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本文引用的文献

1
Demystifying Open Science in health psychology and behavioral medicine: a practical guide to Registered Reports and Data Notes.揭开健康心理学与行为医学中开放科学的神秘面纱:注册报告和数据说明实用指南
Health Psychol Behav Med. 2024 May 29;12(1):2351939. doi: 10.1080/21642850.2024.2351939. eCollection 2024.
2
A blueprint for patient and public involvement in the development of a reporting guideline for systematic reviews of outcome measurement instruments: PRISMA-COSMIN for OMIs 2024.患者及公众参与制定结局测量工具系统评价报告指南的蓝图:2024年OMIs的PRISMA-COSMIN
Res Involv Engagem. 2024 Mar 21;10(1):33. doi: 10.1186/s40900-024-00563-5.
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The challenges of open data sharing for qualitative researchers.定性研究人员在开放数据共享方面所面临的挑战。
J Health Psychol. 2024 Jun;29(7):659-664. doi: 10.1177/13591053241237620. Epub 2024 Mar 14.
4
Exchanging words: Engaging the challenges of sharing qualitative research data.交流观点:应对分享定性研究数据的挑战
Proc Natl Acad Sci U S A. 2023 Oct 24;120(43):e2206981120. doi: 10.1073/pnas.2206981120. Epub 2023 Oct 13.
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Opportunities, challenges and tensions: Open science through a lens of qualitative social psychology.机遇、挑战与矛盾:透过质性社会心理学视角看开放科学
Br J Soc Psychol. 2023 Oct;62(4):1581-1589. doi: 10.1111/bjso.12628. Epub 2023 Jan 31.
6
Qualitative Data Sharing: Participant Understanding, Motivation, and Consent.定性数据共享:参与者的理解、动机和同意。
Qual Health Res. 2022 Jan;32(1):182-191. doi: 10.1177/10497323211054058. Epub 2021 Dec 1.
7
Is It Time to Share Qualitative Research Data?是时候分享定性研究数据了吗?
Qual Psychol. 2018 Nov;5(3):380-393. doi: 10.1037/qup0000076. Epub 2017 Mar 16.
8
The FAIR Guiding Principles for scientific data management and stewardship.科学数据管理和保存的 FAIR 指导原则。
Sci Data. 2016 Mar 15;3:160018. doi: 10.1038/sdata.2016.18.
9
SCIENTIFIC STANDARDS. Promoting an open research culture.科学标准。促进开放的研究文化。
Science. 2015 Jun 26;348(6242):1422-5. doi: 10.1126/science.aab2374.
10
Guidance for developers of health research reporting guidelines.健康研究报告规范开发者指南。
PLoS Med. 2010 Feb 16;7(2):e1000217. doi: 10.1371/journal.pmed.1000217.

制定定性健康与社会护理研究数据集的数据记录报告指南(DeNOTE研究):一项研究方案。

Developing a Data Note reporting guideline for qualitative health and social care research datasets (the DeNOTE study): A study protocol.

作者信息

Long Hannah A, Toomey Elaine, Stevenson Fiona, Brooks Joanna M, Stewart Andrew J, French David P

机构信息

Healthier Futures Research Platform, School of Health Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.

Centre for Health Research Methodology, School of Nursing, and Midwifery, University of Galway, Galway, Ireland.

出版信息

Health Psychol Behav Med. 2025 Jul 21;13(1):2532792. doi: 10.1080/21642850.2025.2532792. eCollection 2025.

DOI:10.1080/21642850.2025.2532792
PMID:40697405
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12281645/
Abstract

BACKGROUND

Data Note articles describe openly available research datasets. They detail how and why the data were created, with the aim of increasing research transparency and facilitating data reuse. However, existing guidelines and templates for Data Note articles have been designed for quantitative research datasets and are unsuitable for qualitative research datasets. As qualitative health and social care datasets have unique sensitivities, they must be treated and reported differently to quantitative datasets.

AIM

To describe the protocol for developing a novel reporting guideline for Data Note articles describing qualitative health and social care datasets (i.e. the DeNOTE reporting guideline).

METHODS

The DeNOTE study includes (i) a rapid scoping exercise of existing documents and expert knowledge to identify and synthesise relevant reporting 'items' or 'statements' for a Data Note article describing qualitative health and social care data, (ii) an online questionnaire with expert participants to rate their agreement with items identified in (i) and to propose new or amended items, (iii) an online workshop with participants to co-develop the reporting items and reach consensus, (iv) eliciting participant feedback on the draft reporting guideline, and (v) finalising the guideline.

CONCLUSION

Our plans to develop the DeNOTE reporting guideline are registered on the EQUATOR (Enhancing the QUAlity and Transparency Of health Research) Network. The guideline will support researchers producing Data Note articles describing qualitative health and social care data. We will create a tailored resource to address the needs of qualitative researchers to facilitate transparency and to support data reuse.

摘要

背景

数据说明文章描述了公开可用的研究数据集。它们详细说明了数据的创建方式和原因,目的是提高研究透明度并促进数据重用。然而,现有的数据说明文章指南和模板是为定量研究数据集设计的,不适用于定性研究数据集。由于定性健康和社会护理数据集具有独特的敏感性,因此必须以与定量数据集不同的方式进行处理和报告。

目的

描述为描述定性健康和社会护理数据集的数据说明文章制定新的报告指南(即DeNOTE报告指南)的方案。

方法

DeNOTE研究包括:(i)对现有文献和专家知识进行快速范围界定,以识别和综合描述定性健康和社会护理数据的数据说明文章的相关报告“项目”或“陈述”;(ii)向专家参与者发放在线问卷,以评估他们对(i)中确定的项目的认同度,并提出新的或修订的项目;(iii)与参与者举办在线研讨会,共同制定报告项目并达成共识;(iv)征求参与者对报告指南草案的反馈意见;(v)最终确定指南。

结论

我们制定DeNOTE报告指南的计划已在EQUATOR(提高健康研究的质量和透明度)网络上注册。该指南将支持研究人员撰写描述定性健康和社会护理数据的数据说明文章。我们将创建一个量身定制的资源,以满足定性研究人员的需求,促进透明度并支持数据重用。