- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07371195
Relationship Between Upper Cervical Mobility and Temporomandibular Joint Range of Motion in Patients With Temporomandibular Disorders
Study Overview
Status
Detailed Description
Temporomandibular disorders (TMD) are multifactorial conditions involving the temporomandibular joint, masticatory muscles, or both. Prior research indicates a strong association between TMD and cervical spine dysfunction, with patients frequently exhibiting neck pain, reduced cervical motion, and muscular tenderness.
This study explores how upper cervical mobility (flexion, extension, and rotation) correlates with TMJ range of motion (mouth opening, lateral excursion, and protrusion). The aim is to identify whether cervical spine hypomobility contributes to restricted jaw movement in TMD patients.
A total of 50 participants with TMD will undergo standardized clinical measurements of cervical mobility using a CROM device and TMJ motion using a ruler or caliper. Pearson or Spearman correlation coefficients will be applied to evaluate the association between cervical and TMJ movement parameters.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Demiana Hany Habib
- Phone Number: +201229435551
- Email: demianahany7@gmail.com
Study Locations
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Menia Governorate
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Minya, Menia Governorate, Egypt
- faculty of physical therapy, Deraya University
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Contact:
- Aliaa Gamal Hussien
- Phone Number: +201003041632
- Email: aliaa.gamal@deraya.edu.eg
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Medically stable individuals who consent to participate in the study.
- Age between 18 and 50 years.
- Both male and female participants.
- Patients diagnosed with temporomandibular joint (TMJ) dysfunction for at least three months.
Exclusion Criteria:
- Presence of systemic diseases.
- Body mass index (BMI) greater than 30 kg/m².
- Pregnancy.
- Recent physical therapy for cervical spine disorders, headaches, or temporomandibular dysfunction.
- Cervical radiculopathy or other neurological disorders.
- History of trauma or major psychological problems.
- Generalized joint hypermobility.
- Down syndrome.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Temporomandibular Disorder Group
Fifty patients with temporomandibular disorder will undergo evaluation of upper cervical spine mobility (flexion, extension, and rotation) and TMJ range of motion (opening, lateral excursion, and protrusion) using standardized instruments (CROM device and ruler/caliper).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Upper Cervical Spine Mobility
Time Frame: Single assessment session (baseline only)
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Upper cervical spine mobility (flexion, extension, and left and right rotation) will be measured in degrees using a CROM device.
Participants will be seated in an upright position, and each movement will be measured twice following standardized procedures.
The mean value of both readings will be used for analysis.
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Single assessment session (baseline only)
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Temporomandibular Joint Range of Motion (TMJ ROM)
Time Frame: Single assessment session (baseline only)
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TMJ range of motion will be measured in millimetres using a standard ruler or digital calliper.
Measurements include maximum mouth opening, lateral excursion (left and right), and protrusion.
Each measurement will be taken twice, and the average will be recorded in millimetres to ensure reliability.
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Single assessment session (baseline only)
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Correlation Between Upper Cervical Mobility and TMJ Range of Motion
Time Frame: Single assessment session (baseline only)
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The relationship between upper cervical spine mobility (measured in degrees using the CROM device) and TMJ range of motion (measured in millimetres using a ruler or calliper) will be analysed statistically.
Pearson or Spearman correlation coefficients will be applied, depending on data normality, to determine the strength and direction of association.
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Single assessment session (baseline only)
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Musculoskeletal Diseases
- Stomatognathic Diseases
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Muscular Diseases
- Joint Diseases
- Jaw Diseases
- Headache Disorders
- Mandibular Diseases
- Craniomandibular Disorders
- Myofascial Pain Syndromes
- Headache Disorders, Secondary
- Temporomandibular Joint Disorders
- Temporomandibular Joint Dysfunction Syndrome
- Post-Traumatic Headache
Other Study ID Numbers
- Upper Cervical Mobility
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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