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The Effectiveness of Integrated Interactive Digital Health Application and Telemonitoring in Patients with Heart Failure and Reduced Ejection Fraction

H

Hsiao Fu-Chih

Status

Not yet enrolling

Conditions

Health Behavior
Heart Failure

Treatments

Behavioral: Interactive digital health application

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Patient Source: Patients discharged from the cardiology ward with heart failure.

Intervention Group: Prior to discharge, patients will be provided with and instructed on how to use the "Intelligent Interactive Personal Management System for Heart Failure" as well as a "Bluetooth-enabled blood pressure monitor and scale for remote data transmission."

Control Group: Patients will receive standard medical care.

Assessment Method: The Health-Related Quality of Life Questionnaire (EQ-5D), Kansas City Cardiomyopathy Questionnaire (KCCQ-12), and Functional Assessment of Chronic Illness Therapy - Spiritual Well-Being; The 12-item Spiritual Well-Being Scale (FACIT-Sp-12) will be completed before discharge, and at 1 month, 6 months, and 12 months post-discharge. The average time to complete the questionnaires is 10-15 minutes. Additionally, cardiovascular events and readmission rates will be tracked and analyzed over a 1-year period.

Enrollment

100 estimated patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Diagnosed with heart failure

Exclusion criteria

Inability to independently stand or get out of bed. Unstable condition

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

100 participants in 2 patient groups

Interactive digital health care
Experimental group
Description:
The "Intelligent Interactive Personal Management System for Heart Failure" and Bluetooth-enabled devices for remote monitoring of blood pressure and weight.
Treatment:
Behavioral: Interactive digital health application
Standard care
No Intervention group
Description:
The control group will continue to receive standard medical care.

Trial contacts and locations

1

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Central trial contact

Fu-Chih Hsiao Doctor of Medicine

Data sourced from clinicaltrials.gov

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