VR lets doctors walk in Patients' shoes to fight mental health stigma
NCT ID NCT07375199
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a short virtual reality experience can reduce stigma toward people with schizophrenia among healthcare workers and students. Participants will watch two VR videos that simulate hallucinations and paranoid thoughts, then researchers measure changes in attitudes and biases. The goal is to see if immersive perspective-taking can foster empathy and reduce discrimination in healthcare settings.
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 simulation of psychotic symptoms
- What this could lead to
- If it works, this could point toward a new training tool to reduce stigma and improve empathy among healthcare workers.
- What could go wrong
- This is an early-stage study with only 128 participants, and it measures attitudes rather than clinical outcomes. The effect may be small or not last long-term.
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 128 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 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 to 65 years
- 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.
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 between 18 and 65 * currently employed as a healthcare professional or enrolled as a advanced-grade student in medicine, nursing, or psychology * no history of psychiatric or addictive disorders (except for tobacco dependence) * covered by French social security * able to provide informed written consent after receiving appropriate information. Exclusion Criteria: * current or past psychiatric or addictive disorder (except tobacco dependence) * use of antipsychotic medication; first-degree family history of schizophrenia; cognitive impairment * susceptibility to cybersickness * recent (\<1 year) or acute neurological disorders * history of epilepsy * known otorhinolaryngologic conditions causing vertigo, nausea or vomiting * pregnancy or breastfeeding * legal protection measures * any condition, in the investigator's opinion that would prevent valid questionnaire completion.
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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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Unité de Recherche Clinique (URC), Centre Hospitalier Henri Laborit
Poitiers, 86000, France
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Other studies related to the condition(s) this trial covers.
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