Continued Study of Artificial Vision: Evaluation of the BrainPort® System and Investigation of Visual Ambulation
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 7
- 试验地点
- 1
- 主要终点
- Average Time to completion of obstacle path (over 25 trials) in seconds
研究概览
简要总结
The purpose of this study is to evaluate the use of an artificial vision system called Brainport system in blind patients To investigate visual, and oculomotor (eye motion) mechanisms involved in the use of the Brainport system.
详细描述
The prevalence of blindness in the US adult population is 0.8% and ranges from about 3/10000 to 15/10000 in children. Data from world health organization show that about 500,000 children become blind each year. The annual cost of blindness to the federal government is $4 billion and the cost of a lifetime of support and unpaid taxes for a blind person is about $1 million.
There is a need to restore vision for blind patients. Research on vision restoration develops fast. There are multiple types of approaches toward producing useful artificial vision. One of them directly sends images from a video camera to the visual cortex via an electrode array that is intracranially placed on the visual cortex of blind patients. Another one surgically places an electrode array beneath the retina for patients whose optic nerves are still healthy. Both of them require major surgery and have high risks, and neither is available for routine clinical application.
The one that is non-invasive and easy to use is called the BrainPort® system. The BrainPort® system is manufactured by Wicab, Inc. It is commercially available and affordable to any consumer. This system is a novel, bionic, non-invasive, vision bypass system that conveys environment images from a spectacle-frame-mounted video-camera to the brain via an electro-tactile tongue array. The electro-tactile stimulation delivered by the tongue-array placed on the tongue allows users to interpret the images of objects in their camera's visual field.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 10 Years 至 24 Years（Child, Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Less than 25 years of age and be able to cooperate for full study protocol
- •Have a clinical diagnosis of blindness (light perception or worse), or 20/20 vision corrected or otherwise.
- •Have completed a complete ophthalmic evaluation.
- •Patients recruited must be able to undergo the training to use the BrainPort® system.
- •Sign informed consent (family) or assent (patient).
排除标准
- •Have any neurologic disease, developmental delay, congenital genetic syndromes, congenital organ malformation, malformation syndromes or metabolic disease.
- •Be on any medications known to affect the visual system
研究组 & 干预措施
Group A - Blind
Subjects will be trained to ambulate through a 40-foot obstacle course by the occupational therapy colleagues at Akron Children's Hospital after which they will be scored on their performance while using the BrainPort® system.
干预措施: BrainPort (Device)
Group C - Control
Subjects will be trained to ambulate through a 40-foot obstacle course by the occupational therapy colleagues at Akron Children's Hospital after which they will be scored on their performance while using the BrainPort® system.
干预措施: BrainPort (Device)
结局指标
主要结局
Average Time to completion of obstacle path (over 25 trials) in seconds
时间窗: 1 month
To evaluate the usefulness of an artificial vision system called BrainPort® system in blind patients
次要结局
- Average Number of errors during each trial (over 25 trials)(1 month)