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Transcranial direct current stimulation (a-tCDS) after subacromial injections in patients with subacromial pain syndrome: a randomized controlled pilot study.
Larrivée, Samuel; Balg, Frédéric; Léonard, Guillaume; Bédard, Sonia; Tousignant, Michel; Boissy, Patrick.
Afiliação
  • Larrivée S; Research Center on Aging CIUSSS Estrie CHUS, Sherbrooke, QC, Canada.
  • Balg F; Department of Surgery, Division of Orthopedics, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.
  • Léonard G; Department of Surgery, Division of Orthopedics, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.
  • Bédard S; Research Center CRCHUS, CIUSSS Estrie CHUS, Sherbrooke, QC, Canada.
  • Tousignant M; Research Center on Aging CIUSSS Estrie CHUS, Sherbrooke, QC, Canada.
  • Boissy P; School of Rehabilitation, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.
BMC Musculoskelet Disord ; 22(1): 265, 2021 Mar 11.
Article em En | MEDLINE | ID: mdl-33706729
BACKGROUND: Subacromial pain syndrome (SAPS) is a common complaint in orthopaedics. Subacromial corticosteroid injections (CSI) can relieve pain in the short term. Anodal transcranial direct current stimulation (a-tDCS) has been used for symptomatic pain relief in a variety of chronic pain conditions. The aim of this pilot study was to assess whether the application a-tDCS could enhance the symptomatic relief provided by CSI in patients affected by SAPS. METHODS: Thirty-eight participants (18 to 65-year-old) suffering from SAPS were recruited to have a CSI and randomly allocated to receive, 1 weeks post CSI, real a-tDCS (r-tDCS), sham tDCS (s-tDCS) or no intervention (Control). Upper limb function was measured 1 week prior to the CSI, at the 2- and 4-week follow-ups using self-administered questionnaires and physical measures. Self-reported pain and activity during each day were logged by the participants using visual analog scales (VAS). Differences between groups were tested using repeated-measures ANOVAs. RESULTS: Pain VAS and the Single Assessment Numeric Evaluation scale (SANE) showed significant improvement from baseline 2 weeks and 4 weeks after CSI in all groups (p < 0.05). There were no significant group X time interaction 2 weeks following tDCS treatment in any of the variables. CONCLUSION: All groups showed significant improvement in pain VAS and SANE scores following the CSI. One session of a-tDCS treatment 2 weeks following CSI did not result in any additive or potentializing effects when compared to a s-tDCS or a control group. TRIAL REGISTRATION: ClinicalTrials.gov, NCT03967574 . Registered 30 May 2019 - Retrospectively registered.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor Crônica / Estimulação Transcraniana por Corrente Contínua Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor Crônica / Estimulação Transcraniana por Corrente Contínua Idioma: En Ano de publicação: 2021 Tipo de documento: Article