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Effect of an Adult EDUcation Program on CArdiovascular ouTcomEs in Post-myocardial-infarction Patients

Effect of an Adult Education Program on Cardiovascular Outcomes in Post-myocardial-infarction Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04007887
Acronym
EDUCATE
Enrollment
320
Registered
2019-07-05
Start date
2017-10-15
Completion date
2020-06-30
Last updated
2019-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myocardial Infarction

Brief summary

A non-MD-led adult education program consisting in 10 one-hour sessions designed to provide information and motivation will be offered to patients who have recently been hospitalized for acute myocardial infarction (STEMI and NSTEMI), regarding the management of their treatment and strategies to aggressively optimize control of cardiovascular risk factors.. The intervention arm will be compared to a control group of patients treated with usual care.

Interventions

OTHERAdult education program

A 10-hour program embodying major adult education principles, designed to achieve cognitive involvement of patients in their treatment

Sponsors

National and Kapodistrian University of Athens
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* History of acute ST-elevation myocardial infarction (STEMI) or non-ST-elevation myocardial infarction (NSTEMI), Type Ι, according to the 3rd Universal Definition of MI, within the preceding 6 weeks * Absence of substantial cognitive dysfunction (Mini Mental State examination score ≥24)

Exclusion criteria

\- Age \>80 years or \<18 years

Design outcomes

Primary

MeasureTime frameDescription
Time to death or myocardial infarction or cerebrovascular event or unplanned hospitalization for cardiovascular reasons24 monthsTime from randomization to the composite endpoint of death or myocardial infarction or cerebrovascular event or unplanned hospitalization for cardiovascular reasons

Secondary

MeasureTime frameDescription
MACCE24 monthsMajor cardio-/cerebro-vascular events (cardiovascular death, myocardial infarction, cerebrovascular event)

Other

MeasureTime frameDescription
Change in LDL-chol12 monthsChange from baseline to 12 months in LDL-cholesterol concentration
Change in body-mass index12 monthsChange from baseline to 12 months in the body-mass index
Change in arterial pressure12 monthsChange from baseline to 12 months in systolic arterial pressure (the mean of 3 office measurements)

Countries

Greece

Contacts

Primary ContactSpyridon Deftereos, MD
spdeftereos@med.uoa.gr00302105832352

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026