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Effects of Instrument-assisted Soft Tissue Mobilization on Musculoskeletal Properties

PURPOSE: Instrument-assisted soft tissue mobilization (IASTM) has been reported to improve joint range of motion (flexibility). However, it is not clear whether this change in the joint range of motion is accompanied by any alterations in the mechanical and/or neural properties. This study aimed to...

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Autores principales: IKEDA, NAOKI, OTSUKA, SHUN, KAWANISHI, YOZO, KAWAKAMI, YASUO
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6798743/
https://www.ncbi.nlm.nih.gov/pubmed/31083046
http://dx.doi.org/10.1249/MSS.0000000000002035
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author IKEDA, NAOKI
OTSUKA, SHUN
KAWANISHI, YOZO
KAWAKAMI, YASUO
author_facet IKEDA, NAOKI
OTSUKA, SHUN
KAWANISHI, YOZO
KAWAKAMI, YASUO
author_sort IKEDA, NAOKI
collection PubMed
description PURPOSE: Instrument-assisted soft tissue mobilization (IASTM) has been reported to improve joint range of motion (flexibility). However, it is not clear whether this change in the joint range of motion is accompanied by any alterations in the mechanical and/or neural properties. This study aimed to investigate the effects of IASTM in plantarflexors and Achilles tendon on the mechanical and neural properties of them. METHODS: This randomized, controlled, crossover study included 14 healthy volunteers (11 men and 3 women, 21–32 yr). IASTM was performed on the skin over the posterior part of the lower leg for 5 min and targeted the soft tissues (gastrocnemii, soleus, and tibialis posterior muscles; overlying deep fascia; and Achilles tendon). As a control condition, the same participants rested for 5 min between pre- and postmeasurements without IASTM on a separate day. The maximal ankle joint dorsiflexion angle (dorsiflexion range of motion), the peak passive torque (stretch tolerance), and the ankle joint stiffness (slope of the relationship between passive torque and ankle joint angle) during the measurement of the dorsiflexion range of motion and muscle stiffness of the triceps surae (using shear wave elastography) were measured before and immediately after the interventions. RESULTS: After IASTM, the dorsiflexion range of motion significantly increased by 10.7% ± 10.8% and ankle joint stiffness significantly decreased by −6.2% ± 10.1%. However, peak passive torque and muscle stiffness did not change. All variables remained unchanged in the repeated measurements of controls. CONCLUSION: IASTM can improve joint range of motion, without affecting the mechanical and neural properties of the treated muscles.
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spelling pubmed-67987432019-11-18 Effects of Instrument-assisted Soft Tissue Mobilization on Musculoskeletal Properties IKEDA, NAOKI OTSUKA, SHUN KAWANISHI, YOZO KAWAKAMI, YASUO Med Sci Sports Exerc Applied Sciences PURPOSE: Instrument-assisted soft tissue mobilization (IASTM) has been reported to improve joint range of motion (flexibility). However, it is not clear whether this change in the joint range of motion is accompanied by any alterations in the mechanical and/or neural properties. This study aimed to investigate the effects of IASTM in plantarflexors and Achilles tendon on the mechanical and neural properties of them. METHODS: This randomized, controlled, crossover study included 14 healthy volunteers (11 men and 3 women, 21–32 yr). IASTM was performed on the skin over the posterior part of the lower leg for 5 min and targeted the soft tissues (gastrocnemii, soleus, and tibialis posterior muscles; overlying deep fascia; and Achilles tendon). As a control condition, the same participants rested for 5 min between pre- and postmeasurements without IASTM on a separate day. The maximal ankle joint dorsiflexion angle (dorsiflexion range of motion), the peak passive torque (stretch tolerance), and the ankle joint stiffness (slope of the relationship between passive torque and ankle joint angle) during the measurement of the dorsiflexion range of motion and muscle stiffness of the triceps surae (using shear wave elastography) were measured before and immediately after the interventions. RESULTS: After IASTM, the dorsiflexion range of motion significantly increased by 10.7% ± 10.8% and ankle joint stiffness significantly decreased by −6.2% ± 10.1%. However, peak passive torque and muscle stiffness did not change. All variables remained unchanged in the repeated measurements of controls. CONCLUSION: IASTM can improve joint range of motion, without affecting the mechanical and neural properties of the treated muscles. Lippincott Williams & Wilkins 2019-10 2019-09-13 /pmc/articles/PMC6798743/ /pubmed/31083046 http://dx.doi.org/10.1249/MSS.0000000000002035 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American College of Sports Medicine. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Applied Sciences
IKEDA, NAOKI
OTSUKA, SHUN
KAWANISHI, YOZO
KAWAKAMI, YASUO
Effects of Instrument-assisted Soft Tissue Mobilization on Musculoskeletal Properties
title Effects of Instrument-assisted Soft Tissue Mobilization on Musculoskeletal Properties
title_full Effects of Instrument-assisted Soft Tissue Mobilization on Musculoskeletal Properties
title_fullStr Effects of Instrument-assisted Soft Tissue Mobilization on Musculoskeletal Properties
title_full_unstemmed Effects of Instrument-assisted Soft Tissue Mobilization on Musculoskeletal Properties
title_short Effects of Instrument-assisted Soft Tissue Mobilization on Musculoskeletal Properties
title_sort effects of instrument-assisted soft tissue mobilization on musculoskeletal properties
topic Applied Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6798743/
https://www.ncbi.nlm.nih.gov/pubmed/31083046
http://dx.doi.org/10.1249/MSS.0000000000002035
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