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临床试验/ISRCTN17308399
ISRCTN17308399已完成未知

Automated virtual reality (VR) cognitive therapy for patients with psychosis who have anxious avoidance of social situations: a single-blind parallel group randomised controlled trial (gameChange)

niversity of Oxford0 个研究点目标入组 346 人开始时间: 2019年5月2日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
346

研究概览

简要总结

2019 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/31462489 protocol (added 30/08/2019) 2022 Results article in https://pubmed.ncbi.nlm.nih.gov/35395204/ (added 02/09/2022) 2022 Results article in https://pubmed.ncbi.nlm.nih.gov/36399379/ Economic analysis (added 21/11/2022) 2023 Results article in https://doi.org/10.2196/38065 Qualitative results (added 17/01/2023) 2021 Protocol article in https://doi.org/10.2196/31742 Automated Virtual Reality Cognitive Therapy for People With Psychosis: Protocol for a Qualitative Investigation Using Peer Research Methods (added 24/06/2024) 2020 Protocol article in https://doi.org/10.2196/20300 Virtual Reality Cognitive Therapy in Inpatient Psychiatric Wards: Protocol for a Qualitative Investigation of Staff and Patient Views Across Multiple National Health Service Sites (added 24/06/2024) 2022 Results article in https://doi.org/10.2196/20300 Agoraphobic avoidance in patients with psychosis: Severity and response to automated VR therapy in a secondary analysis of a randomised controlled clinical trial (added 24/06/2024) 2022 Results article in https://doi.org/10.1017/s0033291722001167 Virtual reality (VR) therapy for patients with psychosis: satisfaction and side effects (added 24/06/2024)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Adults aged 16 years or older
  • 2. Attending a NHS mental health trust for the treatment of psychosis
  • 3. Clinical diagnosis of schizophrenia spectrum psychosis (F20-29) or an affective diagnosis with psychotic symptoms (F31.2, 31.5, 32.3, 33.3) (ICD-10, WHO, 2010)
  • 4. Having self-reported difficulties going outside their home primarily due to anxiety that they would like treated
  • 5. Participant is willing and able to give informed consent for participation in the trial

排除标准

  • 1. Unable to attempt an Oxford-Behavioural Assessment Task (O-BAT) (the primary outcome measure) at baseline (e.g. due to being unpermitted to leave a psychiatric ward)
  • 2. Photosensitive epilepsy
  • 3. Significant visual, auditory, or balance impairment
  • 4. Current receipt of another intensive psychological therapy (or about to start it within the 6-week trial therapy window)
  • 5. Insufficient comprehension of English
  • 6. In forensic settings or Psychiatric Intensive Care Unit (PICU)
  • 7. Organic syndrome
  • 8. Primary diagnosis of alcohol or substance disorder or personality disorder
  • 9. Significant learning disability
  • 10. Current active suicidal plans
  • (added 31/03/2021) When ethical approval was received on 03/09/2020 to restart the trial following the pause due to COVID-19, this was with a continuing recruitment suspension in place for participants who were at moderate or high risk for a severe course of COVID-19. From 16/02/2021 patients who were at moderate or high risk for a severe course of COVID-19 could join the trial if they had received the COVID-19 vaccine (subject to medical advice)

研究者

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