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

Temporomandibular Joint Dysfunction Syndrome Clinical Trial

Official title:

Effects of Manual Therapy and Exercises Applied to Cervical Spine in Patients With Temporomandibular Disorders: Pilot Study

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01954511
• Other study ID #: U1111-1139-4055
• Secondary ID: 0300.0.135.000-1
• Status: Withdrawn
• Phase: N/A
• Start date: July 2012
• Est. completion date: December 2012

Study information

• Verified date: September 2019
• Source: Universidade Federal de Sao Carlos
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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 information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 2012
• Est. primary completion date: December 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 25 Years

Eligibility

Inclusion Criteria:

• Patients diagnosed with myogenic or mixed temporomandibular disorders

Exclusion Criteria:

• Patients diagnosed with arthrogenic or discogenic temporomandibular disorders

Related Conditions & MeSH terms

• Joint Diseases
• Temporomandibular Joint Disorders
• Temporomandibular Joint Dysfunction Syndrome

Intervention

Other:
• Manual 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 ?rst ?nger and medial aspect of the hand, and other hand over the frontal region of the patient's head. The mobilizing force was delivered by ?exing 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
• Manual therapy
The patient was prone with the cervical spine in a neutral position. The therapist placed the tips of his thumbs on the posterior surface of the C5 spinous process, while the other ?ngers rested gently around the patients' neck. This technique was applied for 9 minutes

Device:
• Pressure 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

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Universidade Federal de Sao Carlos

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Changing in Mandibular Function Impairment Questionnaire -MFIQ	To evaluated mandibular function was used the Mandibular Function Impairment Questionnaire	Before and 5 days follow-up intervetion
Primary	Changing in maximum mouth opening pain free	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)	Before and 5 days follow-up intervetion
Secondary	Changing of Pain	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.	Before and 5 days follow-up intervetion