The purpose of this study is to evaluate the efficacy of repetitive transcranial magnetic stimulation (rTMS) in improving depressive symptoms in patients with Parkinson's Disease (PD). Participants will be randomly assigned to either an active rTMS group or a sham-control group. The study aims to establish an optimal treatment protocol using a neuronavigation system and to validate treatment responses through various digital biomarkers such as facial expression analysis and eye-tracking.
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Beck Depression Inventory-II (BDI-II)
Timeframe: Change from Baseline (T0) at 1 week (T1) and 5 weeks (T2, 1-month follow-up)
Neuropsychiatric Inventory (NPI)
Timeframe: Change from Baseline (T0) at 1 week (T1) and 5 weeks (T2, 1-month follow-up)