Recruiting

RURAL-HFmHealth-enabled Home-based Cardiac Rehabilitation Program for Rural Heart Failure Patients

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Study Aim

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.

What is being tested

Movn app

+ Accelerometer

Device
Who is being recruted

Cardiovascular Diseases

+ Heart Diseases

+ Heart Failure

Over 18 Years
+12 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 3
Interventional
Study Start: August 2025
See protocol details

Summary

Principal SponsorUniversity of Texas Southwestern Medical Center
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleImplementing a Home-based Cardiac Rehabilitation Program Among Rural Patients With Heart Failure
NCT06349941
Principal SponsorUniversity of Texas Southwestern Medical Center
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

332 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

Cardiovascular DiseasesHeart DiseasesHeart Failure

Criteria

5 inclusion criteria required to participate
Adults aged 18 years or older

History of hospitalization for acute heart failure with ejection fraction ≥ 35%

Ability to participate in telemedicine visits

Access to smartphone or device capable of running the mHealth application

Show More Criteria

7 exclusion criteria prevent from participating
Heart failure with reduced ejection fraction (ejection fraction < 35%)

Inability to participate in physical exercise or cardiac rehabilitation due to medical contraindications

Inability to provide informed consent

Lack of access to required technology (smartphone, internet connectivity)

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Cardiac rehabilitation delivered through Movn app through the use of mHealth.

Group II

Active Comparator
This group will receive a wearable device for step count tracking and will get periodic check ins to minimize differential attention between groups. They will not receive an exercise plan.

Study 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

Recruiting

University of Texas Southwestern Medical Center

Dallas, United StatesOpen University of Texas Southwestern Medical Center in Google Maps
Recruiting soon

Baylor Scott and White Health System

Dallas, United States
Recruiting
2 Study Centers