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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.

調査の概要

研究の種類

介入

入学 (推定)

74

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • California
      • San Diego、California、アメリカ、92127
        • UCSD Interventional Psychiatry
        • コンタクト:
        • コンタクト:
          • UCSD Interventional Psychiatry Clinic
          • 電話番号:858-207-0938

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~70年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

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).

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:トリプル

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ: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).

偽コンパレータ: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Active vs Sham spaced tDCS Efficacy as measured by the Montgomery-Åsberg Depression Rating Scale
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Changes in MADRS with active versus sham spaced tDCS during all post treatment visits
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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
時間枠: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.

その他の成果指標

結果測定
メジャーの説明
時間枠
Biomarker Discovery: Short-Interval Intracortical Inhibition (SICI) and Long-Interval Intracortical Inhibition (LICI) via TMS-EMG
時間枠: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
時間枠: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)
時間枠: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
時間枠: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)
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年10月15日

一次修了 (推定)

2031年10月15日

研究の完了 (推定)

2031年10月15日

試験登録日

最初に提出

2026年9月10日

QC基準を満たした最初の提出物

2026年9月16日

最初の投稿 (実際)

2026年9月22日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月22日

QC基準を満たした最後の更新が送信されました

2026年9月16日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 814732
  • 1K23MH144148-01 (米国 NIH グラント/契約)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

はい

米国で製造され、米国から輸出された製品。

はい

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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