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Integrated cognitive behavioral therapy for chronic pain: An open-labeled prospective single-arm trial

BACKGROUND: We aimed to examine the feasibility of our newly-developed, integrated, and high-intensity individual cognitive behavioral therapy (CBT) protocol for treatment-resistant chronic pain. METHODS: We conducted an open-labeled prospective single-arm trial for patients aged 18 years and above,...

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Autores principales: Taguchi, Kayoko, Numata, Noriko, Takanashi, Rieko, Takemura, Ryo, Yoshida, Tokiko, Kutsuzawa, Kana, Yoshimura, Kensuke, Shimizu, Eiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886449/
https://www.ncbi.nlm.nih.gov/pubmed/33578513
http://dx.doi.org/10.1097/MD.0000000000023859
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author Taguchi, Kayoko
Numata, Noriko
Takanashi, Rieko
Takemura, Ryo
Yoshida, Tokiko
Kutsuzawa, Kana
Yoshimura, Kensuke
Shimizu, Eiji
author_facet Taguchi, Kayoko
Numata, Noriko
Takanashi, Rieko
Takemura, Ryo
Yoshida, Tokiko
Kutsuzawa, Kana
Yoshimura, Kensuke
Shimizu, Eiji
author_sort Taguchi, Kayoko
collection PubMed
description BACKGROUND: We aimed to examine the feasibility of our newly-developed, integrated, and high-intensity individual cognitive behavioral therapy (CBT) protocol for treatment-resistant chronic pain. METHODS: We conducted an open-labeled prospective single-arm trial for patients aged 18 years and above, suffering from chronic pain, and diagnosed with somatic symptom disorder with predominant pain. We provided 16 weekly sessions of CBT, each lasting for 50 minutes, which included 4 new strategies: attention shift, memory work, mental practice, and video feedback. For comparison, the study had a pre-test post-test design. The primary outcome was the change from baseline (week 1) to 16, as indicated by the Numerical Rating Scale and Pain Catastrophizing Scale. In addition, we evaluated depression, anxiety, disability, and quality of life as secondary outcomes. RESULTS: Sixteen patients with chronic pain underwent our CBT program. Though there was no reduction in pain intensity, catastrophic cognition showed statistically significant improvement with a large effect size. Depression, anxiety, and disability demonstrated statistically significant improvements, with small to moderate effect sizes. No adverse events were reported. CONCLUSION: Our newly integrated CBT program for chronic pain may improve catastrophic cognition, depression, anxiety, and disability. Large-scale randomized controlled studies are necessary to investigate the program's effectiveness in the future.
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spelling pubmed-78864492021-02-17 Integrated cognitive behavioral therapy for chronic pain: An open-labeled prospective single-arm trial Taguchi, Kayoko Numata, Noriko Takanashi, Rieko Takemura, Ryo Yoshida, Tokiko Kutsuzawa, Kana Yoshimura, Kensuke Shimizu, Eiji Medicine (Baltimore) 5000 BACKGROUND: We aimed to examine the feasibility of our newly-developed, integrated, and high-intensity individual cognitive behavioral therapy (CBT) protocol for treatment-resistant chronic pain. METHODS: We conducted an open-labeled prospective single-arm trial for patients aged 18 years and above, suffering from chronic pain, and diagnosed with somatic symptom disorder with predominant pain. We provided 16 weekly sessions of CBT, each lasting for 50 minutes, which included 4 new strategies: attention shift, memory work, mental practice, and video feedback. For comparison, the study had a pre-test post-test design. The primary outcome was the change from baseline (week 1) to 16, as indicated by the Numerical Rating Scale and Pain Catastrophizing Scale. In addition, we evaluated depression, anxiety, disability, and quality of life as secondary outcomes. RESULTS: Sixteen patients with chronic pain underwent our CBT program. Though there was no reduction in pain intensity, catastrophic cognition showed statistically significant improvement with a large effect size. Depression, anxiety, and disability demonstrated statistically significant improvements, with small to moderate effect sizes. No adverse events were reported. CONCLUSION: Our newly integrated CBT program for chronic pain may improve catastrophic cognition, depression, anxiety, and disability. Large-scale randomized controlled studies are necessary to investigate the program's effectiveness in the future. Lippincott Williams & Wilkins 2021-02-12 /pmc/articles/PMC7886449/ /pubmed/33578513 http://dx.doi.org/10.1097/MD.0000000000023859 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle 5000
Taguchi, Kayoko
Numata, Noriko
Takanashi, Rieko
Takemura, Ryo
Yoshida, Tokiko
Kutsuzawa, Kana
Yoshimura, Kensuke
Shimizu, Eiji
Integrated cognitive behavioral therapy for chronic pain: An open-labeled prospective single-arm trial
title Integrated cognitive behavioral therapy for chronic pain: An open-labeled prospective single-arm trial
title_full Integrated cognitive behavioral therapy for chronic pain: An open-labeled prospective single-arm trial
title_fullStr Integrated cognitive behavioral therapy for chronic pain: An open-labeled prospective single-arm trial
title_full_unstemmed Integrated cognitive behavioral therapy for chronic pain: An open-labeled prospective single-arm trial
title_short Integrated cognitive behavioral therapy for chronic pain: An open-labeled prospective single-arm trial
title_sort integrated cognitive behavioral therapy for chronic pain: an open-labeled prospective single-arm trial
topic 5000
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886449/
https://www.ncbi.nlm.nih.gov/pubmed/33578513
http://dx.doi.org/10.1097/MD.0000000000023859
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