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Clinical Trials in Spain / NCT07408622
Active, not recruiting Not applicable

Virtual Reality Therapy for Wrist and Hand Injury Recovery

NCT07408622 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2026-04-01
Last updated
2026-06-03

Condition(s) studied

Wrist InjuriesHand and Upper Limb TraumaMuskuloskeletan Pain

Investigational drug(s) / intervention(s)

Virtual reality

Virtual reality: The AOT+VR intervention is distinguished by its novel application of immersive first-person perspective virtual reality combined with action observation therapy specifically during the immobilization period in traumatic wrist and hand injuries, targeting the critical early window (first 12-48 hours) when maladaptive neuroplasticity begins. Unlike previous studies focused on neurological patients or post-immobilization phases, this protocol integrates longitudinal assessment of sensorimotor cortical activity using electroencephalography (EEG) alongside functional and psychosocial measures, establishing direct correlations between cortical preservation and clinical recovery not previously documented in traumatic upper limb injuries.

Study summary

The goal of this randomized clinical trial is to find out whether an early neuro-functional rehabilitation program using virtual reality and action observation can improve recovery after a traumatic injury of the wrist or hand that requires immobilization in a cast or splint.

After a fracture or other traumatic injury, the wrist and hand often have to be immobilized for several weeks. This rest is necessary for the bone and soft tissues to heal, but it also has negative effects. The muscles become weaker, joint movement is reduced, and the sense of position and movement (proprioception) worsens. Immobilization also produces fast changes in the brain areas that control movement, which may slow down recovery and increase the risk of long-lasting pain, stiffness, and disability.

This study will compare two rehabilitation programs:

Control group: participants will receive conventional rehabilitation after the cast or splint is removed, following the usual care of the hand therapy and traumatology services.

Experimental group: in addition to conventional rehabilitation, participants will follow a specific program that combines action observation therapy with immersive virtual reality (AOT+VR). During each session, patients will watch first-person videos of functional wrist and hand movements through a virtual reality headset and then practice these same movements. The program includes about 12 sessions of 45 minutes over 6 weeks, starting during the immobilization period and continuing after the cast or splint is removed.

Adults between 18 and 70 years with traumatic injuries of the wrist and/or hand (such as distal radius, carpal or metacarpal fractures, or tendon and ligament injuries) who need immobilization for 2 to 8 weeks will be invited to participate.

Researchers will measure:

Sensorimotor cortical activity associated with action observation and execution using electroencephalography (EEG), pain, disability, and function of the upper limb using validated questionnaires, Physical measures such as wrist range of motion, grip strength, and proprioception, Psychological factors such as fear of movement and pain catastrophizing, Feasibility, adherence to the program, side effects, and patient satisfaction. The main hypothesis is that the AOT+VR program, started early during immobilization, will help maintain brain excitability, reduce pain and psychological barriers, and lead to faster and more complete functional recovery of the wrist and hand compared with conventional rehabilitation alone.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Age 18-70 years old. * Diagnosis of traumatic wrist and/or hand injury within 5 days of injury onset. * Traumatic injury types include: distal radius fractures, scaphoid fractures, metacarpal fractures, phalangeal fractures, other carpal bone fractures, tendinous injuries, or ligamentous injuries. * Require immobilization with cast or splint for 2-8 weeks. * Ability to provide written informed consent. * Ability to understand and follow study instructions. * Sufficient mobility and residual manual capacity to participate in virtual reality sessions and physical assessments. Exclusion Criteria: * History of neurological disease affecting motor control (stroke, Parkinson's disease, multiple sclerosis). * Severe psychiatric disorders (psychosis, severe depression requiring hospitalization). * Current involvement in other rehabilitation protocols or clinical trials. * Contraindications for using virtual reality.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Universidad de Málaga Málaga Málaga

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07408622 on ClinicalTrials.gov ↗ ← All trials in Spain