Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/42584
Title: Physiotherapy-led care for acute low back pain in Belgium: Protocol with preliminary results
Authors: DENIS, Corentin 
SEVERIJNS, Pieter 
Dankaerts, Wim
TIMMERMANS, Annick 
Roussel, Nathalie
GOOSSENS, Nina 
FOURRE, Antoine 
VERSCHUEREN, Pieter 
Pitance, Laurent
JANSSENS, Lotte 
Issue Date: 2023
Source: 11th Congress of the Belgian Back Society, Brussels, Belgium, 02-12-2023
Abstract: Abstract Background Low back pain (LBP) is the leading cause of disability worldwide, presenting a substantial societal burden. This calls for the optimization of care pathways to enhance the efficacy of the management of LBP. Physiotherapists (PT), who have unique expertise in movement and the musculoskeletal system, can adopt a central role in the primary care for LBP. International research has shown that PT-led care for musculoskeletal conditions improved clinical efficacy, reduced waiting times, resulted in higher satisfaction among patients and referrers, and was not associated with increased harm. However, PT-led care still needs to be explored in Belgium despite its acceptance in 72% of World Confederation for Physical Therapy (WCPT) member countries, encompassing various European nations. Purpose The primary objective is to examine the clinical efficacy of PT-led care compared to General Practitioner (GP)-led care for patients with acute LBP in Belgium. The secondary objective is to identify which patients’ biopsychosocial factors determine the clinical efficacy of PT-led care. Methods In a quasi-randomized controlled trial, 640 subjects with acute LBP will receive PT-led care or GP-led care. Demographics and risk of chronicity (Start Back Tool [SBT]) will be assessed at baseline. LBP-related disability (Oswestry Disability Index [ODI]), pain intensity (Numeric Pain Rating Scale [NRS]) and pain extent (Pain Drawing) will be evaluated at baseline, every week from the first to the sixth week and at three months, six months, one year and two years. Attitudes and beliefs (Fear-Avoidance Beliefs Questionnaire [FABQ] and Back Pain Attitudes Questionnaire [Back-PAQ]) and self-efficacy (General Self-Efficacy Scale [GSES]) will be assessed at baseline, three months, six months, one year and two years. Baseline group characteristics will be displayed using descriptive statistics. Based on a data normality check, parametric or non-parametric statistics will be performed and the significance level of α=0.05 will be used. Clinical efficacy of PT-led care will be assessed with linear mixed models and multiple linear regression analysis for variable relationships. Results In October 2023, 26 participants were included (French-speaking: n= 14, Dutch-speaking: n= 12) and directly allocated to PT-led care. Within-group improvement was found at 3 months for NRS (-3.9, SD = 2.7, P < 0.01) and ODI (- 19.9, SD = 15.6, p < 0.01), with a prominent improvement in the first week (P < 0.001). Moreover, the improvement in NRS was associated with baseline pain extent (P < 0.001), FABQ (P < 0.001), Back-PAQ (P < 0.001) and GSES (P < 0.001) scores. Improvement in ODI is associated with the SBT subgroup (P = 0.032), pain extent (P = 0.002) and Back-PAQ (P = 0.002). Conclusion Preliminary results indicate that PT-led care is effective for acute LBP in reducing pain and disability and seems a promising and feasible pathway, deserving further investigation in Belgium. Implication Study findings may pave the way for enhancing acute LBP treatment and influence policy changes regarding direct access to PT in Belgium.
Keywords: low back pain;direct access;care pathway
Document URI: http://hdl.handle.net/1942/42584
Category: C2
Type: Conference Material
Appears in Collections:Research publications

Files in This Item:
File Description SizeFormat 
Poster - Direct physio trial - BBS 2023.pdfConference material209.62 kBAdobe PDFView/Open
Show full item record

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.