Manual Therapy and Exercises Applied to Cervical Spine in Patients With Temporomandibular Disorders
- Conditions
- Temporomandibular Joint Dysfunction Syndrome
- Interventions
- Other: Manual therapyDevice: Pressure biofeedback device
- Registration Number
- NCT01954511
- Lead Sponsor
- Universidade Federal de Sao Carlos
- 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
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- Female
- Target Recruitment
- Not specified
- Patients diagnosed with myogenic or mixed temporomandibular disorders
- Patients diagnosed with arthrogenic or discogenic temporomandibular disorders
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Manual therapy Pressure biofeedback device Upper cervical flexion mobilization, C5 central posterior-anterior mobilization, Pressure biofeedback device Manual therapy Manual therapy Upper cervical flexion mobilization, C5 central posterior-anterior mobilization, Pressure biofeedback device
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.