Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
100 participants
OBSERVATIONAL
2020-04-07
2027-12-07
Brief Summary
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Detailed Description
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Patients will be examined during three times - in the acute myocardial infarction period (Day 1-3), before dismissal (Day 5-14) and after 6 months for a follow-up. During all times they will be given questionnaires asking about their levels of stress, anxiety and general well-being as well as tests checking their cognitive abilities (thus to find out if they decrease over time). Moreover, blood samples checking cortisol levels as well as metanephrine levels will be taken in order to objectify the levels of stress that are stated by the patients. Furthermore, clinical evaluations, laboratory runs (troponin), ECGs and echocardiographies will be done at all three points in time.
The goal is to detect the biopsychosocial relations and to develop better prevention.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients with MCI
Patients with myocardial infarction (STEMI/NSTEMI) aged 19-90
No intervention
Questionnaires, lab-run
Interventions
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No intervention
Questionnaires, lab-run
Eligibility Criteria
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Inclusion Criteria
* men and women 19-90
* after myocardial infarctions
* no psychiatric disease before myocardial infarction
* no other severe disease influencing the immune system
* non-compliant patients (dementia, delirium)
* steroid-therapy
19 Years
90 Years
ALL
Yes
Sponsors
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Medical University of Graz
OTHER
Responsible Party
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Locations
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Medical University of Graz
Graz, Styria, Austria
Countries
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Central Contacts
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Hans-Bernd Rothenhäusler, MD
Role: CONTACT
Facility Contacts
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Other Identifiers
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31-478 ex 18/19
Identifier Type: OTHER
Identifier Source: secondary_id
7479
Identifier Type: -
Identifier Source: org_study_id
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