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临床试验/NCT07711626
NCT07711626招募中不适用

Efficacy of Foot Reflexology and Transcutaneous Auricular Vagus Nerve Stimulation on Pain, Xerostomia, Fatigue, Sleep, and Treatment-Related Symptoms in Head and Neck Cancer Patients Receiving Concurrent Chemoradiotherapy: A Randomized, Single-Blind, Sham-Controlled Trial

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7月13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 Numeric Rating Scale (NRS) for pain

研究概览

简要总结

Head and neck cancer (HNC) patients undergoing concurrent chemoradiotherapy (CCRT) frequently experience pain, xerostomia, fatigue, sleep disturbance, and other treatment-related toxicities that impair quality of life and treatment adherence, with incomplete relief from current supportive care. This randomized, single-blind, sham-controlled trial evaluates whether foot reflexology (FR), transcutaneous auricular vagus nerve stimulation (ta-VNS), and auricular acupressure (AA) reduce pain, xerostomia, fatigue, sleep disturbance, and treatment-related symptoms in HNC patients receiving cisplatin-based CCRT, 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 1, 2, and 4.

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 patients with pathologically confirmed HNC (clinical stage II-IVA) scheduled to receive a second cycle of cisplatin-based CCRT are stratified by CRT dose (<66 Gy vs ≥66 Gy) and randomized using a computer-generated sequence with block size 4 or 8, in a 1:1:1 ratio, 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 twice weekly for 20 minutes over two weeks and comprises a relaxation phase, a head-neck/gastrointestinal 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) twice weekly for 20 minutes over two 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 1), T2 (week 2), and T3 (week 4). 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
Supportive Care
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Pathologically confirmed head and neck cancer, clinical stage II-IVA, age 30-75 years, conscious, able to communicate and comprehend, and able to comply with study procedures
  • Scheduled to receive a second cycle of cisplatin-based concurrent chemoradiotherapy
  • ECOG performance status ≤2

排除标准

  • Severe cognitive impairment or psychiatric illness precluding comprehension or cooperation
  • 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
  • Severe bone-marrow suppression (WBC <2,000/µL or platelets <50,000/µL)
  • 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 Numeric Rating Scale (NRS) for pain

时间窗: T0 baseline, T1 week 1, T2 week 2, T3 week 4

0-10 scale; 0 = no pain, 10 = worst pain.

次要结局

未报告次要终点

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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