CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 836 enrolled
Drug / intervention
Beta-blocker adherence after an AMIbehavioral
Likely dose
Not stated in record
Key inclusion· 4
  • Clinical diagnosis of acute myocardial infarction (AMI)
  • AMI diagnosed between December 1, 2003 and May 31, 2004
  • Beta-blocker dispensed following AMI
  • Beta-blocker dispensed prior to intervention date
Key exclusion· 0

None specified.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00211172
NCT00211172N/ACompleted

The HMO Research Network CERT: Acute Myocardial Infarction

Kaiser Permanente·interventional·Posted Sep 21, 2005·Updated Oct 9, 2014

In Brief

A clinical study evaluating Beta-blocker adherence after an AMI for Acute Myocardial Infarction (AMI). Completed, enrolled 836 participants across 4 sites.

Detailed Summary

The primary goal of this study is to evaluate the effectiveness of direct-to-patient mailings designed to increase patient's adherence to prescribed beta-blockers following an acute myocardial infarction (AMI). Prior to developing patient materials, focus groups were conducted with patient who had previously suffered an acute myocardial infarction (AMI) to identify the issues and information that patients felt were important to include in our materials as well as the best way to present the information. Additionally, patient materials were "pre-tested" with AMI patients to ensure that the materials were clear and easy to read and that the key messages were understood.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 21, 2005
Enrollment StartOct 1, 2003
Primary CompletionDec 1, 2005
Study CompletionMay 1, 2009
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 20.8 years ago

Interventions

Beta-blocker adherence after an AMIbehavioral

The intervention consisted of 2 mailed communications. A personalized letter was mailed first, followed approximately 2 months later by a similar letter and an accompanying brochure. Both mailings also included a wallet card that suggested questions for the patient to ask their clinician, space to list their medications, and space to record additional queries.