Efficacy of Foot Reflexology and Transcutaneous Auricular Vagus Nerve Stimulation on Tinnitus in Non-Cancer Adult Populations
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
- 否
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)
Procedure: True Foot Reflexology
干预措施: True Foot Reflexology (Procedure)
Arm B: Foot Reflexology - Sham (n=36)
Procedure: Sham Foot Reflexology
干预措施: Sham Foot Reflexology (Procedure)
Arm C: ta-VNS - True (n=36)
Device: True ta-VNS + Procedure: Auricular Acupressure
干预措施: True ta-VNS (Device)
Arm C: ta-VNS - True (n=36)
Device: True ta-VNS + Procedure: Auricular Acupressure
干预措施: True Auricular Acupressure (Procedure)
Arm D: ta-VNS - Sham (n=36)
Device: Sham ta-VNS + Procedure: Sham Auricular Acupressure
干预措施: Sham ta-VNS (Device)
Arm D: ta-VNS - Sham (n=36)
Device: Sham ta-VNS + Procedure: Sham Auricular Acupressure
干预措施: Sham Auricular Acupressure (Procedure)
Arm E: Usual Care (n=36)
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
Chun Hou Huang
Associate Professor
Tzu Chi University
