RURAL-HFmHealth-enabled Home-based Cardiac Rehabilitation Program for Rural Heart Failure Patients
This study aims to evaluate the effectiveness of a home-based, mobile health-enabled cardiac rehabilitation program for heart failure patients living in rural areas, focusing on improving quality of life, reducing hospitalizations, and decreasing all-cause mortality.
Movn app
+ Accelerometer
Cardiovascular Diseases
+ Heart Diseases
+ Heart Failure
Treatment Study
Summary
Study start date: August 15, 2025
Actual date on which the first participant was enrolled.This study aims to improve heart health care for rural patients who have heart failure by testing a home-based cardiac rehabilitation program. Rural areas often face challenges like a lack of access to specialized health care services, which results in fewer options for heart disease treatment and rehabilitation. This study is particularly important because it uses modern technology, like smartphones and remote health monitoring, to help bridge these gaps. By introducing a digital rehabilitation program, the study seeks to offer an accessible alternative that could enhance the quality of life for many people living in areas with limited medical facilities. Participants in this study are adults recently hospitalized with heart failure. They are split into two groups: one receives the mHealth cardiac rehabilitation program and the other an attention control. Those in the rehabilitation program use a smartphone app connected to devices like a blood pressure monitor and a wearable fitness tracker to participate in exercise sessions and consult with coaches remotely. The control group receives a FitBit to track activity and has regular phone calls discussing general health. The study evaluates the effectiveness of the program by looking at outcomes like mortality rates, hospitalizations, and quality of life improvements. Additionally, aspects like physical activity levels and mental health are monitored to assess the overall impact of the intervention.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.332 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 2 locations
University of Texas Southwestern Medical Center
Dallas, United StatesOpen University of Texas Southwestern Medical Center in Google MapsBaylor Scott and White Health System
Dallas, United States