Hypothesis / aims of study
Overactive bladder (OAB) is associated with aberrant supraspinal network activity involving the supplementary motor area (SMA) and dorsolateral prefrontal cortex (dlPFC). Current OAB therapies primarily target peripheral pathways. Repetitive transcranial magnetic stimulation (rTMS) is a non-invasive neuromodulation therapy that can induce neuroplastic changes by altering cortical excitability. We hypothesized that a combined protocol of inhibitory low-frequency (LF) rTMS to the SMA and excitatory high-frequency (HF) rTMS to the dlPFC would be feasible, safe, and associated with improvements in OAB symptom burden.
Study design, materials and methods
This was a prospective, single-arm pilot trial of adults with idiopathic OAB. Inclusion criteria included ≥8 voids and ≥3 urgency episodes per 24 hours on bladder diary. Participants completed five daily 40-minute neuronavigated rTMS sessions targeting bilateral pelvic SMA (1 Hz) and right dlPFC (10 Hz). Clinical outcomes were measured using validated patient-reported outcome measures (Overactive Bladder Questionnaire Short Form (OAB-qSF), Lower Urinary Tract Symptoms Network Symptom Index-10 (LURN SI-10), Patient Perception of Bladder Condition (PPBC) and Hospital Anxiety and Depression Scale (HADS)) and bladder function parameters were derived from standardized 2-day bladder diaries. Outcomes were assessed at baseline, immediately post-treatment, and at 3-week and 6-week follow-up intervals. Linear mixed models evaluated longitudinal changes from baseline.
Interpretation of results
The significant and sustained clinical improvements across multiple validated scales suggest that rTMS effectively reduces OAB symptom burden. The reduction in both subjective bother and objective diary events, such as urgency episodes and pad use, indicates that targeting the SMA and dlPFC provides a meaningful therapeutic effect. The durability of these clinical improvements through the 6-week mark suggests potential for lasting benefit beyond the immediate treatment period.