About this trial
The goal of this clinical trial is to test whether an accelerated deep Transcranial Magnetic Stimulation (dTMS) protocol can reduce depressive symptoms in older adults (ages 60-85) with Major Depressive Disorder (MDD) who have not tolerated or responded to antidepressant medications. The study will evaluate whether accelerated dTMS administered over 5 consecutive days is safe and well-tolerated in this population, and whether it produces greater reductions in depressive symptoms compared to placebo stimulation.
Eligibility criteria
Qualifiers
are between 60- 85 years old (on the day of randomization)
have been diagnosed with DSM5 Major Depressive Disorder, with the current episode longer than 4 weeks but less than 5 years
did not respond to/did not tolerate, or failed to achieve remission with at least one antidepressant trial of 8 week minimum duration
are willing to provide informed consent
Disqualifiers
have a metal plate in your head (such as an ear implant, implanted brain stimulators, aneurysm clips). Dental devices and implants that are non-magnetic are safe
have known increased pressure or a history of increased pressure in their brain, which may increase their risk for having seizures
have a cardiac pacemaker
have an implanted medication pump
Trial design
Treatments tested in this trial
- Active Brainsway H7-Coil Deep TMS System
- Sham Brainsway H1-Coil Deep TMS System