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临床试验/NCT05856006
NCT05856006已完成不适用

Effects of Upper Trapezius Stretching With and Without Mid Lower Trapezius Strenghthening Exercises on Pain, Disability and Quality of Life in Female Desk Workers With Trapezius Myalgia

Riphah International University2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
2
主要终点
SF-36 for Quality of life

研究概览

简要总结

A Randomized controlled trial will be conducted. Non-probability convnience sampling will be used to collect the data. Sample size of 42 subjects with age group between 18 to 40 years will be taken. Data will be collected by using tools Numeric Pain Rate Scale (NPRS) for pain, Neck Disability Index (NDI) for disability and SF-36 for Quality of life. An informed consent will be taken. A total of 20 subjects will be selected by following inclusion and exclusion criteria and will equally divided in to two groups by random number generator table. Both groups will come thrice per week for a total of 4 weeks.

详细描述

Trapezius myalgiais the complaint of pain, stiffness, and tightness of the upper trapezius muscle. It is characterised by acute or persistent neck-shoulder pain. In today's society, due to the increased use of computers, where the neck and shoulders are maintained in static abnormal postures to look at the computer screens and become vulnerable to cause neck pain. The aim of the study is to determine effects of upper trapezius stretching with and without mid lower trapezius strengthening exercises on pain, disability and quality of life in females with work related trapezius myalgia.

A Randomized controlled trial will be conducted in physiotherapy outpatient department of Bahria International Hospital Lahore. Non-probability convnience sampling will be used to collect the data. Sample size of 42 subjects with age group between 18 to 40 years will be taken. Data will be collected by using tools Numeric Pain Rate Scale (NPRS) for pain, Neck Disability Index (NDI) for disability and SF-36 for Quality of life. An informed consent will be taken. A total of 20 subjects will be selected by following inclusion and exclusion criteria and will equally divided in to two groups by random number generator table. Both groups will come thrice per week for a total of 4 weeks. The data will be analysed using SPSS software version 25. After assessing normality of data by Shapiro-Wilk test, it will be decided either parametric or non-parametric test will be used within a group or between two groups.

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 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • • Females between the age range of 18-40 years
  • Examination-Symptoms provoked by neck movement and palpation of Trapezius musculature.
  • Positive Trapezius Strength Test

排除标准

  • Participants who present with dizziness and vertigo
  • Infection or febrile state at the time of performing the test;
  • Anxiety or extreme emotional tension;
  • pharmacological treatment (analgesics, muscle relaxants, anxiolytics, antidepressants)
  • Disc lesions

研究组 & 干预措施

Stretching Group

Active Comparator

upper trapezius stretching plus neck isometrics

干预措施: upper trapezius stretching plus neck isometrics (Other)

Stretching plus strengthening Group

Experimental

upper trapezius stretching with mid-lower trapezius strengthening exercises plus neck isometrics

干预措施: upper trapezius stretching with mid-lower trapezius strengthening exercises plus neck isometrics (Other)

结局指标

主要结局

SF-36 for Quality of life

时间窗: up to 4 weeks

The SF-36 is a 36-item scale constructed to survey health status and quality. The SF-36 assesses eight health concepts: limitations in Quality of lifephysical activities because of health problems; limitations in social activities because of physical or emotional problems; limitations in usual role activities because of physical health problems); bodily pain; general mental health (psychological distress and well-being); limitations in usual role activities because of emotional problems; vitality (energy and fatigue); and general health perceptions. The standard form of the instruments asks for participants to reply to questions according to how they have felt over the previous week. The items use Likert-type scales, some with 5 or 6 points and others with 2 or 3 pointsmotions

Numeric Pain Rate Scale (NPRS)

时间窗: up to 4 weeks

Patient level of pain will be assessed using this scale. This scale ranges from 0to10."0"indicates "no pain" and "10" indicates "worst pain".

Neck Disability Index

时间窗: up to 4 weeks

NDI is a 10-item questionnaire that measures a patient's self-reported neck pain related disability

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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