Effectiveness of Myofascial Release and Exercises Therapy in the Treatment of Temporomandibular Disorders: a Randomized Clinical Trial
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Temporomandibular Joint Disorders
- Sponsor
- Universidad de Almeria
- Enrollment
- 64
- Primary Endpoint
- Intensity of pain (100-mm VAS)
- Status
- Completed
- Last Updated
- 10 years ago
Overview
Brief Summary
Objectives: The aim of this research is to compare the effectiveness of myofascial release therapy and exercise therapy on pain, quality of sleep, anxiety, trigger points, and joint sounds in individuals with temporomandibular disorders and myofascial pain-dysfunction syndrome.
Material and Methods: A single-blind randomized clinical trial will be conducted in a university research clinic. Sixty-four subjects with temporomandibular disorders and myofascial pain-dysfunction syndrome will be randomly assigned to physical therapy group (myofascial release protocol and Rocabado exercise therapy) and control group (exercise therapy). Intensity of pain, quality of life, quality of sleep, anxiety, trigger points, and joint sounds will be collected at baseline, and forty-eight hours after the intervention phase.
Investigators
Adelaida María Castro-Sánchez
PhD (Lecturer)
Universidad de Almeria
Eligibility Criteria
Inclusion Criteria
- •Presence of myofascial pain with or without jaw opening limitation (Ia and Ib) according to the Research Diagnostic Criteria for Temporomandibular Disorders (RDC / TMD).
- •A chief complaint of acute pain (duration \< 6 months) in the temporomandibular joint on at least one side.
- •The presence of joint clicking during jaw opening that was eliminated on protrusive opening.
- •Agreement to attend evening therapy sessions.
Exclusion Criteria
- •Subjects with dental pain or tender muscles caused by systemic diseases.
- •Major psychological disorders.
- •A recent history of trauma in the face and neck area.
- •Subjects wearing full or partial dentures.
- •Edentulism.
- •Therapeutic co-interventions during treatment.
- •Indication for surgical treatment of temporomandibular joint.
Outcomes
Primary Outcomes
Intensity of pain (100-mm VAS)
Time Frame: Changes from baseline in intensity of pain at twelve weeks
A 100-mm VAS was used for determining pain intensity, ranging from 0 (no pain) to 100 (very severe pain).
Secondary Outcomes
- Physical parameters of active and passive mouth opening(Changes from baseline in active and passive mouth opening at twelve weeks)
- Physical parameters of pain in masseter muscles(Changes from baseline in pain in temporalis muscles at twelve weeks)
- State and trait anxiety (state anxiety questionnaire and trait - STAI)(Changes from baseline in state and trait anxiety at twelve weeks)
- Physical parameters of pain in lateral pterygoid muscles(Changes from baseline in pain in lateral pterygoid muscles at twelve weeks)
- Quality of Sleep (Pittsburgh Sleep Quality Index - PSQI)(Changes from baseline in quality of sleep at twelve weeks)
- Physical parameters of pain in temporalis muscles(Changes from baseline in pain in temporalis muscles at twelve weeks)
- Physical parameters of lateral condyle pole and temporal tendon insertion pain(Changes from baseline in Lateral condyle pole and temporal tendon insertion pain at twelve weeks)
- Physical parameters of clicking sound when opening / close palpation(Changes from baseline in clicking sound when opening / close palpation at twelve weeks)