Pôle de simulation en Santé de Lyon Sud (PL3S)
Oullins, 69921, France
NCT Number: NCT05561283
Health students are the future actors of the health system. They are exposed to many stressors in their journey. The quality of life of medical students is alarming worldwide: 11.1% of undergraduate and postgraduate residents reportedly have suicidal ideation and 27.2% have depressive symptoms. In addition, 44.2% suffer from burn-out syndrome. In the third cycle, 28.8% suffer from depressive symptoms and 35.1% from burn-out syndrome. This finding is shared internationally among medical residents. Health professionals are facing a global problem which it is crucial to act.
At national level, a survey on the mental health of young doctors carried out in 2017 found, among the 7603 residents who responded a prevalence: 22.8% of depressive symptoms, 59.7% of anxiety symptoms, 23.4% of suicidal thoughts, including 5.0% in the month prior to the survey. In 2018, a French report on the quality of life of health by Dr Donata Marra highlighted a real malaise affecting residents and the need to intervene "for residents, for carers and for patients", through the implementation of specific recommendations. The proposal 6 of the report emphasises the prevention of psychosocial risks through educational interventions such as training in collaborative management. On a personal level, the aim is to the leadership of each individual, in terms of stress management, communication, cross-disciplinary skills or even the introduction of relational simulations in the teaching of an awareness of deviant behaviour and harassment. The stress factors are indeed multiple during health studies confrontation with death, competition, increasing responsibilities… Perceived stress has a negative impact on the quality of life and burnout. Effective stress management strategies could therefore help to improve the quality of life of residents.
In this context, the analysis of the literature highlights three main areas of intervention that could contribute to resident leadership in favour of their quality of life: stress management, healthy living and the construction of a professional identity.
The Junior Leadership programme for residents from the beginning of their professional formation designed to provide basic knowledge and skills in healthcare leadership and to develop cross-disciplinary skills. The aim is to provide the necessary support for the success of the resident's professional project by participating in the improvement of their quality of life and the prevention of psycho-social risks.
The study therefore propose to evaluate the feasibility of training in leadership and meditation on the satisfaction of resident.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Oullins, 69921, France
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Self-questionnaires on satisfaction, burn-out, depression, anxiety, relational skills and sleep quality
Time frame: At 4 months (at the end of the training that lasts around 4 months)
The satisfaction of the residents will be evaluated by a self-questionnaire according to model recommended by the Haute Autorité de Santé (HAS)and used in the framework of the SAMSEI programme (SAMSEI="Stratégies d'Apprentissage des Métiers de Santé en Environnement Immersif" that means in English "Learning Strategies for Healthcare Professions in an Immersive Environment") and the Lyon South Health Simulation Centre. The questionnaire will evaluate the interest, practical usefulness, density of information information, conformity with the objectives, the material conditions of the training, the activity of the participants and the motivation to continue the training.
Time frame: Before training (baseline) and 3 months, 6 months and 1 year after training
The proportion of residents showing symptoms of burn-out will be assessed by the Maslach's burn-out inventory before training and 3 months, 6 months and 1 year after training.
Time frame: Before training (baseline) and 3 months, 6 months and 1 year after training
Anxiety and depression symptoms will be assessed by Hospital Anxiety and Depression Scale (HADS) before training and at 3 months, 6 months and 1 year after training.
Time frame: Before training (baseline) and 3 months, 6 months and 1 year after training
The stress of residents in their work environment will be assessed using the Karasek scale, which evaluates psychosocial risk factors at work before training and at 3 months, 6 months and and 1 year after the training
Time frame: Before training (baseline) and 3 months, 6 months and 1 year after training
Caregivers' interpersonal skills will be assessed by Cungi and Rey's communication scale at 3 months, 6 months and 1 year after the training.
Time frame: Before training (baseline) and 3 months, 6 months and 1 year after training
The sleep quality of the residents will be assessed by the LEEDS scale before training and at 3 months, 6 months and 1 year after training
Time frame: Before training (baseline) and 3 months, 6 months and 1 year after training
The use of psychoactive substances will be collected from residents before the training and at 3 months, 6 months and 1 year after the training
Time frame: Before training (baseline) and 3 months, 6 months and 1 year after training
The use of medical/psychological support will be collected from residents before the training and at 3 months, 6 months and 1 year after the training.
Time frame: Before training (baseline) and 3 months, 6 months and 1 year after training
The number of days off sick will be collected from the residents before the training and at 3 months, 6 months and 1 year after the training.
Hospices Civils de Lyon
Other
Evaluation of the Satisfaction and Relevance of Leadership Training for Residents - START Study
Acronym: START
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.
NCT06750692
Brain Diseases, Cardiovascular Diseases
Afyonkarahisar, Turkey (Türkiye)
View Trial DetailsNCT07720752
Behavior, Climate Change Anxiety
Islamabad, Pakistan
View Trial DetailsNCT06654869
Cancer, Neoplasms
Erzurum, Yakutiye, Turkey (Türkiye)
View Trial DetailsNCT05379504
Disabilities Multiple, Quality of Life
Columbia, Missouri, United States
View Trial Details