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临床试验/NCT05420896
NCT05420896已完成不适用

Electromyographic Evaluation of the Efficacy of Manual Therapy in Temporomandibular Joint

Bahçeşehir University2 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2021年6月10日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
34
试验地点
2
主要终点
Visual Analogue Scale (VAS)

研究概览

简要总结

Individuals with temporomandibular joint dysfunction (TMD) may experience changes in muscle activation as a result of symptoms such as pain and limitation of movement. The aim of this study is to examine the efficacy of manual therapy electromyographically in patients with TMD.

详细描述

TMD is a common condition in the community. It may occur due to factors such as trauma, stress, occlusal disorders. Symptoms include pain, limitation in mouth opening, joint voice, postural and psychosocial disorders. TMD/RDC diagnostic criteria are used in the classification of TMD, and accordingly, it is stated that it may originate from the joint, disc and chewing muscles. In the treatment, conservative treatments such as patient education, manual therapy and exercises are applied first.

Manual therapy is an effective physiotherapy method on pain and muscle dysfunctions in musculoskeletal problems. In our study, electromyographic changes of masticatory muscles will be examined by applying manual treatment to the masticatory muscles and cervical region in myofascial TMD patients according to TMD/RC.

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • No cognitive impairment
  • Diagnosed with temporomandibular joint(TMJ) dysfunction of myofascial origin,
  • Volunteers aged 18-65

排除标准

  • Malignancy and fracture of the cervical region and/or TMJ
  • Active infection
  • Patients actively receiving cervical and/or TMJ-related therapy

结局指标

主要结局

Visual Analogue Scale (VAS)

时间窗: Change from initial assessment to 4 weeks after initial assessment.

A Visual Analogue Scale (VAS) is one of the pain rating scales used for the first time in 1921 by Hayes and Patterson. It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms.

次要结局

  • Maximum Mouth Opening (MMO)(Change from initial assessment to 4 weeks after initial assessment.)
  • Functional Limitation Scale of the Jaw-8(Change from initial assessment to 4 weeks after initial assessment.)
  • TAMPA(Change from initial assessment to 4 weeks after initial assessment.)
  • Hospital Anxiety Depression Scale (HADS)(Change from initial assessment to 4 weeks after initial assessment.)
  • Electromyography (EMG)(Change from initial assessment to 4 weeks after initial assessment.)
  • Pain Pressure Threshold (PPT)(Change from initial assessment to 4 weeks after initial assessment.)

研究者

发起方
Bahçeşehir University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Kumru Ateş

PhD-C

Bahçeşehir University

研究点 (2)

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