Virtual reality and music may ease ICU suffering

NCT ID NCT04017299

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 electronic distractions like music, virtual reality, or TV can reduce discomfort in ICU patients. Sixty awake, non-delirious adults tried each device for 15 minutes. Researchers measured changes in pain, anxiety, thirst, shortness of breath, and insomnia. The goal is to find safe, effective tools to improve patient comfort.

What this could mean

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

Active substance
electronic distraction devices (music therapy, virtual reality, radio, television)
What this could lead to
If successful, this could point toward simple, non-drug ways to reduce suffering for ICU patients.
What could go wrong
This is a small feasibility study with only 60 patients, so results may not apply to all ICU patients. It tests short-term use and does not yet prove long-term benefits.

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

Jul 2019

Finished

Dec 2019

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 years and older

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: * patient admitted in intensive care unit, * adult, * French speaking, * awake (RASS ≥ -1), * not delirious (CAM-ICU negative), Exclusion Criteria: * patient refusal * psychosis or preexisting cognitive dysfunction * cerebral injury, * hygiene/microbiological harm, * pregnancy, * decision of withdrawal of care

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Conditions

The condition(s) this trial relates to.

anxiety disorder Dyspnea Pain

As listed by the trial registrant

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

Contacts and locations

Locations

  • University of Montpellier Hospital

    Montpellier, 34295, France

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