Temporomandibular Joint Dysfunction Syndrome
Conditions
Keywords
Stomatognathic diseases;, Temporomandibular Joint Dysfunction Syndrome
Brief summary
The objective of this study was to investigate the effect of a manual therapy and exercise program, focused on the rehabilitation of cervical function, on clinical signs and mandibular function in subjects with TMD.
Detailed description
Temporomandibular disorder (TMD) is a general term that refers to disorders associated with the temporomandibular joint (TMJ) and the masticatory muscles. Among the main symptoms are pre-auricular pain (in the region of the TMJ) and/or pain in the masticatory muscles. It's usual to observe that subjects with TMD also present cervical alteration. Beside this, cervical postural alterations produced by muscle tension can influence mandibular position. The intervention protocol was based on manual therapy, stabilization exercises and stretching. The technique are:. 1. Upper cervical flexion mobilization; 2. C5 central posterior-anterior mobilization; 3. Stabilization exercise: Cranio-cervical flexor stabilization exercise 4. Stretching of muscles: upper trapezius, scalenes, semispinalis capitis; splenius capitis, sternocleidomastoid
Interventions
OTHERManual therapy
The patient was supine with the cervical spine in a neutral position. The therapist brought about a contact of the occipital bone with the first finger and medial aspect of the hand, and other hand over the frontal region of the patient's head. The mobilizing force was delivered by flexing the upper cervical region using a combination of cephalic traction with the occipital hand and caudal pressure with the frontal hand. This technique was applied for 10 minutes
DEVICEPressure biofeedback device
Device: Stabilizer - Chattanooga Group Inc., Chattanooga, Tennessee, USA The cranio-cervical flexor stabilization exercise was done 10 times holding 10 seconds the flexing position graded through feedback from a pressure biofeedback device
Sponsors
Universidade Federal de Sao Carlos
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 25 Years
Healthy volunteers
Yes
Inclusion criteria
* Patients diagnosed with myogenic or mixed temporomandibular disorders
Exclusion criteria
* Patients diagnosed with arthrogenic or discogenic temporomandibular disorders
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changing in maximum mouth opening pain free | Before and 5 days follow-up intervetion | The clinical signs was based on Research Diagnostic Criteria protocol and it was measured maximum mouth opening pain free using a caliper ((Somet, 150mm, Inox, Czechoslovakia) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changing of Pain | Before and 5 days follow-up intervetion | To evaluate pain it was applied a scale from Research Diagnostic Criteria protocol, that consists of a line scored from 0 to 10, where 0 represents no pain and 10 the worst pain that the subject has experienced, allowing it to check the number that features their pain at the moment. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Changing in Mandibular Function Impairment Questionnaire -MFIQ | Before and 5 days follow-up intervetion | To evaluated mandibular function was used the Mandibular Function Impairment Questionnaire |
Outcome results
None listed