About this trial
PURPOSE:
The purpose of the study is to investigate the effect of the breather device on ventilatory effort and in patients with myogenic temporomandibular joint disorders To investigate the effect of the breather device on craniocervical angle and oral Health quality in patients with myogenic temporomandibular joint disorders
BACKGROUND:
TMDs affect between 5% and 12% of the population which is presented by symptoms such as pain in the masticatory muscles with a decrease in the mandible's movement. Other symptoms include ear pain, headache, joint sounds with mandible movement, and/or functional limitations in the jaw like swallowing difficulties commonly found. (Hatice ., et al 2023) Increased prevalence of TMDs has been linked to physical, psychological, and hormonal changes throughout pubertal development. The age predisposes to the development of masticatory system problems in students since symptoms peak between the ages of 20 and 40 years. Women of breeding age are the majority of TMD sufferers. The prevalence of TMD increases globally throughout adolescence and may vary from 7% to 30% of the population (Loster ., et al2017). Alterations of body posture, upper thoracic breathing pattern, and mouth breathing constitute causal factors for the overuse of the accessory inspiratory musculature, which generates hyperactivity and consequently, alteration of head position, and mandibular traction. (Kim., et al 2017)
HYPOTHESES:
There will be no significant effect of the breather device on ventilatory effort in patients with myogenic temporomandibular joint disorders.
There will be no significant effect of the breather device on a craniocervical angle and oral Health quality in patients with myogenic temporomandibular joint disorders RESEARCH QUESTION: Does the breather device can improve ventilatory effort in patients with myogenic temporomandibular joint disorders?.
Eligibility criteria
Qualifiers
Sixty female patients who fulfilled the RDC/TMD criteria of myofascial pain and the presence of parafunctional habits, such as bruxism, teeth grinding, mouth breathing, and lip biting.
The Patient's ages will range from 20 to 40 years.
Disqualifiers
patients undergo surgery or trauma in the orofacial region; systemic or degenerative odontologic disease.
The patient has Surgery or trauma in the spine and upper limb.
Patients suffering from rheumatic diseases and other severe comorbidities.
Patients suffering from any respiratory diseases (restrictive, obstructive, suppurative diseases).
Trial design
Treatments tested in this trial
- the breather device
- conventional exercise program
Treatment groups
Locations
Sponsors and collaborators
Cairo University
Lead sponsor
Misr University for Science and Technology
Sponsor institution