Virtual reality goggles could soothe Pre-Surgery jitters
NCT ID NCT05718661
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether watching a virtual reality video before abdominal surgery could reduce anxiety. 96 adult patients scheduled for elective surgery were randomly assigned to watch a VR video or a plain video. Their anxiety and stress levels were measured using a questionnaire and a smart bracelet. The goal was to see if VR distraction helps patients feel calmer before going into the operating room.
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 video
- What this could lead to
- If it works, this could offer a simple, drug-free way to help patients feel calmer before surgery.
- What could go wrong
- This is a small, completed trial with 96 patients. The results may not apply to everyone, and the effect might be small or temporary.
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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96 people
The number who actually took part.
- Started
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Jan 2023
- 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.
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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 Scheduled for elective abdominal surgery (e.g., appendectomy, ileal/bowel surgery, hernia repair, gallbladder/pancreas surgery) Awaiting transfer to the operating room on the morning of surgery Able to communicate effectively Able to provide informed consent Exclusion Criteria Patients scheduled for abdominal cancer surgery Patients undergoing unplanned or emergency surgery Patients in isolation Patients with visual and/or auditory impairments Patients with neurological conditions such as vertigo
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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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Trakya University Hospital
Edirne, 22000, Turkey (Türkiye)
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