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Virtual reality and nerve stimulation to aid early stroke recovery

Tests virtual reality with electrical nerve stimulation in adults recovering from a recent stroke.

Plain-language title generated from the registry record
Registry title: Virtual Reality and Neurostimulation for Early Stroke Rehabilitation

Key facts

Where
Vienna, AustriaSee the site

Could this be for you?

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  • Are you between 18 and 80 years old?

Source: NCT06887231, who can take part

Where in Austria

  • Medical University of Vienna, Department of NeurologyVienna, AustriaTaking people

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Trial details

Who runs it
Medical University of Vienna
Trial code
NCT06887231
Record updated
6 April 2025
Original description
Stroke is one of the leading causes of disability, leaving millions of individuals each year impaired with lasting motor and sensory impairments. In the subacute phase, which goes from the first week to 3 months post-stroke, the patient has the highest recovery, which could be boosted by proper technologies intended for the rehabilitation of the patients. The impairments that the patients experience are extremely heterogeneous and go from muscle weakness to spasticity of the paretic side of the body. Beyond motor deficits, stroke survivors also suffer from sensory impairment (they do not properly feel with the paretic side of their body), impaired body representation (misjudging the size, position, and movement of their affected limb), which can further hinder recovery.Read full original descriptionShow less

Virtual Reality (VR) Platform and Transcutaneous Electrical Nerve Stimulation (TENS) for Early Stroke Rehabilitation

Stroke is one of the leading causes of disability, leaving millions of individuals each year impaired with lasting motor and sensory impairments. In the subacute phase, which goes from the first week to 3 months post-stroke, the patient has the highest recovery, which could be boosted by proper technologies intended for the rehabilitation of the patients. The impairments that the patients experience are extremely heterogeneous and go from muscle weakness to spasticity of the paretic side of the body. Beyond motor deficits, stroke survivors also suffer from sensory impairment (they do not properly feel with the paretic side of their body), impaired body representation (misjudging the size, position, and movement of their affected limb), which can further hinder recovery.

Traditional rehabilitation primarily targets motor function, often without considering at all the role of sensory feedback and body perception in the recovery process. However, growing evidence suggests that the combination of multiple sensory modalities towards a multifaceted rehabilitation can enhance neuroplasticity and improve rehabilitation outcomes.

To address this, the investigators have developed a novel rehabilitation approach that integrates immersive virtual reality (VR) with transcutaneous electrical nerve stimulation (TENS). This system allows stroke patients to interact with a virtual environment while receiving synchronized tactile stimulation, reinforcing sensorimotor integration. Unlike conventional therapy, which relies on passive or repetitive exercises, this approach engages patients in active, goal-oriented movements, tailored to their individual recovery progress.

By focusing on the subacute stroke population, this project aims to leverage the brain's heightened plasticity during early recovery to maximize functional improvements. The VR-based intervention will adapt to each patient's motor abilities, providing real-time feedback to encourage precise movements and enhance sensory processing. Through this multisensory experience, the investigators seek to improve not only motor control but also sensory and body representation measures.

Inclusion: Confirmed diagnosis of ischemic or hemorrhagic stroke; In the subacute phase (from 7 days to 3 months from last stroke onset); Fugl-Meyer-Upper Extremity (FMUE) scale for the motor part: FMUE ≥ 10; Ability to sit in an upright position; Age between 18 and 80 years.

Exclusion: Pacemaker or other electronic implants; Other neurological or physical impairment or mental condition that, in the judgment of the investigator, does not allow participation in the study; Epilepsy; Mini-Mental State Examination (MMSE) < 24; Nausea, headaches or fatigue due to VR-generated environment ("virtual reality motion sickness"); Peripheral nerve damage in the affected arm or hand.

ClinicalTrials.gov NCT06887231