Recruiting

EBP in NursingEvidence-Based Practice for Ventilator-Associated Pneumonia in ICU Patients

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What is being tested

This is a pre- and post- quasi-experimental study.

+ Education with EBP

Behavioral
Who is being recruted

Healthcare-Associated Pneumonia+9

+ Cross Infection

+ Iatrogenic Disease

Over 18 Years
See all eligibility criteria
How is the trial designed

Services Research Study

Interventional
Study Start: October 2024
See protocol details

Summary

Principal SponsorHiroshima University
Study ContactNahida Akhter, Ph. D FellowMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleEffect of Implementing Evidence-based Practice and Nurse's Behavior Change on Quality of Care in Intensive Care Unit: Focus on Ventilator Associated Pneumonia in a Tertiary Hospital in Bangladesh
NCT06624540
Principal SponsorHiroshima University
Study ContactNahida Akhter, Ph. D FellowMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

272 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Services Research Study

These studies look at how healthcare is delivered, managed, and organized. They aim to improve care quality, patient experience, and access to treatment.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

Healthcare-Associated PneumoniaCross InfectionIatrogenic DiseaseInfectionsLung DiseasesPathologic ProcessesPneumoniaRespiratory Tract DiseasesRespiratory Tract InfectionsPathological Conditions, Signs and SymptomsDisease AttributesPneumonia, Ventilator-Associated

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.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Nurses: All nurses who work at GICU of DMCH Patients: all patients who will admit at the assigned GICU during the study period of DMCH

Study 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

Recruiting

Dhaka Medical College Hospital

Dhaka, BangladeshOpen Dhaka Medical College Hospital in Google Maps
Recruiting soon

Hiroshima University

Hiroshima, Japan
Recruiting
2 Study Centers