Your session is about to expire
← Back to Search
Neonatal Resuscitation Booster Training for Newborn Breathing Issues
N/A
Waitlist Available
Led By Priya Sharma, MD
Research Sponsored by University of Texas Southwestern Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 month and 9 month assessments
Awards & highlights
Study Summary
This trial will compare the percentage of mask leak in medical providers who receive positive pressure ventilation skills training with a booster training six months later to those who only receive the initial training.
Who is the study for?
This trial is for healthcare providers who have a Neonatal Resuscitation Program card from University of Texas Southwestern, Stanford University, or St. Louis University. It's not open to beginners who haven't completed an NRP course because they need to be familiar with the resuscitation equipment.Check my eligibility
What is being tested?
The study is testing if booster training using a special cart improves skills in neonatal resuscitation six months after initial training. Providers are randomly chosen to either receive this extra training or not, and their performance will be compared.See study design
What are the potential side effects?
Since this trial involves educational booster training rather than medical treatments, there are no direct side effects like you'd expect with drugs or surgeries.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 month and 9 month assessments
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 month and 9 month assessments
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Mask Leak
Secondary outcome measures
Peak Inspiratory Pressure score
Positive End Expiratory Pressure score
Positive Pressure Ventilation composite score
+2 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Booster Training GroupExperimental Treatment1 Intervention
Participants randomized to intervention will undergo booster training sessions with the RQI cart (including audiovisual feedback) at 3, 6 and 9 months post instructor-led training session. Following each of these booster sessions, the participants will undergo 1 minute assessments, without feedback.
Group II: No Booster Training GroupActive Control1 Intervention
Participants randomized to the control group will undergo 1 minute assessments, without feedback, at 6 and 9 months. Participants will not be able to access the RQI cart outside of their assessment.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Booster Training with the Neonatal Resuscitation Quality Improvement Cart
2022
N/A
~160
Find a Location
Who is running the clinical trial?
University of Texas Southwestern Medical CenterLead Sponsor
1,044 Previous Clinical Trials
1,053,419 Total Patients Enrolled
American Academy of PediatricsOTHER
40 Previous Clinical Trials
1,016,313 Total Patients Enrolled
Priya Sharma, MDPrincipal InvestigatorUniversity of Texas
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- People who have never taken a Neonatal Resuscitation Program course will be excluded because they may not be familiar with the equipment needed to help a baby breathe without being shown by an instructor in person.
Research Study Groups:
This trial has the following groups:- Group 1: Booster Training Group
- Group 2: No Booster Training Group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
How many subjects are involved in this research endeavor?
"Indeed, the information hosted on clinicaltrials.gov confirms that this research is actively recruiting participants. This study was initially posted on April 18th 2022 and had its most recent update occur on the same day. 150 patients will be accepted at a single medical centre for participation in this trial."
Answered by AI
Are there any vacancies available in this medical research program?
"Clinicaltrials.gov indicates that recruitment for this medical experiment is underway, with the initial posting having been made on April 18th 2022 and the last amendment occurring likewise."
Answered by AI
Recent research and studies
Other Trials to Consider
Popular Categories
Share this study with friends
Copy Link
Messenger