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Phone app spots seizures in kids

NCT ID NCT06093490

Diagnosis Sponsor: Eysz, Inc. 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested a smartphone app that guides children through deep breathing (hyperventilation) and records their face and sounds to detect absence seizures. 65 children with and without seizure history participated. The app's accuracy was compared to standard EEG monitoring. The goal is to provide a simple, accessible tool for seizure detection.

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.

Participants

65 people

The number who actually took part.

Started

Dec 2023

Finished

Jul 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

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

Who is studied

Children undergoing routine EEG as part of clinical care at risk or known to have childhood absence epilepsy who will be undergoing hyperventilation

Ages

4 to 12 years

Sex

Anyone

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: * typical absence seizure during use of the Eysz Hyperventilation Recorder or Control Exclusion Criteria: * Other seizure type besides typical absence seizure during use of the Eysz Hyperventilation Recorder * subclinical seizure activity * inability to participate with study procedures * contraindications to hyperventilation including history of subarachnoid hemorrhage, sickle cell anemia, recent cerebrovascular accident or myocardial infarction, significant cardiopulmonary disease, active asthma, known aneurysm, known moyamoya disease, or pregnancy. * People who have a history of generalized tonic clonic convulsions (GTCs) provoked by hyperventilation

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Conditions

The condition(s) this trial relates to.

childhood absence epilepsy childhood-onset epilepsy syndrome epilepsy Epilepsy, Absence Hyperventilation visual epilepsy

As listed by the trial registrant

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

Absence epilepsy Absence epilepsy, childhood Absence seizures Epilepsy in children Seizures Staring

Contacts and locations

Locations

  • Cincinnati Children's Hospital

    Cincinnati, Ohio, 045229, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.