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。

非特异性颈部疼痛个体的离心肌肉训练和本体感觉神经肌肉促进技术的比较

2026年8月11日 更新者:Doç.Dr.Ömer Şevgin、Uskudar University
其目的是比较对非特异性颈部疼痛患者的颈部肌肉进行离心运动训练和本体感觉神经肌肉促进(PNF)技术对疼痛、耐力和功能的影响。

研究概览

详细说明

该研究计划作为一项定量研究。 年龄在18-65岁之间患有非特异性颈部疼痛的志愿者将被纳入研究中,参与者将被随机分为3组。 对照组(n=15)、本体感觉神经肌肉促进技术应用组(n=15)、离心肌肉训练技术应用组(n=15)。 参与研究的人员将被详细解释,并被要求签署一份经伦理委员会批准的自愿同意书。 将首先记录所有三个组中个人的人口统计信息。 所有三组的参与者都将在申请开始和结束时接受评估。 在我们的研究中,参与者使用麦吉尔疼痛问卷进行评估,以评估疼痛的性质和特点,使用深颈屈肌耐力测试(DBFET)评估他们的身体健康状况,使用颈部残疾指数(NEI)评估他们与日常生活活动相关的功能,以及世界卫生组织生活质量简表 (WHOYKA-CF) 的生活质量。 ) 坦帕运动恐惧症量表 (TKÖ) 和用于颈椎关节运动范围测量的测角仪将用于评估运动恐惧症,即对疼痛和再次受伤的恐惧,以及对活动和身体运动的焦虑。 这项研究将计划每周进行五次,持续六周。 对照组将进行伸展和稳定练习,共 3 组,每组 10 次。

研究类型

介入性

注册 (实际的)

45

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。

学习地点

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

  • 成人
  • 年长者

接受健康志愿者

不

描述

纳入标准

  • 年龄在18-65岁之间
  • 颈部疼痛持续至少 7 天的病史
  • 同意参加研究
  • 具有读写土耳其语的能力。 排除标准
  • 颈部神经根病和结构紊乱,
  • 颈部手术,
  • 炎症性疾病,
  • 严重的心理疾病,
  • 颈椎骨和软组织存在感染,
  • 恶性肿瘤,
  • 晚期骨质疏松症,
  • 那些有上肢病变的人,
  • 患有无法接受治疗的神经系统疾病
  • 之前接受过颈椎和脊柱手术
  • 在过去 6 个月内参加了颈部和背部区域的物理治疗计划,
  • 其定义为在过去 24 小时内服用 NSAID(非甾体抗炎药)和阿片类药物等药物。

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:本体感觉
本体感觉神经肌肉促进技术应用
本体感觉神经肌肉促进技术组;除了对参与者和对照组进行练习之外,还将使用等张收缩和动态稳定相结合的促进技术,并使用保持放松技术作为抑制技术。
实验性的:偏心
离心肌训练技术应用
离心肌肉训练技术:除了对照组的练习外,参与者还将接受离心肌肉训练。 使用前,会对颈部进行5分钟的热身运动。 偏心肌肉训练将应用于参与者颈部的肌肉。 离心运动会加强颈部肌肉在各个平面的运动方向,即屈/伸和侧屈。 首先将向患者解释和演示这些动作。
有源比较器:Control
Participants performed a cervical stretching and stabilisation exercise programme only, without any additional technique.
Cervical stretching and stabilisation exercise programme. Stretching was applied in flexion, extension, rotation and lateral flexion (30-second hold, 10 repetitions). Stabilisation exercises were performed with the participant applying self-resistance from a seated position (10-second contraction, 15-second rest). Both components were performed in 3 sets of 10 repetitions with 1-minute rest between sets, in 45-minute sessions, 5 days per week for 6 weeks. This programme was also delivered as the base programme to both experimental groups.

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
Cervical Deep Flexor Muscle Endurance Test
大体时间:Baseline (before the first session) and 6 weeks (immediately after the final session of the intervention period). No further follow-up.
Patients were asked to lie in a supine position with knees flexed at 90° and hands on the abdomen in a hook position. A 0.5 kilogram (kg) weight was placed on the forehead with the help of a band passed over the ears. The patients were asked to first perform cervical retraction and then 10° cervical flexion, and the degree of flexion was determined with the help of a goniometer. The patients were asked to maintain this position and the time was determined with a stopwatch and recorded in seconds. Patients must be able to maintain this position for 60 seconds (sec) in order to have sufficient muscle endurance. Those below this period have insufficient muscle endurance. Cervical flexion for 60 seconds. Patients holding it above were considered to have sufficient endurance and were not included in the study.
Baseline (before the first session) and 6 weeks (immediately after the final session of the intervention period). No further follow-up.
World Health Organization Quality of Life Survey Short Form
大体时间:Baseline (before the first session) and 6 weeks (immediately after the final session of the intervention period). No further follow-up.
The scale measures 28 general health, physical, psychological, social and environmental well-being and consists of 26 questions. Turkey version consists of 27 questions. The 27th question is the national question that determines the Environmental Score. Since each domain expresses the quality of life in its own field independently of each other, domain scores are calculated between 4-20. As the score increases, the quality of life increases.
Baseline (before the first session) and 6 weeks (immediately after the final session of the intervention period). No further follow-up.
Neck Disability Index
大体时间:Baseline (before the first session) and 6 weeks (immediately after the final session of the intervention period). No further follow-up.
Neck Disability Index will be used to evaluate the disability specific to neck pain. The Neck Disability Index has been modified from the Oswestry Disability Index. It consists of 10 sections: pain intensity, personal care, weight bearing, reading, headache, concentration, working, driving, sleep and recreational activities. Each section consists of 6 answers and is scored from 0, no disability, to 5, representing total disability. According to total score; 0-4: no limitation, 5-14: mild limitation, 15-24: moderate limitation, 25-34: severe limitation, 34 and above: completely limited.
Baseline (before the first session) and 6 weeks (immediately after the final session of the intervention period). No further follow-up.
Tampa Kinesiophobia Scale
大体时间:Baseline (before the first session) and 6 weeks (immediately after the final session of the intervention period). No further follow-up.
Tampa Kinesiophobia Scale was used to evaluate kinesiophobia, which is a state of anxiety that develops against activity and physical movement due to fear of pain and re-injury. It was developed to differentiate between non-excessive fear and phobia in patients with chronic musculoskeletal pain. It is frequently used in the literature to evaluate movement-related fear and anxiety. The scale is a 17-item scale that includes parameters of injury, re-injury and fear-avoidance in work-related activities. As the score increases, it is accepted that the kinesiophobia of the individual with pain increases.Results consist of a total raw score (range between 17 and 68) A low score indicates low kinesiophobia.
Baseline (before the first session) and 6 weeks (immediately after the final session of the intervention period). No further follow-up.
Cervical joint goniometric measurements
大体时间:Baseline (before the first session) and 6 weeks (immediately after the final session of the intervention period). No further follow-up.
Goniometric measurements in the neck are methods used to evaluate and record neck joint range of motion. These measurements are important to evaluate the patient's condition during the treatment process, follow the progress and create the treatment plan.
Baseline (before the first session) and 6 weeks (immediately after the final session of the intervention period). No further follow-up.

次要结果测量

结果测量
措施说明
大体时间
McGill Pain Questionnaire (long form)
大体时间:Baseline (before the first session) and 6 weeks (immediately after the final session of the intervention period).
The long-form McGill Pain Questionnaire was used to characterise the multidimensional quality of pain, including pain localisation, the sensory, affective and evaluative word-descriptor dimensions, the number of words chosen, the pain-time relationship, and present pain intensity. Higher scores indicate greater pain.
Baseline (before the first session) and 6 weeks (immediately after the final session of the intervention period).

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。

调查人员

  • 学习椅:Büşra SÖKMEN YILDIRIM、Uskudar University

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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)

2024年5月9日

初级完成 (实际的)

2024年7月30日

研究完成 (实际的)

2025年1月10日

研究注册日期

首次提交

2024年5月6日

首先提交符合 QC 标准的

2024年5月6日

首次发布 (实际的)

2024年5月9日

研究记录更新

最后更新发布 (实际的)

2026年8月14日

上次提交的符合 QC 标准的更新

2026年8月11日

最后验证

2026年8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

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