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临床试验/NCT07711639
NCT07711639招募中不适用

Efficacy of Foot Reflexology and Transcutaneous Auricular Vagus Nerve Stimulation on Tinnitus in Non-Cancer Adult Populations

Tzu Chi University1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2026年4月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
180
试验地点
1
主要终点
Change in Tinnitus Handicap Inventory (THI) score

研究概览

简要总结

Tinnitus is a common neurosensory symptom affecting 12-30% of adults and is closely associated with anxiety, sleep disturbance, and autonomic dysregulation. Current pharmacologic treatments offer limited efficacy and notable side effects, prompting interest in non-pharmacological approaches. This randomized, single-blind, sham-controlled trial evaluates whether foot reflexology (FR), transcutaneous auricular vagus nerve stimulation (ta-VNS), and auricular acupressure (AA) improve tinnitus severity, psychological distress, sleep quality, and autonomic indicators (heart rate variability and salivary cortisol) in non-cancer adults with tinnitus, compared with usual care. Participants are randomized to a foot reflexology group, an auricular vagus nerve stimulation group (each with true and sham subgroups), or a usual-care control group, and are followed at baseline and weeks 2, 4, and 8.

详细描述

This is a three-arm parallel, repeated-measures randomized controlled trial conducted in the otolaryngology outpatient and inpatient settings of Hualien Tzu Chi Hospital. Eligible non-cancer adults with tinnitus as the sole chief complaint and normal pure-tone thresholds are stratified by age and sex, then randomized by computer-generated random number tables to the FR group, the ta-VNS group, or the usual-care control group; the FR and ta-VNS groups are further randomized to true or sham subgroups. The foot reflexology intervention is delivered once weekly for 20 minutes over four sessions (one month) and comprises a relaxation phase, an inner-ear/autonomic regulation phase, and a circulation/detoxification phase; the sham condition applies light, non-specific touch. The ta-VNS intervention stimulates the left tragus, cymba conchae, and cavum conchae (pulse width 250 µs, 25 Hz, 0.5-5 mA individualized to a tingling sensation, 30 s on/off) once weekly for 20 minutes over four weeks; the sham condition stimulates the left earlobe at 0.5 mA. Auricular acupressure with magnetic beads is self-administered three times daily. Outcomes are assessed at T0 (baseline), T1 (week 2), T2 (week 4), and T3 (week 8). Data are analyzed with generalized estimating equation (GEE) models.

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-75 years, conscious, able to communicate and comprehend, and able to complete questionnaires and comply with study procedures
  • Tinnitus as the sole chief complaint, with pure-tone thresholds ≤25 dB HL bilaterally at 500, 1000, 2000, and 4000 Hz

排除标准

  • Objective tinnitus, peripheral vestibular disease, central nervous or cardiovascular causes, or other organic ear pathology
  • Open wounds or skin lesions of the foot or ear, lower-limb edema, history of deep vein thrombosis, or diabetes with most recent HbA1c >7.5%
  • Cardiac pacemaker or other implanted electronic device, or other severe cardiovascular disease
  • Foot reflexology or vagus nerve stimulation within the past 3 months
  • Pregnant or breastfeeding women
  • History of epilepsy or seizures
  • Physically frail condition

研究组 & 干预措施

Arm A: Foot Reflexology - True (n=36)

Experimental

Procedure: True Foot Reflexology

干预措施: True Foot Reflexology (Procedure)

Arm B: Foot Reflexology - Sham (n=36)

Sham Comparator

Procedure: Sham Foot Reflexology

干预措施: Sham Foot Reflexology (Procedure)

Arm C: ta-VNS - True (n=36)

Experimental

Device: True ta-VNS + Procedure: Auricular Acupressure

干预措施: True ta-VNS (Device)

Arm C: ta-VNS - True (n=36)

Experimental

Device: True ta-VNS + Procedure: Auricular Acupressure

干预措施: True Auricular Acupressure (Procedure)

Arm D: ta-VNS - Sham (n=36)

Sham Comparator

Device: Sham ta-VNS + Procedure: Sham Auricular Acupressure

干预措施: Sham ta-VNS (Device)

Arm D: ta-VNS - Sham (n=36)

Sham Comparator

Device: Sham ta-VNS + Procedure: Sham Auricular Acupressure

干预措施: Sham Auricular Acupressure (Procedure)

Arm E: Usual Care (n=36)

Active Comparator

Other: Usual Care

干预措施: Usual Care (Other)

结局指标

主要结局

Change in Tinnitus Handicap Inventory (THI) score

时间窗: T0 baseline, T1 week 2, T2 week 4, T3 week 8

25-item scale across functional, emotional, and catastrophic subscales; total 0-100, higher = greater handicap.

Change in Tinnitus Functional Index (TFI) score

时间窗: T0 baseline, T1 week 2, T2 week 4, T3 week 8

25-item scale; total 0-100, higher = greater impact.

次要结局

  • Change in Distress Thermometer (DT)(T0 baseline, T1 week 2, T2 week 4, T3 week 8)
  • Change in Pittsburgh Sleep Quality Index (PSQI)(T0 baseline, T1 week 2, T2 week 4, T3 week 8)
  • Change in Heart Rate Variability (HRV)(T0 baseline, T1 week 2, T2 week 4, T3 week 8)
  • Change in salivary cortisol concentration(T0 baseline, T1 week 2, T2 week 4, T3 week 8)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Chun Hou Huang

Associate Professor

Tzu Chi University

研究点 (1)

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