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Clinical Trial Summary

The objective of the study is to determine if Obstetric Life Support Program (OBLS) has an effect on the confidence and skills knowledge in participants.


Clinical Trial Description

Enrolled participants with healthcare experience will be randomized to intervention with an electronic curriculum and instructor-led course or placebo first and then will be crossed over to receive the intervention. Participants will undergo assessments pre and post intervention, as well as repeat assessments after three washout periods separated by six months each. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05355519
Study type Interventional
Source UConn Health
Contact Laurie Kavanagh, MPH
Phone 206-399-0531
Email kavanagh@uchc.edu
Status Recruiting
Phase N/A
Start date October 21, 2021
Completion date July 2024

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