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Simulation-based Education for Managing Stress in ICU Nurses

Completed
Conditions
Professional Stress
Interventions
Other: Simulation during the study (5-day specific training with dedicated scenario done by an ICU expert simulation team)
Other: questionnaire to define the presence of job strain at 6 months
Other: questionnaire to define the presence of job strain at 12 months
Registration Number
NCT02672072
Lead Sponsor
Assistance Publique Hopitaux De Marseille
Brief Summary

I. Main outcome Decrease of the stress evaluated 6 months after training. Stress is defined as the presence of job strain as defined by Karasek.

II. Main secondary outcomes

* ICU nurses stress at one year

* Burnout

* Intent-to-leave the ICU

* Quality of life

III. Design

Prospective, randomized, open study comparing 2 groups of ICU nurses:

Simulation group and Control group

Nurses from 9 different adult ICUs will be included. Stratification by ICU will be done (to take into account differences between the ICUs regarding organization, activity, patients...).

This study is observational because nurses can participate to this training when they want. The fact that nurses are in control group delays their participation to this training but does not forbid them to particpate. The nurses from control group will participate to training at the end of study.

IV. Specific measures Control group: none

Simulation group: 5-day specific training with dedicated scenario done by an ICU expert simulation team

V. Study duration 48 months

VI. Ethical aspects - Reglementary concerns

* Study accepted by the Comité Consultatif sur le Traitement de l'Information en matière de Recherche dans le domaine de la Santé (CCTIRS) and by the Commission Nationale de l'Informatique et des Libertés (CNIL)

* Information to the participants prior inclusion

VII. Study population Job strain evaluated in a French study was 59% . The same rate was observed in a survey done in our institution (Assistance Publique Hôpitaux de Marseille). We therefore hypothesized that the intervention (simulation) should be able to reduce the job strain from 59% to 45% of the participants. With a power of 80% and a risk a of 5%, this study needs to include 185 patients per arm. To take into account few participants who will not complete the study, we aimed to include a total of 400 ICU nurses.

VIII Results An interim analysis will be performed after 200 inclusions

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
198
Inclusion Criteria
  • ICU nurses from adult ICUs with a professional experience in the actual ICU of at least 6 months and no decision to leave the ICU at the time of enrollment

Non inclusion Criteria:

  • Less than 6 months of professional activity in the actual ICU at the time of enrollment
  • Intent-to-leave in the next 6-month period
  • Previous experience of this simulation program
  • Pregnant women

Exclusion Criteria :

  • ICU nurses who leave their city during the study period
  • Pregnant women who miss their job during at least 4 weeks during the study period
Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Simulation groupquestionnaire to define the presence of job strain at 12 months5-day specific training with dedicated scenario done by an ICU expert simulation team
Simulation groupquestionnaire to define the presence of job strain at 6 months5-day specific training with dedicated scenario done by an ICU expert simulation team
Control groupquestionnaire to define the presence of job strain at 6 months5-day specific training with dedicated scenario done by an ICU expert simulation team after the period of the study
Simulation groupSimulation during the study (5-day specific training with dedicated scenario done by an ICU expert simulation team)5-day specific training with dedicated scenario done by an ICU expert simulation team
Control groupquestionnaire to define the presence of job strain at 12 months5-day specific training with dedicated scenario done by an ICU expert simulation team after the period of the study
Primary Outcome Measures
NameTimeMethod
Presence of job stain evaluated by the French version of the Karasek scale6 months

Presence of job strain: psychological demand of work \> 21 and decision latitude \< 72

Secondary Outcome Measures
NameTimeMethod
Stress evaluated by the Karasek scaleenrollment and 1 year

Karasek questionnaire

Psychosocial risks (Copenhagen Psychosocial Questionnaire)enrollment, 6 months and one year

French version of the COPSOQ (Copenhagen Psychosocial Questionnaire)

Burnout (Maslach Burnout Inventory)enrollment, 6 months and one year

French version of the Maslach Burnout Inventory

Intent-to-leave (Number of enrolled nurses who leave the actual ICU)enrollment, 6 months and one year

Number of enrolled nurses who leave the actual ICU

Quality of life (visual analogic scale)enrollment, 6 months and one year

visual analogic scale from 0 to 10

Trial Locations

Locations (1)

AP-HM

🇫🇷

Marseille, France

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