Temporomandibular Joint Dysfunction Syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Volunteer women; age between 18 and 45 years; diagnosis of painful TMD for more than 3 months.
Exclusion criteria
Exclusion criteria: Volunteers undergoing any type of treatment for painful Temporomandibular Dysfunction; previous history of tumors; previous history of trauma or head and neck surgery; presence of neurological disorders; presence of psychiatric disorders; volunteers who use controlled medications, such as anxiolytics, antidepressants and anticonvulsants; pregnant volunteers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Painful reduction resulting from chronic painful Temporomandibular Disorder,immediately after the end of the intervention, as well as epigenetic changes. Pain reduction will be assessed by quantitative sensory tests such as the pressure pain threshold and hyperalgesia (using a digital algometer) and allodynia (using a rotating electric toothbrush, with a 5-second stimulation). The three tests will be applied at the same pre points -determined). The epigenetic analysis will be performed by global DNA methylation and by methylation analysis of single nucleotide polymorphisms (SNPs), previously identified related to chronic painful temporomandibular disorder. | — |
Secondary
| Measure | Time frame |
|---|---|
| Cognitive-behavioral-emotional changes, measured by validated, self-applicable and specific protocols. They will be evaluated immediately after completion of the intervention. | — |
Countries
Brazil
Contacts
Universidade de São Paulo-Faculdade de Filosofia Ciências e Letras de Ribeirão Preto