Burnout, ProfessionalPSY-DESARNCT04350151
National French Survey on Psychological Distress at Work of Anesthesia and Intensive Care Residents
An observational study of Burnout, Professional and Intensive Care, run by Facteurs Humains en Santé at 1 site in France.
Trial summary
Psychological distress is a significant problem for healthcare professionals and students in training. The investigator question the prevalence of this problem in French residents in anaesthesia and intensive care training. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Burnout, Professional, Intensive Care, Anesthesia
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 519 participants
- Where
- 1 siteFrance
- Study dates
- 2 Feb 2019to 1 May 2019
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: French resident of intensive care and anesthesia
Who may be able to join
- resident of intensive care or anesthesia, french
Who cannot join
- none
Trial locations and contacts
1 site in 1 country.
About this study
Psychological distress is a significant problem for healthcare professionals and students in training. The investigator question the prevalence of this problem in French residents in anaesthesia and intensive care training.
Read the detailed description
The investigator performed an observational study on the national population of anaesthesia residents. A questionnaire was sent to all residents composed with validated questionnaires analyzing psychological distress (Hospital Anxiety and Depression Scale (HADS), Copenhagen Burnout Inventory (CBI), Perceived Stress Scale (PSS), Karasek's questionnaire; work-related questions (work hours per week, night shift per month, application of safety rest after night shift, average time to start and end work, break time and time for food per day; two semi-open work-related questions (main stressor during internship, professional orientation); a free verbatim.
- Conditions
- Burnout, Professional, Intensive Care, Anesthesia, Depression, Anxiety, Stress, Psychological, Fatigue
- Being tested
- no intervention
- Medical subject headings
- Burnout, Professional, Depression, Anxiety Disorders, Stress, Psychological, Fatigue
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
no interventionBehavioural
no intervention
What is being measured
The primary outcome is the main question the study is designed to answer.
Hospital Anxiety and Depression Scale (HADS)
Investigation of the anxiety and depression with 14 questions, the cut-off score is more than 11 for anxiety or depression
Measured: baseline
Copenhagen Burnout Inventory (CBI)
Investigation of the burnout on 3 axes: personal, professional and relational with 19 questions, the cut-off score is 50 to identify a burnout
Measured: baseline
Karacek's questionnaire
Investigation of the stress at work
Measured: baseline
Perceived Stress Scale (PSS)
Investigation of the stress with 10 questions
Measured: baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Apr 2020
- Study start2 Feb 2019
- Primary completion1 May 2019
- Study completion1 May 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Burnout, ProfessionalStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Retrospective
- Enrolment
- 519 participants (actual)
Sponsor and investigators
- Lead sponsor
- Facteurs Humains en Santé
- Sponsor type
- University, hospital or other
- Collaborators
- Dominique FLETCHER MD-PhD, François Marty MD, Dinh Phong Nguyen MD, Loic Druette MD, Benoit Plaud MD-PhD, Clément Duret MD
- Responsible party
- Principal investigator, François JAULIN, Facteurs Humains en Santé
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04350151
- Sponsor's protocol ID
- 20200316
- Acronym
- PSY-DESAR
- Status last verified
- Apr 2020
- First submitted
- 16 Mar 2020
- Last updated
- 16 Apr 2020
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: At the end of the survey
Study at a glance
From the registry record, last updated by the sponsor on 16 Apr 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- National French Survey on Psychological Distress at Work of Anesthesia and Intensive Care Residents
- ClinicalTrials.gov ID
- NCT04350151
- Acronym / sponsor ID
- PSY-DESAR / 20200316
- Conditions
- Burnout, Professional, Intensive Care, Anesthesia, Depression, Anxiety, Stress, Psychological, Fatigue
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 519 participants (actual)
- Lead sponsor
- Facteurs Humains en SantéUniversity, hospital or other
- Collaborators
- Dominique FLETCHER MD-PhD, François Marty MD, Dinh Phong Nguyen MD, Loic Druette MD, Benoit Plaud MD-PhD, Clément Duret MD
- Study start
- 2 Feb 2019 (actual)
- Primary completion
- 1 May 2019 (actual)
- Study completion
- 1 May 2019 (actual)
- First posted
- 16 Apr 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Psychological distress is a significant problem for healthcare professionals and students in training. The investigator question the prevalence of this problem in French residents in anaesthesia and intensive care training.
Detailed description
The investigator performed an observational study on the national population of anaesthesia residents. A questionnaire was sent to all residents composed with validated questionnaires analyzing psychological distress (Hospital Anxiety and Depression Scale (HADS), Copenhagen Burnout Inventory (CBI), Perceived Stress Scale (PSS), Karasek's questionnaire; work-related questions (work hours per week, night shift per month, application of safety rest after night shift, average time to start and end work, break time and time for food per day; two semi-open work-related questions (main stressor during internship, professional orientation); a free verbatim.
Study design
- Observational model
- Other
- Time perspective
- Retrospective
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- French resident of intensive care and anesthesia
Key inclusion criteria (1 listed)
- resident of intensive care or anesthesia, french
Key exclusion criteria (1 listed)
- none
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| no interventionno intervention | Behavioural | – |
Primary outcome
Hospital Anxiety and Depression Scale (HADS)
Time frame: baseline
Investigation of the anxiety and depression with 14 questions, the cut-off score is more than 11 for anxiety or depression
Copenhagen Burnout Inventory (CBI)
Time frame: baseline
Investigation of the burnout on 3 axes: personal, professional and relational with 19 questions, the cut-off score is 50 to identify a burnout
Karacek's questionnaire
Time frame: baseline
Investigation of the stress at work
Perceived Stress Scale (PSS)
Time frame: baseline
Investigation of the stress with 10 questions
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Apr 2020.
- Individual participant dataSharing planned: Yes. At the end of the survey
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Burnout, Professional and Intensive Care, run by Facteurs Humains en Santé at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 16 Apr 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Hospital Anxiety and Depression Scale (HADS) (time frame: baseline). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Apr 2020.