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临床试验/NCT02292355
NCT02292355已完成不适用

Effect of the Method Pilates in Women With Temporomandibular Disorders - Clinical Trial

Federal University of Rio Grande do Sul1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2015年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
Pain Intensity Measure

研究概览

简要总结

Introduction: the influence of temporomandibular disorders (TMD) related to postural changes are yet no consensus, but it is believed that the imbalances of a system can influence another. Several techniques have been used to treat TMD and its associated problems, however there is a paucity of studies evaluating the effects of global treatments, such as Pilates, in individuals with TMD literature. Objective: To evaluate changes in the level of pain, the severity of TMD, the EMG activity of masticatory muscles and posture of young women undergoing training in Pilates, as well as correlating postural changes, pain level, severity of TMD and EMG activity of masticatory muscles. A randomized clinical trial with blinded assessors will be held. 40 patients divided randomly into two groups will be assessed, the control group (CG) who receive conventional treatment with occlusal splint and intervention group (IG), which in addition to conventional treatment will undergo Pilates sessions. Both groups will be formed for women aged 18 to 35 years with TMD and pain. The IG will receive treatment with the Pilates Method for 15 weeks with frequency of twice weekly and use occlusal splint as directed by the dentist. The CG will make use of occlusal splint alone. At the beginning and end of the 15 weeks the individuals are evaluated to verify the presence of TMD, TMD severity, pain, EMG evaluation of masticatory muscles and body posture. Data will be analyzed statistically.

详细描述

t-test or Mann-Whitney test will be used to compare data before and after 15 weeks of treatment.

Multiple Two-Way ANOVAs will be used to compare treatment and evaluation period, for each depended variable: effects of pain, severity of TMD, EMG activity of masticatory muscles and posture.

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 (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Women between 18 and 35 years old;
  • •Possess temporomandibular disorder diagnosed by the Research Diagnostic Criteria for Temporomandibular Disorders (RDC / TMD) and classified into categories of severity of functional limitation through the Mandibular Function Impairment Questionnaire MFIQ
  • •Owning a complaint of pain in the TMJ region, classified as greater than 2.5 (moderate to high) by the Visual Analog Scale.

排除标准

  • •Have greater than 35 kg / m2 body mass index (BMI);
  • •Diagnosis of other disorders of the stomatognathic system;
  • •Have a history of any surgical procedure on the face, teeth and spine in the last six months;
  • •Possess severe pathologies of the spine (fractures, inflammatory diseases or tumors);
  • •Provide framework for intellectual disability or inability to give consistent information;
  • •Being in treatment for TMD, be it physical therapy, medical or dental care throughout the study period.
  • •Being practicing Pilates in the last six months;
  • •Being pregnant;
  • •Make use of dental prosthesis or appliance;
  • •Have a history of trauma to the face and temporomandibular joint in the last six months;
  • •Having presented temporomandibular joint dislocation in the last six months;
  • •Possess dental flaws between canines and molars.
  • •Provide cross bite, overbite or open bite;
  • •Presenting undershot or overshot jaw;
  • •Present vestibular disorders that may interfere with the balance
  • •Make use of continuous medication for pain or inflammation.

研究组 & 干预措施

Pilates

Experimental

Intervention group will undergo Pilates sessions in addition to conventional treatment with occlusal splint

干预措施: Pilates (Other)

Occlusal splint

No Intervention

Control group who receive conventional treatment with occlusal splint

结局指标

主要结局

Pain Intensity Measure

时间窗: 15 weeks

Pain intensity will be assessed using visual analog scale (VAS), which consists of a 10-cm horizontal line in which "0" means "No pain" and "10" means "The worst pain I can imagine".

次要结局

  • Posture(15 weeks)
  • Severity of TMD(15 weeks)
  • EMG activity of masticatory muscles(15 weeks)

研究者

发起方
Federal University of Rio Grande do Sul
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jefferson Fagundes Loss

Doctor

Federal University of Rio Grande do Sul

研究点 (1)

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