Mental Health Outcomes in Healthcare Workers During COVID-19

Sponsor
University Health Network, Toronto (Other)
Overall Status
Completed
CT.gov ID
NCT04397848
Collaborator
William Osler Health System (Other), University of Toronto (Other), Sunnybrook Health Sciences Centre (Other)
3,852
1
1.6
2344.9

Study Details

Study Description

Brief Summary

An online survey will be sent to healthcare workers (HCWs) in acute care hospitals to explore a variety of risk factors for negative psychological outcomes and levels of anxiety, depression and post-traumatic stress symptoms using validated scales. It is important to understand the sources of negative psychological impact on HCWs during this COVID-19 pandemic before hospitals and organizations can address and develop support programs to mitigate the stresses experienced by healthcare workers. Addressing and supporting the needs of our HCWs will be paramount in this COVID-19 pandemic and future outbreaks.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Previous work conducted by our group during the 2003 SARS outbreak demonstrated symptoms of post-traumatic stress disorder (PTSD) and depression in healthcare workers (HCWs) working in high-risk areas. Similar reports are emerging with regards to HCWs during COVID-19 which may affect staff mental health outcomes which may have effects on staff absenteeism and retention.

    The study is a cross-sectional, multi-centered, hospital-based online survey conducted at several Toronto hospitals. Participants will be recruited to participate in the voluntary study via an internal e-mail that will contain a short description of the study and a link to the online survey. The survey will take approximately 25 minutes to complete. The study group will include HCW s from high-risk units (Emergency, ICU, and COVID-19 units) with a comparison group of HCWs who are not directly involved in the assessment or management of patients with COVID-19.

    This study will evaluate the psychological impact of the COVID-19 pandemic on HCW's and identify risk factors that may place HCWs at greater risk for negative psychological outcomes. The survey will gather information such as s basic, non-identifying demographic information, hospital and unit of work, quarantine and isolation, work with patients diagnosed with COVID-19, loss of loved ones to COVID-19, understanding of the reasons for PPE/ infection control directives, perceptions of risk to self and family, sources of support. As well, Toronto is in the unique situation of having been at the centre of the 2003 Canadian SARS outbreak and presently experiencing the impact of the COVID-19. The investigators propose that COVID-19 might have a differential impact on the psychological wellbeing of current HCWs depending on whether they practiced during SARS. Our survey will explore the differences of the psychological impact of the COVID-19 pandemic on healthcare workers who lived through the SARS outbreak and those who did not. The following validated scales are embedded in the survey to evaluate the psychological impact of the COVID pandemic: Impact of Event Scale-Revised (IES-R), Generalized Anxiety Disorder -7 (GAD-7) , and Patient Health Questionnaire (PHQ-9). Open-ended questions will also provide respondents the opportunity to relate aspects of working during the COVID-19 pandemic that are most difficult and to provide additional comments on their unique experiences.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    3852 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Hearing and Supporting the Healthcare Workers: Mental Health Outcomes in Healthcare Workers During COVID-19
    Actual Study Start Date :
    May 14, 2020
    Actual Primary Completion Date :
    Jul 3, 2020
    Actual Study Completion Date :
    Jul 3, 2020

    Outcome Measures

    Primary Outcome Measures

    1. Impact of Event Scale - Revised (IES-R) [Two weeks]

      Scale to evaluate Post-traumatic Stress Disorder symptoms

    2. General Anxiety Disorder (GAD-7) [Two weeks]

      Scale to evaluate anxiety symptoms

    3. Patient Health Questionnaire (PHQ-9) [Two weeks]

      Scale to evaluate depressive symptoms

    Secondary Outcome Measures

    1. Qualitative Data [Two weeks]

      Qualitative data will be coded and analyzed to show emerging themes.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    HCW currently working at Toronto based hospitals: University Health Network (UHN), Sunnybrook Health Sciences and William Osler Health System.

    Exclusion Criteria: Not a healthcare worker

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Health Network Toronto Ontario Canada M5G 2C4

    Sponsors and Collaborators

    • University Health Network, Toronto
    • William Osler Health System
    • University of Toronto
    • Sunnybrook Health Sciences Centre

    Investigators

    • Principal Investigator: Rima Styra, MD, MEd, University Health Network, Toronto

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Rima Styra, Dr. Rima Styra, MD,MEd, FRCPC, ABPN, University Health Network, Toronto
    ClinicalTrials.gov Identifier:
    NCT04397848
    Other Study ID Numbers:
    • 3189
    First Posted:
    May 21, 2020
    Last Update Posted:
    Nov 3, 2020
    Last Verified:
    Nov 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Rima Styra, Dr. Rima Styra, MD,MEd, FRCPC, ABPN, University Health Network, Toronto
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 3, 2020