NECK DISABILITY AND WORK ROLE FUNCTIONING IN OFFICE WORKERS (ND-WRF)

February 26, 2026 updated by: Gizem Soylu, Hacettepe University

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

Not yet recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

50

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

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.

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Neck Disability (NDI Score)
Time Frame: Baseline (single assessment)
Neck-related disability will be assessed using the Neck Disability Index (NDI). Higher scores indicate greater disability.
Baseline (single assessment)
Work Role Functioning
Time Frame: baseline
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)
Time Frame: Baseline (single assessment)
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)
Time Frame: Baseline (single assessment)
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)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

February 27, 2026

Primary Completion (Estimated)

March 27, 2026

Study Completion (Estimated)

March 27, 2026

Study Registration Dates

First Submitted

February 26, 2026

First Submitted That Met QC Criteria

February 26, 2026

First Posted (Actual)

March 3, 2026

Study Record Updates

Last Update Posted (Actual)

March 3, 2026

Last Update Submitted That Met QC Criteria

February 26, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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