Could virtual reality calm anxious kids at the doctor?
NCT ID NCT07280910
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study examined whether virtual reality (VR) can help lower anxiety in children aged 6-15 during medical procedures. Researchers analyzed data from 168 pediatric patients who used VR as part of a quality improvement program. They measured changes in heart rate, blood pressure, and fear scores before and after VR use.
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 (VR) distraction therapy
- What this could lead to
- If successful, this could support using VR as a simple, drug-free way to ease children's anxiety during medical procedures.
- What could go wrong
- This was a small, completed study that only looked back at existing data, not a controlled trial. Results may not apply to all children or 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.
- Participants
-
168 people
The number who actually took part.
- Started
-
Oct 2023
- Finished
-
Jun 2024
- 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.
Who is studied
The study involved pediatric patients who received VR intervention as part of the original QI initiative. Data protection and de-identification procedures were rigorously applied throughout the study
- Ages
-
6 years and older
- 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 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.
Pediatric Subjects Inclusion Criteria: * pediatric patients who received VR intervention as part of the original QI initiative. * pediatric patients who were eligible and received VR during the QI initiative aged 6-15 years. Exclusion Criteria: * Patients with developmental delays, head injuries, or seizures were excluded from the study. * Only those pediatric patients who met the inclusion criteria and did not exhibit the specified exclusion conditions were included. Data protection and de-identification procedures were rigorously applied throughout the study Caregivers/Parents Inclusion Criteria: \- pediatric patients who were eligible and received VR during the QI initiative, aged 6-15 years Exclusion Criteria: \- N/A Nurses Inclusion Criteria: * nurses of pediatric patients who were eligible and received VR during the QI initiative, aged 6-15 years Exclusion Criteria: * N/A
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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
-
Virginia Commonwealth University
Richmond, Virginia, 23298, United States
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