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Impact of COVID-19 Pandemic Burnout on Cardiovascular Risk in Healthcare Professionals Study Protocol: A Multicenter Exploratory Longitudinal Study.
Al Tunaiji, Hashel; Al Qubaisi, Mai; Dalkilinc, Murat; Campos, Luciana Aparecida; Ugwuoke, Nnamdi Valbosco; Alefishat, Eman; Aloum, Lujain; Ross, Ramzy; Almahmeed, Wael; Baltatu, Ovidiu Constantin.
Afiliación
  • Al Tunaiji H; Zayed Military Hospital, Abu Dhabi, United Arab Emirates.
  • Al Qubaisi M; Zayed Military Hospital, Abu Dhabi, United Arab Emirates.
  • Dalkilinc M; Zayed Military Hospital, Abu Dhabi, United Arab Emirates.
  • Campos LA; College of Health Sciences, Abu Dhabi University, Abu Dhabi, United Arab Emirates.
  • Ugwuoke NV; Center of Innovation, Technology and Education (CITE), Sao Jose dos Campos Technology Park, Sao Jose dos Campos, Brazil.
  • Alefishat E; Institute of Biomedical Engineering, Anhembi Morumbi University-Laureate International Universities, Sao Jose dos Campos, Brazil.
  • Aloum L; College of Medicine & Health Sciences, Khalifa University, Abu Dhabi, United Arab Emirates.
  • Ross R; College of Medicine & Health Sciences, Khalifa University, Abu Dhabi, United Arab Emirates.
  • Almahmeed W; College of Medicine & Health Sciences, Khalifa University, Abu Dhabi, United Arab Emirates.
  • Baltatu OC; Myriad Global Solutions, Abu Dhabi, United Arab Emirates.
Front Med (Lausanne) ; 7: 571057, 2020.
Article en En | MEDLINE | ID: mdl-33415114
ABSTRACT

Introduction:

The coronavirus disease 2019 (COVID-19) pandemic has created new and unpredictable challenges for healthcare systems. Healthcare professionals are heavily affected by this rapidly changing situation, especially frontline healthcare professionals who are directly engaged in the diagnosis, treatment, and care of patients with COVID-19 and may experience psychological burdens. The objective of this study is to explore the evolution of psychosocial, cardiovascular, and immune markers in healthcare professionals with different levels of exposure to the COVID-19 pandemic. Methods and

Analysis:

This is a STROBE compliant, blended, exploratory study involving online and onsite approaches that use wearable monitoring. A planned random probability sample of residents, staff physicians, nurses, and auxiliary healthcare professionals will be recruited. The study sample will be stratified by exposure to the COVID-19 pandemic. As a first step, recruitment will be conducted online, with e-consent and using e-surveys with Maslach Burnout Inventory, Fuster-BEWAT score, and sociodemographic characteristics. Onsite visits will be planned for the second step where participants will receive a wearable setup that will measure heart rate, actimetry, and sleep quality monitoring, which will be used together with blood sampling for immune biomarkers. Steps 1 and 2 will then be repeated at 2-3 months, and 6 months. Power BI and Tableau will be used for data visualization, while front-end data capture will be used for data collection using specific survey/questionnaires, which will enable data linkage between e-surveys, internet of things wearable devices, and clinical laboratory data. Clinical Trial Registration ClinicalTrials.gov; Identifier NCT04422418.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Med (Lausanne) Año: 2020 Tipo del documento: Article País de afiliación: Emiratos Árabes Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Med (Lausanne) Año: 2020 Tipo del documento: Article País de afiliación: Emiratos Árabes Unidos