EBP in NursingEvidence-Based Practice for Ventilator-Associated Pneumonia in ICU Patients
This is a pre- and post- quasi-experimental study.
+ Education with EBP
Healthcare-Associated Pneumonia+9
+ Cross Infection
+ Iatrogenic Disease
Services Research Study
Summary
Study start date: October 10, 2024
Actual date on which the first participant was enrolled.This study focuses on improving the quality of care in intensive care units (ICUs) by reducing infections like ventilator-associated pneumonia (VAP), which are common in these settings. It aims to implement evidence-based practices (EBP) to lower infection rates and improve patient outcomes by changing how nurses work through specialized training. The research targets ICU patients and seeks to enhance their care by using new technologies and training nurses to adhere to EBP, ultimately aiming to reduce infections and improve survival rates. The study involves three phases, starting with observing current ICU practices and infection rates to establish baseline data. In the second phase, nurses receive one month of EBP training, followed by two months of observing changes in their practice. This training includes using advanced equipment like suction devices and special brushes for patient care. The final phase evaluates the effectiveness of these changes by comparing infection rates before and after the training. The study seeks to determine if these interventions lead to better patient outcomes, such as reduced infections and shorter ICU stays.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.272 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Services Research Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study 2: Inclusion criteria: * Who will be a registered nurse in Bangladesh. * Who will agree to participate in this study and the EBP training. Exclusion criteria: * Who will not directly involve patient care in ICU. Study 3: Inclusion Criteria: * Irrespective of age and sex, participant must be 18 years old. * Legal guardian of a patient consents to participation in the study * Intubated patients after admission. Exclusion Criteria: * Who stays less than 2 days at the GICU. * Who dies or is extubated within 2 days after admitted in the GICU. * ICU readmission.
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 2 locations
Hiroshima University
Hiroshima, Japan