Evaluation the Preoperative Anxiety Level of the Surgeons

February 3, 2022 updated by: Tuna Şahin, Adana City Training and Research Hospital
Many studies are present about the preoperative anxiety among patients. But the preoperative anxiety of the surgeons is not studied yet. The aim of this study is to evaluate the preoperative anxiety of the surgeons.100 surgeons consisted of performing operations in general surgery, obstetric and gynecology , orthopedic surgery ,ophthalmology, otorhinolaryngology, plastic and reconstructive surgery, urology, gynecologic oncology, surgical oncology, cardiovascular surgery, pediatric surgery and neurosurgery will be participated in the study. Surgeons will be chosen from the specialist doctor, assistant doctor, doctor lecturer, associate professor and professors.15 minutes prior to the first elective operation of the day, salivary cortisol samples will be taken from the surgeons and they will be asked to fill the evaluation form and State-Trait Anxiety Inventory Form (STAI).

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Detailed Description

100 surgeons between the ages of 25-55 years will be participated in the study. Surgeons will be consisted of performing operations in general surgery, obstetric and gynecology, orthopedic surgery, ophthalmology, otorhinolaryngology, plastic and reconstructive surgery, urology, gynecologic oncology, surgical oncology, cardiovascular surgery, pediatric surgery and neurosurgery.They will be chosen from the specialist doctor, assistant doctor, doctor lecturer, associate professor and professors. Oral and written informed consent will be obtained from the surgeons.15 minutes prior to the first elective operation of the day salivary cortisol samples will be taken from the surgeons and they will be asked to fill the evaluation form and State-Trait Anxiety Inventory Form (STAI). The evaluation form will include the age, gender of the surgeon, surgical department, academic superscription, years of clinical experience in medical sciences and professions and the name of the surgery which is going to be done.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Observational

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
100

Contacts and Locations

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

Study Locations

  • Turkey
      • Adana, Turkey
        • Tuna Şahin

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

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

25 years to 55 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Surgeons will be consisted of performing operations in general surgery, obstetric and gynecology, orthopedic surgery, ophtalmology, otorhinolaryngology, plastic and reconstructive surgery, urology, gynecologic oncology, surgical oncology, cardiovascular surgery, pediatric surgery and neurosurgery.They will be chosen from the specialist doctor, assistant doctor, doctor lecturer, associate professor and professors.

Description

Inclusion Criteria:

  • Accepting to participate the study
  • Surgeons planning first elective operation of the day
  • 25-55 years

Exclusion Criteria:

  • Non volunteers
  • Neurological and psychological disorders
  • History of anxiolytic , antidepressant drug usage

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

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
State Trait Anxiety Inventory (STAI)
Time Frame: up to 15 minutes
State Trait Anxiety Inventory (STAI) form
up to 15 minutes
Serum cortisol sample
Time Frame: up to 5 minutes
Samples will be taken 15 minutes prior to the first elective surgery of the day
up to 5 minutes

Collaborators and Investigators

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

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Adana City Training and Research Hospital

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Principal Investigator: Tuna Şahin, Adana City Training and Research Hospital

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 (ACTUAL)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
July 28, 2020

Primary Completion (ACTUAL)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
December 20, 2021

Study Completion (ACTUAL)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
December 31, 2021

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
May 31, 2020

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
May 31, 2020

First Posted (ACTUAL)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
June 4, 2020

Study Record Updates

Last Update Posted (ACTUAL)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
February 4, 2022

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
February 3, 2022

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
February 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • 746

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug 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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