Actively Recruiting
Virtual Reality and Artificial Intelligence in Treatment for Patients With Psychosis
Led by Oslo University Hospital · Updated on 2025-03-25
150
Participants Needed
2
Research Sites
190 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Virtual Reality (VR) has gained momentum in the treatment of various mental health conditions. Despite its potential and emphasis on better use of technology in healthcare strategies, VR therapy for severe mental illness remains underdeveloped and understudied. This will be the first randomized controlled trial to combine cognitive behavioral therapy-based VR with state-of-the-art Artificial Intelligence. Reduced quality of life, social withdrawal and inactivity found in psychotic disorders may be largely explained by avoidance due to severe symptoms of anxiety, present in as many as two-thirds of patients with schizophrenia. Alleviating anxiety may thus be key to help improve functional outcomes. The aim of this study is to provide novel information about VR therapy in psychosis employing the newly developed RecoVRy application. Study objectives are to examine short- and long-term effects on real-world functioning, psychiatric symptoms, and quality of life. A total of 150 participants will be recruited from five Norwegian hospitals. Participants will be randomly assigned to either receive the RecoVRy intervention (N=75) alongside treatment as usual or a control intervention (N=75) in which they engage with three distinct VR games. RecoVRy will generate new and important knowledge to improve mental health services in psychosis and hopefully improve existing practise and facilitate personalized treatment. RecoVRy will fill knowledge gaps concerning anxiety in psychosis, as this is often left untreated and consequently create societal benefits by increasing social and functional participation. Finally, knowledge from RecoVRy can easily be generalized to other patient groups and health sectors.
CONDITIONS
Official Title
Virtual Reality and Artificial Intelligence in Treatment for Patients With Psychosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 17 and 65 years
- Receiving psychosis treatment at a participating hospital clinic
- Clinical diagnosis of schizophrenia spectrum psychosis (ICD-10 codes F20-F29) or affective disorder with psychotic symptoms (F31.2, F31.5, F32.3, F33.3)
- Self-reported difficulties going outside or engaging in everyday activities
- Willing and able to provide written informed consent to participate
You will not qualify if you...
- Photosensitive epilepsy
- Significant impairments in vision, hearing, or balance
- Insufficient understanding of Norwegian language
- Currently receiving treatment in a forensic setting or Psychiatric Intensive Care Unit
- Primary diagnosis of alcohol or substance use disorder, personality disorder, or organic syndrome
- Clinically significant learning disability
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
Oslo University Hospital
Oslo, Norway, Norway
Actively Recruiting
2
Oslo University Hospital
Nydalen, Norway, Postboks 4959
Active, Not Recruiting
Research Team
J
Jan Ivar Røssberg, Professor
CONTACT
J
June U Lystad, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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