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Video games on the floor may ease kids' post-surgery pain

NCT ID NCT06571123

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether an interactive floor projection — where kids step on virtual balloons to pop them — could reduce pain and help them move sooner after surgery. 84 children aged 3-6 were randomly assigned to use the interactive floor or receive standard care. Researchers measured pain scores and how long children were able to mobilize. The goal was to see if distraction through play could improve recovery.

What this could mean

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

Active substance
interactive floor projection system
What this could lead to
If it works, this could give hospitals a simple, fun way to help children feel less pain and move earlier after surgery without extra medication.
What could go wrong
This is a small, completed trial with 84 children, so results may not apply to all surgeries or ages. The effect may be modest and not replace standard pain 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

84 people

The number who actually took part.

Started

Oct 2024

Finished

Jul 2025

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

3 to 6 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Speak and understand Turkish * Children whose parents agreed to participate in the study, * Between 3 and 6 years old, * Mobilization for the first time after surgical intervention * No previous experience with other surgical procedures * Ability to walk independently * Children with vesico-uretero renal reflux, torsion of the ovarian pedicle of the ovary and fallopian tube, hypospadias, hirschsprung's disease, undescended testis, persistent cloaca, hydronephrosis, ureteropelvic junction obstruction, appendicitis, anus atresia/stenosis/fistula, biliary atresia, circumcision, phimosis and paraphimosis, post-traumatic surgery Exclusion Criteria: * Daily surgical procedures performed * Having a health problem that prevents him/her from walking * Serious complications after the operation * Having any visual, auditory and mental problems * The physician reports a problem that may prevent him/her from walking

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Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

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

Contacts and locations

Locations

  • Istanbul Aydin University

    Istanbul, Istanbul, 34295, Turkey (Türkiye)

  • Istanbul University Cerrahpaşa Cerrahpasa Faculty of Medicine

    Bakırköy, Istanbul, 34295, Turkey (Türkiye)

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