Evaluation of the Relationship Between Neck Pain and Temporomandibular Disorders in Office Workers

November 9, 2021 updated by: Tugba Sahbaz
The current study aimed to explore the associations between neck pain and temporomandibular disorders in office workers

Study Overview

Status

Completed

Detailed Description

This is a cross-sectional study. All participants will provide informed consent before participating in the study. The study will be conducted in accordance with the Helsinki Declaration criteria. Data will be collected using questionnaires, which include information on demographic, clinical conditions.

Study Type

Observational

Enrollment (Actual)

500

Contacts and Locations

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

Study Locations

    • Kucukcekmece
      • Istanbul, Kucukcekmece, Turkey
        • University of Health Sciences, Kanuni Sultan Süleyman Training and Research Hospital,

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

18 years to 55 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

aged between 18 and 55, working on computer, having neck pain at least three months with or without temporomandibular pain

Description

Inclusion Criteria:

  • Aged between 18 and 55,
  • Working on computer,
  • Having neck pain at least three months.

Exclusion Criteria:

  • Reporting pregnancy,
  • Having a history of accidents,
  • Trauma or surgery in the neck region and temporomandibular region,
  • Congenital anomaly of the spine or temporomandibular joint,
  • Rheumatologic disease,
  • Osteoporosis,
  • Spondylosis,
  • Spondylolisthesis,
  • Infection of the spine or temporomandibular joint
  • Cervical disc herniation,
  • Tumor

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
Neck pain
Diagnostic Test: A self-administered questionnaire A self-administered questionnaire will be used to screen VAS scores, bournemouth neck questionnaire, demographic information and for temporomandibular pain Diagnostic Criteria for Temporomandibular Disorders: Assessment Instruments Axis I TMD Pain Screener, Symptom questionnaire and Axis II PHQ-4, Oral Behaviors Checklist .
Neck pain with temeporomandibular pain
Diagnostic Test: A self-administered questionnaire A self-administered questionnaire will be used to screen VAS scores, bournemouth neck questionnaire, demographic information and for temporomandibular pain Diagnostic Criteria for Temporomandibular Disorders: Assessment Instruments Axis I TMD Pain Screener, Symptom questionnaire, Clinical Examination Form, Axis II Pain Drawing Graded Chronic Pain (version 2), JFLS-8 ,PHQ-4 Oral Behaviors Checklist.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Neck Bournemouth Questionnaire
Time Frame: 1 interview day
The NBQ consists of 7 questions that examine the pain intensity, daily life activities, social activities, anxiety, emotional aspects of depression, kinesiophobia, and the ability to control pain. The items in the questionnaire are specific to patients with neck pain and each question evaluates a different parameter.The score for each measure are added. This can produce a value between a minimum score of 0, and a maximum score of 70. The higher the score reflects the degree of impact on a patient's life.
1 interview day
Diagnostic Criteria for Temporomandibular Disorders: Assessment Instruments
Time Frame: 1 interview day
Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) is a dual-axis framework for the assessment and diagnosis of Axis I physical diagnoses for the most common TMDs and Axis II self-report psychosocial and behavioral screening questionnaires.
1 interview day

Collaborators and Investigators

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

Sponsor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 (Actual)

May 20, 2021

Primary Completion (Actual)

June 20, 2021

Study Completion (Actual)

July 20, 2021

Study Registration Dates

First Submitted

May 20, 2021

First Submitted That Met QC Criteria

May 20, 2021

First Posted (Actual)

May 25, 2021

Study Record Updates

Last Update Posted (Actual)

November 10, 2021

Last Update Submitted That Met QC Criteria

November 9, 2021

Last Verified

November 1, 2021

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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