VR headsets tested to ease End-of-Life distress
NCT ID NCT07109050
First seen Jun 26, 2026 · Last updated Jul 07, 2026 · Updated 2 times
Summary
This study tests whether using a virtual reality headset can help people receiving palliative care achieve personal goals, such as relaxation or bucket-list experiences. Up to 12 patients and their companions will try up to 3 VR sessions. Researchers will track mood, anxiety, and goal progress to see if VR is effective.
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 headset
- What this could lead to
- If it works, this could show that VR is a useful tool for improving wellbeing and achieving personal goals in palliative care.
- What could go wrong
- This is a very small study (12 people) with no control group, so results may not apply widely. It only measures short-term effects, and VR may not help everyone.
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
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8 people
The number who actually took part.
- Started
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Aug 2025
- Finished
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May 2026
- 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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Accepted
You do not need to have the condition being studied to take part.
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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: Participants recieving palliative care must be: * Aged 18 or over (no upper age limit due to the service being lifelong). * Patients deemed to be palliative, receiving specialist care at the designated hospice as either an inpatient or outpatient. * Willing and able to engage in VR interventions as determined by the patients' usual care team. * Able to consent to the research, as assessed by the clinical psychologist supporting recruitment and the primary researcher delivering the VR intervention. Participant companions (carers, relatives) must be: * Aged 18 or over (no upper age limit). * Willing and able to engage in VR interventions and travel to the designated hospice site. * Able to consent to the research, as assessed by the clinical psychologist supporting recruitment and the primary researcher delivering the VR intervention. Exclusion criteria: * Lacking capacity to consent to take part in research as assessed by both the clinical psychologist supporting recruitment and the primary researcher delivering VR. * Exhibiting contraindications as set out by care team including eyesight impairments or neurological conditions such as epilepsy or dementia.
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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 Lincoln
Lincoln, United Kingdom
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