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
1 other identifier
observational
50
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Feb 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 26, 2026
CompletedStudy Start
First participant enrolled
February 27, 2026
CompletedFirst Posted
Study publicly available on registry
March 3, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 27, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 27, 2026
CompletedMarch 3, 2026
February 1, 2026
28 days
February 26, 2026
February 26, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Neck Disability (NDI Score)
Neck-related disability will be assessed using the Neck Disability Index (NDI). Higher scores indicate greater disability.
Baseline (single assessment)
Work Role Functioning
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.
baseline
Perceived Stress (PSS Total Score)
Perceived stress will be assessed using the Perceived Stress Scale (PSS). Higher scores indicate higher perceived stress.
Baseline (single assessment)
Health Status (NHP Section I Total Score)
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.
Baseline (single assessment)
Study Arms (1)
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.
Eligibility Criteria
The study population consists of full-time desk-based office workers aged between 18 and 65 years. Participants are required to have sufficient proficiency in Turkish to understand and complete the study questionnaires and must voluntarily agree to participate by providing written informed consent. Individuals with neurological, orthopedic, or systemic conditions causing functional impairment, history of spinal surgery, malignant disease, acute infection, pregnancy, or illiteracy will be excluded.
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hacettepe University
Ankara, Select, 06000, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Asisstant
Study Record Dates
First Submitted
February 26, 2026
First Posted
March 3, 2026
Study Start
February 27, 2026
Primary Completion
March 27, 2026
Study Completion
March 27, 2026
Last Updated
March 3, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share