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Clinical Trials in Norway / NCT07147660
Recruiting Not applicable

Vision on the Road: Vision Rehabilitation for Driving After Stroke

NCT07147660 · tracked via the Priya Life Science Norway tracker
Sponsor
University of South-Eastern Norway
Phase
Not applicable
Started
2025-03-28
Last updated
2025-08-29

Condition(s) studied

StrokeVisual Field LossHemianopia

Investigational drug(s) / intervention(s)

Compensatory scanning trainingDelayed Compensatory scanning training

Compensatory scanning training: Individual home-based vision training exercises for 20 minutes every day for 8 weeks. A training program with online and manual oculomotor exercises, scanning and visual search-exercises. Weekly short follow up-conversation by telephone to check in and keep the motivation high with the participants.

Delayed Compensatory scanning training: Delayed track start. Individual home-based vision training exercises for 20 minutes every day for 8 weeks. A training program with online and manual oculomotor exercises, scanning and visual search-exercises. Weekly short follow up-conversation by telephone to check in and keep the motivation high with the participants.

Study summary

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

Eligibility

Sex
ALL
Min age
20 Years
Max age
85 Years
Healthy volunteers
No
Inclusion criteria: * 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 Exclusion criteria: * 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

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
University of South-Eastern Norway Kongsberg Norway Recruiting
Lovisenberg Diaconal hospital Oslo Norway Recruiting

More University of South-Eastern Norway trials in Norway

Virtual Nature as a Health-promoting Intervention for Nursing Home Residents With Dementia Active, not recruiting
Strength Training and Eating Disorders Enrolling by invitation

Other trials for the same condition

Decentralized Imaging by REmote Computer Tomography for Cerebral Infarct Thrombolysis Recruiting
Left Atrial Appendage Occlusion Versus Novel Oral Anticoagulation for Stroke Prevention in Atrial Fibrillation Recruiting
Predisposing Factors for Post-stroke Epilepsy Recruiting
Prevention of Stroke by Left Atrial Appendage Closure in Atrial Fibrillation Patients After Intracerebral Hemorrhage Active, not recruiting
Population-based Atrial Fibrillation Screening in Individuals With NT-proBNP Above Median in the Tromsø Study Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07147660 on ClinicalTrials.gov ↗ ← All trials in Norway