Stress and ETS: Measuring the neuroendocrine stress response of participants in a hospital disaster response simulation.

Stress and ETS: Measuring the neuroendocrine stress response of participants in a hospital disaster response simulation. - Stress and ETS

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON30907

Enrollment

Registered

2007-10-02

Start date

2007-09-01

Completion date

Unknown

Last updated

2024-05-13

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

Conditions

Omgang met stress Stress response / stress coping

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Participating in an ETS training, informed consent

Exclusion criteria

Exclusion criteria: No specific exclusion criteria will be used.

Design outcomes

Primary

Measure	Time frame
The main study endpoint is the neuro-endpcrine stress response to the ETS training. The response is measured by the cortisol and amylase levels in the saliva, the heart rate and variability in the heart rate, the answers to the questionnaires, and the stress perception as measured by the VAS.	—

Secondary

Measure	Time frame
Secundary outcome measures are the influence of chronic strecc, sensitivity to stress, task, and experience with MCI situations on the course of the neuro-endocrine stress response.	—

Countries

Netherlands

Outcome results