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dc.contributor.authorPaula, Tânia Maria Hendges dept_BR
dc.contributor.authorCastro, Mariane Schäfferpt_BR
dc.contributor.authorMedeiros, Liciane Fernandespt_BR
dc.contributor.authorPaludo, Rodrigo Hernandespt_BR
dc.contributor.authorCouto, Fabricia Fritzpt_BR
dc.contributor.authorCosta, Taina Ramires dapt_BR
dc.contributor.authorFortes, Juliana Pereirapt_BR
dc.contributor.authorSalbego, Maiara de Oliveirapt_BR
dc.contributor.authorBehnck, Gabriel Schardosimpt_BR
dc.contributor.authorMoura, Thielly Amaral Mesquita dept_BR
dc.contributor.authorTarouco, Mariana Lenzpt_BR
dc.contributor.authorCaumo, Wolneipt_BR
dc.contributor.authorSouza, Andressa dept_BR
dc.date.accessioned2024-12-21T06:55:24Zpt_BR
dc.date.issued2023pt_BR
dc.identifier.issn0034-7094pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/282654pt_BR
dc.description.abstractIntroduction Fibromyalgia is a complex, generalized, and diffuse chronic musculoskeletal pain. Pharmacological approaches are widely used to relieve pain and increase quality of life. Low-Dose Naltrexone (LDN) was shown to increase the nociceptive threshold in patients with fibromyalgia. Transcranial Direct Current Stimulation (tDCS) is effective for pain management. Objective The purpose of this study was to evaluate the analgesic and neuromodulatory effects of a combination of LDN and tDCS in patients with fibromyalgia. Methods This was a randomized, double-blinded, parallel, placebo/sham-controlled trial (NCT04502251; RBR-7HK8N) in which 86 women with fibromyalgia were included, and written informed consent was obtained from them. The patients were allocated into four groups: LDN + tDCS (n = 21), LDN + tDCS Sham (n = 22), placebo + tDCS (n = 22), and placebo+tDCS Sham (n = 21). The LDN or placebo (p.o.) intervention lasted 26 days; in the last five sessions, tDCS was applied (sham or active, 20 min, 2 mA). The following categories were assessed: sociodemographic, Visual Analog Pain Scale (VAS), Pain Catastrophizing Scale (PCS), State-Trait Anxiety Inventory (STAI), Fibromyalgia Impact Questionnaire (FIQ), Beck Depression Inventory (BDI-II), Profile of Chronic Pain Scale (PCP:S), Pain Pressure Threshold (PPT), and Conditioned Pain Modulation (CPM). Blood samples were collected to analyze BDNF serum levels. Results At baseline, no significant difference was found regarding all measurements. VAS pain was significantly reduced in the LDN + tDCS (p = 0.010), LDN + tDCS Sham (p = 0.001), and placebo+tDCS Sham (p = 0.009) groups. In the PCP:S, the LDN+tDCS group showed reduced pain frequency and intensity (p = 0.001), effect of pain on activities (p = 0.014) and emotions (p = 0.008). Depressive symptoms reduced after all active interventions (p > 0.001). Conclusion Combined LDN+tDCS has possible benefits in reducing pain frequency and intensity; however, a placebo effect was observed in pain using VAS, and further studies should be performed to analyze the possible association.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoporpt_BR
dc.relation.ispartofBrazilian journal of anesthesiology. Rio de Janeiro. Vol. 73, n. 4 (2023), p. 409−417pt_BR
dc.rightsOpen Accessen
dc.subjectFibromialgiapt_BR
dc.subjectFibromyalgiaen
dc.subjectNaltrexoneen
dc.subjectDorpt_BR
dc.subjectEstimulação transcraniana por corrente contínuapt_BR
dc.subjectPainen
dc.subjectTranscranial direct current stimulationen
dc.subjectNaltrexonapt_BR
dc.titleAssociation of low-dose naltrexone and transcranial direct current stimulation in fibromyalgia : a randomized, double-blinded, parallel clinical trialpt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001213949pt_BR
dc.type.originNacionalpt_BR


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