This study aims to test if the VR games could be a form of upper limb rehabilitation for people with arm/hand problems due to SCI while they are in hospital. Participants who have had a spinal cord injury and have tetraplegia will be recruited from the Queen Elizabeth National Spinal Injuries Unit. After they have provided informed consent, they will receive 12 weeks of either standard upper limb therapy ('control group'), or both the VR activities and standard treatment ('VR Group'). Participants who receive VR activities will engage in immersive VR games that have been designed in co-production with people with tetraplegia and spinal cord injury specialists. The games aim to help participants improve the use of their arms and hands while they are undergoing primary rehabilitation within the Queen Elizabeth National Spinal Injuries Unit (QENSIU). The participants who are in the control group will receive their usual rehabilitation and will be given the opportunity to try the VR games after the completion of their involvement in the trial. This study will measure the feasibility (the 'primary outcome') and explore the effectiveness (the 'secondary outcome') of the VR intervention. Feasibility will be measured by recording how often the VR games are used and whether or not participants use the games for the full duration of the trial. Participants and therapists will be interviewed at the end of the trial.
Age range
18 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Number of VR Sessions Completed
Timeframe: Measured over 12 weeks of participation.
Time spent in VR
Timeframe: Measured over 12 weeks of participation.
Number of completed assessments
Timeframe: Measured over 12 weeks of participation.
Participant retention
Timeframe: Measured over 12 weeks of participation.
Participant recruitment rate per month
Timeframe: Measured over 12 weeks of participation.
Participant eligibility
Timeframe: Measured over 12 weeks of participation.
Adverse event monitoring and reporting
Timeframe: Measured over 12 weeks of participation.
Semi-structured Interviews
Timeframe: Completed at week 12 after the last VR session has been completed.
Usefulness, Satisfaction, and Ease of use Questionnaire (USE Questionnaire)
Timeframe: Completed at week 12 after the last VR session has been completed.
Handedness (Treatment Parameter)
Timeframe: Completed at week 12 after the last VR session has been completed.
Target Movement (Treatment Parameters)
Timeframe: Completed at week 12 after the last VR session has been completed.
Number of Repetitions (Treatment Parameters)
Timeframe: Completed at week 12 after the last VR session has been completed.
Choice of Game (Treatment Parameters)
Timeframe: Completed at week 12 after the last VR session has been completed.
Input Device choices (Treatment Parameters)
Timeframe: Completed at week 12 after the last VR session has been completed.