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Active, not recruiting Observational

Respiratory and Physical Outcomes in Different Types of Office Workers

NCT06216431 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2024-02-28
Last updated
2025-05-18

Condition(s) studied

Work-related Illness

Investigational drug(s) / intervention(s)

Physical Evaluations of individuals

Physical Evaluations of individuals: 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 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. 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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

  • Handgrip strength — up to 5 minutes
    Hand grip strength will be measured using the Jamar hand dynamometer.

Trial sites (1)

FacilityCityRegionStatus
Izmir Democracy University Izmir Turkey (Türkiye)
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06216431 on ClinicalTrials.gov ↗ ← All trials in Turkey