ICU-specific virtual reality for mental health after critical illness: an international three-arm randomized clinical trial

Survivors of critical illness frequently experience symptoms of post-intensive care syndrome (PICS), including post-traumatic stress disorder (PTSD), anxiety, and depression, with downstream impact on health-related quality of life (HRQoL). We evaluated whether an intensive care unit-specific virtual reality (ICU-VR) video improves mental health outcomes and whether timing (early vs. late) matters. We conducted an international, three-arm, multicentre randomized clinical trial across eleven hospitals. Adults (≥ 18 years) with ICU stay ≥ 72 h and mechanical ventilation ≥ 24 h were randomized 1:1:1 to (1) standard care, (2) early ICU-VR (within 7–15 days post-ICU), or (3) late ICU-VR (≈ 3 months, during aftercare). The primary endpoint was PTSD symptom severity at six months (T3) measured by the Impact of Event Scale-Revised (range 0–88). Secondary endpoints included anxiety/depression severity and prevalence, and HRQoL. We randomized 344 participants (median age 61 years; 62% male); follow-up among survivors at six months (T3) was 80%. At six months, PTSD symptom severity did not differ between early ICU-VR and control (β = 0.32; 95% CI –3.38 to 4.02; p = 0.87) nor late ICU-VR and control (–0.82; 95% CI –4.62 to 2.97; p = 0.67). No between-group differences were observed for anxiety, depression, or HRQoL (all adjusted p > 0.05). Patients rated ICU-VR highly for improving understanding of the ICU experience and overall satisfaction (median 8/10). In this multicentre randomized clinical trial, a single ICU-VR video did not improve PTSD, anxiety, depression, or HRQoL at six months versus standard care. Findings should not be generalized to multi-session, therapist-guided, or personalized VR interventions. Future trials should target high-risk patients, make multi-session mandatory, and personalize ICU-VR. This study was prospectively registered Netherlands: Trial Register/International Clinical Trials Registry Platform, NL9812, October 21, 2021.

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Publication Details

Journal
Critical Care
Published
2026-07-24
DOI
https://doi.org/10.1186/s13054-026-06186-4
Primary Topic
Intensive Care Unit Cognitive Disorders
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article
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article

ICU-specific virtual reality for mental health after critical illness: an international three-arm randomized clinical trial

Fabio Silvio Taccone, Jasper van Bommel, Adrienne Raben, Christian Jung et al.
Critical Care
Intensive Care Unit Cognitive Disorders
article

ICU-specific virtual reality for mental health after critical illness: an international three-arm randomized clinical trial

Fabio Silvio Taccone, Jasper van Bommel, Adrienne Raben, Christian Jung, Johan H. Vlake, Tim I.M. Korevaar, Barbara Festen, Anna FC Schut, Michel E. van Genderen, Denise E. Hilling, Corstiaan A. den Uil, Jan H Elderman, Sefanja Achterberg, Ralph K. L. So, Marianne Devroey, Margo van Mol, Evert‐Jan Wils, Diederik A M P J Gommers, Denzel L. Q. Drop, Annemieke Dijkstra
article en

Abstract

Survivors of critical illness frequently experience symptoms of post-intensive care syndrome (PICS), including post-traumatic stress disorder (PTSD), anxiety, and depression, with downstream impact on health-related quality of life (HRQoL). We evaluated whether an intensive care unit-specific virtual reality (ICU-VR) video improves mental health outcomes and whether timing (early vs. late) matters. We conducted an international, three-arm, multicentre randomized clinical trial across eleven hospitals. Adults (≥ 18 years) with ICU stay ≥ 72 h and mechanical ventilation ≥ 24 h were randomized 1:1:1 to (1) standard care, (2) early ICU-VR (within 7–15 days post-ICU), or (3) late ICU-VR (≈ 3 months, during aftercare). The primary endpoint was PTSD symptom severity at six months (T3) measured by the Impact of Event Scale-Revised (range 0–88). Secondary endpoints included anxiety/depression severity and prevalence, and HRQoL. We randomized 344 participants (median age 61 years; 62% male); follow-up among survivors at six months (T3) was 80%. At six months, PTSD symptom severity did not differ between early ICU-VR and control (β = 0.32; 95% CI –3.38 to 4.02; p = 0.87) nor late ICU-VR and control (–0.82; 95% CI –4.62 to 2.97; p = 0.67). No between-group differences were observed for anxiety, depression, or HRQoL (all adjusted p > 0.05). Patients rated ICU-VR highly for improving understanding of the ICU experience and overall satisfaction (median 8/10). In this multicentre randomized clinical trial, a single ICU-VR video did not improve PTSD, anxiety, depression, or HRQoL at six months versus standard care. Findings should not be generalized to multi-session, therapist-guided, or personalized VR interventions. Future trials should target high-risk patients, make multi-session mandatory, and personalize ICU-VR. This study was prospectively registered Netherlands: Trial Register/International Clinical Trials Registry Platform, NL9812, October 21, 2021.

Critical Care
Université Libre de Bruxelles (BE), Bethesda Hospital (IN), Erasmus MC (NL), Sint Franciscus Gasthuis (NL), Düsseldorf University Hospital (DE), Albert Schweitzer Ziekenhuis (NL), Medisch Centrum Haaglanden (NL), Ikazia Ziekenhuis (NL), Maasstad Ziekenhuis (NL), Ziekenhuis Gelderse Vallei (NL), IJsselland Ziekenhuis (NL), Groene Hart Ziekenhuis (NL), Erasmus MC Cancer Institute (NL), Heinrich Heine University Düsseldorf (DE), Erasmus University Rotterdam (NL)
Good health and well-being
Openalex Percentile: Top 8%
Intensive Care Unit Cognitive Disorders
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