RecruitingNot ApplicableNCT06854367

Accelerated vs. Conventional Theta Burst Stimulation for Late-life Depression


Sponsor

Centre for Addiction and Mental Health

Enrollment

280 participants

Start Date

Mar 27, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this trial is to compare the treatment efficacy (improvement in depressive symptoms) of accelerated TBS protocol (where participants receive multiple TBS treatments daily) to conventional TBS protocol (where participants receive a single TBS treatment daily) in late life depression. In addition, the study also aims to determine if specific patterns of stimulation are more or less effective. To do this, all participants will receive active treatments, but some of the participants in this study will receive accelerated TBS and some will receive once daily TBS.


Eligibility

Min Age: 60 Years

Plain Language Summary

Simplified for easier understanding

This study compares two schedules of transcranial magnetic stimulation (TMS) — a non-invasive brain stimulation treatment — for older adults aged 60 and above with depression that has not responded to antidepressant medications. One group receives the usual treatment schedule; the other gets a compressed, faster schedule. **You may be eligible if:** - You are 60 years or older - You have been diagnosed with major depressive disorder with a current depressive episode - You have tried at least one antidepressant at an adequate dose in this episode but it did not work - You are an outpatient (not currently hospitalized) - You have a depression score of 10 or higher on the PHQ-9 questionnaire - Your antidepressant medications have been stable (no changes) for at least 4 weeks **You may NOT be eligible if:** - You have a history of seizures or a brain implant (e.g., a pacemaker, cochlear implant, or metal in the skull) - You have signs of dementia - You have bipolar disorder, a psychotic disorder, or active suicidal intent - You have not responded to electroconvulsive therapy (ECT) in this episode - You are currently taking anticonvulsant medications or high doses of benzodiazepines Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DEVICETBS

Repetitive transcranial magnetic stimulation (rTMS) is a form of non-invasive neurostimulation that uses focused magnetic field pulses to directly stimulate cortical neurons. Theta burst stimulation (TBS) is a briefer form of patterned rTMS that has been shown to be effective against major depressive disorder. Each treatment will consist of either 1) cTBS of right DLPFC followed by iTBS of left DLPFC; or 2) iTBS of left DLPFC.


Locations(2)

Sunnybrook Health Sciences Centre

Toronto, Ontario, Canada

Centre for Addiction and Mental Healh

Toronto, Ontario, Canada

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06854367


Related Trials