Evaluation the Preoperative Anxiety Level of the Surgeons

NCT04413981 | Completed

• 1 other identifier: 746
• Study Type: observational
• Target: 100
• Locations: 1 country
• Sites: 1

Brief Summary

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).

Conditions

Preoperative Anxiety

Keywords

surgeon; cortisol; anxiety

Outcome Measures

Primary Outcomes (2)

• State Trait Anxiety Inventory (STAI)

  State Trait Anxiety Inventory (STAI) form

  up to 15 minutes

• Serum cortisol sample

  Samples will be taken 15 minutes prior to the first elective surgery of the day

  up to 5 minutes

Eligibility Criteria

• Age: 25 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)
• 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.

You may qualify if:

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

You may not qualify if:

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

Sponsors & Collaborators

• Adana City Training and Research Hospital: lead

Study Sites (1)

Tuna Şahin

Adana, Turkey (Türkiye)

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

salivary cortisol

MeSH Terms

Conditions

Anxiety Disorders

Condition Hierarchy (Ancestors)

Mental Disorders

Study Officials

• Tuna Şahin

  Adana City Training and Research Hospital

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Specialist of Anesthesiology and Reanimation

Study Record Dates

• First Submitted: May 31, 2020
• First Posted: June 4, 2020
• Study Start: July 28, 2020
• Primary Completion: December 20, 2021
• Study Completion: December 31, 2021
• Last Updated: February 4, 2022

Record last verified: 2022-02

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)