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OpenTrials
Completed

NCT Number: NCT02672072

Simulation-based Education for Managing Stress in ICU Nurses

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

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

AP-HM

Marseille, France

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

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

Other

Primary outcomes

  1. Presence of job stain evaluated by the French version of the Karasek scale

    Time frame: 6 months

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

Secondary outcomes

  1. Stress evaluated by the Karasek scale

    Time frame: enrollment and 1 year

    Karasek questionnaire

  2. Psychosocial risks (Copenhagen Psychosocial Questionnaire)

    Time frame: enrollment, 6 months and one year

    French version of the COPSOQ (Copenhagen Psychosocial Questionnaire)

  3. Burnout (Maslach Burnout Inventory)

    Time frame: enrollment, 6 months and one year

    French version of the Maslach Burnout Inventory

  4. Intent-to-leave (Number of enrolled nurses who leave the actual ICU)

    Time frame: enrollment, 6 months and one year

    Number of enrolled nurses who leave the actual ICU

  5. Quality of life (visual analogic scale)

    Time frame: enrollment, 6 months and one year

    visual analogic scale from 0 to 10

Sponsors and collaborators

Lead sponsor

Assistance Publique Hopitaux De Marseille

Other

Registry information

Acronym: SISTRESSREA

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Feb 3, 2016
Registry last updated
May 30, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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