Awareness of Surgeons

December 14, 2025 updated by: İlke Dolgun, Istinye University

Evaluation of Surgical Physicians' Awareness of Preoperative Patient Preparation

It aims to objectively reveal the current knowledge levels of surgical physicians, to increase their awareness, and to contribute to in-house training processes with the results obtained and to fill an important gap in the literature.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Turkey (Türkiye)
    • Merkez Mahallesi
      • Istanbul, Merkez Mahallesi, Turkey (Türkiye), 34250
        • Istinye University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The population of this study consists of all surgical specialists (both residents and specialists) working at Sultangazi Haseki Training and Research Hospital. The study will include physicians working in general surgery, orthopedics, neurosurgery, urology, ENT, and other surgical disciplines.

Description

Inclusion Criteria:

  • Individuals who voluntarily approved the participation form,
  • Those who fully participated in the training and testing.

Exclusion Criteria:

  • Those who did not complete the voluntary consent form,
  • Those who did not participate in any phase of the training or testing,
  • Participants with incomplete or inaccurate data.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Difference between pre- and post-training test scores (knowledge/awareness increase)
Time Frame: 1 hour
The outcome is defined as the difference between the post-training and pre-training test scores assessing surgical awareness. Test scores range from 0 to 100, with higher scores indicating greater surgical awareness and knowledge. A positive difference reflects an increase in awareness following the training.
1 hour

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Istinye University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

December 10, 2025

Primary Completion (Estimated)

December 17, 2025

Study Completion (Estimated)

December 31, 2025

Study Registration Dates

First Submitted

December 2, 2025

First Submitted That Met QC Criteria

December 2, 2025

First Posted (Estimated)

December 15, 2025

Study Record Updates

Last Update Posted (Actual)

December 19, 2025

Last Update Submitted That Met QC Criteria

December 14, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 244-2025

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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