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A 20-Minute VR forest stroll might melt Pre-Surgery jitters

NCT ID NCT07774156

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 19, 2026 · Last updated Aug 21, 2026 · Updated 2 times

Summary

This trial tests whether a single 20-minute virtual reality session featuring calming nature scenes can reduce fear and anxiety in adults scheduled for bariatric (weight-loss) surgery. Participants will view 360° footage of forests, seas, and landscapes in their hospital room shortly before the operation. Researchers will measure changes in surgical fear and state anxiety using standard questionnaires to see if this simple, non-drug approach helps patients feel more at ease.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
A single 20-minute immersive virtual reality session showing 360° nature footage (forest, sea, landscape) designed to relax patients before surgery.
What this could lead to
If effective, this could offer a simple, drug-free way to ease anxiety and fear in patients awaiting surgery, potentially improving their experience and recovery.
What could go wrong
This is a small, early-stage trial, and the effect may be modest or not last. Some people may not find VR relaxing, and results may not apply to all surgical 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

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

120 people

The number who actually took part.

Started

Mar 2025

Finished

Jul 2026

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 60 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: * 18 years or older * scheduled for elective bariatric surgery * able to communicate verbally * without visual or hearing impairment * without a diagnosed psychiatric disorder * not concurrently using any other non-pharmacological anxiety-reduction method Exclusion Criteria: * younger than 18 years * those with visual or hearing impairment * those using another non-pharmacological method during the study period were excluded

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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

  • Firat Universty

    Elâzığ, 23119, Turkey (Türkiye)

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