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临床试验/NCT06598826
NCT06598826已完成不适用

Graston Technique Versus Kinesio Taping on Myofascial Pain Syndrome After Neck Dissection Surgery

Cairo University1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2024年5月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
52
试验地点
1
主要终点
Range of motion (ROM) (cervicallateralflexion)

研究概览

简要总结

This study was conducted to investigate the effect of Graston technique versus Kinesiotaping on myofascial pain syndrome after neck dissection surgery.

详细描述

Fifty two patients from both genders who had cervical Myofascial pain syndrome following a neck dissection surgery participated in this Study. Their ages ranged from 30 to 50 years. They had been selected from the National Cancer Institute, Cairo University. They were assigned randomly into two groups (A) and (B), equal in number. Group (A) received Graston technique (IASTM), in addition to traditional treatment (range of motion exercises, stretching exercises and strengthening exercises) for 12 Sessions performed in a period of 4 weeks (three times weekly). While Group (B) Received kinesiotaping, in addition to traditional treatment (range of motion exercises, stretching exercises and strengthening exercises) for 8 sessions performed in a period of 4 weeks (twice weekly). Pressure pain threshold, visual analogue scale and cervical lateral flexion and rotation were measured pre and post 4 weeks of treatment.

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
None

入排标准

年龄范围
30 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • The subjects were selected according to the following criteria:
  • The patient's ages ranged from 30 to 50 years participated in this study. Both genders participated in this study. All patients had a history of MPS at UTM from 3 to 5 months. All patients had moderate to severe pain (VAS score >4). Informed consent was obtained from every patient enrolled in the trial. All patients had myofascial pain syndrome after unilateral modified radical neck dissection surgery.

排除标准

  • The potential participants were excluded if they meet one of the following criteria:
  • A wound in the affected area A cervical disk lesion Myelopathy or radiculopathy Cervical spine fracture or spondylolisthesis Rheumatoid arthritis Epilepsy or any psychological disorders Contraindications to IASTM. Contraindications to Kinesiotaping. Coagulopathy. Hemophilia or other clotting disorders.

结局指标

主要结局

Range of motion (ROM) (cervicallateralflexion)

时间窗: Pretreatment, post treatment ( after 4 weeks of treatment)

Universal Goniometer is a reliable instrument used to evaluate Range of motion in degrees

Range of motion (ROM) (cervical rotation)

时间窗: Pretreatment, post treatment ( after 4 weeks of treatment)

Universal Goniometer is a reliable instrument used to evaluate Range of motion in degrees

Pressure pain threshold

时间窗: Pretreatment, post treatment ( after 4 weeks of treatment)

Pressure Algometer with a spring is used. They maintain a peak force or pressure (KP (kilopond) = 10 N, Newton = 100 kPa (kilopascal)) until tared

Assessment of pain

时间窗: Pretreatment, post treatment ( after 4 weeks of treatment)

Vasual Analogue Scale(VAS) is used technique for assessing pain intensity , a continuous scale with a vertical or horizontal line of 100 mm, from 0 to10, whose extremes are designated "no pain" and "worst imaginable pain" (0= no pain; 10= most painful imaginable pain).

次要结局

未报告次要终点

研究者

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

Hasnaa Abd-Elfatah Mohamed

Physiotherapy specialist

Cairo University

研究点 (1)

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