Transcranial Magnetic Stimulation for Binge Eating Disorder (TMS for BED)
Binge-Eating Disorder
About this trial
This is an interventional treatment trial for Binge-Eating Disorder focused on measuring Transcranial Magnetic Stimulation
Eligibility Criteria
Inclusion Criteria: English speaking (EPSI and Binge Eating Disorder Scale available only in English) Diagnosed with binge eating disorder as defined by the DSM-5 and in treatment for at least 6 months Stable doses of medications for at least 6 weeks Female subjects of childbearing age must consent to pregnancy tests at the beginning of each treatment session; will be counseled to use barrier methods during the course of this study Exclusion Criteria: Contraindications to receiving TMS such as: Aneurysm clips or coils Stents in the neck or brain Deep brain stimulators Electrodes to monitor brain activity Metallic implants in ears and eyes Shrapnel or bullet fragments in or near the head Facial tattoos with metallic or magnetic-sensitive ink Other metal devices or object implanted in or near the head
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Experimental
Experimental
Experimental
Group A
Group B
Group C
Group D
Patients with BED not undergoing symptom provocation
Patients with BED not undergoing symptom provocation
Patients with BED undergoing symptom provocation
Patients with BED undergoing symptom provocation