Evaluation of the Accuracy and Usability of the Minuteful - Kidney Urine Analysis Test System in the Lay User Hands

NCT ID: NCT05838872

Last Updated: 2023-05-03

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 216 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-12-09
• Study Completion Date: 2022-07-15

Brief Summary

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.

Detailed Description

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.

Conditions

Albuminuria; Chronic Kidney Diseases; Diabetes; Hypertension

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

Minuteful - Kidney Urine Analysis Test System

Group Type: EXPERIMENTAL

Minuteful - Kidney Urine Analysis Test System

Intervention Type: DEVICE

Urine samples were collected and tested by a lay user, using the Minuteful - Kidney test device. The lay user test results were compared to the results obtained by testing the same urine sample on the comparison device, the URiSCAN Optima.

Interventions

Minuteful - Kidney Urine Analysis Test System

Urine samples were collected and tested by a lay user, using the Minuteful - Kidney test device. The lay user test results were compared to the results obtained by testing the same urine sample on the comparison device, the URiSCAN Optima.

Intervention Type: DEVICE

Other Intervention Names

Minuteful - Kidney; Minuteful - Kidney Test Device; ACR | U.S. Urine Analysis Test System

Eligibility Criteria

Inclusion Criteria

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
• Obesity
• 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

Exclusion Criteria

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Healthy.io Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

AccuMed research associates

Garden City, New York, United States

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

ACR-US-MCU-SUP

Identifier Type: -

Identifier Source: org_study_id