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NCT05006963

Tele-Rehabilitation in Patients With Temporomandibular Dysfunction

Recruiting now NA Last updated 4 March 2025
What this trial tests

NA trial testing manual therapy and therapy by exercise in Temporomandibular Disorder in 50 participants. Currently enrolling.

Timeline
30 September 2021
Primary endpoint
30 December 2026
30 March 2027

Quick facts

Lead sponsorUniversity of Nove de Julho
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment50
Start date30 September 2021
Primary completion30 December 2026
Estimated completion30 March 2027
Sites1 location across Brazil

Drugs / interventions tested

Conditions studied

Sponsor

University of Nove de Julho

Who can join

Adults 18 to 60, any sex, with Temporomandibular Disorder or Temporomandibular Joint Disorders. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Temporomandibular Disorder

Currently open trials in the same condition.

Other University of Nove de Julho trials

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Data sources for this page

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