Virtual reality and music may ease ICU suffering
NCT ID NCT04017299
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
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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
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60 people
The number who actually took part.
- Started
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Jul 2019
- Finished
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Dec 2019
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Montpellier Hospital
Montpellier, 34295, France
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