Remote Monitoring of Chronic Illness Patients With a IHAP Home Wireless Hub and Vitals Measurements

Chronic Disease of Cardiovascular System Clinical Trial

— REMOTE-HUB-1  

Official title:

Remote Monitoring of Chronic Illness Patients (REMOTE-HUB-1) Study - to Assess Utility of a Mobile Device for Improved Management of At-risk Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06330714
• Other study ID #: AV.RMH.v01-01
• Status: Completed
• Start date: July 1, 2018
• Est. completion date: December 30, 2018

Study information

• Verified date: March 2024
• Source: Aventyn, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This is planned as a feasibility study. The primary objective is to evaluate a specially designed patient monitoring software Vitalbeat and standard mobile device hub termed Intel Health Application Platform (IHAP) in terms of its reliability, seamless data transmission and early data availability to the physician to improve patient physician interaction. The second objective is assessing patient response to use of mobile device monitoring and patient self-monitoring skills to transmit vital signs data using the IHAP wireless home hub device

Description:

The proposed study is a prospective single-center clinical feasibility study. All patients shall be monitored for a total period of 30 days from their date of recruitment. A total of 10 patients will be recruited from one center. The center will be provided with mobile devices which would be activated by a local mobile service provider. Additionally a tablet computer will be provided to the local investigator for monitoring patient's data, providing portability and immediate access of information. An automated blood pressure (BP) monitoring apparatus and a weighing scale will be provided to the patient. Vitalbeat software, with a mobile device home hub having a specially designed patient personalized software application ("Vitalbeat" from Aventyn, USA) for remote monitoring and a clinician monitoring software will be tested in the proposed study. The software has been developed in a manner which provides easy navigation and use, with provision of regular data entry of basic parameters used in chronic illness monitoring. The entered data is instantaneously available on the software monitored at the physician's end. This study is targeted towards chronic patients. A "chronic" patient is defined as a patient who has had within the last six months symptoms of chronic illness before enrollment. All patients above 18 years hospitalized and discharged alive with a primary diagnosis of a chronic illness shall be considered for recruitment. Upon enrollment into the study, patients will have mobile device monitoring along with existing standard care monitoring available at the local center.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: December 30, 2018
• Est. primary completion date: November 30, 2018
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Subjects of either gender and 18 years or older
• The subject is able and willing to provide written informed consent prior to enrollment in the study
• Symptoms of chronic illness.

Exclusion Criteria:

• Disability of fingers or upper limbs (unable to use devices)
• Visually impaired
• Those unable to read and write
• Hearing dysfunction
• Significant cognitive disabilities / mental illness
• Those who are unable to handle electronic devices
• Those residing in places outside mobile phone coverage
• Patients who may not come for follow up or likely to drop out of the study
• Any illness which may preclude regular follow up

Related Conditions & MeSH terms

• Chronic Disease
• Chronic Disease of Cardiovascular System

Intervention

Other:
• Symptoms of chronic illness.
The patient is advised to monitor BP and body weight daily in a standardized fashion as described below: Body weight should be measured in the morning without clothes or shoes after emptying the urinary bladder but before breakfast. BP should be measured in the morning preferably using the right arm, sitting comfortably in a chair after 5 minutes of rest in the seated position.

Locations

Country	Name	City	State
United States	Institute for Liver Health	Chandler	Arizona

Sponsors (2)

Lead Sponsor	Collaborator
Aventyn, Inc.	Intel Corporation

Country where clinical trial is conducted

United States, 

References & Publications (1)

Thorvaldsen T, Benson L, Stahlberg M, Dahlstrom U, Edner M, Lund LH. Triage of patients with moderate to severe heart failure: who should be referred to a heart failure center? J Am Coll Cardiol. 2014 Feb 25;63(7):661-671. doi: 10.1016/j.jacc.2013.10.017. Epub 2013 Oct 30. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mobile Home Device Hub Data Resiliency	he primary objective is to evaluate a specially designed patient monitoring software and standard mobile device hub in terms of its reliability, seamless data transmission and early data availability to the physician to improve patient physician interaction once per day for 30 days.	30 Days
Secondary	Patient Self Monitoring	The second objective is assessing patient response to use of mobile device monitoring and patient self-monitoring skills to transmit vital signs data using a home hub device once per day for 30 days	30 Days

External Links

•   Abstract 18895: Utility of Remote Monitoring Using a Mobile Phone in Patients with Heart Failure: the REMOTE-HF-1 Study
•   Assess Measurements of Wireless Cardiac Output Device (Remote-CO-1)