The purpose of this study is to evaluate whether repetitive transcranial magnetic stimulation (rTMS) treatment is an effective adjunct treatment to mood stabilizers and Bupropion.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
45
150mg daily for first week, 300mg daily thereafter for a total of 8 weeks
Daily left DLPFC, at 110% motor threshold, with a frequency of 10 Hz. Stimulation will be applied in 5-second trains with a 10-second inter-train interval, for 30 trains per session. This treatment will be provided for the first 4 weeks of the study.
150mg daily first week, 300mg daily thereafter for a total of 8 weeks.
Allan Memorial Institute
Montreal, Quebec, Canada
Change in Montgomery-Asberg Depression Rating Scale (MADRS) from baseline at 8 weeks
Time frame: 8 weeks
Change in Beck Depression Inventory (BDI-II) from baseline at 8 weeks
Time frame: 8 weeks
Change in Young Mania Rating Scale (YMRS) from baseline at 8 weeks
Time frame: 8 weeks
Alcohol use disorder identification test (AUDIT Assessment)
Time frame: At intake
Drug abuse screen test (DAST Assessment)
Time frame: At intake
Clinical Global Impression (CGI) & Analog scale
Time frame: 8 weeks
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Sham rTMS will also begin their treatment 5 times a week for 4 weeks in junction with pharmacotherapy (Wellbutrin). Sham rTMS will be delivered at a frequency of 10 Hz and stimulation will be applied in 5-second trains with a 20-second inter-train interval, for 30 trains per session.