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Open-label placebo treatment in chronic low back pain: a randomized controlled trial
This randomized controlled trial was performed to investigate whether placebo effects in chronic low back pain could be harnessed ethically by adding open-label placebo (OLP) treatment to treatment as usual (TAU) for 3 weeks. Pain severity was assessed on three 0- to 10-point Numeric Rating Scales,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113234/ https://www.ncbi.nlm.nih.gov/pubmed/27755279 http://dx.doi.org/10.1097/j.pain.0000000000000700 |
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author | Carvalho, Cláudia Caetano, Joaquim Machado Cunha, Lidia Rebouta, Paula Kaptchuk, Ted J. Kirsch, Irving |
author_facet | Carvalho, Cláudia Caetano, Joaquim Machado Cunha, Lidia Rebouta, Paula Kaptchuk, Ted J. Kirsch, Irving |
author_sort | Carvalho, Cláudia |
collection | PubMed |
description | This randomized controlled trial was performed to investigate whether placebo effects in chronic low back pain could be harnessed ethically by adding open-label placebo (OLP) treatment to treatment as usual (TAU) for 3 weeks. Pain severity was assessed on three 0- to 10-point Numeric Rating Scales, scoring maximum pain, minimum pain, and usual pain, and a composite, primary outcome, total pain score. Our other primary outcome was back-related dysfunction, assessed on the Roland–Morris Disability Questionnaire. In an exploratory follow-up, participants on TAU received placebo pills for 3 additional weeks. We randomized 97 adults reporting persistent low back pain for more than 3 months' duration and diagnosed by a board-certified pain specialist. Eighty-three adults completed the trial. Compared to TAU, OLP elicited greater pain reduction on each of the three 0- to 10-point Numeric Rating Scales and on the 0- to 10-point composite pain scale (P < 0.001), with moderate to large effect sizes. Pain reduction on the composite Numeric Rating Scales was 1.5 (95% confidence interval: 1.0-2.0) in the OLP group and 0.2 (−0.3 to 0.8) in the TAU group. Open-label placebo treatment also reduced disability compared to TAU (P < 0.001), with a large effect size. Improvement in disability scores was 2.9 (1.7-4.0) in the OLP group and 0.0 (−1.1 to 1.2) in the TAU group. After being switched to OLP, the TAU group showed significant reductions in both pain (1.5, 0.8-2.3) and disability (3.4, 2.2-4.5). Our findings suggest that OLP pills presented in a positive context may be helpful in chronic low back pain. |
format | Online Article Text |
id | pubmed-5113234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-51132342016-11-23 Open-label placebo treatment in chronic low back pain: a randomized controlled trial Carvalho, Cláudia Caetano, Joaquim Machado Cunha, Lidia Rebouta, Paula Kaptchuk, Ted J. Kirsch, Irving Pain Research Paper This randomized controlled trial was performed to investigate whether placebo effects in chronic low back pain could be harnessed ethically by adding open-label placebo (OLP) treatment to treatment as usual (TAU) for 3 weeks. Pain severity was assessed on three 0- to 10-point Numeric Rating Scales, scoring maximum pain, minimum pain, and usual pain, and a composite, primary outcome, total pain score. Our other primary outcome was back-related dysfunction, assessed on the Roland–Morris Disability Questionnaire. In an exploratory follow-up, participants on TAU received placebo pills for 3 additional weeks. We randomized 97 adults reporting persistent low back pain for more than 3 months' duration and diagnosed by a board-certified pain specialist. Eighty-three adults completed the trial. Compared to TAU, OLP elicited greater pain reduction on each of the three 0- to 10-point Numeric Rating Scales and on the 0- to 10-point composite pain scale (P < 0.001), with moderate to large effect sizes. Pain reduction on the composite Numeric Rating Scales was 1.5 (95% confidence interval: 1.0-2.0) in the OLP group and 0.2 (−0.3 to 0.8) in the TAU group. Open-label placebo treatment also reduced disability compared to TAU (P < 0.001), with a large effect size. Improvement in disability scores was 2.9 (1.7-4.0) in the OLP group and 0.0 (−1.1 to 1.2) in the TAU group. After being switched to OLP, the TAU group showed significant reductions in both pain (1.5, 0.8-2.3) and disability (3.4, 2.2-4.5). Our findings suggest that OLP pills presented in a positive context may be helpful in chronic low back pain. Wolters Kluwer 2016-12 2016-10-13 /pmc/articles/PMC5113234/ /pubmed/27755279 http://dx.doi.org/10.1097/j.pain.0000000000000700 Text en © 2016 International Association for the Study of Pain This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Research Paper Carvalho, Cláudia Caetano, Joaquim Machado Cunha, Lidia Rebouta, Paula Kaptchuk, Ted J. Kirsch, Irving Open-label placebo treatment in chronic low back pain: a randomized controlled trial |
title | Open-label placebo treatment in chronic low back pain: a randomized controlled trial |
title_full | Open-label placebo treatment in chronic low back pain: a randomized controlled trial |
title_fullStr | Open-label placebo treatment in chronic low back pain: a randomized controlled trial |
title_full_unstemmed | Open-label placebo treatment in chronic low back pain: a randomized controlled trial |
title_short | Open-label placebo treatment in chronic low back pain: a randomized controlled trial |
title_sort | open-label placebo treatment in chronic low back pain: a randomized controlled trial |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113234/ https://www.ncbi.nlm.nih.gov/pubmed/27755279 http://dx.doi.org/10.1097/j.pain.0000000000000700 |
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