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临床试验/NCT02498795
NCT02498795已完成不适用

Comparative Research Among 3 Action Protocol in Other to Approach Chronic Patellar Tendinopathy

Universidad de Zaragoza2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2019年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
2
主要终点
Change from baseline in functionality at 8 weeks as measured by Visa-p

研究概览

简要总结

The accomplishment of a treatment with Intratissue Percutaneous Electrolysis of additional form to the accomplishment of eccentric exercise's program in patients with chronic patellar tendinopathy is more effective than the accomplishment of an additional treatment with dry needling or eccentric exercise's program realized of isolated form.

详细描述

Experimental study randomized with double blind, whose purpose is to compare three protocols in those who apply different protocols of physical therapy to themselves in three groups of intervention with patients with chronic patellar tendinopathy.

There take part in this study young women of both sexes, of Zaragoza and of different sports clubs of entity 18 and 40 years, that they realize of habitual form (minimum 3 times a week) a sport. All of them present chronic patellar tendinopathy.

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
Triple (Participant, 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

  • Age understood between 18 and 40 years.
  • To practise any sport of habitual form.
  • Patients diagnosed of chronic patellar tendinopathy with a minimum of 3 months of evolution and with stable symptomatology.
  • Pain to the palpation of the tendon in the low pole of the knee and during the training or competition.
  • Punctuation of the questionnaire VISA-P under 80.

排除标准

  • Patient had an operation on the knee affected in the last 6 months.
  • Infiltrations in the knee affected in the last 3 months.
  • Patient who has received pharmacological treatment or physical therapy in the last 48 hours.
  • Pathology with less than 3 months of evolution.
  • To present bilateral chronic tendinopathy.
  • Punctuation of the questionnaire major or equal Visa - p of
  • Inability to apply someone of the techniques of treatment or valuation for absolute or relative contraindication.

结局指标

主要结局

Change from baseline in functionality at 8 weeks as measured by Visa-p

时间窗: 8 weeks

This scale consists of eight questions, the first six questions of which employ an analogical visual scale in order to assign a score of 0 to 10, where 10 represents the optimum state, for the purpose of quantifying pain and function in different activities, whereas the last two questions assess the level of functionality and ability to perform physical activity.

次要结局

  • Pain, as measured by Visual Analog Scale(0, 8 and 20 weeks)
  • Quality of life by SF-36(0, 8 and 20 weeks)
  • Thickness of the tendon, as measured by ultrasound scan(0, 8 and 20 weeks)
  • Height of the jump(0, 8 and 20 weeks)
  • Concentric force of the low members(0, 8 and 20 weeks)
  • Speed of the jump(0, 8 and 20 weeks)
  • Functionality, as measured by Visa-p(0 and 20 weeks)
  • Hypervascularity, as measured by ultrasound scan(0, 8 and 20 weeks)

研究者

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

Maria Pilar López Royo

Graduate

Universidad de Zaragoza

研究点 (2)

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