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临床试验/CTRI/2026/01/102237
CTRI/2026/01/102237尚未招募不适用

Effect of gong mobilization on cervical range of motion, deep cervical flexor muscle function, kinesiophobia and symptom inventory in patients with cervicogenic headache : a randomised control trial

bazila1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2026年2月4日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
32
试验地点
1

研究概览

简要总结

This study aims to evaluate the effect of gong mobilization on cervical range of motion deep cervical flexor muscle function and kinesiophobia in patients with cervicogenic headache. Cervicogenic headache is a secondary headache disorder originating from the cervical spine and is commonly associated with reduced neck mobility impaired muscle function and fear of movement. This prospective randomized controlled trial will include patients diagnosed with cervicogenic headache who meet the inclusion criteria. Participants will be randomly allocated into an experimental group receiving gong mobilization along with conventional physiotherapy and a control group receiving conventional physiotherapy alone. Outcome measures will include cervical range of motion deep cervical flexor muscle function and kinesiophobia assessed at baseline and after completion of the intervention. The findings of this study will help determine the effectiveness of gong mobilization as an adjunct intervention in the management of cervicogenic 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
Participant Blinded

入排标准

年龄范围
20.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • 1.Participants between age group of 20-40 years.
  • 2.Diagnosis based on the International Classification of Headache Disorders (ICHD)
  • Unilateral pain, usually starting in the neck and radiating to the front of the neck.
  • 4.Headache associated with neck stiffness, reduced Cervical ROM or dysfunction at C1 C2 segment.
  • 5.Positive Cervical Flexion-Rotation test (FRT) eg: less than 32 rotation towards symptomatic side 6.Both genders will be included.
  • 7.Patient who will give informed consent & will be able to attend SGT hospital for treatment & assessment.

排除标准

  • Patient with evidence of CNS involvement, cervical radiculopathy, myelopathy, Disc herniation or peripheral neuropathies.
  • 2.Known history of high-level spinal cord injury, malignancy & Central pain syndrome (e.g., Fibromyalgia).
  • Subjects diagnosed with any severe cardiovascular conditions.
  • Any recent major surgeries.
  • Cognitive impairment or psychiatric disorder.
  • Unwillingness to adhere to the intervention protocol.

研究者

发起方
bazila
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Bazila

school of physiotherapy

研究点 (1)

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