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临床试验/NCT04827147
NCT04827147已完成不适用

Randomized Controlled Multicenter Clinical Trial of Multi-Periscopic Prism Glasses for Homonymous Hemianopia

Massachusetts Eye and Ear Infirmary8 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2023年4月3日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
64
试验地点
8
主要终点
Improvement in Blind-side Detection Rate for Hazards Approaching at a Bearing Angle of 40 Degrees

研究概览

简要总结

This clinical trial will evaluate the efficacy of two types of high-power prism glasses that provide field of view expansion for patients with homonymous hemianopia (the complete loss of half the field of vision on the same side in both eyes).

详细描述

Patients with hemianopic field loss may be unaware of objects in their blind (non-seeing) hemi-field and often experience difficulties with hazards, such as walking into obstacles on the side of the field loss. Prism glasses that provide field of view expansion may be helpful in detecting hazards on the blind side. In this clinical trial, two types of high power prism glasses will be evaluated. A new design of prisms, Multi-Periscopic Prisms (MPP), will be compared to commercially-available permanent Fresnel peripheral prism (FPP) glasses. The extent to which the prismatic devices improve detection of hazards on the side of the field loss and are helpful when walking will be evaluated.

Participants will try each type of prism glasses at home for 4 weeks in counterbalanced order. Prism glasses will be fitted by Low Vision Practitioners at vision rehabilitation clinics. Participants will attend in-office study visits before and after wearing each type of prism glasses. At the in-office visits they will complete a test that involves detecting pedestrian hazards in a video simulating a walk through a busy shopping mall (virtual reality, VR, walking simulator test). In addition, they may be asked to complete questionnaires to record their experiences of using the prism glasses.

After wearing the second pair of prism glasses, participants will be asked to complete a questionnaire comparing the two types of prism glasses and to select their preferred type. A clinical decision will be made as to whether the participant should continue to use either the first or second pair of prism glasses (e.g. if a participant finds one pair of prism glasses helpful for obstacle avoidance when walking). For participants who continue with the prism glasses, telephone follow-up interviews will be conducted after about 6 and 12 months.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • •Homonymous hemianopia with or without macular sparing for at least 3 months
  • •Visual acuity of at least 20/50 in each eye, with correction if needed
  • •Refractive error in the -12D to +5D range
  • •Able to walk independently, using a cane or walker if needed
  • •Able to communicate in English sufficiently to understand the study procedures and how to use the prisms

排除标准

  • •Central visual field loss in the seeing hemifield of either eye (e.g. from macular degeneration, glaucoma, diabetic retinopathy or other maculopathies)
  • •Hemi-spatial neglect
  • •Significant cognitive impairment
  • •Any other physical or mental disabilities, or general health problems that could impair the ability to be independently mobile (i.e., walk ), participate in the VR walking simulator test or use the prism glasses

研究组 & 干预措施

MPP first, FPP second

Experimental

Participants in this arm will receive the MPP in the first period of the crossover and the FPP in the second period.

干预措施: Multi-Periscopic Prism (MPP) glasses (Device)

MPP first, FPP second

Experimental

Participants in this arm will receive the MPP in the first period of the crossover and the FPP in the second period.

干预措施: Fresnel Peripheral Prism (FPP) glasses (Device)

FPP first, MPP second

Experimental

Participants in this arm will receive the FPP in the first period of the crossover and the MPP in the second period.

干预措施: Multi-Periscopic Prism (MPP) glasses (Device)

FPP first, MPP second

Experimental

Participants in this arm will receive the FPP in the first period of the crossover and the MPP in the second period.

干预措施: Fresnel Peripheral Prism (FPP) glasses (Device)

结局指标

主要结局

Improvement in Blind-side Detection Rate for Hazards Approaching at a Bearing Angle of 40 Degrees

时间窗: Immediately after each 4-week intervention

Improvement in detection rate with prism glasses for hazards approaching from the blind side at a bearing angle of 40 degrees in the VR walking simulator test. Improvement is a binary outcome, defined as blind-side detection rate (number of pedestrians detected as a percentage of the total number of pedestrian events) which is significantly higher (z-test for two proportions) with than without prism glasses at the same visit.

次要结局

  • Improvement in Blind-side Detection Rate for Hazards Approaching at a Bearing Angle of 20 Degrees(Immediately after each 4-week intervention)
  • Device Preference(Immediately after the second 4-week intervention)

研究者

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

Eli Peli

Senior Scientist

Massachusetts Eye and Ear Infirmary

研究点 (8)

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