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Acupuncture for irritable bowel syndrome: A protocol for a pragmatic randomised controlled trial
BACKGROUND: There is insufficient evidence on the effectiveness of acupuncture for irritable bowel syndrome (IBS) for conclusions to be drawn. Given the current interest in acupuncture by patients, it is in the public interest to establish more rigorous evidence. Building on the positive findings fr...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909152/ https://www.ncbi.nlm.nih.gov/pubmed/20565790 http://dx.doi.org/10.1186/1471-230X-10-63 |
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author | MacPherson, Hugh Bland, Martin Bloor, Karen Cox, Helen Geddes, David Kang'ombe, Arthur Reynolds, Julie Stamuli, Eugena Stuardi, Tracey Tilbrook, Helen Torgerson, David Whorwell, Peter |
author_facet | MacPherson, Hugh Bland, Martin Bloor, Karen Cox, Helen Geddes, David Kang'ombe, Arthur Reynolds, Julie Stamuli, Eugena Stuardi, Tracey Tilbrook, Helen Torgerson, David Whorwell, Peter |
author_sort | MacPherson, Hugh |
collection | PubMed |
description | BACKGROUND: There is insufficient evidence on the effectiveness of acupuncture for irritable bowel syndrome (IBS) for conclusions to be drawn. Given the current interest in acupuncture by patients, it is in the public interest to establish more rigorous evidence. Building on the positive findings from a pilot study, in this paper we present the protocol for a fully-powered trial designed to establish whether or not acupuncture is effective and cost-effective. METHODS/DESIGN: In this pragmatic randomised controlled trial we will randomise patients recruited directly from GP databases to either 10 sessions of acupuncture plus usual GP care or to usual GP care alone. The primary clinical outcome will be the IBS Symptom Severity Score (SSS) (maximum score 500) at three months, and at 12 month assessing whether there is an overall benefit. We estimate the sample size required to detect a minimum clinical difference at 90% power and 5% significance to be 188 patients. To allow for loss to follow up we will recruit 220 patients drawn from an estimated primary care population of 140 000. Analysis will be by intention-to-treat, and multiple imputation is to be used for missing data. In a nested qualitative study using in-depth interviews, we will explore how patients, acupuncturists, and GPs explain and subsequently understand acupuncture to work. We will use purposive sampling to identify patients and flexible topic guides for the interviews. The data analysis will lead to a thematic description of how patients and practitioners explain how acupuncture works, and whether or not the explanations influence treatment outcome and/or referrals. We will undertake a cost-effectiveness analysis at 12 months by comparing resource use in the two groups with any treatment benefit. We will use the EQ-5D to measure health-related quality of life and convert into quality adjusted life years (QALYs). We will generate cost effectiveness acceptability curves (CEACs) exploring the probability that acupuncture will produce an acceptable cost per QALY at different cost-effectiveness thresholds. DISCUSSION: The trial has received NHS ethics approval and recruited 233 patients between November 2008 and June 2009. Results are expected in 2011. TRIAL REGISTRATION: Current Controlled Trials ISRCTN08827905 |
format | Text |
id | pubmed-2909152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29091522010-07-24 Acupuncture for irritable bowel syndrome: A protocol for a pragmatic randomised controlled trial MacPherson, Hugh Bland, Martin Bloor, Karen Cox, Helen Geddes, David Kang'ombe, Arthur Reynolds, Julie Stamuli, Eugena Stuardi, Tracey Tilbrook, Helen Torgerson, David Whorwell, Peter BMC Gastroenterol Study Protocol BACKGROUND: There is insufficient evidence on the effectiveness of acupuncture for irritable bowel syndrome (IBS) for conclusions to be drawn. Given the current interest in acupuncture by patients, it is in the public interest to establish more rigorous evidence. Building on the positive findings from a pilot study, in this paper we present the protocol for a fully-powered trial designed to establish whether or not acupuncture is effective and cost-effective. METHODS/DESIGN: In this pragmatic randomised controlled trial we will randomise patients recruited directly from GP databases to either 10 sessions of acupuncture plus usual GP care or to usual GP care alone. The primary clinical outcome will be the IBS Symptom Severity Score (SSS) (maximum score 500) at three months, and at 12 month assessing whether there is an overall benefit. We estimate the sample size required to detect a minimum clinical difference at 90% power and 5% significance to be 188 patients. To allow for loss to follow up we will recruit 220 patients drawn from an estimated primary care population of 140 000. Analysis will be by intention-to-treat, and multiple imputation is to be used for missing data. In a nested qualitative study using in-depth interviews, we will explore how patients, acupuncturists, and GPs explain and subsequently understand acupuncture to work. We will use purposive sampling to identify patients and flexible topic guides for the interviews. The data analysis will lead to a thematic description of how patients and practitioners explain how acupuncture works, and whether or not the explanations influence treatment outcome and/or referrals. We will undertake a cost-effectiveness analysis at 12 months by comparing resource use in the two groups with any treatment benefit. We will use the EQ-5D to measure health-related quality of life and convert into quality adjusted life years (QALYs). We will generate cost effectiveness acceptability curves (CEACs) exploring the probability that acupuncture will produce an acceptable cost per QALY at different cost-effectiveness thresholds. DISCUSSION: The trial has received NHS ethics approval and recruited 233 patients between November 2008 and June 2009. Results are expected in 2011. TRIAL REGISTRATION: Current Controlled Trials ISRCTN08827905 BioMed Central 2010-06-17 /pmc/articles/PMC2909152/ /pubmed/20565790 http://dx.doi.org/10.1186/1471-230X-10-63 Text en Copyright ©2010 MacPherson 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 cited. |
spellingShingle | Study Protocol MacPherson, Hugh Bland, Martin Bloor, Karen Cox, Helen Geddes, David Kang'ombe, Arthur Reynolds, Julie Stamuli, Eugena Stuardi, Tracey Tilbrook, Helen Torgerson, David Whorwell, Peter Acupuncture for irritable bowel syndrome: A protocol for a pragmatic randomised controlled trial |
title | Acupuncture for irritable bowel syndrome: A protocol for a pragmatic randomised controlled trial |
title_full | Acupuncture for irritable bowel syndrome: A protocol for a pragmatic randomised controlled trial |
title_fullStr | Acupuncture for irritable bowel syndrome: A protocol for a pragmatic randomised controlled trial |
title_full_unstemmed | Acupuncture for irritable bowel syndrome: A protocol for a pragmatic randomised controlled trial |
title_short | Acupuncture for irritable bowel syndrome: A protocol for a pragmatic randomised controlled trial |
title_sort | acupuncture for irritable bowel syndrome: a protocol for a pragmatic randomised controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909152/ https://www.ncbi.nlm.nih.gov/pubmed/20565790 http://dx.doi.org/10.1186/1471-230X-10-63 |
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