Evaluate the Working Environments of Individuals Working From Home During Covid-19 Outbreak

February 16, 2022 updated by: Gamze Polen Akşimşek, Istanbul University-Cerrahpasa
The study aims to evaluate the working environments of individuals working from home during the covid-19 outbreak and the effect of the working environments on their musculoskeletal system.

Study Overview

Status

Completed

Detailed Description

The study will include people between the ages of 18-65 who work from home (works in the office before isolation) as a part of the Covid-19 isolation measure. The working environment of the individuals participating in the study will be evaluated with The Rapid Office Strain Assessment (ROSA). Musculoskeletal symptoms will be analyzed by using the Standardised Nordic Questionnaires (NMQ). Pain will be analyzed by using the Visual Analogue Scale (VAS) .

Study Type

Observational

Enrollment (Actual)

259

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

      • Istanbul, Turkey
        • Istanbul University Cerrahpasa

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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

The study will include people between the ages of 18-65 who works from home (works in the office before isolation) as a part of Covid-19 isolation measure

Description

Inclusion Criteria:

  • between the ages of 18-65
  • works from home
  • works in the office before isolation

Exclusion Criteria:

  • have any systemic disease that may affect on musculoskeletal system such as fibromyalgia, myofacial pain syndrome, etc.
  • have any vision problem
  • have difficulty of understanding and following online survey
  • have any physical disability
  • have self-reported computer use for less than four hours on a typical workday

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

  • Observational Models: Case-Only
  • Time Perspectives: Cross-Sectional

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Rapid Office Strain Assessment (ROSA)
Time Frame: 30 minutes
The working environment of the individuals participating in the study will be evaluated with The Rapid Office Strain Assessment (ROSA). ROSA is a picture-based posture checklist designed to quantify exposure to risk factors in an office work environment. In ROSA, three subsections (A-chair height, depth, armrest, and backrest; B-monitor and telephone; C-mouse and keyboard) of the office work environment are assessed. After completing the ROSA checklist, the related tables are used to calculate the score from each part, and eventually, the final ROSA score is derived. If the final score is ≤4; the risk of musculoskeletal disorders is low (low risky). If the final score is ≥5 the risk of musculoskeletal disorders risk is high (high risky).
30 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Standardised Nordic Questionnaries (NMQ)
Time Frame: 15 minutes
The NMQ includes 27 items exploring the presence of musculoskeletal symptoms for the last 12 months covering nine different parts of the body. It also has items about severity grades, determined according to functional status and the presence of musculoskeletal symptoms during the 7 days. Symptoms indicate musculoskeletal disorders in different body regions among the working population. The NMQ section that questions the last 7 days will be used in the study. In that section consists additional questions relating to the neck, the shoulders, and the lower back further detail relevant issues. Twenty-five forced-choice questions elicit any accidents affecting each area, functional impact at home and work (change of job or duties), duration of the problem, assessment by a health professional, and musculoskeletal problems in the last 7 days.
15 minutes

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Visual Analog Scale (VAS)
Time Frame: 2 minutes
Pain will be analyzed by using the Visual Analogue Scale (VAS). VAS is a scale assessing pain intensity and composed of a horizontal or vertical line and anchored at both ends by words indicative of extremes of magnitude, such as "no pain" to "most intense pain sensation imaginable". In the current study, at the last 1 year and last 7 days, pain intensity was assessed by using horizontal lined VAS. Higher values show higher pain.
2 minutes

Collaborators and Investigators

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

Investigators

  • Study Director: Ayşe Zengin Alpözgen, PhD, Istanbul University-Cerrahpasa

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.

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)

May 29, 2020

Primary Completion (Actual)

July 1, 2020

Study Completion (Actual)

August 1, 2020

Study Registration Dates

First Submitted

April 7, 2020

First Submitted That Met QC Criteria

April 9, 2020

First Posted (Actual)

April 10, 2020

Study Record Updates

Last Update Posted (Actual)

March 4, 2022

Last Update Submitted That Met QC Criteria

February 16, 2022

Last Verified

February 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • GPA1347

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

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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