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Not yet recruitingNCT07447778ND-WRFUpdated Mar 3, 2026

NECK DISABILITY AND WORK ROLE FUNCTIONING IN OFFICE WORKERS

An observational study in Neck Pain, sponsored by Hacettepe University. Not yet recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-03-03.

Sponsored by Hacettepe University · Observational

From the registry’s dates

  • Primary completion was expected by Mar 2026, 6 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
50
Ages
18 Years to 65 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Neck Pain

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Keywords

  • Neck Disability
  • Work Role Functioning
  • Office Workers
  • Perceived Stress
  • Occupational Health
  • Work Productivity
  • Cross-Sectional Study
03

In context

Neck Pain

1,232 studies on the registry are indexed under Neck Pain; 255 are open to participants now.

This study's planned enrollment of 50 is below the median of 90 across 213 observational studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

Hacettepe University is the lead sponsor of 983 studies on the registry; 212 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

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.

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

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

05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
50 participants (estimated)
Patient registry
No

Groups and cohorts

  • 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.

06

What researchers measure

Primary outcomes

  1. Neck Disability (NDI Score)

    Neck-related disability will be assessed using the Neck Disability Index (NDI). Higher scores indicate greater disability.

    Time frame: Baseline (single assessment)

  2. 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.

    Time frame: baseline

  3. Perceived Stress (PSS Total Score)

    Perceived stress will be assessed using the Perceived Stress Scale (PSS). Higher scores indicate higher perceived stress.

    Time frame: Baseline (single assessment)

  4. 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.

    Time frame: Baseline (single assessment)

07

Study locations

1 site
  • Hacettepe University
    Ankara, Select 06000, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07447778
Lead sponsor
Hacettepe University
Responsible party
Gizem Soylu (Research Asisstant, Hacettepe University) — Principal investigator
First posted
Mar 3, 2026
Start date
Feb 27, 2026 (estimated)
Primary completion
Mar 27, 2026 (estimated)
Completion
Mar 27, 2026 (estimated)
Last update
Mar 3, 2026

Study contacts

Gizem Soylu
Contact
fztgizemsoylu@gmail.com
+905380844943

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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