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OpenTrials
Completed

NCT Number: NCT02395588

Improving Heart Failure Outcomes Rural

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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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Riverside Shore Memorial Hospital, Nassawadox, Virginia, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Guideline based care

Other

Patient education using guideline based teaching guides

Primary outcomes

  1. Self-management

    Time frame: 7 Days

    Self-care of Heart Failure Index

Secondary outcomes

  1. Readmission

    Time frame: 7 and 30 days post discharge

    Readmission to the hospital (all cause and heart failure related)

Sponsors and collaborators

Lead sponsor

University of Maryland, Baltimore

Other

Registry information

Official study title

Improving Heart Failure Outcomes (IHO)

Acronym: IHO Rural

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Mar 23, 2015
Registry last updated
May 11, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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