- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05605626
Learning Skills in Young Specialists and Residents in Operative Vaginal Delivery Using Simulator Models
Operative Vaginal Delivery in Residents and Young Specialists
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
CH
-
Chieti, CH, Italy, 66100
- University of Chieti
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria: residents or young specialists (less than 5 years after ending of residency) -
Exclusion Criteria: medical students before MD
-
Study Plan
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
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- ObGynEASC001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Delivery Complication
-
Rambam Health Care CampusRecruitingCesarean Delivery Affecting Fetus | Delivery ComplicationIsrael
-
Alzahraa Ismail Ragheb GodaUnknownDelivery ,Complications,Maternal | Delivery,Complication,FetalEgypt
-
Central Hospital, Nancy, FranceNot yet recruitingDelivery Complication
-
The Reading Hospital and Medical CenterRecruitingPregnancy Related | Cesarean Delivery Affecting Fetus | Delivery ComplicationUnited States
-
Ariel UniversityCompletedPregnancy Related | Delivery ComplicationIsrael
-
Oslo University HospitalVestre Viken Hospital Trust; Helse Stavanger HF; Haukeland University Hospital; Sorlandet Hospital HF and other collaboratorsCompletedDelivery Complication | Induced; Birth | Indications for Care in Pregnancy; Labor; and DeliveryNorway
-
University Hospital, CaenRecruitingPregnancy Related | Delivery Complication | Labor LongFrance
-
The George Washington University Biostatistics...Eunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsRecruitingObstetrical Complications | Cesarean Delivery | Labor and Delivery ComplicationUnited States
-
OASIS Diagnostics S.A.CompletedObstetric Complication | Delivery Complication | Obstetric Anal Sphincter InjuryPoland
-
OASIS Diagnostics S.A.National Center for Research and Development, PolandCompletedObstetric Complication | Delivery Complication | Obstetric Anal Sphincter InjurySpain, Czechia, Poland, Slovakia
Clinical Trials on the better retaining of skills
-
G. d'Annunzio UniversityEnrolling by invitationForceps Delivery Affecting Fetus or Newborn | Ventouse Extraction;Liveborn | Birth; ForcedItaly
-
McMaster UniversityHealth CanadaRecruitingCommunication | Palliative Care | Education of Primary Care CliniciansCanada
-
Lokman Hekim UniversityCompletedHealth Knowledge, Attitudes, Practice | SexualityTurkey (Türkiye)
-
Karamanoğlu Mehmetbey UniversityCompletedSexual Behavior | Climactericum | Sexuality EducationTurkey (Türkiye)
-
Boston University Charles River CampusNational Institute of Mental Health (NIMH)CompletedSchizophrenia | Schizoaffective Disorder | Bipolar Disorder | Major Depression | Chronic Mental DisorderUnited States
-
Kutahya Health Sciences UniversityGazi UniversityCompletedHysterectomy | Sexual Function | Sexual Health | PLISSIT Model | Sexual Health Quality of LifeTurkey (Türkiye)
-
Capogna GiorgioCompleted
-
University of WashingtonNational Institute of Mental Health (NIMH)CompletedDementia | Alzheimer DiseaseUnited States
-
Northwestern UniversityWithdrawnCoronary Artery Disease | Coronary Artery Bypass | Surgery | Hemorrhage Postoperative | Patient Care Team