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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05006963
Other study ID # Tele-Reabilitação em TMD
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 30, 2021
Est. completion date August 30, 2024

Study information

Verified date March 2024
Source University of Nove de Julho
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Temporomandibular disorder or TMD is characterized by a set of symptoms such as: pain, decreased range of motion and joint noise. It's origin is multifactorial, which may be related to biological aspects, environmental and psychosocial. The multimodal approach has been widely used in physiotherapy for the treatment of TMDs. Physiotherapy has been walking together with technology so that telerehabilitation can be a reality, contributing so that quality care reaches the patient, in the impossibility office-to-face service. The objective of this study is to verify the effect of telerehabilitation on pain outcomes, range of motion, functionality and biopsychosocial aspects in individuals with temporomandibular disorders. Will be a randomized, controlled and blinded clinical trial was carried out. The study will be divided into two moments: evaluation and intervention. Evaluations will be carried out using the Diagnostic Criteria for Temporomandibular Disorders: Clinical Protocol and Assessment Instruments (DC/TMD), the Fonseca Anamnesis Index (IAF), the Numerical Pain Scale (END) and the Functional Limitation Questionnaire (MFIQ). Individuals will be randomized into 2 groups: Group A (in person) Group B (telerehabilitation). Both groups will receive treatment physical therapy for 12 weeks. After collecting the data, they will be tabulated and analyzed using a 5% significance level.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date August 30, 2024
Est. primary completion date August 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility 1. Age between 18 and 60 years; 2. presence of pain in the facial region in the last 6 months; 3. diagnosis of myalgia, arthralgia, headache attributed to temporomandibular disfunction and/or subluxation temporomandibular joint.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
manual therapy and therapy by exercise
In general, patients will receive extra-oral massage and intraoral massage, myofascial release in the cranio-cervical musculature, mobilization of the hyoid bone and may also receive unspecific joint mobilization. Will bemouth opening exercise was also performed with the tongue on the palate, proprioceptive lateralization and protrusion exercises with hyperboloid and exercises with combinations of movements of laterality and opening, or protrusion and opening.

Locations

Country Name City State
Brazil University Nove de Julho São Paulo

Sponsors (1)

Lead Sponsor Collaborator
University of Nove de Julho

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Score in Numerical Pain Scale intensity of pain The level of pain at 12 weeks
Primary Score in Numerical Pain Scale intensity of pain The level of pain at 6 months
Primary measure range of motion range of motion The range of motion at range of motion at 12 weeks .
Primary measure range of motion range of motion The range of motion at 6 months.
Secondary measure Functionality Mandibular Functional Limitation Questionnaire The functionality at 12 weeks .
Secondary measure Functionality Mandibular Functional Limitation Questionnaire The functionality at 6 months.
Secondary Biopsychosocial analysis. Axis II of the diagnostic criterion for temporomandibular disorders The biopsychosocial analysis at 12 weeks .
Secondary Biopsychosocial analysis. Axis II of the diagnostic criterion for temporomandibular disorders The biopsychosocial analysis at 6 months.
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