Trial of a Tailored Message Program to Implement CHF Guidelines
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|ClinicalTrials.gov Identifier: NCT00013026|
Recruitment Status : Completed
First Posted : March 16, 2001
Last Update Posted : April 7, 2015
|Condition or disease||Intervention/treatment||Phase|
|Heart Failure||Behavioral: CHF Self-management Education (Web-based Education)||Not Applicable|
Congestive heart failure is a serious health problem in the United States and is associated with excessive morbidity and mortality. Several classes of medications have been shown to improve mortality in patients with CHF. Despite this these medications are widely under prescribed. Guidelines have been shown to improve patient outcomes and several guidelines on the management of CHF have been published. Implementation of guidelines is challenging and most strategies have focused on changing physician behavior. Patient-based interventions have been shown to be effective in implementing guidelines on CHF but they have been very labor intensive. A computer based intervention to implement CHF guidelines, if effective, would be beneficial.
Patients with CHF consume a significant proportion of healthcare resources, with exacerbations of CHF being the second most common reason for medical admission to VA medical centers. Therefore, the main objective is to understand the impact of a tailored education message program designed for direct use by patients on medical resource use. Other objectives include understanding the tools impact on patient compliance and quality of life.
Patients have been randomized to one of two groups: 1) intervention group or the 2) control group. The intervention group receives the tailored education messages program. This program assesses patients� beliefs about compliance with medications, diet, and self-monitoring. Based on identified barriers to compliance, intervention patients receive a tailored educational message to dispel these beliefs and improve compliance. The control group interacts with a generic healthcare website. Patients in both groups are monitored for hospitalization; emergent care visits, compliance with prescribed treatment and quality of life
Project work is ongoing.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||700 participants|
|Intervention Model:||Parallel Assignment|
|Official Title:||Trial of a Tailored Message Program to Implement CHF Guidelines|
|Actual Study Completion Date :||March 2004|
|Arm 1||Behavioral: CHF Self-management Education (Web-based Education)|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00013026
|United States, Alabama|
|Birmingham VA Medical Center, Birmingham, AL|
|Birmingham, Alabama, United States, 35233|
|Principal Investigator:||Terrence M. Shaneyfelt, MPH MD||Birmingham VA Medical Center, Birmingham, AL|
|Principal Investigator:||Catarina I. Kiefe, PhD MD||Birmingham VA Medical Center, Birmingham, AL|