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Temporomandibular Disorders (TMD)NCT07371195

Relationship Between Upper Cervical Mobility and Temporomandibular Joint Range of Motion in Patients With Temporomandibular Disorders

An observational study of Temporomandibular Disorders (TMD) and Temporomandibular Joint Dysfunction Syndrome, run by Deraya University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Upper cervical spine mobility plays a crucial role in temporomandibular joint (TMJ) function. This observational study investigates the relationship between upper cervical spine mobility and TMJ range of motion in patients diagnosed with temporomandibular disorders (TMD). Read more about this study

Who is it for?
Ages 18 to 50 years
How many people
50 participants
Where
1 siteEgypt
Study dates
15 Feb 2026to 20 Aug 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 50 years
  • All sexes
  • No healthy volunteers
  • Adult

Study population: Participants will be adult patients (both male and female) aged 18 to 50 years who have been clinically diagnosed with temporomandibular joint (TMJ) dysfunction for more than three months. All participants will be recruited from the outpatient clinic of the Faculty of Physical Therapy, Deraya University, Minya, Egypt. Eligible participants will be medically stable and free from systemic or neurological disorders that could affect cervical or temporomandibular mobility.

Who may be able to join

  • 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.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • faculty of physical therapy, Deraya University

    Minya, Menia Governorate

Other trials in Egypt

About this study

Upper cervical spine mobility plays a crucial role in temporomandibular joint (TMJ) function. This observational study investigates the relationship between upper cervical spine mobility and TMJ range of motion in patients diagnosed with temporomandibular disorders (TMD). Cervical hypomobility may restrict mandibular movement and contribute to TMJ dysfunction through shared biomechanical and neuromuscular mechanisms.

Read the 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.

Keywords
Temporomandibular Joint, Temporomandibular Disorders, Upper Cervical Spine, Cervical Mobility
Medical subject headings
Temporomandibular Joint Disorders, Temporomandibular Joint Dysfunction Syndrome, Post-Traumatic Headache

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07371195
Study groupRoleWhat they receive
Temporomandibular Disorder GroupFifty 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).

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Upper Cervical Spine Mobility

    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.

    Measured: Single assessment session (baseline only)

  2. Temporomandibular Joint Range of Motion (TMJ ROM)

    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.

    Measured: Single assessment session (baseline only)

  3. Correlation Between Upper Cervical Mobility and TMJ Range of Motion

    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.

    Measured: Single assessment session (baseline only)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Jan 2026
  2. Study start15 Feb 2026
  3. Primary completion15 Aug 2026
  4. Study completion20 Aug 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07371195
Sponsor's protocol ID
Upper Cervical Mobility
Status last verified
Aug 2026
First submitted
19 Jan 2026
Last updated
28 Aug 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Temporomandibular Disorders (TMD) and Temporomandibular Joint Dysfunction Syndrome, run by Deraya University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Upper Cervical Spine Mobility (time frame: Single assessment session (baseline only)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Aug 2026.

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