E-field Guided iTBS for Treatment Resistant Depression

The purpose of this study is to establish how personalization of rTMS can change markers of brain activity and improve treatment response in major depressive disorder (MDD). All participants will receive up to 30 iTBS treatments to the left dorsolateral prefrontal cortex (DLPFC), delivered daily, 5 days per week, for 6 weeks. Participants will be randomized to either a standard treatment arm, in which the iTBS targeting will be via the Beam F3 method to identify the left DLPFC location, and intensity will be determined as 120% of the resting motor threshold, or a personalized arm, in which the left DLPFC will be identified via functional magnetic resonance imaging (fMRI), the optimal coil position and stimulus intensity will be derived through E-Field modeling pipelines.

Inclusion criteria

• are outpatients;
• are voluntary and competent to consent to treatment;
• have a Diagnostic and Statistical Manual for Mental Disorders, 5th edition major depressive episode based on the Mini International Neuropsychiatric Interview (MINI)
• are 18yo to 65yo;
• have a score of ≥18 on the Hamilton Rating Scale for Depression (HRSD-17) item at screening
• have not had a clinical response to an adequate dose of an antidepressant based on an Antidepressant Treatment History Form (ATHF) score of ≥ 3 in the current episode or have been unable to tolerate at least 2 separate trials of antidepressants of inadequate dose and duration (ATHF 1 or 2);
• are agreeable to keeping their current medication constant during the study
• are able to adhere to the study and treatment schedules
• meet TMS and MRI safety criteria

Exclusion criteria

• have a concomitant unstable medical illness
• are pregnant or intend to become pregnant during the study
• have a current MINI diagnosis of bipolar disorder, psychotic disorder, obsessive compulsive disorder, concurrent substance use disorder (aside from nicotine) or post-traumatic stress disorder (current or within the last year)
• have failed a course of electroconvulsive therapy within the current depressive episode due to the lower likelihood of response to rTMS;
• have any significant neurological disorder (e.g., space occupying brain lesion, history of stroke, cerebral aneurysm, seizure disorder, Parkinson's disease, Huntington's chorea, multiple sclerosis) or confirmed diagnosis of dementia or cognitive impairment
• present with a medical condition, medication, or laboratory abnormality that could cause a major depressive episode in the opinion of the investigator
• have an intracranial implant or any other metal object that cannot be safely removed, precluding safety of TMS or MRI exposure within or near the head, excluding the mouth
• require benzodiazepine equivalent to lorazepam 2 mg/day or higher or any anticonvulsant due to the potential of these medications to limit the efficacy of rTMS [45]
• have inadequate English fluency to complete clinical assessments.
• are participating in a new course psychotherapy initiated within the last 3 months or finishing prior to the end of scheduled treatments;
• have a non-correctable clinically significant sensory impairment (i.e., cannot hear well enough to cooperate with interview).