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Clinical Trials in Spain / NCT07633769
Recruiting Not applicable

Virtual Reality-based Rehabilitation for Traumatic Hand and Wrist Injuries

NCT07633769 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2026-02-01
Last updated
2026-06-08

Condition(s) studied

Wrist InjuryHand and Upper Limb TraumaHand and Forearm TraumaMuskuloskeletal Diseases

Investigational drug(s) / intervention(s)

Immersive Virtual Reality Action Observation TherapyConventional Rehabilitation

Immersive Virtual Reality Action Observation Therapy: Participants observe and subsequently perform functional wrist and hand movements within immersive virtual reality environments using a Meta Quest Pro headset. The intervention is delivered twice weekly for six weeks, with sessions lasting approximately 45 minutes.

Conventional Rehabilitation: Standard rehabilitation program for traumatic wrist and hand injuries including active and passive mobilization, strengthening exercises, functional training, and pain management.

Study summary

This randomized controlled trial aims to evaluate the effectiveness of immersive virtual reality (VR)-based Action Observation Therapy (AOT) as an adjunct to conventional rehabilitation in patients with traumatic wrist and hand injuries. Participants will receive standard rehabilitation treatment, and the intervention group will additionally undergo a six-week VR program involving observation and execution of functional hand and wrist movements. Outcomes related to hand function, grip strength, pain, proprioception, disability, and psychological factors will be assessed to determine the potential benefits of incorporating VR into rehabilitation programs.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18 years or older. * Diagnosis of a traumatic wrist and/or hand injury. * Referred for rehabilitation treatment at the participating hand therapy unit. * Ability to understand study procedures and provide written informed consent. * Ability to participate in the virtual reality intervention. Exclusion Criteria: * Previous injury affecting the same hand. * Associated upper-limb conditions, including tenosynovitis or Dupuytren's disease. * Previous surgery involving the affected hand before the current traumatic injury. * Corticosteroid or other therapeutic injection in the affected hand within the previous 3 weeks. * Any physical, neurological, visual, vestibular, or medical condition that prevents safe use of the virtual reality device. * Inability to comply with the study procedures or assessments.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
UMA Málaga Spain Recruiting

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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 NCT07633769 on ClinicalTrials.gov ↗ ← All trials in Spain