Virtual reality assessment for asylum seekers with paranoid delusions
Official title: Paranoid Behaviour & Threat Evaluation in Asylumseekers Diagnosed With a Psychotic Disorder and Experiencing Paranoid Delusions: A Phenomenological Qualitative Virtual Reality Study
Run by University Medical Center Groningen · NCT06692530 · Data updated 2026-11-12
This study tests whether virtual reality can help understand the thoughts and feelings of asylum seekers with paranoid delusions to improve their treatment.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 15 (estimated) |
| Sponsor | University Medical Center Groningen Academic / other |
| Locations | 1 site (Balkbrug, Overijssel) |
| Status | Recruiting |
| Started | November 22, 2024 |
| Main results expected | May 1, 2025 |
| Study ends | July 1, 2025 |
| Registry record updated | April 2, 2025 |
| Trial ID | NCT06692530 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are asylum seekers aged 18 and over, diagnosed with paranoid delusions and receiving treatment at CTP Veldzicht.
✕Probably not a fit
Patients who are acutely psychotic or unable to provide informed consent will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to explore the behaviors and threat evaluations of asylum seekers experiencing paranoid delusions through the use of virtual reality (VR). By leveraging VR technology, researchers intend to assess thoughts, behaviors, and emotions in real-time, addressing the challenges posed by language and cultural differences in traditional diagnostic assessments. The study focuses on individuals aged 18 and over who are receiving treatment for psychotic disorders at CTP Veldzicht in the Netherlands. The goal is to evaluate the applicability of VR as a diagnostic tool for this vulnerable population.
Why it matters
Potential benefit: If successful, this study could enhance diagnostic accuracy and treatment approaches for asylum seekers experiencing paranoid delusions.
How similar studies have gone: While the use of VR in psychiatric assessments is emerging, this specific application for asylum seekers with paranoid delusions is relatively novel and has not been extensively tested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Aged 18 or over * Receiving treatment from CTP Veldzicht * Seeking asylum in the Netherlands, registered with Centraal Opvang Asielzoekers (COA) * Classification (primary or subsidiary classification) of a disorder categorized within the 'schizophreniaspectrum- and other psychotic disorders' (DSM-V) * Diagnosed with the symptom of paranoid delusion, defined as a PANSS score on the delusion item (P6) \>2 Exclusion Criteria: * Unable to provide informed consent * Acutely psychotic, which means overwhelmed by psychotic symptoms, agitated, not able to participate in an interview, as judged by a therapist or socio-therapist.
Where it's running
-
CTP Veldzicht
Balkbrug, Overijssel, Netherlands Recruiting
Study contacts
- Study coordinator: Ron Haarms, MSc
- Email: r.haarms@umcg.nl
- Phone: 650070910
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Transition Support for First-Episode Psychosis
A team-based program helps people experiencing their first psychotic episode move from hospital to outpatient care to see if they stay engaged and feel better.
-
SEEG-guided DBS for Schizophrenia
This study tests whether SEEG-guided deep brain stimulation can help people with treatment-resistant schizophrenia see if symptoms improve.
-
Using an epigenetic drug to boost virtual reality cognitive training for middle-aged and older adults with depression or bipolar disorder
This trial will test whether daily sodium butyrate combined with three weeks of virtual reality cognitive training improves thinking skills in symptomatically stable adults aged 40–75 with depression or bipolar disorder.
-
Medical and psychiatric profiling of adults admitted to general adult psychiatry wards
This project will collect questionnaires, rating scales, and case-note information from adults admitted to general adult psychiatry wards to see what their physical and mental health profiles look like.
-
iTEST: a blended mobile program to improve introspective accuracy (accurate self-judgment of abilities)
This trial tests whether iTEST — daily mobile cognitive training plus coaching that focuses on accurate self-judgment — helps adults with schizophrenia-spectrum or other psychotic disorders improve community functioning.
-
VR avatar therapy for psychosis: linking thinking, self-awareness, and social cognition
This project will test whether cognitive, metacognitive, and social-cognition factors relate to how well VR-based avatar therapy helps people with schizophrenia who have persistent auditory hallucinations.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.