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临床试验/NCT07670325
NCT07670325招募中不适用

Funzionalità e Sicurezza di un Dispositivo di Ginocchio Per Riabilitazione Della Deambulazione Con Pazienti Neurologici

Scuola Superiore di Studi Universitari e di Perfezionamento Sant'Anna1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2026年6月22日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
20
试验地点
1
主要终点
Number of device-related adverse events

研究概览

简要总结

This clinical investigation aims to evaluate the safety, feasibility, and preliminary performance of the AKO-R wearable robotic device for knee assistance during walking. The study involves participants performing treadmill and overground gait training under supervised conditions, with the device providing assistive torque to support movement. Clinical and functional outcomes are assessed using validated measurement tools, while additional data are collected to characterize user performance and interaction with the device. The study is designed as an exploratory investigation to gather evidence supporting the clinical use and further development of the device. Primary outcomes regards safety of the device and preliminary clinical benefit on gait symmetry.

详细描述

The study is structured in 5 sessions. The first and last session are the assessment. the 2nd session is the session for calibration of the exoskeleton parameters. The 3rd session is for exo familiarization and the 4th exo is for exo-assisted condition evaluation.

研究设计

研究类型
Interventional
分配方式
Na
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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • diagnosed stroke with fMRI
  • within 2 years from stroke event
  • height [1.5 - 2]m
  • weigth <= 100 Kg

排除标准

  • Pregnancy
  • Implanted cardiac devices, such as pacemakers or implantable cardioverter defibrillators (ICDs)
  • Recent or current participation in research studies that, in the opinion of the Principal Investigator, may affect the subject's response to the study intervention
  • Severe aphasia

结局指标

主要结局

Number of device-related adverse events

时间窗: through study completion, an average of 1 year

Step Length Symmetry Index Change

时间窗: Day 4

The Step Length Symmetry Index (SI) will be compared across conditions. Descriptive data are averaged across \>20 steps. Score closer to 0 means a better outcome.

Stance Time Symmetry Index Change

时间窗: Day 4

The Stance Time Symmetry Index (SI) will be compared across conditions. Descriptive data are averaged across \>20 steps. Score closer to 0 means a better outcome.

次要结局

  • Range of motion Change(Day 4)
  • Self-selected velocity Change(Day 5)
  • Endurance(Day 5)
  • Usability score(Day 5)
  • Acceptability(Day 5)
  • Satisfaction Score(Day 5)

研究者

发起方
Scuola Superiore di Studi Universitari e di Perfezionamento Sant'Anna
申办方类型
Other
责任方
Sponsor

研究点 (1)

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