Dry Needling and Manual Therapy for the Management o Cervicogenic Headache.
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 150
- 试验地点
- 1
- 主要终点
- Â Pain (Numerical Pain Rating scale).
研究概览
简要总结
The cause of CGH isthought to lie in any of the structures that are innervated by the first three cervicalnerves. This study examines about the dry needling and manual therapy for themanagement of patient with Cervicogenic Headache. As previous studies fails toinvestigate about the dry needling and manual therapy for the management ofpatient with Cervicogenic Headache, this study intends to discuss in detail aboutthe proposed topic and also proposes the model. This study will help the futureresearchers to know about how dry needling and manual therapy helps in themanagement of patient with Cervicogenic Headache as combined modality.Analyzing the existing researches, this research aims to provide a clear overview easymanagementofcervicogenicheadache.
Effects of dryneedling andmanual therapyImprovement in headachedisability index ,Improved range of motion ,Improved quality of life, reduce pain and tenderness for the management of patient withCervicogenic Headache.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Investigator Blinded
入排标准
- 年龄范围
- 20.00 Year(s) 至 50.00 Year(s)（—）
- 性别
- All
入选标准
- •Based on the following conditions the individuals are included in the study:
- •Both male and female with the age group of 20-50 years.
- •Persons fulfilling the diagnostic criteria given by IHS (international headache society.
- •Positive FRT (flexion-rotation test) and restricted ROM.
排除标准
- •Following participants were excluded from the study:
- •Cervical spine injury, fracture or surgery.
- •Congenital spinal deformity.
- •The participants not meeting age criteria for inclusion.
- •Cervical radiculopathy or presenting neurological deficit.
- •Participants with history of recent trauma.
- •Participants suffering from dizzy spells.
- •Vertebral malignancy.
- •Vertebral-basilar insufficiency.
- •Bone infections.
- •10 Any participants who were taking anti-inflammatory or muscle relaxant medication were excluded.
- •Any participants who failed to comply with the consent form were excluded.
结局指标
主要结局
 Pain (Numerical Pain Rating scale).
时间窗: Before and After the treatment( duration is 4 weeks)
Subjective outcome measures:
时间窗: Before and After the treatment( duration is 4 weeks)
Quality of life (QOL Questionnaire)
时间窗: Before and After the treatment( duration is 4 weeks)
Headache disability index (HDI questionnaire)
时间窗: Before and After the treatment( duration is 4 weeks)
Objective outcome measures:
时间窗: Before and After the treatment( duration is 4 weeks)
Tenderness (PPT Algometer)
时间窗: Before and After the treatment( duration is 4 weeks)
Cervical range of motion
时间窗: Before and After the treatment( duration is 4 weeks)
次要结局
- Not Applicable(NA)