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临床试验/NCT02567123
NCT02567123终止不适用

The Effects of Gait Retraining in Runners With Patellofemoral Pain: A Randomized Trial

University of New Mexico2 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2014年11月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
21
试验地点
2
主要终点
Pain

研究概览

简要总结

The purpose of this study is to determine whether changing foot strike pattern from a rearfoot strike to a forefoot strike reduces chronic running-related knee pain. It is believed that switching foot strike pattern from a rearfoot strike to a forefoot strike pattern will reduce associated running-related patellofemoral knee pain.

详细描述

Runners will come to the Gait Analysis Lab on north campus of the University of New Mexico, HSSB 168, for the first running trial. During this time you will fill out a health questionnaire, receive an assessment by a physical therapist, and be given a new pair of running shoes to use for the duration of the study.

Runners will be equipped with several reflective markers, which will be placed on your lower body. Runners will then complete several passes across a runway while we record your running with a motion analysis system. Runners will be equipped with a mouthpiece and nose clip. You will run for 10 minutes while we collect the gases you breathe.Twenty-four hours after you complete this running trial, you will come to our Exercise Physiology lab in Johnson Center, B143 to perform the training sessions. During this time you will run for about 10-30 minutes in front of a mirror and receive feedback from the research team. You will perform these training sessions eight times over two weeks. Twenty-four hours after your last training session, you will perform another follow-up running trial, which will be the same as the first trial. After completing the second running trial, you will be allowed to return to your normal running routine for about one month. After one month, you will return to the Gait Analysis lab to perform a final running trial, which will be the same as the first and second running trials.

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 44 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Presence of patellofemoral pain
  • No history of any cardiovascular issues.
  • Currently running as part of training program

排除标准

  • No patellofemoral pain present.
  • Not currently running as part of training program
  • Other lower extremity pain and/or injury that interferes with ability to run.
  • Not in the selected age ranges
  • Presence of cardiovascular or cardiopulmonary diseases

结局指标

主要结局

Pain

时间窗: 6 weeks

次要结局

  • Patellofemoral Stress(6 weeks)
  • Knee range of motion(6 weeks)
  • ankle range of motion(6 weeks)
  • Patellofemoral contact force(6 weeks)
  • Knee abduction(6 weeks)
  • ankle flexion(6 weeks)
  • Knee flexion(6 weeks)
  • Achilles tendon force(6 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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