- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05173766
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
Conditions
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.
Sponsor
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
- Cassidy, S. and P. Eachus, Developing the computer user self-efficacy (CUSE) scale: Investigating the relationship between computer self-efficacy, gender and experience with computers. Journal of educational computing research, 2002. 26(2): p. 133-153.
- Punnett L, Wegman DH. Work-related musculoskeletal disorders: the epidemiologic evidence and the debate. J Electromyogr Kinesiol. 2004 Feb;14(1):13-23. Review.
- Wahlstrom J. Ergonomics, musculoskeletal disorders and computer work. Occup Med (Lond). 2005 May;55(3):168-76. doi: 10.1093/occmed/kqi083.
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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