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A controlled trial of a virtual reality experience to support wellbeing in healthcare students

A controlled trial of a virtual reality experience to support wellbeing in healthcare students

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN51742331
Enrollment
120
Registered
2025-05-06
Start date
2023-11-06
Completion date
Unknown
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety/stress Mental and Behavioural Disorders

Interventions

Overview The study employed an unblinded, parallel randomised controlled trial (RCT) design with university students. A clinically informed multi-sensory hypnotherapy-based experience using an immersi
a deliberate decision was made not to exclude students with mental health concerns. 131 participants were recruited and randomly allocated to VR (n=67) or video (n=64). Participants received sixty p

Sponsors

St George's, University of London
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Over the age of 18 2. Enrolled student at St George's University of London

Exclusion criteria

Exclusion criteria: 1. History of seizures 2. History of pacemakers

Design outcomes

Primary

MeasureTime frame
1. Momentary negative and positive affective states, and participants’ level of immersion were measured using a 10-point numerical analogue scale (VAS) at baseline and a 2-week follow-up 2. Cybersickness was measured using the Simulator Sickness Questionnaire (SSQ) before and after the intervention on the final trial session 3. The following short-term outcomes in perceived stress, wellbeing, and depressive symptoms measures using standardised questionnaires at baseline and a 2-week follow-up: 3.1. Global perceived level of stress was measured with the 10-item version of the Perceived Stress Scale (PSS) 3.2. Positive states of being, thinking, behaving and feeling in the last 2 weeks were measured using the Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS) 3.3. Depression symptoms were measured using the Patient Health Questionnaire-2 (PHQ2) 4. Intervention satisfaction: At the end of the trial, participants were asked which group they would have preferred to be in. Satisfaction with the intervention for participants completing VR or Video interventions was measured using the VAS, measuring levels of agreement (with anchors 1=‘do not agree’, 10=‘totally agree’) that the experience made them feel calmer, had a positive effect and is one they would recommend to other students. Participants were also asked to describe the impact the experience had on them personally, if it is something they could see themselves using and to provide any other comments/feedback in an open-ended manner. At 2-week follow-up, participants rated levels of agreement (on VAS scales) that the intervention helped to manage stressful situations and is a resource they would see themselves using in the future.

Secondary

MeasureTime frame
Use of mental health and support services measured using a study questionnaire at baseline, post-intervention and 2-week follow-up

Countries

England, United Kingdom

Contacts

Public ContactAileen O'Brien
aobrien@sgul.ac.uk+44 (0)7961174521

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026