Ergonomic Considerations on Musculoskeletal Disorders and Posture in Software Developers.

December 9, 2022 updated by: Riphah International University

Effects of Ergonomic Considerations on Musculoskeletal Disorders and Posture in Software Developers.

The human and computer interface is becoming increasingly intuitive, but for the inexperienced user still poses formidable problems. Musculoskeletal symptoms of VDU users are believed to have a multifactorial aetiology. Software developers don't have knowledge of ergonomic principles. Faulty postures had an effect on posture.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Data will be collected from software developer companies in Lahore at questionnaire include demographic data and data collection tools. The software developer will be guided about basic ergonomic principles and data will be collected at the start of the study and in 2 stages with a 2-week interval. A quasi-experiment study will be used. The sample size will be323 (margin of error 5%, confidence level 95%, population size 2000, and dist. 50%) by Rao software. A convenient sampling technique will be used. Data will be analyzed using SPSS 21 by comparing mean and correlating variables

Study Type

Interventional

Enrollment (Actual)

323

Phase

  • Not Applicable

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
      • Lahore, Punjab, Pakistan, 54700
        • I leads Software house

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 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Software engineers who have experience of more than 2 years, in the same company.
  • Software engineers with the age less than 40 years and both gender.

Exclusion Criteria:

  • Software engineers who had a past history of spine surgery or diseases in the Spine like disc prolapse, discitis, arthritis etc.
  • Orthopedically physically challenged
  • Pregnant women.

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

  • Primary Purpose: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Ergonomic Principals
Ergonomic Principal for computer users will be used.
Ergonomic principles for posture correction in office for computer users.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Rapid Entire Body Assessment (REBA)
Time Frame: Change from Baseline Rapid Entire Body Assessment at 3 week
The Rapid Entire Body Assessment (REBA) was developed to "rapidly" evaluate risk of musculoskeletal disorders (MSD) associated with certain job tasks. Change from Baseline Rapid Entire Body Assessment at 3 week
Change from Baseline Rapid Entire Body Assessment at 3 week
The Nordic Musculoskeletal Questionnaire (NMQ)
Time Frame: Change from Baseline for musculoskeletal disorders Assessment at 3 week.
The NMQ can be used as a questionnaire or as a structured interview for musculoskeletal disorders. Change from Baseline for musculoskeletal disorders Assessment at 3 week.
Change from Baseline for musculoskeletal disorders Assessment at 3 week.
Computer Workstations Tool
Time Frame: Change from Baseline Computer Workstations Assessment at 3 week.
provided by Occupational Safety and Health Administration. Change from Baseline Computer Workstations Assessment at 3 week.
Change from Baseline Computer Workstations Assessment at 3 week.

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

November 10, 2021

Primary Completion (Actual)

February 10, 2022

Study Completion (Actual)

March 10, 2022

Study Registration Dates

First Submitted

December 1, 2021

First Submitted That Met QC Criteria

December 29, 2021

First Posted (Actual)

December 30, 2021

Study Record Updates

Last Update Posted (Estimate)

December 12, 2022

Last Update Submitted That Met QC Criteria

December 9, 2022

Last Verified

December 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/Lhr/20/1041/Hafiz Muhammad

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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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