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临床试验/NCT05684809
NCT05684809已完成不适用

Efficacy of Cervical Mobilization With Post Isometric Relaxation in Managing Mechanical Neck Pain Associated With Myofascial Trigger Points: a Randomized Comparative Study

Najran University3 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2022年10月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
33
试验地点
3
主要终点
Pain intensity

研究概览

简要总结

purpose of the study: to determine the effectiveness of cervical mobilization with PIR in reducing pain and improving neck ROM and function in people with mechanical neck pain associated with MTrPs

详细描述

This study will be based on a randomized controlled design which will be comparative in nature. Participants will be recruited using the convenience sampling method and will be randomly divided into two groups A and B respectively. Thirty participants of mechanical neck pain associated with upper Trapezius trigger point pain will be recruited from the Physiotherapy department, at the Najran University, Saudi Arabia. Study objectives and procedure will be properly explained and written informed consent will be obtained at the beginning of the study. All the participants will be randomly assigned into two equal groups A and B.

Group A will be receiving the hot pack, active Stretching, isometric exercise intervention, and PIR technique while group B will receive the hot pack, active Stretching, isometric exercise intervention, and cervical Mobilization.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • age 20-40 years,
  • having mechanical neck pain located in the neck or scapular regions along with 1-2 MTrPs which,
  • on palpation replicated their chief complaints in the upper Trapezius muscle (unilateral).

排除标准

  • known cases of fibromyalgia syndrome,
  • cervical radiculopathy or myelopathy,
  • history of cervical spine surgery,
  • congenital or acquired postural deformity, presence of MTrPs in bilateral upper Trapezius muscles,
  • patients who received any treatment for their pain one month prior to the study.

结局指标

主要结局

Pain intensity

时间窗: 3 Weeks

The pain intensity was assessed Using a numeric pain rating scale (NPRS), Its a 11 point scale, where zero indicates no pain and 10 indicates severe pain

Neck Disability Index

时间窗: 3 Weeks

The Neck Disability was assessed using a neck disability index (NDI) questionnaire, the minimum value 0- and the maximum value is 50

Range of Motion

时间窗: 3 Weeks

The Neck Side Flexion range of motion was assessed using cervical range of motion(CROM) device

Pain Pressure Threshold

时间窗: 3 Weeks

The Pain Pressure Threshold (PPT) was assessed using an algometer algometer

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

Hashim Ahmed

Assistant Professor

Najran University

研究点 (3)

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