Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06911671

EMG Control Assistance Virtual Reality Interface Coupled With Cerebellar-iTBS for Arm Recovery After Stroke (ERICA)

Led by I.R.C.C.S. Fondazione Santa Lucia · Updated on 2026-02-03

45

Participants Needed

1

Research Sites

130 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The investigators hypothesize that a myoelectric (EMG) controlled virtual reality (VR) interface allows for effective upper limb motor recovery of stroke patients. EMG control offers the possibility to alter visual feedback according to the recorded muscle activity in real-time. By manipulating the motion of a virtual hand associated with the recorded muscle patterns, assistance can be provided to stroke patients by correcting the error between the actual (dysfunctional) and a reference (functional) muscle pattern. Thus, through such an assistive EMG control algorithm, patients will be able to perform reaching movements with the virtual hand despite their motor impairment. By gradually reducing assistance, it is hypothesized that the salient error in the task space provided as visual feedback will systematically change the muscle patterns, thereby driving adaptation of the dysfunctional muscle patterns, enhancing motor recovery. Moreover, due to its relevant role in motor learning, it is expected that cerebellar stimulation will favor the underlying processes of adapting cerebello-cortical plasticity involved in motor learning. Therefore, it is hypothesized that an assistive EMG control algorithm in combination with cerebellar transcranial magnetic stimulation will further enhance upper limb recovery.

CONDITIONS

Official Title

EMG Control Assistance Virtual Reality Interface Coupled With Cerebellar-iTBS for Arm Recovery After Stroke (ERICA)

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • First ever ischemic stroke with mild to moderate motor impairment of upper limb
  • Left or right sub-cortical or cortical lesion of the middle cerebral artery
  • Age above 18 and below 80 years
  • No visuospatial, cognitive, or attention deficits
  • Fugl-Meyer score less than 56
Not Eligible

You will not qualify if you...

  • History of seizures
  • Treatment with Benzodiazepines or Baclofen
  • Pregnancy
  • Intracranial metal implant
  • Cardiac pacemaker
  • Orthopedic limitation of the upper limb
  • Upper limb pain
  • Neurological diseases other than stroke or neuropsychiatric/neuropsychological disorders affecting consent or compliance

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

IRCCS Santa Lucia Foundation

Roma, Rome, Italy, 00179

Actively Recruiting

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Research Team

G

Giacomo Koch, Prof.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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