Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06148818

Effect of Progressive Neck Motor Control Exercises on Temporomandibular Joint Dysfunction

The primary aim of this study was to investigate the effects of progressive neck motor control exercises on craniocervical pain, posture, function and kinesiophobia in different types of temporomandibular dysfunction. The secondary aim of the study was to examine the differences between the effects of progressive neck motor control exercises on different types of temporomandibular dysfunction.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Karadeniz Technical University

Trabzon, Turkey (Türkiye)

Location status: Recruiting

Location contact

Nurhayat Korkmaz, Msc

CONTACT

+90462377 ext. 2471

Nurhayat korkmaz, Msc

PRINCIPAL_INVESTIGATOR

About this study

In this randomised controlled study, the effects of progressive neck motor control exercise therapy on craniocervical pain, posture, function and kinesiophobia in individuals with different types of temporomandibular dysfunction (myofascial, disc displacement with reduction, disc displacement without reduction) and their differences with the control group will be compared. Participants diagnosed by a dentist according to three different types of temporomandibular dysfunction will be included in the study. Participants will be divided into groups by block randomisation method. A total of 6 groups will be included in the study, including participants with three different types of temporomandibular dysfunction who voluntarily agree to participate in the study and meet the inclusion criteria, and the control group of each group. The study groups will receive the same treatment and patient education for 6 weeks, while the control groups will receive only patient education.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 to 55 years old,
  • Temporomandibular joint-related complaints for at least 3 months,
  • Temporomandibular dysfunction is diagnosed as a result of clinical and radiological evaluation by the dentist,
  • Neck pain of 3 or more according to the numeric pain scale

Exclusion criteria

  • Cognitive problems,
  • The one with the splint,
  • Those who have used painkillers or muscle relaxants for temporomandibular dysfunction complaints in the last 1 week,
  • With any systematic joint or muscle disease (e.g. fibromyalgia, rheumatoid arthritis),
  • Those with serious systemic diseases,
  • Any neurological disorder (e.g. trigeminal neuralgia),
  • Pregnancy or breastfeeding,
  • Treated for Temporomandibular joint or orofacial muscle pain in the last 3 months,
  • Has undergone an operation/trauma to the cervical region and/or temporomandibular joint,
  • Positive vertebrobasilar artery test

Treatment and study plan

Progressive neck motor control exercise therapy

Other

The exercise programme will be conducted as a single session two days a week for 6 weeks. The sessions will always be conducted by the same physiotherapist. Each exercise session will consist of 10 minutes of warm-up exercises, 40 minutes of neck motor control exercises and 10 minutes of cool down exercises. Each exercise will be performed as 2 sets of 10 repetitions.

Patient Education

Other

The content of this education consists of information about the disease and symptoms, chewing recommendations, dietary changes, parafunctional habits, activities to be avoided, posture recommendations.

Primary outcomes

  1. Fonseca Anamnestic Index

    Time frame: 1st, sixth week, first mont

    Assessment of Temporomandibular Dysfunction Severity

  2. Numeric Pain Scale

    Time frame: 1st, sixth week, first mont

    Assessment of Pain, 0: No pain, 10: Maximum pain

  3. Pressure pain threshold

    Time frame: 1st, sixth week, first mont

    Assessment of Pressure pain threshold

  4. Range of motion

    Time frame: 1st, sixth week, first mont

    Assessment of Temporomandibular joint and neck range of motion

  5. Joint position error test

    Time frame: 1st, sixth week, first mont

    Assessment of Cervical proprioception

  6. Endurance

    Time frame: 1st, sixth week, first mont

    Assessment of Deep neck flexor endurance

  7. Photographic Posture Analysis

    Time frame: 1st, sixth week, first mont

    Assessment of head and neck posture

  8. Mandibular Function Impairment Questionnaire

    Time frame: 1st, sixth week, first mont

    Assessment of Mandibular Function

Secondary outcomes

  1. Tampa kinesiophobia scale

    Time frame: 1st, sixth week, first mont

    Assessment of kinesiophobia for temporomandibular joint, 12 points: low kinesiophobia; 48 points:high kinesiophobia

Study contacts

Contact information is provided by the study sponsor or research team.

Nurhayat Korkmaz, MSc

CONTACT

[email protected]

+90538736 ext. 9062

nurhayat korkmaz, PhDstudent

CONTACT

[email protected]

+90538736 ext. 9062

Sponsors and collaborators

Lead sponsor

Karadeniz Technical University

Other

Registry information

Official study title

Investigation of the Effect of Progressive Neck Motor Control Exercises on Craniocervical Pain, Posture, Function and Kinesiophobia in Different Types of Temporomandibular Joint Dysfunction

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Nov 28, 2023
Registry last updated
Jan 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.