Major Depressive Disorder (MDD) has a high prevalence, is the leading cause of disability, and currently available interventions are associated with side effects and high treatment resistance. There is an urgent need for the development of novel interventions for MDD with alternate mechanisms of action. Temporal Interference (TI) stimulation is a newly emerging form of transcranial alternating current stimulation (tACS) that involves the application of two high-frequency currents at slightly different kHz frequencies. Since neurons, due to their intrinsic low-pass filtering, do not respond to high frequencies (i.e. \> 100 Hz), TI relies on the 'beat' interaction leading to neuromodulation at any given location, resulting in a much smaller focus and allowing for better targeting. The subgenual cingulate cortex (SCC) appears to be critical in the pathophysiology of depression and treatment response, especially in treatment-resistant cases. Non-invasive treatments, however, are not able to accurately target SCC due to its deep location within the brain. In this trial, 30 participants meeting the diagnostic criteria for MDD will be randomized to receive 10 sessions of 130 Hz TI delivered daily for 30 minutes, or 10 sessions of sham stimulation. During the stimulation, participants will be watching emotional film clips to enhance target engagement. The investigators will collect metrics of SCC target engagement using the resting-state fMRI and EEG technologies, and determine feasibility, tolerability, safety, and therapeutic efficacy of TI stimulation in MDD. The results of this trial will inform the TI technology as a therapeutic tool for network-based psychiatric disorders, including MDD, and be vital for the design and development of a large-scale randomized-controlled trial.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
30
TI involves simultaneous delivery of independent currents to the brain at slightly different kHz frequencies, which are individually too high to recruit neural firing. However, the difference ('beat') frequency where the currents overlap (i.e., temporally interfered) is low enough to drive neural activity. The interferometrically derived low frequencies have been demonstrated to activate neurons at a selected focus without activation of surrounding regions in awake mice. The safety of the TI paradigm has been demonstrated in over 60 healthy human volunteers, and finite element modeling of simulations of TI fields in human anatomical models suggests that large subcortical structures such as the hippocampus or SCC could be selectively targeted. However, the precise TI parameters for selective engagement of SCC in healthy participants and in MDD is currently unknown.
Electrodes will be placed in the same location on the head as that for the TI intervention; 0 mA of electrical current will be delivered to the brain (compared to 2 mA in the active intervention arm), therefore it is expected to elicit no changes in neural activity.
Interventional Psychiatry Program, St. Michael's Hospital - Unity Health Toronto
Toronto, Ontario, Canada
RECRUITINGNeuroimaging - Signal variance
Signal variance within SCC to demonstrate SCC target engagement to TI stimulation
Time frame: End of 2nd week of intervention
Neuroimaging - Functional connectivity
Seed-based resting-state functional connectivity of SCC to demonstrate SCC target engagement to TI stimulation
Time frame: End of 2nd week of intervention
Neuroimaging - Anatomical connectivity
Anatomical connectivity of SCC to demonstrate SCC target engagement to TI stimulation
Time frame: End of 2nd week of intervention
Neuroimaging - Perfusion metrics
Cerebral blood flow within SCC to demonstrate SCC target engagement to TI stimulation
Time frame: End of 2nd week of intervention
Clinical change in depression symptoms
Change in symptoms of depression measured by the 17-item Hamilton Depression Rating Scale (HAM-D); scores range from 0 to 53, and higher scores indicate more severe depression symptoms.
Time frame: Baseline, end of 1st week of intervention, end of 2nd week of intervention, 1 week post-intervention, and 4 weeks post-intervention
Clinical change in depression symptoms
Change in symptoms of depression measured by the 16-item Quick Inventory of Depressive Symptomatology; scores range from 0 to 48, and higher scores indicate more severe depression symptoms.
Time frame: Baseline, each intervention visit (5 times/week for 2 weeks), 1 week post-intervention, and 4 weeks post-intervention
EEG Signals - Time domain features
Changes in time domain features of gamma oscillation on resting-state EEG Changes in time domain features of theta oscillation on resting-state EEG
Time frame: Baseline, end of 1st week of intervention, and end of 2nd week of intervention
EEG Signals - Frequency domain features
Changes in frequency domain features of gamma oscillation on resting-state EEG Changes in frequency domain features of theta oscillation on resting-state EEG
Time frame: Baseline, end of 1st week of intervention, and end of 2nd week of intervention
EEG Signals - Functional connectivity
Changes in functional connectivity on resting-state EEG
Time frame: Baseline, end of 1st week of intervention, and end of 2nd week of intervention
Correlation between EEG and depression symptoms
Correlation between changes in features of gamma or theta oscillations (EEG) and changes in depression symptoms measured by the HAM-D
Time frame: Baseline, end of 1st week of intervention, and end of 2nd week of intervention
EEG Signals - MMN event-related potential
Changes in mismatch negativity (MMN) event-related potential amplitude and latency
Time frame: Baseline, end of 1st week of intervention, and end of 2nd week of intervention
Tolerability - Adverse events
Incidence of treatment-emergent adverse events
Time frame: End of 1st week of intervention, end of 2nd week of intervention, 1 week post-intervention, and 4 weeks post-intervention
Trial Feasibility - Dropout rate
The proportion of participants who discontinue participation in the study before completion
Time frame: End of 1st week of intervention, end of 2nd week of intervention, 1 week post-intervention, and 4 weeks post-intervention
Trial Feasibility - Recruitment rate
The number of participants enrolled into the study per month
Time frame: Enrollment
Trial Feasibility - Intervention adherence
Percentage of participants who completed ≥80% of scheduled intervention sessions
Time frame: End of 2nd week of intervention
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