Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT05732116

PTSD of Surgeons or Anesthesiologists on Prognosis of Surgical Patients

Led by Xijing Hospital · Updated on 2025-04-04

10000

Participants Needed

2

Research Sites

149 weeks

Total Duration

On this page

Sponsors

X

Xijing Hospital

Lead Sponsor

N

Ningbo No.2 Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

The objective of this prospective cohort study is to explore the association between the development of post-traumatic stress disorder (PTSD) in surgeons and anesthesiologists and postoperative prognosis in surgical patients they care for during the COVID-19 pandemic. There are 2 cohorts included in this study. The first cohort consists of registered surgeons and anesthesiologists in the study center. The development of PTSD will be evaluated with a series of questionnaires and scales. This cohort defines exposure (with PTSD). The second cohort consists of surgical patients managed by the surgeons and anesthesiologists in the first cohort. The postoperative outcome of these patients will be evaluated thus to explore the association between PTSD in physicians and adverse patient outcomes. The second cohort defines the outcomes( response).

CONDITIONS

Official Title

PTSD of Surgeons or Anesthesiologists on Prognosis of Surgical Patients

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Registered surgeons and anesthesiologists at the study center
Not Eligible

You will not qualify if you...

  • Surgeons and anesthesiologists planning to change practice locations during the study period
  • Refusal to sign written informed consent or complete evaluation questionnaires

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Ningbo NO.2 hospital

Ningbo, Zhejiang, China

Actively Recruiting

2

Xijing Hospital

Xi'an, China, 710032

Actively Recruiting

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Research Team

C

Chong Lei, MD, phd

CONTACT

L

Lini Wang, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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