跳至主要内容
临床试验/NCT04914104
NCT04914104Unknown不适用

Accessible Support in Surgical Training During a Pandemic Study

University of Ottawa0 个研究点目标入组 60 人开始时间: 2021年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
60
主要终点
Stress

研究概览

简要总结

The COVID-19 pandemic has fundamentally changed the surgical trainee experience by exacerbating the difficulty of this notoriously stressful training, while limiting access to traditional avenues of mental health support. The investigators propose the application of a mobile app-based mindfulness program to address stress and burnout in the surgical training.

The proposed study is a prospective randomized, observer-blinded study including surgical trainees at the University of Ottawa in their first and second years of training. The intervention group will receive free access to the mobile app Headspace and will be encouraged to access the app three times a week for 15 minutes.

详细描述

The COVID-19 pandemic has fundamentally changed the surgical trainee experience. The personal risks and uncertainties of this environment have compounded the difficulty of this notoriously stressful training. Burnout in the medical profession is prolific, and health care workers are not immune to the adverse mental health effects of the pandemic. Of all health professionals, surgical trainees frequently report the highest rates of burnout and severe stress. In particular, high burnout is associated with profoundly increased rates of depression and suicidal ideation in these trainees. In addition to the adverse effects of burnout and stress on the mental health wellbeing of trainees, excessive stress in the operating room can threaten patient safety and slow motor skill acquisition.

In response, many organizations have sought out methods to mitigate the negative mental health effects of surgical training. One promising intervention is mindfulness-based stress reduction. The perception of stress in surgical trainees is mediated by both cognitive and behavioural factors, which demonstrates an opportunity for mindfulness-based stress reduction (MBSR) interventions to modulate the perceived stress. In-person MBSR has been investigated in previous randomized trials of first year surgical residents. These pilot reports describe promising feasibility and adherence to mindfulness practice, with improved stress and cognitive control in the interventional arms.

Mindfulness techniques lend themselves to self-guided instruction provided by mobile apps and are a widely available resource. Mobile app-based mindfulness practice demonstrates comparable improvements in self-reported well-being when compared with in-person mindfulness sessions. When time is a scarce commodity, participant adherence is crucial to the effectiveness of any intervention. Mindfulness-based interventions have typically boasted strong adherence exceeding an average of 16 minutes per day after 3 months, particularly when self-directed. Specifically, adherence to optional online mindfulness-based practice is promising in medical trainees, with over half of trainees voluntarily adhering to regularly scheduled online mindfulness meditation after 8 weeks. In Canadian medical students, a pilot study demonstrated improved self-compassion from mindfulness-based interventions with an average adherence of only 20 minutes per week. When compared with a traditional weekly 8-session intensive mindfulness program, an abbreviated 4-session program demonstrated comparable improvements in perceived stress and empathy.

Ironically during a pandemic when stress levels at their highest, traditional wellness programs such as in-person counselling are not available due to the social distancing protocols. The investigators propose mindfulness-based therapy in the form of a mobile app to fill this void in high risk health professionals. This study investigates the effectiveness of mindfulness therapy delivered by a mobile app in surgical residents to reduce burnout and associated repercussions during the COVID-19 pandemic.

The primary objective of this investigation is to determine if access to mindfulness therapy delivered by a mobile app is effective in improving the mental well-being in surgical trainees, when compared with the current standard of care. Mental well-being encompasses a variety of factors including stress, burnout, depression and anxiety. Additional secondary objectives include adherence to mindfulness therapy and subject satisfaction.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

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

  • •First and second year surgical residents
  • •Enrolled in the Surgical Foundations program at the University of Ottawa

排除标准

  • 未提供

研究组 & 干预措施

Intervention

Experimental

The intervention group will receive free access to the mobile app Headspace and directed to access the app three times a week for at least 15 minutes.

干预措施: Mindfulness Training - Headspace App (Behavioral)

Control

No Intervention

The control group will receive standard of care, which does not involve routine in-person or free access to mobile mindfulness therapy.

结局指标

主要结局

Stress

时间窗: 18 weeks

Perceived Stress Questionnaire (PSQ) (0 - 40, where low is better)

Burnout

时间窗: 18 weeks

Maslach Burnout Inventory - HSS-For Medical Personnel (MBI) (0 to 6)

Anxiety

时间窗: 18 weeks

DASS-21 (Depression, Anxiety and Stress Scale) (0 to 63, where low is better)

Stress

时间窗: 6 weeks

Perceived Stress Questionnaire (PSQ) (0 - 40, where low is better)

Stress

时间窗: 12 weeks

Perceived Stress Questionnaire (PSQ) (0 - 40, where low is better)

Burnout

时间窗: 6 weeks

Maslach Burnout Inventory - HSS-For Medical Personnel (MBI) (0 to 6)

Burnout

时间窗: 12 weeks

Maslach Burnout Inventory - HSS-For Medical Personnel (MBI) (0 to 6)

Anxiety

时间窗: 6 weeks

DASS-21 (Depression, Anxiety and Stress Scale) (0 to 63, where low is better)

Anxiety

时间窗: 12 weeks

DASS-21 (Depression, Anxiety and Stress Scale) (0 to 63, where low is better)

次要结局

  • Adherence(12 weeks)
  • Satisfaction with App Usage(12 weeks)
  • Adherence(6 weeks)
  • Satisfaction with App Usage(6 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mark Rockley

Co-Investigtor

University of Ottawa

相似试验