Urdu Version Of Cornell Musculoskeletal Discomfort Questionnaire: Reliability And Validity Study

Musculoskeletal Pain Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05207540
• Other study ID #: REC-FSD-00299
• Status: Completed
• Start date: May 30, 2021
• Est. completion date: February 2, 2022

Study information

• Verified date: March 2022
• Source: Riphah International University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 150
• Est. completion date: February 2, 2022
• Est. primary completion date: January 31, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Participants having an age limit of 18 to 55.
• Could read and understand the Urdu language.
• Both males and females working more than 6 hours in sitting and standing positions.

Exclusion Criteria:

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

Related Conditions & MeSH terms

• Musculoskeletal Pain

Locations

Country	Name	City	State
Pakistan	Ripah International University	Faisalabad	Punjab

Sponsors (1)

Lead Sponsor	Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cornell Musculoskeletal Discomfort Questionnaire	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.	1st day
Primary	Nordic Musculoskeletal Questionnaire	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.	1st day
Primary	Visual Analogue Scale	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".	1st day