Evaluation of Different Treatment Modalities in Children With Myalgia or Arthralgia in the Temporomandibular Region - a Randomized, Single-blinded, Controlled Non-inferiority Study
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 入组人数
- 150
- 试验地点
- 2
- 主要终点
- Responders to treatment - median weekly pain intensity
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Investigator)
盲法说明
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
入排标准
- 年龄范围
- 7 Years 至 13 Years(Child)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •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.
排除标准
- •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.
研究组 & 干预措施
Jaw exercises
Resistance exercises to do twice a day
干预措施: Jaw exercises (Behavioral)
Jaw exercises
Resistance exercises to do twice a day
干预措施: Counseling (Behavioral)
Counseling
Just information at the first visit
干预措施: Soft occlusal appliance (Device)
Counseling
Just information at the first visit
干预措施: Jaw exercises (Behavioral)
Counseling
Just information at the first visit
干预措施: Counseling (Behavioral)
Jaw exercises
Resistance exercises to do twice a day
干预措施: Soft occlusal appliance (Device)
Soft occlusal appliance
Individually casted appliances
干预措施: Soft occlusal appliance (Device)
Soft occlusal appliance
Individually casted appliances
干预措施: Jaw exercises (Behavioral)
Soft occlusal appliance
Individually casted appliances
干预措施: Counseling (Behavioral)
结局指标
主要结局
Responders to treatment - median weekly pain intensity
时间窗: 1-6 months
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
时间窗: 1-6 months
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
次要结局
- Change in emotional status(1-6 months)
- Daily activities(1-6 months)
- Change in physical functioning using the Graded Chronic Painscale (GCPS)(1-6 months)
研究者
Nikolaos Christidis
Associate professor, Senior Lecturer, Senior Consultant
Karolinska Institutet
