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Individualized Temporally Interfering Electrical Stimulation in Major Depressive Disorder

2026年11月6日 更新者:Xianyun Kang、Tianjin Medical University General Hospital

Closed-Loop Bio-Machine Interaction System and Applications in Psychiatric Diagnosis and Treatment

Temporally interfering (TI) electrical stimulation is a novel noninvasive neuromodulation technique with high spatial resolution. Although its effects on human brain function and behavior have been increasingly investigated, its clinical utility in major depressive disorder (MDD) has not been established. This trial aims to evaluate the efficacy and safety of TI electrical stimulation in MDD patients.

研究概览

详细说明

This is a multicenter, double-blind, randomized, sham-controlled trial including three parallel arms: (1)single-target active stimulation targeting the right primary auditory cortex (A1); (2) dual-target active stimulation targeting the right A1 and the right dorsolateral prefrontal cortex (DLPFC); (3)sham stimulation. All interventions will be delivered over two consecutive weeks, comprising ten treatment visits, with 20 minutes of stimulation applied to each target.

研究类型

介入性

注册 (估计的)

75

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Fujian
      • Fuzhou、Fujian、中国、350007
        • 招聘中
        • Fuzhou Neuropsychiatric Hospital Affiliated to Fujian Medical University
        • 接触:
    • Tianjin Municipality
      • Tianjin、Tianjin Municipality、中国、300222
        • 招聘中
        • Tianjin Anding Hospital
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 65年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Meets Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) diagnostic criteria for MDD, confirmed independently by two psychiatrists;
  2. Currently experiencing a depressive episode;
  3. Hamilton Depression Rating Scale 17-item (HAMD-17) score ≥ 17;
  4. Aged between 18-65 years;
  5. No restrictions on sex or gender;
  6. Attained at least junior high school education; lower education permitted if cognitive capacity is confirmed by a physician;
  7. Normal or corrected-to-normal vision and normal hearing;
  8. No use of antidepressant within two weeks prior to enrollment, or ongoing antidepressant treatment judged by a psychiatrist to be in a stable treatment phase;
  9. Ability to read and understand informed consent and self-report assessment scales;
  10. Willingness to participate in the study, with written informed consent provided by the participant or a legal guardian.

Exclusion Criteria:

  1. History of any psychiatric disorder other than MDD;
  2. History of traumatic brain injury or coma;
  3. History of organic brain disease or severe systemic medical illness;
  4. History of cochlear implants, pacemakers, or other implanted brain devices;
  5. History of epileptic seizures or family history of epilepsy;
  6. Obvious suicidal or impulsive violent behavior;
  7. Receipt of electroconvulsive therapy (ECT), transcranial magnetic stimulation (TMS), or other neuromodulation therapies within the past six months;
  8. History of alcohol use disorder or use of other psychoactive substances;
  9. Participation in other interventional clinical trials;
  10. Any condition precluding informed consent or compliance with study procedures.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:single-target active TI electrical stimulation group

Single-target active stimulation targeting the right primary auditory cortex (A1), each target stimulation phase will last 20 minutes, including a 30-second ramp-up at onset and a 30-second ramp-down at termination. Alternating currents with frequencies of f1 = 2000 Hz and f2 = 2040 Hz will be delivered through the two electrode pairs, and the total current intensity across the two electrode pairs will be fixed at 4 mA (AC, peak-to-base). The intervention will be administered over two consecutive weeks, with participants receiving stimulation on five days per week.

实验性的:dual-target active TI electrical stimulation group

Dual-target active stimulation targeting the right A1 and the right dorsolateral prefrontal cortex (DLPFC), each target stimulation phase will last 20 minutes, including a 30-second ramp-up at onset and a 30-second ramp-down at termination. For each target, two pairs of electrodes will be used; the alternating current frequency and total stimulation intensity will be the same as those in the single-target active TI electrical stimulation group.The intervention will be administered over two consecutive weeks, with participants receiving stimulation on five days per week.

假比较器:sham TI electrical stimulation group

Sham TI electrical stimulation group will follow the same session duration, treatment frequency, and procedural setup as the active stimulation groups. However, electrical stimulation will be limited to an initial 30-second ramp-up followed immediately by a 30-second ramp-down, after which no current will be delivered for the remainder of the session.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Hamilton Depression Rating Scale 17-item (HAMD-17)
大体时间:Baseline, Week 1, Week 2, Week 4.

Total scores range from 0 to 52, with higher scores indicating greater depressive symptom severity (worse outcomes).

Baseline, Week 1, Week 2, Week 4.

次要结果测量

结果测量
措施说明
大体时间
Patient Health Questionnaire-9 (PHQ-9)
大体时间:Baseline, Week 1, Week 2, Week 4.

Total scores range from 0 to 27, with higher scores indicating greater depressive symptom severity (worse outcomes).

Baseline, Week 1, Week 2, Week 4.
Hamilton Anxiety Rating Scale (HAMA)
大体时间:Baseline, Week 1, Week 2, Week 4.

Total scores range from 0 to 56, with higher scores indicating greater anxiety symptom severity (worse outcomes).

Baseline, Week 1, Week 2, Week 4.
Generalized Anxiety Disorder 7-item (GAD-7)
大体时间:Baseline, Week 1, Week 2, Week 4.

Total scores range from 0 to 21, with higher scores indicating greater anxiety symptom severity (worse outcomes).

Baseline, Week 1, Week 2, Week 4.
Young Mania Rating Scale (YMRS)
大体时间:Baseline, Week 1, Week 2, Week 4.

Total scores range from 0 to 60, with higher scores indicating greater manic symptom severity (worse outcomes).

Baseline, Week 1, Week 2, Week 4.
Electroencephalographic (EEG) Power in the Gamma Frequency Band
大体时间:Baseline, Week 1, Week 2, Week 4.

Gamma-band EEG power will be assessed using spectral analysis of EEG recordings.

Baseline, Week 1, Week 2, Week 4.
40-Hz Auditory Steady-State Response (ASSR) Event-Related Spectral Perturbation (ERSP)
大体时间:Baseline, Week 1, Week 2, Week 4.

The 40-Hz ASSR will be assessed using electroencephalography (EEG). Event-related spectral perturbation (ERSP) quantifies stimulus-induced changes in oscillatory power relative to a prestimulus baseline. ERSP will be expressed in decibels (dB), with higher values indicating greater stimulus-related power enhancement.

Baseline, Week 1, Week 2, Week 4.
40-Hz Auditory Steady-State Response (ASSR) Inter-Trial Coherence (ITC)
大体时间:Baseline, Week 1, Week 2, Week 4.

The 40-Hz ASSR will be assessed using electroencephalography (EEG). Inter-trial coherence (ITC) quantifies the consistency of oscillatory phase across repeated auditory stimulus presentations. ITC values range from 0 to 1, with higher values indicating greater phase consistency.

Baseline, Week 1, Week 2, Week 4.
Magnetic Resonance Imaging (MRI)
大体时间:Baseline, Week 2.

Changes in brain structure and functional organization, assessed using MRI, will be included as secondary neuroimaging outcomes.

Baseline, Week 2.

其他结果措施

结果测量
措施说明
大体时间
Athens Insomnia Scale (AIS)
大体时间:Baseline, Week 1, Week 2, Week 4.

Total scores range from 0 to 24, with higher scores indicating greater insomnia symptom severity (worse outcomes).

Baseline, Week 1, Week 2, Week 4.
Attention Control Scale (ACS)
大体时间:Baseline, Week 1, Week 2, Week 4.

The ACS consists of 20 items assessing two dimensions of attentional control: Attentional Focusing and Attentional Shifting. Total scores range from 20 to 80, with higher scores indicating better overall attentional control abilities (better outcomes). Attentional Focusing reflects the ability to maintain attention and resist distractions, whereas Attentional Shifting reflects the ability to flexibly shift attention between tasks or stimuli.

Baseline, Week 1, Week 2, Week 4.
Chinese 10-item Rumination Response Scale (RRS-10)
大体时间:Baseline, Week 1, Week 2, Week 4.

The RRS-10 consists of 10 items assessing two dimensions of rumination: Brooding and Reflection, each comprising five items. Total scores range from 10 to 40, with higher scores indicating greater overall rumination (generally worse outcomes). Brooding reflects maladaptive rumination, whereas Reflection reflects purposeful self-focused thinking and does not necessarily indicate worse outcomes.

Baseline, Week 1, Week 2, Week 4.
Emotion Regulation Questionnaire (ERQ) - Cognitive Reappraisal Subscale
大体时间:Baseline, Week 1, Week 2, Week 4.

The Cognitive Reappraisal subscale of the ERQ consists of 6 items assessing the tendency to regulate emotions by reinterpreting emotional situations. Total scores range from 6 to 42, with higher scores indicating greater use of cognitive reappraisal, generally considered a more adaptive emotion regulation strategy (better outcomes).

Baseline, Week 1, Week 2, Week 4.
Emotion Regulation Questionnaire (ERQ) - Expressive Suppression Subscale
大体时间:Baseline, Week 1, Week 2, Week 4.

The Expressive Suppression subscale of the ERQ consists of 4 items assessing the tendency to inhibit outward emotional expression. Total scores range from 4 to 28, with higher scores indicating greater use of expressive suppression, generally considered a less adaptive emotion regulation strategy (worse outcomes).

Baseline, Week 1, Week 2, Week 4.
Cognitive Flexibility Inventory (CFI)
大体时间:Baseline, Week 1, Week 2, Week 4.

The CFI consists of 20 items assessing two dimensions of cognitive flexibility: Alternatives (13 items) and Control (7 items). Total scores range from 20 to 100, with higher scores indicating greater cognitive flexibility (better outcomes). Alternatives reflects the ability to generate multiple explanations and solutions to difficult situations, whereas Control reflects the tendency to perceive difficult situations as controllable.

Baseline, Week 1, Week 2, Week 4.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2025年3月11日

初级完成 (估计的)

2027年6月15日

研究完成 (估计的)

2027年6月15日

研究注册日期

首次提交

2026年11月3日

首先提交符合 QC 标准的

2026年11月6日

首次发布 (实际的)

2026年11月9日

研究记录更新

最后更新发布 (实际的)

2026年11月9日

上次提交的符合 QC 标准的更新

2026年11月6日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

其他研究编号

  • XY1895

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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