VR to Improve Psychological Recovery After Critical Illness

  • Research type

    Research Study

  • Full title

    Use of Virtual Reality to Improve Psychological Recovery Following Critical Illness

  • IRAS ID

    299663

  • Contact name

    Jacqueline Twamley

  • Contact email

    jacqueline.twamley@lthtr.nhs.uk

  • Sponsor organisation

    Lancashire Teaching Hospitals NHS Foundation Trust

  • Duration of Study in the UK

    0 years, 3 months, 31 days

  • Research summary

    Critical care survivors face significant barriers in their recovery, experiencing a high incidence of anxiety, depression and post-traumatic stress disorder (PTSD). PTSD is caused by very stressful, frightening or distressing events. This can result in the avoidance of contact with healthcare settings and staff and can affect a patient's willingness to engage in rehabilitation activities, and affect their relationships and ability to work.

    Virtual reality (VR) has been used to treat PTSD in veterans of conflicts such as soldiers. Virtual reality allows progressive exposure in a safe and controlled way, where the patient can feel in control of the situation. The proposal is to develop the VR equivalent of our CrCU (Critical Care Unit) and use this to prevent or to treat PTSD and other psychological/emotional responses to critical illness in former CrCU patients.

    This innovative study has the potential for helping both our own critical care patients and also critical care patients nationally and perhaps worldwide. The study could also be used to inform and support families of CrCU patients, who are the main carers for patients during their recovery, and to train healthcare professionals about the patient experience.

    Using a co-design approach, this VR content development study will take place at Lancashire Teaching Hospitals from July to October 2021 and will involve the creation of a Virtual CrCU environment and define the scope of its use in clinical practice.

    Working with former CrCU patients and CrCU staff from the VR development will involve patient and staff consultation to inform the design and delivery of the VR intervention. Patients and staff will each be asked to take part in 1 focus group meeting and, if willing, a co-design meeting. On completion of this study we will have created the VR prototype to test in clinical practice.

  • REC name

    North West - Greater Manchester West Research Ethics Committee

  • REC reference

    21/NW/0204

  • Date of REC Opinion

    19 Aug 2021

  • REC opinion

    Further Information Favourable Opinion