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Telerehabilitation and face-to-face multimodal intervention: Randomized controlled clinical trial in adolescents with Temporomandibular Disorder

Exercises applied on line and face-to-face multimodal intervention: Randomized controlled clinical trial in adolescents with Temporomandibular Dysorder

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5scd5tm
Enrollment
Unknown
Registered
2023-05-19
Start date
2022-11-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Temporomandibular Disorder

Interventions

This is a randomized controlled clinical trial, which will be carried out in Florianópolis region. It will be a longitudinal study with a quantitative, analytical character, which will be carried out
E02.760.169.063.500.891)

Sponsors

Universidade do Estado de Santa Catarina
Lead Sponsor
Universidade do Estado de Santa Catarina
Collaborator

Eligibility

Age
10 Years to 18 Years

Inclusion criteria

Inclusion criteria: Participants aged between 10 and 18 years; be regularly enrolled and attending formal school activities at the chosen educational establishment; presence of Temporomandibular Disorders (TMD) confirmed by the Diagnostic Criteria for Temporomandibular Disorders (DC/TMD)

Exclusion criteria

Exclusion criteria: Participantes who have neurological, respiratory or musculoskeletal disorders that may interfere with any of the assessments; who received physical therapy care in the 3 months prior to the evaluation; history of trauma or dislocation to the face and/or TMJ; who using an orthodontic appliance (mobile or fixed) or myorelaxant plate; who make use of analgesics, anxiolytics and/or muscle relaxants 24 hours before the evaluation, inability to understand and/or perform the assessment protocol

Design outcomes

Primary

MeasureTime frame
To assess peripheral muscle oxygenation in the masseter muscles. To verify this result, near infrared spectroscopy will be used. It is expected to find improvement in oxygenation after the intervention performed, through the peripheral saturation index. The higher this index, the better the oxygenation.;Verify the intensity of pain in the temporomandibular region in adolescents with TMD. It is expected to find a decrease in pain after the intervention performed. And to verify this outcome, the numerical pain scale (0-10), the graduated chronic pain scale (0-10) and the algometer will be used. The higher the score on these scales, the greater the degree of pain.

Secondary

MeasureTime frame
To verify the presence of kinesiophobia in adolescents with TMD, through the Tampa Scale instrument (TSK/TMD). It is expected to find a decrease in kinesiophobia after the intervention performed, kscore that can range from 18-72. The higher the score on this scale, the greater the degree of kinesiophobia. ;Check the presence of anxiety in adolescents with TMD using the GAD-7 scale. Adolescents with TMD are expected to present higher degree of anxiety.The higher the score on this scale, the greater the degree of anxiety, which can range from 0-21, with 10 being the general cutoff point for identifying generalized anxiety disorder.

Countries

Brazil

Contacts

Public ContactAndreza Paes

Universidade do Estado de Santa Catarina

andrezagarrett@gmail.com+55(48)984180888

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 4, 2026