Actively Recruiting
Rehabilitation of Visual Function After Brain Injury
Led by University Hospital, Gentofte, Copenhagen · Updated on 2024-12-09
56
Participants Needed
1
Research Sites
521 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Gentofte, Copenhagen
Lead Sponsor
T
The Institute for the Blind and Partially Sighted (IBOS)
Collaborating Sponsor
AI-Summary
What this Trial Is About
In Denmark, about 120,000 people suffer from brain damage, of whom approx. 75,000 with brain damage after stroke. Serious and often lasting vision impairments affect 20% to 35% of people after stroke. Vision is the most important sense in humans, and even smaller permanent injuries can drastically reduce quality of life. Vision impairments after brain damage inhibits rehabilitation and enhances other invalidating effects. Reduced vision results in impaired balance, increased risk of serious falls, increased support needs, reduced quality of life, and impaired ability to perform activities of daily living. Restoration of visual field impairments occur only to a small extent during the first month after brain damage, and therefore the time window for spontaneous improvements is very limited. Hence, brain-impaired persons with visual impairment will most likely experience chronically impaired vision already 4 weeks after brain injury and the need for visual compensatory rehabilitation is substantial. Neuro Vision Technology (NVT) is an supervised training course where people with visual impairments are trained in compensatory techniques using special equipment. Through the NVT process, the individual's vision problems are carefully investigated and personal data is used to organize individual training sessions that practice the individual in coping with situations that cause problems in everyday life. The purpose of this study is to investigate whether rehabilitation with NVT can cause significant and lasting improvement in functional capacity in persons with chronic visual impairments after brain injury. Improving eyesight is expected to increase both physical and mental functioning, thus improving the quality of life. Participants included in the project will be investigated in terms of both visual and mental functions, including quality of life, cognition and depression. Such an investigation has not been performed previously and can have a significant impact on vision rehabilitation both nationally and internationally.
CONDITIONS
Official Title
Rehabilitation of Visual Function After Brain Injury
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 14 years or older with brain injury
- Persons who experience significant vision impairment
- Eye sight 6/18 or better
- Time from symptom onset to study inclusion is between 6 weeks and 9 months
You will not qualify if you...
- Cognitive dysfunction
- Anosognosia or severe neglect
- Inability to move independently at least 35 meters with or without assistance
- Inability to understand Danish or communication disorders preventing test participation
- Terminal or other progressive disorders
- Significant abuse of alcohol or narcotic drugs
- Serious mental illness, especially severe depression
- New brain injury or significant disorders after study inclusion
- Vision impairment not caused by brain damage or not permanent or not causing significant disability
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
The Institute for the Blind and Partially Sighted (IBOS)
Copenhagen, Hellerup, Denmark, 2900
Actively Recruiting
Research Team
N
Nanna F Mikkelsen, OT
CONTACT
R
Rune S Rasmussen, MA, Ph.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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