AI therapist in virtual reality aims to treat depression
NCT ID NCT07172113
First seen Jun 26, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This pilot study tests a virtual reality (VR) therapy session guided by an AI-powered virtual therapist to help reduce depression symptoms. Sixty Chinese young adults with mild to severe depression will either receive the VR therapy or join a waitlist. The goal is to see if this digital approach can make cognitive behavioral therapy (CBT) more accessible and engaging.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- AI-powered virtual reality cognitive behavioral therapy
- What this could lead to
- If successful, this could provide a more accessible and interactive digital therapy option for depression, reducing stigma and cost barriers.
- What could go wrong
- This is a small pilot study with only 60 participants, so results may not apply broadly. The virtual therapist may not be as effective as in-person therapy, and long-term benefits are unknown.
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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2025
- Expected to finish
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Sep 2025
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 40 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.
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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: 1. Chinese young adult aged 18-40 years 2. Native Cantonese speaker 3. Presence of depressive symptoms, as indicated by a score of 10 or higher on the depression sub-scale of the Depression Anxiety Stress Scale 21 (DASS-21). 4. Able and willing to comply with the requirements of the study protocol Exclusion Criteria: 1. A current or history of any psychiatric disorder(s) other than depressive disorder and anxiety disorder, such as bipolar disorder, psychotic disorders, and substance use disorder 2. A current or history of any voice, speech, and language disorders 3. A current or history of non-suicidal self-injury or suicidality 4. Incompetent in giving informed consent for participation in the study 5. A current or history of significant motion sickness, active nausea, and vomiting or epilepsy. 6. A current or history of color vision deficiency 7. Subject who is preparing for pregnancy or pregnant
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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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The Chinese University of Hong Kong
RECRUITINGHong Kong, Hong Kong
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