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Tech toys tested to calm kids' nerves at the hospital

NCT ID NCT06924814

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
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 Results may not be published yet.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 This study
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This status has not been confirmed recently, so it may be out of date.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 Aug 19, 2026 · Updated 3 times

Summary

This study will test whether using technology like virtual reality headsets, tablets with games, or other gadgets can help reduce anxiety and pain in children aged 4 to 17 during minor procedures such as lumbar punctures or heart catheterizations. About 200 kids will be randomly assigned to use a tech distraction or standard care (no tech). Their anxiety and pain levels will be measured before and after the procedure.

What this could mean

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

Active substance
technology-based distractions (VR headsets, AR headsets, haptic devices, tablets with games)
What this could lead to
If successful, this could provide a simple, non-drug way to ease anxiety and pain for children during medical procedures.
What could go wrong
This is an early-stage study with no phase, so results are uncertain. The effect may be small or no better than 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.

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Apr 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

4 to 17 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 patient age between 4-17 * English speaking * Parental consent/patient assent * Undergoing minor procedure(s) at LPCH or Stanford Hospital Exclusion Criteria: * Patient does not consent * Legal guardian not present to obtain consent * Patient with a significant neurological condition or major developmental disability * Patient experiencing nausea * Patient with active infection of the face or hand * A history of severe motion sickness * A history of visual problems * A history of seizures caused by flashing light * Major surgery within the last 48 hours * Patients who are clinically unstable or require urgent/emergent intervention * Patient or parental preference for general anesthesia

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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.

Contacts and locations

Locations

  • Lucile Packard Children's Hospital Stanford

    Palo Alto, California, 94304, United States

More trials for these conditions

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