A randomised controlled trial of the use of a respiratory function monitor to teachneonatal mask ventilation to healthcare professionals in a simulation setting

Not Applicable

Recruiting

• Conditions: eonatal resuscitation; Neonatal resuscitation; Reproductive Health and Childbirth - Complications of newborn; Public Health - Health service research

• Registration Number: ACTRN12616000542493
• Lead Sponsor: Centre for Research Excellence and Newborn Research Centre, Royal Women's Hospital Melbourne

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-04-27
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 382

Inclusion Criteria

Each participant must meet the following criteria to be enrolled in the study:
1. Over 18 years of age
2. One of the following healthcare professionals: Doctors from any specialty, midwives, nurses, physiotherapists, occupational therapists, paramedics, or a medical, nursing or midwifery student
3. Attending the Victorian Neonatal Resuscitation training program. Attendees of both the first response program (3 hours’ duration) and the Advanced Resuscitation (7 hours’ duration) are eligible.

Exclusion Criteria

1. Unable or unwilling to provide written informed consent
2. Attendees who are not one of the healthcare professional groups or student groups listed above will not be included

Study & Design

• Study Type: Interventional
• Study Design: Not specified