About this trial
This study aimed to aim to investigate the efficacy of individualized rTMS according to lateralization index on motor recovery and cortical excitability in subacute stroke patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Unilateral ischemic or hemorrhagic stroke
Stroke within 3 months
Medical Research Council Scale for Muscle Strength in upper limb ≤ 3
No previous stroke, seizure, dementia, Parkinson's disease or other degenerative neurological diseases.
Disqualifiers
Previous stroke, traumatic brain injury, brain tumor
With central nervous system disease (spinal cord injury, Parkinson's disease)
Any contraindication to rTMS (seizure, alcoholism, metal implant, pacemaker)
Patients unable to cooperate the treatment
Trial design
Parallel
Treatments tested in this trial
Repetitive transcranial magnetic stimulation
DeviceRepetitive transcranial magnetic stimulation (rTMS) is a non-invasive neuromodulation technology. High and low frequencies of rTMS could modulate the excitability of the cerebral cortex.
Treatment groups
Trial outcomes
Primary outcomes
Fugl-Meyer Assessment
Fugl-Meyer Assessment motor function set, score: 0-66, higher scores indicate a better outcome.
Secondary outcomes
Medical Research Council (MRC) Scale for Muscle Strength
Medical Research Council (MRC) Scale for Muscle Strength, assessing muscle strength from Grade 5 (normal) to Grade 0 (no visible contraction).
National Institutes of Health Stroke Scale
National Institutes of Health Stroke Scale, The maximum possible score is 42, with the minimum score being a 0. Higher scores indicate a worse outcome.
Barthel Index
Barthel Index, score 100-0. Higher scores indicate a better outcome.
Modified Rankin Scale
Modified Rankin Scale, score from 0 to 6. Higher scores indicate a worse outcome.
Locations
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Sponsors and contacts
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