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.
Age range
13 Years – 18 Years
Sex
ALL
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Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Proportion of Patients in the Target Population Who Agree to Participate
Timeframe: Baseline
Proportion of Patients in the Target Population Excluded Due to Motion Sickness Screening
Timeframe: Baseline
Proportion of Participants Who Complete All Study Procedures
Timeframe: up to 3-weeks following hospital discharge
Average Number of Hours to Complete Assessments at Each Time Point
Timeframe: up to 3-weeks following hospital discharge
Average Number of Minutes to Complete Each Intervention Session
Timeframe: Baseline
Percentage of Adolescent Participants in Which Intervention Delivered With Greater Than or Equal to 80% Fidelity
Timeframe: Baseline
Percentage of Adolescent Participants With Average Acceptability Scores Less Than or Equal to 2
Timeframe: Baseline
Adolescents' Perceptions of Acceptability
Timeframe: Baseline