Virtual reality may replace painkillers during procedures
NCT ID NCT07779083
First seen Aug 21, 2026 · Last updated Aug 21, 2026
Summary
This trial tests whether virtual reality (VR) distraction can reduce pain, anxiety, and the need for pain medications during prone pain procedures, compared to standard care alone. About 230 adults undergoing such procedures at a pain clinic will be randomly assigned to either use a VR headset showing calming nature scenes or receive usual care. The study measures pain and anxiety scores and whether opioid or sedative medications are needed, aiming to see if VR offers a non-drug way to improve patient comfort.
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) audiovisual distraction using a commercially available Meta Quest 3 headset with calming nature scenes and an ergonomic cushion/support
- What this could lead to
- If effective, VR distraction could offer a drug-free way to ease pain and anxiety during medical procedures, potentially reducing the need for opioids and sedatives.
- What could go wrong
- This is a single-site trial, and results may not apply broadly. VR may not work for everyone, and some people may experience motion sickness or discomfort.
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 230 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
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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18 years and older
- 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: * Patients aged 18 years old or older * Male and female gender * Referred to UC Davis Pain Medicine Clinic and require a prone pain procedure * English speaking and with the ability to understand oral and written instructions Exclusion Criteria: * Pregnant women * Prisoners * Patients who have high risk of motion sickness * Seizure disorder * Visual/hearing impairment
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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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UC Davis Pain Clinic
Sacramento, California, 95817, United States
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Other studies related to the condition(s) this trial covers.
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