Actively Recruiting

Age: 18Years - 65Years
All Genders
NCT06874816

Masseter Thickness, Bruxism, and Oral Behaviors in Chronic Neck Pain

Led by Beylikduzu State Hospital · Updated on 2025-03-26

60

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

A total of 30 patients aged 18-65 years who present with chronic non-specific neck pain and 30 healthy volunteers will be included in the study. Patients with symptoms persisting for at least 3 months will be eligible for inclusion. Necessary information will be provided to all participants, and informed consent will be obtained. To assess pain severity before treatment, participants will be asked to rate their complaints using the Visual Analog Scale (VAS), a linear scale for pain assessment. The Neck Disability Index will be used to determine the level of disability. The Jaw Functional Limitation Scale-20 (JFLS-20), Patient Health Questionnaire-9 (PHQ-9), Patient Health Questionnaire-15: Physical Symptoms, Generalized Anxiety Disorder-7 (GAD-7), and the Oral Behaviors Checklist-included in Axis 2 of the DC/TMD form developed for evaluating temporomandibular joint dysfunction-will be used to assess patients' psychosocial characteristics and parafunctional habits. Additionally, masseter muscle thickness will be evaluated using ultrasonographic measurement.

CONDITIONS

Official Title

Masseter Thickness, Bruxism, and Oral Behaviors in Chronic Neck Pain

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with chronic non-specific neck pain
  • Aged between 18-65 years
  • Symptoms persisting for at least 3 months
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Presence of psychiatric or neurological diseases
  • Use of psychiatric medications
  • Cognitive impairment
  • History of neck injection or surgery within the last 6 months
  • Presence of rheumatic diseases
  • Spinal stenosis
  • Cervical disc herniation
  • Advanced degeneration detected in radiological imaging
  • History of fracture or surgery in the temporomandibular joint
  • Presence of inflammatory, rheumatologic diseases, or malignancy affecting the temporomandibular joint

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Beylikdüzü State Hospital

Istanbul, Beylikdüzü, Turkey (Türkiye), 34147

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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