Skip to content

Effectiveness of Cervical Stabilization Exercises in Individuals With Temporomandibular Joint Disorder

Effectiveness of Cervical Stabilization Exercises in Individuals With Temporomandibular Joint Disorder

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06472141
Enrollment
30
Registered
2024-06-24
Start date
2024-06-24
Completion date
2025-03-21
Last updated
2025-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Temporomandibular Joint Disorders

Keywords

Temporomandibular Joint Disorders

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.

Interventions

Cervical Stabilization Exercises will be performed 3 days a week for 8 weeks.

OTHERStandard treatment (Education + home exercises)

Individuals will be informed about TMJ disorders, parafunctional activities (chewing gum, nail/pen biting, etc.) and recommendations. In addition, Rocabado exercises will be given as a home program.

Sponsors

Bitlis Eren University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

This study was planned as a randomized controlled trial. The individuals included in the study will be divided into 2 groups as Stabilization and Control group by block randomization method.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Numeric Pain Rating Scale (NPRS)Change from baseline at 8 weeksTMJ 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)Change from baseline at 8 weeksIt 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 PostureChange from baseline at 8 weeksCervical posture will be evaluated from the craniovertebral angle.
Cervical MobilityChange from baseline at 8 weeksFor cervical mobility, normal joint movements of the neck will be evaluated with a goniometer.
Cervical Muscle PerformanceChange from baseline at 8 weeksCervical muscle performance will be evaluated with the craniocervical flexion test.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026