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癌症幸存者数字健康干预中的患者参与策略:一项范围综述

Patient engagement strategies in digital health interventions for cancer survivors: A scoping review.

作者信息

Ren Maria, Orsso Camila E, Ghomashchi Homa, da Silva Bruna R, Aubrey Christa, Nielssen Ingrid, Pin Sophia, McNeely Margaret L, Tandon Puneeta, Prado Carla M

机构信息

Department of Agricultural, Food & Nutritional Science, University of Alberta, Edmonton, Canada.

Department of Obstetrics & Gynecology, University of Alberta, Edmonton, Canada.

出版信息

PLOS Digit Health. 2025 May 30;4(5):e0000871. doi: 10.1371/journal.pdig.0000871. eCollection 2025 May.

Abstract

Individuals can face various mental and physical health challenges after a cancer diagnosis. Digital health platforms can address some of these challenges by providing self-management tools for improving lifestyle behaviors, while reducing the burden on healthcare systems and enhancing healthcare access to underserved populations. Involving individuals with a history of cancer, termed here as "cancer survivors", in the development and evaluation of digital health platforms can improve their effectiveness. This scoping review aimed to explore the state of patient engagement in research on digital health platforms for cancer survivors, including strategies for engagement, characteristics, and identifying gaps and barriers. A systematic search was conducted in OVID Medline, OVID EMBASE, and Scopus from inception until May 2023. The review followed Joanna Briggs Institute's guidance for scoping reviews. Eligible studies actively involved cancer survivors in the development or evaluation of digital health platforms. These studies focused on self-management digital health platforms delivering nutrition, physical activity, and/or mental health interventions. Reporting of patient engagement was evaluated according to the Guidance for Reporting Involvement of Patients and the Public 2 (GRIPP2). The search strategy captured 7 studies using various patient engagement approaches, with patient and public involvement being the most frequently used (43%, n = 3). Studies were conducted in 6 countries and most focused on the development or evaluation of web-based digital health platforms (71%, n = 5). Few studies reported all elements of GRIPP2's reporting checklist (29%, n = 2). We further identified barriers and areas of improvement for patient engagement in digital health research. Patient engagement improves digital health platforms, but few studies have meaningfully included patients, therefore reporting and evaluation of patient engagement is necessary to support its adoption in digital health research projects. In addition to exploring the gaps in patient engagement practices, this scoping review serves as a foundation for future research to advance patient-oriented digital health interventions for cancer survivors.

摘要

癌症确诊后,个人可能会面临各种身心健康挑战。数字健康平台可以通过提供自我管理工具来改善生活方式行为,从而应对其中一些挑战,同时减轻医疗系统的负担,并改善弱势群体获得医疗服务的机会。让有癌症病史的个人(本文称为“癌症幸存者”)参与数字健康平台的开发和评估,可以提高其有效性。本综述旨在探讨癌症幸存者参与数字健康平台研究的现状,包括参与策略、特征,以及找出差距和障碍。从数据库建立至2023年5月,在OVID Medline、OVID EMBASE和Scopus中进行了系统检索。该综述遵循乔安娜·布里格斯研究所的综述指南。符合条件的研究积极让癌症幸存者参与数字健康平台的开发或评估。这些研究聚焦于提供营养、身体活动和/或心理健康干预的自我管理数字健康平台。根据《患者及公众参与报告指南2》(GRIPP2)对患者参与情况的报告进行评估。检索策略共纳入7项采用不同患者参与方法的研究,其中患者和公众参与是最常用的方法(43%,n = 3)。研究在6个国家开展,且大多数聚焦于基于网络的数字健康平台的开发或评估(71%,n = 5)。很少有研究报告GRIPP2报告清单的所有要素(29%,n = 2)。我们进一步确定了患者参与数字健康研究的障碍和改进领域。患者参与可改善数字健康平台,但很少有研究真正纳入患者,因此有必要对患者参与情况进行报告和评估,以支持其在数字健康研究项目中的应用。除了探索患者参与实践中的差距外,本综述还为未来研究推进针对癌症幸存者的以患者为导向的数字健康干预奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6365/12124549/f667f63d2dbe/pdig.0000871.g001.jpg

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