此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Kinesiology Taping Versus Self-Mobilization for Neck Pain Related to Prolonged Electronic Device Use

2026年11月2日 更新者:Emrah Zirek、Istanbul University - Cerrahpasa

Effects of Kinesiology Taping Versus Self-Sustained Natural Apophyseal Glide Mobilization on Pain, Neck Disability, Cervical Proprioception, Respiratory Muscle Strength, and Upper Trapezius Muscle Activity in Individuals With Neck Pain Related to Prolonged Electronic Device Use: A Randomized Controlled Trial

The goal of this clinical trial is to learn whether kinesiology taping or self-mobilization better reduces neck pain in adults who use electronic devices for long periods each day. The main questions it aims to answer are:

  • Does kinesiology taping or self-mobilization lead to greater reduction in neck pain after 4 weeks?
  • Do the two treatments differ in their effects on neck-related disability, neck position sense, breathing muscle strength, and upper trapezius muscle activity?

Researchers will compare kinesiology taping with self-sustained natural apophyseal glide (self-SNAG) mobilization to see which approach is more effective.

Participants will:

  • Be randomly assigned to one of the two treatment groups
  • Receive kinesiology tape applied to the back of the neck every 4 days for 4 weeks, or learn and perform a towel-assisted neck self-mobilization exercise for 4 weeks
  • Receive education on posture and self-management
  • Complete assessments of pain, neck disability, neck position sense, breathing muscle strength, and neck-shoulder muscle activity at the start of the study, after 4 weeks, and 1 month later

研究概览

详细说明

Prolonged use of electronic devices is associated with sustained cervical flexion and altered activation of the cervicoscapular musculature, particularly the upper trapezius. Kinesiology taping and Mulligan self-mobilization are commonly used conservative approaches; however, their comparative effects on pain, cervical proprioception, respiratory muscle strength, and muscle activity in this population remain unclear.

In this single-blind, two-arm, parallel-group randomized controlled trial, adults with neck pain (VAS > 3/10) and a history of electronic device use of at least 4 hours per day during the preceding year will be randomized to kinesiology taping (8 applications over 4 weeks) or self-SNAG mobilization performed with mirror-based visual feedback. Both groups will receive standardized education on posture and self-management.

Bilateral upper trapezius surface electromyography will be recorded during isometric shoulder elevation using a wireless sEMG system, with electrode placement according to SENIAM guidelines, and normalized to maximum voluntary isometric contraction. A bilateral upper trapezius EMG asymmetry index will be derived from the normalized right- and left-side values.

Primary and secondary outcomes will be analyzed using linear mixed-effects models with random intercepts for participants. As a pre-specified secondary analysis, the association between baseline bilateral upper trapezius EMG asymmetry and change in pain intensity will be examined, including its interaction with treatment group.

研究类型

介入性

注册 (估计的)

27

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Emrah Zirek Assistant Professor, Ph. D.
  • 电话号码:+905446457700
  • 邮箱:ezirek@bingol.edu.tr

学习地点

    • Bingöl
      • Bingoel、Bingöl、土耳其(türkiye)、12000
        • 招聘中
        • Bingol University, Faculty of Physical Therapy and Rehabilitation

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Age 18 years or older
  • Neck pain with an intensity greater than 3 on a 10-point Visual Analog Scale
  • Use of electronic devices for at least 4 hours per day during the preceding year
  • Willingness to participate and provision of written informed consent

Exclusion Criteria:

  • Cervical or shoulder surgery within the past 6 months
  • Previously diagnosed cervical pathology, including whiplash-associated disorder, cervical spondylolisthesis, disc herniation, or rheumatoid arthritis
  • Current use of analgesics, opioids, or corticosteroids
  • Skin allergy, open wounds, or skin lesions in the cervical region that preclude kinesiology tape application

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Kinesiology Taping

Participants receive kinesiology tape (5 cm wide, 0.5 mm thick, water-resistant) applied to the posterior cervical region in a seated neutral position. A Y-strip is applied over the cervical extensors from T1-T2 to C1-C2 with approximately 25% tension, and a second strip is applied perpendicularly across C3-C6. The tape is reapplied every 4 days by a trained physiotherapist for a total of 8 applications over 4 weeks. Participants also receive standardized education on posture and self-management.

Elastic therapeutic tape applied to the posterior cervical region (Y-strip over the cervical extensors with approximately 25% tension and a perpendicular strip across C3-C6), reapplied every 4 days for 8 applications over 4 weeks.

有源比较器:Self-SNAG Mobilization

Participants are trained by an experienced physiotherapist to perform towel-assisted self-administered sustained natural apophyseal glide (self-SNAG) mobilization at the C5 level, with mirror-based visual feedback. The end-range rotation position is sustained for 3 seconds, with 10 repetitions per session within a pain-free range, [frequency, e.g., once daily] for 4 weeks. Participants also receive standardized education on posture and self-management.

Towel-assisted self-administered sustained natural apophyseal glide at C5 with mirror-based visual feedback, 10 repetitions per session with 3-second end-range holds, performed over 4 weeks.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in Neck Pain Intensity (Visual Analog Scale)
大体时间:Baseline and week 4 (end of intervention)

Neck pain intensity is assessed using a 10-point Visual Analog Scale (0 = no pain, 10 = worst imaginable pain). Higher scores indicate greater pain.

Baseline and week 4 (end of intervention)

次要结果测量

结果测量
措施说明
大体时间
Change in Neck-Related Disability (Neck Disability Index)
大体时间:Baseline, week 4, and week 8

Self-reported neck-related disability is assessed using the 10-item Neck Disability Index (total score 0-50). Higher scores indicate greater disability.

Baseline, week 4, and week 8
Change in Cervical Joint Position Sense Error
大体时间:Baseline, week 4, and week 8

Cervical joint position sense error is measured in centimeters using a head-mounted laser pointer and a target placed 90 cm from the seated participant, following active cervical flexion, extension, and left and right rotation. The mean deviation across five repetitions per direction is recorded. Higher values indicate poorer proprioceptive accuracy.

Baseline, week 4, and week 8
Change in Upper Trapezius Muscle Activity (Surface Electromyography)
大体时间:Baseline, week 4, and week 8

Bilateral upper trapezius activity is recorded with wireless surface electromyography during isometric shoulder elevation (three 7-second contractions) and expressed as root-mean-square amplitude normalized to maximum voluntary isometric contraction (%MVIC).

Baseline, week 4, and week 8
Bilateral Upper Trapezius EMG Asymmetry Index
大体时间:Baseline, week 4, and week 8

EMG asymmetry is calculated from normalized right- and left-side upper trapezius activity as |Right - Left| / [(Right + Left) / 2] x 100. A value of 0% indicates perfect symmetry; higher values indicate greater bilateral imbalance. Baseline asymmetry will be examined as a predictor of change in pain intensity.

Baseline, week 4, and week 8

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年11月3日

初级完成 (估计的)

2026年11月13日

研究完成 (估计的)

2026年12月15日

研究注册日期

首次提交

2026年10月11日

首先提交符合 QC 标准的

2026年10月11日

首次发布 (实际的)

2026年10月16日

研究记录更新

最后更新发布 (实际的)

2026年11月4日

上次提交的符合 QC 标准的更新

2026年11月2日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

Individual participant data will not be shared publicly. De-identified data may be made available from the principal investigator upon reasonable request.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅