Virtual reality training to prevent aggression in psychiatric patients
Feasibility and Pilot Study of Virtual Reality Aggression Prevention Training (VRAPT) for (Forensic) Psychiatric Patients
NA · University Hospital, Basel, Switzerland · NCT05293834
This study is testing a new virtual reality training program to see if it can help reduce aggressive behaviors in psychiatric patients, both those in the justice system and those receiving regular care.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 68 (estimated) |
| Ages | 12 Years and up |
| Sex | All |
| Sponsor | University Hospital, Basel, Switzerland (other) |
| Locations | 1 site (Basel, Canton of Basel-City) |
| Trial ID | NCT05293834 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of Virtual Reality Aggression Prevention Training (VRAPT) for both forensic and non-forensic psychiatric patients in Switzerland. It aims to address the high prevalence of violent and aggressive behaviors in these populations by implementing a novel virtual reality intervention. The study will assess the feasibility of VRAPT and gather data on its impact on aggressive behaviors among adult and juvenile patients. Previous research has shown some promise for VRAPT in reducing aggression, and this study seeks to expand its application in a new setting.
Who should consider this trial
Good fit: Ideal candidates include forensic and non-forensic psychiatric in- and out-patients exhibiting aggressive behavior problems.
Not a fit: Patients with insufficient German language skills, intellectual disabilities, epilepsy, or those in an acute psychotic state may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce aggressive behaviors in psychiatric patients, leading to improved safety and rehabilitation outcomes.
How similar studies have performed: Previous studies on VRAPT in other countries have shown some initial success, indicating potential for effectiveness in this new context.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * forensic and non-forensic psychiatric in- and out-patients of the Forensic Department or Adult Department of the Psychiatric University Hospitals Basel with aggressive behavior problems according to their clinical treatment team (which includes senior medical doctor, therapist, nursing staff). Exclusion Criteria: * insufficient German language skills (in speech or reading); * intellectual disabilities (IQ \< 70); * epilepsy; * acute psychotic state.
Where this trial is running
Basel, Canton of Basel-City
- Psychiatric University Hospitals (UPK) Basel — Basel, Canton of Basel-City, Switzerland (RECRUITING)
Study contacts
- Principal investigator: Cyril Boonmann, PhD — Psychiatric University Hospitals (UPK) Basel
- Study coordinator: Cyril Boonmann, PhD
- Email: cyril.boonmann@upk.ch
- Phone: +41 61 325 82 91
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Forensic Psychiatry, Aggression Prevention, Virtual Reality, Virtual Reality Aggression Prevention Training