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临床试验/CTRI/2025/02/081009
CTRI/2025/02/081009已完成不适用

Efficacy of multimodal physiotherapy on pain, range of motion and functional disability in subjects with cervicogenic headache: A Randomized Controlled Trial

Jiya Kharbe1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2025年4月1日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
32
试验地点
1
主要终点
1. flexion rotation test

研究概览

简要总结

This study aims to assess the effectiveness of multimodal physiotherapy in reducing pain, improving cervical range of motion, and decreasing functional disability in individuals with cervicogenic headache through a randomized controlled trial (RCT). Conducted at NITTE Deemed to be University, Mangaluru, the study includes 32 participants, randomized into two groups: the experimental group (receiving multimodal therapy plus conventional therapy) and the control group (receiving only conventional therapy). The intervention spans four weeks with two sessions per week, and assessments are conducted at baseline, week two, and week four by a blinded assessor. The control group undergoes TENS (10 minutes) and strengthening exercises, while the experimental group receives TENS (15 minutes, 100Hz frequency) with electrodes on C4 and C7 spinous processes, cervical SNAG mobilization on C2 facet joint, patient education, and strengthening exercises targeting cervical and scapular muscles. Data will be analyzed statistically to determine whether multimodal therapy provides superior benefits over conventional therapy alone in managing cervicogenic headache.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
19.00 Year(s) 至 25.00 Year(s)(—)
性别
All

入选标准

  • University students of various institution under Nitte Deemed to be University
  • Age 19-25 years old
  • Pain intensity on NPRS with a score between 3 to 8
  • One episode of pain in last 3 months
  • Flexion rotation test positive if restrictions more than 32 to 33 degrees
  • Headache impact test positive with score of 50 and above
  • Who are willing to participate in the given study.

排除标准

  • neuralgia) 2) Vertebrobasilar insufficiency 3) Trauma to neck in past 2 years 4) Surgery in past 2 years 5) History of neurological, cardiovascular and cerebral palsy 6) Long term corticosteroids 7) Severe operation around neck region.

结局指标

主要结局

1. flexion rotation test

时间窗: at baseline, 2nd week and 4th week

2. numerical pain rating scale

时间窗: at baseline, 2nd week and 4th week

次要结局

  • headache impact test-6(neck disability index)

研究者

发起方
Jiya Kharbe
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Jiya Kharbe

NITTE Deemed to be University

研究点 (1)

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