The value of qualitative research in randomized controlled trials involving drugs and medical devices: a systematic mapping review.

IF 3 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Yuan-Tao Huang, Benjamin Gregory, Sharon Greenwood, Evi Germeni
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引用次数: 0

Abstract

Objective: The use of qualitative research with randomized controlled trials (RCTs) has grown exponentially over the last decade, but little is known about how it is contributing to trial procedures and interventions. This review systematically mapped the value that qualitative research has had in RCTs of drugs and medical devices.

Methods: We searched five electronic databases (MEDLINE, EMBASE, PsycINFO, CINAHL, and ASSIA) and the NIHR Journals Library to identify original, peer-reviewed qualitative research conducted in the context of specific RCTs (pilot or full). Drawing on studies published between January 2019 and December 2020, we identified and classified examples illustrating how qualitative research had contributed to the trial. This created a list of questions qualitative methods can address in RCTs.

Results: Of 207 included studies, only 22 percent explicitly articulated their value. Most frequently reported contributions included: (a) explaining trial findings; (b) ensuring that interventions meet the needs of key stakeholders; and (c) making the trial feasible and viable (e.g., through improved trial design and conduct). A total of 776 examples demonstrating how qualitative methods had enhanced the trial were classified into twenty-seven subcategories. A list of sixty potential questions was developed to assist future research design.

Conclusions: The value of qualitative research in trials is expanding. While qualitative methods have traditionally been associated with complex interventions, this review highlights their relevance to trials involving drugs and devices. Future trials could benefit from expanding the use of qualitative methods to deepen understanding of outcomes, strengthen measurement validity, and capture experiences of conditions.

定性研究在涉及药物和医疗器械的随机对照试验中的价值:一个系统的制图回顾。
目的:在过去十年中,随机对照试验(rct)定性研究的使用呈指数级增长,但人们对它如何促进试验程序和干预措施知之甚少。本综述系统地描绘了定性研究在药物和医疗器械随机对照试验中的价值。方法:我们检索了5个电子数据库(MEDLINE、EMBASE、PsycINFO、CINAHL和ASSIA)和NIHR期刊库,以确定在特定rct(试点或完整)背景下进行的原始的、同行评审的定性研究。根据2019年1月至2020年12月期间发表的研究,我们确定并分类了一些例子,说明定性研究如何对试验做出贡献。这创建了一个定性方法可以在随机对照试验中解决的问题列表。结果:在207项纳入的研究中,只有22%明确表达了它们的价值。最常见的报告贡献包括:(a)解释试验结果;(b)确保干预措施满足主要利益攸关方的需求;(c)使试验可行和可行(例如,通过改进试验设计和实施)。共有776个例子证明定性方法如何提高了试验被分为27个子类别。拟定了一份包含60个潜在问题的清单,以协助未来的研究设计。结论:定性研究在临床试验中的价值正在扩大。虽然定性方法传统上与复杂的干预措施有关,但本综述强调了它们与涉及药物和设备的试验的相关性。未来的试验可以从扩大定性方法的使用中受益,以加深对结果的理解,加强测量的有效性,并捕捉对条件的经验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Technology Assessment in Health Care
International Journal of Technology Assessment in Health Care 医学-公共卫生、环境卫生与职业卫生
CiteScore
4.40
自引率
15.60%
发文量
116
审稿时长
6-12 weeks
期刊介绍: International Journal of Technology Assessment in Health Care serves as a forum for the wide range of health policy makers and professionals interested in the economic, social, ethical, medical and public health implications of health technology. It covers the development, evaluation, diffusion and use of health technology, as well as its impact on the organization and management of health care systems and public health. In addition to general essays and research reports, regular columns on technology assessment reports and thematic sections are published.
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