Anxiety, Stress and Pain & Myocardial Infarction

NCT ID: NCT04130269

Last Updated: 2025-09-29

Study Results

Results pending

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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Recruitment Status

RECRUITING

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-04-07

Study Completion Date

2027-12-07

Brief Summary

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People often experience the acute phase of a myocardial infarction as a stressful and traumatic event that seems lifethreatening. Such anxiety, pain and stress can lead to the development of posttraumatic stress disorder in the long run. Previous studies suggest that there might be a relevant percentage of people developing Posttraumatic Stress Disorder (PTSD) after a myocardial infarction. Posttraumatic stress disorder is a risk factor for the development of coronary heart disease. The goal of this study is to detect the percentage of people that develop symptoms of anxiety, stress, and PTSD after an acute myocardial infarction.

Detailed Description

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People often experience the acute phase of a myocardial infarction as a stressful and traumatic event that seems lifethreatening. Such anxiety, pain and stress can lead to the development of posttraumatic stress disorder in the long run. Previous studies suggest that there might be a relevant percentage of people developing PTSD after a myocardial infarction. Posttraumatic stress disorder is a risk factor for the development of coronary heart disease. The goal of this study is to detect the percentage of people that develop symptoms of anxiety, stress and PTSD after an acute myocardial infarction.

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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Myocardial Infarction

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients with MCI

Patients with myocardial infarction (STEMI/NSTEMI) aged 19-90

No intervention

Intervention Type OTHER

Questionnaires, lab-run

Interventions

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No intervention

Questionnaires, lab-run

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* willingness to participate in the study
* 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
Minimum Eligible Age

19 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Medical University of Graz

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Medical University of Graz

Graz, Styria, Austria

Site Status RECRUITING

Countries

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Austria

Central Contacts

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Andreas Baranyi, MD

Role: CONTACT

004331638513612

Hans-Bernd Rothenhäusler, MD

Role: CONTACT

004331638513612

Facility Contacts

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Andreas Baranyi, Prof. MD

Role: primary

+4331638586241

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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