跳至主要内容
临床试验/NCT07530601
NCT07530601尚未招募不适用

Multidimensional Assessment of a New Ankle-Foot Prosthesis in Daily Use: User Comfort, Safety, and Biomechanical Performance

Vrije Universiteit Brussel2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2026年4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
尚未招募
入组人数
120
试验地点
2
主要终点
Comparative Scales: Comfort, Safety, Fatigue and Pain

研究概览

简要总结

This clinical investigation aims to evaluate a new articulated prosthetic foot during daily-life activities.

详细描述

This clinical investigation aims to evaluate a new articulated prosthetic foot during daily-life activities.

The primary objective of this clinical investigation is to evaluate the safety, effectiveness, and comfort of the new prosthetic foot, along with user satisfaction and its impact on quality of life during daily-life activities. The study aims to determine whether the prosthetic foot can be safely and effectively integrated into the users' routine mobility, while also providing a comfortable experience that enhances overall well-being. In addition to these primary outcomes, the study will address several secondary objectives to gain a more comprehensive understanding of the device's performance. These include assessing the biomechanical characteristics of walking with the new prosthetic foot, specifically focusing on gait parameters. The investigation also aims to evaluate the device's shock absorption capabilities and its ability to support multi-axial movement, both of which are important for natural and efficient locomotion. Furthermore, the study will explore the attentional demand required when walking with the new prosthetic foot, providing insight into how the device affects mental engagement during ambulation. Lastly, the influence of prosthetic alignment on performance and user experience will be examined to optimize fitting and functionality.

Overall, the new prosthetic foot will be assessed during a variety of daily-life activities, with varying familiarization periods, allowing for a holistic evaluation of the prosthetic foot in realistic and diverse usage conditions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
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

入选标准

  • Age: 18 - 80 years
  • Gender: Men and Women
  • Level of amputation:
  • Unilateral / bilateral
  • Transtibial / transfemoral / knee disarticulation / hip disarticulation
  • Cause of amputation:
  • Vascular, traumatic, cancer and congenital
  • Medicare Functional Classification Level: K2-K3-K4
  • Completion of post-amputation rehabilitation

排除标准

  • Any neurological disease
  • Excessive residual limb pain and wounds

研究组 & 干预措施

New Articulated Prosthetic Foot

Experimental

Participants will be fitted with the new articulated prosthetic foot and follow the protocol

干预措施: New Articulated Prosthetic Foot (Device)

Current Prosthetic foot

Active Comparator

Participants will be fitted with their current prosthetic foot and follow the protocol

干预措施: Current Prosthetic foot (Device)

结局指标

主要结局

Comparative Scales: Comfort, Safety, Fatigue and Pain

时间窗: Through study completion, a period of 3 hours.

Visual Analog Scale (VAS) during different activities: walking on flat ground, walking on slopes, climbing and descending stairs, and walking on uneven terrain. VAS is between 0 and 100. Higher scores indicate higher comfort, safety, fatigue or pain.

Preference questionnaire: 5 points Likert scale

时间窗: Through study completion, a period of 3 hours.

Comparison between the current foot and the new articulated foot in several areas : Mobility \& Functionality, Comfort \& Fit, Stability \& Safety, Mechanical Performance. Likert scale is between 1 and 5, where 1 indicates "Much worse", and 5 indicates "Much better".

User satisfaction questionnaire: 5 points Likert scale

时间窗: Through study completion, a period of 3 hours.

Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST-device). Satisfaction scale is between 1 and 5, where 1 indicates "Not satisfied at all", and 5 indicates "Very satisfied".

次要结局

  • Temporal Gait parameters(Through study completion, a period of 3 hours.)
  • Hill assessment index(Through study completion, a period of 3 hours.)
  • Stair assessment index(Through study completion, a period of 3 hours.)
  • Ankle Joint angles and angular velocities(Through study completion, a period of 3 hours.)
  • Ankle Joint Moment(Through study completion, a period of 3 hours.)
  • Ankle Joint Power(Through study completion, a period of 3 hours.)
  • Shock absorption(Through study completion, a period of 3 hours.)
  • Multi-axial movement(Through study completion, a period of 3 hours.)
  • Attentional demand(Through study completion, a period of 3 hours.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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