Stimulation of iM1 |
• Direct enhancement of the reduced participation in the incompletely recovered motor network after stroke |
• Higher risk of adverse effects due to induction of excitotoxicity in the penumbra and shunting of electrical current |
Stimulation of cM1 |
• Stimulation of intact cortical areas |
• Inhibitory stimulation might also impair complex motor function |
Stimulation of secondary sensorimotor areas |
• Stimulation of intact cortical areas |
• More difficult to target |
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• Modulation of cortico-cortical connections to M1 |
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Stimulation of the cerebellum |
• Stimulation of intact cortical areas |
• More difficult to target |
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• Alternative target within the motor learning network |
• Comparable high discomfort of cerebellar rTMS protocols |
Simultaneous application of a motor training paradigm |
• Simultaneous modulation of LTP-/LTD-like mechanisms |
• Unfavorable homeostatic interactions |
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• Not feasible for most rTMS protocols |
Stimulation in the acute or sub-acute phase |
• Enhanced adaptive plasticity |
• Higher risk of adverse effects |
Stimulation in the chronic phase |
• More stable deficit |
• Reestablished growth/plasticity inhibition |
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• Lower risk of adverse effects |
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Multi-session stimulation |
• Enhancement of plasticity, e.g., induction of late-phase LTP/LTD-like neuroplasticity |
• More complex and time-consuming |
Multifocal stimulation |
• Modulation of multiple nodes of the motor network |
• Higher risk of adverse effects, e.g., shunting of current |
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• Induction of additive or supra-additive effects |
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Sequential stimulation |
• Time-dependent modulation of multiple nodes of the motor network |
• More complex setup |
Patterned rTMS protocols |
• Shorter delivery time |
• Higher risk of adverse effects |
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• Proposed potent modulatory aftereffect |
• Need of a more complex and expensive setup |
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• Mixed results |