Pregnancy
Conditions
Brief summary
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..
Interventions
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
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
Sponsors
Study design
Eligibility
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 \-
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| education | 3 months | after educational course for each group (SCIM and Video), students' competency in neonatal resuscitation would be evaluated through an OSCE in each group. the competency between group (before and after education) and in each group would be comapared before and after education. |
Countries
Iran