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Can a smartphone app ease Parents' fears about childhood epilepsy?

NCT ID NCT06402526

Knowledge-focused Sponsor: McGill University Health Centre/Research Institute of the McGill University Health Centre 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 mobile app designed to educate parents and caregivers of children with epilepsy. The app provides information about the condition, tracks symptoms, and helps manage appointments. Researchers wanted to see if using the app for one month would increase parents' knowledge and reduce their anxiety compared to standard care. 72 caregivers took part in the study at a single hospital in Canada.

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

72 people

The number who actually took part.

Started

Jun 2024

Finished

Dec 2024

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 years and older

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: * Parents/caregivers whose children are between 1-17 years old; * Parents/caregivers whose child was diagnosed with epilepsy at least 2 months ago; * At least one primary caregiver is comfortable interacting in English or French; and * At least one primary caregiver owns and uses a smartphone on a daily basis. Exclusion Criteria: \- Inability to provide informed consent for any reason.

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Conditions

The condition(s) this trial relates to.

anxiety anxiety disorder Behavior childhood-onset epilepsy syndrome epilepsy

As listed by the trial registrant

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

Anxiety Epilepsy Epilepsy in children Knowledge, attitudes, practice

Contacts and locations

Locations

  • Montreal Children's Hospital

    Montreal, Quebec, H4A 3J1, Canada

  • Research Institute of the McGill University Health Centre

    Montreal, Quebec, H4A 3J1, Canada

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