- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02948595
Video Feedback Versus Verbal Feedback
September 16, 2019 updated by: Naomi Y Swanson, University of New Mexico
Video Feedback Versus Verbal Feedback in Simulated Laparoscopic Vaginal Cuff Closure
The long term goal of our research is to develop a curriculum for Obstetrics and Gynecology resident physicians that regularly employs use of video assessment to improve surgical skills.
Regular use of video feedback may enable improved self-assessment and allow for formal documentation of proficiency.
The overall objective is to compare the use of video feedback to use of structured verbal feedback in the simulated task of laparoscopic vaginal cuff closure.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
19
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Resident Physician in the Department of Obstetrics and Gynecology
Exclusion Criteria:
- Not a resident physician in the Department of Obstetrics and Gynecology
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Video feedback then verbal feedback
Video feedback followed by structured verbal feedback
|
Video feedback followed by structured verbal feedback
|
|
Experimental: Verbal feedback then video feedback
Structured verbal feedback followed by video feedback
|
Structured verbal feedback followed by video feedback
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improvement in ob/gyn resident physician self-efficacy as measured by self-efficacy questionnaire in video versus verbal feedback for simulated laparoscopic vaginal cuff closure
Time Frame: up to 18 months
|
Resident physicians will report their self-efficacy in completion of simulated laparoscopic vaginal cuff closure using an adaptation of a previously validated self-efficacy questionnaire.
Their self-efficacy will be compared after completion of the task incorporating verbal feedback from a proctor to completion of the task incorporating review of video feedback provided by proctor.
|
up to 18 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improvement in time of simulated laparoscopic vaginal cuff closure with video versus verbal feedback
Time Frame: up to 18 months
|
Resident physicians will be timed (in minutes) for completion of simulated laparoscopic vaginal cuff closure.
Time will be compared in completion of the task after verbal feedback from a proctor versus completion of task after video feedback from a proctor.
|
up to 18 months
|
|
Improvement in skill of simulated laparoscopic vaginal cuff closure as measured by Objective Structured Assessment of Technical Skills (OSATS) global rating scale with video versus verbal feedback
Time Frame: up to 18 months
|
Two advanced gynecologic laparoscopists will review the films of the tasks for each resident physician.
They will rate level of skill for each participant based on Objective Structured Assessment of Technical Skills (OSATS) global rating scale.
The reviews will generate two scores for each participant: the score for the task completed after the resident receives verbal feedback and the score for the task completed after the resident receives video feedback.
The two scores will then be compared for each participant.
|
up to 18 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 18, 2016
Primary Completion (Actual)
May 3, 2017
Study Completion (Actual)
May 3, 2017
Study Registration Dates
First Submitted
July 21, 2016
First Submitted That Met QC Criteria
October 26, 2016
First Posted (Estimate)
October 28, 2016
Study Record Updates
Last Update Posted (Actual)
September 19, 2019
Last Update Submitted That Met QC Criteria
September 16, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- 16-096
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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