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Published on: August 11, 2015
Intermittent Theta-Burst Stimulation and Depressive Symptoms in Major Depressive Disorder: A Randomized Clinical
Marte C Ørbo1, Ole K Grønli2,3, Mats S Brochs1
1Department of Psychology, Faculty of Health Sciences, UiT The Arctic University of Norway, Tromsø, Norway.
JAMA Network Open
|July 8, 2026
Summary
Intermittent theta-burst stimulation (iTBS) effectively reduced depressive symptoms in adults with major depressive disorder (MDD) during a 10-session treatment. However, these benefits were not sustained at the 4-week follow-up, emphasizing the need for longer treatment durations.
Area of Science:
- Neuroscience
- Psychiatry
- Clinical Trials
Background:
- Intermittent theta-burst stimulation (iTBS) is an established treatment for major depressive disorder (MDD).
- Sham-controlled evidence for once-daily iTBS protocols in MDD is limited.
- Assessing the efficacy of a fixed 10-session once-daily iTBS protocol is crucial.
Purpose of the Study:
- To determine if 10 sessions of once-daily iTBS is superior to sham iTBS for adults with MDD.
- To evaluate the short-term and sustained effects of iTBS on depressive symptoms.
- To compare clinician-rated and self-reported depression scores.
Main Methods:
- A randomized clinical trial involving 73 adults with MDD (MADRS score ≥ 20).
- Participants received 10 weekday sessions of iTBS or sham stimulation targeting the left dorsolateral prefrontal cortex.
- Depression scores (MADRS, BDI-II) were assessed on days 5, 10, and at 4-week follow-up.
Main Results:
- iTBS demonstrated superiority over sham for MADRS scores on day 10 (p=.01) and day 5 (p=.04).
- No significant difference was found between iTBS and sham for BDI-II scores on day 10 (p=.30).
- The observed benefits were not sustained at the 4-week follow-up, with improvements noted in the sham group.
Conclusions:
- A 10-session schedule of once-daily iTBS led to greater reductions in clinician-rated depressive symptoms compared to sham during treatment.
- The treatment was well-tolerated with mild, transient adverse events.
- Findings underscore the importance of treatment duration and extended follow-up in evaluating clinical response for MDD.
