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临床试验/NCT02219230
NCT02219230已完成不适用

Outcomes Associated With Use of Passive, Adaptive, and Active Prosthetic Knees in Persons With Unilateral, Transfemoral Amputation: a Randomized Crossover Trial

University of Washington1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2011年6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
12
试验地点
1
主要终点
Timed Stair Test

研究概览

简要总结

The goals of this study are to assess measured, observed, and self-reported outcomes achieved through the use of passive (mechanical), active(motorized) and adaptive (magnetorheological) prosthetic knee control systems in individuals with unilateral, transfemoral amputation.

详细描述

An interrupted time-series trial with pre/post baseline assessments, randomized crossover of interventions, and within-phase repeated measures is used to evaluate and compare the effectiveness of the Össur Power Knee II and the Össur Rheo Knee in individuals with unilateral, transfemoral amputation. A rigorous and clinically-meaningful experimental protocol is applied to verify study participants receive appropriate training, experience, and assessment in each knee condition. A suite of standardized and ad-hoc physical performance tests, patient-reported questionnaires, and monitoring technologies were carefully selected to assess important, clinically-relevant participant outcomes. Comparative effectiveness of three prosthetic knee interventions are evaluated using direct measurement (i.e., timed tests), observed clinical ratings (i.e., subjective assessments of gait quality) and self-report instruments (i.e., health status surveys). Analyses will focus on identifying differences between control system technologies inherent to each type of prosthetic knee (i.e., passive [mechanical], adaptive [magnetorheological], and active [power]). Outcomes will be used to establish recommendations for which activities and patients knees are most appropriate or likely to produce a desired effect.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
盲法
Single (Participant)

入排标准

年龄范围
45 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •age 45 - 75
  • •body weight less than 275lbs
  • •unilateral amputation between the hip and knee
  • •amputation due to non-vascular causes
  • •no other major limb amputations
  • •amputation occurred at least 2 years prior
  • •stable limb volume (i.e., at least 6 months on an unmodified prosthetic socket)
  • •intact skin tissue without open wounds or sores for at least 2 months
  • •physiologically stable medical condition (i.e., non-degenerative)
  • •possession and regular (i.e., daily) use of a prosthesis with a prosthetic knee with non-microprocessor (i.e., mechanical or fluid) stance control
  • •Medicare functional classification level (MFCL or "K-level") 3

排除标准

  • •expect to receive or are expected to require a replacement prosthetic socket within 15 months
  • •complete reliance on an assistive device (i.e., cane or walker) for ambulation

研究组 & 干预措施

Prosthetic knee

Experimental

Subjects crossed over between interventions (three different prosthetic knees). Knee conditions include 1) Active knee (Ossur Power Knee II); 2) Adaptive knee (Ossur Rheo); and 3) Passive knee (Various manufacturers)

干预措施: Passive knee (Various manufacturers) (Device)

Prosthetic knee

Experimental

Subjects crossed over between interventions (three different prosthetic knees). Knee conditions include 1) Active knee (Ossur Power Knee II); 2) Adaptive knee (Ossur Rheo); and 3) Passive knee (Various manufacturers)

干预措施: Active knee (Ossur Power Knee II) (Device)

Prosthetic knee

Experimental

Subjects crossed over between interventions (three different prosthetic knees). Knee conditions include 1) Active knee (Ossur Power Knee II); 2) Adaptive knee (Ossur Rheo); and 3) Passive knee (Various manufacturers)

干预措施: Adaptive knee (Ossur Rheo) (Device)

结局指标

主要结局

Timed Stair Test

时间窗: Change from Baseline (mean score at weeks 1, 2, 3, and 4) to Follow-Up (mean score at weeks 8, 12, 16, 20, 24, and 28)

Timed performance test that involves walking up and down 6 steps.

Step activity

时间窗: Change from Baseline (mean score at weeks 1, 2, 3, and 4) to Follow-Up (mean score at weeks 8, 12, 16, 20, 24, and 28)

Average daily step counts measured by an accelerometer-based device.

Obstacle course time

时间窗: Change from Baseline (mean score at weeks 1, 2, 3, and 4) to Follow-Up (mean score at weeks 8, 12, 16, 20, 24, and 28)

Time to walk a 1/2-mile outdoor walking course.

Timed Up and Go

时间窗: Change from Baseline (mean score at weeks 1, 2, 3, and 4) to Follow-Up (mean score at weeks 8, 12, 16, 20, 24, and 28)

Timed performance test that measures rising from a chair, walking 3m, and returning to a seated position.

Timed Ramp Test

时间窗: Change from Baseline (mean score at weeks 1, 2, 3, and 4) to Follow-Up (mean score at weeks 8, 12, 16, 20, 24, and 28)

Timed performance test that involves walking up and down a 14ft ramp.

次要结局

  • Reported Falls(Change from Baseline (mean score at weeks 1, 2, 3, and 4) to Follow-Up (mean score at weeks 8, 12, 16, 20, 24, and 28))
  • Prosthesis Evaluation Questionnaire (PEQ)(Change from Baseline (mean score at weeks 1, 2, 3, and 4) to Follow-Up (mean score at weeks 8, 12, 16, 20, 24, and 28))
  • Activities Specific Balance Confidence Scale (ABC)(Change from Baseline (mean score at weeks 1, 2, 3, and 4) to Follow-Up (mean score at weeks 8, 12, 16, 20, 24, and 28))
  • Patient Reported Outcomes Measurement Information System (PROMIS)(Change from Baseline (mean score at weeks 1, 2, 3, and 4) to Follow-Up (mean score at weeks 8, 12, 16, 20, 24, and 28))

研究者

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

Brian Hafner

Associate Professor

University of Washington

研究点 (1)

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