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临床试验/NCT05072210
NCT05072210已完成不适用

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 Toronto1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2021年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
13
试验地点
1
主要终点
Perceived Stress Scale

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Participant, Investigator)

盲法说明

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.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •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)

排除标准

  • •Non-Unity Health Toronto staff

研究组 & 干预措施

Mobile Intervention Group

Experimental

One half of the participants will receive personalized automated alerts throughout their involvement.

干预措施: Mobile Intervention (Other)

Control Group

No Intervention

For 4 weeks, the other half of the participants will not receive personalized automated alerts. After 4 weeks, these alerts will be enabled.

结局指标

主要结局

Perceived Stress Scale

时间窗: 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.

次要结局

  • Perceived Stress Scale(At 12 weeks from baseline)
  • Active Data - Generalized Anxiety Disorder Scale(At 4 weeks from baseline)
  • Active Data - Patient Health Questionnaire(At 4 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)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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