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Use of Wii Fit (TM) to Increase Compliance With Home Exercises in Treating Patellofemoral Syndrome

2012年8月27日 更新者:University of Manitoba

The Use of Wii Fit ™ to Increase Compliance With Home Exercises for Treatment of Patellofemoral Syndrome in Adolescent Females

To determine the utility of the Wii Fit TM interactive video game program in patellofemoral symptom resolution, development of increased muscle strength and flexibility as a result of increased compliance with home exercises in adolescent females with patellofemoral syndrome.

研究概览

详细说明

Patellofemoral syndrome (PFS) is a very common diagnosis amongst adolescents and young adults. Symptoms can be chronic in nature and interfere with sporting activity and activities of daily living. Current treatment consists of home exercises to increase muscular strength and flexibility. Adolescents are known to have poor compliance with treatments for chronic illnesses.

There is a paucity of published literature surrounding the Wii TM Interactive Video Game. There has been one published report of the use of Wii Fit TM in rehabilitation where participants used the Wii Fit TM to train proprioception after ankle injury. Individuals that participated in the Wii Fit TM group found improvement in their balance on objective measures as well as increased enjoyment with their treatment plan. One anecdotal report used the Wii TM video game in physiotherapy treatments of a college athlete and found a dramatic increase in attendance compliance after introduction of the video game.

This randomized controlled study will determine if using the Wii Fit TM for home exercise completion will increase compliance and subsequently improve symptoms related to patellofemoral syndrome in adolescent females.

研究类型

介入性

注册 (实际的)

22

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Manitoba
      • Winnipeg、Manitoba、加拿大、R2M 5L6
        • Legacy Sport Medicine

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

11年 至 17年 (孩子)

接受健康志愿者

有资格学习的性别

女性

描述

Inclusion Criteria:

  • Female between ages of 11 and 17 years of age
  • A diagnosis of patellofemoral syndrome with one or more of the following symptoms: anterior knee pain, positive theater sign, stairs provoking knee pain.
  • No physiotherapy or regular, structured home exercise program is being followed
  • Parental/guardian consent to participate
  • Patient assent to participate

Exclusion Criteria:

  • Patients participating in physiotherapy at the time of initial assessment or have had physiotherapy in the last 6 months for patellofemoral syndrome
  • Patients performing regular home exercise program prescribed by physician, physiotherapist, or other allied health professional for patellofemoral syndrome at time of initial assessment
  • Patients who have additional knee pathology (e.g. acute patellar dislocation; acute internal knee derangement (i.e. meniscal, ligament injury); osteochondritis dissecans; severe apophysitis or tendinitis) that could interfere with rehabilitation exercises due to pain or instability from these conditions
  • Individuals with history of knee surgery
  • Individuals that have a Wii Fit TM video game at home
  • Individuals for whom consent and assent is not obtained

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Wii Fit (TM) Interactive Video Game
Use of interactive video game exercise program on a daily basis focusing on quadriceps and hamstring flexibility along with VMO strengthening.
其他名称:
  • Nintendo Wii Fit (TM)
有源比较器:Traditional Home Exercise Program
Completion of daily home exercise program for quadriceps and hamstring flexibility and VMO strengthening.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Percentage of Exercise Days Completed.
大体时间:3 months
Calculated for the 12 week period as daily exercise completion rate as percentage
3 months

次要结果测量

结果测量
大体时间
Changes in Patellofemoral Symptoms
大体时间:3 months
3 months
Change in Hamstring Flexibility
大体时间:3 months
3 months
Change in Quadriceps Flexibility
大体时间:3 months
3 months
Change in Vastus Medialis Oblique Muscle Strength
大体时间:3 months
3 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Erika B Persson, MD、University of Manitoba

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2009年10月1日

初级完成 (实际的)

2010年9月1日

研究完成 (实际的)

2010年9月1日

研究注册日期

首次提交

2009年11月3日

首先提交符合 QC 标准的

2009年11月3日

首次发布 (估计)

2009年11月4日

研究记录更新

最后更新发布 (估计)

2012年9月27日

上次提交的符合 QC 标准的更新

2012年8月27日

最后验证

2010年6月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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