Stress and ETS: Measuring the neuroendocrine stress response of participants in a hospital disaster response simulation.
- Conditions
- Omgang met stressStress response / stress coping
- Registration Number
- NL-OMON30907
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 18
Inclusion Criteria
Participating in an ETS training, informed consent
Exclusion Criteria
No specific exclusion criteria will be used.
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The main study endpoint is the neuro-endpcrine stress response to the ETS<br /><br>training. The response is measured by the cortisol and amylase levels in the<br /><br>saliva, the heart rate and variability in the heart rate, the answers to the<br /><br>questionnaires, and the stress perception as measured by the VAS. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Secundary outcome measures are the influence of chronic strecc, sensitivity to<br /><br>stress, task, and experience with MCI situations on the course of the<br /><br>neuro-endocrine stress response. </p><br>