Heart Failure Clinical Trial

Improving Heart Failure Outcomes Rural

Summary

This study will test if standardized care helps patients feel better, if it can be implemented in rural hospitals, and find out which healthcare processes and outcomes are most important to heart failure patients.

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Full Description

The aims of this research are to: 1) Conduct a quasi-experimental study of rural hospitals to test if guideline-based care (standardized patient education, making a post discharge appointment with the patient's provider and calling the patient at 48 hours to reinforce HF education) improves patient outcomes (better self-care, and lower readmissions at 7 and 30 days post discharge); 2) Identify hospital (staffing, practice environment, costs) and provider (evidence-based practices) characteristics associated with better implementation of heart failure patient care processes; and 3) Determine which healthcare processes and outcomes are most important to heart failure patients. A quasi-experimental study with mixed methods will be used. The sample consists of HF patients (N=40, 20 each hospital) and nurses who care for HF patients on study units (N=90, 45 each hospital) from 2 rural hospitals. Survey data will be collected from patients (baseline, discharge, 48 hours and 7 days post discharge) and nurses (baseline, during patient education, on patient discharge). Secondary data will be collected quarterly on nurse staffing and once for patient readmission within 30 days of discharge. Structured patient interviews will be conducted with 10 HF patients in person to determine which health care processes and outcomes are most important to them. Both patients and nurses will be engaged to inform study procedures and outcomes consistent with the tenants of patient-centered outcomes research.

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Eligibility Criteria

Inclusion Criteria:

Admitted to hospital with a diagnosis of heart failure
Age > 20
Cognitively intact
English speaking
Plan for discharge to home, assisted living or intermediate care

Exclusion Criteria:

Patients with planned discharge to sub-acute or nursing home facilities
Patients enrolled in another research study to test interventions to improve heart failure knowledge, self-management or reduce readmission to the hospital within 30 days post discharge
Patients that are cognitively impaired
Patients that are transferred to another unit in the hospital, and will be discharged from that unit
Patients who undergo or have a planned surgical intervention during their hospital stay

Study is for people with:

Heart Failure

Estimated Enrollment:

26

Study ID:

NCT02395588

Recruitment Status:

Completed

Sponsor:

University of Maryland, Baltimore

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There are 2 Locations for this study

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Riverside Shore Memorial Hospital
Nassawadox Virginia, 23413, United States
Riverside Tappahannock Hospital
Tappahannock Virginia, 22560, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Estimated Enrollment:

26

Study ID:

NCT02395588

Recruitment Status:

Completed

Sponsor:


University of Maryland, Baltimore

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