NCT07447778

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Feb 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Completed
1 day until next milestone

Study Start

First participant enrolled

February 27, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

March 3, 2026

Completed
24 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 27, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 27, 2026

Completed
Last Updated

March 3, 2026

Status Verified

February 1, 2026

Enrollment Period

28 days

First QC Date

February 26, 2026

Last Update Submit

February 26, 2026

Conditions

Keywords

Neck DisabilityWork Role FunctioningOffice WorkersPerceived StressOccupational HealthWork ProductivityCross-Sectional Study

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

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-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.

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)

Location

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

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

Locations