About this trial
Goal: This clinical study aims to investigate how the range of motion of the temporomandibular joints (TMJ) changes in relation to the patient's head posture. Furthermore, we will assess the efficacy of a specific physiotherapy program in improving TMJ mobility and influencing head alignment in patients undergoing orthodontic treatment or prosthetic reconstruction.
Scope: The project will evaluate TMJ function and head alignment in orthodontic or prosthetic patients aged 11-65. The core focus is to analyze the correlation between head posture and TMJ mobility and to measure changes in these parameters before and after the manual physiotherapy intervention.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients aged 11 to 13 years with a confirmed occlusion class (Class I, II, or III) with parental/legal guardian consent.
Patients aged 13 to 17 years with personal assent and parental/legal guardian consent.
Adult patients (up to 65 years of age) who have provided informed consent.
Disqualifiers
Inability to perform required study tests or procedures.
Positive safety tests indicating contraindications to manual intervention.
History of surgeries or trauma to the maxillofacial region.
Genetic defects or neurological disorders.
Trial design
Single group
Treatments tested in this trial
Manual therapy
Other intervention1. Performance of 2 manual therapy techniques immediately following the participant's initial examination. The participant remains secured in the device. The examiner performs manual therapy on each temporomandibular joint (TMJ) sequentially. The following procedures are performed consecutively: 6 sec. of Grade II distraction (traction) according to F. Kaltenborn on the TMJ, repeated 6 times; 6 seconds of Grade II lateral glide on the TMJ, repeated 6 times. Following the completed physiotherapy intervention, the digital axiograph examination is performed again. A comparative analysis of the performed examinations will be conducted 2. Instruction on homework exercises performed by the patient. The exercises are performed 6 times per day, each in a series of 6 repetitions, for a period of 4 to 6 weeks. They include: a) Head flexion in the cranio-cervical joint - Standing position near a door frame; the patient performs maximum head flexion while simultaneously resting the occiput against
Treatment groups
Trial outcomes
Primary outcomes
CROM device
Cervical spine movements
JMA (Jaw Motion Analyzer) Axiograph
TMJ movements
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: