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硬皮病患者为中心干预网络(SPIN)队列:一项队列多项随机对照试验(cmRCT)设计的方案,旨在支持在罕见病背景下进行心理社会和康复干预的试验。

The Scleroderma Patient-centered Intervention Network (SPIN) Cohort: protocol for a cohort multiple randomised controlled trial (cmRCT) design to support trials of psychosocial and rehabilitation interventions in a rare disease context.

机构信息

Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, Québec, Canada.

出版信息

BMJ Open. 2013 Aug 7;3(8):e003563. doi: 10.1136/bmjopen-2013-003563.

Abstract

INTRODUCTION

Psychosocial and rehabilitation interventions are increasingly used to attenuate disability and improve health-related quality of life (HRQL) in chronic diseases, but are typically not available for patients with rare diseases. Conducting rigorous, adequately powered trials of these interventions for patients with rare diseases is difficult. The Scleroderma Patient-centered Intervention Network (SPIN) is an international collaboration of patient organisations, clinicians and researchers. The aim of SPIN is to develop a research infrastructure to test accessible, low-cost self-guided online interventions to reduce disability and improve HRQL for people living with the rare disease systemic sclerosis (SSc or scleroderma). Once tested, effective interventions will be made accessible through patient organisations partnering with SPIN.

METHODS AND ANALYSIS

SPIN will employ the cohort multiple randomised controlled trial (cmRCT) design, in which patients consent to participate in a cohort for ongoing data collection. The aim is to recruit 1500-2000 patients from centres across the world within a period of 5 years (2013-2018). Eligible participants are persons ≥18 years of age with a diagnosis of SSc. In addition to baseline medical data, participants will complete patient-reported outcome measures every 3 months. Upon enrolment in the cohort, patients will consent to be contacted in the future to participate in intervention research and to allow their data to be used for comparison purposes for interventions tested with other cohort participants. Once interventions are developed, patients from the cohort will be randomly selected and offered interventions as part of pragmatic RCTs. Outcomes from patients offered interventions will be compared with outcomes from trial-eligible patients who are not offered the interventions.

ETHICS AND DISSEMINATION

The use of the cmRCT design, the development of self-guided online interventions and partnerships with patient organisations will allow SPIN to develop, rigourously test and effectively disseminate psychosocial and rehabilitation interventions for people with SSc.

摘要

简介

心理社会和康复干预措施越来越多地用于减轻慢性病患者的残疾程度并提高其健康相关生活质量(HRQL),但通常不适用于罕见病患者。针对罕见病患者开展严格、充分有力的此类干预措施试验非常困难。硬皮病患者为中心干预网络(SPIN)是一个由患者组织、临床医生和研究人员组成的国际合作组织。SPIN 的目标是建立一个研究基础设施,以测试易于使用且成本低廉的自我指导在线干预措施,从而减少患有罕见病系统性硬化症(SSc 或硬皮病)患者的残疾并改善其 HRQL。经过测试后,有效的干预措施将通过与 SPIN 合作的患者组织提供给患者。

方法和分析

SPIN 将采用队列多项随机对照试验(cmRCT)设计,在该设计中,患者同意参与队列研究以进行持续的数据收集。目标是在 5 年内(2013-2018 年)从全球各中心招募 1500-2000 名患者。符合条件的参与者是年龄≥18 岁且诊断为 SSc 的人。除了基线医疗数据外,参与者还将每 3 个月完成一次患者报告的结果测量。一旦入组该队列,患者将同意在未来被联系参加干预研究,并同意其数据将被用于与其他队列参与者进行测试的干预措施的比较。一旦开发出干预措施,将从队列中随机选择患者并向其提供干预措施,作为实用随机对照试验的一部分。接受干预措施的患者的结果将与未接受干预措施的符合试验条件的患者的结果进行比较。

伦理和传播

cmRCT 设计的使用、自我指导在线干预措施的开发以及与患者组织的合作,将使 SPIN 能够为 SSc 患者开发、严格测试和有效传播心理社会和康复干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/3740254/35c2ca2b71b5/bmjopen2013003563f01.jpg

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