Can a VR headset beat numbing cream for Children's needle pain?
NCT ID NCT07763132
First seen Aug 13, 2026 · Last updated Aug 14, 2026 · Updated 1 time
Summary
This trial tests whether virtual reality can reduce pain during blood draws in children aged 3 to 15. It compares three approaches: VR distraction with a headset showing a wildlife video, topical numbing cream (EMLA), and standard care. Pain is measured right after the procedure using a simple faces scale. The goal is to see if VR offers a better, drug-free way to ease needle-related discomfort.
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 using a VR headset, compared with topical lidocaine-prilocaine cream (EMLA) and standard care.
- What this could lead to
- If VR works well, it could offer a drug-free, needle-free way to reduce pain and anxiety for children during blood draws and similar procedures.
- What could go wrong
- The trial is relatively small and early, and VR may not outperform the numbing cream or standard care. Some children may not tolerate the headset, and results may not apply to all settings.
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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About 450 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2024
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- 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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3 to 15 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * Children aged 3 to 15 years. * Clinical indication for venipuncture. * Written informed consent provided by a parent or legal guardian and verbal or written assent from the child, as appropriate for age and cognitive ability. Exclusion Criteria: * Known hypersensitivity to local anesthetics. * Diagnosed mental disorder. * Current treatment with analgesic or anxiolytic medications. * Venipuncture not successful on the first attempt.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Krajska zdravotni, a.s. - Masarykova nemocnice v Usti nad Labem
RECRUITINGÚstí nad Labem, Ústí nad Labem Region, 40011, Czechia
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