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Glove-based Care in the NICU to Prevent Late Onset Sepsis (GloveCare)

Primary Purpose

Sepsis Newborn, Infection

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Glove based care
Standard of Care - Hand Hygiene
Sponsored by
Hamilton Health Sciences Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Sepsis Newborn focused on measuring Late onset sepsis, glove based care, NICU, Non sterile gloves, infection control

Eligibility Criteria

1 Minute - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Infants admitted to the NICU at participating sites for > 2 days until discharge

Exclusion Criteria:

  • Babies requiring contact precautions due to other reasons (as glove based care would be occurring)

Sites / Locations

  • McMaster Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Glove based care

Standard care

Arm Description

The intervention is the use of non-sterile gloves, after standard hand hygiene for all routine patient care needs.

The control group will provide standard care, that is, hand hygiene before all patient, bed, and intravenous catheter contact.

Outcomes

Primary Outcome Measures

Late onset sepsis events
The anticipated incidence of LOS is 10% of patients based on Canadian Neonatal Network retrospective data. Infection is defined as blood stream, urinary tract, or cerebrospinal fluid infection based on 1 or more positive cultures with a bacterial or fungal pathogen (2 cultures required for Coagulase negative staphylococcus), at least 2 compatible signs and symptoms (including temperature instability, hemodynamic changes, respiratory distress and increased inflammatory markers), and the need for antimicrobial treatment.

Secondary Outcome Measures

Time to first infection
Time from admission to NICU to first infection in days
Length of stay
Time from admission to discharge (days)
All-cause mortality
Number of deaths (number of patients who die during study)
Proportion colonized by antibiotic resistant organisms at any point during their NICU stay
Proportion of infants who become colonized with antibiotic resistant organisms during surveillance screening as part of routine care (number of patients)

Full Information

First Posted
February 1, 2017
Last Updated
August 8, 2018
Sponsor
Hamilton Health Sciences Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT03078335
Brief Title
Glove-based Care in the NICU to Prevent Late Onset Sepsis
Acronym
GloveCare
Official Title
Non-Sterile Glove Based Care to Prevent Late Onset Sepsis in The NICU - Cluster Crossover Randomized Controlled Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
June 5, 2017 (Actual)
Primary Completion Date
June 1, 2018 (Actual)
Study Completion Date
June 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hamilton Health Sciences Corporation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Babies that get an infection after 3 days of age while in the Neonatal Intensive Care Unit is not related to their delivery but to the hospital environment. Preventing these infections results in shorter hospital stays for babies, less risk of long term health problems and less health care resources required to care for them. Hand washing alone doesn't remove all bacteria from the hands of healthcare workers, and studies have shown that infections in adults and children admitted to hospital decrease if health care providers use clean, non- sterile gloves when treating patients. The main focus of this study will be to find out if using gloves when caring for newborns in the NICU is better than washing hands alone. McMaster Children's Hospital and The Hospital for Sick Children will be the pilot sites to participate in a future larger study where some infants will be cared for using non-sterile gloves, and others will be cared for using the standard hand washing method.
Detailed Description
Late onset sepsis (LOS) is defined as infection occurring after 72 hours of life in neonates admitted to the Neonatal Intensive Care Unit (NICU). LOS can lead to severe complications including death, major neurologic sequelae, and contribute to increased length of stay and costs of care. These hospital acquired infections are largely preventable. Hand washing prior to any patient care is considered the cornerstone of prevention and is the standard of care in the NICU. Adherence to hand washing however is difficult to achieve, with estimates of compliance among health care workers ranging from 30% to 60%. Observational studies in at-risk critically ill children suggest a reduction in hospital acquired infections and central line associated bloodstream infections with glove based care in addition to hand hygiene. One small single-centre randomized trial of glove based care versus hand hygiene alone to assess LOS rates in extremely premature infants in the NICU showed a reduction in gram positive infections and central line infections with glove-based care. We propose to test the effect of glove based care in an adequately powered, rigorously designed and conducted, cluster randomized controlled trial (RCT) after completing a feasibility pilot study. This pilot study will include all babies in the NICU being randomized to 6 months of glove based care or standard of care, and then the following 6 months will be the opposite arm. All health care provider contact with the infant will require gloves in the intervention arm, but families of infants admitted to the NICU will not be required to wear gloves. The main outcome measured will be the number of episodes of infections in the blood, urinary tract, and cerebrospinal fluid comparing the glove intervention arm against the control arm. Invasive infections are an important challenge for infants admitted to the NICU and reducing this risk can improve the quality and quantity of neonatal survivors from the NICU.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sepsis Newborn, Infection
Keywords
Late onset sepsis, glove based care, NICU, Non sterile gloves, infection control

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
This pilot study is a single centre NICU based cluster-randomized crossover trial, with 2 crossover periods each lasting 6 months, and a 2-week washout period in between.
Masking
Outcomes Assessor
Masking Description
The final adjudication of events will be completed by two of the investigators blinded to study arm, based on a summary report of each event after completion of the pilot.
Allocation
Randomized
Enrollment
786 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Glove based care
Arm Type
Experimental
Arm Description
The intervention is the use of non-sterile gloves, after standard hand hygiene for all routine patient care needs.
Arm Title
Standard care
Arm Type
Active Comparator
Arm Description
The control group will provide standard care, that is, hand hygiene before all patient, bed, and intravenous catheter contact.
Intervention Type
Other
Intervention Name(s)
Glove based care
Intervention Description
Described in Experimental Arm: Glove based care
Intervention Type
Other
Intervention Name(s)
Standard of Care - Hand Hygiene
Intervention Description
Hand Hygiene - hand washing with soap and water, or alcohol based hand rub
Primary Outcome Measure Information:
Title
Late onset sepsis events
Description
The anticipated incidence of LOS is 10% of patients based on Canadian Neonatal Network retrospective data. Infection is defined as blood stream, urinary tract, or cerebrospinal fluid infection based on 1 or more positive cultures with a bacterial or fungal pathogen (2 cultures required for Coagulase negative staphylococcus), at least 2 compatible signs and symptoms (including temperature instability, hemodynamic changes, respiratory distress and increased inflammatory markers), and the need for antimicrobial treatment.
Time Frame
Weeks of admission to the NICU. Infection must occur at >72 hours of age, throughout neonatal admissions for the 6 month duration of each study arm
Secondary Outcome Measure Information:
Title
Time to first infection
Description
Time from admission to NICU to first infection in days
Time Frame
Time from admission to NICU to discharge (days to months) throughout neonatal admissions for the 6 month duration of each study arm]
Title
Length of stay
Description
Time from admission to discharge (days)
Time Frame
Time from admission to discharge (days to months) throughout neonatal admissions for the 6 month duration of each study arm]
Title
All-cause mortality
Description
Number of deaths (number of patients who die during study)
Time Frame
Duration of study (1 year)
Title
Proportion colonized by antibiotic resistant organisms at any point during their NICU stay
Description
Proportion of infants who become colonized with antibiotic resistant organisms during surveillance screening as part of routine care (number of patients)
Time Frame
Weeks of admission to NICU, for the duration of study (1 year)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Minute
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Infants admitted to the NICU at participating sites for > 2 days until discharge Exclusion Criteria: Babies requiring contact precautions due to other reasons (as glove based care would be occurring)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sarah Khan, MD, FRCPC
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
McMaster Children's Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N3Z5
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
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Glove-based Care in the NICU to Prevent Late Onset Sepsis

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