Changes in masticatory mechanosensitivity, mouth opening and head posture after intervention with a myofascial induction protocol
- Conditions
- Forward head postureMuscular MechanosensitivityMouth mobilityPhysical Medicine / Rehabilitation - PhysiotherapyMusculoskeletal - Other muscular and skeletal disordersOral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
- Registration Number
- ACTRN12612000733875
- Lead Sponsor
- niversity of Sevilla (Spain)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 48
(I) older than 25 years old; (II) absence of symptoms in the cervical spine, upper limbs and craniofacial area within the past four weeks previous to data collection; (II) willingness to participate in the study as declared in signing the informed consent form.
(I) a history of whiplash injury;
(II) a history of degenerative disorders of the central and/or peripheral nervous system;
(III) a history of cranial vault, craniofacial, temporomandibular joint, or any level of spinal fractures and/or surgery;
(IV) suffering or having suffered osteitis, or cranial-vault, craniofacial, or temporomandibular joint rheumatic or tumoural diseases; and
(V) consumption of analgesics or anti-inflammatory drugs within 48 hours prior to data collection
(VI) receiving soft tissue therapy within the year before the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method IMPROVEMENT OF CRANIOVERTEBRAL ANGLE IN AT LEAST 15%<br><br>The craniovertebral angle (CVA) is measured to be that between a horizontal line that crosses the body of the seventh cervical vertebra (C7) and the line from the tragus of the ear to the spinal apophysis of C7. Two lateral photographs are taken of the subject seated and standing still. For the first photograph, the subjects are asked to sit with their arms on their legs, and to rest their back and buttocks on the back of the chair, with both feet on the ground. The examiner instructs them to fix their gaze on an imaginary point on the wall directly in front. For the second photograph, the subjects stand still in a posture as natural as possible, with arms resting along the body, and directing their gaze as in the previous case.[AFTER INTERVENTION]
- Secondary Outcome Measures
Name Time Method INCREASE OF VERTICAL MOUTH OPENING(VMO) IN AT LEAST 10%<br><br>The maximum amplitude of VMO is measured using a digital gauge (Fino Digital Caliper, Model 59112, Germany) with a sensitivity of 0.01 mm. Measurements are made in two positions: (i) the subject supine with flexed hips and knees, and hands resting on the abdomen; and (ii) subject seated with back support and feet resting on the floor. The instruction given to the subject is simple: Open your mouth as much as possible without there being any sensation of pain or discomfort. The examiner then placed one end of the calliper on the middle incisor of the upper jaw incisor and the other on the central incisor of the jaw line. Three consecutive measurements were made, with a resting period of 30 seconds between each. The mean of the three measurements was taken as the value for the subsequent analyses. This procedure has proven to have high intra-examiner reliability (ICC=0.90-0.98)[AFTER INTERVENTIOn]