VR headsets beat Pre-Surgery jitters in heart patients
NCT ID NCT07263659
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a virtual reality (VR) experience could reduce anxiety in 75 patients scheduled for a heart valve repair procedure called TEER. Patients either got standard education or standard education plus a VR tour of the procedure and hospital. The researchers measured anxiety levels right after the education and again a week before the procedure. The goal was to see if VR could help patients feel calmer and more prepared.
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) experience
- What this could lead to
- If it works, this could offer a simple, drug-free way to ease anxiety before heart procedures.
- What could go wrong
- This is a small, completed study with only 75 participants. The effect may depend on timing and may not apply to all patients or procedures.
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
-
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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75 people
The number who actually took part.
- Started
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Oct 2021
- Finished
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Dec 2024
- 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: * Adults scheduled for elective mitral (M-TEER) or tricuspid (T-TEER) transcatheter edge-to-edge repair procedures. Exclusion Criteria: * Insufficient proficiency in Dutch. * Severe visual or auditory impairment that would prevent full engagement with the VR content. * Any mental or physical condition that, in the judgment of the clinical team, significantly interferes with participation (e.g., advanced cognitive decline, acute psychological distress, or inability to tolerate wearing a VR headset).
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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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Amsterdam UMC
Amsterdam, 1105 AZ, Netherlands
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