Get Back, a person-centred digital programme targeting physical activity for patients undergoing spinal stenosis surgery-a study protocol of a randomized feasibility study

被引:0
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作者
Karlsson, Emelie [1 ]
Hanafi, Rikard [1 ,2 ,3 ]
Brisby, Helena [4 ,5 ]
Fors, Andreas [6 ,7 ,8 ]
Kemani, Mike [1 ,3 ,9 ]
Hedman, Hakan [7 ]
Nijs, Jo [2 ,10 ,11 ]
Lundberg, Mari [1 ,2 ,6 ,7 ]
机构
[1] Sophiahemmet Univ, Dept Hlth Promoting Sci, Back Mot Res Grp, Box 5605, S-11486 Stockholm, SE, Sweden
[2] Vrije Univ Brussel, Fac Phys Educ & Physiotherapy, Dept Physiotherapy Human Physiol & Anat, Pain Mot Res Grp PAIN, B-1050 Brussels, Belgium
[3] Karolinska Univ Hosp, Med Unit Med Psychol, Theme Womens Hlth & Allied Hlth Profess, Solna, Sweden
[4] Univ Gothenburg, Inst Clin Sci, Sahlgrenska Acad, Dept Orthopaed, Gothenburg, Sweden
[5] Sahlgrens Univ Hosp, Dept Orthopaed, Gothenburg, Sweden
[6] Univ Gothenburg, Inst Hlth & Care Sci, Sahlgrenska Acad, Gothenburg, Sweden
[7] Univ Gothenburg, Sahlgrenska Acad, Ctr Person Centred Care GPCC, Gothenburg, Sweden
[8] Reg Vastra Gotaland, Res Educ Dev & Innovat, Primary Hlth Care, Gothenburg, Sweden
[9] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
[10] Univ Hosp Brussels, Dept Phys Med & Physiotherapy, Chron Pain Rehabil, B-1050 Brussels, Belgium
[11] Univ Gothenburg, Dept Hlth & Rehabil, Unit Physiotherapy, Inst Neurosci & Physiol,Sahlgrenska Acad, Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
Spine disease; eHealth; Physical activity; Physiotherapy; Feasibility; BEHAVIOR-CHANGE; SELF-EFFICACY; LUMBAR; DISABILITY; OUTCOMES; FEAR; PERFORMANCE; MOVEMENT; CAPACITY; IMPROVE;
D O I
10.1186/s40814-023-01433-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundSpinal stenosis is the most common reason for elective spine surgery, and the cardinal symptom is leg pain and discomfort when walking. Patients with spinal stenosis have a decreased level of physical activity and thereby an increased risk of poor health. Get Back is a person-centred digital programme that strives to support patients being physically active after surgery. The aim is to explore if Get Back, in its present format (referred to as Get Backfeasibility), is feasible and contributes to detectable change in variables related to intervention content.MethodsThirty patients planned for decompression surgery due to central lumbar spinal stenosis who present with low physical activity, pain catastrophizing or fear of movement, will be included in a randomized feasibility study. All patients will be randomly allocated to either Get Backfeasibility or usual physical therapy. Get Backfeasibility aims to increase the patient's physical activity level by combining a person-centred and cognitive behavioural approach. It comprises 10 video and telephone sessions led by a physical therapist over 12 weeks (pre/postoperatively). Outcomes are treatment fidelity (treatment dose, adherence, and content), process feasibility (recruitment, intervention use, and acceptability of measurements and intervention), and variables related to the intervention content (steps per day, physical activity level, pain catastrophizing, fear of movement, and general self-efficacy). Treatment fidelity and feasibility data will be assessed during the full study period (12 weeks). Physical activity, physical capacity, and patient-reported outcomes will be assessed digitally at baseline (2 weeks preoperatively) and 11-12 weeks postoperatively. Variables related to the intervention content will be monitored weekly through a digital application. Feasibility data will be analysed descriptively and inferentially using a nonparametric approach, data from repeated measures will be displayed graphically and data from telephone interviews will be analysed using content analysis with a descriptive manifest approach.DiscussionThe results will provide information on whether Get Back in its present format is feasible and can be evaluated for effectiveness in a larger randomized controlled trial, for patients with a low physical activity level and a high fear of movement who are undergoing decompression surgery.Trial registrationRegistered at ClinicalTrails.gov 04/08/2023, registration no. NCT05806593.
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页数:12
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