Could VR headsets make ICU recovery less miserable?
NCT ID NCT07089134
First seen Jun 24, 2026 · Last updated Sep 16, 2026 · Updated 3 times
Summary
This study tests whether using an immersive virtual reality headset during physical therapy can improve satisfaction and recovery for patients in the intensive care unit. Ninety adult ICU patients will be randomly assigned to either traditional rehab or rehab with VR. The goal is to see if VR makes the experience more pleasant and helps patients get better faster.
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 headset
- What this could lead to
- If it works, this could make ICU rehabilitation more pleasant and engaging, potentially improving recovery and reducing stress.
- What could go wrong
- This is a small, early-stage trial with only 90 patients. The benefits may not be large or may not apply to all ICU patients. Virtual reality may cause discomfort or side effects like dizziness.
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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About 90 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2026
- Expected to finish
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Oct 2028
An estimate. End dates often move.
- 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: * Aged ≥18 years * Glasgow Coma Scale (GCS) score ≥14 * Richmond Agitation-Sedation Scale (RASS) score between -1 and +1 * Negative for delirium according to the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) * Estimated ICU stay of ≥72 hours * Able to communicate in Portuguese * Understand and follow verbal instructions * Have no psychotic disorders, visual impairment or hearing loss. Exclusion Criteria: * Hemodynamic instability * Signs of respiratory distress * Contact isolation for infectious diseases * Conditions that limit head and neck movement
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hospital Sírio Libanês
RECRUITINGSão Paulo, São Paulo, 01308050, Brazil
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