Brain study tests if sound or touch can replace sight
NCT ID NCT07450677
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study at Stanford University will test how the brain responds when visual information is turned into patterns of sound or touch. Two hundred blind and sighted participants will use special devices (BrainPort and AI Sight) for 5 weeks. Researchers will use brain scans and performance tasks to see how people learn and adapt to these sensory substitutions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Electrotactile display (BrainPort) and vision-to-sound converter (AI Sight) devices
- What this could lead to
- If successful, this could help improve assistive technologies for blind individuals by understanding how the brain processes non-visual sensory information.
- What could go wrong
- This is an early-stage observational study, not a treatment trial. It may not lead to any direct clinical benefit, and results may not apply to all types of blindness.
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
-
About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Jun 2026
An estimate. Start dates often move.
- Expected to finish
-
Aug 2030
An estimate. End dates often move.
- 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
-
8 to 85 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: 1. 8-85 years old for blind individuals; or 18-85 years old for sighted controls. 2. (a) Blind due to ocular impairment (documented visual acuity of light perception or worse) in both eyes, or (b) sighted healthy adult controls with corrected visual acuity of 20/40 or better and with no known vision disorders. 3. Able to hear the Informed Consent Form being read out to him or her, to understand it, and sign the Informed Consent Form. 4. Able to undergo functional neuroimaging tests. 5. Able to walk and stand independently. 6. Able to understand and remember the training protocols involved in the research study. 7. Willing and able to use the provided sensory substitution system to solve simple visual tasks. 8. Willing and able to complete simple tactile or auditory tasks. 9. Able to communicate by telephone and/or computer with research staff. Exclusion Criteria: 1. Prior use with the sensory substitution device under investigation. This applies to both the auditory and tactile stimulators. 2. Presence of any foreign metal in the body, except for dental fillings (will need to be pre-screened by a radiologist prior to signing the informed consent and enrollment). 3. Pregnant or breastfeeding by self-report or urine test. 4. Is a prisoner or has any required movements legally restricted. 5. Unwilling or unable to adhere to all study requirements, including completion of the training period and any evaluation tests. 6. Implanted electrical medical devices such as pacemakers. 7. Claustrophobia that would prevent functional neuroimaging. 8. Obesity preventing placement in the MRI scanner. 9. No known neurological disorders or any medical condition that can possibly lead to emergency medical care (e.g., history of seizures, family history of epilepsy, stroke, severe headaches, use of medication for neurological or psychiatric conditions). 10. Documented or suspected brain damage resulting in significant cognitive or sensory impairment (e.g., traumatic brain injury).
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Blindness are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The study's own enquiry address
This study publishes an address for enquiries. See it below .
-
The places running it
2 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
Genom att skicka in godkänner du våra Användarvillkor
Locations
-
Byers Eye Institute at Stanford University
Palo Alto, California, 94303, United States
-
LUCAS Center for Imaging
Stanford, California, 94305, United States
Contact Email: •••••@•••••
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Could stem cells restore sight in damaged eyes?
- Scientists test brain chip to restore sight in the blind
- Tiny brain implant could give blind people a 'Limited sense of Sight'
- Sound-Guided gaze: new device aims to sharpen eye imaging for the visually impaired
- Blind cane study reveals how tools become part of the body
- Experimental eye drug hopes to restore sight in rare blindness