Actively Recruiting

Phase Not Applicable
Age: 14Years +
All Genders
NCT03160131

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

Age: 14Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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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

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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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