- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03551353
Checkout Procedure, Airway Practices, Video Based Feedback
Checkout Procedure Before Airway Practices To Provide Clinical Practice With Video Based Feedback
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Video-assisted feedback (VAF) is an educational method used by educators in various areas of medicine. It is possible to gain technical and non-technical skills for practical applications such as cardiopulmonary resuscitation and surgical procedures . VAF is an objective proof of an individual's performance because by giving feedback it provides non debatable, accurate, real-time data. By allowing awareness on certain issues it helps correcting the mistakes . Studies have shown improvement in clinical skills after VAF .
Inaccurate or incomplete control of anesthesia equipment before use is associated with serious postoperative morbidity and mortality risk. For this reason, a number of control methods have been developed before the anesthesia application. This is one of these methods that checklists are created and repeated in intermittent periods.
American society of anesthesiologists (ASA) published a guideline to improve patient safety in 2008 . This guideline is summarized as mentioned below.
ASA Checklist:
1.Verify Auxiliary Oxygen Cylinder and Self-inflating Manual Ventilation Device are Available & Functioning 2: Verify patient suction is adequate to clear the airway 3: Turn on anesthesia delivery system and confirm that ac power is available 4: Verify availability of required monitors, including alarms. 5: Verify that pressure is adequate on the spare oxygen cylinder mounted on the anesthesia machine 6: Verify that the piped gas pressures are ≥ 50 psig 7: Verify that vaporizers are adequately filled and, if applicable, that the filler ports are tightly closed. 8: Verify that there are no leaks in the gas supply lines between the flowmeters and the common gas outlet 9: Test scavenging system function. 10: Calibrate, or verify calibration of, the oxygen monitor and check the low oxygen alarm.
11: Verify carbon dioxide absorbent is not exhausted 12: Breathing system pressure and leak testing. 13: Verify that gas flows properly through the breathing circuit during both inspiration and exhalation.
14: Document completion of checkout procedures. 15: Confirm ventilator settings and evaluate readiness to deliver anesthesia care. (ANESTHESIA TIME OUT)
Ten anesthesia residents will be included in this study. Preoperative evaluation in terms of general anesthesia will be completed for a patient before anesthesia induction. After receiving informed consent from the patient resident will complete the preparations by checking the above-mentioned list (anesthesia machine, operating room desk, monitorization methods, aspirator systems, operating room gas systems, waste systems and other anesthesia equipment) then induction will be started. All these steps will be recorded with a camera system. Once the anesthetic application is completed and all stages are recorded, the video records will be evaluated in terms of ASA guideline. Before the second phase of the study, the resident will be informed about the guideline by a staff. Then induction of general anesthesia in another patient will be recorded at all stages. Once the anesthesia application is complete, the camera record will be monitored. Differences and developments or possible similar mistakes between the records will be discussed. After evaluating the records -twice for each resident- the applicability and effectiveness of the VAF training course will be investigated in the direction of the results of 20 records, before and after VAF.
The aim of the study is to assess the compliance of anesthesiology and reanimation residents with the ASA guideline in Kocaeli Derince Training and Research Hospital.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- anesthesia residents will be included in this study
Exclusion Criteria:
- not to work in anesthesia clinic
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Group before Video-assisted feedback
Ten anesthesia residents will be included in this group.
Preoperative evaluation in terms of general anesthesia will be completed for a patient before anesthesia induction.
After receiving informed consent from the patient resident will complete the preparations by checking the above-mentioned list (anesthesia machine, operating room desk, monitorization methods, aspirator systems, operating room gas systems, waste systems and other anesthesia equipment) then induction will be started.
All these steps will be recorded with a camera system.
Once the anesthetic application is completed and all stages are recorded, the video records will be evaluated in terms of ASA guideline
|
Ten anesthesia residents will be included in this group.
Preoperative evaluation in terms of general anesthesia will be completed for a patient before anesthesia induction.
After receiving informed consent from the patient resident will complete the preparations by checking the above-mentioned list (anesthesia machine, operating room desk, monitorization methods, aspirator systems, operating room gas systems, waste systems and other anesthesia equipment) then induction will be started.
All these steps will be recorded with a camera system.
Once the anesthetic application is completed and all stages are recorded, the video records will be evaluated in terms of ASA guideline
|
|
Group after Video-assisted feedback
Before the second phase of the study, the resident will be informed about the guideline (checkout procedure) by a staff.
Then induction of general anesthesia in another patient will be recorded at all stages.
Once the anesthesia application is complete, the camera record will be monitored.
Differences and developments or possible similar mistakes between the records will be discussed.
|
Before the second phase of the study, the resident will be informed about the guideline (checkout procedure) by a staff.
Then induction of general anesthesia in another patient will be recorded at all stages.
Once the anesthesia application is complete, the camera record will be monitored.
Differences and developments or possible similar mistakes between the records will be discussed.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Success rates of anesthesia residents after video assisted feedback (VAF) educational method
Time Frame: at month two after first measurement for each participant
|
Researchers will record video of participants during practical application and the video will asses by the checklist that American society of anesthesiologists (ASA) published in 2008 to improve patient safety
|
at month two after first measurement for each participant
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Success rates of anesthesia residents before video assisted feedback (VAF) educational method
Time Frame: on day 1 for each participant
|
Researchers will record video of participants during practical application and the video will asses by the checklist that American society of anesthesiologists (ASA) published in 2008 to improve patient safety
|
on day 1 for each participant
|
Collaborators and Investigators
Investigators
- Principal Investigator: tahsin md şimşek, KOCAELİ DERİNCE EĞİTİM VE ARAŞTIRMA HASTANESİ
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2018-111
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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