- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00743223
The Frequency Forward Head Posture in Subjects With Temporomandibular Disorder
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Postural habit is defined as "the attitude of the body" being characterized as good when the parts of the body muscles and bones are lined up and work together in a harmonious form protecting the body of injury or gradual deformity and independently the attitude. The bad posture is a bad habit, but it can be which results in the disagreement of some parts of the body. These are at risk of injury or pain due to and increased tension that the disagreement imposes to the support structures. Several study confirm this occurrence relating that this the attitude can alter itself principally if a discomfort occurs. When it occurs there will be the installation of alterations, limitation of movements or even deformity, leading it to the development of an abnormal of posture of the body which will be able to reduce the functional capacity of various structures and organs of the human body.
The forward head posture is a common abnormality in cervical spine that can contribute to perpetuation the trigger points in muscles of the head as well as some kinds of temporomandibular disorder. It was suggested its influence in the treatment of patients with orofacial pain and TMD the FHP may occur a result of an acute trauma or if develop itself gradually because of an inadequate position.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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São Paulo, Brazil, 04023-062
- Federal University of São Paulo
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Study group
The criteria of inclusion of the individuals for this group were:
- Individuals whose main complaint were pain in the muscles of the chew or the TMJ
- To present pain of the muscle or to articulate during the functional tests
- Maximum opening interincisal equal or minor than 40 mm
Crontrol group
The criteria of inclusion of the individuals for this group were:
- Individuals who underwent routine dental treatment
- Individuals without TMD complaint
- Maximum opening interincisal bigger than 40 mm
Exclusion Criteria:
- There are not
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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1
Study-group: The volunteers were selected on a randomized form among the individuals who went to the clinic of orofacial pain and temporomandibular disorders of São Paulo Hospital.
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The investigation of the cervical position consisted of locating the individual in side view with the parallel feet in erect position and tracing an imprisoned plumb wire to the ceiling and tangent to the kyphosis curve of the thoracic column.
With a ruler it was verified at a distance of this line until the point deepest of the cervical lordosis curve.
Other Names:
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2
Control-group: The volunteers were selected on a randomized form among the individuals who went to the dental offices of the researchers.
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The investigation of the cervical position consisted of locating the individual in side view with the parallel feet in erect position and tracing an imprisoned plumb wire to the ceiling and tangent to the kyphosis curve of the thoracic column.
With a ruler it was verified at a distance of this line until the point deepest of the cervical lordosis curve.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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Outcome Measure: frequency of the forward head posture
Time Frame: one year
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one year
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Collaborators and Investigators
Investigators
- Principal Investigator: GUSTAVO VINHOLI, DENTIST, Federal University of São Paulo
Study record dates
Study Major Dates
Study Start
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CEP-UNIFESP1175/06
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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