Anxiety Clinical Trial
Official title:
Low Field Magnetic Stimulation: Open Label Study.
To assess the effects of daily LFMS treatments for those suffering from affective or anxiety symptoms. We hypothesize a reduction in affective and or anxiety symptoms after active treatment over the period of one week, with improvement through the following week.
The Low Field Magnetic Stimulation (LFMS) procedure is an application of a series of
electromagnetic pulses to the brain. The field and timing parameters of the LFMS pulses,
such as pulse timing, duration, frequency, and electric and magnetic field distribution and
direction are different from other neurostimulation methods. LFMS electromagnetic fields are
significantly weaker (< 100x) than those used in ECT and rTMS.
LFMS was discovered at McLean Hospital and has thus far been studied as an experimental
antidepressant treatment at McLean Hospital. LFMS is also being studied at Massachusetts
General Hospital and 5 other hospitals in an NIH sponsored trial (RAPID) as well as in
studies at Cornell-Weill School of Medicine. The mechanism of action for the antidepressant
effects of LFMS is hypothesized to be an interaction between the electromagnetic fields and
neurons in cortical regions, brought about by low level electrical stimulation applied with
particular timing.
The current study proposes to assess the effects of daily LFMS treatments in participants
suffering from affective disorders and/or anxiety. This is an open-label study. All subjects
will receive active LFMS treatments. Potential subjects will be referred to the study by
their clinicians and will be pre-screened by phone.
;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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