Actively Recruiting

Phase Not Applicable
Age: 13Years - 18Years
All Genders
NCT07186543

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

Age: 13Years - 18Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

UNC Adolescent Psychiatry Inpatient Unit

Chapel Hill, North Carolina, United States, 27599

Actively Recruiting

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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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