跳至主要内容
临床试验/NCT06670989
NCT06670989进行中(未招募)不适用

Training to Modify Fixational Eye Movements for Optimizing Visual Performance

National Eye Institute (NEI)2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
30
试验地点
2
主要终点
Fixation stability

研究概览

简要总结

People with central vision loss almost all have exaggerated fixational eye movements when compared with people with normal vision (e.g. larger amplitudes of microsaccades and ocular drifts). Central vision loss primarily results from eye diseases or disorders that affect the macular region of the retina, such as age-related macular degeneration (AMD) and Stargardt disease. The clinical wisdom is that exaggerated fixational eye movements are detrimental to vision. This forms the basis of the increasing number of clinical trials that use fixation stability (variability of eye positions during fixation) as an outcome measure to evaluate the effectiveness of interventions on age-related macular degeneration or other retinal diseases, despite the lack of causal evidence supporting or refuting a relationship between fixational eye movements and functional vision. If excessive fixational eye movements are indeed detrimental to vision for people with central vision loss, can we reduce the amount of their fixational eye movements, thus improve their fixation stability? And if so, does that lead to improved functional vision? The goal of this study is to examine the hypothesis that retinal image motion due to abnormal fixational eye movements can be modified through fixation training, with accompanied improvements in functional vision as a result.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
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

  • Participants with normal vision:
  • age 18 or above
  • best corrected visual acuity of at least 20/20 in each eye
  • cataracts, if present, must be minimal (grade 1 or below according to the Lens Opacity Classification System)
  • normal contrast sensitivity for their ages
  • stereoacuity at least 40 seconds of arc
  • no history or signs of any retinal diseases
  • Participants with macular disorders:
  • age 18 or above
  • macular disorder present in both eyes
  • presence of at least one scotoma within the central 5 degrees of the visual field and with best corrected visual acuity of at least 20/400 in the better-seeing eye
  • no foveal island of vision left (i.e. absolute scotoma must include the foveal area)
  • cataracts, if present, must be grade 2 or lower according to the Lens Opacity Classification System II

排除标准

  • Participants with normal vision:
  • younger than 18 years of age
  • best corrected visual acuity worse than 20/20 in each eye
  • cataracts worse than grade 1 according to the Lens Opacity Classification System II
  • abnormal contrast sensitivity for their ages
  • stereoacuity worse than 40 seconds of arc
  • history or signs of any retinal diseases
  • Participants with macular disorders:
  • younger than 18 years of age
  • macular disorder absent in at least one eye
  • no scotoma within the central 5 degrees of the visual field in the better-seeing eye
  • best corrected visual acuity of worse than 20/400 in the better-seeing eye
  • foveal island of vision
  • cataracts worse than grade 2 according to the Lens Opacity Classification System II

结局指标

主要结局

Fixation stability

时间窗: Data will be collected immediately before (within 1 hour) the first training session and immediately after (within 1 hour) the last training session. Data will be reported when analysis is completed for all participants (target date: by June 2025).

Eye positions measured while participants looked at a stationary fixation target for 10 seconds, quantified as the area that captures 68% of eye positions (unit: deg\^2).

次要结局

  • Visual acuity(Data will be collected immediately before (within 1 hour) the first training session and immediately after (within 1 hour) the last training session. Data will be reported when analysis is completed for all participants (target date: by June 2025).)
  • Contrast sensitivity(Data will be collected immediately before (within 1 hour) the first training session and immediately after (within 1 hour) the last training session. Data will be reported when analysis is completed for all participants (target date: by June 2025).)
  • Reading performance: Maximum reading speed(Data will be collected immediately before (within 1 hour) the first training session and immediately after (within 1 hour) the last training session. Data will be reported when analysis is completed for all participants (target date: by June 2025).)
  • Reading performance: critical print size(Data will be collected immediately before (within 1 hour) the first training session and immediately after (within 1 hour) the last training session. Data will be reported when analysis is completed for all participants (target date: by June 2025).)
  • Orientation judgement accuracy: low spatial-frequency(Data will be collected immediately before (within 1 hour) the first training session and immediately after (within 1 hour) the last training session. Data will be reported when analysis is completed for all participants (target date: by June 2025).)
  • Orientation judgement accuracy: high spatial-frequency(Data will be collected immediately before (within 1 hour) the first training session and immediately after (within 1 hour) the last training session. Data will be reported when analysis is completed for all participants (target date: by June 2025).)
  • Characteristics of fixational eye movements: microsaccade rate(Data will be collected immediately before (within 1 hour) the first training session and immediately after (within 1 hour) the last training session. Data will be reported when analysis is completed for all participants (target date: by June 2025).)
  • Characteristics of fixational eye movements: microsaccade amplitude(Data will be collected immediately before (within 1 hour) the first training session and immediately after (within 1 hour) the last training session. Data will be reported when analysis is completed for all participants (target date: by June 2025).)

研究者

申办方类型
Nih
责任方
Principal Investigator
主要研究者

Susana Chung

Professor

National Eye Institute (NEI)

研究点 (2)

Loading locations...

相似试验