Can sound help restore sight? small study tests new rehab device for hemianopia
NCT ID NCT04963075
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This small proof-of-concept study tested a non-invasive device that uses sound and light to help people with hemianopia (blindness in half of the visual field). Five adults with stable hemianopia underwent training sessions where they were exposed to matching sound and visual cues in their blind area. The goal was to see if this multisensory approach could improve visual detection. Results are very early and limited.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- multisensory rehabilitation device
- What this could lead to
- If it works, this could point toward a non-invasive way to improve vision in people with hemianopia.
- What could go wrong
- This was a very small proof-of-concept study with only 5 participants. Results may not apply to everyone, and the approach is still experimental.
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
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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
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5 people
The number who actually took part.
- Started
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Sep 2021
- Finished
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Sep 2025
- Lead sponsor
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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
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18 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * adults (\<85) of either sex * diagnosis of a stable homonymous hemianopia (\>6 months) with absence of hemineglect * lesion encompassing at least primary visual cortex but sparing parietal cortex * normal auditory and cognitive function * willingness to participate in the three month program * ability to perform the visual discriminations in their intact field Exclusion Criteria: * adults (\>85) * normal auditory and cognitive function * unwilling to participate in the three month program * inability to perform the visual discriminations in their intact field
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Wake Forest Health Sciences
Winston-Salem, North Carolina, 27157, United States
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Other studies related to the condition(s) this trial covers.
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