Could virtual reality help treat anorexia? new study aims to find out
NCT ID NCT07353151
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a short virtual reality (VR) program is safe and acceptable for adults with anorexia nervosa. Participants will use VR for about 20-30 minutes each weekday for one week, while continuing their usual care. The goal is to see if people are willing to try it and complete the sessions, and if it helps with anxiety or motivation around food.
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 program
- What this could lead to
- If this works, it could point toward a new, engaging way to help people with anorexia manage food-related anxiety and improve motivation.
- What could go wrong
- This is a very early, small feasibility study with only 45 participants. It may not show clear benefits, and some people might experience side effects like nausea or dizziness from VR.
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 45 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2027
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: * Adults ≥18 years. * Anorexia nervosa receiving or awaiting treatment as usual (TAU) within South London and Maudsley NHS Foundation Trust (inpatient, day service, or outpatient). * Medically stable and clinically suitable to take part in brief VR sessions alongside TAU (as judged by the treating team). * Able to give informed consent. Exclusion Criteria: * Current or recent (within 12 months) serious self-harm with suicidal intent, or behaviour that posed a risk to life (e.g., overdose, deep cutting, swallowing sharp objects), or self-harm likely to cause lasting impairment. * Active suicidality or high risk of suicide. * Untreated or unstable epilepsy. * Psychotic disorder. * Outpatient participants with BMI \< 10. * Current participation in another research study or clinical trial.
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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 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.
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