Article Text

Protocol
Evidence-based digital support during 1 year after an Interdisciplinary Pain Rehabilitation Programme for persons with chronic musculoskeletal pain to facilitate a sustainable return to work: a study protocol for a registry-based multicentre randomised controlled trial
  1. Christina Turesson1,
  2. Gunilla Liedberg1,
  3. Linda Vixner2,
  4. Monika Lofgren3,
  5. Mathilda Björk1
  1. 1Department of Health Medicine and Caring Sciences, Linkoping University, Linkoping, Sweden
  2. 2School of Health and Welfare, Dalarna University, Falun, Sweden
  3. 3Department of Clinical Sciences and Department of Rehabilitation Medicine Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden
  1. Correspondence to Dr Christina Turesson; christina.turesson{at}liu.se

Abstract

Introduction Chronic musculoskeletal pain (CMSP) severely affects the individual’s quality of life, functioning and ability to work, and comes with significant societal costs for sick leave and productivity loss. After rehabilitation, patients with CMSP often experience lack of support when responsibility for the return-to-work process is taken over by the employer. Therefore, we aim to evaluate the effectiveness of a digital support (Sustainable WorkEr digital support for Persons with chronic Pain and their Employers (SWEPPE)) for promoting a sustainable return-to-work for persons with CMSP and to facilitate the employers’ supportive role and responsibilities in the process.

Methods and analysis In this registry-based multicentre randomised controlled trial, 360 patients with CMSP will be randomised to either receive the smartphone application SWEPPE (n=180) or to a control group (n=180). The intervention group will use SWEPPE for 1 year and the control group will not receive any intervention for return to work (RTW). Participants will be recruited from approximately 10 specialist and primary care level units connected to the Swedish National Quality Registry for Pain Rehabilitation providing Interdisciplinary Pain Rehabilitation Programmes (IPRP) for CMSP. Eligibility criteria are age 18–65 years and a need for support in RTW or continued support at work for creating a sustainable work situation. Baseline data will be collected when the participants have completed the IPRP. Final assessment will be performed after 12 months. The primary outcome will be a number of days with sickness cash benefit. Secondary outcomes and explanatory variables including important domains affected by CMSP such as health-related quality of life, functioning and work ability will be collected.

Ethics and dissemination The Swedish Ethics Review Board approved the study (Dnr 2020-01593, Dnr 2021-01854). The study findings will be disseminated through publication, national and international conferences, and meetings to be available for patients, healthcare providers or stakeholders.

Trial registration number NCT05058547.

  • Clinical trials
  • PAIN MANAGEMENT
  • REHABILITATION MEDICINE
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Footnotes

  • Twitter @ChristinaTures1

  • Contributors MB and GL formed the original research concept. CT, MB and GL contributed to the study design and CT will coordinate the project in cooperation with MB and GL. CT, ML and LV will be responsible for the unit coordinators at each participating unit and the inclusion of participants. All authors will collect and manage data during the trial. CT, MB and GL have written and revised this protocol with critical input from ML and LV. All authors have contributed important intellectual content to the manuscript.

  • Funding This study was supported by the Swedish Research Council for Health, Working Life and Welfare (Dnr 2019-01264).

  • Competing interests None declared.

  • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.