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