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临床试验/NCT05683288
NCT05683288已完成不适用

Comparison of the Efficiency of Instrument Assisted Soft Tissue Mobilization and Myofascial Release Techniques in Individuals With Chronic Neck Pain

KTO Karatay University2 个研究点 分布在 2 个国家目标入组 48 人开始时间: 2022年12月28日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
48
试验地点
2
主要终点
Change from Baseline Cervical Pain assessed by Numeric Pain Scale.

研究概览

简要总结

The aim of this study is to determine whether EYYDM and myofascial applications have short and long-term effects on pain and disability in individuals diagnosed with chronic neck pain.

详细描述

Participants will be randomly assigned to IASTM, myofascial release and control groups. In addition to conventional treatment, IASTM and myofascial release groups will be treated twice a week for 4 weeks. Conventional treatment will be applied to the control group for 4 weeks.

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
18 Years 至 44 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • having a diagnosis of chronic neck pain,
  • To have given at least 3 values to the pain with the Numerical Pain Scale
  • having bilateral muscle spasms in the cervical region

排除标准

  • those who are taking any analgesic medication,
  • those with acute injury or infection,
  • those with open wounds,
  • osteoporosis,
  • fracture,
  • hematoma,
  • those with acute cardiac, liver and kidney problems,
  • those with connective tissue disease,
  • rheumatoid arthritis, osteoarthritis,
  • those with circulation problems,
  • those with peripheral vascular disease,
  • epilepsy,
  • history of surgery in the cervical region

结局指标

主要结局

Change from Baseline Cervical Pain assessed by Numeric Pain Scale.

时间窗: Baseline, 4 weeks

Pain will be evaluated with a 10-point Likert Numerical Pain Scale. 0 means no pain, 10 means unbearable pain.

次要结局

  • Change from Baseline Cervical Disability assessed by Neck Disability Index(Baseline, 4 weeks)

研究者

发起方
KTO Karatay University
申办方类型
Other
责任方
Sponsor

研究点 (2)

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