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Individualized Temporally Interfering Electrical Stimulation in Major Depressive Disorder

2026년 11월 6일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (추정된)

75

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Fujian
      • Fuzhou, Fujian, 중국, 350007
        • 모병
        • Fuzhou Neuropsychiatric Hospital Affiliated to Fujian Medical University
        • 연락하다:
    • Tianjin Municipality
      • Tianjin, Tianjin Municipality, 중국, 300222
        • 모병
        • Tianjin Anding Hospital
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 더블

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.

실험적: 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.

가짜 비교기: 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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Hamilton Depression Rating Scale 17-item (HAMD-17)
기간: 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.

2차 결과 측정

결과 측정
측정값 설명
기간
Patient Health Questionnaire-9 (PHQ-9)
기간: 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)
기간: 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)
기간: 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)
기간: 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
기간: 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)
기간: 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)
기간: 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)
기간: Baseline, Week 2.

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

Baseline, Week 2.

기타 결과 측정

결과 측정
측정값 설명
기간
Athens Insomnia Scale (AIS)
기간: 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)
기간: 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)
기간: 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
기간: 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
기간: 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)
기간: 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.

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2025년 3월 11일

기본 완료 (추정된)

2027년 6월 15일

연구 완료 (추정된)

2027년 6월 15일

연구 등록 날짜

최초 제출

2026년 11월 3일

QC 기준을 충족하는 최초 제출

2026년 11월 6일

처음 게시됨 (실제)

2026년 11월 9일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 11월 9일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 11월 6일

마지막으로 확인됨

2026년 11월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • XY1895

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