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Home-based rehabilitation training with human key point detection for chronic low back pain patients: a randomized controlled trial protocol
BACKGROUND: Core stability exercise (CSE) is a globally acknowledged intervention for managing chronic low back pain. However, the sustained adherence of patients with chronic low back pain to CSE can be challenging, mainly due to the absence of supervision and guidance from physical therapists duri...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680338/ https://www.ncbi.nlm.nih.gov/pubmed/38012740 http://dx.doi.org/10.1186/s13063-023-07805-z |
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author | Fuming, Zheng Zhicheng, Li Huanjie, Huang Xinna, Zhang Rong, Chen Jiahui, Peng Liming, Yang Xi, Chen Chuhuai, Wang |
author_facet | Fuming, Zheng Zhicheng, Li Huanjie, Huang Xinna, Zhang Rong, Chen Jiahui, Peng Liming, Yang Xi, Chen Chuhuai, Wang |
author_sort | Fuming, Zheng |
collection | PubMed |
description | BACKGROUND: Core stability exercise (CSE) is a globally acknowledged intervention for managing chronic low back pain. However, the sustained adherence of patients with chronic low back pain to CSE can be challenging, mainly due to the absence of supervision and guidance from physical therapists during home-based exercise sessions. Consequently, exercise compliance tends to decline, resulting in suboptimal long-term effectiveness of the intervention. In this trial, our primary aim is to evaluate the potential therapeutic equivalence between home-based rehabilitation training employing key point identification technology and exercise guidance administered in a hospital setting. METHODS: In this trial, we will randomly assign 104 adults with chronic low back pain (CLBP) to either an intervention or control group, with 52 participants in each group. Both interventions will consist of three weekly 0.5-h sessions of core stability exercise (CSE). The intervention group will engage in home rehabilitation training utilizing key identification technology for movement, while the control group will perform supervised exercises in a hospital setting. Outcome assessments will be conducted at 4 weeks and 16 weeks after randomization. The primary outcome measure will be the change in pain intensity based on numeric rating scale (NRS scores) from baseline to 4 weeks. Secondary outcomes will include changes in physical function (measured by the Oswestry Disability Index (ODI)) and lumbar spine mobility as well as activity participation and treatment satisfaction. DISCUSSION: If home-based rehabilitation method is demonstrated to be non-inferior or even superior to traditional face-to-face exercise guidance, it could significantly advance the adoption of digital medical care and contribute to improving the overall health of the population. TRIAL REGISTRATION: NCT05998434. Registered on 16 August 2023. |
format | Online Article Text |
id | pubmed-10680338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106803382023-11-27 Home-based rehabilitation training with human key point detection for chronic low back pain patients: a randomized controlled trial protocol Fuming, Zheng Zhicheng, Li Huanjie, Huang Xinna, Zhang Rong, Chen Jiahui, Peng Liming, Yang Xi, Chen Chuhuai, Wang Trials Study Protocol BACKGROUND: Core stability exercise (CSE) is a globally acknowledged intervention for managing chronic low back pain. However, the sustained adherence of patients with chronic low back pain to CSE can be challenging, mainly due to the absence of supervision and guidance from physical therapists during home-based exercise sessions. Consequently, exercise compliance tends to decline, resulting in suboptimal long-term effectiveness of the intervention. In this trial, our primary aim is to evaluate the potential therapeutic equivalence between home-based rehabilitation training employing key point identification technology and exercise guidance administered in a hospital setting. METHODS: In this trial, we will randomly assign 104 adults with chronic low back pain (CLBP) to either an intervention or control group, with 52 participants in each group. Both interventions will consist of three weekly 0.5-h sessions of core stability exercise (CSE). The intervention group will engage in home rehabilitation training utilizing key identification technology for movement, while the control group will perform supervised exercises in a hospital setting. Outcome assessments will be conducted at 4 weeks and 16 weeks after randomization. The primary outcome measure will be the change in pain intensity based on numeric rating scale (NRS scores) from baseline to 4 weeks. Secondary outcomes will include changes in physical function (measured by the Oswestry Disability Index (ODI)) and lumbar spine mobility as well as activity participation and treatment satisfaction. DISCUSSION: If home-based rehabilitation method is demonstrated to be non-inferior or even superior to traditional face-to-face exercise guidance, it could significantly advance the adoption of digital medical care and contribute to improving the overall health of the population. TRIAL REGISTRATION: NCT05998434. Registered on 16 August 2023. BioMed Central 2023-11-27 /pmc/articles/PMC10680338/ /pubmed/38012740 http://dx.doi.org/10.1186/s13063-023-07805-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Study Protocol Fuming, Zheng Zhicheng, Li Huanjie, Huang Xinna, Zhang Rong, Chen Jiahui, Peng Liming, Yang Xi, Chen Chuhuai, Wang Home-based rehabilitation training with human key point detection for chronic low back pain patients: a randomized controlled trial protocol |
title | Home-based rehabilitation training with human key point detection for chronic low back pain patients: a randomized controlled trial protocol |
title_full | Home-based rehabilitation training with human key point detection for chronic low back pain patients: a randomized controlled trial protocol |
title_fullStr | Home-based rehabilitation training with human key point detection for chronic low back pain patients: a randomized controlled trial protocol |
title_full_unstemmed | Home-based rehabilitation training with human key point detection for chronic low back pain patients: a randomized controlled trial protocol |
title_short | Home-based rehabilitation training with human key point detection for chronic low back pain patients: a randomized controlled trial protocol |
title_sort | home-based rehabilitation training with human key point detection for chronic low back pain patients: a randomized controlled trial protocol |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680338/ https://www.ncbi.nlm.nih.gov/pubmed/38012740 http://dx.doi.org/10.1186/s13063-023-07805-z |
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