Evidence map›Paper›PMID 40071237›Full record

ArticleWearable technologies2025

Predictive control of musculotendon loads across fast and slow-twitch muscles in a simulated system with parallel actuation.

Mahdi Nabipour, Gregory S Sawicki, Massimo Sartori

Abstract read
In one paragraph

Article in Wearable technologies, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Mahdi NabipourNeuromuscular Robotics Laboratory, Department of Biomechanical Engineering, University of Twente, Enschede, the Netherlands.ORCID https://orcid.org/0000-0002-6263-4469
Gregory S SawickiHuman Physiology of Wearable Robotics (PoWeR) laboratory, George W. Woodruff School of Mechanical Engineering, School of Biological Sciences and Institute for Robotics and Intelligent Machines, Georgia Institute of Technology, Atlanta, GA, USA.
Massimo SartoriNeuromuscular Robotics Laboratory, Department of Biomechanical Engineering, University of Twente, Enschede, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Research in lower limb wearable robotic control has largely focused on reducing the metabolic cost of walking or compensating for a portion of the biological joint torque, for example, by applying support proportional to estimated biological joint torques. However, due to different musculotendon unit (MTU) contractile speed properties, less attention has been given to the development of wearable robotic controllers that can steer MTU dynamics directly. Therefore, closed-loop control of MTU dynamics needs to be robust across fiber phenotypes, that is ranging from slow type I to fast type IIx in humans. The ability to perform closed-loop control the in-vivo dynamics of MTUs could lead to a new class of wearable robots that can provide precise support to targeted MTUs for preventing onset of injury or providing precision rehabilitation to selected damaged tissues. In this paper, we introduce a novel closed-loop control framework that utilizes nonlinear model predictive control to keep the peak Achilles tendon force within predetermined boundaries during diverse range of cyclic force production simulations in the human ankle plantarflexors. This control framework employs a computationally efficient model comprising a modified Hill-type MTU contraction dynamics component and a model of the ankle joint with parallel actuation. Results indicate that the closed-form muscle-actuation model's computational time is in the order of microseconds and is robust to different muscle contraction velocity properties. Furthermore, the controller achieves tendon force control within a time frame below , aligning with the physiological electromechanical delay of the MTU and facilitating its potential for future real-world applications.

Indexed as

achilles tendonankle plantarflexorshill-type musclehoppinginjury preventionlocomotionmuscle fiber phenotypemusculotendon unitpredictive force controlwalkingwearable robotics

Identifiers

PMID40071237
PMCPMC11894420

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.