Phase
Condition
Affective Disorders
Depression
Depression (Major/severe)
Treatment
Theta burst stimulation
Clinical Study ID
Ages 18-55 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Men or women aged 18 to 55 years of age
Mini-International Neuropsychiatric Interview-confirmed diagnosis of MDD, as asingle or recurring episode
Symptoms of MDD have not improved after ≥ 1 but ≤ 7 adequate dose(s) ofantidepressant trial(s) in the current depressive episode
A baseline score of ≥ 15 on the 17-item Hamilton Rating Scale for Depression (HRSD-17)
Have received a stable antidepressant regimen for at least four weeks prior toentering trial
Are voluntary and competent to consent to study
Can speak and read English
Exclusion
Exclusion Criteria:
Current or past (< 3 months) substance (including nicotine) or alcoholabuse/dependence, as defined in DSM-5 criteria
Positive urine test for illegal substances, cannabis, or cotinine
Suicide attempt in the past three months and/or active suicidal intent
Pregnancy (confirmed by urine test) and/or lactation
Psychotic features in the current episode
Any comorbid mental health disorders (including, but not limited to lifetime historyof psychotic disorders, OCD, PTSD and/or bipolar I or II disorder) with theexception of anxiety/panic disorders and ADHD
Significant unstable medical or neurologic illness confirmed by medical history andblood test at baseline (e.g. uncontrolled diabetes, or renal dysfunction)
Organic cause to the depressive symptoms (e.g. thyroid dysfunctions), as ruled outby the referring physician
Contraindication for TMS (e.g., personal history of epilepsy or convulsion, metallichead implant, pacemaker)
Contraindication for MRI (e.g. metallic implant, claustrophobia)
Have undergone a prior PET or SPECT research study
ECT or rTMS treatment in the current depressive episode
Benzodiazepine use
Have a body mass index (BMI) higher then 35 or lower then 18
Any other condition that, in the opinion of the investigators, would adverselyaffect the participant's ability to complete the study
Study Design
Study Description
Connect with a study center
The Royal Ottawa Mental Health Centre
Ottawa, Ontario K1Z 7K4
CanadaActive - Recruiting
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