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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00375037
Other study ID # 05-277
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2007
Est. completion date July 2008

Study information

Verified date October 2018
Source McMaster University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This randomized controlled trial will evaluate the effect of a multifaceted intervention including performance feedback on adherence to hand hygiene among healthcare workers. A key component of the study is to demonstrate whether improved adherence to hand hygiene leads to a reduction in rates of infection.


Description:

A cluster randomized controlled trial of the intervention will be conducted where hospital units (wards) in three hospitals will be allocated to either the intervention or usual practise. We will stratify by hospital site in order to minimize confounding by hospital-level factors. The unit of allocation, intervention, and analysis will be at the level of the hospital unit. Thirty hospital units will be randomized to either the intervention or comparison arm. We will compare adherence to hand hygiene, MRSA rates, and other outcomes between the two study arms.


Recruitment information / eligibility

Status Completed
Enrollment 1500
Est. completion date July 2008
Est. primary completion date July 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility A. Study units Inclusion: Medical and subspecialty units, surgical units, critical care units

Exclusion: pediatric units, neonatal intensive care units

B. Healthcare workers

Inclusion: any hospital staff with direct patient care who are affiliated with a single unit (includes registered nurses, nursing assistants, environmental aides, allied health professionals (occupational, physical, and respiratory therapists), and some physicians

C. Patients Clinical outcomes will be measured in patients on study units.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
feedback

Education

Other:
usual care


Locations

Country Name City State
Canada Hamilton General Hospital Hamilton Ontario
Canada Henderson Hospital Hamilton Ontario
Canada McMaster University Medical Centre Hamilton Ontario

Sponsors (2)

Lead Sponsor Collaborator
Hamilton Health Sciences Corporation The Physicians' Services Incorporated Foundation

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of MRSA 12 months
Primary Adherence to hand hygiene 12 months
Secondary Incidence of multi-resistant bacteria other than MRSA 12 months
Secondary Catheter-related blood stream infections 12 months
Secondary Clostridium difficile related diarrhea 12 months
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