Proposed categories for reporting of service organization in rehabilitation in clinical trials: a discussion paper.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-07 DOI:10.23736/S1973-9087.24.08494-6
Cecilie Røe, Christoph Gutenbrunner, Andrea Bökel, Marit Kirkevold, Boya Nugraha, Nada Andelic, Juan Lu, Erik Bautz-Holter, Paul B Perrin, Audny Anke, Reidun Jahnsen, Grethe Månum, Emilie Howe, Line Kildal Bragstad, Helene L Soberg
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Abstract

Background: The lack of standardized reporting for crucial organizational factors in rehabilitation poses a significant barrier to understanding their impact on patient outcomes in clinical trials and meta-analyses.

Aim: Based on the categories in the International Classification of Service Organization in Rehabilitation (ICSO-R 2.0), we aimed to develop reporting standards specifically for organizational factors in clinical trials.

Methods: A comprehensive two-step process was conducted. In Step 1, important categories were identified. The identification was based on previous results from a Delphi survey with international stakeholder participation, two systematic literature reviews and results from focus groups with users in Germany, Indonesia and Norway. Step 2 involved the necessary reduction of categories and the proposal of reporting specifications, achieved through two voting rounds among key researchers, stakeholders and users.

Results: The suggested minimum reporting set comprises Context and Setting as well as Quality assurance and management. The Context and Setting is proposed to include whether the intervention is delivered by Hospital, Community or Other service providers. The Mode of delivery is proposed to be specified as Inpatient, Outpatient, In-home, or Tele-rehabilitation. Furthermore, the Level of specialization (Primary/Secondary) and the Phase of service delivery Acute, Subacute or Long-term rehabilitation services should be reported. The Quality assurance and management should be reported as Yes or No, with the option Yes requiring description of the quality assurance applied in the methods section.

Conclusions: This study proposed a compulsory and standardized reporting of organizational factors in clinical trials to facilitate the generation of scientific evidence regarding effective service provision and delivery in rehabilitation medicine. Authors are encouraged to consider the proposed reporting set to testing, criticism, and modification to enhance its applicability and robustness.

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临床试验中康复服务组织报告的拟议类别:讨论文件。
背景:目的:根据《国际康复服务组织分类》(ICSO-R 2.0)中的分类,我们旨在制定专门针对临床试验中组织因素的报告标准:方法:分两步进行。第一步,确定重要类别。确定的依据是之前由国际利益相关者参与的德尔菲调查的结果、两篇系统文献综述以及德国、印度尼西亚和挪威用户焦点小组的结果。第二步是对类别进行必要的缩减,并通过主要研究人员、利益相关方和用户之间的两轮投票,提出报告规范:结果:建议的最低报告要求包括 "背景和环境 "以及 "质量保证和管理"。背景和环境建议包括干预是否由医院、社区或其他服务提供者提供。提供服务的方式建议明确为住院、门诊、居家或远程康复。此外,还应报告专业水平(初级/中级)和服务提供阶段(急性、亚急性或长期康复服务)。质量保证和管理应报告为是或否,选项 "是 "要求在方法部分描述所采用的质量保证:本研究建议对临床试验中的组织因素进行强制性和标准化报告,以促进产生有关康复医学中有效服务提供和交付的科学证据。我们鼓励作者考虑对建议的报告集进行测试、批评和修改,以提高其适用性和稳健性。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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