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临床试验/NCT06537661
NCT06537661进行中(未招募)不适用

VIRTUAL REALITY and TEMPOROMANDIBULAR DISORDER FOLLOWING MAXILLOFACIAL SURGERY

Cairo University2 个研究点 分布在 1 个国家目标入组 2 人开始时间: 2024年3月10日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
2
试验地点
2
主要终点
Measure pain

研究概览

简要总结

Sixty eight patients who have TMJ pain and ROM restriction after maxillofacial surgery participated in this study , they are selected from government hospitals (general and insurance ).

Will be randomly divided into two equal groups ( group A, group B ). Their ages range from 20 - 35 years.

The Purpose of the study is to evaluate the therapeutic efficacy of VR in decreasing pain and improve ROM for Patients after maxillofacial surgery.

详细描述

Sixty eight patients who have TMJ pain and ROM restriction after maxillofacial surgery participated in this study , they are selected from government hospitals (general and insurance ).

Will be randomly divided into two equal groups ( group A, group B ). Their ages range from 20 - 35 years.

The VR glasses which were the source of visual and auditory feedback, were connected by Bluetooth to a mobile phone and all the videos of selected tasks (tasks of Active mobility exercises and isometric contraction exercises, massage exercises) were turned on. Active mobility exercises (jaw opening 6 times of 30 s; lateralization 10 times of 5 s; protrusion 10 times Of 5 s).

  • Self-massage masticatory Muscles, After each session.
  • Isometric contraction exercises The Purpose of the study is to evaluate the therapeutic efficacy of VR in decreasing pain and improve ROM for Patients after maxillofacial surgery.

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
Double (Participant, Investigator)

入排标准

年龄范围
30 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • The subject selection will be according to the following criteria:
  • Patients after Arthrocentesis .
  • Patients after Temporomandibular joint condylar discopexy.
  • Age ranges between 30 - 45 years.
  • All patients will have informed consent .

排除标准

  • • Surgery That conducted on the temporomandibular joint (meniscectomy, arthroscopy, etc.).
  • oral surgery (e.g., surgery for impaction of the third molar), as well as patients with concomitant systemic or neurological conditions.

结局指标

主要结局

Measure pain

时间窗: 6weeks

Measure by visual analog scale (VAS) 0: low in pain 10:high in pain

次要结局

  • Maximum mouth opnening (MMO )(6weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nehal mohamed soliman Elbkery

Principal investigator

Cairo University

研究点 (2)

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