Comparative, Controlled Study to Evaluate the Clinical Accuracy and Usability Performance of the Minuteful - Kidney Urine Analysis Test System Conducted by Lay Users
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 216
- 试验地点
- 1
- 主要终点
- Accuracy Evaluation: The Degree of Agreement (%) of the Minuteful - Kidney Urine Analysis Test System as Compared to the Comparator Device
研究概览
简要总结
The purpose of this study was to collect additional performance and clinical data on the Minuteful - Kidney test device (previously "ACR | U.S. Urine Analysis Test System"), following the original data collection (NCT04626271).
This method comparison and usability study was designed to evaluate the agreement levels of the Minuteful - Kidney Test with the comparator device (URiSCAN Optima) as well as the device's usability including the lay user's ability to understand and implement the device instructions. It also evaluates the ease of use of the device under actual use conditions in a simulated home environment.
详细描述
Eligible subjects meeting the inclusion criteria were recruited at the designated site by the study personnel. Following subject consent, the Minuteful - Kidney test kit, in its original packaging, along with the Minuteful - Kidney smartphone application were provided to the subject in a simulated home- use environment. All subjects were requested to follow the in-app instructions to complete the test, without any guidance from the study staff before, during or after testing. After each subject completed the test, the urine sample was tested by a professional user at the clinical site on the URiSCAN Optima device. Each urine sample was tested twice: once using the Minuteful - kidney test by the lay user and once using the comparator device (URiSCAN Optina) by the professional user.
To evaluate the usability of the device, study staff on-site were asked to observe and document the user performance on key tasks in the study flow as well as information regarding the user behavior while performing the test. Subjects were also asked to answer a usability post-test questionnaire.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •A) Males and Females 18-80 years of age
- •B) Subjects with a known, well-established medical condition and/or risk factor for kidney damage, that can potentially present as an abnormal concentration of urine albumin:
- •Diabetes (Type I/Type II, or Gestational Diabetes)
- •High Blood Pressure (i.e., Hypertension)
- •Cardiovascular Diseases
- •Family History of Kidney Disease
- •History of Acute Kidney Injury (AKI)
- •C) Or; subjects with other medical conditions and/or risk factors that impact kidney function:
- •Dyslipidemia
- •Heavy smoking
- •Inherited kidney disease (e.g. Polycystic kidney disease)
- •Prolonged obstruction of the urinary tract from different conditions (e.g. enlarged prostate)
- •Malignancies
- •Recurrent kidney infections
- •Other relevant conditions
- •D) Subjects who are able to use both hands
- •E) Subjects who are familiar with the use of a smartphone
- •F) Subjects who are capable of comprehending and following instructions in English
排除标准
- •A) Subjects with a major cognitive impairment (e.g.: dementia, memory loss, severe mental disorder)
- •B) Subjects who are not able to collect urine in a receptacle
- •C) Subjects who are visually impaired (i.e., cannot read the user manual)
- •D) Any additional reason that disqualifies the subject from participating in the study according to the study physician
研究组 & 干预措施
Minuteful - Kidney Urine Analysis Test System
干预措施: Minuteful - Kidney Urine Analysis Test System (Device)
结局指标
主要结局
Accuracy Evaluation: The Degree of Agreement (%) of the Minuteful - Kidney Urine Analysis Test System as Compared to the Comparator Device
时间窗: 10 months
The primary objective of the study is to evaluate the % exact match (percent agreement) and the % ±1 block match (percent agreement) of Minuteful - kidney test (tested by the lay user) compared to the URiSCAN Optima Urine Analyzer (the comparator device, tested by a healthcare professional user), for all reported values (blocks).
次要结局
- Usability Evaluation: User Performance Analysis(10 months)