None listed
Conditions
Brief summary
We hypothesized that, in decreasing muscular mechanosensitivity will have a positive impact in parameters that are strongly related to the functionality of the cranio mandibular axis. So after the intervention protocol, we will find an immediate increase in vertical mouth opening and head posture
Interventions
MYOFASCIAL INDUCTION PROTOCOL The protocol began with an induction technique in the deep fascia of the temporal region. The subject was placed supine and the therapist sat at the head of the table. The therapist places one of her hands on the temporal muscle and the other one at the zygomatic arch. Maintaining this position, the cranial hand exerts a slight pressure in cranial direction and the caudal hand does the same in caudal direction. After reaching the relaxation of the tissue (about 4 minutes of time), the caudal hand moves toward the chest respecting any soft tissue restrictions during this advance. The technique was applied bilaterally (first in the dominant side and then in the non-dominant side of the body). Then, it was performed a myofascial technique in the masseter muscle. Remaining at the therapist-patient position, the therapist places one hand at the zygomatic arch and the other one just below, performing a cranial traction with her cranial hand and a caudal traction with the other hand. The technique lasts approximately 4 minutes. Having performed this maneuver in both sides, the protocol was completed with the masster muscle induction in a transverse direction. For this, the therapist places three fingers on the insertion of the muscle in both zygomatic arches and sustained pressure is applied to the midline of the face. The whole protocol lasted approximately 20 minutes and involved only a single session
Sponsors
Study design
Eligibility
Inclusion criteria
(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.
Exclusion criteria
(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