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Treatment of Temporomandibular Disorders in Children and Adolsecents (TMD/PED)

Primary Purpose

Temporomandibular Disorder, Myalgia, Arthralgia of TMJ

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Soft occlusal appliance
Jaw exercises
Counseling
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Temporomandibular Disorder focused on measuring Children, Mixed dentition, Primary dentition, Adolescents, Myalgia, Arthralgia of TMJ, Treatment, Side-effects

Eligibility Criteria

7 Years - 13 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age 7-14 years
  • a diagnosis of myalgia or arthralgia according to DC/TMD
  • self-assessed average TMD pain intensity of ≥ 30 mm on a 100-mm visual analogue scale (VAS) during one week prior to examination.

The patients will remain included with one or several co-diagnoses of:

  • disc displacement with or without reduction according to DC/TMD
  • degenerative joint disease.

Exclusion Criteria:

  • diagnosed systemic muscular or joint diseases (e.g. fibromyalgia, rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis)
  • whiplash associated disorder (WAD)
  • neuropathic pain or neurological disorders (e.g. myasthenia gravis, orofacial dystonia)
  • history of psychiatric disorders, and 5) pain of dental origin.

Sites / Locations

  • Karolinska Institutet, Department of Dental MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Soft occlusal appliance

Jaw exercises

Counseling

Arm Description

Individually casted appliances

Resistance exercises to do twice a day

Just information at the first visit

Outcomes

Primary Outcome Measures

Responders to treatment - median weekly pain intensity
30% decrease in median weekly pain intensity using a numeric rating scale 0-10 rating the worst pain daily
Responders to treatment - Patients global impression change scale
The patients global impression change scale (PGIC) will be used. PGIC is a 7-point scale with the following options: 0 = eliminated, 1 = much improved, 2 = improved, 3 = unchanged, 4 = impaired, 5 = much impaired and 6 = very much impaired

Secondary Outcome Measures

Change in physical functioning using the Graded Chronic Painscale (GCPS)
The graded chronic pain scale include 3 questions regarding pain intensity and 3 questions regarding physical functioning. The mean of the 3 questions regarding provide us with the characteristic pain intensity while the mean of the physical functgioning questions together with sick leave (from work/school) provide us with information about how pain affects physical functioning. Characteristic pain intensity ranges from 0-100 while physical functioning is graded from 0-IV. The lower, the better outcome for all subscales. GCPS is a stanrd tool in the Diagnostic Criteria for temporomandibular disorders (DC/TMD) and part of Axis II which also the questionnaires for the emotional status in Oiutcome 3 are.
Change in emotional status
Changed scores in questionnaires from Axis II in DC/TMD, including stress using the Perceived Stress Scale-4 (PSS-4), anxiety/depression using the Patient Health Questionnaire-4 (PHQ-4) and the psychosocial situation using the Youth Self-report (YSR) Lower scores in these questionnair represent a better outcome The PSS and PHQ-scales are not combained and ranges from 0-4 for each questions. The YSR is based on several subscales, including the DCM-IV.
Daily activities
This outcome is based on a daily question of school attendance as well as free-time activities. The question is did you attend at school today or did you stay at home due to your orofacial pain. Question 2. Did you do your free-time activity or did you stay at hom due to your orofacial pain

Full Information

First Posted
February 20, 2019
Last Updated
October 3, 2023
Sponsor
Karolinska Institutet
Collaborators
Folktandvården Stockholms län AB
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1. Study Identification

Unique Protocol Identification Number
NCT03849534
Brief Title
Treatment of Temporomandibular Disorders in Children and Adolsecents
Acronym
TMD/PED
Official Title
Evaluation of Different Treatment Modalities in Children With Myalgia or Arthralgia in the Temporomandibular Region - a Randomized, Single-blinded, Controlled Non-inferiority Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2023 (Actual)
Primary Completion Date
December 31, 2026 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Folktandvården Stockholms län AB

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Children and adolescents are treated with routine treatment approaches for adults and one of the most commonly used treatments are occlusal appliances. The use of occlusal appliances in managing orofacial pain conditions is supported by evidence, but only for adults. However, the efficacy of the treatment approaches and any possible side-effects/impairment of mandibular growth are absent. Therefore, the aim of this project is to investigate the effectiveness and possible side-effects of different treatment modalities, such as an occlusal appliance, jaw exercises, NSAID for the conditions myalgia orarthralgia in the orofacial region in children with primary or mixed dentition.
Detailed Description
It is well known that the impact of pain in the orofacial region is not only the unpleasant sensory experience but also an emotional experience with feelings of failure, misery, guilt, alienation, and co-morbid depression. TMD is a collective term embracing chronic pain conditions affecting the temporomandibular joint or the masticatory muscles as well as their associated structures. TMD has a prevalence of approximately 10-20% and is 1.5 to 2 times more prevalent in women. It is often associated with restricted mouth opening capacity, pain upon chewing, muscle soreness and headache, thus affecting quality of life considerably although it is not life threatening. The prevalence of reported chronic pain in children and adolescents is high, and similar to the prevalence in adults. The worldwide variation in the prevalence of TMD in children and adolescents ranges from 6% to 69%. Many studies reported that TMD, headache and abdominal pain are the most common chronic pain affecting children and adolescents. Children and adolescents are treated with routine treatment approaches for adults and one of the most commonly used treatments are occlusal appliances. The use of occlusal appliances in managing orofacial pain conditions is supported by evidence, but only for adults. However, the efficacy of the treatment approaches and any possible side-effects/impairment of mandibular growth are absent. To our knowledge the only two high-quality studies present have investigated adolescents with permanent dentition (12-19 years), but there are no studies in the growing child with primary or mixed dentition (7-14 years). Hence, there is no knowledge if there is an effective treatment and if such a treatment with a resilient occlusal appliance impair the mandibular growth in these children. Taken together there is immense need for research on treatment of children/adolescents with orofacial pain and following their growth in order to be able to provide effective and safe treatment. Also, to investigate the knowledge-base among care-givers, giving the opportunity to improve the content of the education which in turn would lead to better, faster management of these children/adolescents who actually are our future. Therefore, the aim of this non-inferiority project is to investigate the effectiveness and possible side-effects of different treatment modalities, such as an occlusal appliance, jaw exercises, NSAID for the conditions myalgia orarthralgia in the orofacial region in children with primary or mixed dentition. The hypotheses are that: 1) there will be no significant differences in treatment outcome between the use of a soft occlusal appliance and standardized jaw exercises in children with myalgia but that the soft occlusal appliance and the standardized jaw exercises are superior to instructions of self-care; 2) the soft occlusal appliance does not affect the mandibular growth nor the dental eruption pattern; 3) there will be no significant differences in treatment outcome between the use of a soft occlusal appliance, or NSAIDs in children with arthralgia, but that the soft occlusal appliance and the NSAIDs are superior to instructions of self-care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Temporomandibular Disorder, Myalgia, Arthralgia of TMJ
Keywords
Children, Mixed dentition, Primary dentition, Adolescents, Myalgia, Arthralgia of TMJ, Treatment, Side-effects

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Non-inferiority study with two patient arms that are randomized to one of three different treatment arms. 75 children with TMD myalgia are randomized to one of three treatment arms 75 children with TMD arthralgia are randomized to one of three treatment arms
Masking
Investigator
Masking Description
The investigator is blinded to treatment that is performed by a specialist in orofacial pain. The patient is instructed to not reveal the treatment to the investigator
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Soft occlusal appliance
Arm Type
Active Comparator
Arm Description
Individually casted appliances
Arm Title
Jaw exercises
Arm Type
Active Comparator
Arm Description
Resistance exercises to do twice a day
Arm Title
Counseling
Arm Type
Active Comparator
Arm Description
Just information at the first visit
Intervention Type
Device
Intervention Name(s)
Soft occlusal appliance
Intervention Description
According to Best Practice in Sweden the soft occlusal appliance is ranked as gold standard for children with mixed or primary dentition
Intervention Type
Behavioral
Intervention Name(s)
Jaw exercises
Intervention Description
The participants do three exercises twice a day. Open and closing mouth against resistance as well as stretch
Intervention Type
Behavioral
Intervention Name(s)
Counseling
Intervention Description
The patients are instructed to minimize jaw parafunctions, chewing chewing gum etc, to do exercises, to take pain-killers or NSAIDs etc.
Primary Outcome Measure Information:
Title
Responders to treatment - median weekly pain intensity
Description
30% decrease in median weekly pain intensity using a numeric rating scale 0-10 rating the worst pain daily
Time Frame
1-6 months
Title
Responders to treatment - Patients global impression change scale
Description
The patients global impression change scale (PGIC) will be used. PGIC is a 7-point scale with the following options: 0 = eliminated, 1 = much improved, 2 = improved, 3 = unchanged, 4 = impaired, 5 = much impaired and 6 = very much impaired
Time Frame
1-6 months
Secondary Outcome Measure Information:
Title
Change in physical functioning using the Graded Chronic Painscale (GCPS)
Description
The graded chronic pain scale include 3 questions regarding pain intensity and 3 questions regarding physical functioning. The mean of the 3 questions regarding provide us with the characteristic pain intensity while the mean of the physical functgioning questions together with sick leave (from work/school) provide us with information about how pain affects physical functioning. Characteristic pain intensity ranges from 0-100 while physical functioning is graded from 0-IV. The lower, the better outcome for all subscales. GCPS is a stanrd tool in the Diagnostic Criteria for temporomandibular disorders (DC/TMD) and part of Axis II which also the questionnaires for the emotional status in Oiutcome 3 are.
Time Frame
1-6 months
Title
Change in emotional status
Description
Changed scores in questionnaires from Axis II in DC/TMD, including stress using the Perceived Stress Scale-4 (PSS-4), anxiety/depression using the Patient Health Questionnaire-4 (PHQ-4) and the psychosocial situation using the Youth Self-report (YSR) Lower scores in these questionnair represent a better outcome The PSS and PHQ-scales are not combained and ranges from 0-4 for each questions. The YSR is based on several subscales, including the DCM-IV.
Time Frame
1-6 months
Title
Daily activities
Description
This outcome is based on a daily question of school attendance as well as free-time activities. The question is did you attend at school today or did you stay at home due to your orofacial pain. Question 2. Did you do your free-time activity or did you stay at hom due to your orofacial pain
Time Frame
1-6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age 7-14 years a diagnosis of myalgia or arthralgia according to DC/TMD self-assessed average TMD pain intensity of ≥ 30 mm on a 100-mm visual analogue scale (VAS) during one week prior to examination. The patients will remain included with one or several co-diagnoses of: disc displacement with or without reduction according to DC/TMD degenerative joint disease. Exclusion Criteria: diagnosed systemic muscular or joint diseases (e.g. fibromyalgia, rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis) whiplash associated disorder (WAD) neuropathic pain or neurological disorders (e.g. myasthenia gravis, orofacial dystonia) history of psychiatric disorders, and 5) pain of dental origin.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nikolaos Christidis, PhD
Phone
+46700374967
Email
nikolaos.christidis@ki.se
First Name & Middle Initial & Last Name or Official Title & Degree
Sofia Louca Jounger, PhD
Phone
+46852488229
Email
sofia.louca@ki.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nikolaos Christidis, PhD
Organizational Affiliation
Karolinska Institutet, Department of Dental Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska Institutet, Department of Dental Medicine
City
Huddinge
ZIP/Postal Code
141 04
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nikolaos Christidis, PhD, DDS
Phone
+46852488000
Email
nikolaos.christidis@ki.se
First Name & Middle Initial & Last Name & Degree
Nikolaos Christidis, PhD, DDS
First Name & Middle Initial & Last Name & Degree
Georgios Tsilingaridis, Professor
First Name & Middle Initial & Last Name & Degree
Idil Alatli Burt, PhD, DDS
First Name & Middle Initial & Last Name & Degree
Sofia Louca, PhD, DDS
First Name & Middle Initial & Last Name & Degree
Raghdah Abduljabbar, DDS

12. IPD Sharing Statement

Learn more about this trial

Treatment of Temporomandibular Disorders in Children and Adolsecents

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