myMedidata Registries

临床试验通常一次只围绕一项研究进行设计。这种传统方法难以实现患者的长期留存,使得试验前招募与试验后长期随访存在断层。

myMedidata Registries 是一款统一的患者登记库和门户网站,支持贯穿研究前、中和后的全周期的持续患者互动,从而打破单一试验的周期局限,确保跨研究项目的患者连接。

下载概述
Video transcript: Clinical trials are vital to creating innovative medicines that save lives, and patients play a crucial role in making these trials successful. Patients are the true heroes, selflessly dedicating their time and energy to participate in clinical trials, all while managing their own health challenges and juggling the demands of everyday life. If these challenges weren't enough to deter them from participating, consider this: Patients are often unaware of clinical trials as a viable care option, restricting their health care choices. Moreover, the process of finding an appropriate trial involves navigating various resources, causing confusion about how to enroll or who to contact. And in the event that a patient manages to participate, once the trial is over, they're often left in the dark about outcomes, uncertain of its impact on their medical care and disconnected from future trials. This lack of information leaves them uncertain, missing out on opportunities to improve their health and wondering whether it was worth their time. For sponsors of the trial, all of these challenges impact patient recruitment and retention, increasing costs and reducing the chance of clinical trial success. In response, My Metadata Registries was developed by patients, for patients to address these challenges, engaging patients before they've considered joining a trial and supporting them after they've participated. Here's how it works. Allison is directed to a My Metadata Registry website by her healthcare provider, patient advocacy group, or through social media advertising. Here, she learns about the benefits of joining the registry and discovers specific study opportunities presented in easy to understand language and with useful information to help her decide if the study is right for her. By creating a MyMetadata lifetime account, she gains access to all clinical trial support, equipping her with the necessary tools to successfully complete her trials. After creating her account, she completes custom eligibility assessments for one or more trials. If she meets the criteria, she's referred to a trial site for further screening and enrollment. After successfully completing a trial, Allison is informed of trial outcomes and notified of future study opportunities. She's now empowered in her healthcare journey, bringing information back to her family and caregivers to decide on next steps. MyMetadataRegistries empowers patients with expanded health care choices, presenting clinical trial opportunities as an option. This benefits both patients and sponsors, mitigating recruitment and retention challenges by creating a community of empowered, research ready patients. Together, we continue to celebrate patients as the true heroes in advancing medical knowledge and improving patient care. Learn more at mymetadata dot com slash registry.

为患者提供一站式信息获取与互动平台

当患者拥有一个单一、可信赖的平台来探索临床试验机会并保持长期联系时,他们往往展现出更高的参与并继续的意愿。Registries 让试验前与试验后的全周期患者互动变得轻松高效。

扩大患者触达范围
加速患者招募进程
集合参与就绪的患者群体
支持患者长期参与

构建患者信任纽带,而非单纯的数据收集

患者

患者早在研究开始前就已准备就绪

Registries 为患者提供的单一平台,方便他们了解临床试验机会、明确参与的具体流程,并于研究团队保持长期联系。

通过提升信息透明度与沟通效率,它赋予患者充分的自主权,让他们能够根据自身实际情况,更从容地开启试验参与之旅。

下载产品简介
Video transcript: Clinical trials are vital to creating innovative medicines that save lives, and patients play a crucial role in making these trials successful. Patients are the true heroes, selflessly dedicating their time and energy to participate in clinical trials, all while managing their own health challenges and juggling the demands of everyday life. If these challenges weren't enough to deter them from participating, consider this: Patients are often unaware of clinical trials as a viable care option, restricting their health care choices. Moreover, the process of finding an appropriate trial involves navigating various resources, causing confusion about how to enroll or who to contact. And in the event that a patient manages to participate, once the trial is over, they're often left in the dark about outcomes, uncertain of its impact on their medical care and disconnected from future trials. This lack of information leaves them uncertain, missing out on opportunities to improve their health and wondering whether it was worth their time. For sponsors of the trial, all of these challenges impact patient recruitment and retention, increasing costs and reducing the chance of clinical trial success. In response, My Metadata Registries was developed by patients, for patients to address these challenges, engaging patients before they've considered joining a trial and supporting them after they've participated. Here's how it works. Allison is directed to a My Metadata Registry website by her healthcare provider, patient advocacy group, or through social media advertising. Here, she learns about the benefits of joining the registry and discovers specific study opportunities presented in easy to understand language and with useful information to help her decide if the study is right for her. By creating a MyMetadata lifetime account, she gains access to all clinical trial support, equipping her with the necessary tools to successfully complete her trials. After creating her account, she completes custom eligibility assessments for one or more trials. If she meets the criteria, she's referred to a trial site for further screening and enrollment. After successfully completing a trial, Allison is informed of trial outcomes and notified of future study opportunities. She's now empowered in her healthcare journey, bringing information back to her family and caregivers to decide on next steps. MyMetadataRegistries empowers patients with expanded health care choices, presenting clinical trial opportunities as an option. This benefits both patients and sponsors, mitigating recruitment and retention challenges by creating a community of empowered, research ready patients. Together, we continue to celebrate patients as the true heroes in advancing medical knowledge and improving patient care. Learn more at mymetadata dot com slash registry.
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常见问题

myMedidata Registries 旨在将患者参与从单次试验的“事务性模式”扩展为涵盖试验前与试验后的全周期互动。由此,申办方可以与患者互动并开展研究宣讲,在试验启动前建立通过预筛选的潜在患者候选库,并在试验结束后持续跟进未来的试验参与机会。

myMedidata Registries 旨在将患者参与从单次试验的“事务性模式”扩展为涵盖试验前与试验后的全周期互动。由此,申办方可以与患者互动并开展研究宣讲,在试验启动前建立通过预筛选的潜在患者候选库,并在试验结束后持续跟进未来的试验参与机会。

支持。myMedidata Registries 可为患者提供便捷的问卷,并根据其回答在线评估其是否符合条件参与试验。此外,myMedidata Registries 还提供与 Circuit Clinical 联合打造的 MD Prescreen 专属招募管家服务。该增值服务由具备资质的护士及医疗专业人员开展更深度的患者预筛选与试验匹配,从而优化患者、研究中心及申办方的招募流程。

是的。作为 Medidata 多样性计划的一部分,myMedidata Registries 有助于申办方招募、互动并留存代表性不足的患者群体。通过将社区互动功能与研究中心级的人口统计学数据相结合,赋能研究团队达成多样性患者入组目标,并满足相关监管指南的要求。

是的。Medidata 为客户及合作伙伴提供多种培训方案,包括自学课程与讲师授课课程。如需查看可用课程并获取相关资源,请访问 Medidata 全球教育与培训中心。

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