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临床试验/NCT01954511
NCT01954511撤回不适用

Effects of Manual Therapy and Exercises Applied to Cervical Spine in Patients With Temporomandibular Disorders: Pilot Study

Universidade Federal de Sao Carlos0 个研究点开始时间: 2012年7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
撤回
发起方
主要终点
Changing in maximum mouth opening pain free

研究概览

简要总结

The objective of this study was to investigate the effect of a manual therapy and exercise program, focused on the rehabilitation of cervical function, on clinical signs and mandibular function in subjects with TMD.

详细描述

Temporomandibular disorder (TMD) is a general term that refers to disorders associated with the temporomandibular joint (TMJ) and the masticatory muscles. Among the main symptoms are pre-auricular pain (in the region of the TMJ) and/or pain in the masticatory muscles.

It's usual to observe that subjects with TMD also present cervical alteration. Beside this, cervical postural alterations produced by muscle tension can influence mandibular position.

The intervention protocol was based on manual therapy, stabilization exercises and stretching.

The technique are:.

  1. Upper cervical flexion mobilization;
  2. C5 central posterior-anterior mobilization;
  3. Stabilization exercise: Cranio-cervical flexor stabilization exercise
  4. Stretching of muscles: upper trapezius, scalenes, semispinalis capitis; splenius capitis, sternocleidomastoid

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients diagnosed with myogenic or mixed temporomandibular disorders

排除标准

  • Patients diagnosed with arthrogenic or discogenic temporomandibular disorders

研究组 & 干预措施

Manual therapy

No Intervention

Upper cervical flexion mobilization, C5 central posterior-anterior mobilization, Pressure biofeedback device

干预措施: Manual therapy (Other)

Manual therapy

No Intervention

Upper cervical flexion mobilization, C5 central posterior-anterior mobilization, Pressure biofeedback device

干预措施: Pressure biofeedback device (Device)

结局指标

主要结局

Changing in maximum mouth opening pain free

时间窗: Before and 5 days follow-up intervetion

The clinical signs was based on Research Diagnostic Criteria protocol and it was measured maximum mouth opening pain free using a caliper ((Somet, 150mm, Inox, Czechoslovakia)

次要结局

  • Changing of Pain(Before and 5 days follow-up intervetion)

研究者

发起方
Universidade Federal de Sao Carlos
申办方类型
Other
责任方
Principal Investigator
主要研究者

Bruno Leonardo da Silva Grüninger

Pt

Universidade Federal de Sao Carlos

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