Descriptive Study of Biological Stress and Perceived Stress at the Center 15 (RegulStress)

Centre Hospitalier Régional Metz-Thionville

Status: Completed

Conditions: Psychological Stress; Physiological Stress

Treatments: Other: salivary sampling by a biomnis swab

Study type: Interventional

Funder types: Other

Identifiers

NCT02075424

2013-02-CHRMT

2013-A01725-40 (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to describe biological stress (cortisolemia) and perceived stress in Emergency Call Center Operators and Doctors while processing a center 15 call.

Full description

Sample description : qualitative variables be expressed as percentages, numbers and 95% confidence intervals Quantitative variables will be expressed as means, standard deviations or medians, range, interquartile intervals Description of biological stress : it will be described by calculating the difference between the observed peek or peeks of cortisol ans the cortisol level measured at rest (means, standard deviations or medians, range, interquartile intervals) Description of perceived stress : the AVS will be described in terms of means and standard deviation Comparison of the peek-delta/base level of cortisol in the 3 different workstations of the call center operators according to the non parametrical Kruskall Wallis test. Same for the lengthof service of the call operator, the severity of the call and the status of the doctor The AVS score (perceived stress) will be compared to the peek-delta/base level of cortisol (biological stress) thanks to the Spearmann correlation coefficient.

Enrollment: 40 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• medical and paramedical staff from the center 15 (call operators, emergency doctors and general practitioners)
• healthy volunteers having received the specific information letter regarding the sudy and having signed the clarified consent form
• healthy volunteers are affiliated to the french social welfare

Exclusion criteria

• chronic alcoholism
• women under oestroprogestative hormonal treatment
• high level athletes
• healthy volunteers under steroids treatment
• healthy volunteers suffering from a mental health related disorder
• fever on the day the sample is taken
• healthy volunteers with endocrine disorders

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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40 participants in 1 patient group

salivery sampling by a biomnis swab

Experimental group

Description:

Each call operator will have a series of salivary sampling taken when assigned to call reception, to the unit deployment station and to the assessment station. Only one sampling will occur to doctors who are assigned to a single workstation. Sampling will be taken every 15 minutes during one hour and half and one last sample will be taken 2 hours after the call For each participant, a serie of control-samples will be taken during a day off and during a security break.

Treatment:

Other: salivary sampling by a biomnis swab