Learning Skills in Young Specialists and Residents in Operative Vaginal Delivery Using Simulator Models

October 30, 2022 updated by: Claudio Celentano, G. d'Annunzio University

Operative Vaginal Delivery in Residents and Young Specialists

Evaluation of different learning programs on persistence of skills in operative vaginal delivery

Study Overview

Status

Completed

Detailed Description

Investigators enrolled residents and young specialist randomly exposed to simulation of operative vaginal delivery or a lecture before and after experience on simulator program. The two groups were exposed after 8-12 weeks to a second experience of simulator program due to evaluate the improve, deterioration of skills in operative vaginal delivery.

12-months persistence of skills were evaluated

Study Type

Observational

Enrollment (Actual)

24

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

    • CH
      • Chieti, CH, Italy, 66100
        • University of Chieti

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

25 years to 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

participants were residents in ObGyn or young specialists in ObGyn (less than 5 years)

Description

Inclusion Criteria: residents or young specialists (less than 5 years after ending of residency) -

Exclusion Criteria: medical students before MD

-

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

  • Observational Models: Case-Crossover
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Simulator training before
group exposed directly to simulator training without knowing the topic of obstetric emergency
identify which teaching program has the better retaining of skills
lesson before simulation training
group undergoing formal lecture before the vacuum delivery simulation on mannequin
identify which teaching program has the better retaining of skills

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
improving and retaining skills in two different groups of teaching programs
Time Frame: 12 weeks and 1 year
evaluate video recorded simulations using items and total value during the operative vaginal delivery on manequin
12 weeks and 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
improve skills in obstetric emergencies considering year of formation and teaching programs
Time Frame: 12 weeks and 1 year
Comparison of quality scale per items
12 weeks and 1 year

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)

June 15, 2021

Primary Completion (Actual)

October 30, 2021

Study Completion (Actual)

April 1, 2022

Study Registration Dates

First Submitted

March 26, 2022

First Submitted That Met QC Criteria

October 30, 2022

First Posted (Actual)

November 4, 2022

Study Record Updates

Last Update Posted (Actual)

November 4, 2022

Last Update Submitted That Met QC Criteria

October 30, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

Simulation in EASC

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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