Temporomandibular Joint Dysfunction Syndrome
Conditions
Keywords
TEMPOROMANDIBULAR JOINT, Cervical Posture, wind Musician
Brief summary
Temporomandibular dysfunction (TMD) consists of a series of multifactorial signs and symptoms that occur in the orofacial region, with pain being the most common symptom. There is a close biomechanical and anatomical relationship between the cervical region and the temporomandibular joint (TMJ) through the trigemino-spinal nucleus. Objectives: To comparatively assess the improvement in subjects with TMD when adding cervical manual therapy to a postural treatment. Additionally, to determine if both cervical treatments separately produce changes in the TMJ. Materials and methods: An experimental study of randomized controlled clinical trial type was conducted. The study involved 30 wind instrument players randomly assigned to an experimental group (EG) and a control group (CG). After obtaining consent, measurements were taken for maximum mouth opening (MMO), cervical range of motion, and pain threshold to pressure (PTP) in the masseter and temporalis muscles. Both groups underwent active cervical postural treatment for 4 weeks, and the EG additionally received a cervical manual therapy protocol. An initial assessment was conducted before the intervention, and a final assessment was done one week after the last intervention. The statistical program SPSS was used for data analysis.
Interventions
OTHERManual therapy
Within the manual therapy protocol carried out in the experimental group, we performed a series of passive maneuvers. The patient remains in supine position on a treatment table throughout the treatment, while the therapist sits at the head of the patient on a stool. The sequence of application is as follows: Suboccipital inhibition technique Cervical spinal mobilization Posterior fascia stretching
OTHERPostural exercises
The treatment plan includes active postural exercises for the cervical spine.
Sponsors
Universidad de Murcia
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)
Masking description
Using the Random Team Generator mobile application.
Intervention model description
The present study is an experimental, analytical, longitudinal, and prospective controlled randomized clinical trial.
Eligibility
Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No
Inclusion criteria
* Acceptance of written informed consent. * Playing a wind instrument. * Age between 18-40 years. * Pain in the cranio-cervico-mandibular region and/or masticatory muscles. * Hypertrophy in the masticatory muscles.
Exclusion criteria
* History of trauma and/or fracture in the cranial and/or facial region. * Rheumatic injury or degenerative disease. * Surgical intervention on the temporomandibular joint (TMJ). * Malformations of the cervical or cranial spine. * Vestibular, circulatory, or neurological disorders. * Degenerative or infectious joint diseases. * Current orthodontic treatment. * Receiving physiotherapy treatment during the two weeks prior to the study or during the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Cranio facial pain and disability inventory | a week after treatment | CF-PDI (Craniofacial Pain and Disability Inventory): This questionnaire focuses on pain as a common symptom of TMD (Temporomandibular Disorders). It is self-administered and designed to assess patients' perception of their physical and psychosocial health in relation to craniofacial pain. It consists of 21 questions regarding the impact of pain on activities involving the use of the temporomandibular joint, with a scoring range from 0 to 63 in ascending order, where 0 indicates no impact and 63 indicates maximum impact. This questionnaire demonstrates good structure, internal consistency, reproducibility, and validity, making it an objective tool that can be used in research and clinical practice for evaluating patients with craniofacial pain and disability. It is easy to administer and requires a short amount of time. The CF-PDI was created and developed in Spain, based on a biopsychosocial approach. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Maximum mouth opening. | a week after treatment | The measurement of maximum mouth opening (MMO) is the distance in centimeters between the upper and lower incisor teeth when the subject actively opens their mouth. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Pain pressure threshold in myofascial trigger points of the masticatory muscles. | a week after treatment | In TMD, myofascial pain of the masticatory muscles is the most relevant clinical entity that affects the masticatory system. It will be measured using a pressure algometer. |
Countries
Spain
Outcome results
None listed