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Virtual reality headsets bring calm and brain games to ICU patients

NCT ID NCT06876168

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jul 21, 2026 · Updated 3 times

Summary

This study tests whether virtual reality (VR) can help patients in the intensive care unit (ICU) relax, improve their mood, and keep their minds active. Participants will use a VR headset for about 15 to 45 minutes each day for up to 5 days, doing breathing exercises, brain games, and relaxation tasks. The study includes 32 adults with acute respiratory failure or sepsis. The main goal is to see if the VR approach is easy to use and practical in the ICU setting.

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 sessions with breathing exercises, brain games, and relaxation techniques
What this could lead to
If it works, this could point toward a simple, drug-free way to help ICU patients feel better and think clearer during recovery.
What could go wrong
This is a very small, early feasibility study with only 32 people. It is designed to see if the approach is practical, not to prove it works. Results may not apply to all ICU 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.

Participants

27 people

The number who actually took part.

Started

Jul 2025

Finished

May 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.

Who is studied

Patients in the intensive care unit at University of Kentucky with sepsis or acute respiratory failure.

Ages

18 to 99 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: * Admitted to ICU at University of Kentucky for acute respiratory failure, sepsis or other Exclusion Criteria: * Are less than 18 years of age * Have a pre-existing neurologic disorder * Have a pre-existing emotional or personality disorder * Have a history or active mental health disorder or disease * Experienced an acute neurologic event (e.g., stroke) * Are currently pregnant * Are a prisoner * Receiving hospice care * Have existing open wounds or pressure ulcers on head or neck

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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

  • University of Kentucky

    Lexington, Kentucky, 40536, United States

More trials for these conditions

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