The Effect of SCIM on Neonatal Resuscitation

Pregnancy Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02082964
• Other study ID #: training
• Status: Completed
• Phase: N/A
• First received: February 13, 2014
• Last updated: March 8, 2014
• Start date: December 2011
• Est. completion date: March 2012

Study information

• Verified date: March 2014
• Source: Mashhad University of Medical Sciences
• Contact: n/a
• Is FDA regulated: No
• Health authority: Iran: Ethics Committee
• Study type: Interventional

Clinical Trial 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..

Recruitment information / eligibility

• Status: Completed
• Enrollment: 48
• Est. completion date: March 2012
• Est. primary completion date: March 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 22 Years to 32 Years

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

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor)

Related Conditions & MeSH terms

• Pregnancy

Intervention

Other:
• SCIM
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
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

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Mashhad University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	education	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.	3 months	No