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The Effect of SCIM on Neonatal Resuscitation

M

Mashhad University of Medical Sciences

Status

Completed

Conditions

Pregnancy

Treatments

Other: SCIM
Other: video

Study type

Interventional

Funder types

Other

Identifiers

NCT02082964
training

Details and patient eligibility

About

In this randomized controlled trial 48 students were randomly allocated in three groups SCIM, Video training (VT) and control group(no training). They had a workshops based on NRP and lasted 6 hours for each group. Before and after the workshops and one month later all students participated in a 7 station OSCE..

Enrollment

48 patients

Sex

All

Ages

22 to 32 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

healthy, without any history of severe stress in the past 6 months prior to the study. Accepts Healthy Volunteers

Exclusion Criteria:severe stress

Trial design

48 participants in 2 patient groups

SCIM
Experimental group
Description:
after lecture students had rotation in 6 groups through 6 stations, trained and practiced under supervision of 6 instructors about Initial Steps, Positive Pressure Ventilation(PPV), Intubation, Chest Compressions, Medications and management of advanced resuscitation
Treatment:
Other: SCIM
video
Experimental group
Description:
video about neonatal resuscitation presented then students repeated the video. Workshops was based on NRP and lasted 6 hours for each group the contentof the video was based on the educational content of the course.
Treatment:
Other: video

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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