Use of the PREPARE (PREhabilitation, Physical Activity and exeRcisE) program to improve outcomes after lumbar fusion surgery for severe low back pain: a study protocol of a person-centred randomised controlled trial

BMC Musculoskeletal Disorders

Study Protocol

Max Jakobsson¹  Helena Brisby²  Mari Lundberg³  Olle Hägg⁴  Hanna Lotzke⁵  Lars-Eric Olsson⁶  Rob Smeets⁷  Marlies den Hollander⁸  Annelie Gutke⁹ 

[1] Department of Orthopaedics, Institute of Clinical Science, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden;District Department North, Division of Rehabilitation, Borås Stad, Borås, Sweden;Department of Orthopaedics, Institute of Clinical Science, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden;Division of Physiotherapy, Department of Neurobiology, Care Sciences and Sociology, Karolinska Institutet, Stockholm, Sweden;Department of Orthopaedics, Institute of Clinical Science, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden;Division of Physiotherapy, Department of Neurobiology, Care Sciences and Sociology, Karolinska Institutet, Stockholm, Sweden;Department of Orthopaedics, Sahlgrenska University Hospital, Gothenburg, Sweden;Department of Orthopaedics, Institute of Clinical Science, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden;Spine Center Göteborg, Västra Frölunda, Sweden;Department of Orthopaedics, Institute of Clinical Science, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden;Spine Center Göteborg, Västra Frölunda, Sweden;Physiotherapy Department Spine Center AB, 430 21, Västra Frölunda, Sweden;Department of Orthopaedics, Sahlgrenska University Hospital, Gothenburg, Sweden;Institute of Health and Care Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden;Gothenburg Centre for Person-Centred Care (GPCC), University of Gothenburg, Gothenburg, Sweden;Department of Rehabilitation Medicine, Maastricht University, Maastricht, The Netherlands;Libra Rehabilitation and Audiology, Eindhoven/Weert, The Netherlands;Department of Rehabilitation Medicine, Maastricht University, Medical Centre, Maastricht, The Netherlands;Department of Clinical Psychological Science, Maastricht University, Maastricht, The Netherlands;Division of Physiotherapy, Department of Health and Rehabilitation, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden;

关键词: Prehabilitation;    Rehabilitation;    Spinal fusion surgery;    Physiotherapy;    Cognitive behavioural approach;    Person-centred;    Chronic low back pain;    Physical activity;   

DOI  :  10.1186/s12891-016-1203-8

 received in 2016-01-29, accepted in 2016-08-04,  发布年份 2016

来源: Springer

【 摘 要 】

BackgroundFollowing lumbar fusion surgery, a successful outcome is empirically linked to effective rehabilitation. While rehabilitation is typically postoperative, the phase before surgery – termed prehabilitation – is reportedly an ideal time to prepare the patient. There are presently no guidelines for prehabilitation before lumbar fusion surgery. Physical activity has well-known health benefits, and staying physically active despite pain is a major principle in non-pharmacological chronic low back pain treatment. Psychological factors such as fear of movement, pain catastrophizing and low self-efficacy are known to be barriers to staying active. No studies have investigated prehabilitation protocols that promote physical activity and target psychological risk factors before lumbar fusion surgery. The aim of our proposed randomised controlled trial is to investigate whether patients who undergo lumbar fusion surgery for degenerative disc disease experience better functioning with a physiotherapeutic prehabilitation program (PREPARE) based on a cognitive behavioural approach compared to conventional care.Methods/DesignWe will recruit 110 patients between 18–70 years of age with degenerative disc disease who are waiting for lumbar fusion surgery. These patients will be randomly assigned to receive either PREPARE or conventional care. PREPARE uses a person-centred perspective and focuses on promoting physical activity and targeting psychological risk factors before surgery. The primary outcome will be disability measured using the Oswestry Disability Index 2.0. Secondary outcomes will include functioning (patient-reported and performance-based), physical activity (accelerometer), health-related quality of life, back and leg pain intensity, pain catastrophizing, kinesiophobia, self-efficacy, depression, anxiety, satisfaction with treatment results and health economic factors. Data will be collected at baseline (preoperatively) after the intervention (preoperatively), 3 and 8 weeks, 3, 6, 12, 24 and 60 months postoperatively.DiscussionWe hypothesise that the focus on promoting physical activity and targeting psychological risk factors before surgery will decrease disability and help the patients to be more active despite pain both before and after surgery. We will use a combination of outcome measures both patient-reported and performance-based, as well as accelerometer data. This will provide a more comprehensive picture of the patient’s functioning than just patient-reported outcomes alone.Trial registrationCurrent Controlled Trials ISCRTN17115599, Retrospectively Registered 18 May 2015.

【 授权许可】

CC BY   
© The Author(s). 2016