Can a VR headset prevent Post-Surgery confusion in seniors?
NCT ID NCT06232317
First seen Jun 24, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tested whether a virtual reality game called ReCognitionVR could help older adults (60+) stay mentally alert after abdominal surgery. Thirty participants used the VR headset or standard orientation methods. The goal was to see if the VR approach is safe, acceptable, and feasible for preventing post-operative delirium.
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 software (ReCognitionVR) delivered via Oculus Quest 2
- What this could lead to
- If it works, this could point toward a non-drug way to prevent confusion and delirium in older patients after surgery.
- What could go wrong
- This is a very small feasibility study with only 30 participants, so results may not apply broadly. The VR approach may not be practical or effective for all 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.
- 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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30 people
The number who actually took part.
- Started
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Dec 2023
- Finished
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May 2024
- 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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60 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * ≥60 years of age * Scheduled to undergo the following abdominal surgeries (open or laparoscopic or robotic assisted): small bowel and large bowel surgery; cholecystectomy; Whipple procedure; pancreatectomy; splenectomy. * Richmond Agitation-Sedation Scale (RASS) Score 0 Exclusion Criteria: * Subjects with baseline cognitive impairment * Person with active psychiatric disorders and being treated with medications, especially schizophrenia * Person who is deaf or blind * Person with an underlying cognitive disorder or associated phobias (e.g., claustrophobia) * Person participating in other clinical trials involving drugs, biologics, devices, or behavioral interventions * Active seizure disorders
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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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Houston Methodist Research Institute
Houston, Texas, 77030, United States
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Other studies related to the condition(s) this trial covers.
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