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临床试验/ACTRN12617000675325
ACTRN12617000675325终止未知

The correlation of changes in the neural mechanisms associated with pain and patient reported improvement in pain and function in mid-portion Achilles tendinopathy: A mechanistic cohort study

The University of Notre Dame Australia0 个研究点目标入组 9 人开始时间: 2017年5月10日最近更新:
适应症

试验速览

阶段
未知
状态
终止
入组人数
9

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 60 Years(—)
性别
All

入选标准

  • Recreational or competitive runner
  • *Can have ceased running due to AT
  • *No limit on distance or running duration per week
  • Reported pain for greater than 3 months
  • Reported local Achilles Pain (<2 fingers width)
  • Reported local Achilles Stiffness
  • Reported impairment of functional activity
  • *Local A-P Thickening of the mid-portion AT
  • *Hyperechoic area of the mid-tendon with colour Doppler signal within the area
  • Ability to given informed consent
  • Able to complete questionnaires
  • Able to begin Baseline Testing and Intervention within 2 weeks of recruitment

排除标准

  • - VISA-A score of greater than 80/100, 12 week wash out from other treatments,
  • - Corticosteroid injection within the past 12 months,
  • - Bilateral Achilles Tendinopathy,
  • - Insertional Achilles Tendinopathy,
  • - Previous Fracture lower limb within 12 months,
  • - Systemic Disease (Diabetes, Rheumatic Conditions, Circulatory Disorders, Neurological Disorders),
  • - Foot or Ankle Surgery in the previous 6 months,
  • - Regular intake of medication which may have an influence on outcome (Statins, Fluoroquinolones),
  • - Confounding lower limb or ankle injury,
  • - Confounding Injury for CPM (chronic lumbar pain, recurrent or chronic tension headache, migraine, whiplash, painful OA etc),
  • - Current Radiculopathy
  • - Contra-indications to Cold application (Cold Uticaria, Raynaud’s Phenomenon, Skin Conditions).

研究者

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