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Effect of Educational Program About Preventive Care Bundle for Prevention of Ventilator Associated Pneumonia Among Newborns

Effect of Educational Program for Nurses About Preventive Care Bundle for Prevention of Ventilator Associated Pneumonia Among Newborns

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06066489
Enrollment
137
Registered
2023-10-04
Start date
2023-10-31
Completion date
2024-03-31
Last updated
2023-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ventilator Associated Pneumonia

Keywords

newborn

Brief summary

This study is designed to investigate the effect of educational program for nurses about preventive care bundle for prevention of ventilator associated pneumonia among newborns.

Detailed description

Neonatal ventilator associated pneumonia (VAP) is a common nosocomial infection and a frequent reason for empirical antibiotic therapy in NICUs. Ventilator associated pneumonia (VAP) is defined as a nosocomial lower airway infection in intubated patients with onset after 48 h or more of invasive mechanical ventilation.Prevention of VAP has been primarily achieved by the bundle approach; this involves the simultaneous application of several preventive strategies for all patients.In Egypt and other developing countries, reports on the success of VAP intervention strategies, particularly among neonates, are scarce. So, it is important to conduct educational programs for nurses about VAP to decrease its incidence.

Interventions

OTHEReducational program about VAP

An educational program about VAP that includes VAP bundle from CDC as core measures , equipment related measures and general measures.

Sponsors

Damanhour University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

A prospective, quasi-experimental, pre- and post-study with a one month baseline period; one month intervention period and three months post-intervention period

Eligibility

Sex/Gender
ALL
Age
3 Days to 30 Days
Healthy volunteers
No

Inclusion criteria

* Gestational age ≥34 weeks * Intubated newborns and those expected to receive mechanical ventilation for more than 48 hours.

Exclusion criteria

* Newborns with diagnosis of pneumonia at the time of admission. * Newborns developed pneumonia in the first 48 hours of mechanical ventilation. * Newborns subjected to reintubation. * Immunosuppressed newborns.

Design outcomes

Primary

MeasureTime frameDescription
prevalence of VAP among newborns ( the number of newborns diagnosed with VAP during the study periodbefore intervention as baseline ( Day 1), immediately after the intervention, 3 months later after interventionprevalence of VAP will be compared before application of educational program for nurses about preventive care bundle for prevention of VAP and after the program ( immediately, 3 months later) by using centers for disease control and prevention PNU-1

Secondary

MeasureTime frameDescription
nurses practices about prevention of ventilator associated pneumonia after implementing the training program will be compared by their practices before the intervention using Observational Checklistbefore intervention as baseline(Day 1), immediately after the intervention, 3 months later after interventionnurses practices will be assessed before and after the intervention immediately and 3 months later using Observational Checklist about their practices and then results compared before and after the intervention by mean percent score

Contacts

Primary ContactBasma Ibrahim Khamis, Doctoral
basmaaibrahim@yahoo.com01221880646

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026