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Surgical Coaching for Enhancing Laparoscopic Skills in ObGyn Residents
N/A
Waitlist Available
Led By Cara King, D.O.
Research Sponsored by The Cleveland Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 day
Awards & highlights
Study Summary
This trial aims to evaluate the effectiveness of video-based surgical coaching to help Obstetrics and Gynecology residents learn laparoscopic suturing skills. Participants will practice the skill on a validated trainer and be assessed on their technical skills.
Who is the study for?
This trial is for Cleveland Clinic Obstetrics and Gynecology residents who are looking to improve their laparoscopic skills, specifically in suturing the vaginal cuff. There are no specific exclusion criteria mentioned, so it appears open to all residents within this department.Check my eligibility
What is being tested?
The study is testing whether surgical coaching can help ObGyn residents get better at laparoscopic suturing. Residents will be split into two groups: one that just practices with videos and a trainer, and another that gets extra video-based coaching sessions.See study design
What are the potential side effects?
Since this trial involves educational interventions rather than medical treatments or drugs, there aren't traditional side effects. However, participants may experience varying levels of stress or anxiety related to performance improvement.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 day
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 day
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Global Operative Assessment Laparoscopic Skills (GOALS-PLUS)
Secondary outcome measures
Amount of tracking months
Enjoyment in the operating room
Experience undergoing surgical coaching
+7 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Comparison groupExperimental Treatment1 Intervention
Resident participants who do receive video-based surgical coaching
Group II: Control groupActive Control1 Intervention
Resident participants who do not receive video-based surgical coaching
Find a Location
Who is running the clinical trial?
The Cleveland ClinicLead Sponsor
1,026 Previous Clinical Trials
1,366,048 Total Patients Enrolled
Cara King, D.O.Principal InvestigatorThe Cleveland Clinic
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Eligibility Criteria:
This trial includes the following eligibility criteria:- Not applicable.
Research Study Groups:
This trial has the following groups:- Group 1: Control group
- Group 2: Comparison group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Does this research endeavor currently need new participants?
"Unfortunately, the trial hosted on clinicaltrials.gov is not presently recruiting participants; although this study was published on July 1st 2022 and last modified on June 12th 2023, there are still 21 other trials open to enrolment at the current time."
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