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Clinical Trials/NCT02395588
NCT02395588
Completed
Not Applicable

Improving Heart Failure Outcomes (IHO)

University of Maryland, Baltimore2 sites in 1 country26 target enrollmentApril 2014
ConditionsHeart Failure

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Failure
Sponsor
University of Maryland, Baltimore
Enrollment
26
Locations
2
Primary Endpoint
Self-management
Status
Completed
Last Updated
4 years ago

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
April 2014
End Date
June 2015
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

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

Outcomes

Primary Outcomes

Self-management

Time Frame: 7 Days

Self-care of Heart Failure Index

Secondary Outcomes

  • Readmission(7 and 30 days post discharge)

Study Sites (2)

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