Attentionnal Performance of Shift Health Workers in Emergency Department

NCT06492928 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 69

Last updated 2024-10-16

No results posted yet for this study

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.

Conditions

  • Work-Related Condition

Interventions

OTHER

Psychomotor Vigilance Task

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 & Collaborators

  • Boulogne sur Mer Hospital Center

    collaborator OTHER
  • Centre Hospitalier de l'Arrondissement de Montreuil-sur-mer

    collaborator UNKNOWN
  • Centre Hospitalier Saint-Omer

    collaborator UNKNOWN
  • Centre Hospitalier de Bethune

    collaborator NETWORK
  • Centre Hospitalier de Lens

    collaborator OTHER
  • Polyclinique de la Clarence

    collaborator UNKNOWN
  • Centre hospitalier de Dunkerque

    collaborator UNKNOWN
  • Centre Hospitalier de Douai

    collaborator OTHER
  • Centre Hospitalier de Valenciennes

    collaborator NETWORK
  • Centre Hospitalier d'Hazebrouck

    collaborator UNKNOWN
  • Centre Hospitalier de Watrelos

    collaborator UNKNOWN
  • Centre Hospitalier de Denain

    collaborator UNKNOWN
  • Tourcoing Hospital

    collaborator OTHER
  • GHICL

    collaborator UNKNOWN
  • Polyclinique de Grande Synthe

    collaborator UNKNOWN
  • Centre Hospitalier de Roubaix

    lead OTHER

Principal Investigators

  • Remy Diesnis, MD · Centre Hospitalier de Roubaix

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-12
Primary Completion
2024-06-13
Completion
2024-07-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06492928 on ClinicalTrials.gov