Respiratory and Physical Outcomes in Different Types of Office Workers

May 16, 2025 updated by: Gulsah Bargi, Izmir Democracy University

Investigation of Respiratory System, Musculoskeletal System, Physical Activity Level and Quality of Life in Different Types of Office Workers.

There are no studies in the literature reporting the posture, chest mobility, dyspnea, flexibility, quality of life and physical activity levels of emergency call center employees. The aims of this observational study are; 1) to evaluate posture, chest mobility, strength, dyspnea, flexibility, musculoskeletal disorders, physical activity and quality of life in emergency call center workers and office workers, 2) to reveal the relationships between these parameters of both research groups and 3) The aim is to compare these measurement parameters in emergency call center workers and office workers.

Study Overview

Status

Active, not recruiting

Detailed Description

Over time, there has been an increase in the number of office workers and the use of computers. Working in a static position for long working hours and improper working postures can lead to loss of flexibility in the muscles, decrease in thoracic mobility, pain in the musculoskeletal system and deterioration of ideal posture. Emergency call center employees work long hours, in shifts that require serious attention, where stress is intense and the circadian rhythm is disrupted. There is no study in the literature that evaluates the posture, chest mobility, dyspnea, flexibility and physical activity levels of emergency call center employees. Therefore, the aim of our study is; It is a comparative evaluation of posture, chest mobility, cough strength, dyspnea flexibility, musculoskeletal disorders, physical activity level and quality of life in emergency call center operators and desk workers.

Study Type

Observational

Enrollment (Actual)

52

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

      • İzmir, Turkey, 35140
        • Izmir Democracy University

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

At least 27 individuals will be included in the emergency call center workers group and at least 25 individuals will be included in the office workers group.

Description

Inclusion Criteria for Emergency Call Center Workers

  • Being an operator at Izmir 112 Emergency Call Center
  • Being 18 years or older
  • Volunteering to participate in the study
  • Being able to understand and answer surveys

Inclusion Criteria for Office Workers

  • Being actively working at a desk
  • Being 18 years or older
  • Volunteering to participate in the study
  • Being able to understand and answer surveys

Exclusion Criteria:

  • Have any history of acute/chronic infection, physical or mental disability/disease and/or cognitive impairment that would prevent measurement.
  • Being pregnant
  • Being able to exercise regularly

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
Emergency call center workers
This group will consist of individuals working as operators at Izmir 112 Emergency Call Center.
Participants will be evaluated on posture, chest mobility, cough strength, flexibility, hand grip strength and pinch strength. They will be asked to answer the Modified Medical Research Council Scale, Cornell Musculoskeletal Disorders Questionnaire, International Physical Activity Questionnaire Short Form and Short Form -36. The data to be obtained from all these evaluations are planned to be collected face to face from the participants at once and within a maximum of 1 hour.
Office workers
This group will consist of office workers who work actively at a desk.
Participants will be evaluated on posture, chest mobility, cough strength, flexibility, hand grip strength and pinch strength. They will be asked to answer the Modified Medical Research Council Scale, Cornell Musculoskeletal Disorders Questionnaire, International Physical Activity Questionnaire Short Form and Short Form -36. The data to be obtained from all these evaluations are planned to be collected face to face from the participants at once and within a maximum of 1 hour.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Handgrip strength
Time Frame: up to 5 minutes
Hand grip strength will be measured using the Jamar hand dynamometer.
up to 5 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Thoracic mobility
Time Frame: up to 5 minutes
Individuals will be asked to sit in an upright sitting position with their arms slightly open, and their chest circumference will be measured with a tape measure at three different levels (axillary, epigastric, subcostal) at rest, deep breathing (maximum inspiration) and deep exhalation (maximum expiration). The difference between measurements will be recorded in centimeters.
up to 5 minutes
Cough strength
Time Frame: up to 2-3 minutes
Cough strength will be evaluated using a PEFmeter.
up to 2-3 minutes
Dyspnea
Time Frame: up to 1 minute
Dyspnea will be assessed using the Modified Medical Research Council (MMRC) Scale. This scale is a five-item scale based on various physical activities that cause a feeling of shortness of breath (dyspnea). As the score an individual gets from the scale increases, the perception of shortness of breath also increases.
up to 1 minute
Posture
Time Frame: up to 5 minutes
Posture will be evaluated with sensorless posture analysis software based on the artificial intelligence concept created by Fizyosoft and Becure.
up to 5 minutes
Musculoskeletal pain
Time Frame: up to 5 minutes
Musculoskeletal pain will be assessed using the Turkish version of the Cornell Musculoskeletal Disorders Questionnaire. The score is obtained by multiplying the weighted scores corresponding to the individual's answer. The scores obtained for each region range between 0 and 90, and higher scores indicate higher levels of pain disorder.
up to 5 minutes
Flexibility
Time Frame: up to 5 minutes
Flexibility will be evaluated with sit-reach test, pectoral shortness tests, and shoulder adductor and internal rotator shortness tests.
up to 5 minutes
Pinch strength
Time Frame: up to 5 minutes
Pinch strength will be evaluated using a hydraulic pinch dynamometer.
up to 5 minutes
Physical activity level
Time Frame: up to 2 minutes
Physical activity level will be assessed using the Turkish version of the International Physical Activity Questionnaire Short Form."MET-min/week" scores were obtained by multiplying the minutes, days, and MET (which is set by convention at 3.5 milliliter of oxygen per kilogram per minute) values of each activity. According to these scores, individuals were classified as inactive, minimally active, and sufficiently active.
up to 2 minutes
Health-related quality of life
Time Frame: up to 5 minutes
Quality of life will be assessed using the SF-36. It consists of eight subscales including physical function, role limitations due to physical health and emotional problems, vitality, emotional well-being, social function, bodily pain, and general health. Each subscale is scored between 0 (poorer health) and 100 (better health).
up to 5 minutes

Collaborators and Investigators

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

Investigators

  • Study Director: GÜLŞAH BARĞI, Assoc.Dr., Izmir Democracy University
  • Principal Investigator: BERFİN KİŞİN, MSc, Izmir Emergency Call Center
  • Principal Investigator: ÖZLEM ÇİNAR ÖZDEMİR, Assoc.Dr., Izmir Democracy University

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)

February 28, 2024

Primary Completion (Estimated)

April 15, 2026

Study Completion (Estimated)

December 15, 2026

Study Registration Dates

First Submitted

December 29, 2023

First Submitted That Met QC Criteria

January 10, 2024

First Posted (Actual)

January 22, 2024

Study Record Updates

Last Update Posted (Actual)

May 18, 2025

Last Update Submitted That Met QC Criteria

May 16, 2025

Last Verified

May 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • Different Office Workers

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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