Accelerated Neuromodulation of Anterior Cingulate Cortex for Depression

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age60-85
SponsorRotman Research Institute at Baycrest

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

Treatment groups

24 Participants
are divided into 2 treatment groups