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临床试验/NCT01691170
NCT01691170已完成1 期

Quadriceps Femoris Strengthening Versus Hamstring Stretching for Patellofemoral Pain Syndrome: A Randomized Clinical Trial.

University of Sao Paulo2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2008年3月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
20
试验地点
2
主要终点
Numeric Pain Rating Scale

研究概览

简要总结

The patellofemoral pain syndrome (PFPS) is defined as a painful complaint in the anterior aspect of the knee, although peripatellar pain and / or retropatellar are also common. In general, conservative treatment is the initial option of choice for patients with PFPS, however, the lack of a specific causal factor makes it difficult to choose the best treatment so early. This way, the purpose of this study is investigate the effects of the quadriceps femoris strengthening versus hamstring stretching in patients with pattellofemoral pain.

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
None

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

  • Symptoms of anterior knee pain for at least 1 moth;
  • Average pain level of 3 or more on a 10-cm visual analogue scale during stepping up and down a 25-cm height;
  • Anterior or retropatellar knee pain on at least 2 of the following activities: prolonged sitting, climbing stairs, squatting, running, kneeling, and hopping/jumping;
  • Presence of 2 of the following clinical criteria on assessment: pain during apprehension test, pain during the patellar compression test, and crepitation during the compression test.

排除标准

  • Previous knee surgery or arthritis;
  • History of patellar dislocation or subluxation, malalignment, or ligament laxity;
  • Patellar tendon pathology or chondral damage;
  • Spinal referred pain;
  • History of other abnormalities such as leg length inequalities (>2 cm);
  • Medication as a part of the treatment;
  • Previous physical therapy or acupuncture treatment for the knee within the previous 30 days.

结局指标

主要结局

Numeric Pain Rating Scale

时间窗: Participants will be followed for the duration of 8 weeks.

Pain was assessed using an 11-point numeric pain rating scale (NPRS), on which 0 denoted an absence of pain and 10 denoted unbearable pain.

次要结局

  • Lysholm Scale(Participants will be followed for the duration of 8 weeks.)

研究者

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

Gabriel Peixoto Leão Almeida, PT

Principal Investigator

University of Sao Paulo

研究点 (2)

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