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Remote Home Prothrombin Time (PT)/International Normalized Ratio (INR) Monitoring and Patient Management System

Use of a Novel Remote Home PT/INR-monitoring Device for Long-Term Anticoagulation Management

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00978445
Acronym
vMetrics-AMS
Enrollment
25
Registered
2009-09-17
Start date
2009-09-30
Completion date
2010-08-31
Last updated
2013-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Venous Thromboembolism

Keywords

Systemic embolic events, Thromboembolic Complications with Atrial Fibrillation, Prophylaxis with Atrial Fibrillation, Mechanical Cardiac Valve Replacement

Brief summary

Long-term anticoagulation is indicated in patients for the prophylaxis and/or treatment of the thromboembolic complications associated with atrial fibrillation and/or mechanical cardiac valve replacement, prevention or treatment of venous thromboembolism (deep vein thrombosis and pulmonary embolism), to prevent thromboembolic events post-myocardial infarction, and in patients with systemic embolic events. Currently the only approved oral medication for anticoagulation is warfarin (Coumadin, Bristol-Myers Squibb and generic warfarin. Dosage is controlled by periodic determinations of the prothrombin time (PT)/International Normalized Ratio (INR). Under treatment may lead to venous or arterial thrombotic events or stroke, while over treatment may lead to major bleeding and even death. Patients require frequent INR monitoring to maintain a therapeutic level of anticoagulation. The therapeutic INR range varies by clinical indication, most commonly an INR 2-3 goal, but ranging from 1.5-4.0. Bleeding complications are more likely to occur above an INR value of 4.0. The vMetrics - Anticoagulation Management System is a remote patient management solution for Oral Anticoagulation Care patients. This system provides confirmation of patient question and testing protocols as well as virtual patient management care capability for dosage and patient scheduling. This trial will provide end points to ascertain efficiency against standard care protocol and confirm equivalent care standards.

Detailed description

The creation of optimal devices for patient self-testing protocols for anticoagulation management is an area of active medical research. The current pilot study represents the initial step in the development of a new customized device for this purpose, the vMetrics - Anticoagulation Monitoring System. The v-Metrics Anticoagulation Monitoring System (vMetrics AMS) is defined by: 1. A PT/INR home monitoring unit which interfaces to FDA approved PT/INR home monitors such as the Hemosense INRatio device, and 2. an anticoagulation clinic patient management application which manages patient communications, database of prior test results, testing schedules, and communication to an EMR. The INR home-monitoring system to be tested in this study will address several of the limitations of currently available technologies and practices for standard and home INR self-testing. The proposed project will develop a self-testing device that maximizes safety and efficiency for both the patient and the health care provider. The monitoring device (vMetrics) allows the wireless transmission of the INR result from an approved home INR measuring monitoring device (ex:HemoSense - INRatio) to a secure database in a health care provider staffed anticoagulation clinic. The device will also collect yes/no responses to a set of standard questions from the subject to assure patient safety and determine optimal Coumadin dosing. Upon receipt of the patient data, the Coumadin provider can review the INR result and responses to the questions and use standard Coumadin dosing protocols and clinical judgment to transmit dosing instructions back to the patient through the device. A calendar schedule of dosing until the next scheduled INR check will be transmitted to the patient. In certain instances (i.e., high INR \> 5), the device will transmit instructions to call the Coumadin clinic. The subject will confirm receipt of the Coumadin dose sent to him/her by pressing a button on the device (which transmits the confirmation back to the database). This process may reduce inconvenience to the subject, the INR value is reported directly from the device reducing the possibility of error, two-way communication is wireless and will reduce the need for telephone contact, thus potentially saving health care provider and patient time. In addition, the data from the encounter will be available in a form that can be entered into the patient's electronic medical record. The patient will enter data into the device using a 4-digit passcode that will allow for security of data. In addition to coordinating INR transmission through the home INR device, a customized database will provide a platform for the anticoagulation clinic patient management application (Wireless Home Coumadin clinic). This platform which will organize the workflow of the Coumadin provider to more easily determine which patients are due (or overdue) for monitoring, and which patients have transmitted an INR value and questionnaire and are awaiting a response.

Interventions

OTHERvMetrics protocol

use vmetrics protocol and device or use standard in clinic monitoring

Sponsors

The Cleveland Clinic
CollaboratorOTHER
ZIN Technologies, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Ages 18-80 years * Requires long-term oral anticoagulation therapy for one of the following indications: * Venous thromboembolism (deep vein thrombosis or pulmonary embolism) * Arterial thromboembolic event(s) * Atrial fibrillation * Mechanical heart valve * INR goal set at 2-3 by supervising physician * Subject has been followed in the Vascular Medicine Coumadin program for at least 3 months * No INR values \> 7, and no major thrombotic or bleeding complications within the preceding 3 months of follow-up in the Coumadin program. * Subject has been compliant with INR monitoring during period of enrollment in the Vascular Medicine Coumadin program. * Physically able and willing to perform finger stick INR measurements on self * Able to use the hand-held monitoring device and have adequate vision to read information on the device screen

Exclusion criteria

* Inability to speak and read English * Anticipated interruption in anticoagulation within the next 6 months (e.g., for elective major surgery, pregnancy) * Cognitive impairment which makes ability to perform necessary procedures related to the remote home monitoring device unlikely

Design outcomes

Primary

MeasureTime frameDescription
Time Spent Per PT/INR Monitoring EncounterOnce per week during 12 week studyminutes spent measuring coagulation time of blood on standard versus home protocol

Secondary

MeasureTime frameDescription
Change in Quality of Life - Based on Quality of Life Scores PSQ-18 (Short Form Patient Satisfaction Questionnaire) Duke Anticoagulation Satisfaction Scale SF-12 (Short Form 12 Version 2) Quality of Life QuestionnaireDuring study vist number 2 after 12 week study period, repeated after second study 12 week period study visit #3we are interested in the relative measure of quality of life by comparing quality of life measures through use of PSQ-18 and other measures listed. Higher scores indicate a better quality of life.

Countries

United States

Participant flow

Recruitment details

Inrolled 25 patients in two arms of 12 weeks from patient population of Cleveland Clinic Foundation

Pre-assignment details

Clear enrollement criteria were created only real exclusion was if physician did not believe patient could perform protocol and if outside of age criteria.

Participants by arm

ArmCount
All Participants
all participants recieved all interventions during study
25
Total25

Baseline characteristics

CharacteristicAll Participants
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
25 Participants
Age Continuous53.7 years
STANDARD_DEVIATION 11.7
Region of Enrollment
United States
25 participants
Sex: Female, Male
Female
10 Participants
Sex: Female, Male
Male
15 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 25
serious
Total, serious adverse events
0 / 25

Outcome results

Primary

Time Spent Per PT/INR Monitoring Encounter

minutes spent measuring coagulation time of blood on standard versus home protocol

Time frame: Once per week during 12 week study

Population: through minimum power study

ArmMeasureValue (MEAN)Dispersion
All Participants-Home ProtocolTime Spent Per PT/INR Monitoring Encounter19.4 minutesStandard Deviation 2.3
All Particpants - Standard ProtocolTime Spent Per PT/INR Monitoring Encounter47 minutesStandard Deviation 2.6
Secondary

Change in Quality of Life - Based on Quality of Life Scores PSQ-18 (Short Form Patient Satisfaction Questionnaire) Duke Anticoagulation Satisfaction Scale SF-12 (Short Form 12 Version 2) Quality of Life Questionnaire

we are interested in the relative measure of quality of life by comparing quality of life measures through use of PSQ-18 and other measures listed. Higher scores indicate a better quality of life.

Time frame: During study vist number 2 after 12 week study period, repeated after second study 12 week period study visit #3

Population: power analysis

ArmMeasureGroupValue (MEAN)Dispersion
All Participants-Home ProtocolChange in Quality of Life - Based on Quality of Life Scores PSQ-18 (Short Form Patient Satisfaction Questionnaire) Duke Anticoagulation Satisfaction Scale SF-12 (Short Form 12 Version 2) Quality of Life QuestionnairePSQ-1851.1 scores on a scaleStandard Deviation 0.7
All Participants-Home ProtocolChange in Quality of Life - Based on Quality of Life Scores PSQ-18 (Short Form Patient Satisfaction Questionnaire) Duke Anticoagulation Satisfaction Scale SF-12 (Short Form 12 Version 2) Quality of Life QuestionnaireDASS47.5 scores on a scaleStandard Deviation 2.6
All Particpants - Standard ProtocolChange in Quality of Life - Based on Quality of Life Scores PSQ-18 (Short Form Patient Satisfaction Questionnaire) Duke Anticoagulation Satisfaction Scale SF-12 (Short Form 12 Version 2) Quality of Life QuestionnairePSQ-1850.8 scores on a scaleStandard Deviation 0.6
All Particpants - Standard ProtocolChange in Quality of Life - Based on Quality of Life Scores PSQ-18 (Short Form Patient Satisfaction Questionnaire) Duke Anticoagulation Satisfaction Scale SF-12 (Short Form 12 Version 2) Quality of Life QuestionnaireDASS49.7 scores on a scaleStandard Deviation 2.7

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026