Stress Response in Emergency Among Physicians in Helicopter and Ambulance Based Emergency Medical Systems

NCT ID: NCT03422952

Last Updated: 2018-11-09

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

COMPLETED

Total Enrollment

25 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-04-30

Study Completion Date

2018-11-01

Brief Summary

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Stress reactions in emergency physicians will be measures using cortol-awakening-reaction, heart-rate-variability and standardised stress questionnaires

Detailed Description

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In a field study with within-subject design, there will be conducted the hormonal and physiological stress strain of emergency physicians working in rescue helicopters or van on different days of service on different headquarters. The investigation of the parameter of stress will be conducted on two days of rescue service, on two days of clinical service and as a control on two days off. The quantification of the hormonal stress strain will be carried out with the cortisol awakening response, there will be conducted 3 saliva samples with identical interval after getting up within 30 minutes. While the labour time on the rescue service and on the clinical service and the whole day off, the heart rate variability will show the degree of physiological stress. This will be measured with a pulse-belt on the chest, which the participant will carry the whole day. In addition, participants will fill out a set of questionnaire on the first day of measurement.

Conditions

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Hormone Disturbance Stress Reaction Stress Related Disorder

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Medical Doctor working in rescue helicopter or van

Exclusion Criteria

* Metabolic disease
* Autoimmune disease
* Heart disease
* Blood disease
* Mental disease
* Endocrinologic disease
* BMI\>30
* \>10 cigarettes/day
* Taking cortisone medication
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Insel Gruppe AG, University Hospital Bern

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Lorenz Theiler, PD Dr. med

Role: PRINCIPAL_INVESTIGATOR

attending anaesthesiologist

Locations

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Bern University Hospital and University of Bern

Bern, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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2017-00561

Identifier Type: -

Identifier Source: org_study_id

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