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Clinical Trials/NCT06472141
NCT06472141
Completed
Not Applicable

Effectiveness of Cervical Stabilization Exercises in Individuals With Temporomandibular Joint Disorder

Bitlis Eren University1 site in 1 country30 target enrollmentJune 24, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Temporomandibular Joint Disorders
Sponsor
Bitlis Eren University
Enrollment
30
Locations
1
Primary Endpoint
Numeric Pain Rating Scale (NPRS)
Status
Completed
Last Updated
last year

Overview

Brief Summary

It is planned to examine the effect of cervical stabilization exercises on Temporomandibular Joint (TMJ) symptoms in individuals with TMJ disorder.

Detailed Description

Individuals included in the study will be divided into 2 groups, Stabilization and Control groups, by block randomization method. A standard treatment program (Education + home exercises) will be applied to both groups. In addition to the stabilization group, cervical stabilization exercises will be applied. Individuals will be evaluated with the Sociodemographic Data Form before the application. Before and after the application, individuals were assessed for TMJ pain with the Numeric Pain Rating Scale (NPRS), TMJ symptom severity with the Fonseca Anamnestic Index (FAI) and cervical posture, mobility and muscle performance will be evaluated with craniovertebral angle, goniometer and craniocervical flexion test.

Registry
clinicaltrials.gov
Start Date
June 24, 2024
End Date
March 21, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Bitlis Eren University
Responsible Party
Principal Investigator
Principal Investigator

Mesut Arslan

Assistant Professor

Bitlis Eren University

Eligibility Criteria

Inclusion Criteria

  • Having a TMJ disorder according to the TMJ Disorders Research Diagnostic Criteria (RDC/TMD),
  • Being between the ages of 18-65,

Exclusion Criteria

  • Neurological diseases (such as Multiple Sclerosis, Parkinson's disease),
  • Metabolic and systemic diseases (such as Hypothyroidism, Hypercalcemia, Diabetes mellitus, Celiac disease),
  • Rheumatologic diseases (such as Rheumatoid arthritis, Scleroderma),
  • History of head and spine trauma/surgery in the last 6 months,
  • History of malignancy and pregnant women will be excluded.

Outcomes

Primary Outcomes

Numeric Pain Rating Scale (NPRS)

Time Frame: Change from baseline at 8 weeks

TMJ pain will be evaluated at rest with the NPRS scale. It is a scale scored between 0-10 points and '0 points means 'I have no pain' and '10 points means 'I have unbearable pain'. NRS score between 1-3 points indicates mild pain, between 4-6 points indicates moderate pain and between 7-10 points indicates severe pain.

Fonseca Anamnestic Index (FAI)

Time Frame: Change from baseline at 8 weeks

It assesses TMJ disorder and its severity. The index includes three options: "yes" (10 points), "sometimes" (5 points) and "no" (0 points). A total score of 0-15 is considered as no TMJ disorder, 20-40 as mild, 45-65 as moderate, and 70-100 as severe.

Cervical Posture

Time Frame: Change from baseline at 8 weeks

Cervical posture will be evaluated from the craniovertebral angle.

Cervical Mobility

Time Frame: Change from baseline at 8 weeks

For cervical mobility, normal joint movements of the neck will be evaluated with a goniometer.

Cervical Muscle Performance

Time Frame: Change from baseline at 8 weeks

Cervical muscle performance will be evaluated with the craniocervical flexion test.

Study Sites (1)

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