Evaluation of Temporal Interference in Target Engagement of Subgenual Cingulate Cortex in the Treatment of Major Depressive Disorder
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 30
- 试验地点
- 2
- 主要终点
- Neuroimaging - Perfusion metrics
研究概览
简要总结
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
盲法说明
The following roles will be blinded: i) Investigators and care providers; ii) Enrolled participants; iii) Outcome assessors; iv) MRI technician
入排标准
- 年龄范围
- 18 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Neuroimaging - Perfusion metrics
时间窗: End of 2nd week of intervention
Cerebral blood flow within SCC to demonstrate SCC target engagement to TI stimulation
Neuroimaging - Signal variance
时间窗: End of 2nd week of intervention
Signal variance within SCC to demonstrate SCC target engagement to TI stimulation
Neuroimaging - Functional connectivity
时间窗: End of 2nd week of intervention
Seed-based resting-state functional connectivity of SCC to demonstrate SCC target engagement to TI stimulation
Neuroimaging - Anatomical connectivity
时间窗: End of 2nd week of intervention
Anatomical connectivity of SCC to demonstrate SCC target engagement to TI stimulation
次要结局
- Tolerability - Adverse events(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(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(Enrollment)
- Trial Feasibility - Intervention adherence(End of 2nd week of intervention)
- Clinical change in depression symptoms(Baseline, each intervention visit (5 times/week for 2 weeks), 1 week post-intervention, and 4 weeks post-intervention)
- EEG Signals - Frequency domain features(Baseline, end of 1st week of intervention, and end of 2nd week of intervention)
- EEG Signals - Functional connectivity(Baseline, end of 1st week of intervention, and end of 2nd week of intervention)
- Correlation between EEG and depression symptoms(Baseline, end of 1st week of intervention, and end of 2nd week of intervention)
- EEG Signals - MMN event-related potential(Baseline, end of 1st week of intervention, and end of 2nd week of intervention)
- EEG Signals - Time domain features(Baseline, end of 1st week of intervention, and end of 2nd week of intervention)
