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临床试验/CTRI/2023/11/059436
CTRI/2023/11/059436已完成1 期

Comparative Effect of Wet Cupping and Rigid Taping on Individuals with Migraine Induced Trapezitis: A Randomised Clinical Trial

KLE Academy of Higher Education and Research1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2023年8月11日最近更新:

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
32
试验地点
1
主要终点
Headache Impact Test (HIT-6)

研究概览

简要总结

Aim: Todetermine the effect of wet cupping and rigid taping inindividuals with migraine induced trapezitis.

Inclusion Criteria:  Willingto participate, Agebetween 18 and 50 years, Intensityof 3 points and more on the Numerical Pain Rating Scale., Clinicallydiagnosed with migraine induced trapezitis.

Exclusion Criteria: Anyhistory of muscular or neurological disorders (except for migraine), Pregnancy,Diabetes Mellitus, Historyof allergy to tape, open wounds, Hypersensitiveskin, Any skin allergy, Anycontraindication to use cupping.

Ou  Outcome Measure: Headache Impact Test (HIT-6), Migrainedisability assessment (MIDAS) questionnaire, Rangeof Motion using Universal Goniometer, NumericalPain Rating Scale (NPRS), PainPressure Threshold

Procedure: GROUP A will be given wet cupping and conventional treatment and Group B will be given rigid taping  and conventional treatment this will last for 2 weeks with thrice per week.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • Willing to participate Age between 18 and 50 years Intensity of 3 points and more on the Numerical Pain Rating Scale.
  • Clinically diagnosed with migraine induced trapezitis.

排除标准

  • any history of muscular or neurological disorders (except for migraine) Pregnancy, Diabetes Mellitus History of allergy to tape, open wounds Hypersensitive skin Any skin allergy Any contraindication to use cupping.

结局指标

主要结局

Headache Impact Test (HIT-6)

时间窗: pre - at baseline | post - after 2 weeks

Migraine disability assessment (MIDAS) questionnaire

时间窗: pre - at baseline | post - after 2 weeks

Range of Motion using Universal Goniometer

时间窗: pre - at baseline | post - after 2 weeks

Numerical Pain Rating Scale (NPRS)

时间窗: pre - at baseline | post - after 2 weeks

Pain Pressure Threshold

时间窗: pre - at baseline | post - after 2 weeks

次要结局

未报告次要终点

研究者

发起方
KLE Academy of Higher Education and Research
申办方类型
Private medical college

研究点 (1)

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