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New Eye-Training game may help stroke survivors see better

NCT ID NCT01730560

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested a computer-based training for people who lost part of their vision after a stroke or brain injury. The training used a moving target to help patients automatically look into their blind area. 22 adults with hemianopia (blindness in half the visual field) completed the training. The goal was to see if this automatic approach could improve visual search and reading more than traditional methods.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
computer-based visual training task
What this could lead to
If it works, this could offer a new, easier way to improve vision-related daily activities like reading and finding objects.
What could go wrong
This was a very small, early study with only 22 participants, so results may not apply widely. The training may not lead to meaningful real-world improvements.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

22 people

The number who actually took part.

Started

Nov 2010

Finished

Jun 2018

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 80 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Male/Female * Stroke (ischemia or hemorrhage) documented by CTscan or MRI * Traumatic brain injury (TBI) documented by CTscan or MRI * Right or Left hemianopia defined by perimetry * All subjects must be between the ages of 18-80 * Aetiology of visual field defect : Stroke (ischemia or hemorrhage) * Delay post-stroke : at least 6 months * Only one lesion on CTscan or MRI (performed in a maximal delay of 6 months) * Corrected monocular visual acuity \> 5/10 * Possible understanding of experimental conditions * Patient being able to be quiet and sit during at least 2 hours * Having given written informed consent prior to any procedure related to the study * Availability for the period of the study * Covered by a Health System where applicable, and/or in compliance with the recommendations of the national laws in force relating to biomedical research Exclusion Criteria: * Ophthalmologic criteria : monocular visual acuity \< 4/10, strabismus , diplopia , ocular instability , nystagmus, maculopathy , glaucoma , retinopathy , orthoptic rehabilitation * Neurologic criteria : sever phasic disturbances , neurologic degenerative affection , non controlled seizure , severe handicap non compatible with prolonged sit position or concentration during 30 consecutive minutes * No command of french language * Non stabilized medical situation * Females who are pregnant, nursing, or planning a pregnancy during the study period, or females of childbearing potential, not using a reliable means of contraception. * Not under any administrative or legal supervision

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Service de Médecine Physique et de Réadaptation,Hôpital Henry Gabrielle

    Saint-Genis-Laval, 69235, France