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Home-Based Exercise Program Using Mobile Technology After Left Ventricular Assist Device Implantation

RECRUITINGN/ASponsored by University of Pennsylvania
Actively Recruiting
PhaseN/A
SponsorUniversity of Pennsylvania
Started2024-08-14
Est. completion2028-06-30
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations4 sites

Summary

The goal of this clinical trial is to evaluate the effects of a home-based exercise program using mobile technology on physical activity and capacity, frailty and muscle mass, and quality of life in patients with a newly implanted HeartMate 3 left ventricular assist device (HM3 LVAD). Researchers will compare the effects of an exercise intervention vs. usual care on physical activity and capacity, frailty and muscle mass, and quality of life.

Eligibility

Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria:

1. ≥ 18 years of age
2. Newly implanted with a HeartMate 3™ LVAD for the first time
3. Able to ambulate independently (with or without the use of an assistive device)
4. Owns a smartphone with Internet connection
5. Patient will be discharged home with LVAD or patient will be living at home with LVAD within 45 days of index discharge

Exclusion Criteria:

1\. Major comorbidities or limitations that may interfere with exercise training (including significant orthopedic/neurologic limitations, decompensated heart failure, uncontrolled arrhythmias, unstable angina)

Conditions2

Heart DiseaseHeart Failure

Locations4 sites

Michigan

1 site
Henry Ford Health
Detroit, Michigan, 48202
Clinical Research Coordinator

Ohio

1 site
Cleveland Clinic Foundation
Cleveland, Ohio, 44195
Clinical Research Coordinator

Pennsylvania

1 site
University of Pennsylvania
Philadelphia, Pennsylvania, 19104
Clinical Research Coordinator

Utah

1 site
University of Utah Health
Salt Lake City, Utah, 84112
Clinical Research Coordinator

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