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The Predictors of Depression and Burnout Among Surgical Residents: A Cross-sectional Study From Kuwait

2021年3月19日 更新者:Waleed burhamah、Ministry of Health, Kuwait
To assess the prevalence and risk factors for depression and burnout among residents across surgical specialties in Kuwait.

研究概览

详细说明

This is a questionnaire based cross-sectional study conducted in Kuwait from jan 2021- February 2021 An online questionnaire was sent to the residents enrolled to the surgical residency programs in Kuwait. Residency training in Kuwait provides programs in both medical and surgical specialties. Specialties included in our cohort were: general surgery, orthopedic surgery, urology, neurosurgery, Obstetrics and Gynecology and otolaryngology.

The email sent to our participants included an invitation letter detailing the reason behind the questionnaire and that it is confidential and anonymous. Consent was obtained from participants.

Variables:

Variables collected included; age, gender, marital status, smoking history, exercise, specialty, year of training, on-call frequency, assessment of burnout and assessment of depression symptoms.

研究类型

观察性的

注册 (实际的)

80

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Outside U.S./Canada
      • Kuwait、Outside U.S./Canada、科威特、00000
        • Mubarak Al Kabeer hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人
  • 年长者

接受健康志愿者

不适用

有资格学习的性别

全部

取样方法

非概率样本

研究人群

surgical residents across 4 specialties.

描述

Inclusion Criteria:

- residents enrolled in surgical training in Kuwait. Across all surgical specialties From R1-R5

Exclusion Criteria:

Recently accepted candidates that have not yet started residency.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
general surgery residents
no intervention, this is an observational cross sectional study
orthopedic surgery residents
no intervention, this is an observational cross sectional study
urology residents
no intervention, this is an observational cross sectional study
OBGYN residents
no intervention, this is an observational cross sectional study

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Symptoms of depression were assessed using the 9-item Patient Health Questionnaire (PHQ-9) score
大体时间:1 month
(PHQ-9) score, a self-report questionnaire that is commonly used as a screening tool for depression. It is composed of 9 questions assessing the frequency of depressive symptoms on a 4-point Liker-scale ranging from 0 (never) to 3 (nearly every day). The total score was calculated for each patient and was interpreted as follows: minimal (1-4), mild (5-9), moderate (10-14), moderately severe (15-21), severe (20-27). A standard cutoff of score of 10 was used, indicating a diagnosis of depression.
1 month
Burnout symptoms were assessed using 9-item form of the Maslach Burnout Inventory - Human Services Survey (aMBI-HSS)
大体时间:1 month
The aMBI is a 9-item questionnaire each question is rated on a 7-point Liker scale ranging from 0 to 6, which indicates the frequency of symptoms in question. Response options include; Every day, A few times a week, Once a week, A few times a month, Once a month, A few times a year, or Never. The questions grouped into 3 subscales (emotional exhaustion EE, depersonalization D and personal accomplishment PA) are evaluated and scored separately with each score ranging from 0 to 18. We used the cut off points set by Lebares et al. for EE and D. The cut off points for high burnout among U.S. surgery residents were: EE score ≥ 9 and D score ≥ 6. A PA score ≤ 12 was chosen as a cut-off for high burnout.
1 month

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2021年1月1日

初级完成 (实际的)

2021年2月1日

研究完成 (实际的)

2021年2月1日

研究注册日期

首次提交

2021年3月18日

首先提交符合 QC 标准的

2021年3月19日

首次发布 (实际的)

2021年3月22日

研究记录更新

最后更新发布 (实际的)

2021年3月23日

上次提交的符合 QC 标准的更新

2021年3月19日

最后验证

2021年3月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • MOHKWMKH21

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 共享支持信息类型

  • 研究方案
  • 树液
  • 国际碳纤维联合会
  • 分析代码
  • 企业社会责任

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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