Could a family video or VR nature trip calm ICU patients?
NCT ID NCT07794696
First seen Aug 31, 2026 · Last updated Sep 02, 2026 · Updated 2 times
Summary
This trial tests whether watching short family videos or virtual reality nature scenes can reduce anxiety, agitation, and pain in adults staying in intensive care. Researchers will randomly assign 72 participants to one of three groups: family videos, family videos plus VR nature videos, or standard care. They will measure anxiety, agitation, pain, and vital signs before and after the sessions on the second and third days in the ICU.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Family videos and virtual reality-based nature videos
- What this could lead to
- If effective, these simple, non-drug interventions could offer a safe way to reduce anxiety, agitation, and pain in intensive care patients without relying on sedatives.
- What could go wrong
- This is a small trial with 72 participants, so results may not apply broadly. The effects may be modest, and some patients might not tolerate the VR headset or find the videos helpful.
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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
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72 people
The number who actually took part.
- Started
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Oct 2024
- Finished
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Mar 2025
- 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 to 80 years
- 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 18-80 years * Hospitalized in an intensive care unit * Conscious and able to communicate * Willing to participate in the study * At least literate * Able to speak Turkish * No diagnosed psychiatric disorder * Hospitalized in the intensive care unit for at least two days Exclusion Criteria: Visual or hearing impairment * Being intubated * Cognitive, sensory, or verbal impairment preventing communication * Use of sedative, anxiolytic, or similar medications
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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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Istanbul Ministry of Health Goztepe Training and Research Hospital
Istanbul, Istanbul, 34010, Turkey (Türkiye)
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