Actively Recruiting
Co-Designing a Virtual Reality Intervention to Enhance Skill Development
Led by University of North Carolina, Chapel Hill · Updated on 2025-10-15
26
Participants Needed
1
Research Sites
54 weeks
Total Duration
On this page
Sponsors
U
University of North Carolina, Chapel Hill
Lead Sponsor
M
MQ Mental Health Research
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study is refining and pilot testing a novel Virtual Reality (VR) supplement for inpatient treatment: the Practice Experiences for School Reintegration (PrESR) program. The PrESR provides immersive school and social experiences for inpatient adolescents (with suicidal-related admissions) to practice skills in real-world settings with the guidance of a trained clinician within the confines of a hospital. The initial intervention was based on feedback from adolescent hospitalized for suicide-related crises, and school and hospital professionals, but did not provide tailored experiences to address the individual needs of ethnic-racial, gender, and sexual minoritized adolescents. Therefore, the VR environment of PrESR was adapted based on input from adolescents with previous suicide-related crises identifying as ethnic, racial, sex, or gender minoritized. This pilot randomized controlled trial (RCT) aims to explore the feasibility, acceptability, and facilitators/barriers to implementation of the adapted version of PrESR for improving outcomes in hospitalized adolescents. This study is not powered to test hypotheses; however, in addition to assessing feasibility, acceptability, and barriers/facilitators, this pilot trial will assess candidate intermediary and outcome measures.
CONDITIONS
Official Title
Co-Designing a Virtual Reality Intervention to Enhance Skill Development
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Current hospitalization for suicidal thoughts and behaviors
- Ages 13 to 18 years
- Approval from a clinician to participate
- Ability to speak, read, and understand English well enough to complete study procedures
- Consent from a parent or legal guardian in English or Spanish (for minors)
- Adolescent assent or consent in English
You will not qualify if you...
- Presence of active psychosis
- Presence of intellectual disability
- Risk for cybersickness at or above the 50th percentile based on the Motion Sickness Susceptibility Questionnaire
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
UNC Adolescent Psychiatry Inpatient Unit
Chapel Hill, North Carolina, United States, 27599
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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