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Can a gentle screen soothe a Child's fear in the ER?

NCT ID NCT07761637

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 12, 2026 · Last updated Aug 13, 2026 · Updated 1 time

Summary

This trial tests whether a non-wearable audiovisual display, like a mobile screen showing calming content, can reduce anxiety in children aged 6 to 12 during emergency department procedures such as blood draws or stitches. Participants are randomly assigned to either use the distraction device or receive standard care, while their anxiety is measured through physiological signals and behavioral observation. The goal is to see if this simple, non-drug approach can make emergency visits less stressful for young patients.

What this could mean

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

Active substance
Non-wearable audiovisual distraction using a mobile display system (LG StanbyME) providing gentle, low-stimulation content during emergency department procedures.
What this could lead to
If effective, this could offer a simple, drug-free way to ease anxiety in children during emergency procedures, potentially improving their experience and outcomes.
What could go wrong
The trial is relatively small and early-stage, and results may not apply to all pediatric settings. The distraction may not significantly reduce anxiety compared to standard care.

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 90 people

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

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Sep 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

6 to 12 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: * Pediatric patients aged 6 to 12 years presenting to the Emergency Department. * Requiring invasive medical procedures (e.g., blood sampling, intravenous line insertion, or laceration repair/suturing). * Patient and legal guardian/parent willing and able to provide informed assent/consent and comply with study protocols. Exclusion Criteria: * Patients with severe developmental delay, cognitive impairment, or neurological disorders affecting communication or behavioral assessment. * Patients with severe visual or hearing impairment that prevents interaction with the non-wearable display system. * Hemodynamically unstable patients or those requiring immediate life-saving resuscitation. * Patients with severe upper body or facial injuries that prevent the placement or operation of continuous ECG recorders.

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Conditions

The condition(s) this trial relates to.

anxiety disorder Pain, Procedural

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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. 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 ↗

  3. 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

Locations

  • National Taiwan University Hospital Yunlin Branch

    Douliu, Yunlin County, 640203, Taiwan

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