Learning Skills in Shoulder Dystocia Delivery Using Simulator Models

January 30, 2024 updated by: Claudio Celentano, G. d'Annunzio University

Shoulder Dystocia Delivery and Learning Skills on Mannequin

Learning skills on shoulder dystocia on doctor and midwife

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Active learning on mannequin for shoulder dystocia deliveries on doctor and midwife using role play approach and its effect on clinical practice using questionnaires after first training and 6 months training

Study Type

Observational

Enrollment (Actual)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Italy
    • Italia
      • Pescara, Italia, Italy, 65100
        • Claudio Celentano

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

Sampling Method

Non-Probability Sample

Study Population

residents specialists midwies

Description

Inclusion Criteria:

  • residents and specialists in obstetrics and gynecology
  • midwives

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
time 0 and 6 months answers
questionnaire answers after first training and after re-training on shoulder dystocia model
Other: modification of clinical approach in clinical practice at time 0
evaluation of modification in clinical approach after training
Other Names:
  • questionnaire for evaluation of modification in clinical approach
Other: modification of clinical approach in clinical practice at 6 months
evaluation of modification in clinical approach after retraining
Other Names:
  • questionnaire for evaluation of modification in clinical approach

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Management of SD
Time Frame: 6 months
incidence of personal management of SD and fetal and neonatal outcomes in previous experiences and in successive
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Clinical approach in labor ward in identification and management of SD (with previous SD)
Time Frame: 6 months
modification in approach if previous experience occurred
6 months
Clinical approach in labor ward in identification and management of SD (without previous SD)
Time Frame: 6 months
modification in approach without previous experience
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

G. d'Annunzio University

Collaborators

Claudio Crescini, MD Humanitas Milan Italy
Federico Prefumo, Istituto Giannina Gaslini
Claudio Meloni, University of Florence

Investigators

  • Principal Investigator: Claudio Celentano, MD, EASC

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)

January 1, 2023

Primary Completion (Actual)

December 30, 2023

Study Completion (Actual)

December 31, 2023

Study Registration Dates

First Submitted

June 8, 2023

First Submitted That Met QC Criteria

June 25, 2023

First Posted (Actual)

June 27, 2023

Study Record Updates

Last Update Posted (Estimated)

February 1, 2024

Last Update Submitted That Met QC Criteria

January 30, 2024

Last Verified

July 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • ObGynEASC002

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

recruiting residents, specialists and midwives in University of Chieti and Pescara Hospital

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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