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Coaching to Help Adults With Heart Failure Exercise More

Tests whether coaching in person or by video helps adults with HFpEF exercise.

Plain-language title generated from the registry record
Registry title: HEART Camp Connect -Promoting Exercise in Adults With Heart Failure With Preserved Ejection Fraction

Key facts

Where
Charlottesville, Detroit, and Omaha, United StatesSee the 3 sites

Where in United States

  • University of VirginiaCharlottesville, United StatesNot yet recruiting
  • Henry Ford Health SystemDetroit, United StatesTaking people
  • University of Nebraska Medical CenterOmaha, United StatesTaking people

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Trial details

Who runs it
University of Nebraska
Trial code
NCT05784753
Record updated
10 November 2026
Original description
The goal of this study is to learn more about patients with heart failure with preserved ejection fraction (HFpEF) and exercise. Investigators want to see if meeting with a coach in person or by video conference will help these patients exercise, feel better, and change markers in their blood. Participants will be randomly placed in one of three groups for 18 months. All groups will have access to a fitness center and be given a watch and heart rate monitor to wear during exercise. The usual care group (control group) will have access to exercise videos via the medical fitness center and will not meet with a coach. The HEART Camp group will exercise and meet with their coach in-person at the medical fitness center. The HEART Camp Connect group will have access to exercise videos via the medical fitness center and will meet with their coach via videoconferencing. All participants will take part in an exercise test and study training prior to being randomized. At four data collection time points, participants will wear an activity monitor for 7 days each, have their blood drawn, and answer questions related to heart failure and exercise. Participants will also wear a heart rate monitor when they exercise and fill out a daily exercise diary.Read full original descriptionShow less

HEART (Heart Failure Exercise and Resistance Training) Camp Connect: Promoting Adherence to Exercise in Adults With Heart Failure With Preserved Ejection Fraction

The goal of this study is to learn more about patients with heart failure with preserved ejection fraction (HFpEF) and exercise. Investigators want to see if meeting with a coach in person or by video conference will help these patients exercise, feel better, and change markers in their blood. Participants will be randomly placed in one of three groups for 18 months. All groups will have access to a fitness center and be given a watch and heart rate monitor to wear during exercise. The usual care group (control group) will have access to exercise videos via the medical fitness center and will not meet with a coach. The HEART Camp group will exercise and meet with their coach in-person at the medical fitness center. The HEART Camp Connect group will have access to exercise videos via the medical fitness center and will meet with their coach via videoconferencing. All participants will take part in an exercise test and study training prior to being randomized. At four data collection time points, participants will wear an activity monitor for 7 days each, have their blood drawn, and answer questions related to heart failure and exercise. Participants will also wear a heart rate monitor when they exercise and fill out a daily exercise diary.

Inclusion: Diagnosis of heart failure with an ejection fraction greater than or equal to 50; Echocardiogram in prior 24 months; Stable pharmacologic therapy in the past 30 days; Any of the following evidence to confirm HFpEF - Score< 6 on Heavy Hypertensive Atrial Fibrillation, Pulmonary Hypertension, Elder, Filling Pressure algorithm, invasive hemodynamic evidence of HFpEF(i.e., elevated pulmonary wedge pressure), or a confirmed clinical diagnosis of HFpEF.

Exclusion: Myocardial infarction, coronary artery bypass graft, or biventricular pacemaker in prior 6 weeks; Life-limiting illness precluding study completion; Clinical evidence of decompensated heart failure; Unstable angina or marked shortness of breath on exertion at less than 2 metabolic equivalents; Orthopedic or neuromuscular disorders preventing aerobic exercise; Cardiopulmonary exercise test results that preclude safe exercise; Unwilling/unable to complete pre-randomization procedures; Pregnancy; Implantable cardioverter defibrillator.

ClinicalTrials.gov NCT05784753