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VR goggles could speed up recovery after major surgery

NCT ID NCT07493499

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Aug 12, 2026 · Updated 3 times

Summary

This study tests whether using virtual reality (VR) before and after major abdominal surgery can improve recovery and shorten hospital stays. Sixty adults will either receive standard care or add VR sessions with guided relaxation and breathing exercises. The goal is to see if this drug-free approach reduces pain, anxiety, and time in the hospital.

What this could mean

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

Active substance
Immersive virtual reality (VR) sessions with nature and relaxation content
What this could lead to
If it works, VR could become a simple, drug-free way to help people recover faster and feel better after major abdominal surgery.
What could go wrong
This is a small, early-stage trial with only 60 people, so results may not apply to everyone. VR might cause side effects like dizziness or nausea 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

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

Mar 2026

Finished

Jun 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: * Adult patients aged 18 to 60 years. * Scheduled for elective major abdominal surgery (e.g., colorectal, gastric, or hepatobiliary procedures). * Physical and cognitive ability to provide informed consent. * Ability to use and interact with Virtual Reality (VR) equipment (head-mounted display). * Followed the standardized Enhanced Recovery After Surgery (ERAS) protocol at the hospital. Exclusion Criteria: \- Patients with a history of epilepsy or photosensitive seizures. * Significant cognitive impairment or diagnosed psychiatric disorders that may interfere with study participation. * Severe visual or auditory impairments that prevent effective interaction with VR content. * Patients with pre-existing motion sickness or severe vertigo. * Presence of open wounds or infections in the head or face area that prevent wearing the VR headset.

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Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Alexandria University Hospital, Faculty of Nursing

    Alexandria, Alexandria Governorate, 21511, Egypt

More trials for these conditions

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