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NCT05979701 Clinical Trial

Simulation for the Retention of Skills in the Management of Obstetric Hemorrhages

Postpartum Hemorrhage Clinical Trial

— SimHPP  

Official title:
Use of Simulation Training Versus Theoretical Learning for the Retention of Knowledge and Skills in the Management of Postpartum Hemorrhage: A Multicenter, Comparative Study in Eastern DRCongo.

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05979701
Other study ID # 001
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 15, 2023
Est. completion date May 15, 2024

Study information
Verified date June 2023
Source Université Evangélique enAfrique
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the retention of knowledge and skills after theory+simulation training versus theoretical training alone in postpartum haemorrhage immediately, 3 months and 6 months after training in South Kivu, in the east of the Democratic Republic of Congo.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 30
Est. completion date May 15, 2024
Est. primary completion date January 15, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Work in one of the selected maternity units - Have two years' experience - Be either a gynaecologist, obstetrician, general practitioner, midwife, nurse, anaesthetist or laboratory technician. Exclusion Criteria: -

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Simulation training
The intervention will consist of training participants through simulation in addition to theoretical training. The simulation will cover 3 themes, including diagnosis of haemorrhage, communication between healthcare providers, management of post-partum haemorrhage and transfusion monitoring.

Locations
Country Name City State
n/a

Sponsors (2)
Lead Sponsor Collaborator
Université Evangélique enAfrique University Hospital, Angers

Outcome
Type Measure Description Time frame Safety issue
Primary Score obtained before training and immediatly after training Difference of mean score obtained before training, immediatly after training using validate qestionnaire Before and immediatly after training
Primary Score obtained before training and 3 months after training Difference of mean score obtained before training and 3 months after training using validated questionnaire 3 months after training
Primary Score obtained before training and 6 months after training Difference of mean score obtained before training and 6 months after training using validated questionnaire 6 months after training
Secondary OSCE (Objective Structural Clinical Exam) Score Difference of OSCE mean score obtained before training and 6 months Immediatly and 6 months after training
See also
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Completed NCT05429580 - Prophylactic Tranexamic Acid Use After Vaginal Delivery N/A
Terminated NCT03064152 - Rotational Thromboelastometry for the Transfusion Management of Postpartum Hemorrhage After Vaginal or Cesarean Delivery N/A
Recruiting NCT05382403 - Novel Vacuum-Induced Hemorrhage Control for Postpartum Hemorrhage N/A
Not yet recruiting NCT02853552 - Misoprostol as First Aid Measure to Address Excessive Postpartum Bleeding Phase 4
Completed NCT02805426 - Effectiveness of Tranexamic Acid When Used as an Adjunct to Misoprostol for the Treatment of Postpartum Hemorrhage Phase 4
Completed NCT03344302 - Oxytocin Administration During Cesarean Section Phase 4