Trial of an Interactive CD-Program on 6 Months Readmission Rate in Patients With Heart Failure

Not Applicable

Completed

• Conditions: Heart Failure

• Registration Number: NCT00311194
• Lead Sponsor: Swedish Heart Lung Foundation

Brief Summary

The purpose of this study is to determine whether extra education of patients with chronic heart failure can reduce 6 months readmission rate to hospital.

Detailed Description

The prevalence of heart failure (HF) has increased in the western world and is a major concern due to increasing prevalence and rising health care costs. The prognosis remains poor despite improvement in survival due to treatment with ACE-inhibitors and beta-receptor antagonists. HF has a high rate of readmission and hospitalisation. Some readmissions are ascribed to patients' lack of compliance, insufficient knowledge about diet, medication and symptoms of heart failure. Education of patients has become an important component in order to increase the patients' self-care and compliance. Intense education and counselling of patients is recommended in both European and American guidelines for HF.

Several systematic reviews of studies on strategies for improvement of outcomes of heart failure patients after discharge have been published, but very little emphasis has been put on methodological issues, e.g. methods of education. In most programs the methods and equipment used for education and information have only consisted of verbal and written material; computer-based tools seem to be relatively new.

Interactive CD-ROM programs for HF patients can increase patients' knowledge about heart failure and its treatment. However, no studies have examined the clinical outcome, e.g. rate of readmission.

Comparison: Extra educated patients (interactive CD-ROM education) compared to standard educated patients on readmission rate or death during 6 months.

Study Timeline

• Study Start: 1998-02
• Status Verified: 2002-05
• Study Completion: 2002-07
• Study First Submitted: 2006-04-03
• Study First Submitted QC: 2006-04-03
• Last Update Submitted: 2006-04-03
• Study First Posted: 2006-04-05
• Last Update Posted: 2006-04-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 206

Inclusion Criteria

• Inpatients treated for heart failure with left ventricular ejection fraction (LVEF) < 40 % at echocardiography or at least two of the criteria pulmonary rates, peripheral oedema, a third heart sound and signs of heart failure at chest X-ray.

Exclusion Criteria

• Somatic disease or physical handicap with difficulties to communicate or handle the technical equipment, patients with only little knowledge in Swedish, patients with expected problems with compliance due to alcohol/drug abuse or major psychiatric illness, and participation in a trial.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Readmission and death rate at 6 months' follow up.

Secondary Outcome Measures

Name	Time	Method
Knowledge regarding heart failure and its treatment

Trial Locations

Locations (1)

Drug and Therapeutics Committee, Malmoe University Hospital; 🇸🇪 Malmo, Sweden