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临床试验/NCT05665452
NCT05665452已完成不适用

Efficacy of Adding Patellar Mobilization to Hip and Knee Exercises in Patients With Patellofemoral Pain Syndrome

Cairo University1 个研究点 分布在 1 个国家目标入组 59 人开始时间: 2023年1月15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
59
试验地点
1
主要终点
Changes in functional disability

研究概览

简要总结

Patellofemoral pain syndrome is a common source of anterior knee pain. The causes of PFPS may be multifactorial such as biomechanical disorders, muscle weakness which affect the dynamic stability of lower limb and alter patellar tracking in trochlear groove. Moreover, the syndrome associated with muscular tightness of iliotibial band, gastrocnemius, soleus, hamstring and quadriceps. Strengthening and stretching exercises are effective in improving patient's symptoms. However, they do not sufficient in correction of kinematic changes associated with PFPS. Patellar mobilization is effective in improving patient'symptoms in cases with PFPS. However, studies that conducted patellar mobilization were either low quality studies or no study combined patellar mobilization with hip and knee exercises.

Therefore, APTA guidelines recommended for conducting high quality study to investigate the effect of adding patellar mobilization to exercise therapy to support the definite recommendation delivered to therapists.

详细描述

this is interventional study in which patients will receive stretching and strengthening exercises in control group. in addition, experimental group will receive the same exercises of control group in addition to patellar mobilization, retinacula release and deep friction message.

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 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age ranging between 18 and 35 years
  • Tenderness of medial and lateral borders of patella
  • Retropatellar pain
  • Duration of symptoms of patellofemoral pain syndrome is greater than 4 weeks
  • Positive patellar compression test
  • Pain intensity is more than 3 at visual analogue scale
  • Had a history of insidious onset
  • Had anterior knee pain during 2 or more of provocative activities that include stair ascent or descent, kneeling, prolonged sitting, or squatting

排除标准

  • Previous patellar realignment surgery or patellar fracture
  • Had a history of traumatic patellar dislocation
  • Had a history of previous knee surgery
  • Had any form of inflammatory arthritis that include osteoarthritis or rheumatoid arthritis
  • Had a history of knee menisci, ligaments, bursae, or synovial plica syndrome dysfunction
  • Taking corticosteroids or nonsteroidal anti-inflammatory medication
  • Inability to attend treatment program to the end of sessions

结局指标

主要结局

Changes in functional disability

时间窗: It will be assessed one week before and after treatment

Functional disability will be assessed using Kujala questionnaire.The scale ranges from 0 to 100 score where 100 represents no functional limitation.

Changes in pain that felt during ascending, descending, squatting and prolonged sitting

时间窗: It will be assessed one week before and after treatment

Pain during ascending, descending, squatting and prolonged sitting will be assessed using visual analogue scale, it is a horizontal line from 0 to 10, where 0 no pain and 10 maximum pain.

次要结局

  • changes in hamstring flexibility(It will be assessed one week before and after treatment)
  • Changes in hip external rotators strength(It will be assessed one week before and after treatment)
  • changes in quadriceps strength(It will be assessed one week before and after treatment)
  • changes in functional performance(It will be assessed one week before and after treatment)
  • changes in gastrocnemius flexibility(It will be assessed one week before and after treatment)
  • changes in foot pronation(It will be assessed one week before and after treatment)
  • Changes in hip abductors strength(It will be assessed one week before and after treatment)
  • changes in knee valgus(It will be assessed one week before and after treatment)

研究者

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

Nadia Abdo Mohamed Abdelhafez

Assistant lecturer at orthopedic department of faculty of physical therapy

Cairo University

研究点 (1)

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