Including Young Children in the Development and Testing of Patient Reported Outcome (PRO) Instruments: A Scoping Review of Children's Involvement and Qualitative Methods.

IF 3.4 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Victoria Gale, Jill Carlton
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引用次数: 0

Abstract

Background: Qualitative research during the development/testing of Patient Reported Outcome Measures (PROMs) is recommended to support content validity. However, it is unclear if and how young children (≤ 7 years) can be involved in this research because of their unique cognitive needs.

Objectives: Here we investigate the involvement of children (≤ 7 years) in qualitative research for PROM development/testing. This review aimed to identify (1) which stages of qualitative PROM development children ≤ 7 years had been involved in, (2) which subjective health concepts had been explored within qualitative PROM development with this age group, and (3) which qualitative methods had been reported and how these compared with existing methodological recommendations.

Methods: This scoping review systematically searched three electronic databases (searches re-run prior to final analysis on 29 June 2022) with no date restrictions. Included studies had samples of at least 75% aged ≤ 7 years or reported distinct qualitative methods for children ≤ 7 years in primary qualitative research to support concept elicitation or PROM development/testing. Articles not in English and PROMs that did not enable children ≤ 7 years to self-report were excluded. Data on study type, subjective health and qualitative methods were extracted and synthesised descriptively. Methods were compared with recommendations from guidance.

Results: Of 19 included studies, 15 reported concept elicitation research and 4 reported cognitive interviewing. Most explored quality of life (QoL)/health-related quality of life (HRQoL). Some concept elicitation studies reported that creative/participatory activities had supported children's engagement, but results and reporting detail varied considerably across studies. Cognitive interviewing studies reported less methodological detail and fewer methods adapted for young children compared with concept elicitation studies. They were limited in scope regarding assessments of content validity, mostly focussing on clarity while relevance and comprehensiveness were explored less.

Discussion: Creative/participatory activities may be beneficial in concept elicitation research with children ≤ 7 years, but future research needs to explore what contributes to the success of young children's involvement and how researchers can adopt flexible methods. Cognitive interviews with young children are limited in frequency, scope and reported methodological detail, potentially impacting PROM content validity for this age group. Without detailed reporting, it is not possible to determine the feasibility and usefulness of children's (≤ 7 years) involvement in qualitative research to support PROM development and assessment.

Abstract Image

将幼儿纳入患者报告结果(PRO)工具的开发和测试:儿童参与和定性方法的范围审查。
背景:建议在开发/测试患者报告结果测量(PROMs)期间进行定性研究以支持内容效度。然而,目前尚不清楚幼儿(≤7岁)是否以及如何参与这项研究,因为他们有独特的认知需求。目的:在这里,我们调查了儿童(≤7岁)在早PROM发展/测试的定性研究中的参与情况。本综述旨在确定(1)≤7岁的儿童参与了质性早PROM发展的哪些阶段,(2)在该年龄组的质性早PROM发展中探讨了哪些主观健康概念,以及(3)报告了哪些质性方法,以及如何将这些方法与现有的方法建议进行比较。方法:本综述系统地检索了三个电子数据库(检索在2022年6月29日最终分析之前重新运行),没有日期限制。纳入的研究至少有75%的样本年龄≤7岁,或者在主要的定性研究中报告了针对≤7岁儿童的不同定性方法,以支持概念启发或PROM发展/测试。非英文文章和不允许≤7岁儿童自我报告的prom被排除。对研究类型、主观健康和定性方法的数据进行提取和描述性综合。方法与指南中推荐的方法进行比较。结果:纳入的19项研究中,概念启发研究15项,认知访谈研究4项。大多数探索生活质量(QoL)/健康相关生活质量(HRQoL)。一些概念启发研究报告说,创造性/参与性活动支持了儿童的参与,但不同研究的结果和报告细节差别很大。与概念启发研究相比,认知访谈研究报告的方法论细节较少,适用于幼儿的方法也较少。它们在内容效度评估方面的范围有限,主要关注清晰度,而相关性和全面性的探讨较少。讨论:创造性/参与性活动在≤7岁儿童的概念启发研究中可能是有益的,但未来的研究需要探索是什么促成了幼儿参与的成功,以及研究人员如何采用灵活的方法。对幼儿的认知访谈在频率、范围和报告的方法细节上都是有限的,这可能会影响该年龄组PROM内容的有效性。如果没有详细的报告,就不可能确定儿童(≤7岁)参与支持PROM发展和评估的定性研究的可行性和有用性。
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来源期刊
Patient-Patient Centered Outcomes Research
Patient-Patient Centered Outcomes Research HEALTH CARE SCIENCES & SERVICES-
CiteScore
6.60
自引率
8.30%
发文量
44
审稿时长
>12 weeks
期刊介绍: The Patient provides a venue for scientifically rigorous, timely, and relevant research to promote the development, evaluation and implementation of therapies, technologies, and innovations that will enhance the patient experience. It is an international forum for research that advances and/or applies qualitative or quantitative methods to promote the generation, synthesis, or interpretation of evidence. The journal has specific interest in receiving original research, reviews and commentaries related to qualitative and mixed methods research, stated-preference methods, patient reported outcomes, and shared decision making. Advances in regulatory science, patient-focused drug development, patient-centered benefit-risk and health technology assessment will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in The Patient may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances. All manuscripts are subject to peer review by international experts.
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