- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04291534
Quality of Life and Addiction Among Hospital Night Workers (ALADDIN)
Quality of Life and Addiction Among Hospital Night Workers - Descriptive Study of APHP Workers in Paris
The current context of the Covid-19 health crisis leads to an over-solicitation of health systems, with hospital staff in the front line. These personnel are undergoing high levels of stress, an alteration of their life rhythm, but also of their health status and quality of life at work. In addition, night work, through the disruption of circadian rhythms, has consequences on physical and mental health. The more frequent worsening of the condition of certain patients at night increases the burden and responsibilities of night staff. Increasing the use of psychoactive substances (SPAs) can become a solution for managing stress, work rhythms, sleep disorders and their consequences. This self-medication behaviour is not without risks, neither for staff nor for patients.
The ALADDIN study is a project made up of 2 waves of questionnaires - one during and the other after the Covid "hospital" crisis - filled in by the hospital night staff of AP-HP. This project will assess the impact of the Covid-19 epidemic on the quality of work life, mental health disorders, post-traumatic stress and substance use of hospital night staff.
The main objectives of this study is to evaluate the prevalence of psychoactive substance consumption among the night shift healthcare workers of the AP-HP and to describe the participants' quality of working life.
Methods The study is prospective study using an online self-completed questionnaire. The questionnaire was elaborated on the basis of the validated scales ASSIST (Alcohol, Smoking, and Substance Involvement Screening Test), AUDIT-C (Alcohol Use Disorder Test, shortened version) and HAD (for anxiety and depression) and on qualitative interviews conducted among care staff working the night shift.
The questionnaire will be completed at t0 (baseline) and 18 months after. This study will provide data on the consumption psychoactive substances by night hospital workers adn their quality of working life. It will also allow us to compare their consumption with the general population, and to describe the risk factors influencing the consumption.
Study Overview
Status
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Lorraine COUSIN, PhDc
- Phone Number: 0683586227
- Email: cousinlorraine@gmail.comlorraine.cousin-ext@aphp.fr
Study Contact Backup
- Name: Olivia Rousset Torrente, MD
- Phone Number: 0140274689
- Email: olivia.rousset-torrente-ext@aphp.fr
Study Locations
-
-
-
Le Kremlin-Bicêtre, France, 94275
- Recruiting
- Hopital de Bicetre
-
Contact:
- Aïchata F Dara, MD
- Phone Number: 33 0140275544
- Email: adara.proqol@gmail.com
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Paris, France, 75004
- Recruiting
- Assistance Publique des Hopitaux de Paris
-
Contact:
- Lorraine COUSIN, PhDc
- Phone Number: 0144841777
- Email: lorraine.cousin-ext@aphp.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- hospital workers at APHP, working at night or night and day alternance (working at least 3 hours between 9 p.m and 6 a.m, 2 times a week)
Exclusion Criteria:
- Hospital workers working during the day
- Workers working less than 3 hours a night two time a week
- Doctors
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Substance use prevalence
Time Frame: at T0 month : baseline
|
Prevalence in APHP health workers of psychoactive substance consumption during the Covid 19 outbreak
|
at T0 month : baseline
|
Quality of working life scale
Time Frame: at T0 month : baseline
|
Evaluation of the quality of working life during the Covid 19 outbreak using a validated scale
|
at T0 month : baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Intervention preference
Time Frame: at T0 month
|
Identify the preferences for intervention to improve the quality of life or change the addictive risk of night hospital staff at the APHP.
Preferences for intervention methods and ranking of the least preferred.
|
at T0 month
|
Psychoactive substance consumption and associated factors
Time Frame: at T0 month
|
Describe the risk factors associated with the consumption of psychoactive substances (PAS). Logistic or fish linear regression depending on the type of variable taken into account. |
at T0 month
|
Impact of substance consumption on quality of life at work
Time Frame: at T0 month
|
Evaluate the impact of substance use on quality of life at work Principal component analysis and classification to see if there are consumer groups for the night and / or day population.
Method for taking into account missing, unused or invalid data
|
at T0 month
|
Risk factors associated with tobacco use
Time Frame: at T0 month
|
Describe the risk factors associated with tobacco use among night hospital workers,
|
at T0 month
|
Impact of sleep quality on quality of working life and perceived health
Time Frame: at T0 month
|
Evaluate the impact of sleep quality on the quality of working life and perceived health of night staff
|
at T0 month
|
Impact of anxiety and depressive symptoms on sleep and QWL.
Time Frame: at T0 month
|
Describe the links between QWL and sleep, anxiety, depressive syndromes, and workplace upheaval.
|
at T0 month
|
Impact of sleep and workplace upheaval on anxiety and depressives symptoms
Time Frame: at T month
|
Describe the links between anxiety/depressive syndromes and workplace disruption, sleep, and the Covid epidemic.
|
at T month
|
Modification of quality of working life score and psychoactive substances consumption prevalences
Time Frame: T18 months
|
Comparison between the baseline score and prevalences and the score and prevalences 18 months after
|
T18 months
|
Comparison of modification of quality of life score and declared quality of life modification after 18 month
Time Frame: T18 months
|
Analysis of the relation between declared change and evolution of the quality of life score
|
T18 months
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ALADDIN-QoLHospWork
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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