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临床试验/NCT03455933
NCT03455933已完成不适用

Action Mechanisms Responsibles for the Effects of Shock Waves on the Pressure Pain Thresholds

Centro Universitario La Salle2 个研究点 分布在 1 个国家目标入组 63 人开始时间: 2018年5月7日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
63
试验地点
2
主要终点
Pressure pain threshold

研究概览

简要总结

The aim of this study is to evaluate whether the intensity of pain perceived during the application of extracorporeal shockwave therapy (ESWT) is determinant for producing changes in pressure pain threshold (PPT) in asymptomatic subjects. The investigators will perform a single controlled random trial to three groups. Two of them will receive ESWT whereas the third group will get a cold pressure test (CPT).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Absence of pain or illness
  • No changes in cognitive ability
  • Good command of Spanish, both spoken and written

排除标准

  • People with systemic diseases, tumors, infections, pacemakers, clotting disorders, skeletally immature, fibromyalgia, whiplash history, dizziness or in physiotherapeutic or pharmacological treatment
  • Pregnant women

研究组 & 干预措施

Shockwave Light Pain Group

Experimental

Sham Comparator. It will received a light intensity shockwave in the lateral epicondyle regulated until reach a 3/10 in the Visual Analog Scale (VAS) scale.

干预措施: Sham Comparator (Other)

Shockwave Moderate Pain Group

Experimental

Experimental Intervention. It will received a moderate intensity shockwave in the lateral epicondyle regulated until reach a 6/10 in the Visual Analog Scale (VAS) scale.

干预措施: Experimental Intervention (Other)

Cold Pressure Group

Other

Control Group. The cold pressure test will be apply to this group. The investigators will use a container with an outer part filled with ice and an inner part filled with water, both separated by a screen that prevents direct contact between the ice and the hand. The water will be regularly stirred to maintain the temperature near to 0.7ºC.

干预措施: Control Group (Other)

结局指标

主要结局

Pressure pain threshold

时间窗: through study completion, an average of 1 month

The investigators will use a digital algometer (Force Ten FDX Wagner) to measure when pressure becomes pain.

次要结局

未报告次要终点

研究者

发起方
Centro Universitario La Salle
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ibai López de Uralde Villanueva

Clinical Professor and Principal Investigator

Centro Universitario La Salle

研究点 (2)

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