, contrast sensitivity and visual acuity. The NEI-VFQ 15 Quality of Life Questionnaire will be used to measure patients perception of how well they are doing.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • All patients 18 yrs of age and older
  • must understand and respond to spoken English and be fully literate.

排除标准

  • Patients with significant neurological problems (like Parkinson's disease), motor problems (like arthritis) or other significant illnesses that may prevent them from completing the testing involved in the study (like advanced heart failure).
  • Patients who have received training related to low vision.

结局指标

主要结局

the reproducibility of AARV, and its relationship to standard clinical tests

时间窗: Day 1, 1 week, 6 months, 1 year

次要结局

  • A better estimate of the reproducibility of standard clinical tests.(Day 1, 1 week, 6 months, 1 year)

研究者

发起方
Wills Eye
申办方类型
Other
责任方
Principal Investigator
主要研究者

George L. Spaeth MD

Principal Investigator

Wills Eye

相似试验

Assessment of Ability Related to Vision | 临床试验