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临床试验/NCT05207540
NCT05207540已完成不适用

A Reliability and Validity Study of Urdu Version Of Cornell Musculoskeletal Discomfort Questionnaire

Riphah International University1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2021年5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
150
试验地点
1
主要终点
Cornell Musculoskeletal Discomfort Questionnaire

研究概览

简要总结

The study aims to translate and adapt Cornell Musculoskeletal Discomfort Questionnaire cross-culturally into the Urdu language for the Pakistani population for investigating the reliability and validity of Cornell Musculoskeletal Discomfort Questionnaire in the Pakistani population and to study the correlation between Nordic Musculoskeletal Questionnaire and the Visual Analogue Scale.

详细描述

The English version of the Cornell Musculoskeletal Discomfort Questionnaire will be translated into Urdu and culturally adapted, as per a previous recommendation. The Cornell Musculoskeletal Discomfort Questionnaire will be given to one hundred and fifty workers of Masood Textile Mills, who would be chosen based on convenience sampling and inclusion and exclusion criteria. The inter-observer and intra-observer reliability of the Cornell Musculoskeletal Discomfort Questionnaire, Nordic Musculoskeletal Questionnaire, and Visual Analog Scale will be evaluated in this study. On the same day, the questionnaire will be filled out created two times. An Inter - observer assessment will be done with 2 hour break between distributions of questionnaires. The initial observer then will gather a third assessment over one-week period (intra-observer assessment). For data entry and analysis, Statistical Package of Social Sciences Version 24 will be utilized. Internal consistency will be checked using the Cronbach alpha value, and test retest reliability will be assessed using the Intraclass coefficient.

研究设计

研究类型
Observational
观察模型
Ecologic Or Community
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Participants having an age limit of 18 to
  • Could read and understand the Urdu language.
  • Both males and females working more than 6 hours in sitting and standing positions.

排除标准

  • Having any fracture in any part of the body.
  • Having any congenital or acquired disability that restricts them in their daily living.

结局指标

主要结局

Cornell Musculoskeletal Discomfort Questionnaire

时间窗: 1st day

This questionnaire is used to access discomfort caused by Musculoskeletal disorders. It has 3 scales, frequency, severity and interference scale. It has 3 versions on the basis of the nature of work place and activity level i.e. Sedentary workers, standing workers and hand discomfort. Sedentary workers don't include the "foot" domain while the standing worker has this domain. The hand discomfort version is used to access only hand problems. Its interpretation can be done by multiplying all the scale score.

Visual Analogue Scale

时间窗: 1st day

The Visual Analogue Scale was created to represent the concept of a fundamental continuity. A Visual Analogue Scale is typically a straight stripe measuring 100 mm long, with word descriptions for each end. The patient draws a line through the spot on the line which they believe best describes their present state. The Visual Analogue Scale score is calculated by calculating in millimeters as from the line's left side to the point marked by that of the patient. It usually ranges from "0" indicating "no pain" to the "10" indicating "worst pain".

Nordic Musculoskeletal Questionnaire

时间窗: 1st day

The Nordic Questionnaire is an internationally recognized tool for standardization research on Musculoskeletal symptom assessment. Its goal is to use an ergonomically approach to analyze Musculoskeletal problems. The very first component of this instrument includes questions on body parts that correlate to nine anatomical regions. The questions were structured in the following sequence: yearly and weekly prevalence; functional disability; and seeking medical treatment in the last year. This questionnaire can be used in an examination or by the individual who is now being assessed.

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 (1)

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