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Acupuncture for functional dyspepsia: study protocol for a two-center, randomized controlled trial

BACKGROUND: Functional dyspepsia (FD) is a common health problem currently without any optimal treatments. Acupuncture has been traditionally sought as a treatment for FD. The aim of this study is to investigate whether acupuncture treatment helps improve symptoms of FD. METHODS/DESIGN: A two-center...

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Autores principales: Han, Gajin, Ko, Seok-Jae, Park, Jae-Woo, Kim, Jinsung, Yeo, Inkwon, Lee, Hyejung, Kim, Song-Yi, Lee, Hyangsook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994398/
https://www.ncbi.nlm.nih.gov/pubmed/24655542
http://dx.doi.org/10.1186/1745-6215-15-89
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author Han, Gajin
Ko, Seok-Jae
Park, Jae-Woo
Kim, Jinsung
Yeo, Inkwon
Lee, Hyejung
Kim, Song-Yi
Lee, Hyangsook
author_facet Han, Gajin
Ko, Seok-Jae
Park, Jae-Woo
Kim, Jinsung
Yeo, Inkwon
Lee, Hyejung
Kim, Song-Yi
Lee, Hyangsook
author_sort Han, Gajin
collection PubMed
description BACKGROUND: Functional dyspepsia (FD) is a common health problem currently without any optimal treatments. Acupuncture has been traditionally sought as a treatment for FD. The aim of this study is to investigate whether acupuncture treatment helps improve symptoms of FD. METHODS/DESIGN: A two-center, randomized, waitlist-controlled trial will be carried out to evaluate whether acupuncture treatment improves FD symptoms. Seventy six participants aged 18 to 75 years with FD as diagnosed by Rome III criteria will be recruited from August 2013 to January 2014 at two Korean Medicine hospitals. They will be randomly allocated either into eight sessions of partially individualized acupuncture treatment over 4 weeks or a waitlist group. The acupuncture group will then be followed-up for 3 weeks with six telephone visits and a final visit will be paid at 8 weeks. The waitlist group will receive the identical acupuncture treatment after a 4-week waiting period. The primary outcome is the proportion of responders with adequate symptom relief and the secondary outcomes include Nepean dyspepsia index, EQ-5D, FD-related quality of life, Beck’s depression inventory, state-trait anxiety inventory questionnaire, and level of ghrelin hormone. The protocol was approved by the participating centers’ Institutional Review Boards. DISCUSSION: Results of this trial will help clarify not only whether the acupuncture treatment is beneficial for symptom improvement in FD patients but also to elucidate the related mechanisms of how acupuncture might work. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT01921504.
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spelling pubmed-39943982014-05-07 Acupuncture for functional dyspepsia: study protocol for a two-center, randomized controlled trial Han, Gajin Ko, Seok-Jae Park, Jae-Woo Kim, Jinsung Yeo, Inkwon Lee, Hyejung Kim, Song-Yi Lee, Hyangsook Trials Study Protocol BACKGROUND: Functional dyspepsia (FD) is a common health problem currently without any optimal treatments. Acupuncture has been traditionally sought as a treatment for FD. The aim of this study is to investigate whether acupuncture treatment helps improve symptoms of FD. METHODS/DESIGN: A two-center, randomized, waitlist-controlled trial will be carried out to evaluate whether acupuncture treatment improves FD symptoms. Seventy six participants aged 18 to 75 years with FD as diagnosed by Rome III criteria will be recruited from August 2013 to January 2014 at two Korean Medicine hospitals. They will be randomly allocated either into eight sessions of partially individualized acupuncture treatment over 4 weeks or a waitlist group. The acupuncture group will then be followed-up for 3 weeks with six telephone visits and a final visit will be paid at 8 weeks. The waitlist group will receive the identical acupuncture treatment after a 4-week waiting period. The primary outcome is the proportion of responders with adequate symptom relief and the secondary outcomes include Nepean dyspepsia index, EQ-5D, FD-related quality of life, Beck’s depression inventory, state-trait anxiety inventory questionnaire, and level of ghrelin hormone. The protocol was approved by the participating centers’ Institutional Review Boards. DISCUSSION: Results of this trial will help clarify not only whether the acupuncture treatment is beneficial for symptom improvement in FD patients but also to elucidate the related mechanisms of how acupuncture might work. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT01921504. BioMed Central 2014-03-22 /pmc/articles/PMC3994398/ /pubmed/24655542 http://dx.doi.org/10.1186/1745-6215-15-89 Text en Copyright © 2014 Han et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Study Protocol
Han, Gajin
Ko, Seok-Jae
Park, Jae-Woo
Kim, Jinsung
Yeo, Inkwon
Lee, Hyejung
Kim, Song-Yi
Lee, Hyangsook
Acupuncture for functional dyspepsia: study protocol for a two-center, randomized controlled trial
title Acupuncture for functional dyspepsia: study protocol for a two-center, randomized controlled trial
title_full Acupuncture for functional dyspepsia: study protocol for a two-center, randomized controlled trial
title_fullStr Acupuncture for functional dyspepsia: study protocol for a two-center, randomized controlled trial
title_full_unstemmed Acupuncture for functional dyspepsia: study protocol for a two-center, randomized controlled trial
title_short Acupuncture for functional dyspepsia: study protocol for a two-center, randomized controlled trial
title_sort acupuncture for functional dyspepsia: study protocol for a two-center, randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994398/
https://www.ncbi.nlm.nih.gov/pubmed/24655542
http://dx.doi.org/10.1186/1745-6215-15-89
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