- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01184950
Virtual Reality Laparoscopy Training
November 7, 2022 updated by: TriHealth Inc.
Prospective Randomized Trial of Virtual Reality Simulator Training in an Obstetrics and Gynecology Residency
The use of virtual reality simulation training in obstetrics and gynecology has not been widely studied.
The investigators hypothesized that residents randomized to the trainer would not perform differently when compared with those who are not randomized.
Residents in Obstetrics and gynecology are randomized to a 4 month training course on our simulator.
They are objectively evaluated performing various laparoscopy tasks prior to and after the course.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ohio
-
Cincinnati, Ohio, United States, 45220
- Good Samaritan Hospital
-
-
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
N/A
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Resident in OB/Gyn at TriHealth
Exclusion Criteria:
- None
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
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Trainer Curriculum
|
|
|
No Intervention: No Curriculum
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
observed structured assessment of technical skills (OSATS) Score
Time Frame: 0 Months
|
The residents are timed in seconds on various laparoscopy tasks.
They are also rated by an objective blinded observer in several performance categories and given a score by the observer.
These times and scores are recorded upon entry into the study, after randomization to intervention or no intervention.
|
0 Months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
observed structured assessment of technical skills (OSATS) score
Time Frame: 4 Months
|
The residents are timed in seconds on various laparoscopy tasks.
They are also rated by an objective blinded observer in several performance categories and given a score by the observer.
These times and scores are recorded 4 months after entry into the study.
|
4 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 Registration Dates
First Submitted
August 11, 2010
First Submitted That Met QC Criteria
August 18, 2010
First Posted (Estimate)
August 19, 2010
Study Record Updates
Last Update Posted (Actual)
November 9, 2022
Last Update Submitted That Met QC Criteria
November 7, 2022
Last Verified
August 1, 2010
More Information
Terms related to this study
Other Study ID Numbers
- 10019
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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