- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05143749
Pandemic and Gynecological Surgery Education
The Effects of Video Use and Self-evaluation on Gynecological Surgery Education in the Light of Current Technological Developments in the Pandemic
SarsCov2/COVID19 virus emerged in Wuhan, China in December 2019, and cases were seen in our country about 3 months later, causing a worldwide pandemic. In this process, both the stress caused by the risk of contracting the disease and the social restrictions affected life deeply.
578 / 5000 Çeviri sonuçları This study will be beneficial for the assistant doctors in recognizing technical errors in gynecological operations, reducing the risks and improving the results.
Surgical operation trainings such as hysterectomy and oophorectomy fistula surgery can be given with laparotomy-guided simulators, which can offer interactive training for gynecological operations in adult female sizes and show high adaptability. However, it is not possible to train major vaginal surgical operations with this method today. At this point, video tutorials can be used. This study was planned with the aim of increasing the level of anxiety about the training of the residents during the pandemic period, with the aim of making positive changes in order to increase the assistant's own skills, realize his mistakes and reduce the level of anxiety with video training.
Study Overview
Detailed Description
Our study is a Prospective Cross-sectional Case Control study. Our study is a training study and our assistants included in the study will consist of two groups. Group 1: A total of 10 assistants who have just completed the gynecological surgery training, which is in the last 4 months of a total of 8 months of training during the pandemic process, and Group 2 is 4 . It will consist of 10 assistants who have just started their surgical training after the first month. The assistants in Group 2 will videotape their first, fifth, tenth, fifteenth and twentieth gynecological operations, then watch their own operations to test their skills. Written consent will be obtained from the patients for the video recording of the operations, stating that the operations will be used for educational purposes only before the operation.
Operations are planned as abdominal hysterectomy, vaginal hysterectomy and myomectomy, which are the most performed gynecological operations.
Video applied to the residents in Group 1, who completed their training in the last 4 months of the pandemic process, and to the residents in Group 2, who completed their training by watching the video footage of their own operations, by applying the Self-Confidence Scale, General Self-Efficacy Scale, State Anxiety Inventory (DCI) and Trait Anxiety Inventory (SCI) scales. The effect of education on residents' anxiety, competence and self-confidence will be investigated.
After the training, the operations performed by the residents will be analyzed and the average operation time, intraoperative and postoperative major and minor complication rates, bleeding amounts in the operations, preoperative and postoperative hemogram amounts, postoperative hospital stay of the patients, postoperative analgesia need parameters will be evaluated and a comparison will be made between the two groups. In this way, the effect of video training on the lurning curve will be investigated.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Ankara, Turkey, 06800
- Ankara City Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria: training as a gynecological assistant -
Exclusion Criteria:not yet receive gynecological assistant training
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Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: 10 assistant doctors who received video training
10 assistant doctors who receive video training will be the intervention arm
|
get video tutorial
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No Intervention: 10 assistant doctors who did not receive video training
10 assistant doctors who did not receive video training will be the control arm
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
self confidence
Time Frame: minimum 3 months
|
Self-confidence level will be tested in the group receiving video training.
|
minimum 3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Rahime Bedir Findik, Ankara City Hospital Bilkent
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- AnkaraCHBilkent-MH-RBF-03
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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