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VR goggles teach Post-Surgery Self-Care in new trial

NCT ID NCT07283432

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Updated 1 time

Summary

This study tested whether using virtual reality glasses for discharge education helps patients better care for themselves after bariatric surgery. Sixty adults who had laparoscopic weight-loss surgery were split into two groups: one received standard care, the other watched a 15-20 minute VR training video before leaving the hospital. Researchers measured self-care ability using a questionnaire before surgery and at 1 and 3 months after. The goal was to see if VR makes learning easier and more effective.

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 point toward a more engaging way to teach patients how to care for themselves after weight-loss surgery.
What could go wrong
This is a small, early-stage study with only 60 patients. The effect on long-term health or weight loss is not measured, and VR may cause discomfort in some users.

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

60 people

The number who actually took part.

Started

Aug 2025

Finished

Dec 2025

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 65 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Patients who are 18 years of age or older, 65 years of age or younger, * Who have undergone laparoscopic sleeve gastrectomy or laparoscopic gastric bypass surgery, * Who have not developed any complications during or after the surgical procedure, * Who volunteer to participate in the study will be included in the study. Exclusion Criteria: * Patients who have not undergone laparoscopic surgery, * Patients with neurological or psychological problems, * Patients who have been transferred to the intensive care unit after surgery, - Emergency and unplanned cases, * Patients diagnosed with cancer, * Patients with visual, auditory or systemic disorders, * Patients with balance problems, * Patients diagnosed with hypertension and hypotension, * Patients diagnosed with anxiety disorder or epilepsy will be excluded from the study.

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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

  • Ankara Yıldırım Beyazıt University

    Ankara, Turkey (Türkiye)

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