Efficacy and Biological Targets of Response to rTMS Therapy in Youth Depression
NCT ID: NCT02472470
Last Updated: 2017-10-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
20 participants
INTERVENTIONAL
2015-06-30
2017-05-31
Brief Summary
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Detailed Description
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Investigators propose to examine the efficacy of repetitive transcranial magnetic stimulation (rTMS) for youth depression. There are several reasons for pursuing this treatment: 1) rTMS applied to the dorsolateral prefrontal cortex (DLPFC), a cortical region implicated in pathophysiology of depression, is a safe and FDA approved treatment for adults with medication-resistant depression; 2) Young age is suggested to be a good predictor of response to rTMS treatment; 3) rTMS trials in adolescence and youth with medication resistant depression provide evidence that rTMS is a safe efficacious and well tolerated treatment for adolescents that does not increase suicidal thoughts. Additionally, recently rTMS parameter developments such as theta burst stimulation (i.e., TBS) provide compelling evidence for efficacy in less of the time it takes to administer conventional rTMS, thus lowering the overall costs and increasing the number of patients that can be treated.
It is imperative that research investigate treatment related biological mechanisms, such that increases in understanding can lead to enhanced efficacy. Investigators will utilize a novel and powerful in vivo brain mapping technique of TMS combined with electroencephalography (TMS-EEG) that permits non-invasive assessment of inhibitory, connectivity and plasticity mechanisms from the DLPFC. The pathophysiology of depression has been linked to impairment in neural plasticity and connectivity and neural and behavioral inhibition - mechanisms that can be measured through TMS-EEG and maybe changed by TBS treatment. Therefore, investigating the association between TBS-related changes in plasticity, connectivity and inhibition may be key to understanding both the treatment mechanisms involved in youth depression and predictors of treatment response in this disorder.
Therefore the specific aims in this study are twofold:
1. To examine the efficacy of TBS applied to the DLPFC for youth depression, and
2. To identify biological targets and predictors of response to TBS applied to the DLPFC for youth depression.
Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Treatment
intermitten TBS (iTBS) rTMS applied to the left Dorsolateral Prefrontal Cortex (DLPFC) + continuous TBS (cTBS) rTMS applied to the right DLPFC. The order will be counterbalanced. Administration of this treatment takes roughly 10 minutes. This treatment will be applied daily, 5 days/week, for 2 weeks.
rTMS
Participants will receive 10 active TBS rTMS sessions once daily on weekdays for 2 weeks.
Interventions
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rTMS
Participants will receive 10 active TBS rTMS sessions once daily on weekdays for 2 weeks.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* between the ages of 16 and 24
* competent to consent to study participation
* Mini-International Neuropsychiatric Interview (MINI) confirmed diagnosis of MDD single or recurrent
* no change in treatment (psychotherapy or medication) for at least four weeks prior to participation in the study
* HRSD-17 score of 20 and higher
* at least one failed/refused/intolerant to antidepressant trial in the current episode as determined by Antidepressant Treatment History Form (ATHF)
* No safety concerns endorsed on TMS Screening and Information Form
Exclusion Criteria
* history of substance use disorders (moderate to severe) within the last 3 months as determined by MINI
* concomitant major unstable medical illness
* acutely suicidal or high risk for suicide as assessed by a study psychiatrist
* not eligible to receive TMS or MRI as indicated by TMS Screening and Information Form
* a change in treatment status during the study trial that will be considered a confound to the study. This includes change in medication or Cognitive Behavioral Therapy, each reviewed case by case by the study psychiatrists.
* medications that are considered a confound to the study including benzodiazepines, antipsychotics, mood stabilizers, stimulants and anticonvulsants.
* missing more than 20% of the treatment sessions consecutively (i.e., 2 sessions in a row) or 40% (i.e., 4 sessions) within two weeks
* have failed brain stimulation in the past
16 Years
24 Years
ALL
No
Sponsors
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Centre for Addiction and Mental Health
OTHER
Responsible Party
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Faranak Farzan
Independent Scientist
Principal Investigators
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Faranak Farzan
Role: PRINCIPAL_INVESTIGATOR
Centre for Addiction and Mental Health
Locations
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Center for Addiction and Mental Health
Toronto, Ontario, Canada
Countries
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References
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Dhami P, Moreno S, Croarkin PE, Blumberger DM, Daskalakis ZJ, Farzan F. Baseline markers of cortical excitation and inhibition predict response to theta burst stimulation treatment for youth depression. Sci Rep. 2023 Nov 4;13(1):19115. doi: 10.1038/s41598-023-45107-1.
Dhami P, Atluri S, Lee J, Knyahnytska Y, Croarkin PE, Blumberger DM, Daskalakis ZJ, Farzan F. Neurophysiological markers of response to theta burst stimulation in youth depression. Depress Anxiety. 2021 Feb;38(2):172-184. doi: 10.1002/da.23100. Epub 2020 Oct 1.
Related Links
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Information about research at the Centre for Addiction and Mental Health, Canada's largest mental health and addiction teaching
Other Identifiers
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# 076/2014-01
Identifier Type: -
Identifier Source: org_study_id