Viewing Study NCT04692753



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Last Modification Date: 2024-10-26 @ 1:53 PM
Study NCT ID: NCT04692753
Status: UNKNOWN
Last Update Posted: 2021-01-05
First Post: 2020-12-29

Brief Title: Effect of Education of Health Care Workers on the Maintenance of Venous Access Devices
Sponsor: Post Graduate Institute of Medical Education and Research Chandigarh
Organization: Post Graduate Institute of Medical Education and Research Chandigarh

Study Overview

Official Title: Effect of Intensive Training and Education of Health Care Workers on the Maintenance of Venous Access Devices in Critically Ill Patients at a Tertiary Care Academic Hospital
Status: UNKNOWN
Status Verified Date: 2021-01
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: In intensive care units ICU critically ill patients require various venous access devices for fluid resuscitation drug therapy or renal replacement therapy RRT These include peripheral intravenous catheters PIVC specialized venous ports like central venous catheters CVCs and hemodialysis ports The investigators plan to do this pre- and post-intervention study to know the effect of intensive training and education of HCW doctors and nurses on the condition of venous access devices in critically ill patients
Detailed Description: Phase 1 pre-intervention The first twelve weeks will include 25 random visits to main ICU and point observations of all venous access devices under parameters like condition of dressing connectors and documentation This will also include the comparison of incidence of CLABSI in the pre and post intervention phase

Phase 2 intervention Next four weeks will be an intervention in the form of intensive training and education of the HCW doctors and nurses The intensive training will be in the form of an online presentation in which the investigators would have videos on care and maintenance of venous access devices and the importance of documentation of days of insertion and change of dressing

Phase 3 post-intervention Another twelve weeks post-intervention again 25 random visits will be done to collect point observations about the same parameters of venous access devices and documentation as done in phase 1

Statistical analysis Each of these point observation parameters for central or peripheral venous access will be finally categorized as appropriateinappropriate as per guidelines for best practice

The compiled data from pre and post intervention phases would be compared All the categorical parameters appropriateinappropriate will be compared using chi-square test All the quantitative parameters eg incidence of CLABSI will be compared using a paired t-test

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None