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Can sound and light help stroke patients see again?

NCT ID NCT07317739

Symptom relief Sponsor: Fondazione David Chiossone - Impresa Sociale Source: ClinicalTrials.gov ↗

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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looks at how common vision loss is after a stroke and tests a new rehab method. 300 stroke patients will either get standard rehab or standard rehab plus audio-visual stimulation training using a special device. The goal is to see if this extra training helps improve their visual field defects.

What this could mean

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

Active substance
audio-visual stimulation training using the AV DESK Flexi device
What this could lead to
If it works, this could offer a non-invasive way to help stroke survivors regain some lost vision.
What could go wrong
This is an early-stage study with no phase, so results are uncertain. The training may not improve vision more than standard rehab alone.

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 300 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Mar 2027

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

18 to 99 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: 1. Patients aged 18 to 99 years with stroke (excluding isolated cerebellar, brainstem, or spinal cord strokes), admitted to Neurology in IRCCS San Martino Polyclinic Hospital with the ability to understand and sign the informed consent for study participation. 2. Mobility of at least one upper limb. Exclusion Criteria: 1. Presence of cognitive impairment (with an MMSE score less than 24), which limits the understanding of the informed consent or the ability to perform the test. 2. Difficulty moving both upper limbs. 3. Presence of ocular comorbidity that could affect visual field assessment before stroke. 4. Presence of fluent aphasia, neglect, or head and gaze deviation. 5. Presence of disturbances in the state of consciousness 6. Presence of delirium

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Conditions

The condition(s) this trial relates to.

Hemianopsia stroke disorder

As listed by the trial registrant

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

Hemianopia Visual field defect following cerebrovascular accident

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  2. 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.

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