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Manual Therapy and Exercises Applied to Cervical Spine in Patients With Temporomandibular Disorders

Not Applicable
Withdrawn
Conditions
Temporomandibular Joint Dysfunction Syndrome
Interventions
Other: Manual therapy
Device: 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WITHDRAWN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
Inclusion Criteria
  • Patients diagnosed with myogenic or mixed temporomandibular disorders
Exclusion Criteria
  • Patients diagnosed with arthrogenic or discogenic temporomandibular disorders

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Manual therapyPressure biofeedback deviceUpper cervical flexion mobilization, C5 central posterior-anterior mobilization, Pressure biofeedback device
Manual therapyManual therapyUpper cervical flexion mobilization, C5 central posterior-anterior mobilization, Pressure biofeedback device
Primary Outcome Measures
NameTimeMethod
Changing in maximum mouth opening pain freeBefore 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
NameTimeMethod
Changing of PainBefore 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.

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