Clinical Research Directory

Browse clinical research sites, groups, and studies.

Sites Groups Studies

Back to Studies

RECRUITING

NCT06152705

Comparing the Efficacy of fMRI-Guided vs. Standard iTBS in Treating Depression

Sponsor: The Royal Ottawa Mental Health Centre

View on ClinicalTrials.gov

Summary

In this triple-blind randomized controlled trial, we ask if targeting intermittent theta burst stimulation (iTBS) based on individual resting state connectivity improves treatment outcomes in major depressive disorder (MDD). For the trial, we will recruit 210 patients with major depressive disorder. Each patient will undergo a 30-40-minute MRI scan, after which they will receive a 6-week standard iTBS treatment. Participants will be randomized to receive iTBS either to the standard neuronavigated target (a technique for treatment location targeting, based on group-average connectivity) or to a personalized connectivity-guided target selected based on individual functional connectivity scans. The main outcome of this trial is response rate as determined by ≥ 50% reduction in Grid HRSD-17 scores. Secondary outcomes include remission rate, change in depression, anxiety and anhedonia symptoms, quality of life, and biological measures of heart rate variability, objective sleep measures and daily activity as a proxy of anhedonia - defined as a reduced ability to experience pleasure.

Official title: Triple-blind Randomized Trial Comparing the Efficacy of fMRI-Guided vs. Standard iTBS in Treating Depression

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

210

Start Date

2024-09-16

Completion Date

2027-10-01

Last Updated

2025-12-17

Healthy Volunteers

Conditions

Depression Depressive Disorder, Major Depressive Episode

Interventions

DEVICE

repetitive Transcranial Magnetic Stimulation

Repetitive transcranial magnetic stimulation (rTMS) is a Health Canada approved treatment for major depression. Typical treatments involve 30 to 45 minutes daily sessions delivered over 4 to 6 weeks. Recent technical advances allowed the development of theta burst stimulation (TBS), a novel rTMS paradigm that reduces daily sessions to 3 to 4 minutes while maintaining the same clinical efficacy. This study will specifically be administering intermittent TBS (iTBS), which is a novel refinement of conventional rTMS and consists of bursts of 3 stimulations at 50 Hz at theta frequency (5 Hz).

Inclusion criteria: For inclusion in the study, participants must fulfill all the following criteria: 1. voluntary and competent to consent to study, 2. Adults aged 18 years old or older, 3. can speak and read English, 4. primary and/or predominant diagnosis of major depressive episode without psychotic features in the current episode (confirmed by a Mini-International Neuropsychiatric Interview), 5. depressive symptoms have not improved after ≥ 1 adequate dose of antidepressant trial in the current depressive episode, 6. moderate symptoms in the current depressive episode as indexed by a score of at least 15 on the Grid 17-item Hamilton Rating Scale for Depression (Grid HRSD-17), 7. have been referred to rTMS treatment by their treating physician, and took a free and informed decision to follow this treatment, 8. are able to adhere to treatment schedule, 9. have stable psychotropic medications (including prescribed cannabis) or psychotherapy regimen for at least four weeks prior to entering the trial, 10. have an education-adjusted score of ≥ 24 at the Mini-Mental State Evaluation (MMSE) if they are aged ≥ 65. Exclusion criteria: Participants fulfilling any of the following criteria will be excluded from the study: 1. diagnosis of bipolar I or II disorder, based on the DSM-5 criteria 2. current or past (\< 3 months) substance (excluding caffeine or nicotine) or alcohol use disorder, as defined in DSM-5 criteria. Based on the DSM-5 criteria, mild cannabis or alcohol use disorder would be permissible in the past 3 months, moderate to severe would be an exclusion. 3. current use of illegal substances or cannabis (unless medical use, see note below), confirmed by urine drug screen 4. have a concomitant major unstable medical or neurologic illness (e.g. uncontrolled diabetes or renal dysfunction), 5. organic cause to the depressive symptoms (e.g. thyroid dysfunctions), as ruled out by the referring physician 6. acute suicidality or threat to life from self-neglect, 7. are pregnant or breastfeeding, or thinking of becoming pregnant during course of treatment (pregnancy will be assessed by a urine test), 8. have a specific contraindication for TMS (e.g., personal history of epilepsy or seizure, metallic head implant, pacemaker), 9. unwilling to maintain current antidepressant regimen, 10. are taking more than 1 mg of lorazepam per day or equivalent, 11. any other condition that, in the opinion of the investigators, would adversely affect the participant's ability to complete the study, 12. any contraindications for MRI 13. have failed a course of ECT within the current depressive episode due to the lower likelihood of response to rTMS (if they have had failed ECT in the past, this does not exclude them)

Locations (1)

The Royal's Institute of Mental Health Research

Ottawa, Ontario, Canada