Human Performance Evaluation of a Digital Visual Acuity Device: Visual Acuity-001
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- Mayo Clinic
- 入组人数
- 150
- 试验地点
- 1
- 主要终点
- Number of times the experimental device when measuring visual acuity agreed with standard visual acuity measurements
研究概览
简要总结
The purpose of this research is to validate and determine the accuracy of the experimental device when measuring visual acuity versus our standard visual acuity measurements and to gather voice recordings of letters to help build a special system that recognizes spoken letters.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Screening
- 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
- 是
入选标准
- •Adult patients (≥ 18 years) who come to Ophthalmology Clinic.
- •Willing and able to provide consent.
排除标准
- •Individuals < 18 years of age.
- •Unable to provide consent.
研究组 & 干预措施
Digital Visual Acuity Test
Subjects for an ophthalmological examination that includes a visual acuity examination at Mayo Clinic in Florida have a digital visual acuity test conducted with the FaceScan device.
干预措施: FaceScan (Device)
结局指标
主要结局
Number of times the experimental device when measuring visual acuity agreed with standard visual acuity measurements
时间窗: Baseline
Number of subjects to have agreement between the visual acuity digital device and the clinical assessment
次要结局
- Voice samples(Baseline)
研究者
Antonio J. Forte
Principal Investigator
Mayo Clinic