Actively Recruiting
Vision on the Road: Vision Rehabilitation for Driving After Stroke
Led by University of South-Eastern Norway · Updated on 2025-08-29
52
Participants Needed
2
Research Sites
148 weeks
Total Duration
On this page
Sponsors
U
University of South-Eastern Norway
Lead Sponsor
L
Lovisenberg Diakonale Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn if vision training works to improve functional vision in people with visual field loss after stroke. The investigators want to know more about how people perceive their own functional vision and ability to compensate for visual field loss in daily activities. The main questions the study aims to answer are: * Does vision training improve dimensions of functional vision? * How does vision training affect the participants's perception of functional vision and the ability to compensate for visual field loss? Researchers will compare the effect of home-based vision training to standard care (no vision training) on functional vision. Participants will: * Participate in home-based vision training or standard care for 8 weeks * Be contacted once a week by phone * Keep a training diary
CONDITIONS
Official Title
Vision on the Road: Vision Rehabilitation for Driving After Stroke
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 20-85 years with a visual field defect following stroke
- Norwegian Class 1 driving licence revoked no more than five years ago
- Speak a Scandinavian language
- Able to provide written informed consent
- Motivated and willing to participate in study activities for a total of 20 to 28 weeks
- Own a personal computer (for digital follow-up and online vision training)
- Able to travel to Oslo for data collection
You will not qualify if you...
- Presence of strabismus and/or visual neglect
- Eye disease or other health conditions that do not meet the health requirements for a Norwegian Class 1 driver's license
- Cognitive impairment, dementia, severe psychiatric diagnosis, or inability to provide written informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
University of South-Eastern Norway
Kongsberg, Norway, 3616
Actively Recruiting
2
Lovisenberg Diaconal hospital
Oslo, Norway, 0440
Actively Recruiting
Research Team
M
Marte Rosenvinge, phd-student
CONTACT
H
Helle Falkenberg, Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here