Could a surgeon's mental health impact your surgery outcome?
NCT ID NCT05732116
First seen Aug 05, 2026 · Last updated Aug 06, 2026 · Updated 1 time
Summary
This study looks at whether post-traumatic stress disorder (PTSD) in surgeons and anesthesiologists is linked to higher rates of complications in the patients they operate on. Researchers will screen surgical staff for PTSD using questionnaires and then track the recovery of their patients. The goal is to understand if the mental health of the surgical team might influence patient safety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Screening and diagnosis of PTSD in surgeons and anesthesiologists using questionnaires and scales
- What this could lead to
- If a link is found, it could highlight the importance of mental health support for surgical staff to improve patient safety.
- What could go wrong
- This is an observational study, so it cannot prove cause and effect. Other factors may explain any association found.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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356 people
The number who actually took part.
- Started
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Feb 2023
- Finished
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Dec 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
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 cared by the surgeons and anesthesiologists in the first cohort. The postoperative outcome of these patients will be evaluate thus to explore the association of PTSD in physicians and adverse patient outcomes. The second cohort defines the outcome( response).
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Registered Surgeons and anesthesiologists in the study center Exclusion Criteria: * Surgeons and anesthesiologists with potential practice location changes during the study periods * Refuse to sign written informed consent and fill out the evaluation questionnaire
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Ningbo NO.2 hospital
Ningbo, Zhejiang, China
-
Xijing Hospital
Xi'an, 710032, China
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