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Work-related IllnessNCT06216431

Respiratory and Physical Outcomes in Different Types of Office Workers

An observational study of Work-related Illness, run by Izmir Democracy University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Work-related Illness
What is being tested?
Physical Evaluations of individuals
How many people
52 participants
Where
1 siteTurkey (Türkiye)
Study dates
28 Feb 2024to 3 Nov 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Adult, Older adult

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.

Who may be able to join

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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Izmir Democracy University

    Izmir, 35140

Other trials in Turkey (Türkiye)

About this study

Official title: 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.

Read the 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.

Being tested
Physical Evaluations of individuals
Keywords
office workers, call center operators, musculoskeletal discomfort, dyspnea, posture, thoracic mobility
Medical subject headings
Dyspnea

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Physical Evaluations of individualsOther

    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.

Study groups in NCT06216431
Study groupRoleWhat they receive
Emergency call center workersThis group will consist of individuals working as operators at Izmir 112 Emergency Call Center.
Receives: Other: Physical Evaluations of individuals
Office workersThis group will consist of office workers who work actively at a desk.
Receives: Other: Physical Evaluations of individuals

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Handgrip strength

    Hand grip strength will be measured using the Jamar hand dynamometer.

    Measured: up to 5 minutes

Secondary outcomes (9)
  1. Thoracic mobility

    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.

    Measured: up to 5 minutes

  2. Cough strength

    Cough strength will be evaluated using a PEFmeter.

    Measured: up to 2-3 minutes

  3. Dyspnea

    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.

    Measured: up to 1 minute

  4. Posture

    Posture will be evaluated with sensorless posture analysis software based on the artificial intelligence concept created by Fizyosoft and Becure.

    Measured: up to 5 minutes

  5. Musculoskeletal pain

    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.

    Measured: up to 5 minutes

  6. Flexibility

    Flexibility will be evaluated with sit-reach test, pectoral shortness tests, and shoulder adductor and internal rotator shortness tests.

    Measured: up to 5 minutes

  7. Pinch strength

    Pinch strength will be evaluated using a hydraulic pinch dynamometer.

    Measured: up to 5 minutes

  8. Physical activity level

    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.

    Measured: up to 2 minutes

  9. Health-related quality of life

    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).

    Measured: up to 5 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jan 2024
  2. Study start28 Feb 2024
  3. Primary completion3 Nov 2026
  4. Study completion3 Nov 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
52 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06216431
Sponsor's protocol ID
Different Office Workers
Status last verified
Nov 2026
First submitted
29 Dec 2023
Last updated
5 Nov 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Clemes SA, O'Connell SE, Edwardson CL. Office workers' objectively measured sedentary behavior and physical activity during and outside working hours. J Occup Environ Med. 2014 Mar;56(3):298-303. doi: 10.1097/JOM.0000000000000101.

    PubMed 24603203
  • Heneghan NR, Baker G, Thomas K, Falla D, Rushton A. What is the effect of prolonged sitting and physical activity on thoracic spine mobility? An observational study of young adults in a UK university setting. BMJ Open. 2018 May 5;8(5):e019371. doi: 10.1136/bmjopen-2017-019371.

    PubMed 29730619
  • Janwantanakul P, Pensri P, Jiamjarasrangsri V, Sinsongsook T. Prevalence of self-reported musculoskeletal symptoms among office workers. Occup Med (Lond). 2008 Sep;58(6):436-8. doi: 10.1093/occmed/kqn072. Epub 2008 Jun 10.

    PubMed 18544589
  • Rostamzadeh S, Saremi M, Fereshteh T. Maximum handgrip strength as a function of type of work and hand-forearm dimensions. Work. 2020;65(3):679-687. doi: 10.3233/WOR-203100.

    PubMed 32116266

Questions about this trial

What is this clinical trial studying?

An observational study of Work-related Illness, run by Izmir Democracy University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Handgrip strength (time frame: up to 5 minutes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06216431, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Nov 2026.

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