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临床试验/NCT05812625
NCT05812625招募中不适用

Effectiveness of Myo-kinetic Stretching Exercises Versus Post-isometrics Relaxation Exercise With Traction in Patients of Cervical Radiculopathy

Riphah International University2 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2023年3月10日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
68
试验地点
2
主要终点
Cervical Pain

研究概览

简要总结

The goal of this clinical trial is to examine the effectiveness of Myo-kinetic stretching exercises versus post-isometric relaxation exercise in patients with cervical radiculopathy. Convenient sampling technique will be used to enroll the patients. Patients will be screened on the basis of pre formulated eligibility criteria. Written Consent will be taken from each patient for participation in the trial. The calculated Sample size of this study will be 68 calculated through Epitool. Group A will receive conservative baseline treatment consisted of hot pack therapy for 10 minutes and traction for 8 minutes. Myo-kinetic stretching exercises and group B will receive conservative baseline treatment and post-isometric relaxation exercise. The assessment of patients will be done at baseline, 4th and 8th week. The outcomes from patients will be calculated by using Numeric Pain Rating Scale (NPRS), Goniometer and Neck Disability Index. The comparison between pre-treatment and post-treatment data will be done after 8th week. Data will be analyzed through SPSS 25.

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
Single (Outcomes Assessor)

入排标准

年龄范围
30 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Duration of cervical pain more than 4 weeks.
  • History of positive Spurling test

排除标准

  • History of previous cervical surgery
  • Cervical spine tumor.
  • Rheumatoid arthritis, prolong steroid use and osteoporosis in cervical region.
  • Cervical spine fracture.

结局指标

主要结局

Cervical Pain

时间窗: 8 weeks

Cervical Pain will be measured by Numeric Pain Rating Scale

Neck Disability

时间窗: 8 weeks

Neck disability will be measured by Neck Disability Index

Cervical Range of motion

时间窗: 8 weeks

Cervical Range of motion will be measured by Goniometer

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 (2)

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