MedTrace Logo

Role of Simulators in Improving Obstetric Vaginal Examination Skills

NCT05190692 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 39

Last updated 2022-08-02

No results posted yet for this study

Summary

A prospective study will be performed at the Department of Obstetrics and Gynecology at (VESSALKA unit),at El kasr Al\_Ainy hospital, cairo university. Sample of house officers without obstetric experience in vaginal examination that will begin their clinical rotation in the department will be eligible for inclusion in the study. All patients involved in the study must not be high risk pregnancy nor have any indication of cesarean section and they will be examined by house officers in the first stage of labor. House officers and patients will provide verbal informed consent for participation in the study .all house officers assigned in the obstetric and gynecology department for their clinical rotation at the time of study will receive about a (30-mins) standardized course summarizing how to perform an obstetric vaginal examination . All house officers assigned in the study will be trained on vaginal examination simulators in about (15) training sessions and giving them a score to each one about their performing results on simulators.

Conditions

  • Labour

Interventions

DEVICE

Use simulators in Obstetrics vaginal examination

Two simulators will be used in the study: (1st ) : PROMPT Flex Birthing Simulator Advanced - Light (PRODUCT NO. 80106).UK, 2020 . 2nd): PROMPT Flex Cervical Dilatation \& Effacement Module -Light (PRODUCT NO. 80102),Uk,2020. Both will be used to perform obstetric vaginal examination before examination of patients

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-03-01
Primary Completion
2022-07-10
Completion
2022-07-10

Countries

  • Egypt

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05190692 on ClinicalTrials.gov