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Impact of Burnout on Cardiovascular and Immune Biomarkers in Healthcare Professionals - Covid-19 Pandemic in Abu Dhabi

Multi-Center Prospective Cohort Study: Impact of Burnout on Cardiovascular and Immune Biomarkers Among Frontline Healthcare Professionals During Covid-19 Pandemic in Abu Dhabi Emirate

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04422418
Enrollment
200
Registered
2020-06-09
Start date
2020-07-01
Completion date
2020-12-31
Last updated
2020-11-03

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

Conditions

Burnout, Cardiovascular Risk Factor, Immune Deficiency

Keywords

Pandemics, Healthcare professionals, Burnout, Cardiovascular risk

Brief summary

The main objective of our project is to investigate the evolution of psychosocial, cardiovascular and immune markers in healthcare with different levels of exposure to the COVID-19 pandemic.

Detailed description

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. They may experience psychological burden, especially nurses, women, and frontline health care professionals directly engaged in the diagnosis, treatment, and care for patients with COVID-19. The objective of this study is to investigate the evolution of psychosocial, cardiovascular and immune markers in healthcare professionals with different levels of exposure to the COVID-19 pandemic. The effects of the pandemic work burden on psychological, cardiovascular and immune biomarkers will be stratified per level of exposure to the COVID-19 pandemic, positive diagnosis to COVID-19, profession, sex, age and already existent cardiovascular risk. Methods: A STROBE compliant, blended exploratory study involving online and onsite approach with wearable monitoring will be implemented. A planned random probability sample of residents, staff physicians, nurses and auxiliary healthcare professionals will be recruited from both inpatient and outpatient medicine services will be stratified by exposure to COVID-19 pandemic (frontline versus second line). In a first step, will be an online recruitment with e-consent and e-survey with Maslach Burnout Inventory, Fuster-BEWAT score and sociodemographic characteristics, and planning for onsite visit; in a second step, will be a setup for wearable monitoring of heart rate, actimetry and sleep quality together with blood sampling for immune biomarkers; steps 1 & 2 will be repeated at 2-3 months, 6 months. Power BI & Tableau will be used for data visualization purposes, while the front-end data capture application will be used for data collection and will be built using specific survey/questionnaire related tools for healthcare usage data linkage. Ethics and dissemination: Institutional Review Board approval has been obtained from Khalifa University (protocol # CPRA-2020-034) and Department of Health-Abu Dhabi (protocol # CVDC-20-05/2020-8). Data analysis, release of results and publication of manuscripts are scheduled to start in early 2021. Data and findings may be useful to healthcare policymakers for developing preventive strategies to reduce or prevent burnout, cardiovascular risk and immune dysfunction.

Interventions

None listed

Sponsors

Zayed Military Hospital
CollaboratorOTHER_GOV
Abu Dhabi University
CollaboratorUNKNOWN
Cleveland Clinic Abu Dhabi
CollaboratorOTHER
Sheikh Khalifa Medical City
CollaboratorOTHER
Sheikh Shakhbout Medical City
CollaboratorOTHER
Mediclinic Middle East
CollaboratorINDUSTRY
Myriad Global Solutions
CollaboratorUNKNOWN
Khalifa University for Science and Technology
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* all residents, staff physicians, nurses and auxiliary healthcare professionals from both inpatient and outpatient medicine services who agreed to be a part of the study will be provided with heart rate tracking devices to monitor heart rate.

Exclusion criteria

* not willing to complete written consent form.

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline Through Actigraphy at 2-3 months and 6 monthsbaseline, 2-3 months, 6 monthsData is collected through wearable monitoring technology. Actigraphy data is collected in 1 min epochs using the zero-crossing modes.
Change from Baseline Burnout at 2-3 months and 6 monthsbaseline, 2-3 months, 6 monthsBurnout - through self-reported stress and burnout thoughts, beliefs, emotions, behavior related to Covid-19 using Maslach Burnout Inventory. Maslach Burnout Inventory - is a 22-item survey that covers 3 areas: Emotional Exhaustion (EE), Depersonalization (DP), and low sense of Personal Accomplishment (PA). Each subscale includes multiple questions with frequency rating choices of Never, A few times a year or less, Once a month or less, A few times a month, Once a week, A few times a week, or Every day.
Change from Baseline Cardiovascular Risk Cardiovascular Risk Through Heart Rate Variability Markers at 2-3 months and 6 monthsbaseline, 2-3 months, 6 monthsData is collected through wearable monitoring technology. Cardiovascular risk through monitoring of heart rate variability (HRV) markers. Changes of heart rate variability (HRV) reflecting cardiac autonomic dysfunction are associated with greater risks for cardiac morbidity and mortality.
Change from Baseline Immune Dysfunction at 2-3 months and 6 monthsbaseline, 2-3 months, 6 monthsClassification of the immune function will be screened.
Change from Baseline Through Sleep Quality at 2-3 months and 6 monthsbaseline, 2-3 months, 6 monthsData is collected through wearable monitoring technology. Sleep efficiency is defined as the proportion of the estimated sleep periods spent asleep. Sleep latency is the length of time taken to fall asleep, calculated as the time between 'lights off' to the first period of 3 min of consecutive epochs scored as sleep.
Change from Baseline Cardiovascular Risk Through Fuster-BEWAT score at 2-3 months and 6 monthsbaseline, 2-3 months, 6 monthsCardiovascular risk through Fuster-BEWAT score. The Fuster-BEWAT score will be analyzed as a continuous variable with total score ranging from 0 to 15 points. Additionally, each component will be categorized as ideal (3) or nonideal (0 to 2), and participants will be classified as having poor, intermediate, or ideal cardiovascular health based on the total number of ideal components (0 to 1 = poor, 2 to 3 = intermediate, 4 to 5 = ideal) (Fernández-Alvira et al., 2017).

Secondary

MeasureTime frameDescription
Change from Baseline Cardio-Respiratory Fitness at 2-3 months and 6 monthsbaseline, 2-3 months, 6 monthsSubmaximal field test and maximal oxygen consumption (VO2, mL/kg/min).

Countries

United Arab Emirates

Contacts

Primary ContactOvidiu C Baltatu, MD PhD
ovidiu.baltatu@ku.ac.ae‭+971 2 810 9797
Backup ContactHashel Al Tunaiji, MD MSc
dr.tunaiji@ymail.com+971 50 635 5002

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026