Transcranial direct current stimulation (a-tCDS) after subacromial injections in patients with subacromial pain syndrome: a randomized controlled pilot study.


Journal

BMC musculoskeletal disorders
ISSN: 1471-2474
Titre abrégé: BMC Musculoskelet Disord
Pays: England
ID NLM: 100968565

Informations de publication

Date de publication:
11 Mar 2021
Historique:
received: 01 06 2020
accepted: 28 02 2021
entrez: 12 3 2021
pubmed: 13 3 2021
medline: 15 5 2021
Statut: epublish

Résumé

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. 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. 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. 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. ClinicalTrials.gov, NCT03967574 . Registered 30 May 2019 - Retrospectively registered.

Sections du résumé

BACKGROUND 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 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 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 CONCLUSIONS
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 BACKGROUND
ClinicalTrials.gov, NCT03967574 . Registered 30 May 2019 - Retrospectively registered.

Identifiants

pubmed: 33706729
doi: 10.1186/s12891-021-04139-2
pii: 10.1186/s12891-021-04139-2
pmc: PMC7948354
doi:

Substances chimiques

Adrenal Cortex Hormones 0

Banques de données

ClinicalTrials.gov
['NCT03967574']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

265

Subventions

Organisme : Fond de Recherche en Enseignement en Orthopédie de Sherbrooke (FREOS) (CA)
ID : N/A
Organisme : Université de Sherbrooke Faculty of Medicine and Health Sciences
ID : N/A

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Auteurs

Samuel Larrivée (S)

Research Center on Aging CIUSSS Estrie CHUS, Sherbrooke, QC, Canada.
Department of Surgery, Division of Orthopedics, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.

Frédéric Balg (F)

Department of Surgery, Division of Orthopedics, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.
Research Center CRCHUS, CIUSSS Estrie CHUS, Sherbrooke, QC, Canada.

Guillaume Léonard (G)

Research Center on Aging CIUSSS Estrie CHUS, Sherbrooke, QC, Canada.
School of Rehabilitation, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.

Sonia Bédard (S)

Research Center CRCHUS, CIUSSS Estrie CHUS, Sherbrooke, QC, Canada.

Michel Tousignant (M)

Research Center on Aging CIUSSS Estrie CHUS, Sherbrooke, QC, Canada.
School of Rehabilitation, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.

Patrick Boissy (P)

Research Center on Aging CIUSSS Estrie CHUS, Sherbrooke, QC, Canada. patrick.boissy@usherbrooke.ca.
Department of Surgery, Division of Orthopedics, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada. patrick.boissy@usherbrooke.ca.
Research Center CRCHUS, CIUSSS Estrie CHUS, Sherbrooke, QC, Canada. patrick.boissy@usherbrooke.ca.

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