VR headsets could slash opioid use after surgery
NCT ID NCT07063394
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests whether using a virtual reality headset after heart or chest surgery can lower the amount of strong painkillers (opioids) patients need. Sixty people aged 16 to 40 will be split into three groups: one using interactive VR games, one watching passive VR videos, and one receiving standard care only. The goal is to see if VR's immersive distraction can improve pain control and recovery.
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) headset with interactive games and passive videos
- What this could lead to
- If it works, VR could become a drug-free way to manage pain after surgery, reducing reliance on opioids and their side effects.
- What could go wrong
- This is a small, early-stage trial with only 60 patients. The effect may be small or not work for everyone, and VR might cause discomfort in some patients.
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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2024
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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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16 to 40 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: * Patients undergoing elective cardiac or thoracic surgeries at the Heart Institute (InCor) of the Hospital das Clínicas of the University of São Paulo. * Eligible thoracic surgeries include: pulmonary decortication, thoracic sympathectomy, video-assisted thoracoscopic surgery (VATS), pulmonary biopsy, and pectus excavatum repair using the Nuss procedure. * Patients aged between 16 and 40 years. * Preserved cognitive function, indicated by a Mini-Mental State Examination (MMSE) score of ≥ 25. Exclusion Criteria: * Visual impairments. * Cognitive impairment (MMSE ≤ 24). * Severe upper limb motor limitations. * Claustrophobia. * Spatial disorientation. * Motion sickness or vestibular disorders. * Infectious or contagious diseases.
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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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Incor - Heart Institute - University of Sao Paulo
RECRUITINGSão Paulo, São Paulo, 05403000, Brazil
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