Evidence map›Paper›PMID 37742702›Full record

ArticleThe lancet. Psychiatry2023

Automated virtual reality cognitive therapy versus virtual reality mental relaxation therapy for the treatment of persistent persecutory delusions in patients with psychosis (THRIVE): a parallel-group, single-blind, randomised controlled trial in England with mediation analyses.

Daniel Freeman, Rachel Lister, Felicity Waite, Ushma Galal, Ly-Mee Yu, Sinéad Lambe, Ariane Beckley, Emily Bold, Lucy Jenner, Rowan Diamond and 13 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in The lancet. Psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06876779 (Virtual Reality Based Cognitive Behavioral Therapy for Social Anxiety-Driven Depression Among Youths), which is not on this map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
6.5field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06876779 nanot yet recruitingnot on this mapstarted 2025, after this paper: background citation

Virtual Reality Based Cognitive Behavioral Therapy for Social Anxiety-Driven Depression Among Youths: A Randomized Controlled Trial

TypeinterventionalSponsorHong Kong Shue Yan UniversityRan2025 to 2026Enrolled90ConditionsSocial Anxiety Disorder (SAD), Social PhobiaArmsVR intervention
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 29 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 6 institutions in 2 countries.

Daniel FreemanDepartment of Experimental Psychology, University of Oxford, Oxford, UK; Oxford Health NHS Foundation Trust, Oxford, UK. Electronic address: daniel.freeman@psy.ox.ac.uk.
Rachel ListerDepartment of Experimental Psychology, University of Oxford, Oxford, UK; Black Country Healthcare NHS Foundation Trust, Dudley, UK.
Felicity WaiteDepartment of Experimental Psychology, University of Oxford, Oxford, UK; Oxford Health NHS Foundation Trust, Oxford, UK.
Ushma GalalOxford Primary Care Clinical Trials Unit, Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
Ly-Mee YuOxford Primary Care Clinical Trials Unit, Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
Sinéad LambeDepartment of Experimental Psychology, University of Oxford, Oxford, UK; Oxford Health NHS Foundation Trust, Oxford, UK.
Ariane BeckleyDepartment of Experimental Psychology, University of Oxford, Oxford, UK.
Emily BoldDepartment of Experimental Psychology, University of Oxford, Oxford, UK.
Lucy JennerDepartment of Experimental Psychology, University of Oxford, Oxford, UK.
Rowan DiamondDepartment of Experimental Psychology, University of Oxford, Oxford, UK; Oxford Health NHS Foundation Trust, Oxford, UK.
Miriam KirkhamDepartment of Experimental Psychology, University of Oxford, Oxford, UK.
Eve TwivyDepartment of Experimental Psychology, University of Oxford, Oxford, UK.
Chiara CausierDepartment of Experimental Psychology, University of Oxford, Oxford, UK.
Lydia CarrDepartment of Experimental Psychology, University of Oxford, Oxford, UK.
Simone SaidelDepartment of Experimental Psychology, University of Oxford, Oxford, UK.
Rebecca DayNorthamptonshire Healthcare NHS Foundation Trust, Kettering, UK.
Alejandro BeaccoEvent Lab, Faculty of Psychology Spain, University of Barcelona, Barcelona, Spain; Universitat Politècnica de Catalunya, Barcelona, Spain.
Aitor RoviraDepartment of Experimental Psychology, University of Oxford, Oxford, UK; Oxford Health NHS Foundation Trust, Oxford, UK.
Annabel IvinsNorthamptonshire Healthcare NHS Foundation Trust, Kettering, UK.
Ryan NahNorthamptonshire Healthcare NHS Foundation Trust, Kettering, UK; Central and North West London NHS Foundation Trust, London, UK.
Mel SlaterEvent Lab, Faculty of Psychology Spain, University of Barcelona, Barcelona, Spain; Institute of Neurosciences, University of Barcelona, Barcelona, Spain.
David M ClarkDepartment of Experimental Psychology, University of Oxford, Oxford, UK; Oxford Health NHS Foundation Trust, Oxford, UK.
Laina RosebrockDepartment of Experimental Psychology, University of Oxford, Oxford, UK; Oxford Health NHS Foundation Trust, Oxford, UK.
University of Oxford · GBOxford Health NHS Foundation Trust · GBNorthamptonshire Healthcare NHS Foundation Trust · GBUniversitat de Barcelona · ESBlack Country Healthcare NHS Foundation TrustCentral and North West London NHS Foundation Trust · GB

Funding

Medical Research Council MR/P02629X/1Wellcome Trust
6 · The paper itself

Abstract

backgroundPersecutory delusions are a major psychiatric problem that often do not respond sufficiently to standard pharmacological or psychological treatments. We developed a new brief automated virtual reality (VR) cognitive treatment that has the potential to be used easily in clinical services. We aimed to compare VR cognitive therapy with an alternative VR therapy (mental relaxation), with an emphasis on understanding potential mechanisms of action.

methodsTHRIVE was a parallel-group, single-blind, randomised controlled trial across four UK National Health Service trusts in England. Participants were included if they were aged 16 years or older, had a persistent (at least 3 months) persecutory delusion held with at least 50% conviction, reported feeling threatened when outside with other people, and had a primary diagnosis from the referring clinical team of a non-affective psychotic disorder. We randomly assigned (1:1) patients to either THRIVE VR cognitive therapy or VR mental relaxation, using a permuted blocks algorithm with randomly varying block size, stratified by severity of delusion. Usual care continued for all participants. Each VR therapy was provided in four sessions over approximately 4 weeks, supported by an assistant psychologist or clinical psychologist. Trial assessors were masked to group allocation. Outcomes were assessed at 0, 2 (therapy mid-point), 4 (primary endpoint, end of treatment), 8, 16, and 24 weeks. The primary outcome was persecutory delusion conviction, assessed by the Psychotic Symptoms Rating Scale (PSYRATS; rated 0-100%). Outcome analyses were done in the intention-to-treat population. We assessed the treatment credibility and expectancy of the interventions and the two mechanisms (defence behaviours and safety beliefs) that the cognitive intervention was designed to target. This trial is prospectively registered with the ISRCTN registry, ISRCTN12497310.

findingsFrom Sept 21, 2018, to May 13, 2021 (with a pause due to COVID-19 pandemic restrictions from March 16, 2020, to Sept 14, 2020), we recruited 80 participants with persistent persecutory delusions (49 [61%] men, 31 [39%] women, with a mean age of 40 years [SD 13, range 18-73], 64 [80%] White, six [8%] Black, one [1%] Indian, three [4%] Pakistani, and six [8%] other race or ethnicity). We randomly assigned 39 (49%) participants assigned to VR cognitive therapy and 41 (51%) participants to VR mental relaxation. 33 (85%) participants who were assigned to VR cognitive therapy attended all four sessions, and 35 (85%) participants assigned to VR mental relaxation attended all four sessions. We found no significant differences between the two VR interventions in participant ratings of treatment credibility (adjusted mean difference -1·55 [95% CI -3·68 to 0·58]; p=0·15) and outcome expectancy (-0·91 [-3·42 to 1·61]; p=0·47). 77 (96%) participants provided follow-up data at the primary timepoint. Compared with VR mental relaxation, VR cognitive therapy did not lead to a greater improvement in persecutory delusions (adjusted mean difference -2·16 [-12·77 to 8·44]; p=0·69). Compared with VR mental relaxation, VR cognitive therapy did not lead to a greater reduction in use of defence behaviours (adjusted mean difference -0·71 [-4·21 to 2·79]; p=0·69) or a greater increase in belief in safety (-5·89 [-16·83 to 5·05]; p=0·29). There were 17 serious adverse events unrelated to the trial (ten events in seven participants in the VR cognitive therapy group and seven events in five participants in the VR mental relaxation group).

interpretationThe two VR interventions performed similarly, despite the fact that they had been designed to affect different mechanisms. Both interventions had high uptake rates and were associated with large improvements in persecutory delusions but it cannot be determined that the treatments accounted for the change. Immersive technologies hold promise for the treatment of severe mental health problems. However, their use will likely benefit from experimental research on the application of different therapeutic techniques and the effects on a range of potential mechanisms of action.

fundingMedical Research Council Developmental Pathway Funding Scheme and National Institute for Health and Care Research Oxford Health Biomedical Research Centre.

Identifiers

PMID37742702
PMCPMC7617886
OpenAlexW4386914803

What OpenQuestion holds

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LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.