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      Effectiveness of a Multicomponent Treatment Based on Pain Neuroscience Education, Therapeutic Exercise, Cognitive Behavioral Therapy, and Mindfulness in Patients With Fibromyalgia (FIBROWALK Study): A Randomized Controlled Trial

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          Abstract

          Objective

          The purpose of this study was to evaluate the effectiveness of a 12-week multicomponent treatment based on pain neuroscience education, therapeutic exercise, cognitive behavioral therapy, and mindfulness—in addition to treatment as usual—compared with treatment as usual only in patients with fibromyalgia.

          Methods

          This randomized controlled trial involved a total of 272 patients who were randomly assigned to either multicomponent treatment (n = 135) or treatment as usual (n = 137). The multicomponent treatment (2-hour weekly sessions) was delivered in groups of 20 participants. Treatment as usual was mainly based on pharmacological treatment according to the predominant symptoms. Data on functional impairment using the Revised Fibromyalgia Impact Questionnaire as the primary outcome were collected as were data for pain, fatigue, kinesiophobia, physical function, anxiety, and depressive symptoms (secondary outcomes) at baseline, 12 weeks, and, for the multicomponent group only, 6 and 9 months. An intention-to-treat approach was used to analyze between-group differences. Baseline differences between responders (>20% Revised Fibromyalgia Impact Questionnaire reduction) and nonresponders also were analyzed, and the number needed to treat was computed.

          Results

          At posttreatment, significant between-group differences with a large effect size (Cohen d > 0.80) in favor of the multicomponent treatment were found in functional impairment, pain, kinesiophobia, and physical function, whereas differences with a moderate size effect (Cohen d > 0.50 and <0.80) were found in fatigue, anxiety, and depressive symptoms. Nonresponders scored higher on depressive symptoms than responders at baseline. The number needed to treat was 2 (95% CI = 1.7–2.3).

          Conclusion

          Compared with usual care, there was evidence of short-term (up to 3 months) positive effects of the multicomponent treatment for fibromyalgia. Some methodological shortcomings (eg, absence of follow-up in the control group and monitoring of treatment adherence, potential research allegiance) preclude robust conclusions regarding the proposed multicomponent program.

          Impact

          Despite some methodological shortcomings in the design of this study, the multicomponent therapy FIBROWALK can be considered a novel and effective treatment for patients with fibromyalgia. Physical therapists should detect patients with clinically relevant depression levels prior to treatment because depression can buffer treatment effects.

          Lay Summary

          Fibromyalgia is prevalent and can be expensive to treat. This multicomponent treatment could significantly improve the core symptoms of fibromyalgia compared with usual treatment.

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          Most cited references71

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          The Hospital Anxiety and Depression Scale

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            Is Open Access

            CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials

            The CONSORT statement is used worldwide to improve the reporting of randomised controlled trials. Kenneth Schulz and colleagues describe the latest version, CONSORT 2010, which updates the reporting guideline based on new methodological evidence and accumulating experience
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              The MOS 36-ltem Short-Form Health Survey (SF-36)

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                Author and article information

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                Journal
                Physical Therapy
                Oxford University Press (OUP)
                0031-9023
                1538-6724
                December 01 2021
                December 01 2021
                December 01 2021
                December 01 2021
                September 02 2021
                : 101
                : 12
                Affiliations
                [1 ]Unitat d'Expertesa en Síndromes de Sensibilització Central, Hospital de la Vall d'Hebron, Barcelona, Spain
                [2 ]Escoles Universitàries Gimbernat, Universitat Autònoma de Barcelona, Sant Cugat del Vallès, Spain
                [3 ]Teaching, Research, and Innovation Unit - Parc Sanitari Sant Joan de Déu, Sant Boi de Llobregat, Spain
                [4 ]Department of Basic, Developmental and Educational Psychology. Universitat Autònoma de Barcelona, Cerdanyola del Vallès, Spain
                [5 ]Departament of Clinical & Health Psychology, Universitat Autònoma de Barcelona, Cerdanyola del Vallès, Spain
                [6 ]Department of Methods of Research and Diagnosis in Education, Universitat de Barcelona, Barcelona, Spain
                Article
                10.1093/ptj/pzab200
                34499174
                8710a353-48ec-4144-868e-4228f3d74bd2
                © 2021

                https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model

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