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Clinical Trials/NCT05072210
NCT05072210CompletedNot Applicable

Could Mobile-based Interventions Aid To "Understand and Flatten the Curve" of Stress, Anxiety, Distress and Depression Among Healthcare Providers at Unity Health Toronto During and After the COVID-19 Pandemic?

Unity Health Toronto2 sites in 1 country13 target enrollmentStarted: May 1, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
13
Locations
2
Primary Endpoint
Perceived Stress Scale

Study Overview

Brief Summary

Stress, anxiety, distress and depression are exceptionally high among healthcare providers at the frontline of the COVID-19 pandemic. Knowledge of factors underlying distress and resilience and evidence based interventions to impact the mental wellbeing of frontline healthcare providers is limited. This study will evaluate a novel mobile platform to gather the "distress experience" of healthcare workers at Unity Health Toronto in real time during and after the COVID-19 pandemic, use automated personalized mobile interventions (e.g. routine, sleep, exercise) to nudge active/passive parameters to manage distress.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Double (Participant, Investigator)

Masking Description

Participants will be issued a specific ID number to be used within the mobile app to ensure that any identifiable information within this app will remain anonymous. A master linking log will serve as the only link between participants and the study data collected in the mobile app.

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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 Criteria

  • Non-Unity Health Toronto staff

Outcomes

Primary Outcomes

Perceived Stress Scale

Time Frame: At 4 weeks from baseline

The primary outcome measure will be the ten-item Perceived Stress Scale. Scores range from 0 to 40, and higher scores indicate more severe stress.

Secondary Outcomes

  • Perceived Stress Scale(At 12 weeks from baseline)
  • Active Data - Short UCLA Loneliness Scale(At 4 weeks from baseline)
  • Passive Data - GPS Sample Point Metrics(At 4 weeks from baseline)
  • Active Data - Generalized Anxiety Disorder Scale(At 4 weeks from baseline)
  • Active Data - Patient Health Questionnaire(At 4 weeks from baseline)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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