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临床试验/NCT02190890
NCT02190890已完成不适用

Effects of Different Deep Dry Needling Dosages on Pain and Postneedling Soreness in the Treatment of Patients With Cervical Myofascial Pain

Universidad Rey Juan Carlos0 个研究点目标入组 94 人开始时间: 2013年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
94
主要终点
Postneedling soreness

研究概览

简要总结

The purpose of this study are (1) to determine the effectiveness of different dry needling dosages in the treatment of myofascial trigger points in the upper trapezius muscle in patients with myofascial neck pain, (2) to assess postneedling soreness and tenderness and (3) evaluate the influence of psychological factors on the perception of postneedling soreness.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 53 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of an active myofascial trigger point. Neck pain: Superior to 3 cm in VAS

排除标准

  • Neck area: Fracture, radiculopathy, previous surgery, previous needling treatment in the last 6 months, previous analgesic medication (24 hours), psychiatric disease

结局指标

主要结局

Postneedling soreness

时间窗: 1 week

Visual analog scale. A 100mm VAS, ranging from 0mm (no pain) to 100mm (worst imaginable pain).

Pain

时间窗: 1 week

Visual analog scale. A 100mm VAS, ranging from 0mm (no pain) to 100mm (worst imaginable pain).

次要结局

  • Pressure pain threshold(1 week)
  • Pain in cervical range of motion(1 week)
  • Neck disability(1 week)
  • Cervical range of motion(1 week)
  • Psychological factors(Pre-intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Josue Fernandez Carnero

PhD

Universidad Rey Juan Carlos

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