このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Precision Closed-loop Brain-Computer Interface Neuromodulation for Treatment-Resistant Depression

2026年8月27日 更新者:Lin SUN、Shanghai Mental Health Center

Multi-scenario Clinical Application of Precision Closed-loop Brain-Computer Interface Neuromodulation in Treatment-Resistant Major Depressive Disorder

The goal of this clinical trial is to evaluate whether precision closed-loop neuromodulation treatments can improve depressive symptoms and daily functioning in people with treatment-resistant major depressive disorder (TRD). The study will assess the effectiveness and safety of two neuromodulation approaches: closed-loop deep brain stimulation (DBS) and transcutaneous auricular vagus nerve stimulation (taVNS).

Treatment-resistant major depressive disorder refers to depression that does not improve sufficiently after adequate treatment with standard antidepressant therapies. This study focuses on people with TRD, including individuals with early-onset depression, a history of self-harm or suicidal thoughts, or depression associated with traumatic experiences.

This study aims to answer whether closed-loop DBS and taVNS can reduce depressive symptoms compared with sham stimulation, whether these treatments are safe and well tolerated, and whether changes in brain activity are associated with clinical improvement.

This is a multicenter, prospective clinical study conducted at Shanghai Mental Health Center, Beijing Anding Hospital, and Xuanwu Hospital. Eligible participants with TRD will receive either DBS or taVNS according to patient preference. Within each intervention group, participants will be randomly assigned to active stimulation or sham stimulation groups to assess treatment effects.

During the study, participants will receive neuromodulation treatment and complete regular follow-up assessments. These assessments will include evaluation of depressive symptoms, anxiety symptoms, cognitive function, social functioning, brain electrical activity using electroencephalography (EEG), brain imaging using magnetic resonance imaging (MRI), and monitoring of adverse events.

The study will compare changes in clinical symptoms, brain-related measures, and safety outcomes between active and sham stimulation groups. The findings may help determine whether precision neuromodulation approaches can provide a new treatment option for people with treatment-resistant major depressive disorder.

調査の概要

研究の種類

介入

入学 (推定)

70

段階

  • 適用できない

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

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • Age 18 to 70 years, regardless of sex.
  • At least primary school education and able to understand the content of the assessment scales.
  • Meet the diagnostic criteria for depressive disorders according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5).
  • Have a history of depression lasting at least 24 months and have received adequate-dose and adequate-duration treatment with at least 2 antidepressants for 8 weeks or longer, including electroconvulsive therapy without anesthesia, with a reduction rate in the HAMD-17 score of 20% or less after treatment.
  • Have a HAMD-17 score greater than 17 at baseline.
  • Have been on a stable regimen of the current antidepressant medication for at least 1 month before enrollment.
  • Meet at least one of the following three criteria:

    1. Depression with onset before 18 years of age.

      1. The age at first depressive episode was younger than 18 years, confirmed by a psychiatrist at the attending physician level or above according to the DSM-5 or International Classification of Diseases, 11th Revision (ICD-11) diagnostic criteria for depressive disorders.
      2. The age at onset can be supported by at least one of the following sources: the participant's medical history report, previous medical records, or information about age at onset provided by a guardian.
      3. If the onset age is unclear, confirmation requires consistency between at least two independent sources of information.
    2. A clear history of self-injurious or suicidal behavior:

      1. As confirmed by a guardian or through review of previous medical records, the participant has had clinically significant self-injurious behavior, such as cutting, burning, hitting oneself, involving intentional self-harm without the intent to die; or suicidal behavior or tendencies, such as recurrent suicidal ideation, suicidal planning, or a suicide attempt.
      2. Such behavior or tendencies must be documented in, but not limited to, outpatient or inpatient medical records, psychological assessment records, or school or community referral records. Alternatively, they may be clearly described by a guardian and documented and confirmed in writing by the investigator.
    3. A clear history of traumatic stress:

      1. As confirmed by a guardian or through review of previous medical records, before the onset or worsening of depression, the participant experienced a situation meeting the DSM-5 definition of traumatic events, including but not limited to: actual or threatened death; serious injury; sexual violence; abuse; neglect; bullying; major accidents; war; natural disasters; intimate partner violence.
      2. The traumatic event must have a clearly documented time of occurrence, type of event, and temporal relationship with the onset or worsening of depressive symptoms.
      3. Standardized instruments such as life event questionnaires may be used as supplementary assessments. However, final eligibility determination must be made by the investigator based on comprehensive evaluation of: information provided by the legal guardian; previous medical records; clinical judgment.
  • Participants or their legal guardians must voluntarily sign the informed consent form and must be capable of completing follow-up assessments;
  • Participants assigned to the DBS group must pass preoperative evaluation for DBS surgery and must have no contraindications for neurosurgical procedures;
  • Participants assigned to the taVNS group must pass taVNS eligibility assessment, including: no recent facial or auricular injuries; no metallic implants in the head or heart; no active gastrointestinal symptoms; no acute exacerbation of respiratory disorders; no personal or family history of epilepsy; no frequent or severe headaches.

Exclusion Criteria:

  • Previous diagnosis of: schizophrenia; schizoaffective disorder; substance dependence or drug addiction; mental disorders secondary to other medical conditions; or presence of significant psychotic symptoms, including delusions and hallucinations.
  • Presence of severe or unstable disorders involving the: central nervous system; cardiovascular system; respiratory system; liver; kidney; endocrine system; hematological system; or other major organ systems, which, in the investigator's judgment, make the participant unsuitable for enrollment.
  • Female participants who are: pregnant; breastfeeding; planning pregnancy during the study period or within 8 weeks after the last medication administration; or male participants with plans for reproduction during the study period.
  • Participation in another clinical trial within the previous 3 months.
  • Inability to undergo MRI examination.
  • MRI findings indicating any of the following: more than two lacunar infarcts; regional infarction lesions with a volume >1 cm³; significant white matter lesions; a total Fazekas score of 3.
  • Severe aphasia, visual impairment, hearing impairment, or other conditions preventing completion of study procedures.
  • Any condition that, in the investigator's opinion, makes the participant unsuitable for participation in this study.
  • Contraindications to DBS surgery or chronic vagus nerve stimulation (VNS).
  • High suicide risk determined using the Columbia-Suicide Severity Rating Scale (C-SSRS). Participants will be excluded if any of the following criteria are met:

    1. A suicide attempt within the previous 3 months;
    2. Persistent active suicidal ideation with intent to act, as indicated by the C-SSRS assessment;
    3. Emergency department visit or hospitalization due to suicide risk within 1 month prior to enrollment;
    4. Baseline C-SSRS assessment indicates non-persistent active suicidal ideation, but the investigator determines, based on the intensity of suicidal intent score (C-SSRS Item 5) and clinical evaluation, that the participant has severely impaired impulse control and immediate suicide risk, confirmed by a psychiatric specialist.

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:ダブル

武器と介入

参加者グループ / アーム
介入・治療
実験的:Active DBS
Participants will receive active closed-loop deep brain stimulation (DBS). After DBS implantation surgery, stimulation will be activated 7-14 days after surgery. Participants will receive closed-loop DBS treatment and undergo clinical follow-up assessments for 8 weeks to evaluate changes in depressive symptoms, cognitive function, and safety outcomes.
Closed-loop deep brain stimulation (DBS) is an implanted neuromodulation intervention that delivers electrical stimulation based on real-time neural signals. Participants assigned to the DBS pathway will undergo implantation of a DBS system and receive either active or delayed stimulation according to the randomized study assignment. Clinical outcomes, cognitive function, brain activity, and safety outcomes will be assessed during follow-up.
偽コンパレータ:Sham DB
Participants will receive sham deep brain stimulation (DBS) during the blinded comparison period. After DBS implantation surgery, stimulation will remain inactive until 8 weeks after surgery. Participants will undergo the same clinical follow-up assessments as the active DBS group during the study period.
Closed-loop deep brain stimulation (DBS) is an implanted neuromodulation intervention that delivers electrical stimulation based on real-time neural signals. Participants assigned to the DBS pathway will undergo implantation of a DBS system and receive either active or delayed stimulation according to the randomized study assignment. Clinical outcomes, cognitive function, brain activity, and safety outcomes will be assessed during follow-up.
実験的:Active taVNS
Participants will receive active transcutaneous auricular vagus nerve stimulation (taVNS). Electrical stimulation will be delivered through electrodes placed at the auricular stimulation sites. Participants will receive taVNS treatment and undergo clinical follow-up assessments for 8 weeks to evaluate changes in depressive symptoms, cognitive function, and safety outcomes.
Transcutaneous auricular vagus nerve stimulation (taVNS) is a non-invasive neuromodulation intervention that delivers electrical stimulation through electrodes placed on auricular sites associated with the vagus nerve. Participants assigned to the taVNS pathway will receive either active or sham stimulation according to the randomized study assignment. Clinical outcomes, cognitive function, brain activity, and safety outcomes will be assessed during follow-up.
偽コンパレータ:Sham taVNS
Participants will receive sham transcutaneous auricular vagus nerve stimulation (taVNS). The electrodes will be placed at the same auricular sites as active stimulation, but no therapeutic electrical stimulation will be delivered. Participants will undergo the same clinical follow-up assessments as the active taVNS group.
Transcutaneous auricular vagus nerve stimulation (taVNS) is a non-invasive neuromodulation intervention that delivers electrical stimulation through electrodes placed on auricular sites associated with the vagus nerve. Participants assigned to the taVNS pathway will receive either active or sham stimulation according to the randomized study assignment. Clinical outcomes, cognitive function, brain activity, and safety outcomes will be assessed during follow-up.

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
Change in 17-item Hamilton Rating Scale for Depression (HAMD-17) score
時間枠:Baseline to Week 8
The primary efficacy outcome is the change in the 17-item Hamilton Depression Rating Scale (HAMD-17) score from baseline to week 8 after intervention. The HAMD-17 is used to assess the severity of depressive symptoms, with higher scores indicating greater severity of depressive symptoms. A decrease in HAMD-17 score indicates improvement in depressive symptoms.
Baseline to Week 8

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in Hamilton Anxiety Rating Scale (HAMA) score
時間枠:Baseline to Week 8
The change in Hamilton Anxiety Rating Scale (HAMA) score from baseline to Week 8 will be evaluated to assess changes in anxiety symptom severity. The HAMA total score ranges from 0 to 56, with higher scores indicating greater severity of anxiety symptoms. A decrease in HAMA score indicates improvement in anxiety symptoms.
Baseline to Week 8
Change in Montreal Cognitive Assessment scale (MoCA) score
時間枠:Baseline to Week 8
The change in Montreal Cognitive Assessment (MoCA) score from baseline to Week 8 will be evaluated to assess changes in cognitive function. The MoCA total score ranges from 0 to 30, with higher scores indicating better cognitive function. An increase in MoCA score indicates improvement in cognitive function.
Baseline to Week 8
Change in Montgomery-Asberg Depression Rating Scale (MADRS) score
時間枠:Baseline to Week 8
The change in Montgomery-Åsberg Depression Rating Scale (MADRS) score from baseline to Week 8 will be evaluated to assess changes in depressive symptom severity. The MADRS total score ranges from 0 to 60, with higher scores indicating greater severity of depressive symptoms. A decrease in MADRS score indicates improvement in depressive symptoms.
Baseline to Week 8
Change in Patient Health Questionnaire-9 (PHQ-9) score
時間枠:Baseline to Week 8
The change in Patient Health Questionnaire-9 (PHQ-9) score from baseline to Week 8 will be evaluated to assess changes in depressive symptoms. The PHQ-9 total score ranges from 0 to 27, with higher scores indicating greater severity of depressive symptoms. A decrease in PHQ-9 score indicates improvement in depressive symptoms.
Baseline to Week 8
Change in Generalized Anxiety Disorder-7 (GAD-7) score
時間枠:Baseline to Week 8
The change in Generalized Anxiety Disorder-7 (GAD-7) score from baseline to Week 8 will be evaluated to assess changes in anxiety symptoms. The GAD-7 total score ranges from 0 to 21, with higher scores indicating greater severity of anxiety symptoms. A decrease in GAD-7 score indicates improvement in anxiety symptoms.
Baseline to Week 8
Change in Clinical Global Impression-Improvement (CGI) score, using Clinical Global Impression-Severity (CGI-S)
時間枠:Baseline to Week 8
The change in Clinical Global Impression-Severity (CGI-S) score from baseline to each follow-up assessment will be evaluated to assess changes in overall illness severity. The CGI-S is rated on a 7-point scale from 1 to 7, with higher scores indicating greater illness severity. A decrease in CGI-S score indicates improvement in overall illness severity.
Baseline to Week 8
Change in Clinical Global Impression-Improvement (CGI) score, using Clinical Global Impression-Improvement (CGI-I).
時間枠:Baseline to Week 8
The Clinical Global Impression-Improvement (CGI-I) score will be used to assess overall clinical improvement relative to baseline. The CGI-I is rated on a 7-point scale from 1 to 7, with 1 indicating very much improved, 4 indicating no change, and 7 indicating very much worse. Lower scores indicate greater clinical improvement.
Baseline to Week 8
Change in Personal and Social Performance Scale (PSP) score
時間枠:Baseline to Weeks 1, 2, 4, 6, and 8
The change in Personal and Social Performance (PSP) Scale score from baseline to each follow-up assessment will be evaluated to assess changes in personal and social functioning. The PSP total score ranges from 1 to 100, with higher scores indicating better personal and social functioning. An increase in PSP score indicates improvement in personal and social functioning.
Baseline to Weeks 1, 2, 4, 6, and 8
Change in Social Functioning Rating Scale (SFRS) score
時間枠:Baseline to Week 8
The change in Social Functioning Rating Scale (SFRS) score from baseline to Week 8 will be evaluated to assess changes in social functioning. The SFRS consists of 36 items, with each item scored from 0 to 7, resulting in a total score ranging from 0 to 252. Higher scores indicate poorer social functioning. A decrease in SFRS score indicates improvement in social functioning.
Baseline to Week 8
EEG Delta, Theta, Alpha, and Beta Band Power and Theta/Beta Power Ratio
時間枠:Baseline to Week 8
EEG recordings will be analyzed to quantify changes in spectral power across predefined frequency bands, including delta (0.5-4 Hz), theta (4-8 Hz), alpha (8-13 Hz), beta (13-30 Hz) bands, and theta/beta power ratio from baseline to week 8.
Baseline to Week 8
Changes in neuroimaging measures assessed by magnetic resonance imaging (MRI)
時間枠:Baseline to Week 8
Baseline to Week 8
Number and percentage of participants with adverse events or serious adverse events
時間枠:Baseline to Week 8
Adverse events will be assessed throughout the study period. Clinically significant findings from laboratory tests, vital signs, electrocardiography, and other examinations will be recorded as adverse events when considered clinically significant by the investigator. When a specific clinical diagnosis can be made, the diagnosis will be recorded as the adverse event; when no specific diagnosis can be made, the clinical significance will be determined by the investigator. Adverse events will be classified as mild, moderate, or severe, and their occurrence time, severity, duration, management, and outcome will be recorded. The number and percentage of participants experiencing adverse events will be summarized.
Baseline to Week 8

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。

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8月1日

一次修了 (推定)

2028年12月31日

研究の完了 (推定)

2028年12月31日

試験登録日

最初に提出

2026年8月14日

QC基準を満たした最初の提出物

2026年8月24日

最初の投稿 (実際)

2026年8月25日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月28日

QC基準を満たした最後の更新が送信されました

2026年8月27日

最終確認日

2026年8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

  • 2026-63

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

いいえ

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。

購読する