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VR goggles may ease anxiety during surgery

NCT ID NCT07258420

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether wearing virtual reality glasses during open inguinal hernia surgery with spinal anesthesia could lower anxiety and boost comfort. 84 patients were split into two groups: one watched a video using VR goggles during surgery, the other did not. Researchers measured anxiety and comfort levels using standard scales.

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 glasses
What this could lead to
If it works, this could offer a simple, drug-free way to reduce anxiety and improve comfort during surgery.
What could go wrong
This is a small, completed study with only 84 participants. The results may not apply to all surgeries or patients, and the effect on anxiety might be small.

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

84 people

The number who actually took part.

Started

Sep 2023

Finished

Dec 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.

Ages

18 to 75 years

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: To research; * Planned elective surgery * Those who will undergo inguinal hernia surgery for the first time * Those who do not have vision, hearing and perception problems * Patients who want to participate in the study voluntarily were included. Exclusion Criteria: * Any anesthesia method other than spinal anesthesia was applied during the procedure * Under the age of 18, over the age of 75 * Having advanced vision and hearing problems * Diagnosed with mental and psychological illness * Using anti-depressant/sedative medication * Having stopped watching videos during the surgical procedure

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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

  • Trakya University

    Edirne, Merkez, 22030, Turkey (Türkiye)

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Other studies related to the condition(s) this trial covers.