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Home-Based Randomized Trial of Spaced Transcranial Direct Current Stimulation for Treatment-Resistant Depression

2026年9月16日 更新者:Jean-Philippe Miron、University of California, San Diego

Spaced Transcranial Direct Current Stimulation for Treatment-Resistant Depression: A Home-Based Randomized Sham-Controlled Trial and Mechanistic Exploration

This study aims to evaluate the clinical efficacy and neurophysiological mechanisms of home-based spaced tDCS in TRD through a randomized, double-blind, sham-controlled trial conducted under remote supervision. Specifically, this trial will: (1) compare the efficacy of active versus sham spaced tDCS on depressive symptom severity in individuals with TRD and (2) characterize neurophysiological changes associated with spaced tDCS using TMS-EEG, TMS-EMG and resting state EEG.

研究概览

研究类型

介入性

注册 (估计的)

74

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

    • California
      • San Diego、California、美国、92127
        • UCSD Interventional Psychiatry
        • 接触:
        • 接触:
          • UCSD Interventional Psychiatry Clinic
          • 电话号码:858-207-0938

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 70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:

  • People between the ages of 18 and 70 at the time of screening.
  • Able to read, understand, and provide written, dated informed consent prior to screening. Proficiency in English sufficient to complete questionnaires / follow instructions during interventions. Stated willingness to comply with all study procedures, including availability for the duration of the study, and to communicate with study personnel about adverse events and other clinically important information.
  • Currently diagnosed with Major Depressive Disorder (MDD) and meets criteria for a Major Depressive Episode, according to the criteria defined in the Diagnosis and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5).
  • Medical records confirming a history of at least moderate treatment-resistance as defined on Antidepressant Treatment History Form (ATHF) score for that antidepressant trial of > 2 in the current episode OR have been unable to tolerate at least 2 separate trials of antidepressants of inadequate dose and duration (ATHF score of 1 or 2 on those 2 separate antidepressants) OR have a combination of one failed trial and one not tolerated trial, per the definitions above.
  • MADRS score of ≥20 at screening.
  • Existing relationship with mental health provider and access to ongoing psychiatric care before and after completion of the study.
  • Must be on a stable antidepressant therapeutic regimen for at least 4 weeks prior to study enrollment and agree to continue this regimen throughout the study period. Participants who are not currently on antidepressant treatment are eligible, provided that no discontinuation occurred within the 4 weeks preceding study enrollment.
  • For persons of child-bearing potential: use of highly effective contraception for at least 1 month prior to screening and agreement to use such a method during study participation.
  • Agreement to adhere to Lifestyle Considerations (i.e. must continue with any existing treatments) throughout study duration.
  • For persons of childbearing potential: must take a pregnancy test prior to initiating treatment, with results confirmed as negative by study staff
  • Participants will need to have a stable internet connection and a device compatible with UCSD Microsoft Teams or UCSD Zoom to facilitate remote communication and engagement in study activities.

Exclusion Criteria:

  • Pregnancy this includes breastfeeding or trying to becoming pregnant.
  • History of psychotic or bipolar disorder or depression with psychotic features.
  • Significant borderline personality disorder.
  • Significant comorbid obsessive-compulsive or post-traumatic stress disorder.
  • Previously diagnosed Intellectual Disability or Autism Spectrum Disorder.
  • Current moderate or severe substance use disorder or demonstrating signs of acute substance withdrawal.
  • Clinically significant suicidality.
  • Any history of tDCS.
  • Any history of ECT.
  • History of TMS (greater than 15 sessions) without a clinically meaningful response.
  • History of ketamine (greater than 4 sessions) without a clinically meaningful response.
  • History of significant neurologic disease, including dementia, Parkinson's or Huntington's disease, brain tumor, seizure disorder, subdural hematoma, multiple sclerosis, or history of significant head trauma with persistent symptoms.
  • Untreated or insufficiently treated endocrine disorder.
  • Contraindication to receiving tDCS (e.g., ferromagnetic implant, history of seizure, known brain lesion).
  • Treatment with an investigational drug or other intervention within the study period.
  • Unstable symptoms between screening and baseline as defined by a ≥ 30% change in MADRS score.
  • Require a benzodiazepine with a dose > lorazepam 2 mg/day
  • Has started a new psychotherapeutic process in the past 3 months from screening.
  • Use of potentially irritant topical treatments (ex: retinoids, alpha hydroxy acids).

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:三倍

武器和干预

参与者组/臂
干预/治疗
有源比较器:Active spaced-tDCS

Active tDCS applies low-intensity electrical current to the scalp to modulate cortical excitability through subthreshold shifts in neuronal membrane potentials, influencing synaptic plasticity

Spaced-tDCS will be self-administered at home under the supervision of a trained clinical research coordinator using the Soterix Medical mini-CT device with remote monitoring via a secure videoconferencing platform (e.g., Microsoft Teams).

假比较器:Sham spaced-tDCS

Sham tDCS is a placebo control that simulates the physical sensations of tDCS but does not deliver any actual, prolonged electrical current to the brain.

Soterix Medical mini-CT device sham protocol that match real stimulation parameters will be used.

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
Active vs Sham spaced tDCS Efficacy as measured by the Montgomery-Åsberg Depression Rating Scale
大体时间:Baseline to 4-weeks post treatment

To compare the efficacy of active versus sham spaced tDCS in reducing depressive symptom severity in TRD. Symptom severity will be measured using the MADRS score at four weeks post-treatment.

Baseline to 4-weeks post treatment

次要结果测量

结果测量
措施说明
大体时间
Changes in MADRS with active versus sham spaced tDCS during all post treatment visits
大体时间:1-week post treatment to 10-week post treatment

Clinical outcomes associated with active versus sham spaced tDCS as measured by MADRS response (≥50% reduction) and remission (score ≤10) rates.

1-week post treatment to 10-week post treatment
Changes in Hamilton Depression Rating Scale, 17-item version scores
大体时间:1-week post treatment to 10-week post treatment

Reduction in HAMD-17 scores at all follow-up timepoints. Score range from 0 to 52.

1-week post treatment to 10-week post treatment
Changes in Patient Health Questionnaire-9
大体时间:1-week post treatment to 10-week post treatment

Changes in PHQ scores at all follow-up timepoints. With scores ranging from 0-27

1-week post treatment to 10-week post treatment
Changes in General Anxiety Disorder-7
大体时间:1-week post treatment to 10-week post treatment

Changes in GAD-7 scores at all follow-up timepoints. Score range from 0-21

1-week post treatment to 10-week post treatment
Changes in The Modified Scale for Suicidal Ideation
大体时间:1-week post treatment to 10-week post treatment

Changes in the presence and severity of suicidal thoughts at all follow-up timepoints. Scores ranging from 0-54

1-week post treatment to 10-week post treatment
Feasibility (Recruitment)
大体时间:Baseline clinical assessment to 10 weeks post treatment.

Recruitment rate will be measured as the number of patients enrolled by the conclusion of the study, reported as a whole number.

Baseline clinical assessment to 10 weeks post treatment.
Feasibility (Retention)
大体时间:Baseline clinical assessment to 10 weeks post treatment.

Retention rate will be measured as the percentage of enrolled patients who complete all study visits, reported as a percentage.

Baseline clinical assessment to 10 weeks post treatment.
Feasibility (Adherence)
大体时间:Baseline clinical assessment to 10 weeks post treatment

The proportion of completed sessions relative to the total prescribed sessions, expressed as a percentage.

Baseline clinical assessment to 10 weeks post treatment
Safety of at-home spaced tDCS
大体时间:Baseline clinical assessment to 10 weeks post treatment

Safety will be measured by the number of serious adverse events (SAEs)

Baseline clinical assessment to 10 weeks post treatment
Tolerability to spaced tDCS
大体时间:Baseline clinical assessment to 10 weeks post treatment.

Tolerability will be measured by the number of adverse events (AEs).

Baseline clinical assessment to 10 weeks post treatment.

其他结果措施

结果测量
措施说明
大体时间
Biomarker Discovery: Short-Interval Intracortical Inhibition (SICI) and Long-Interval Intracortical Inhibition (LICI) via TMS-EMG
大体时间:Baseline to 4-weeks post treatment

TMS-EMG will be used to evaluate changes in SICI and LICI.

Baseline to 4-weeks post treatment
Biomarker Discovery: Intracortical Facilitation (ICF) via TMS-EMG
大体时间:Baseline to 4-weeks post treatment

TMS-EMG will be used to evaluate changes in intracortical facilitation

Baseline to 4-weeks post treatment
Biomarker Discovery: Cortical Silent Period (CSP) via Transcranial Magnetic Stimulation-Electromyography (TMS-EMG)
大体时间:Baseline to 4-weeks post treatment

TMS-EMG will be used to assess changes in the cortical silent period (CSP). Unit of Measurement: Duration (milliseconds).

Baseline to 4-weeks post treatment
TMS-Evoked Potential (TEP) Component Amplitudes via TMS-EEG
大体时间:Baseline to 4-weeks post treatment

TMS-EEG will be used to evaluate changes in TMS-evoked potential (TEP) component amplitudes.

Unit of Measurement: Voltage (µV).

Baseline to 4-weeks post treatment
Resting-State Electroencephalography (rsEEG)
大体时间:Baseline to 4-weeks post treatment

rsEEG will be used to analyze changes in brain activity patterns at rest. Unit of Measurement: Frequency (Hz)

Baseline to 4-weeks post treatment

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。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

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 (估计的)

2026年10月15日

初级完成 (估计的)

2031年10月15日

研究完成 (估计的)

2031年10月15日

研究注册日期

首次提交

2026年9月10日

首先提交符合 QC 标准的

2026年9月16日

首次发布 (实际的)

2026年9月22日

研究记录更新

最后更新发布 (实际的)

2026年9月22日

上次提交的符合 QC 标准的更新

2026年9月16日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • 814732
  • 1K23MH144148-01 (美国 NIH 拨款/合同)

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

是的

在美国制造并从美国出口的产品

是的

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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