Assessment of the Efficacy of a Sensorimotor Approach After Maximum Three Sessions in Subjects With TMD With Hypertonia

Osteovox110 enrolled

Overview

The study aims to demonstrate the efficacy of the sensorimotor approach developed by A. Piron (taught to the patient in three sessions) regarding three parameters related to TMD: facial pain, functional incapacities and hypertonia. The subjects in the study are 18 to 77 years old and present the following conditions: a TMD disorder caused or aggravated by hypertonia and responsible for cervico-maxillo-facial pain and/or a functional incapacity in the last 30 days.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

110

Conditions

Temporomandibular Disorder

Interventions

Sensorimotor education with a view to obtaining an optimal FWS further to the relaxation of the masticatory, lingual and labial system. Learning of mandibular micro-movements in 5 directions.BEHAVIORAL

Eligibility

Sex: ALLMin age: 18 YearsMax age: 77 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Male or female subjects aged 18 to 77 years old. Subjects presenting the following 3 characteristics: 1. A TMD disorder (objectivized by the DC/TMD 2014); 2. Facial pain in the last 30 days (objectivized by the Graded Chronic Pain Scale version 2.0 (GCPS v2.0)) and/or functional incapacity (chewing, mobility, verbal and emotional communication) in the last 30 days (objectivized by the Jaw Functional Limitation Scale 20 (JFLS-20)); 3. Hypertonia (objectivized by the Oral Behaviors Checklist (OBC) short version and the Explanatory Model Scale). Subjects who agree to comply with the requirements of the study. Subjects who are of age (and know how to read and write) who have given their informed, explicit consent in advance to any procedure related to the trial, the study or the investigation conducted on human beings, with the objective of developing knowledge specific to the exercise of health care professions, as set out in Royal Decree No. 78 of 10 November 1967 on the practice of the health care professions (Act of 27 December 2005). Subjects insured under social security. Exclusion Criteria: * Any subject presenting at least one of the following criteria may not be included: * Significant medical problems involving the following conditions: Severe or progressive pathology (psychiatric, neurological, cardiopulmonary, renal, hepatic, endocrinological, hematological, neoplastic, infectious, metabolic or allergic). Any acute trauma of the temporomandibular joint (trauma within the last 72 hours). Severe anxiety or severe depression, as defined by a score greater than or equal to 15 on the HAD. * Pregnant women * Criteria related to prior or concurrent treatments: Treatment with antipsychotics, anxiolytics, soporifics or muscle relaxants started within the two months preceding the study. Treatment with intraoral implants during the study or in the two months preceding the study. \- Criteria related to lifestyle: Excessive alcohol consumption (WHO definition: more than two glasses per day for a woman and more than three for a man). Subjects undergoing withdrawal or taking a replacement substance. \- Criteria related to the subject: Subjects unlikely, in the investigator's view, to comply with the instructions in the protocol. Subjects unlikely, on the basis of a score \<2 to question "C" of the Explanatory Model Scale, to comply with the therapy. Subjects who had participated in a clinical trial in the previous month or were participating at the time of selection. Subjects without the linguistic or psychological capacity to understand and sign the informed consent form and complete the psychometric questionnaires and psychological tests. Exclusion criteria after acceptance in the study: In addition to becoming aware a posteriori of an error related to the inclusion or exclusion criteria defined above, the therapist may decide to remove a subject before completion of the study. The motivations for early exit are as follows: * Subject who no longer agrees to comply with the requirements of the study. * Occurrence of a major life stressor (score greater than 40 on the Holmes and Rahe Stress Scale). * Need to redirect the subject to a different treatment. Any early exit from the study, whether decided on by the subject, the therapist or both together, will be recorded on a specific document, indicating the date and the reasons for the early exit.

Locations (6)

Cabinet de Logopédie Liesens-Denis

Berneau, Liège, Belgium

Cabinet d'Ostéopathie PIRON

Beyne-Heusay, Liège, Belgium

Cabinet de groupe LHR

Saive, Liège, Belgium

Cabinet d'Ostéopathie Garcion

Nantes, Loire-Atlantique, France

Outcomes

Primary Outcomes

Overall relief (from 0% to 100%) based on the ratio of "complaint after treatment" to "complaint before treatment". Multiple measurements related to both pain and functional incapacity are aggregated to arrive at one reported value: complaint

Patient's complaint is calculated: * By integrating the weighting of both pain (P) and functional incapacity (FI) parameters in the complaint. 11 possibilities: \[100% P - 0% FI\] OR \[90% P - 10% FI\] OR \[80% P - 20% FI\] etc. * Patient's complaint = Pain and/or functional incapacity * Assessement of pain integrates 2 or 3 or 4 parameters: 2 are constant (intensity and frequency), 2 are optional (quality of life and drugs) because some painful patient don't take drug or don't have an altered quality of life. If there are 2 parameters, each = 50%; if 3 parameters, each = 33,3%; if 4 parameters, each = 25% * The scoring of the 4 pain parameters is based on questionnaires: Intensity: GCPS v2.0 (part 1): Score 0 to 100; Frequency (last month): Score 0 to 30; Drug: number of gram of the most specific medication (last month); Quality of life: GCPS v2.0 (part 2): score 0 to 6 * Assessement of functional incapacity integrates 1 parameter: the JFLS-20 questionnaire (score from 0 to 200)

Time frame: Beginning (day 0); during treatment (day 30 and day 90); end (day 180)

Secondary Outcomes

Evidence of a change from baseline in the "intensity" component of cervico-maxillo-facial pain (a component of the primary outcome measure), on the basis of a questionnaire called "the Graded Chronic Pain Scale Version 2 (GCPS v2.0) (part 1)".

3 Visual Analogic Scales (VAS) \> 0 to 10. The scoring = the mean (0 to 100).

Time frame: Beginning (day 0); during treatment (day 30 and day 90); end (day 180)

Evidence of a change from baseline in the "impact on quality of life" component of facial pain (a component of the primary outcome measure), on the basis of questionnaire called "the Graded Chronic Pain Scale Version 2 (GCPS v2.0) (part 2)".

3 Visual Analogic Scales (VAS) \> 0 to 10 and a 4th question about "how many days did pain keep the patient from doing usual activities" \> 0 to 30 days. These 4 questions lead to a incapacity score from 0 to 6

Data from ClinicalTrials.gov

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