参与痴呆临床研究的能力和意愿:一项定性研究。

IF 3.4 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Nicole Bouranis, Sherril Gelmon, Allison Lindauer
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引用次数: 0

摘要

背景与目的:痴呆临床研究在招募和招募参与者及其研究伙伴方面存在困难。通过召集社区咨询委员会并与之合作,结合痴呆症患者和护理人员的观点,本研究利用社区参与的方法来确定影响痴呆症临床研究参与的因素。方法:在本定性研究中,对24名参与者(12名痴呆症患者和12名护理人员)进行了访谈,其中一半参与了痴呆症临床研究。采用演绎和归纳的方法进行主位分析,以确定主位。结果:将10个主题分为两类。影响参与能力的因素包括症状识别和诊断、对机会的了解、不合格/退出、时间/距离、照顾者负担以及在线搜索学习机会。影响参与意愿的因素包括帮助他人、充分享受生活、照顾者的支持和服用学习药物。结论:当结合在参与能力和意愿的背景下对影响痴呆临床研究入组的因素进行重构时,这些发现可能有助于阐明因素和制定策略,以提高临床研究的参与度,并推进致力于寻找有效治疗痴呆的努力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ability and Willingness to Participate in Dementia Clinical Research: A Qualitative Study.

Background and objective: Dementia clinical research studies have difficulty recruiting and enrolling participants and their study partners. Through convening and working with a community advisory board and the incorporation of the perspectives of people living with dementia and caregivers, this study utilized a community-engaged approach to identify factors affecting dementia clinical research participation.

Methods: In this qualitative study, 24 participants (12 people living with dementia and 12 caregivers), half of whom participated in dementia clinical research, were interviewed. Deductive and inductive approaches to thematic analysis were conducted to identify themes.

Results: Ten themes were organized into two categories. Factors affecting ability to participate include symptom recognition and diagnosis, knowledge of opportunities, ineligibility/disenrollment, time/distance, caregiver burden, and online searches for study opportunities. Factors affecting willingness to participate include helping others, living life to the fullest, caregiver support, and taking study drugs.

Conclusions: When combined with a reframing of factors affecting dementia clinical research enrollment within the context of ability and willingness to participate, these findings may be useful for elucidating factors and developing strategies to enhance participation in clinical research and advance efforts dedicated to finding effective treatments for dementia.

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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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