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- Klinische proef NCT04908007
COvid Pandemic Institutional maNaGement (COPING)
Institutional Management and Professional Experience During the Pandemic COVID-19 by Health Care Institutions in the Auvergne-Rhône-Alpes Region: Assessment and Lessons Learned
Covid-19 has increased organizational tensions within health services (lack of resources, difficulties in recruiting healthcare professionals , elderly and polypathological patients, etc.) and tested the reliability of health facilities. This project aims to draw lessons so that hospitals can transform themselves while improving their reliability to face future crises and other exceptional situations.
Research hypothesis:
Crisis management arrangements lack sensitivity to uncertainty, which manifests itself in lower quality of care and efficiency losses for the entire institution.
The virtuous practices implemented during the crisis spontaneously incorporated principles of the highly reliable organization.
The integration of principles from complexity theory into the management of institutions promotes high reliability organization.
Sustaining these virtuous practices in order to anticipate and cope with crises requires the activation of two interconnected levers: a shared vision (by patients, healthcare professionals, ARS, HAS, and the Ministry in the first place) of the meaning of the action taken by hospitals, and the development of a policy enabling hospitals to become both learning and highly reliable.
Main objective:
To evaluate the management process of the Covid-19 epidemic by the university hospitals of the Auvergne-Rhône-Alpes region, and the structures linked to them (establishments in their territory, ARS, user associations), in terms of points of improvement and good practices. This evaluation concerns the preparation, management and exit phases of the crisis.
Studie Overzicht
Toestand
Conditie
Studietype
Inschrijving (Verwacht)
Contacten en locaties
Studiecontact
- Naam: Julie HAESEBAERT, MD
- Telefoonnummer: +33 4 72 68 49 05
- E-mail: julie.haesebaert01@chu-lyon.fr
Studie Contact Back-up
- Naam: Philippe MICHEL, MD
- Telefoonnummer: +33 4 72 40 71 03
- E-mail: philippe.michel@chu-lyon.fr
Studie Locaties
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Clermont-Ferrand, Frankrijk, 63003
- Werving
- CHU Clermont-Ferrand , Pôle de Santé Publique, unité d'Epidémiologie, Economie de la Santé et Prévention
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Contact:
- Laurent GERBAUD, MD
- E-mail: lgerbaud@chu-clermontferrand.fr
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Grenoble, Frankrijk, 38700
- Werving
- CHU Grenoble, Pôle Santé Publique, service de veille sanitaire
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Contact:
- Patrice FRANCOIS, MD
- E-mail: PFrancois@chu-grenoble.fr
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Lyon, Frankrijk, 69002
- Werving
- Hospices Civils de Lyon, DOQ-RU
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Contact:
- Philippe MICHEL, MD
- Telefoonnummer: +33 4 72 40 71 03
- E-mail: philippe.michel@chu-lyon.fr
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Saint-Étienne, Frankrijk, 42055
- Werving
- CHU Saint-Etienne , Unité de gestion du risque infectieux
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Contact:
- Philippe BERTHELOT, MD
- E-mail: Philippe.berthelot@chu-st-Etienne.fr
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Bemonsteringsmethode
Studie Bevolking
- Professionals and members of the institutions' bodies in the 4 university hospitals: Lyon, St Etienne, Clermont Ferrand, Grenoble
- Adult patients hospitalized for at least 48 hours during the first wave of the pandemic COVID-19 in the 4 university hospitals: Lyon, St Etienne, Clermont Ferrand, Grenoble
Beschrijving
Inclusion Criteria:
Establishments :
- 4 university hospitals: Lyon, St Etienne, Clermont Ferrand, Grenoble
- Establishments in the same territories, public and private
Professionals and members of the institutions' bodies:
- Governance: management and chair of the CME
- Management (care, communication, medical, technical, logistics, IT, personnel)
- Clinical and public health cluster governance
- Medical, paramedical and non-medical staff in the departments most concerned (emergency and EMS reception, intensive care, infectiology, hygiene, virology, imaging, occupational medicine in particular)
- Organizations representing the personnel
- Members of the users' representatives committee
- Adult patients hospitalized for at least 48 hours during the study period (quantitative study by questionnaires).
Exclusion Criteria:
- none
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
Cohorten en interventies
Groep / Cohort |
Interventie / Behandeling |
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Professional qualitative group
Qualitative analysis of crisis management by interviewing professionals most involved during the crisis in each university hospital.
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3 individual interviews with the different categories of professionals most involved during the crisis in each university hospital. In the first phase, the points of improvement identified will be analyzed In the second phase, good practices and innovations will be analyzed. For these first two phases, the duration of one hour was chosen because it is difficult to mobilize the professionals for longer. Individual interviews are preferred, but group interviews are possible with no more than three people so that everyone can express himself or herself. Finally, individual interviews of 15 to 30 minutes will be conducted with some of the people interviewed previously in order to identify the costs of the dysfunctions or problems encountered during the crisis. Questionnaires with establishments associated with the crisis management, the ARS AuRA and France Assos Santé AuRA. Analysis of evidence documents in the university hospitals |
Professional quantitative group
Quantitative analysis of crisis management using the WHO grid adapted sent to the target persons identified within the establishments
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A self-assessment of the three phases of the crisis management process (preparation, crisis management, crisis recovery) will be carried out in the participating establishments using the WHO grid with the target persons identified within the establishments. This step will use the crisis response assessment tool developed by the WHO following the H1N1 pandemic in 2011. This grid will be adapted beforehand to the COVID-19 situation and to the local organization by the study's scientific committee. The dimensions investigated will be : Command and control, Communication, Safety and security, Triage, Surge capacity, Continuity of essential services; Human resources, Logistics and supply management, Post-disaster recovery. The grids will be sent to the 4 university hospitals to be filled in with the target audience recommended by the WHO methodological guide. The results of this self-assessment will be linked to and interpreted with the results of the interviews in phase 1. |
Patient quantitative group
Quantitative analysis of crisis management using a questionnaire sent to patients hospitalized in the first wave asking them about their perception of crisis and post-crisis management.
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A questionnaire of patients' perceptions on the same perimeter (crisis and post-crisis management, from the point of view of points of improvement and good practices) will be constructed and sent by the management of the establishments to all patients hospitalized for 48 hours or more during the first wave and who have left their email address (methods similar to the e-satis survey). The online questionnaire survey is preferred in order to get away from the emotion and for feasibility reasons. This patient experience questionnaire adapted to COVID will be co-constructed with expert/partner patients and user associations. Four dimensions will be investigated : The perception of the quality of the information received by the patient, The nature of the information on the specific health protection protocol from which the patient benefited, The patient's consideration of the overall context, during and after, The effects of the health context on the overall management of the patient |
Tools development
Development of tools to prepare for situations of uncertainty
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Development of tools to prepare for situations of uncertainty : In the third phase of the project, design thinking workshops will be organized (within the HCL) to develop training (in the form of simulation) in order to appropriate virtuous practices in situations of uncertainty. The purpose of these training sessions will be to improve the institution's ability to learn in a situation of uncertainty and thus to develop its reliability. The aim of these workshops is to provide tools for raising awareness of situations of uncertainty to all hospital staff. |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Crisis management process based on a qualitative approach
Tijdsspanne: The Qualitative analysis (intervention 1) will take place from September, 2020 to December, 2021
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The qualitative evaluation (interviews, document review) will make it possible to identify the points of improvement and virtuous practices implemented in the establishments.
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The Qualitative analysis (intervention 1) will take place from September, 2020 to December, 2021
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Crisis management process based on a quantitative approach with the professionals (identified within the establishments)
Tijdsspanne: The Quantitative analysis for professionals (intervention 2) will be conducted from March, 2021 to June 2021.
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The quantitative evaluation will be based on the WHO checklist.
This first part will report, for each hospital, the proportion of items validated in each dimension of the WHO checklist (https://www.who.int/publications/i/item/hospital-emergency-response-checklist):
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The Quantitative analysis for professionals (intervention 2) will be conducted from March, 2021 to June 2021.
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Crisis management process based on a quantitative approach with the patients (hospitalized in the first wave)
Tijdsspanne: The Quantitative analysis for patients (intervention 3) will be conducted from March, 2021 to June 2021. The tool development phase (intervention 4) will be carried out from January, 2022 to June, 2022
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The second quantitative evaluation will be based on patients' perceptions with a constructed questionnaire on theses perimeters: crisis and post-crisis management, from the point of view of points of improvement and good practices. This patient experience questionnaire will be adapted to COVID with expert/partner patients and user associations. |
The Quantitative analysis for patients (intervention 3) will be conducted from March, 2021 to June 2021. The tool development phase (intervention 4) will be carried out from January, 2022 to June, 2022
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Medewerkers en onderzoekers
Sponsor
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Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Verwacht)
Studie voltooiing (Verwacht)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 69HCL20_0466
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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