Preoperative AnxietyNCT04413981
Evaluation the Preoperative Anxiety Level of the Surgeons
An observational study of Preoperative Anxiety, run by Adana City Training and Research Hospital at 1 site in Turkey (Türkiye).
Trial 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 … Read more about this study
- Who is it for?
- Ages 25 to 55 yearsHealthy volunteers can take part
- Conditions the study is for
- Preoperative Anxiety
- How many people
- 100 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 28 Jul 2020to 31 Dec 2021
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 25 to 55 years
- All sexes
- Healthy volunteers accepted
- Adult
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.
Who may be able to join
- Accepting to participate the study
- Surgeons planning first elective operation of the day
- 25-55 years
Who cannot join
- Non volunteers
- Neurological and psychological disorders
- History of anxiolytic , antidepressant drug usage
Trial locations and contacts
1 site in 1 country.
About this study
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).
Read the 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.
- Conditions
- Preoperative Anxiety
- Keywords
- surgeon, cortisol, anxiety
- Medical subject headings
- Anxiety Disorders
What is being measured
The primary outcome is the main question the study is designed to answer.
State Trait Anxiety Inventory (STAI)
State Trait Anxiety Inventory (STAI) form
Measured: up to 15 minutes
Serum cortisol sample
Samples will be taken 15 minutes prior to the first elective surgery of the day
Measured: up to 5 minutes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Jun 2020
- Study start28 Jul 2020
- Primary completion20 Dec 2021
- Study completion31 Dec 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Preoperative AnxietyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Enrolment
- 100 participants (actual)
Sponsor and investigators
- Lead sponsor
- Adana City Training and Research Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Tuna Şahin, Adana City Training and Research Hospital
- Investigators
- Tuna Şahin, Principal investigator, Adana City Training and Research Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04413981
- Sponsor's protocol ID
- 746
- Status last verified
- Feb 2022
- First submitted
- 31 May 2020
- Last updated
- 4 Feb 2022
- Results posted
- No
- FDA-regulated drug
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Feb 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation the Preoperative Anxiety Level of the Surgeons
- ClinicalTrials.gov ID
- NCT04413981
- Acronym / sponsor ID
- 746
- Conditions
- Preoperative Anxiety
- Keywords
- surgeon, cortisol, anxiety
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 100 participants (actual)
- Lead sponsor
- Adana City Training and Research HospitalUniversity, hospital or other
- Study start
- 28 Jul 2020 (actual)
- Primary completion
- 20 Dec 2021 (actual)
- Study completion
- 31 Dec 2021 (actual)
- First posted
- 4 Jun 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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).
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 design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
Who may qualify
- Ages
- 25 to 55 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
- 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.
Key inclusion criteria (3 listed)
- Accepting to participate the study
- Surgeons planning first elective operation of the day
- 25-55 years
Key exclusion criteria (3 listed)
- Non volunteers
- Neurological and psychological disorders
- History of anxiolytic , antidepressant drug usage
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
State Trait Anxiety Inventory (STAI)
Time frame: up to 15 minutes
State Trait Anxiety Inventory (STAI) form
Serum cortisol sample
Time frame: up to 5 minutes
Samples will be taken 15 minutes prior to the first elective surgery of the day
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Feb 2022.
- Individual participant dataSharing planned: No
Related trials for Preoperative Anxiety
Recruiting
Preoperative Music Intervention for Anxiety in Hip and Knee Arthroplasty
Anxiety, Osteoarthritis
Not yet recruitingPhase 4
Effect of Midazolam Given at Induction on Recall of Propofol Injection Pain
Propofol Injection Pain, Postoperative Recall of Pain
RecruitingObservational study
Preoperative Anxiety and One-year Patient-reported Outcomes in Orthopedic Surgery Patients Receiving Enhanced Recovery After Surgery or Conventional Care
Preoperative Anxiety, Orthopedic Surgery
Not yet recruiting
Virtual Reality to Reduce Anxiety During Thoracic Epidural Placement.
Preoperative Anxiety Score
Recruiting
Positive Affirmations and Preoperative Anxiety
Total Joint Replacement Surgery, Preoperative Anxiety
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Tuna Şahin principal investigator
Adana City Training and Research Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Preoperative Anxiety, run by Adana City Training and Research Hospital at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 4 Feb 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
State Trait Anxiety Inventory (STAI) (time frame: up to 15 minutes). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Feb 2022.