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Clinical Trials/NCT05001542
NCT05001542
Completed
Not Applicable

Could Digital Interventions Help Understand And "Flatten The Curve" Of Distress Due To Moral Injury Among Health Care Workers During The COVID Pandemic?

Unity Health Toronto1 site in 1 country15 target enrollmentMay 31, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Moral Injury
Sponsor
Unity Health Toronto
Enrollment
15
Locations
1
Primary Endpoint
Feasibility evaluation of the virtual reality environment
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Stress, anxiety, distress and depression are exceptionally high among healthcare workers at the frontline of the COVID-19 pandemic. Factors underlying distress and resilience are unknown and there are no evidence based interventions to impact the mental wellbeing of frontline healthcare workers. This study will evaluate a novel virtual reality platform to gather the "distress experience" of frontline healthcare workers at Unity Health Toronto in real time during the ongoing COVID pandemic by developing and showing feasibility of digital technology (Virtual Reality (VR) and mobile app) as a digital platform to understand the causes and ultimately reduce the moral distress of healthcare providers during the COVID-19 pandemic. The project will develop innovations which can be used for future pandemics and other contexts prone to producing moral distress and injury.

Registry
clinicaltrials.gov
Start Date
May 31, 2021
End Date
August 30, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Venkat.Bhat

Principal Investigator

Unity Health Toronto

Eligibility Criteria

Inclusion Criteria

  • Staff or healthcare providers working at Unity Health Toronto
  • 18 years of age or older
  • Must own a mobile phone running Android Version 6.0 and higher, or an iPhone 6 running OS 14 and higher)
  • Exclusion Criterion:
  • Non-Unity Health Toronto staff

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Feasibility evaluation of the virtual reality environment

Time Frame: 60 minutes (during the intervention)

The primary outcome measure will be a comparison of MIOS (Moral Injury Outcome Scale) and PSS (Perceived Stress Scale) scores before and after watching an educational video on moral injury; feasibility of this platform will be assessed based on a feasibility questionnaire and changes in score.

Secondary Outcomes

  • Feasibility evaluation of a mobile platform to understand the continuum of stress and moral distress.(Up to 8 weeks)

Study Sites (1)

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