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Attentionnal Performance of Shift Health Workers in Emergency Department

Evaluation of Attentionnal Performance by PVT of Health Workers During Their Shift in Emergency Department

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06492928
Acronym
Emerg-APoSHeW
Enrollment
69
Registered
2024-07-09
Start date
2024-06-12
Completion date
2024-07-30
Last updated
2024-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Work-Related Condition

Keywords

shift-work, PVT, Health worker, Attentionnal performance, Emergency department

Brief summary

Atypical working hours can be a risk factor for workers. In fact, the body is subject to a circadian rhythm, which affects numerous physiological activities. These biological rhythms reflect the need for certain physiological activities to occur at a specific time of day. This cycle can be disrupted and shifted by external factors. This disruption of biological rhythms can manifest itself in the appearance of health effects. The innovative nature of our work lies in the search for an alteration in psychomotor functions in nursing staff (subject to atypical working hours). To this end, we decided to study the concentration of care workers using a reflex-based psychomotor test, the Psychomotor Vigilance Test (PVT). Other factors will be studied in order to assess the factors that may affect this test.

Detailed description

Population : All care staff in the emergency departments of the participating hospitals: physicians, residents, nurses and nursing assistants. The main objective is to evaluate concentration in medical/non-medical staff at the start and end of a work shift. To this end, we will evaluate the Psychomotor Vigilance Test (PVT) and its variation at the start and end of a shift in these personnel. The endpoint is the difference in reflex time to a visual stimulus performed at the beginning and end of the shift with a 3-minute PVT Test. The first secondary objective is to analyze the number of PVT errors. The criterion defining an error is a reaction time greater than 500ms. The second secondary objective is to compare the PVT and its variation in certain subgroups. The subgroups compared will be defined according to the following criteria : * Shift duration: Non-medical staff (\<10h, \>10h), Medical staff (6 to 10h, 10 to 15h, 15 to 24h) Staggered shift: start before 6h or end after 22h, * Type of service: acute care, MCO, SSR (or emergency sector) * Sleep quality (Pittsburgh Sleep Quality Index), * Professional fatigue (Maslach Burnout lnventory), * Anxiety (French official version of the PSS-14), * Chronotype (Morningness-Eveningness Questionnaire).

Interventions

T0 - at the start of the shift: completion of the 1st PVT / socio-demographic and workstation questionnaire T1 - at the end of the shift: completion of the second PVT and questionnaire on the course of the shift that has just taken place T2 - 1 week after the end of the shift: additional questionnaire sent with scales to assess work-related fatigue (MBI), anxiety (PSS), sleep quality (PSQI) and chronotype (MEQ).

Sponsors

Boulogne sur Mer Hospital Center
CollaboratorOTHER
Centre Hospitalier de l'Arrondissement de Montreuil-sur-mer
CollaboratorUNKNOWN
Centre Hospitalier Saint-Omer
CollaboratorUNKNOWN
Centre Hospitalier de Bethune
CollaboratorNETWORK
Centre Hospitalier de Lens
CollaboratorOTHER
Polyclinique de la Clarence
CollaboratorUNKNOWN
Centre hospitalier de Dunkerque
CollaboratorUNKNOWN
Centre Hospitalier de Douai
CollaboratorOTHER
Centre Hospitalier de Valenciennes
CollaboratorNETWORK
Centre Hospitalier d'Hazebrouck
CollaboratorUNKNOWN
Centre Hospitalier de Watrelos
CollaboratorUNKNOWN
Centre Hospitalier de Denain
CollaboratorUNKNOWN
Tourcoing Hospital
CollaboratorOTHER
GHICL
CollaboratorUNKNOWN
Polyclinique de Grande Synthe
CollaboratorUNKNOWN
Centre Hospitalier de Roubaix
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Physicians, * residents, * nurses, * nursing assistants

Exclusion criteria

* Students, * paramedics

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of concentration in medical/non-medical staff at the start and end of a work shift.Day 1To this end, we will evaluate the Psychomotor Vigilance Test (PVT) and its variation at the start and end of a shift in these personnel. The endpoint is the difference in reflex time to a visual stimulus performed at the beginning and end of the shift with a 3-minute PVT Test.

Secondary

MeasureTime frameDescription
The first secondary objective is to analyze the number of PVT errors.Day 1The criterion defining an error is a reaction time greater than 500ms.
Sub-group analysisDay 7The second secondary objective is to compare the PVT and its variation in certain subgroups. The subgroups compared will be defined according to the following criteria Shift duration: Non-medical staff (\<10h, \>10h), Medical staff (6 to 10h, 10 to 15h, 15 to 24h) Staggered shift: start before 6h or end after 22h, Type of service: acute care, MCO, SSR (or emergency sector) Sleep quality (Pittsburgh Sleep Quality Index), Professional fatigue (Maslach Burnout lnventory), Anxiety (French official version of the PSS-14), Chronotype (Morningness-Eveningness Questionnaire).

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026