Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06222736

Evaluation of the Efficacy of Cervical Core Exercises in Persons With Temporomandibular Joint Dysfunction

Led by Istanbul Gelisim University · Updated on 2024-11-19

60

Participants Needed

1

Research Sites

58 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim is to reveal to what extent cervical core exercises affect the results of treatment in patients with Temporomandibular Joint Dysfunction caused by Myofascial pain syndrome. Randomization will be carried out by dividing individuals who agree to participate in the study into 3 groups of 20 people.Participants will be divided into three groups, and all three groups will receive treatment in 30-45 minute sessions a day, 2 days a week for 8 weeks.

CONDITIONS

Official Title

Evaluation of the Efficacy of Cervical Core Exercises in Persons With Temporomandibular Joint Dysfunction

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with Temporomandibular Disorder caused by Myofascial Pain Syndrome
  • Female gender aged 18 and over
  • Volunteering to participate in the study
  • Able to communicate and understand Turkish and the exercises
Not Eligible

You will not qualify if you...

  • History of acute trauma in and around the Temporomandibular Joint
  • Temporomandibular Joint dysfunction caused by neurological disease
  • History of surgical or invasive treatments on the Temporomandibular Joint
  • Presence of infection or tumor within the mouth
  • History of tooth loss or use of prosthetic teeth
  • History of surgical procedures in the cervical area

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Istanbul Gelisim University

Istanbul, Avcılar, Turkey (Türkiye)

Actively Recruiting

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Research Team

T

Tuğçe Bilgic, Msc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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