acute myocardial infarction I21
Conditions
Interventions
Group 1: Interventional:
The intervention group receives a patient agreement listing medication and target values, which is signed by the patient and the treating physician.
Group 2: Control intervent
Sponsors
Stiftung Institut für Herzinfarktforschung
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: acute myocardial infarction Written Informed Consent
Exclusion criteria
Exclusion criteria: 1. participation in another randomised trial 2. forseeable problems to perform 6-month telephon follow-up 3. problems to understand the content of the patient contract
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correct patient knowledge 6 months after discharge: - guideline-compliant target values ??for LDL cholesterol, systolic blood pressure, and the need for physical exercise (simultaneously). | — |
Secondary
| Measure | Time frame |
|---|---|
| correct patient knowledge about individual guideline target values - for LDL-cholesterin - for systolich blood pressure - diet - exercise - smoking cessation Actual target guideline adherent values - LDL-cholesterin - for systolic blood pressure - diet - exercise - smoking cessation | — |
Countries
Germany
Contacts
Public ContactUwe Zeymer
Stiftung Institut für Herzinfarktforschung
Outcome results
None listed