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临床试验/NCT06731114
NCT06731114招募中不适用

"Additional Effects of Sternocleidomastoid Release Along With Suboccipital Muscle Release in Management of Cervicogenic Headache'

Foundation University Islamabad1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2024年7月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
54
试验地点
1
主要终点
Pain Intensity

研究概览

简要总结

This study is a randomised control trial and the purpose of this study is to determine the "Additional effects of sternocleidomastoid release along with suboccipital muscle release in management of cervicogenic headache".

详细描述

Cervicogenic headache is a common headache that causes disability and affects everyday activities. Headache related disorders are the second most common reason for years lived with disability all over the world. According to the latest International Headache Society model, cervicogenicheadache (CGH) is a secondary headache having C1-C2 dysfunction. There is marked limitation in cervical ROM specially rotation. Treatment indicated involves use of electrotherapy and thermal modalities. In addition, use of different manual therapy techniques are advocated to eliminate the root cause i.e. C1-C2 dysfunction treating. patients with cervicogenic headache are mostly presented with forward head posture and weak deep neck flexors which may excerbate the headache symptoms.Therefore The purpose of this study is to determine the ""Additional effects of sternocleidomastoid release along with suboccipital muscle release in management of cervicogenic headache

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
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Participants will be included according to international classification of headache criteria which includes:
  • •Headache with neck stiffness
  • •Headache at least once a month in the last 3 months
  • •Headache with at least 4 score in Numeric Pain Rating Scale(NPRS)
  • •Unilateral headache with no shift of side
  • •Positive flexion rotation test (Rotation restriction is greater than 10 degrees)
  • •C1-C2 dysfunction
  • •Headache precipitated by sustained neck movements,myofacial trigger points palpation in neck
  • •Age group 18-45
  • •Both male and female

排除标准

  • •Cervical spondylosis
  • •Headache of non-cervical origin
  • •Dizziness or visual disturbance
  • •Cervical radiculopathy/ nerve root involvement/ disc herniation
  • •Cervical instability/ fracture
  • •Vertebrobasilar insufficiency
  • •Thoracic outlet syndrome
  • •Cervical spine surgery
  • •Cervical spondylolisthesis
  • •Spinal infection or tumors
  • •Osteoporosis
  • •meningitis
  • •subarachnoid hemorrhage

研究组 & 干预措施

Group A

Experimental

On group A we will perform suboccipital muscle release (3 repititions 3 mins)9 minutes along with conventional physical therapy including TENS and hot pack for 10 mins 6 days a week for consective 2 weeks.

干预措施: Suboccipital muscle release (Procedure)

Group A

Experimental

On group A we will perform suboccipital muscle release (3 repititions 3 mins)9 minutes along with conventional physical therapy including TENS and hot pack for 10 mins 6 days a week for consective 2 weeks.

干预措施: Conventional physical therapy (Procedure)

Group B

Experimental

On group B we will perform sternocleidomastoid release for 5 mins along with suboccipital muscle release and coventional physical therapy including TENS and hot pack for 10 mins 6 days a week for consective 2 weeks .

干预措施: Suboccipital muscle release (Procedure)

Group B

Experimental

On group B we will perform sternocleidomastoid release for 5 mins along with suboccipital muscle release and coventional physical therapy including TENS and hot pack for 10 mins 6 days a week for consective 2 weeks .

干预措施: Conventional physical therapy (Procedure)

Group B

Experimental

On group B we will perform sternocleidomastoid release for 5 mins along with suboccipital muscle release and coventional physical therapy including TENS and hot pack for 10 mins 6 days a week for consective 2 weeks .

干预措施: Sternocleidomastoid release (Procedure)

结局指标

主要结局

Pain Intensity

时间窗: 2 weeks

Pain will be measured on the basis of Numeric Pain Rating Scale score.

ROM

时间窗: 2 weeks

Cervical rotation will be measured through CROM device

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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