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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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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. |
format | Online Article Text |
id | pubmed-6291972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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