Mueller Christian, Schürks Markus, Neußer Thomas, von der Osten Uschi, Weihermüller Daniela, von Arnim Ira, Martin Stephan
Bayer Vital GmbH, Leverkusen, Germany.
Smartpatient GmbH, München, Germany.
JMIR Res Protoc. 2023 Apr 5;12:e44996. doi: 10.2196/44996.
Despite effective treatment options, chronic kidney disease (CKD) has become a major cause of mortality worldwide due to the ever-increasing number of patients with type 2 diabetes mellitus (T2DM). Guideline-compliant, at least, annual screening of patients with T2DM is crucial to prevent renal disease progression. However, data on the prevalence of CKD in patients with T2DM and on screening frequency are limited. SMART-Finder is the first study to exclusively use data provided directly by patients via an adherence app to collect information on the prevalence of CKD, risk factors, disease management, and quality of life of patients with T2DM in Germany.
The primary objective of this study is to determine the proportion of patients with T2DM and an elevated urine albumin-to-creatinine ratio (UACR; albumin-to-creatinine ratio stage A2 and A3) at baseline and after 12 (±3) months. Secondary objectives include the proportion of patients who remain in or switch to another albumin-to-creatinine ratio classification category after 12 months, information on quality of life, disease awareness, and adherence rates, as well as the proportion of patients without any UACR-screening data. Recruitment occurs via push notification among MyTherapy app users with T2DM.
This is a single-arm, retrospective/prospective, observational, digital, patient-centered cohort study, with recruitment and data documentation via a health app. Required routine laboratory data are provided by treating physicians to their patients for data entry. The study population includes adult patients with T2DM documenting their data in the MyTherapy app using their own smartphone or tablet. Study participants are provided with a specifically developed electronic case report form containing questions on demographic and general data, quality of life, disease awareness, and laboratory values including estimated glomerular filtration rate, UACR, hemoglobin 1Ac, and blood pressure. Apart from demographic and general data, all data are collected at baseline and 12 months after the last UACR assessment. An automatically generated push notification reminds participants of the second data entry. The extracted and pseudonymized data are analyzed descriptively.
The enrollment period for this study started in February 2023 and shall end after 12 months or after the enrollment of 5000 patients. An interim analysis is planned 3 months after the inclusion of the first patient and the final analysis after 12 months of follow-up.
Overall, the study will contribute to minimizing the existing data gap on the prevalence of CKD in patients with T2DM in Germany, provide important insights into the current disease management of patients with T2DM in everyday clinical practice in Germany, and support guideline-based care for the participating patients.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): PRR1-10.2196/44996.
尽管有有效的治疗方案,但由于2型糖尿病(T2DM)患者数量不断增加,慢性肾脏病(CKD)已成为全球范围内主要的死亡原因。至少按照指南要求对T2DM患者进行年度筛查对于预防肾脏疾病进展至关重要。然而,关于T2DM患者中CKD的患病率以及筛查频率的数据有限。SMART-Finder是第一项专门使用患者通过依从性应用程序直接提供的数据来收集德国T2DM患者的CKD患病率、危险因素、疾病管理和生活质量信息的研究。
本研究的主要目的是确定基线时以及12(±3)个月后T2DM患者且尿白蛋白与肌酐比值(UACR;白蛋白与肌酐比值A2和A3期)升高的患者比例。次要目标包括12个月后仍处于或转换至另一个白蛋白与肌酐比值分类类别的患者比例、生活质量、疾病知晓率和依从率信息,以及没有任何UACR筛查数据的患者比例。通过向MyTherapy应用程序的T2DM用户推送通知进行招募。
这是一项单臂、回顾性/前瞻性、观察性、数字化、以患者为中心的队列研究,通过健康应用程序进行招募和数据记录。所需的常规实验室数据由治疗医生提供给患者进行数据录入。研究人群包括使用自己的智能手机或平板电脑在MyTherapy应用程序中记录数据的成年T2DM患者。为研究参与者提供一份专门开发的电子病例报告表,其中包含有关人口统计学和一般数据、生活质量、疾病知晓率以及实验室值(包括估算肾小球滤过率、UACR、糖化血红蛋白1Ac和血压)的问题。除人口统计学和一般数据外,所有数据均在基线时以及最后一次UACR评估后12个月收集。自动生成的推送通知会提醒参与者进行第二次数据录入。对提取的匿名化数据进行描述性分析。
本研究的入组期于2023年2月开始,应在12个月后或招募5000名患者后结束。计划在纳入第一名患者3个月后进行中期分析,随访12个月后进行最终分析。
总体而言,该研究将有助于缩小德国T2DM患者中CKD患病率方面现有的数据差距,为德国日常临床实践中T2DM患者当前的疾病管理提供重要见解,并支持对参与研究的患者进行基于指南的护理。
国际注册报告识别码(IRRID):PRR1-10.2196/44996。