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

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.

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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