跳至主要内容
临床试验/NCT05295888
NCT05295888招募中不适用

Evaluation of Temporal Interference in Target Engagement of Subgenual Cingulate Cortex in the Treatment of Major Depressive Disorder

Unity Health Toronto2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年5月15日最近更新:
适应症

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

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)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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