Predictive and Associated Factors of Musculoskeletal Injuries

January 31, 2023 updated by: Riphah International University

Predictive and Associated Factors of Musculoskeletal Injuries in Office Workers.

The aim of this research is to find out the factors associated with musculoskeletal injuries among office workers and also determine whether Functional Movement Screen (FMS) can predict musculoskeletal injuries or not? Prospective Cohort study will be done at the offices of Rawalpindi. The sample size is 208. Study duration will be of 6 months. Non probability Purposive Sampling will be used. Tools used in the study are FMS, Fat Caliper, Weighing machine & Inches tape. Data will be analyzed through SPSS 23.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Musculoskeletal injuries and conditions represent a major public health problem, with significant social, economic, and health consequences. Office workers are forming a major group for musculoskeletal injuries as they have to work for a longer period of time on computer and sitting on a chair. Musculoskeletal discomfort in office workers is commonly caused by poor ergonomic workstation design, psychosocial, physical and organizational risk factor. There are several MSK disorders associated with computer use in people spending more than 9 hours or more every day using computer.

To combat workplace caused mental and physical exhaustion physical activity has been proven to be an efficient. Physical activity is known not to only treat but prevent the occurrence of a fore coming disease. Being physically active will lead to reduced stress levels and increased productivity. The Functional Movement Screen (FMS) is a physical examination used to measure essential movement patterns in a practical and dynamic way. Functional Movement screen was designed with a purpose of identify body asymmetries, assess mobility and stability within the kinetic chain of whole-body movements and to detect poor quality movement patterns. Other tools like modified Y-balance test have also been used to predict injuries.

Literature review: Previously in a study carried out on firefighters Contreras et al reported that 47% of the participants had an FMS score lower than 14 and they accounted for 72% of the total musculoskeletal injuries.

In another study carried out on Collegiate athletic association Division II athletes the overall prognostic accuracy of the FMS offered a slightly better than 50/50 chance of correctly classifying those most at risk for injury.

A study carried out to find the association between functional fitness scores calculated by FMS and musculoskeletal injury in police officers by Liana Lentz et al suggested that of all the participants, females accounted for 17.9% of the injured subjects.

Previously a study carried out by Michal Pan Tanowitz et al to find factors associated with musculoskeletal injuries in an infantry commanders' course suggested that army operators who sustained a spinal injury have a significantly greater BMI than those who did not, and also increased body fat combined with reduced physical fitness may increase the soldier's risk for injury.

Study Type

Observational

Enrollment (Actual)

208

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Punjab
      • Rawalpindi, Punjab, Pakistan, 46000
        • MTBC

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

25 years to 45 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

office workers spending at least 6 hours per day at work

Description

Inclusion Criteria:

  • • Both Genders.

    • 25-45 years.
    • Office workers

Exclusion Criteria:

  • any neuromusculoskeletal injuries

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Office workers
The office workers will do their routine job tasks and will be observed through injury predictor (functional movement screen) at baseline and after actual injuries happened 6 months
Office Workers which will be observed/exposed with different task and different factors

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Functional Movement Screen
Time Frame: 1 day
The assessment of Functional movement screen is based on qualitative analysis with a four-point ranking system (From 0 to 3). To evaluate movement quality, 3-performs the movement correctly without any compensation, complying with standard movement expectations associated with each test; 2-able to complete the movement but must compensate in some way to perform the fundamental movement; 1-unable to complete the movement pattern or is unable to assume the position to perform the movement; 0-pain anywhere in the body.
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 15, 2022

Primary Completion (Actual)

December 30, 2022

Study Completion (Actual)

January 30, 2023

Study Registration Dates

First Submitted

April 11, 2022

First Submitted That Met QC Criteria

April 15, 2022

First Posted (Actual)

April 18, 2022

Study Record Updates

Last Update Posted (Actual)

February 2, 2023

Last Update Submitted That Met QC Criteria

January 31, 2023

Last Verified

January 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • RiphahIU Atif Zulfiqar

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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