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Study protocol for a feasibility study of an online educational programme for people working and living with persistent low back pain. | LitMetric

AI Article Synopsis

  • Low back pain is a leading cause of work absence and activity limitation worldwide, prompting the need for effective management strategies.
  • The study aims to evaluate the usability and effectiveness of a digital education program, called MyRelief, for individuals with persistent LBP in various countries, focusing on ergonomic and self-management techniques.
  • By assessing recruitment, engagement, and outcome metrics, the study seeks to identify challenges in delivering the program and inform future trials on its effectiveness.

Article Abstract

Background: Low back pain (LBP) is the main cause of activity limitation and work absence across the world, leading to a high social and economic burden for individuals, families, the labour market and society. The overall aim of this multicentre study is to test the usability, acceptability and feasibility of an evidence-based, digital education programme for people living and working with persistent LBP who are in sedentary or physically demanding jobs and need advice on ergonomics, self-management of pain and healthy behavioural strategies.

Methods: This is the protocol of a multinational, multicentre, prospective uncontrolled feasibility study targeting people with persistent LBP in Lithuania, Northern Ireland, Italy, Sweden and Portugal. Eligible participants will be offered the opportunity to use the MyRelief educational platform as part of their care and will undergo evaluations at baseline (enrollment) and 1-month follow-up. Feasibility will be assessed using measures of recruitment and retention, intervention engagement, outcome measure completion rates and within-group effect sizes in response to the digital education programme.

Discussion: This study will identify the challenges and implications of delivering a digital training programme in advance of potentially delivering the programme via an online educational platform available on mobile devices. The findings will inform the design of a future randomised controlled trial if it proves feasible.

Trial Registration: ClinicalTrials.gov, NCT04673773 . Registered 17 December 2020.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476405PMC
http://dx.doi.org/10.1186/s40814-023-01382-3DOI Listing

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