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Impostor Phenomenon and Cognitive Complaints in Anesthesiologists

2026年6月11日 更新者:Fusun Gozen

Impostor Phenomenon and Cognitive Complaints in Anesthesiologists: A Neglected Risk for Patient Safety

This prospective observational cross-sectional survey study aims to investigate the relationship between impostor phenomenon and cognitive complaints in anesthesiologists, and to evaluate the role of potential confounding factors such as sleep quality, workload, anxiety, depression, and burnout in this relationship.

研究概览

详细说明

Anesthesiologists are required to make rapid decisions demanding high situational awareness for patient safety and clinical risk management. The Impostor Phenomenon (IP), frequently encountered among healthcare professionals, is defined as perceiving oneself as inadequate despite proven achievements, with persistent fear of being exposed as a fraud. While existing literature has detailed the association of IP with mood symptoms such as anxiety, depression, and burnout, its effect on cognitive complaints has not been sufficiently examined. This study will assess IP using the Clance Impostor Phenomenon Scale (CIPS), cognitive complaints using the Cognitive Failures Questionnaire (CFQ), anxiety and depression using the Hospital Anxiety and Depression Scale (HADS), and sleep quality and workload using single-item subjective scales. Data will be collected anonymously via an online self-administered structured questionnaire from anesthesiologists actively working in clinical practice.

研究类型

观察性的

注册 (实际的)

176

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

      • Bursa、土耳其(türkiye)、16310
        • Bursa Yüksek İhtisas Training and Research Hospital, Bursa, Türkiye

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

  • 成人
  • 年长者

接受健康志愿者

是的

取样方法

非概率样本

研究人群

Anesthesiologists actively working in clinical practice in Turkey, including residents, specialists, and academic staff.

描述

Inclusion Criteria:

Aged 18 years or older Actively working as an anesthesiologist (resident, specialist, or academic staff) Provided written informed consent Completed the survey in full

Exclusion Criteria:

Not actively working in clinical practice Refused to provide informed consent Submitted an incomplete survey

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
Study Cohort
Anesthesiologists actively working in clinical practice, including residents, specialists, and academic staff. Data were collected via an anonymous, self-administered online questionnaire assessing the impostor phenomenon, cognitive complaints, anxiety, depression, sleep quality, and workload.
A structured online self-administered questionnaire including the Clance Impostor Phenomenon Scale (CIPS), Cognitive Failures Questionnaire (CFQ), Hospital Anxiety and Depression Scale (HADS), and single-item scales for sleep quality and workload.

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
Relationship Between Impostor Phenomenon and Cognitive Complaints
大体时间:At the time of survey completion, up to 1 month
Statistical association between the Clance Impostor Phenomenon Scale (CIPS) total score and the Cognitive Failures Questionnaire (CFQ) total score among anesthesiologists.
At the time of survey completion, up to 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。

赞助

调查人员

  • 首席研究员:Füsun Gözen, MD (Anesthesiology)、SBÜ Bursa Yüksek İhtisas Training and Research Hospital

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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)

2026年2月15日

初级完成 (实际的)

2026年5月15日

研究完成 (实际的)

2026年5月15日

研究注册日期

首次提交

2026年6月8日

首先提交符合 QC 标准的

2026年6月11日

首次发布 (实际的)

2026年6月15日

研究记录更新

最后更新发布 (实际的)

2026年6月15日

上次提交的符合 QC 标准的更新

2026年6月11日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

Individual participant data will not be shared. This is a single-center observational survey study conducted at a public hospital. Data were collected anonymously and data sharing is not planned due to institutional privacy regulations and the absence of external funding requiring data sharing.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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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