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临床试验/NCT01397981
NCT01397981已完成1 期

Evaluation of Haptic Technologies for Movement Retraining

Stanford University1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2011年7月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
25
试验地点
1
主要终点
Measure: Knee pain and function

研究概览

简要总结

The purpose of this study is to determine how well people can be trained to produce new and different movements through the use of haptic feedback. One particular application is retraining individuals to walk differently in order to reduce knee joint loads to prevent or treat knee osteoarthritis as an alternative to surgical treatments.

详细描述

During the movement retraining session, you be given different combinations of haptic, visual, and auditory feedback in order to inform you on desired movement changes. This will take place at the Human Performance Laboratory at Stanford University. Motion analysis will be done while you perform movement activities (such as locomotion).

Prior to performing these movement tasks the investigators will attach reflective markers to your body using tape, pre-wrap and/or ace bandages. The investigators will record motion of your body's movements using infrared cameras which capture anatomical data from the reflective markers on your body.

The investigators will provide you with feedback to inform you of desired movement modifications. Haptic feedback devices such as vibration motors and skin stretch devices will be attached to your body via velcro straps and will be used to give "touch" feedback. There will be a computer monitor in front of you during testing to provide visual feedback. Sounds will be played using speakers near the testing area to provide auditory feedback.

The time needed for set up and performance of the above set of tests is approximately 90 minutes. You will be performing walking and other movements for only a small part of that time. The rest of the time will be spent preparing you for the experiment. After the investigators examine your movement data, if some of the data appear inaccurate or the investigators are unable to process the data, the investigators may ask you to repeat the movement analysis at a later time.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Symptoms of medial compartment pain during the previous 6 weeks
  • •Radiographic evidence (AP X-ray) of medial compartment knee osteoarthritis (KL score of 3 or less)
  • •Ability to walk unaided for 25 minutes without rest
  • •Age > 18

排除标准

  • •BMI > 30
  • •Previous injury or surgery on foot, ankle, knee, hip, or back inhibiting ability to adopt different walking gait
  • •Use of shoe insert or hinged knee brace
  • •Corticosteroid injection within the previous 6 weeks
  • •Age > 80

研究组 & 干预措施

Walking modification

Experimental

Changing kinematics for walking

干预措施: Gait retraining (Behavioral)

结局指标

主要结局

Measure: Knee pain and function

时间窗: four weeks

Knee pain and function will be assessed through the standardized KOOS survey

次要结局

  • Learning retention, knee adduction moment(four weeks)

研究者

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

Pete Bradley Shull

Dr.

Stanford University

研究点 (1)

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