NCT07666360

Brief Summary

This cross-sectional study will examine the relationship between mandibular dysfunction, cervical joint position sense, craniovertebral angle, neck pain, and temporomandibular dysfunction (TMD) severity. TMD severity, mandibular function, cervical proprioception, craniovertebral angle, and neck pain history will be assessed using standardized clinical tools and questionnaires. The study will evaluate the associations between these variables and determine the factors that may predict TMD severity.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 18, 2026

Completed
1 day until next milestone

Study Start

First participant enrolled

June 19, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

June 24, 2026

Completed
16 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 10, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 10, 2026

Completed
Last Updated

June 24, 2026

Status Verified

June 1, 2026

Enrollment Period

21 days

First QC Date

June 18, 2026

Last Update Submit

June 18, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Temporomandibular Dysfunction Severity

    TMD severity will be assessed using the Fonseca Anamnestic Index, which evaluates the severity of temporomandibular dysfunction symptoms. It is a 10-item self-report questionnaire. Each item is scored as "Yes" (10 points), "Sometimes" (5 points), or "No" (0 points), with a total score calculated by summing all items.

    Single assessment at baseline (cross-sectional evaluation)

Secondary Outcomes (7)

  • Cervical Extension Joint Position Sense

    Single assessment at baseline (cross-sectional evaluation)

  • Cervical Flexion Joint Position Sense

    Single assessment at baseline (cross-sectional evaluation)

  • Cervical Lateral Flexion Joint Position Sense

    Single assessment at baseline (cross-sectional evaluation)

  • Cervical Rotation Joint Position Sense

    Single assessment at baseline (cross-sectional evaluation)

  • Craniovertebral Angle

    Single assessment at baseline (cross-sectional evaluation)

  • +2 more secondary outcomes

Study Arms (1)

TMD Symptomatic Participants

Participants with temporomandibular dysfunction (TMD) symptoms will be included in the study. All participants will undergo clinical and questionnaire-based assessments to evaluate mandibular function, cervical joint position sense, craniovertebral angle, neck pain history, and TMD severity.

Other: Assessments

Interventions

No intervention was applied.

TMD Symptomatic Participants

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Adults aged 18 years or older with a Fonseca Anamnestic Index (FAI) score of 20 or higher who gave written consent were included. Participants were people with jaw (TMJ) and/or neck complaints. People were excluded if they had recent treatment (last 6 months) for the jaw or neck, used pain or muscle relaxant drugs, had previous neck or jaw surgery or major trauma, jaw dislocation or subluxation, missing teeth or dental prostheses, or neurological, rheumatologic, or systemic inflammatory diseases.

You may qualify if:

  • Fonseca Anamnestic Index score \> 15
  • aged 18 years and older

You may not qualify if:

  • Received medical, orthodontic, or physiotherapy treatment targeting the temporomandibular joint and/or cervical region within the past six months
  • used analgesic, anti-inflammatory, or muscle relaxant medications
  • history of cervical spine or cranio-cervical surgery or major trauma
  • a history of facial or TMJ trauma, TMJ subluxation or dislocation
  • partial or complete dental prostheses
  • had missing teeth
  • neurological, rheumatological, or systemic inflammatory diseases

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara Yıldırım Beyazıt University, Department of Physiotherapy and Rehabilitation

Ankara, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Temporomandibular Joint Disorders

Condition Hierarchy (Ancestors)

Craniomandibular DisordersMandibular DiseasesJaw DiseasesMusculoskeletal DiseasesJoint DiseasesMuscular DiseasesStomatognathic Diseases

Central Study Contacts

Sevilay Seda BAŞ, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Asst. Prof.

Study Record Dates

First Submitted

June 18, 2026

First Posted

June 24, 2026

Study Start

June 19, 2026

Primary Completion

July 10, 2026

Study Completion

July 10, 2026

Last Updated

June 24, 2026

Record last verified: 2026-06

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