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Improving Adherence to VAP Prevention Protocols in ICU Patients A Quality Improvement Study

Effect Of An Adherence Enhancement Program Related To Evidence Based Ventilator Associated Pneumonia (VAP) Prevention Protocols On Early Recognition Of Complications And Clinical Outcomes Among Patients Admitted In Medical Intensive Care Unit Of A Teaching Hospital. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110854
Enrollment
280
Registered
2026-05-21
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: J159- Unspecified bacterial pneumonia

Interventions

Intervention1: Educational Training Programme to healthcare professionals: giving educational training on CDC VAP Bundles
Hand Hygiene protocols
and each components of VAP Bundles Control Intervention1: NOT APPLICABLE: Single arm study with no comparator group

Sponsors

Ms Yagya Koirala
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion Criteria (Patients) Adult patients more than 18 years Receiving invasive mechanical ventilation Admitted to MICU during the study period Inclusion Criteria (Health Care Professionals) Health Professionals working in the Department during the study period and consenting to participate

Exclusion criteria

Exclusion criteria: Exclusion Criteria (Patients) Outside hospital intubation Transfer from another ICU within the same hospital Withdrawal of life support within 24 hours of ICU admission Intubated and extubated within 2 days of admission ICU readmissions & confirmed brain death per Institutional criteria Exclusion Criteria (Health Care Professionals) Health Professionals on Long Term leave during the study period

Design outcomes

Primary

MeasureTime frame
Incidence of Ventilator-Associated Pneumonia (VAP) among mechanically ventilated patients using CDC diagnostic criteriaTimepoint: Baseline (retrospective data from past 12-18 months) and then daily during prospective phase from intubation until extubation or ICU discharge, up to a maximum of 28 days.

Secondary

MeasureTime frame
Adherence rate to evidence-based VAP prevention bundle among ICU nursesTimepoint: Baseline and weekly during intervention period;Early recognition of VAP-related complicationsTimepoint: Daily assessment during ICU stay;Nurses knowledge scores regarding VAP prevention protocolsTimepoint: Pre-intervention and post-intervention

Countries

India

Contacts

Public ContactYagya Koirala

MGM New Bombay Collage of Nursing , Kamothe Navi Mumbai

koiralayagya92492@gmail.com9958926066

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026