开发一种利用双侧踝关节外骨骼估计步行性能的实时控制器
实现机器人踝关节外骨骼个性化辅助的控制器开发
This study is developing and testing a new controller for a robotic ankle exoskeleton (Biomotum) that can adjust itself in real time to better support people while they walk. The system learns how each person moves and automatically changes the amount and timing of assistance to make walking feel easier and more efficient. By using information from the person wearing the device, the exoskeleton can quickly find the level of support that works best for them. The long-term goal is to create personalized walking assistance that can help people with mobility limitations move more comfortably and with less effort.
研究概览
详细说明
This project aims to develop and test a real-time adaptive controller for a robotic ankle exoskeleton (Biomotum) that personalizes assistance to each user by minimizing metabolic cost and optimizing muscle activation patterns during walking. Using human-in-the-loop optimization and advanced musculoskeletal modeling, the controller will dynamically adjust torque magnitude and timing to achieve optimal performance more quickly than current methods.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Farah Fallahtafi, PhD
- 电话号码:4025543075
- 邮箱:ffallahtafti@unomaha.edu
学习地点
-
-
Nebraska
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Omaha、Nebraska、美国、68108
- 招聘中
- Biomechanics Research Building, University of Nebraska at Omaha
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接触:
- Farah Fallahtafti, PhD
- 电话号码:4025543075
- 邮箱:ffallahtafti@unomaha.edu
-
接触:
- Sara Myers, PhD
- 电话号码:4025543246
- 邮箱:samyers@unomaha.edu
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首席研究员:
- Farah Fallahtafti, PhD
-
副研究员:
- Arash Gonabadi, PhD
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副研究员:
- Sara Myers, PhD
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- able to walk independently on a treadmill for 10 minutes,
- free of neurological, cardiovascular, pulmonary, or musculoskeletal conditions that limit walking and exercising,
- no current lower extremity pain or injury,
- able to wear an exoskeleton and safety harness, can provide informed consent
Exclusion Criteria:
- history of neurological disease that affected gait or balance,
- current or recent lower extremity musculoskeletal injury or surgery,
- chronic lower extremity pain during walking,
- inability to participate in moderate-intensity exercise,
- require an assistive device for walking,
- any metabolic or systemic diseases that may be exacerbated by exercise
学习计划
研究是如何设计的?
设计细节
- 主要用途:设备可行性
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Single-Arm Study of a Personalized Robotic Ankle Exoskeleton Controller
This arm employs a within-subject design with two methods of estimating metabolic cost versus the gold standard measure of metabolic cost, wherein a single participant is subjected to two distinct measurements. This design allows for a direct comparison of the effects of each method (i.e., estimation versus gold standard) within the same individual, minimizing intersubject variability and enhancing the statistical power of the analysis. |
This intervention uses a robotic ankle exoskeleton equipped with a real-time adaptive controller that adjusts plantarflexion torque based on each participant's walking mechanics. Unlike standard exoskeleton controllers that use fixed or pre-programmed assistance levels, this system employs human-in-the-loop optimization to continuously update torque magnitude and timing during treadmill walking. The controller integrates metabolic estimations, kinematic data, and musculoskeletal modeling to identify individualized assistance patterns that reduce walking effort and improve muscle activation efficiency. Participants complete multiple walking trials while the controller automatically modifies assistance to determine the optimal personalized settings. |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Successful Real-Time Operation of the Robotic Ankle Exoskeleton Controller
大体时间:through study completion, an average of 1 year
|
Device feasibility will be evaluated by the successful real-time operation of the robotic ankle exoskeleton and adaptive controller during treadmill walking. Feasibility is defined as the controller's ability to continuously generate, update, and apply assistive torque in real time based on incoming biomechanical and physiological data without system failure, interruption, or safety-related termination. Successful operation will be confirmed by continuous controller function and synchronized data acquisition across walking trials. |
through study completion, an average of 1 year
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Net Metabolic Rate During Exoskeleton-Assisted Walking Measured by Indirect Calorimetry
大体时间:through study completion, an average of 1 year
|
Net oxygen consumption (VO₂) and carbon dioxide production (VCO₂) will be measured during treadmill walking using indirect calorimetry (Cosmed K5, Cosmed USA Inc., Chicago, IL). Metabolic rate will be calculated using standard equations during steady-state walking conditions. Measurements will be collected at regular intervals to characterize metabolic demand under different exoskeleton assistance configurations. |
through study completion, an average of 1 year
|
|
Estimated Metabolic Rate Derived From Joint-Space Musculoskeletal Modeling
大体时间:through study completion, an average of 1 year
|
Estimated metabolic rate will be derived from joint-space musculoskeletal models using kinematic and kinetic data collected during treadmill walking. Model-based estimates will be computed on a stride-by-stride basis to provide an indirect estimate of metabolic demand that can be compared with direct measurements from indirect calorimetry. |
through study completion, an average of 1 year
|
|
Estimated Lower-Limb Muscle Activation Derived From Joint-Space Musculoskeletal Modeling
大体时间:through study completion, an average of 1 year
|
Lower-limb muscle activation patterns will be estimated using joint-space musculoskeletal models based on motion capture and ground reaction force data collected during treadmill walking. Estimated muscle activation values will be computed on a stride-by-stride basis to characterize neuromuscular engagement during exoskeleton-assisted gait. |
through study completion, an average of 1 year
|
|
Lower-Limb Muscle Activation Measured by Surface Electromyography During Walking
大体时间:through study completion, an average of 1 year
|
Muscle activation of lower-limb muscles (e.g., tibialis anterior, gastrocnemius medialis, gastrocnemius lateralis, soleus) will be measured during treadmill walking using surface electromyography (Delsys). EMG signals will be collected continuously and processed to quantify muscle activation patterns during exoskeleton-assisted gait. |
through study completion, an average of 1 year
|
|
During treadmill walking trials conducted at a single study visit
大体时间:through study completion, an average of 1 year
|
Controller parameter convergence will be assessed during human-in-the-loop optimization trials by evaluating changes in controller gain and timing parameters across successive walking bouts. Convergence is defined as stabilization of controller parameters within a predefined range during the optimization process. |
through study completion, an average of 1 year
|
合作者和调查者
调查人员
- 首席研究员:Farah Fallahtafti, PhD、Department of Biomechanics, University of Nebraska at Omaha
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- 0587-25-FB
- 55136 (其他赠款/资助编号:Nebraska Research Initiative)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
IPD will not be shared because direct measurements are only taken for baseline measurements that the modeling software will be using. The scripts and code used will be shared through opensource, but that does not include subject data.
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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