Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Mclean Hospital
With
Stanley Medical Research Institute
This study involves a screening visit with the study physician and a treatment visit. Participants will be asked to complete several questionnaires about their mood during both visits. The treatment visit will involve use of the LFMS device. Participants will place the top of their head inside the device for approximately 20 minutes. Participants will receive either the actual treatment or a sham treatment and will not know which they receive. This device produces weak electromagnetic fields. There is no discomfort or even sensation caused by the device. The device has been declared to be a "non-significant risk device" by the FDA, and there are no known risks associated with its use.
Age
18–70
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Diagnosis of Major Depressive Disorder or Bipolar Disorder; must be currently depressed
May be medicated or unmedicated
You may not be if
Contraindication for MRI due to metal in eyes/head
