Actively Recruiting
Impact of Immersive Virtual Reality in Stroke Rehabilitation During the Acute Phase and Correlation With Blood Biomarkers and Genetic Polymorphisms
Led by Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta · Updated on 2026-05-27
120
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Stroke is a leading cause of disability in adults, affecting upper-limb mobility. Researchers are evaluating whether adding immersive virtual reality (IVR) to conventional rehabilitation (CR) can improve motor function, functional status, and quality of life in stroke patients. This single-center, prospective, randomized, controlled, open-label trial with blinded endpoint assessment also explores how IVR affects neuroplasticity biomarkers and the role of genetic polymorphisms in recovery and rehabilitation outcomes. Participants will be adults diagnosed with ischemic or hemorrhagic stroke who have impaired upper-limb mobility and are entering an intensive conventional rehabilitation (ICR) program after hospital discharge. Patients are randomly assigned to receive either ICR alone or ICR combined with IVR therapy. Both groups begin with CR at the hospital followed by ICR at a rehabilitation center, with the intervention group also receiving IVR therapy during these phases. Throughout the one-year study, participants will be assessed at 3 and 12 months for upper-limb motor strength, functional independence, and quality of life. Blood samples taken at baseline and 12 months will be analyzed to identify neuroplasticity-related proteins, microRNAs, and genetic polymorphisms that may predict recovery or influence rehabilitation response. Safety and multiple functional measures will also be monitored during the trial.
CONDITIONS
Brief Title
IVR ON UPPER-LIMB REHABILITATION IN STROKE PATIENTS: A CLINICAL TRIAL
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of ischemic stroke or intracerebral hemorrhage
- Age greater than 18 years
- Less than 7 days between stroke onset and inclusion in the study
- Impairment of mobility in the right or left upper limb due to stroke
- Participation in an intensive conventional rehabilitation program after hospital discharge
- Ability to understand and sign the study informed consent form and biobank consent form
You will not qualify if you...
- Previous upper limb disability from neurological or non-neurological causes
- Previous dementia or any disease with less than 1 year life expectancy
- Language comprehension difficulties
- Difficulty remembering exercise instructions
- History of photosensitive epilepsy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - Up to 7 days after stroke onset
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person)
Duration - Acute phase during hospital stay and continuation post-discharge (duration varies per participant)
Participants receive conventional rehabilitation (CR) at the hospital. Those in the intervention group also receive immersive virtual reality (IVR) therapy. After hospital discharge, all participants continue an intensive conventional rehabilitation (ICR) program at a rehabilitation center; the intervention group continues IVR therapy alongside ICR.
Visits occur during hospital rehabilitation and at the rehabilitation center; frequency depends on individual rehabilitation schedules
Duration - 12 months post-treatment
Participants are assessed for motor function, quality of life, and functional outcomes at 3 and 12 months after the start of the intervention.
2 follow-up visits at 3 and 12 months (in-person)
Trial Site Locations
Total: 1 location
1
Hospital Dr Josep Trueta
Girona, Spain
Actively Recruiting
Research Team
Y
Yolanda Silva, MD PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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