Heart Failure Clinical Trial

NMES in HF Patients to Improve Functional Recovery Following Hospitalization

Summary

The goal of this research study is to understand whether an at-home exercise program started after hospitalization for HFpEF, and continuing for 4 weeks following discharge from the hospital, can preserve or improve physical function.

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Full Description

Heart failure is the leading cause of hospitalization among adults in the US with patients with preserved ejection fraction (HFpEF) comprising half of those admissions. Many patients exhibit chronic fatigue, exercise intolerance and an inability to perform activities of daily living, which is exacerbated by hospitalization. The goal of this research study is to understand whether an at-home exercise program started soon after hospitalization and continuing for 4 weeks following discharge can improve functional recovery in HFpEF patients. Volunteers will be randomly assigned to receive neuromuscular electrical stimulation (NMES) of their quadriceps muscles or not to receive NMES (control group). Volunteers will be evaluated during hospitalization and 4 weeks following discharge. Assessments will include measurements of physical function by 6 minute walk test and the Short Physical Performance Battery, as well as assessment of subjective physical functional capacity and quality of life using the Medical Outcomes Short form 36 and Kansas City Cardiomyopathy questionnaire.

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Eligibility Criteria

Inclusion Criteria:

50-90 years of age
clinical diagnosis of HFpEF being actively managed during hospitalization
live within 30 miles of the medical center
able to perform informed consent

Exclusion Criteria:

rheumatoid arthritis or other inflammatory/autoimmune disease
cancer, excluding non-melanoma skin cancer or low-grade prostate cancer
severe dementia/alzheimer's disease
exercise limiting peripheral vascular disease
neuromuscular disease or neuromuscular dysfunction associated with cerebrovascular event
body mass index ≥40 kg/m2
lower extremity blood clot or implantable cardioverter-defibrillator or pacemaker

Study is for people with:

Heart Failure

Estimated Enrollment:

60

Study ID:

NCT05338437

Recruitment Status:

Recruiting

Sponsor:

University of Vermont Medical Center

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There is 1 Location for this study

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University of Vermont Medical Center
Burlington Vermont, 05405, United States More Info
Sherrie Khadanga
Contact
802-847-2700
[email protected]

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Estimated Enrollment:

60

Study ID:

NCT05338437

Recruitment Status:

Recruiting

Sponsor:


University of Vermont Medical Center

How clear is this clinincal trial information?

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