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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05011435
Other study ID # WP-2021-01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 15, 2021
Est. completion date September 2022

Study information

Verified date August 2021
Source Weprom
Contact Magali BALAVOINE
Phone 241682940
Email m.balavoine@ilcgroupe.fr
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Burnout syndrome has been recognized as a mental illness since 2020. All workers can be affected. The consequences are multiple and often serious, ranging from stoppage of work to depression or even suicide. According to a 2019 survey by Malakoff, 56% of employees are in "professional or personal fragility", but the statistics are incomplete. In the medical community, the burnout rate is doubled compared to the general population. The diagnosis of pre-burnout can precede a burnout by several months, an early treatment can then reduce complications and improve the quality of life at work. On a study model on health data already carried out as part of a cancer detection application in smokers which involved 7000 users and which showed the ability to of such an application to detect curable symptomatic cancers from questionnaires (24% with application against 9% without application), we will carry out a descriptive evaluation of the use of an application to detect pre-burnout, burnout and depressive syndrome in a worker population. In the event of a risk alert of pre-burnout, burnout or depressive syndrome, the application will display a message to the user suggesting that he consult his general practitioner or put him in contact with a doctor through a teleconsultation via a dedicated platform. This first study will assess the feasibility and acceptability of an early detection approach among professionals of a state of "fragility" (pre-burnout, burnout or depressive syndrome). Subsequently, a larger study will evaluate the effectiveness of this application for the early detection of burnout among professionals, its management and the reduction of costs for the healthcare system and society.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date September 2022
Est. primary completion date September 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 64 Years
Eligibility Inclusion Criteria: - Person aged 18 to 64 - Exercising a professional activity - User informed of the use of this data and not objecting to it Exclusion Criteria: - Professionals on sick leave

Study Design


Related Conditions & MeSH terms


Intervention

Device:
web-application for burnout
Use of burnout advisor web-application for detection of professional burnout

Locations

Country Name City State
France ILC Le Mans

Sponsors (2)

Lead Sponsor Collaborator
Weprom Kelindi

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary usefulness number of users who find the application useful 6 months
Secondary alert Description of alerts triggered by algorithms 6 months
Secondary Consultation Number of relevant consultations (or teleconsultations) after an alert 6 months
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