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临床试验/NCT02841384
NCT02841384已完成不适用

McConnell Patellar Taping in Static and Dynamic Postural Control of Women With Patellofemoral Pain Syndrome: Randomized Clinical Trial and Blind

Universidade Estadual de Londrina2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2016年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
2
主要终点
change the balance after the intervention by force platform

研究概览

简要总结

Introduction: Patellofemoral pain syndrome (PFPS) is related to the previous sore knee, change functionality and postural control deficits. One of the possibilities for pain control and better positioning of the patella is the rigid bandage patellar widely used by clinicians and researchers.

Objective: To evaluate the effect of rigid patellar bandage on postural control, pain and function in sedentary women with PFPS.

Methods: The sample will be composed of 30 volunteers, sedentary, between 18 and 55 years; randomized group Bandage Functional Rigid (n = 15) and Banding Placebo (n = 15). All fill the Personal Data Sheet, Visual analog scale Pain Questionnaire Previous Knee Pain Scale; and will be submitted to analysis of postural control (static and dynamic) and carry out the test and sit up in pre conditions and post application of the bandage.

Hypothesis: Expected to observe the effect of rigid patellar bandage in pain, function and postural control in sedentary women with PFPS.

详细描述

This is a randomized controlled trial and blind in the exercise area, postural control and biomechanics.

The subjects with a clinical diagnosis of PFPS will be allocated in two groups: PFPS group with rigid bandage patella (n = 15) and PFPS group with placebo (n = 15).

Procedures: The subjects with a clinical diagnosis of PFPS, will be forwarded to the evaluation protocols. The data collections will be held at University Hospital Physiotherapy Division of the State University of Londrina. Individuals respond to a questionnaire to characterize the sample, EVA and fill the patellofemoral disorders Scale (AKPS).

Data Collection Protocol: will be held to familiarize themselves with the equipment and tests to be used on the force platform and test sitting and standing, voluntary is inserted in one of the groups (PPS + B or PPS + P) through randomisation previously established by www.random.org and stored in opaque and sealed envelopes.

Following the participants carry out, random and drawn at the time way, the static and dynamic tests on the force platform:

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
Single (Participant)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Clinical diagnosis of patellofemoral dysfunction issued by a specialist orthopedic knee and provide anterior knee pain of 3 or more on the Visual Analogue Scale (VAS) for a minimum of 8 weeks prior to evaluation;
  • Previous retropatellar pain or knee, for at least 3 of the following: up / down stairs, squatting, running, kneeling, sitting for long periods and insidious onset of symptoms unrelated to trauma.

排除标准

  • History of severe / traumatic knee injury, surgery history in the locomotor system;
  • Patellar luxation history; clinical evidence of meniscus injury; ligamentous instability; patellar tendinitis.
  • Presence of neurological, cardiovascular or rheumatologic diseases; pregnancy; diabetes,
  • Abnormal sensitivity in the plantar;
  • Medication and / or therapy in the last six months and hypersensitivity or allergy to tape.

研究组 & 干预措施

Group taping McConnell

Other

Taping patellar McConnell: Lateralization correction of the patella with self-adhesive rigid bandage Johnson® positioned lateral border of the patella to the medial condyle of the femur, allowing the lifting of the medial border of the patella and stretching of the knee lateral structures.

干预措施: taping patellar McConnell (Other)

Group placebo taping

Other

Placebo taping through vertical application of patellar rigid taping, with the knee in flexion without medialization of the patella.

干预措施: Placebo taping (Other)

结局指标

主要结局

change the balance after the intervention by force platform

时间窗: before and immediately after the intervention

It will be measured the oscillations through various force platform variables before and after the intervention (taping or placebo, depending on the group) to see if there is change in the balance after the implementation of these interventions.

次要结局

未报告次要终点

研究者

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

Christiane Macedo

First investigator

Universidade Estadual de Londrina

研究点 (2)

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