Actively Recruiting
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
Eligibility Criteria
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
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
Trial Site Locations
Total: 1 location
1
IRCCS Santa Lucia Foundation
Roma, Rome, Italy, 00179
Actively Recruiting
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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