Web-based training and certification of clinical staff during the randomised clinical trial SafeBoosC-III.

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2024-10-23 DOI:10.1186/s13063-024-08530-x
Marie Isabel Skov Rasmussen, Mathias Lühr Hansen, Colin Peters, Gorm Greisen
{"title":"Web-based training and certification of clinical staff during the randomised clinical trial SafeBoosC-III.","authors":"Marie Isabel Skov Rasmussen, Mathias Lühr Hansen, Colin Peters, Gorm Greisen","doi":"10.1186/s13063-024-08530-x","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>SafeBoosC-III is a pragmatic, multinational clinical trial evaluating cerebral oximetry-guided treatment for extremely preterm infants. In total, 1601 infants were randomised across 70 sites in Asia, Europe, and USA. To enhance data quality and patient care, a web-based training program was implemented for staff. We now report on the processes.</p><p><strong>Methods: </strong>All training modules consisted of initial learning material followed by a case-based quiz, with elaborate responses to correct as well as to wrong answers. Modules covered trial introduction, cerebral oximetry monitoring, treatment guidelines, cerebral ultrasound, and Good Clinical Practice. The introduction module was accessible in eight languages on an online platform, while language versions varied for other modules, due to different needs. Certification was earned upon module completion, relevant to the staff category. The training was not mandatory, but for motivational purposes, principal investigators continuously received local certification rate reports.</p><p><strong>Results: </strong>A total of 926 out of 2347 staff (39%) obtained certification. Amongst 295 staff who completed the evaluation, 83% rated the program as overall good and 94% found it relevant to clinical practice. Sites exhibited varying certification rates, with 10 at 0%, 43 between 0.1 and 79.9%, and 17 exceeding 80%. There was no correlation between the rate of certification in individual sites and how often the clinical management was changed due to cerebral hypoxia nor a correlation to site-specific estimates of the intervention effect.</p><p><strong>Conclusion: </strong>Despite language barriers and a low budget, our web-based training and certification program proved feasible. Only a minority of sites reached 80% certification of staff and an impact on the trial could not be detected.</p><p><strong>Trial registration: </strong>The SafeBoosC-III trial is registered at ClinicalTrials.gov NCT03770741. The first participant was randomised in June 2019 and recruitment was completed in December 2021.</p>","PeriodicalId":23333,"journal":{"name":"Trials","volume":"25 1","pages":"711"},"PeriodicalIF":2.0000,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11515472/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Trials","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13063-024-08530-x","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

Background: SafeBoosC-III is a pragmatic, multinational clinical trial evaluating cerebral oximetry-guided treatment for extremely preterm infants. In total, 1601 infants were randomised across 70 sites in Asia, Europe, and USA. To enhance data quality and patient care, a web-based training program was implemented for staff. We now report on the processes.

Methods: All training modules consisted of initial learning material followed by a case-based quiz, with elaborate responses to correct as well as to wrong answers. Modules covered trial introduction, cerebral oximetry monitoring, treatment guidelines, cerebral ultrasound, and Good Clinical Practice. The introduction module was accessible in eight languages on an online platform, while language versions varied for other modules, due to different needs. Certification was earned upon module completion, relevant to the staff category. The training was not mandatory, but for motivational purposes, principal investigators continuously received local certification rate reports.

Results: A total of 926 out of 2347 staff (39%) obtained certification. Amongst 295 staff who completed the evaluation, 83% rated the program as overall good and 94% found it relevant to clinical practice. Sites exhibited varying certification rates, with 10 at 0%, 43 between 0.1 and 79.9%, and 17 exceeding 80%. There was no correlation between the rate of certification in individual sites and how often the clinical management was changed due to cerebral hypoxia nor a correlation to site-specific estimates of the intervention effect.

Conclusion: Despite language barriers and a low budget, our web-based training and certification program proved feasible. Only a minority of sites reached 80% certification of staff and an impact on the trial could not be detected.

Trial registration: The SafeBoosC-III trial is registered at ClinicalTrials.gov NCT03770741. The first participant was randomised in June 2019 and recruitment was completed in December 2021.

在随机临床试验 SafeBoosC-III 期间对临床工作人员进行网络培训和认证。
背景:SafeBoosC-III 是一项务实的跨国临床试验,旨在评估脑氧饱和度指导下对极早产儿的治疗。共有 1601 名婴儿在亚洲、欧洲和美国的 70 个地点接受了随机治疗。为了提高数据质量和患者护理水平,我们对工作人员进行了网络培训。现在,我们将对培训过程进行报告:所有培训模块都包括初始学习材料,然后是基于案例的测验,对正确和错误答案都有详细的回答。培训模块包括试验介绍、脑血氧监测、治疗指南、脑超声和良好临床实践。在在线平台上,介绍模块有八种语言版本,而其他模块的语言版本则因需求不同而各异。完成与工作人员类别相关的模块后可获得认证。培训不是强制性的,但出于激励目的,主要研究人员会不断收到当地的认证率报告:在 2347 名员工中,共有 926 人(39%)获得了认证。在完成评估的 295 名员工中,83% 的人认为该计划总体良好,94% 的人认为该计划与临床实践相关。各培训点的认证率参差不齐,其中 10 个培训点的认证率为 0%,43 个培训点的认证率在 0.1% 至 79.9% 之间,17 个培训点的认证率超过 80%。各医疗点的认证率与因脑缺氧而改变临床管理的频率之间没有相关性,与特定医疗点对干预效果的估计也没有相关性:尽管存在语言障碍且预算较低,但我们的网络培训和认证计划证明是可行的。结论:尽管存在语言障碍且预算较低,但我们的网络培训和认证计划证明是可行的,只有少数地点的员工认证率达到了 80%,而且无法检测到对试验的影响:SafeBoosC-III 试验已在 ClinicalTrials.gov NCT03770741 上注册。第一位参与者于 2019 年 6 月被随机分配,招募工作于 2021 年 12 月完成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信