Heart Failure Clinical Trial

Heart Failure Optimization at Home to Improve Outcomes (Hozho): A Pragmatic in Navajo Nation

Summary

Heart failure causes significant morbidity and mortality, particularly in Navajo Nation. There are well-established evidence of improved mortality and lower heart failure hospitalizations with certain pharmacotherapies for heart failure with reduced ejection fraction (HFrEF). However, these medications are underutilized nationally, including in the Indian Health Service which is one important driver of poor heart failure outcomes. Therefore, as part of an EHR-based pragmatic clinic trial, we are implementing and testing a model that identifies American Indian HFrEF patients receiving care at one large Indian Health Service Site who meet clinical criteria for, but are not on appropriate therapy, and implement a model in which our study team will get patients on appropriate therapy while also supporting primary care providers with cardiology telementorship. We will evaluate the impact of this model to improve uptake of GDMT among HFrEF patients.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Patients with heart failure with reduced ejection fraction with last ejection fraction equal to or less than 40%
Have a primary care physician at Gallup Indian Medical Center or Tohatchi Health Center
Have been seen in the last 12 months at Gallup Indian Medical Center or Tohatchi Health Center

Exclusion Criteria:

On hospice
LVAD/translant
Home inotropes
No visit in last 12 months at Gallup Indian Medical Center or Tohatchi Health Center

Study is for people with:

Heart Failure

Estimated Enrollment:

103

Study ID:

NCT05792085

Recruitment Status:

Completed

Sponsor:

University of Pennsylvania

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There is 1 Location for this study

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Gallup Indian Medical Center
Gallup New Mexico, 87301, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Estimated Enrollment:

103

Study ID:

NCT05792085

Recruitment Status:

Completed

Sponsor:


University of Pennsylvania

How clear is this clinincal trial information?

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