- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07447778
NECK DISABILITY AND WORK ROLE FUNCTIONING IN OFFICE WORKERS (ND-WRF)
NECK-RELATED DISABILITY AS A PREDICTOR OF WORK ROLE FUNCTIONING IN A NON-CLINICAL SAMPLE OF OFFICE WORKERS
This observational cross-sectional study aims to investigate whether neck-related disability predicts work role functioning in a non-clinical sample of office workers.
Office workers frequently experience neck discomfort and functional limitations due to prolonged sitting and computer use. However, the extent to which neck-related disability influences their ability to meet work role demands remains unclear.
Participants will complete validated questionnaires assessing neck disability, perceived stress, general health status, and work role functioning. Demographic information will also be collected. No intervention will be applied.
The findings of this study may help clarify the relationship between neck-related disability and occupational functioning and contribute to the development of preventive strategies in office-based work environments.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Gizem Soylu
- Phone Number: +905380844943
- Email: fztgizemsoylu@gmail.com
Study Locations
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Select
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Ankara, Select, Turkey (Türkiye), 06000
- Hacettepe University
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Contact:
- Gizem SOYLU
- Phone Number: 90538084494
- Email: fztgizemsoylu@gmail.com
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
Full-time office workers performing predominantly desk-based work Individuals aged between 18 and 65 years Individuals who voluntarily agree to participate in the study and sign the informed consent form Individuals with sufficient proficiency in the Turkish language to understand and complete the questionnaires
Exclusion Criteria:
Illiterate individuals
Pregnant individuals
Individuals with acute infection
Individuals with malignant disease
Individuals who have undergone spinal surgery
Individuals with functional impairment due to neurological, orthopedic, or systemic disease
Individuals who decline participation in the study
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Office Workers
This cohort includes non-clinical office workers aged 18 years and older who voluntarily participate in the study.
Participants will complete questionnaires assessing neck-related disability, perceived stress, health status, and work role functioning.
No intervention will be applied.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Neck Disability (NDI Score)
Time Frame: Baseline (single assessment)
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Neck-related disability will be assessed using the Neck Disability Index (NDI).
Higher scores indicate greater disability.
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Baseline (single assessment)
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Work Role Functioning
Time Frame: baseline
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Work role functioning will be assessed using the Work Role Functioning Questionnaire (WRFQ), a validated self-report instrument that evaluates the degree to which health problems interfere with meeting work demands.
The questionnaire provides a total score reflecting overall work role functioning, with higher scores indicating better functioning.
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baseline
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Perceived Stress (PSS Total Score)
Time Frame: Baseline (single assessment)
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Perceived stress will be assessed using the Perceived Stress Scale (PSS).
Higher scores indicate higher perceived stress.
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Baseline (single assessment)
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Health Status (NHP Section I Total Score)
Time Frame: Baseline (single assessment)
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Health status will be assessed using the Nottingham Health Profile (NHP).
Section I total score reflects perceived health problems across multiple domains; higher scores indicate worse perceived health status.
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Baseline (single assessment)
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FTREK24/112
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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