多模式、物理治疗师主导的职业干预对炎症性关节炎患者的有效性和成本效益:物理疗法WORKs试验的研究方案。

IF 2.1 Q3 RHEUMATOLOGY BMC Rheumatology Pub Date : 2023-09-20 DOI:10.1186/s41927-023-00357-4
N F Bakker, S F E van Weely, N Hutting, Y F Heerkens, J A Engels, J B Staal, M van der Leeden, A Boonen, W B van den Hout, T P M Vliet Vlieland, J Knoop
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引用次数: 0

摘要

背景:尽管工作能力下降是炎症性关节炎(IA)患者的一个严重问题,但在临床实践中,工作能力是一个暴露不足的领域。关于IA职业干预的证据有限,但理疗师(PT)提供的有利结果证明需要进一步研究。因此,与常规护理相比,我们的目的是评估多模式、PT主导的职业干预对(自营)就业IA患者的(成本)有效性。方法:这项随机对照试验将包括140名类风湿性关节炎(RA)或轴性脊椎关节炎(axSpA)患者,他们(自营)工作,工作能力下降(工作能力指数-单项量表(WAS) ≤ 7/10)和/或RA/axSpA相关病假(≤ 6个月)。参与者将被1:1随机分配到干预或对照条件下(常规护理)。由初级保健PT提供的干预措施将针对每位患者进行个性化,包括12个月内的10至21次治疗。干预将是多模式的,包括1)运动治疗和体育活动计划,2)教育/自我管理支持,3)指导参与者寻找相关其他护理的工作路线图,以及可选的4)在线自我管理课程和5)工作场所检查。评估将在基线以及3、6和12个月后进行。有效性的主要结果衡量标准是工作能力,在12个月时用WAS进行测量。对于成本效益分析,EuroQol(EQ-5D-5L)、自我报告的医疗保健使用、病假和工作时的生产力将用于从社会角度估计基于试验的成本效用。过程评估,包括依从性和治疗保真度的评估,将在干预组的随机样本中使用PT的注册和12个月随访时的半结构化访谈进行。讨论:这项研究的结果将为多模式、PT主导的职业干预对IA和工作能力下降的人的(成本)有效性提供见解。试验注册:本研究在国际临床试验注册平台(ICTRP)注册,编号为NL9343。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Effectiveness and cost-effectiveness of a multimodal, physiotherapist-led, vocational intervention in people with inflammatory arthritis: study protocol of the Physiotherapy WORKs trial.

Background: Although reduced work ability is a substantial problem among people with inflammatory arthritis (IA), work ability is an underexposed area in clinical practice. Evidence on vocational interventions in IA is limited, but favourable results of delivery by a physiotherapist (PT) warrant the need for further research. Therefore, we aim to evaluate the (cost-)effectiveness of a multimodal, PT-led, vocational intervention in (self-)employed people with IA compared to usual care.

Methods: This randomized controlled trial will include 140 people with rheumatoid arthritis (RA) or axial spondyloarthritis (axSpA) who are (self-)employed and have reduced work ability (Work Ability Index - Single Item Scale (WAS) ≤ 7/10) and/or RA/axSpA related sick leave (≤ 6 months). Participants will be randomized 1:1 to the intervention or control condition (usual care). The intervention, delivered by primary care PTs, will be personalized to each patient, consisting of 10 to 21 sessions over 12 months. The intervention will be multimodal, comprising of 1) exercise therapy and a physical activity plan, 2) education/self-management support, 3) work-roadmap to guide participants in finding relevant other care, with optionally 4) online self-management course and 5) workplace examination. Assessments will be performed at baseline and after 3, 6, and 12 months. The primary outcome measure of effectiveness is work ability, as measured with the WAS at 12 months. For the cost-effectiveness analysis, the EuroQol (EQ-5D-5L), self-reported healthcare use, sick leave and productivity while at work will be used to estimate the trial based cost-utility from a societal perspective. A process evaluation, including assessments of adherence and treatment fidelity, will be undertaken using the registrations of the PTs and semi-structured interviews at 12 months follow-up in a random sample of the intervention group.

Discussion: The results of this study will provide insights in the (cost-)effectiveness of a multimodal, PT-led, vocational intervention in people with IA and a reduced work ability.

Trial registration: This study is registered in the International Clinical Trial Registry Platform (ICTRP) under number NL9343.

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来源期刊
BMC Rheumatology
BMC Rheumatology Medicine-Rheumatology
CiteScore
3.80
自引率
0.00%
发文量
73
审稿时长
15 weeks
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