The study of factors affecting prevention & management of bedsore in ICU patients with nurse education based care in two tertiary care teaching hospitals in coastal Karnataka.
Not Applicable
- Conditions
- Health Condition 1: L89- Pressure ulcer
- Registration Number
- CTRI/2024/03/064872
- Lead Sponsor
- Mr Prasannakumara
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients who have been admitted to ICU expected to stay more than 24 hours
Nurses who work in the selected intensive care units (ICU), With at least six months of ICU experience
Exclusion Criteria
Patients ICU observation patients admitted for less than 24 hours. Patients diagnosed with any stage of PIs in the first 24 hours of admission to the ICU.
Nurses who are not willing to participate in the study and Nursing trainee or nursing students.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie pressure ulcer formation in critically ill ICU patients?
How does a nurse-led HAPI prevention bundle compare to standard-of-care protocols in reducing pressure injuries?
Are there specific biomarkers that identify ICU patients at highest risk for hospital-acquired pressure ulcers?
What adverse events are commonly associated with pressure ulcer prevention strategies in intensive care settings?
What combination approaches show promise in preventing pressure injuries alongside nurse education interventions?