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N/A N=907 Randomized Single-blind Health Services Research

HMO Research Network CERT: Acute Myocardial Infarction

Acute Myocardial Infarction (AMI)

Enrolled (actual)
907
Serious AEs
Results posted
Oct 2014
Primary outcome: Primary: Adjusted Mean Monthly Percent of Days Covered With B-blocker Following Intervention Date — 66.37; 70.62 Adjusted monthly % of days covered

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Beta-blocker adherence after an AMI (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Kaiser Permanente
Primary completion
Dec 2005

Outcome Measures

OutcomeResultp-value
PRIMARY
Adjusted Mean Monthly Percent of Days Covered With B-blocker Following Intervention Date
66.37; 70.62

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.

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of Acute Myocardial Infarction (AMI) from 12/1/03 to 5/31/04
  • Beta-blocker dispensing following AMI
  • Beta-blocker dispensing prior to intervention date

Exclusion Criteria

None

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00211172). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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