Could a VR headset turn a painful IV into a game?
NCT ID NCT07739381
First seen Jul 31, 2026 · Last updated Jul 31, 2026
Summary
This trial tests whether watching an entertaining video through virtual reality glasses or on a tablet can reduce pain, anxiety, and fear in children aged 7 to 12 during intravenous (IV) cannulation in an emergency department. Children are randomly assigned to one of three groups: virtual reality, tablet, or routine care. The study measures pain, anxiety, and fear using validated scales to see if these distraction methods help compared to standard care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Virtual reality distraction and tablet-based cartoon distraction
- What this could lead to
- If effective, these distraction methods could offer simple, drug-free ways to reduce pain and anxiety for children during medical procedures.
- What could go wrong
- The trial is relatively small and results may not apply to all children or settings. The effectiveness of distraction can vary widely between individuals.
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
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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
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132 people
The number who actually took part.
- Started
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Apr 2022
- Finished
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Aug 2022
- Lead sponsor
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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
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7 to 12 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * It was that the child belonged to the 7-12 age group and was fully conscious. Exclusion Criteria: * Children with hearing, cognitive, or visual impairments; children unaccompanied by a parent; children with whom communication cannot be established; and children with critical health issues and/or conditions requiring immediate intervention.
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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
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Kütahya Evliya Çelebi Training and Research Hospital
Kütahya, Kütahya, 4300, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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