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Temporomandibular Joint Dysfunction SyndromeNCT06148818

Effect of Progressive Neck Motor Control Exercises on Temporomandibular Joint Dysfunction

A study testing Patient education in people with Temporomandibular Joint Dysfunction Syndrome, run by Karadeniz Technical University at 1 site in Turkey (Türkiye).

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 55 yearsHealthy volunteers can take part
What is being tested?
Patient education
Could I receive a placebo?
No, everyone receives an active treatment
How many people
75 participants
Where
1 siteTurkey (Türkiye)
Study dates
4 Nov 2024to 30 Jun 2025
Phase
Interventional
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 55 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 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

Who cannot join

  • 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),
Show all 10Show fewer
  • 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

Trial locations and contacts

1 site in 1 country.

nurhayat korkmaz, PhDstudent contact

+90538736 ext. 9062

krkmznrhyt@gmail.com

Nurhayat Korkmaz, MSc contact

+90538736 ext. 9062

krkmznrhyt@gmail.com

Turkey (Türkiye)1 site, 1 recruiting
  • Karadeniz Technical University

    Trabzon

    Nurhayat Korkmaz, Msc, +90462377 ext. 2471

    Nurhayat korkmaz, Msc

    Recruiting

Other trials in Turkey (Türkiye)

About this study

Official 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

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.

Read the detailed description

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.

Being tested
Progressive neck motor control exercise therapy, Patient education
Keywords
Temporomandibular Joint Dysfunction Syndrome, Pain, neck motor control exercise, posture, kinesiophobia, function
Medical subject headings
Temporomandibular Joint Dysfunction Syndrome, Pain, Kinesiophobia

What participants receive

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

  • Progressive neck motor control exercise therapyOther

    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 educationOther

    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.

Study groups in NCT06148818
Study groupRoleWhat they receive
MyofascialExperimentalMyofascial Temporomandibular Dysfunction
Receives: Other: Progressive neck motor control exercise therapy; Other: Patient education
disc displacement with reductionExperimentalTemporomandibular joint disc displacement with reduction
Receives: Other: Progressive neck motor control exercise therapy; Other: Patient education
disc displacement without reductionExperimentalTemporomandibular joint disc displacement without reduction
Receives: Other: Progressive neck motor control exercise therapy; Other: Patient education
Myofascial2OtherMyofascial Temporomandibular Dysfunction
Receives: Other: Patient education
disc displacement with reduction2OtherTemporomandibular joint disc displacement with reduction
Receives: Other: Patient education
disc displacement without reduction2OtherTemporomandibular joint disc displacement without reduction
Receives: Other: Patient education

What is being measured

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

  1. Fonseca Anamnestic Index

    Assessment of Temporomandibular Dysfunction Severity

    Measured: 1st, sixth week, first mont

  2. Numeric Pain Scale

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

    Measured: 1st, sixth week, first mont

  3. Pressure pain threshold

    Assessment of Pressure pain threshold

    Measured: 1st, sixth week, first mont

  4. Range of motion

    Assessment of Temporomandibular joint and neck range of motion

    Measured: 1st, sixth week, first mont

  5. Joint position error test

    Assessment of Cervical proprioception

    Measured: 1st, sixth week, first mont

  6. Endurance

    Assessment of Deep neck flexor endurance

    Measured: 1st, sixth week, first mont

  7. Photographic Posture Analysis

    Assessment of head and neck posture

    Measured: 1st, sixth week, first mont

  8. Mandibular Function Impairment Questionnaire

    Assessment of Mandibular Function

    Measured: 1st, sixth week, first mont

Secondary outcomes (1)
  1. Tampa kinesiophobia scale

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

    Measured: 1st, sixth week, first mont

Timeline

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

  1. First posted28 Nov 2023
  2. Study start4 Nov 2024
  3. Primary completion30 May 2025 (estimated)
  4. Study completion30 Jun 2025 (estimated)

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
75 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06148818
Sponsor's protocol ID
2023/15
Status last verified
Oct 2024
First submitted
20 Nov 2023
Last updated
29 Jan 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Korkmaz Ucuncu N, Yilmaz O, Korkmaz YT, Coskun G. An investigation of the effect of progressive neck motor control exercises on craniocervical pain, posture, function and kinesiophobia in different types of temporomandibular disorders: a randomised controlled study protocol. BMC Oral Health. 2026 Feb 5;26(1):285. doi: 10.1186/s12903-026-07775-z.

    PubMed 41645126

Questions about this trial

What is this clinical trial studying?

A study testing Patient education in people with Temporomandibular Joint Dysfunction Syndrome, run by Karadeniz Technical University at 1 site in Turkey (Türkiye).

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 10 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: status not confirmed, as of the sponsor's last update on 29 Jan 2025. 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 Turkey (Türkiye). 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?

Results are not available in the source record.

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

Contact nurhayat korkmaz, PhDstudent (+90538736 ext. 9062, krkmznrhyt@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Fonseca Anamnestic Index (time frame: 1st, sixth week, first mont). The study lists 8 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06148818, which also lists 1 linked publication.

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 29 Jan 2025.

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