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Motor Imagery and Rehabilitation in Temporomandibular disorders

Graded Motor Imagery as an aditional tool for rehabilitation in Temporomandibular disorders - GMI and temporomandibular disorders

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
REBEC
Registry ID
RBR-82f4tb
Enrollment
Unknown
Registered
2019-06-21
Start date
2019-06-10
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 joint

Interventions

The volunteers will be randomly assigned into two treatment groups: a group that will receive only conventional physiotherapeutic treatment (CONV) that will be the control group of the study (n=32)
and another group that will receive the conventional treatment associated with the GMI techniques (CONV + IMG), which is considered the experimental group (n=32). For conventional treatment it is stab
joint mobilizations
kinesiotherapy for strengthening exercises and stretching of the masticatory and neck muscles. GMI is a 6-week exercise protocol that includes three phases: recognition of laterality, explicit imagery
Behavioural

Sponsors

Universidade Federal de Uberlândia
Lead Sponsor
Universidade Federal de Uberlândia
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Individuals diagnosed with TMD, according to the RDC / TMD classification; who present pain as one of the main symptoms of the dysfunction; for at least 3 months and with intensity of at least 3 according to the Visual Analogue Scale (VAS).

Exclusion criteria

Exclusion criteria: History of previous central pathologies and / or cognitive alterations that make it impossible the comprehension of the methods that will be used

Design outcomes

Primary

MeasureTime frame
To evaluate whether GMI techniques incorporated into conventional physiotherapeutic treatment in individuals with clinical diagnosis of TMD are effective in producing satisfactory primary outcomes in pain reduction and functional improvement of these individuals, when compared to control group. If this is the case, these techniques may be easily incorporated into the treatment of patients with persistent pain which is not responsive to conventional tretaments, which is very common in this population.

Secondary

MeasureTime frame
Reduce fear of pain related to movement and function through gradual exposure of movement.

Countries

Brazil

Contacts

Public ContactJulia Santos

Universidade Federal de Uberlândia

juliasantos@ufu.br553432182929

Outcome results

None listed

Source: REBEC (via WHO ICTRP)