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临床试验/PACTR201904468554670
PACTR201904468554670尚未招募未知

A comparison of the Alfredson and Silbernagel protocols in the management of chronic Achilles tendinopathy.

niversity of Cape Town0 个研究点目标入组 40 人开始时间: 2019年3月29日最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
All

入选标准

  • 1. The participant must be running for more than or equal to one year.
  • 2. They have to be aged between 35-55 years old with a BMI less than or equal to 30.
  • 3. The participants should, on assessment present with posterior lower limb pain in the mid-portion of the Achilles tendon area of at least 3 months duration and additionally fulfill at least one of the following diagnostic criteria;
  • (a) early morning pain over the mid-portion of the Achilles tendon,
  • (b) early morning stiffness over the mid-portion of the Achilles tendon,
  • (c) a history of swelling over the Achilles tendon area,
  • (d) tenderness to palpation of the mid-portion of the Achilles tendon,
  • (e) palpable nodular thickening over the affected Achilles, and/or
  • (f) movement of the painful area in the Achilles tendon with plantar-dorsi-flexion (positive ‘‘shift’’ test)
  • 4. VISA-A (Victorian Institute of Sports Assessment- Achilles) score less than 80.

排除标准

  • 1. Bilateral Achilles tendinopathy.
  • 2. History of current or past fluoroquinolone antibiotic use (within the last 12 months).
  • 3. Previous local corticosteroids injection in the Achilles tendon or the area surrounding the Achilles tendon prior to the onset of symptoms.
  • 4. A history of Achilles tendon rupture.
  • 5. Use of chronic medications
  • 6. Diagnosed connective tissue disorders or any other systemic diseases believed to be associated with tendinopathy, such as, but not limited to, Elhers-Danlos Syndrome, benign hypermobility joint syndrome, rheumatoid arthritis, systemic lupus erythematosus, hyperparathyroidism, renal insufficiency, diabetes mellitus and familial hypercholesterolemia.
  • 7. Insertional Achilles tendinopathy,
  • 8. Congenital or acquired lower limb deformities.
  • 9. Lower limb injury in the last 12 months and/or surgery to the lower limb in the last 2 years.
  • 10. Participants who have performed the exact or similar exercise protocol in the last 4 weeks or received other treatment for their tendinopathy will not be eligible to participate.

研究者

发起方
niversity of Cape Town

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