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Efficacy and safety of thread embedding acupuncture for chronic low back pain: a randomized controlled pilot trial

BACKGROUND: We investigated the efficacy and safety of thread-embedding acupuncture (TEA) for chronic low back pain (LBP) in a randomized controlled pilot trial with the aim of laying the foundation for a large-scale randomized controlled trial on this topic. METHODS: Forty participants were recruit...

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Autores principales: Lee, Hyun-Jong, Choi, Byung Il, Jun, Seungah, Park, Mu Seob, Oh, Se Jung, Lee, Jung Hee, Gong, Han Mi, Kim, Jae Soo, Lee, Young Joon, Jung, So-Young, Han, Chang Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291972/
https://www.ncbi.nlm.nih.gov/pubmed/30541604
http://dx.doi.org/10.1186/s13063-018-3049-x
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author Lee, Hyun-Jong
Choi, Byung Il
Jun, Seungah
Park, Mu Seob
Oh, Se Jung
Lee, Jung Hee
Gong, Han Mi
Kim, Jae Soo
Lee, Young Joon
Jung, So-Young
Han, Chang Hyun
author_facet Lee, Hyun-Jong
Choi, Byung Il
Jun, Seungah
Park, Mu Seob
Oh, Se Jung
Lee, Jung Hee
Gong, Han Mi
Kim, Jae Soo
Lee, Young Joon
Jung, So-Young
Han, Chang Hyun
author_sort Lee, Hyun-Jong
collection PubMed
description BACKGROUND: We investigated the efficacy and safety of thread-embedding acupuncture (TEA) for chronic low back pain (LBP) in a randomized controlled pilot trial with the aim of laying the foundation for a large-scale randomized controlled trial on this topic. METHODS: Forty participants were recruited for this two-arm, assessor-blinded randomized controlled pilot trial. The participants were randomly allocated to a TEA group (experimental group) or an acupuncture group (control group). The TEA group received TEA once every 2 weeks for 8 weeks (four sessions in total), while the acupuncture group received acupuncture twice per week for 8 weeks (16 sessions in total). The primary outcome was the visual analog scale (VAS) score for pain and the secondary outcomes were short-form McGill Pain Questionnaire (SF-MPQ) and Oswestry Disability Index (ODI) scores. Assessments were performed at screening and at 2, 4, 6, 8, and 10 weeks after treatment initiation (the 10-week assessment was conducted at 2 weeks after treatment cessation). RESULTS: Of the 40 participants, 36 completed the study and four dropped out. Both the TEA group and the acupuncture group showed significant improvements in VAS, SF-MPQ, and ODI scores in a time-dependent manner. Furthermore, with regard to ODI, a significant interaction between group and time was observed, with the two groups exhibiting a different pattern of change at 8 weeks according to contrast analysis with Bonferroni’s correction. No serious adverse event occurred, and hematological and biochemical test findings were within normal limits. CONCLUSION: This pilot study has provided basic data for a larger clinical trial to demonstrate the efficacy and safety of TEA for chronic LBP. TRIAL REGISTRATION: Clinical Research Information Service of the Korea National Institute of Health, ID: KCT0001819. Registered on 15 February 2016.
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spelling pubmed-62919722018-12-17 Efficacy and safety of thread embedding acupuncture for chronic low back pain: a randomized controlled pilot trial Lee, Hyun-Jong Choi, Byung Il Jun, Seungah Park, Mu Seob Oh, Se Jung Lee, Jung Hee Gong, Han Mi Kim, Jae Soo Lee, Young Joon Jung, So-Young Han, Chang Hyun Trials Research BACKGROUND: We investigated the efficacy and safety of thread-embedding acupuncture (TEA) for chronic low back pain (LBP) in a randomized controlled pilot trial with the aim of laying the foundation for a large-scale randomized controlled trial on this topic. METHODS: Forty participants were recruited for this two-arm, assessor-blinded randomized controlled pilot trial. The participants were randomly allocated to a TEA group (experimental group) or an acupuncture group (control group). The TEA group received TEA once every 2 weeks for 8 weeks (four sessions in total), while the acupuncture group received acupuncture twice per week for 8 weeks (16 sessions in total). The primary outcome was the visual analog scale (VAS) score for pain and the secondary outcomes were short-form McGill Pain Questionnaire (SF-MPQ) and Oswestry Disability Index (ODI) scores. Assessments were performed at screening and at 2, 4, 6, 8, and 10 weeks after treatment initiation (the 10-week assessment was conducted at 2 weeks after treatment cessation). RESULTS: Of the 40 participants, 36 completed the study and four dropped out. Both the TEA group and the acupuncture group showed significant improvements in VAS, SF-MPQ, and ODI scores in a time-dependent manner. Furthermore, with regard to ODI, a significant interaction between group and time was observed, with the two groups exhibiting a different pattern of change at 8 weeks according to contrast analysis with Bonferroni’s correction. No serious adverse event occurred, and hematological and biochemical test findings were within normal limits. CONCLUSION: This pilot study has provided basic data for a larger clinical trial to demonstrate the efficacy and safety of TEA for chronic LBP. TRIAL REGISTRATION: Clinical Research Information Service of the Korea National Institute of Health, ID: KCT0001819. Registered on 15 February 2016. BioMed Central 2018-12-12 /pmc/articles/PMC6291972/ /pubmed/30541604 http://dx.doi.org/10.1186/s13063-018-3049-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lee, Hyun-Jong
Choi, Byung Il
Jun, Seungah
Park, Mu Seob
Oh, Se Jung
Lee, Jung Hee
Gong, Han Mi
Kim, Jae Soo
Lee, Young Joon
Jung, So-Young
Han, Chang Hyun
Efficacy and safety of thread embedding acupuncture for chronic low back pain: a randomized controlled pilot trial
title Efficacy and safety of thread embedding acupuncture for chronic low back pain: a randomized controlled pilot trial
title_full Efficacy and safety of thread embedding acupuncture for chronic low back pain: a randomized controlled pilot trial
title_fullStr Efficacy and safety of thread embedding acupuncture for chronic low back pain: a randomized controlled pilot trial
title_full_unstemmed Efficacy and safety of thread embedding acupuncture for chronic low back pain: a randomized controlled pilot trial
title_short Efficacy and safety of thread embedding acupuncture for chronic low back pain: a randomized controlled pilot trial
title_sort efficacy and safety of thread embedding acupuncture for chronic low back pain: a randomized controlled pilot trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6291972/
https://www.ncbi.nlm.nih.gov/pubmed/30541604
http://dx.doi.org/10.1186/s13063-018-3049-x
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