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Effect of Education of Health Care Workers on the Maintenance of Venous Access Devices

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
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04692753
Enrollment
400
Registered
2021-01-05
Start date
2020-10-01
Completion date
2021-04-30
Last updated
2021-01-05

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

Conditions

Vascular Access Devices

Keywords

intensive care unit, health care workers, central venous catheters

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 appropriate/inappropriate as per guidelines for best practice. The compiled data from pre and post intervention phases would be compared. All the categorical parameters (appropriate/inappropriate) will be compared using chi-square test. All the quantitative parameters (e.g. incidence of CLABSI) will be compared using a paired t-test

Interventions

Training and education of health care workers in the form of online seminars and bed side demonstration of care and maintenance of venous access devices

Sponsors

Post Graduate Institute of Medical Education and Research, Chandigarh
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* All patients admitted to Main ICU

Exclusion criteria

* Patients who refuse to give consent

Design outcomes

Primary

MeasureTime frameDescription
To study the effect of intensive training and education of health care workers on care and maintenance of venous access devices in critically ill patientsSeven monthsthe maintenance of venous access devices as evident from multiple point observations regarding condition of site ,dressing, connectors

Secondary

MeasureTime frameDescription
effect of intensive training and education on incidence of CLABSI during pre and post intervention phaseseven monthsincidence of central line associated blood stream infection to be compared between pre and post intervention phase

Other

MeasureTime frameDescription
to study improvement in documentation regarding venous access devicesseven monthseffect of training and education will be studied on improvement in documentation of venous access devices in post intervention phase

Countries

India

Contacts

Primary ContactDr. Rubina Sharma, MBBS
rubinasharma7777@gmail.com08427977607
Backup ContactDr. Neeru Sahni, MD
neerunalin@yahoo.com09872646106

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026