Comparison of Cervical and TMJ Parameters in Young Adults With and Without Text Neck Syndrome

September 26, 2026 updated by: Borna Farhoomand

Comparison of Physical Parameters Related to the Cervical Region and Temporomandibular Joint in Young Individuals With and Without Text Neck Syndrome: A Cross-Sectional Study

The aim of this cross-sectional study is to compare temporomandibular joint (TMJ) and cervical spine parameters between young university students aged 18-30 years with and without text neck syndrome, a modern overuse condition caused by prolonged digital device use and repetitive forward head flexion. Given the anatomical, biomechanical, and functional connections between the stomatognathic system and the cervical region, prolonged altered posture may contribute to TMJ dysfunction, pain, and altered physical metrics. Participants are categorized into two groups based on photographic and self-reported text neck severity (levels 3-4 for text neck vs. levels 1-2 for non-text neck) and evaluated across multiple physical parameters, including craniovertebral and cervicothoracic angles, active cervical and mandibular range of motion, cervical joint position sense, neck and TMJ pain intensity via Visual Analog Scale, TMJ dysfunction severity using the Turkish-validated Fonseca Questionnaire, static balance via the single-leg stance test, and dynamic balance via the Y Balance Test.

Study Overview

Study Type

Observational

Enrollment (Estimated)

80

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

1 year to 30 years (Child, Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The study population consists of young adult university students aged 18 to 30 years recruited from a university campus environment. Participants will be sampled from healthy undergraduate and graduate students who routinely use digital devices (such as smartphones and tablets) in their daily academic and personal activities.

Description

Inclusion Criteria:

  • University students aged between 18 and 24 years,
  • Group 1: Individuals with level 3 or level 4 text neck posture based on the self-reported posture assessment diagram,
  • Group 2: Individuals with level 1 or level 2 text neck posture based on the self-reported posture assessment diagram,
  • Being physically and mentally eligible to participate in the study,
  • Willingness to voluntarily participate and provide written informed consent prior to study enrollment.

Exclusion Criteria:

  • History of cervical spine surgery,
  • Ongoing orthodontic treatment,
  • Receiving medical treatment related to the neck or jaw region within the last 3 months,
  • Exposure to trauma related to the neck or jaw region within the last 3 months,
  • Presence of a diagnosed psychiatric disorder.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: COHORT
  • Time Perspectives: CROSS_SECTIONAL

Cohorts and Interventions

Group / Cohort
Text Neck Syndrome Group
Non-Text Neck Group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cervical Posture Angles
Time Frame: Baseline (at a single assessment point)
Baseline (at a single assessment point)
Cervical and Temporomandibular Joint Pain Intensity
Time Frame: Baseline (at a single assessment point).

Description: Will be evaluated using a 10-cm Visual Analog Scale (VAS; 0 = no pain, 10 = worst imaginable pain) for neck pain and TMJ pain (at rest, during activity, and while chewing).

Baseline (at a single assessment point).
Cervical Range of Motion (CROM)
Time Frame: Baseline (at a single assessment point).

Description: Will be evaluated in degrees for active cervical flexion, extension, bilateral lateral flexion, and bilateral rotation using the CROM (Cervical Range of Motion) device.

Baseline (at a single assessment point).
Mandibular Range of Motion
Time Frame: Baseline (at a single assessment point).

Description: Will be measured in millimeters (mm) using a digital caliper and ruler for maximum mouth opening, right/left lateral movements, and protrusion.

Baseline (at a single assessment point).
Text Neck Posture Classification
Time Frame: Baseline (at a single assessment point).

Text neck posture will be assessed using both self-reported perception and standardized photographic analysis.

Baseline (at a single assessment point).

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Temporomandibular Joint Dysfunction Severity
Time Frame: Baseline.

Description: Will be evaluated using the Turkish-validated Fonseca Questionnaire (10 items, total score 0-100; higher scores indicate greater TMD severity).

Baseline.
Cervical Joint Position Sense (JPS)
Time Frame: Baseline

Description: Will be evaluated in degrees using the CROM device across flexion-extension, lateral flexion, and rotation planes to measure absolute error from a target angle

Baseline
Static Balance
Time Frame: Baseline.

Description: Will be measured in seconds with eyes open and eyes closed on a firm surface.

Baseline.
Dynamic Balance Assessment using the Y Balance Test
Time Frame: Baseline
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

October 1, 2026

Primary Completion (Estimated)

November 30, 2026

Study Completion (Estimated)

December 28, 2026

Study Registration Dates

First Submitted

September 22, 2026

First Submitted That Met QC Criteria

September 26, 2026

First Posted (Actual)

October 1, 2026

Study Record Updates

Last Update Posted (Actual)

October 1, 2026

Last Update Submitted That Met QC Criteria

September 26, 2026

Last Verified

September 1, 2026

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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