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    A Semi-Active Dynamic Rapid Evaluate and Adjust Device for Prescribing Custom Foot Orthoses

    Source: Journal of Medical Devices:;2025:;volume( 019 ):;issue: 003::page 31004-1
    Author:
    Rehman, Tanzeel ur
    ,
    Ou, Haihua
    ,
    Johnson, Shane
    DOI: 10.1115/1.4068381
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Traditional custom foot orthoses (CFO) prescription methods often suffer from lengthy processing times, material waste due to refabrication, inconsistent performance due to inaccurate foot alignment, and inadequate consideration of soft tissue impedance. To address these issues, this study proposes a novel framework for CFO prescription that incorporates adjustable devices, dynamic testing, and subject feedback into the design cycle, thereby reducing delivery time. These shortcomings adversely affect the treatment of critical conditions such as foot ulcerations from diabetes, plantar fasciitis, foot deformity, and Achilles tendonitis. The Arch Height Evaluate and Adjust Device (AHEAD), designed for dynamic testing with the human-in-the-loop, was used to assess the performance of varying orthoses arch heights in different subjects. Plantar pressure measurements during gait and subjective feedback were utilized to determine optimal arch heights. Among ten subjects, the mean increase in medial midfoot peak pressure between the maximum comfortable orthoses arch height and the base profile was 37.57(±22.39) kPa, with an acceptable orthoses arch height range of 3.90(±1.26) mm. This framework offers a rapid, quantitative assessment of the relationship between orthotic design variables and dynamic performance, significantly reducing the time required for CFO prescription.
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      A Semi-Active Dynamic Rapid Evaluate and Adjust Device for Prescribing Custom Foot Orthoses

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    http://yetl.yabesh.ir/yetl1/handle/yetl/4308132
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    contributor authorRehman, Tanzeel ur
    contributor authorOu, Haihua
    contributor authorJohnson, Shane
    date accessioned2025-08-20T09:21:04Z
    date available2025-08-20T09:21:04Z
    date copyright5/5/2025 12:00:00 AM
    date issued2025
    identifier issn1932-6181
    identifier othermed_019_03_031004.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4308132
    description abstractTraditional custom foot orthoses (CFO) prescription methods often suffer from lengthy processing times, material waste due to refabrication, inconsistent performance due to inaccurate foot alignment, and inadequate consideration of soft tissue impedance. To address these issues, this study proposes a novel framework for CFO prescription that incorporates adjustable devices, dynamic testing, and subject feedback into the design cycle, thereby reducing delivery time. These shortcomings adversely affect the treatment of critical conditions such as foot ulcerations from diabetes, plantar fasciitis, foot deformity, and Achilles tendonitis. The Arch Height Evaluate and Adjust Device (AHEAD), designed for dynamic testing with the human-in-the-loop, was used to assess the performance of varying orthoses arch heights in different subjects. Plantar pressure measurements during gait and subjective feedback were utilized to determine optimal arch heights. Among ten subjects, the mean increase in medial midfoot peak pressure between the maximum comfortable orthoses arch height and the base profile was 37.57(±22.39) kPa, with an acceptable orthoses arch height range of 3.90(±1.26) mm. This framework offers a rapid, quantitative assessment of the relationship between orthotic design variables and dynamic performance, significantly reducing the time required for CFO prescription.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleA Semi-Active Dynamic Rapid Evaluate and Adjust Device for Prescribing Custom Foot Orthoses
    typeJournal Paper
    journal volume19
    journal issue3
    journal titleJournal of Medical Devices
    identifier doi10.1115/1.4068381
    journal fristpage31004-1
    journal lastpage31004-7
    page7
    treeJournal of Medical Devices:;2025:;volume( 019 ):;issue: 003
    contenttypeFulltext
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