AP-HM
Marseille, France
NCT Number: NCT02672072
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
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Marseille, France
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Non inclusion Criteria:
Exclusion criteria
Time frame: 6 months
Presence of job strain: psychological demand of work > 21 and decision latitude < 72
Time frame: enrollment and 1 year
Karasek questionnaire
Time frame: enrollment, 6 months and one year
French version of the COPSOQ (Copenhagen Psychosocial Questionnaire)
Time frame: enrollment, 6 months and one year
French version of the Maslach Burnout Inventory
Time frame: enrollment, 6 months and one year
Number of enrolled nurses who leave the actual ICU
Time frame: enrollment, 6 months and one year
visual analogic scale from 0 to 10
Assistance Publique Hopitaux De Marseille
Other
Acronym: SISTRESSREA
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.
Published trials that share one or more normalized conditions with this study.
NCT04192097
Anesthesia, Anxiety Disorders
La Tronche, France
View Trial DetailsNCT04199065
Behavior, Behavioral Symptoms
Vitoria-Gasteiz, Araba, Spain
View Trial DetailsNCT04235751
Behavior, Behavioral Symptoms
Rochester, Minnesota, United States
View Trial DetailsNCT04604769
Behavior, Behavioral Symptoms
Liège, Province De Liège, Belgium
View Trial Details