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aser effectiveness in the treatment of local and distant pain in temporomandibular disorder

Not Applicable
Recruiting
Conditions
Temporomandibular disorder
K07.6
Registration Number
RBR-2v6ghb
Lead Sponsor
Faculdade de Odontologia de Ribeirão Preto (FORP) - Universidade de São Paulo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

Women's volunteers; reporting pain in the facial area for at least 03 months; diagnosed with myofascial pain (temporomandibular disorder) according to the criteria of the Research Diagnostic Criteria for Temporomandibular Disorder (RDC/TMD - this diagnosis will be established after an evaluation with the researchers team).

Exclusion Criteria

Women's volunteers who are in any type of treatment for temporomandibular disorder; who have tumor, trauma or head/neck surgery history; previous diagnosis of fibromyalgia and other painful musculoskeletal syndromes (rheumatic diseases, among others); presence of neurological and/or psychiatric disorders; volunteers who use prescription drugs (anxiolytics, antidepressants, and/or anticonvulsants); pregnant women; users of heart pacemaker.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction of pain symptomatology, verified through the Visual Analogue Scale, the application of the Short-form McGill Questionaire and the Pressure Pain Threshold at the pre and posttreatment moments, and the expected reduction is 50% or more in pain intensity and sensitivity for the group that received low intensity laser therapy (LLLT); and 20% or less in the parameters described above for the placebo group.<br>Reduction of the levels of anxiety and stress for both groups (active laser and placebo), verified through the Beck Inventory Questionnaire and the dosage of the morning salivary cortisol at the pre and posttreatment moments, and the expected reduction is 50% or more for both groups.
Secondary Outcome Measures
NameTimeMethod
Secondary outcomes are not expected.
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