招募和保留儿科参与者参与大流行病防备研究:PREMISE EV-D68 试点研究的经验

IF 1.4 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Hai Nguyen-Tran , Alicen B. Spaulding , Kevin Messacar , Matthew R. Vogt , Perdita Permaul , Daniel C. Douek , Abe Mittelman , Careese Thompson , Sandy Grubbs , Christine Magana , Michelle L. Hernandez
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引用次数: 0

摘要

对于前瞻性儿科队列研究,尤其是涉及连续静脉穿刺的研究来说,招募和保留是一项挑战。我们调查了 "通过微生物和免疫监测及流行病学(PREMISE)建立大流行响应库肠病毒 D68(EV-D68)试点研究 "的入组和保留因素,该研究是一项多中心前瞻性纵向队列研究,旨在评估免疫监测在大流行准备中的效用。这项研究对年龄小于 10 岁的儿童进行了两次抽血,分别在 EV-D68 流行季节之前和之后,间隔时间为 6-18 个月。共有 174 名儿童参加了第一组研究,其中 120 名(69%)儿童完成了研究,101 名(58%)参与者获得了后续血样。这些家庭参与研究的主要动机是希望帮助其他儿童,推动科学发展,并为下一次大流行做好更好的准备。在临床指征抽血的基础上增加研究性抽血可提高招募率,多个研究接触点也有助于留住参与者。这些发现可用于改善未来大流行准备工作和纵向儿科队列研究中的招募和保留情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recruitment and retention of pediatric participants for pandemic preparedness research: Experience from the PREMISE EV-D68 Pilot Study

Recruitment and retention are challenges for prospective pediatric cohort studies, particularly those involving serial venipunctures. We investigated factors underlying enrollment and retention in the Pandemic Response Repository through Microbial and Immune Surveillance and Epidemiology (PREMISE) Enterovirus D68 (EV-D68) Pilot Study, a multicenter prospective longitudinal cohort study assessing the utility of immunologic surveillance for pandemic preparedness. This study enrolls children ≤10 years for two blood draws, pre- and post-EV-D68 season, separated by 6–18 months. Overall, 174 children were enrolled in Cohort 1 of the study and 120 (69 %) of children completed the study, with follow-up blood samples obtained from 101 (58 %) of participants. Families were primarily motivated to participate by a desire to help other children, advance science, and better prepare for the next pandemic. Adding research blood draws to clinically indicated blood draws improved enrollment, and multiple study touch points facilitated retention. These findings can be applied to improve recruitment and retention in future pandemic preparedness efforts and longitudinal pediatric cohort studies.

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来源期刊
Contemporary Clinical Trials Communications
Contemporary Clinical Trials Communications Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
2.70
自引率
6.70%
发文量
146
审稿时长
20 weeks
期刊介绍: Contemporary Clinical Trials Communications is an international peer reviewed open access journal that publishes articles pertaining to all aspects of clinical trials, including, but not limited to, design, conduct, analysis, regulation and ethics. Manuscripts submitted should appeal to a readership drawn from a wide range of disciplines including medicine, life science, pharmaceutical science, biostatistics, epidemiology, computer science, management science, behavioral science, and bioethics. Contemporary Clinical Trials Communications is unique in that it is outside the confines of disease specifications, and it strives to increase the transparency of medical research and reduce publication bias by publishing scientifically valid original research findings irrespective of their perceived importance, significance or impact. Both randomized and non-randomized trials are within the scope of the Journal. Some common topics include trial design rationale and methods, operational methodologies and challenges, and positive and negative trial results. In addition to original research, the Journal also welcomes other types of communications including, but are not limited to, methodology reviews, perspectives and discussions. Through timely dissemination of advances in clinical trials, the goal of Contemporary Clinical Trials Communications is to serve as a platform to enhance the communication and collaboration within the global clinical trials community that ultimately advances this field of research for the benefit of patients.
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