Mahajan Raman, Burza Sakib, Bouter Lex M, Sijtsma Klaas, Knottnerus André, Kleijnen Jos, Dael Peter Van, Zeegers Maurice P
Care and Public Health Research Institute, Maastricht University, Maastricht, Netherlands.
Médecins Sans Frontières, New Delhi, India.
JMIR Res Protoc. 2020 Oct 21;9(10):e17864. doi: 10.2196/17864.
Approximately 90% of currently published clinical and public health research is in the form of observational studies. Having a detailed and registered study protocol prior to data collection is important in any empirical study. Without this, there is no reliable way to assess the occurrence of publication bias, outcome reporting bias, and other protocol deviations. However, there is currently no solid guidance available on the information that a protocol for an observational study should contain.
The aim of this study is to formulate the Standardized Protocol Items Recommendations for Observational Studies (SPIROS) reporting guidelines, which focus on 3 main study designs of analytical epidemiology: cohort, case-control, and cross-sectional studies.
A scoping review of published protocol papers of observational studies in epidemiology will identify candidate items for the SPIROS reporting guidelines. The list of items will be extended with the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) checklist items and recommendations from the SPIROS steering committee. This long list serves as the basis for a 2-round Delphi survey among experts to obtain consensus on which items to include. Each candidate item from the long list will be rated on a 5-point Likert scale to assess relevance for inclusion in the SPIROS reporting guidelines. Following the Delphi survey, an expert-driven consensus workshop will be convened to finalize the reporting guidelines.
A scoping review of published observational study protocols has been completed, with 59 candidate items identified for inclusion into the Delphi survey, itself launched in early 2020.
This project aims to improve the timeliness, completeness, and clarity of study protocols of observational studies in analytical epidemiology by producing expert-based recommendations of items to be addressed. These reporting guidelines will facilitate and encourage researchers to prepare and register study protocols of sufficient quality prior to data collection in order to improve the transparency, reproducibility, and quality of observational studies.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): PRR1-10.2196/17864.
目前发表的临床和公共卫生研究中,约90%为观察性研究形式。在任何实证研究中,数据收集前制定详细且已注册的研究方案很重要。没有这个,就没有可靠方法来评估发表偏倚、结果报告偏倚及其他方案偏差的发生情况。然而,目前对于观察性研究方案应包含的信息尚无可靠指导。
本研究旨在制定观察性研究标准化方案条目推荐(SPIROS)报告指南,该指南聚焦于分析性流行病学的3种主要研究设计:队列研究、病例对照研究和横断面研究。
对已发表的流行病学观察性研究方案论文进行范围综述,以确定SPIROS报告指南的候选条目。条目清单将通过加强流行病学观察性研究报告(STROBE)清单条目及SPIROS指导委员会的建议进行扩充。这份长清单作为两轮德尔菲专家调查的基础,以就纳入哪些条目达成共识。长清单中的每个候选条目将按5级李克特量表进行评分,以评估其纳入SPIROS报告指南的相关性。德尔菲调查之后,将召开一次由专家主导的共识研讨会以最终确定报告指南。
已完成对已发表的观察性研究方案的范围综述,确定了59个候选条目纳入2020年初启动的德尔菲调查。
本项目旨在通过给出基于专家的需涵盖条目的建议,提高分析性流行病学中观察性研究方案的及时性、完整性和清晰度。这些报告指南将促进并鼓励研究人员在数据收集前准备并注册高质量的研究方案,以提高观察性研究的透明度、可重复性和质量。
国际注册报告识别号(IRRID):PRR1-10.2196/17864