Transcranial Magnetic Stimulation for Depression
Trial Summary
What is the purpose of this trial?
This study aims to explore how repetitive transcranial magnetic stimulation (rTMS), a treatment for depression, affects brain function. Depression disrupts the brain's complex network or regions that regulate cognition, emotion, and behavior. rTMS targets these disruptions to restore network function. To measure these effects, researchers will use dry quantitative EEG (qEEG), a new technology that records brain electrical activity quickly (15 minutes compared to 1 hour for traditional EEG) without the need for gel or lengthy electrode setups. This study will evaluate a novel qEEG activity developed by iMediSync (Republic of South Korea) in patients treated with neuromodulation for depression before, during, and up to 12 months after treatment to see if changes in brain activity to identify patterns associated with symptomatic improvement and relapse risk. Findings could help personalize depression treatments by predicting patient outcomes and optimizing care.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the study team or your doctor.
What data supports the effectiveness of the treatment Repetitive Transcranial Magnetic Stimulation (rTMS) for depression?
Repetitive transcranial magnetic stimulation (rTMS) has been shown to be effective in treating depression, with over 20 years of clinical trials supporting its use. Studies indicate that rTMS is generally well tolerated and more effective than sham (fake) treatments, with a significant number of patients responding positively.12345
Is transcranial magnetic stimulation (TMS) safe for humans?
How is the treatment rTMS different from other treatments for depression?
Repetitive transcranial magnetic stimulation (rTMS) is unique because it uses magnetic fields to stimulate nerve cells in the brain, which is different from medications that work chemically. It is a non-invasive procedure, meaning it doesn't require surgery or medication, and is typically used when other treatments like antidepressants haven't been effective.15111213
Eligibility Criteria
This clinical trial is for individuals experiencing depression. Participants will undergo a non-invasive treatment called repetitive transcranial magnetic stimulation (rTMS). The study requires participants to have their brain activity monitored using a quick and easy EEG technology.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants undergo an accelerated rTMS protocol over five days, targeting the DLPFC, with pre-treatment imaging to localize the brain region.
Follow-up
Participants are monitored for recurrence of depressive symptoms and undergo maintenance TMS treatment if symptoms worsen.
Maintenance Treatment
Participants receive either a gradually tapering TMS protocol or a cluster protocol to maintain symptom relief.
Treatment Details
Interventions
- Repetitive Transcranial Magnetic Stimulation (rTMS)
Repetitive Transcranial Magnetic Stimulation (rTMS) is already approved in United States, European Union, Canada, Japan for the following indications:
- Depression
- Smoking cessation
- Depression
- Depression
- Depression
Find a Clinic Near You
Who Is Running the Clinical Trial?
Sunnybrook Health Sciences Centre
Lead Sponsor
iMediSync
Collaborator
Mitacs
Industry Sponsor