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临床试验/NCT07469969
NCT07469969尚未招募不适用

Transcutaneous Auricular Vagus Nerve Stimulation Combined With Tailor-Made Notched Music Training Therapy for Chronic Subjective Tinnitus: A Multicenter, Randomized, Controlled, Open-label Trial

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University1 个研究点 分布在 1 个国家目标入组 386 人开始时间: 2026年4月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
386
试验地点
1
主要终点
Tinnitus Improvement Response Rate

研究概览

简要总结

This study is a prospective, multicenter, randomized, controlled, open-label clinical trial designed to evaluate the superiority of transauricular vagus nerve microcurrent stimulation (taVNS) combined with Tailor-Made Notched Music Training (TMNMT) compared with Tinnitus Retraining Therapy (TRT) in patients with chronic subjective tinnitus. A total of 386 participants aged 18-70 years with a tinnitus duration of at least 6 months and a Tinnitus Handicap Inventory (THI) score ≥38 will be enrolled, excluding individuals with severe hearing loss, organic cranial diseases, or other contraindications. Eligible participants will be randomly assigned in a 1:1 ratio to either the experimental group or the control group. The control group will receive standardized TRT, including habituation sound therapy and structured educational counseling, while the experimental group will receive TMNMT combined with taVNS (0.1 Hz pulse-train stimulation, sub-pain threshold intensity of 0.5-10 mA). Although the trial is open-label, outcome assessors and statisticians will remain blinded to group allocation. Baseline and follow-up assessments include THI, visual analog scale (VAS), Beck Anxiety Inventory (BAI), Beck Depression Inventory (BDI), Pittsburgh Sleep Quality Index (PSQI), audiological evaluations, and multimodal neuroimaging using EEG and fMRI. The primary outcome is the tinnitus improvement response rate at 3 months after treatment initiation, defined as a reduction of more than 7 points in the THI score from baseline. Secondary outcomes include treatment response rates at 6 and 12 months, changes in tinnitus severity and tinnitus-related comorbid symptoms, and neuroplasticity-related changes in central neural mechanisms.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients whose primary complaint is tinnitus and who seek medical care for this reason
  • Patients diagnosed with chronic tinnitus for more than 6 months
  • Age between 18 and 70 years
  • Tinnitus frequency within the range of 125-8000 Hz
  • Hearing threshold not exceeding 70 dB HL
  • Tinnitus Handicap Inventory (THI) score ≥ 38 points.

排除标准

  • Patients with conductive hearing loss, history of middle ear surgery, pulsatile tinnitus due to vascular malformations, or tinnitus associated with Meniere's disease
  • History of head trauma, central nervous system disorders, psychiatric disorders, or substance abuse/dependence
  • Patients unwilling or unable to comply with the study protocol requirements
  • Patients with space-occupying lesions in the peripheral auditory pathway or central nervous system (e.g., acoustic neuroma, middle ear cholesteatoma, meningioma) as identified by imaging studies.

研究组 & 干预措施

taVNS + TMNMT

Experimental

transcutaneous auricular vagus nerve stimulation combined with tailor-made notched music training therapy

干预措施: transcutaneous auricular vagus nerve stimulation combined with tailor-made notched music training therapy (Device)

TRT

Active Comparator

Tinnitus Retraining Therapy

干预措施: tinnitus retraining therapy (Device)

结局指标

主要结局

Tinnitus Improvement Response Rate

时间窗: Before treatment and at the end of the 3-month treatment period

The Tinnitus Improvement Response Rate is evaluated based on the change in Tinnitus Handicap Inventory (THI) scores. A higher score indicates greater interference of tinnitus with quality of life. Treatment response is defined as a reduction in the THI score of \>7 points from the baseline assessment after 3 months of treatment, based on the internationally recognized Minimal Clinically Important Difference (MCID) threshold. Calculation Formula: Tinnitus Improvement Response Rate (%) = (Number of Responders / Total Number of Cases in the Corresponding Group) × 100%

次要结局

  • Change in Self-Perceived Tinnitus Loudness assessed by Visual Analogue Scale (VAS) Score(Baseline, Month 3, Month 6, Month 12)
  • Change in Tinnitus Loudness Matching Threshold(Baseline, Month 3, Month 6, Month 12)
  • Number of Participants with Treatment-Related Adverse Events(From Baseline through Month 3)
  • Change in Beck Anxiety Inventory (BAI) Standardized Score(Baseline, Month 3, Month 6, Month 12)
  • Change in Beck Depression Inventory (BDI) Total Score(Baseline, Month 3, Month 6, Month 12)
  • Change in Pittsburgh Sleep Quality Index (PSQI) Global Score(Baseline, Month 3, Month 6, Month 12)
  • Percentage of Participants Achieving Minimal Clinically Important Difference in THI Score(Month 6, Month 12)
  • Change in Quantitative EEG (qEEG) Spectral and Connectivity Metrics (0.5-100 Hz)(Baseline, Month 3, Month 6)
  • Change in Functional MRI (fMRI) BOLD Signal and Network Connectivity(Baseline, Month 3, Month 6)
  • Change in Structural MRI Morphometry (Gray Matter Volume and Cortical Thickness)(Baseline, Month 3, Month 6)
  • Change in Diffusion MRI Metrics and Glymphatic System Activity (DTI-ALPS)(Baseline, Month 3, Month 6)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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