This study evaluated transcranial magnetic stimulation (TMS) for freezing of gait in patients with Parkinson's disease. Participants with Parkinson's disease and freezing of gait received conventional TMS protocols, and their clinical, gait, and neurophysiological outcomes were assessed. Patients who did not achieve sufficient improvement after conventional TMS were further treated with a combined primary motor cortex and cerebellar stimulation protocol. The study aimed to identify factors associated with differential response to conventional TMS and to explore whether cerebellar stimulation could improve symptoms in treatment-resistant patients.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
85
Bilateral lower-limb primary motor cortex stimulation was delivered at 10 Hz and 90% of resting motor threshold, with 2000 pulses per hemisphere. Treatment was administered once daily for five consecutive days per week over two weeks.
Transcutaneous spinal magnetic stimulation was delivered over the T10-T12 segment at 1 Hz, with 1500 pulses. Stimulation intensity was adjusted to produce visible lower-limb muscle contraction.
Supplementary motor area stimulation was delivered at 10 Hz and 90% of resting motor threshold, with 1000 pulses. Treatment was administered as an add-on protocol combined with bilateral lower-limb primary motor cortex stimulation.
Bilateral cerebellar intermittent theta-burst stimulation was delivered using 50-Hz triplets at 5 Hz, with 2-second trains every 10 seconds and a total of 2700 pulses over 15 minutes. This intervention was administered to patients who were treatment-resistant to conventional TMS.
The First Affiliated Hospital with Nanjing Medical University
Nanjing, Jiangsu, China
Freezing of Gait Questionnaire Improvement Rate
The improvement rate of the Freezing of Gait Questionnaire was calculated as \[(pre-treatment FOGQ score at baseline - post-treatment FOGQ score at one-month follow-up) / pre-treatment FOGQ score at baseline\] × 100%. Participants with an improvement rate of at least 30% were classified as treatment responsive.
Time frame: Baseline and 1 month after treatment
Unified Parkinson's Disease Rating Scale Part III Score
Motor symptoms were assessed using the Unified Parkinson's Disease Rating Scale Part III.
Time frame: Baseline, within 24 hours after treatment, and 1 month after treatment
Upper-Limb Short-Interval Intracortical Inhibition
Upper-limb short-interval intracortical inhibition was assessed using paired-pulse transcranial magnetic stimulation and expressed as the conditioned/unconditioned motor evoked potential amplitude ratio.
Time frame: Baseline and within 24 hours after treatment
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